Laboratory and field evaluation of spinosad against the gypsy moth,Lymantria dispar

The toxicity of the naturally derived insecticide spinosad was tested against the gypsy moth, Lymantria dispar. Bioassays using red oak leaf disks, treated with spinosad in a Potter spray tower, yielded an LC₅₀ value of 0.0015 µg AI cm⁻² (3‐day exposure; 13‐day evaluation; 2nd instar larvae). Applied to foliage to run‐off in the laboratory (potted red oak seedlings) and the field (4 m‐tall birch trees), spinosad effectively controlled 2nd instar larvae at concentrations ranging from 3 to 50 mg litre⁻¹. Toxicity in the laboratory, and efficacy and persistence in the field, were comparable to those achieved with the insecticide permethrin. Laboratory studies supported field observations that control was achieved in part by knockdown due to paralysis. In addition, laboratory results demonstrated that crawling contact activity may play an important role in field efficacy; 50% of treated larvae were paralyzed 16 h after a 2‐min crawling exposure to glass coated with a 4 mg litre⁻¹ spinosad solution. © 2000 Society of Chemical Industry     

Beet armyworm (Spodoptera exigua) resistance to spinosad

Susceptibility to spinosad (Success®/Tracer®) of beet armyworm (Spodoptera exigua) from the southern USA and Southeast Asia was determined through exposure of second‐ and third‐instar larvae to dipped cotton leaves. LC₅₀ estimates of susceptibility of second‐ and third‐instar larvae of field populations ranged from 0.279 to 6.14 and 0.589 to 14.0 mg spinosad litre⁻¹, respectively. A Thailand population was 22‐ and 24‐fold less susceptible than the six other US field populations evaluated, and 85‐ and 58‐fold less susceptible than a reference laboratory population, respectively. From these results, we initiated experiments to test the hypothesis that the Thailand population was resistant to spinosad. F₁ crosses between the resistant Thailand population and a susceptible reference strain yielded individuals that were 22‐fold less sensitive to spinosad than the susceptible parent. This same resistant strain exhibited significantly greater survivorship on plants treated with spinosad in the field. Lastly, selection of an Arizona population resulted in a significant reduction in susceptibility to spinosad, further substantiating the hypothesis of a genetic basis for resistance to spinosad. These findings indicate a vulnerability of this new insecticide to resistance development in beet armyworm and should serve as a warning against excessive use of it. © 2000 Society of Chemical Industry     

Comparative SAR Evaluations of Annonaceous Acetogenins for Pesticidal Activity

The activities of 44 Annonaceous acetogenins, which were originally isolated by monitoring plant fractionations with the brine shrimp lethality test (BST), were evaluated in the yellow fever mosquito larvae microtiter plate (YFM) assay. The results clearly demonstrate that most acetogenins have pesticidal properties. The structure–activity relationships indicate that the compounds bearing adjacent bis-THF (tetrahydrofuran) rings with three hydroxyl groups are the most potent. Bullatacin ( 1 ) and trilobin ( 7 ) gave the best activities against YFM with LC₅₀ values of 0·10 and 0·67 mg litre^-1, respectively. Compounds showing LC₅₀ values below 1·0 mg litre^-1 in this assay are usually considered significant as new lead candidates for pesticidal development. In the BST, the corresponding LC₅₀ values were 1·6×10^-3 ( 1 ) and 9·7×10^-3 ( 7 ) mg litre^-1. This is the first report of pesticidal structure–activity relationships for a series of Annonaceous acetogenins which are known to act, at least in part, as potent inhibitors of mitochondrial NADH: ubiquinone oxidoreductase. © of SCI.     

Fumigant Toxicity of Citruspeel Oils against Adult and Immature Stages of Storage Insect Pests

The biological action of citruspeel oils was shown to depend on a strong fumigant action. Bioassays conducted in air-tight glass chambers showed that all the six citrus oils tested had vapour toxicity towards adults of Callosobruchus maculatus F., Sitophilus zeamais Motsch. and Dermestes maculatus Deg. The 24-h LC₅₀ value of limepeel oil (a typical citrus oil) vapour against C. Maculatus was 7·99 μl litre⁻¹ which made it 1·5 and 1·6 times less toxic against the smaller S. zeamais and the larger D. maculatus adult insects. When immature stages were fumigated, limepeel oil vapour had 24-h LC₅₀ values of 7·8 and 21·5 μl litre⁻¹ against eggs of C. maculatus and D. maculatus respectively, and 9·1, 17·8 and 23·1, 23·9 μl litre⁻¹ against early larvae, pupae of C. maculatus and late larvae, pupae of D. maculatus respectively. X-ray studies showed that fumigated C. maculatus larvae within cowpea grains died immediately without further development. The bioactivities of five other citruspeel oils were similar to that of limepeel oil. Bioassays showed that sorption of citruspeel oil fumes occurred in the presence of grains or strips of dried fish, and that this tended to reduce the amount available for fumigant action outside the materials. The problems presented by sorption may hinder the development of citrus oils into practical fumigants for large-scale treatments of stored commodities.     

Susceptibility pattern and development of resistance in the diamondback moth,Plutella xylostella L,to Bacillus thuringiensis Berl var kurstaki in India

Base‐line susceptibility for six‐day‐old larvae of the diamondback moth, Plutella xylostella, against Bacillus thuringiensis var kurstaki (Biobit^®) was studied by a cabbage leaf disc dip bioassay technique. Diamondback moth from 13 locations in seven different states spread over a distance of about 3000 km longitudinally was used for these studies. Forty‐eight‐hour LC₅₀ values varied from 1.0 to 10.97 mg AI litre⁻¹. Further investigations on the development of resistance under laboratory conditions showed an increase in LC₅₀ from 2.76 (for unselected F₁ generation) to 5.28 mg AI litre⁻¹ (for selected F₉ generation), using a selection concentration of 6.4 mg AI litre⁻¹. This suggested a possibility of the development of resistance under field conditions if there were to be extensive and indiscriminate use of B thuringiensis. These findings are discussed in relation to integrated pest management and the mechanisms of resistance in resistance management tactics. © 2000 Society of Chemical Industry     

DPX-MP062—a potent compound for controlling the Egyptian cotton leafworm Spodoptera littoralis (Boisd.)

The effects of DPX-MP062 [methyl 7-chloro-2,3,4a,5-tetrahydro-2-[methoxycarbonyl(4-trifluoromethoxyphenyl)carbamoyl] indeno[1,2-e][1,3,4] oxadiazine-4a-carboxylate] a broad-spectrum insecticide with a novel mode of action, on the Egyptian cotton leafworm, Spodoptera littoralis, were studied in laboratory experiments. Egg hatch was affected by high concentrations (125 mg AI litre^-1) of DPX-MP062. Larvae that hatched from treated eggs were significantly affected at concentrations of 12·5 mg AI litre^-1 and greater. Larvae were fed castor bean leaves treated with DPX-MP062; 1st-instar larvae were the most susceptible development stage. Pupation and adult formation were determined in assays with 5th-instar larvae. There was strong suppression of adult formation; 65 and 91% at 0·5 and 0·75 mg AI litre^-1, respectively. Highly affected larvae died before pupation; slightly affected ones reached pupation 2–4 days later, were smaller than larvae in the untreated control, and were sometimes unable to develop into normal adults. Comparatively high concentrations (50 and 100 mg AI litre^-1) of the test compound were necessary to affect adults by ingestion, but no effects from contact application could be determined at a concentration of 100 mg AI litre^-1. © 1998 Society of Chemical Industry     

The response of pyriproxyfen-resistant and susceptible Bemisia tabaci Genn (Homoptera: Aleyrodidae) to pyriproxyfen and fenoxycarb alone and in combination with piperonyl butoxide

Pyriproxyfen was effective against susceptible Bemisia tabaci eggs at a LC₅₀ of 0.003 mg litre⁻¹ and against nymphs at 0.02 mg litre⁻¹. In comparison, eggs of a laboratory selected, pyriproxyfen-resistant B tabaci strain, originating in an Israeli greenhouse, exhibited 6500-fold resistance and nymphs exhibited 1100-fold resistance. Eggs and nymphs of a strain from an Israeli sunflower field exhibited 450 and 210-fold resistance in comparison to the susceptible standard. Fenoxycarb was generally less effective than pyriproxyfen against B tabaci eggs and nymphs but was unaffected by pyriproxyfen resistance. Piperonyl butoxide (PB) was antagonistic to pyriproxyfen, and this increased with increasing pyriproxyfen resistance. PB had no effect on the toxicity of fenoxycarb. Collectively, these data imply that the modes of action of pyriproxyfen and fenoxycarb are distinct, despite the structural similarities of these molecules. Possible reasons for the antagonism of PB against pyriproxyfen are discussed. © 1999 Society of Chemical Industry     

Effect of the ecdysone agonists,RH-2485 and tebufenozide,on the southwestern corn borer,Diatraea grandiosella

The effect of the ecdysone agonists RH-2485 (proposed name methoxyfenozide) and tebufenozide (RH-5992), was examined on eggs and larvae of the southwestern corn borer, Diatraea grandiosella Dyar. Both compounds exhibited a concentration-dependent ovicidal activity. More than 95% of eggs died when egg masses were dipped in solutions of 100 or 200 mg liter^-1 of either compound in acetone+distilled water (1+1 by volume). Although some eggs treated with 1 or 10 mg liter^-1 of the compounds hatched, the survival rate was low. Newly hatched larvae were fed for seven days on an artificial diet containing RH-2485 or tebufenozide. The LC₅₀ values were 0·049 mg kg^-1 for RH-2485 and 0·185 mg kg^-1 for tebufenozide, showing that RH-2485 was about four times more active than was tebufenozide. Although increasing the time of exposure to either compound decreased the LC₅₀ value significantly, the relative potency of RH-2485 versus tebufenozide was not changed. Newly ecdysed 4th-instar larvae fed with diets containing 0·125, 0·25 or 0·5 mg kg^-1 RH-2485 or tebufenozide ceased feeding approximately 8 h after exposure, indicating that larvae had prematurely entered a molting cycle. Larvae treated with RH-2485 ecdysed earlier and died more quickly than those treated with tebufenozide. Ingestion of sublethal concentrations of RH-2485 (0·005 and 0·01 mg kg^-1) or tebufenozide (0·03 and 0·06 mg kg^-1) retarded larval growth, and decreased pupal weight and adult emergence. Increasing exposure time to tebufenozide tended to increase the larval mortality, significantly retarded larval growth, and decreased the mean weights of male and female pupae and adult emergence. RH-2485 (0·125 and 0·25 mg kg^-1) and tebufenozide (0·25 and 0·5 mg kg^-1) were lethal to newly hatched larvae, even after diets containing these compounds were held for 20 days at 30°C under long days (16 h light: 8 h dark). Our results suggest that field trials to assess the potential of RH-2485 and tebufenozide to control D. grandiosella are warranted. © 1998 SCI     

Pesticidal properties of parthenin (from Parthenium hysterophorus) and related compounds

Eleven sesquiterpene lactone derivatives of parthenin ( 1 ), obtained from wild feverfew, Parthenium hysterophorus, were prepared by chemical and photochemical transformations. The compounds tested were a pyrazoline adduct ( 2 ) of parthenin, its cyclopropyl ( 3 ) and propenyl ( 4 ) derivatives, anhydroparthenin ( 5 ), a dihydro‐deoxygenated product ( 6 ), a formate ( 7 ) and its corresponding alcohol ( 8 ) and acetate ( 9 ), a rearranged product ( 10 ), lactone ( 11 ) and hemiacetal ( 12 ). All these derivatives, along with parthenin, were tried for their antifeedant action against sixth‐instar larvae of Spodoptera litura, for insecticidal activity against the adults of store grain pest Callosobruchus maculatus, for phytotoxic activity against Cassia tora, and for nematicidal activity against the juvenile stage‐II (J₂) of the root knot nematode Meloidogyne incognita. Antifeedent bioassay revealed that parthenin is moderately antifeedant. Among the derivatives, the saturated lactone ( 11 ) was found to be about 2.25 times more active than parthenin. The pyrazoline adduct ( 2 ) was found to be the most effective as an insecticide, with LC₅₀ values after 24, 48 and 72 h of 96, 43 and 32 mg litre⁻¹, respectively, which are comparable with neem extract. Compound 4 was found to be the most effective inhibitor of germination and seedling growth of C tora, with ID₅₀ values for germination, plumule length and radicle length of 136, 326 and 172 compared with 364, 738 and 427 mg litre⁻¹, respectively, for parthenin. Compound 10 was found to be the most effective in terms of nematicidal activity. The LC₅₀ values for this compound were 273 and 104 mg litre⁻¹, respectively, after 48 and 72 h compared with 862 and 512 mg litre⁻¹ observed for parthenin after 48 and 72 h. © 2001 Society of Chemical Industry     

Residual activity of spinosad applied as a soil drench to tomato seedlings for control of Tuta absoluta

BACKGROUND

Tuta absoluta (Lepidoptera: Gelechiidae) is difficult to control by means of foliar insecticides, partly because of the endophytic feeding behavior of its larvae. The biopesticide spinosad is applied as a foliar spray for control of T. absoluta and has systemic properties when applied as a soil drench to the growing medium of tomato plants. The aims of this study were to determine the: (i) instar-dependent tolerance of larvae to spinosad; (ii) efficacy of spinosad drench application for the control of larvae; (iii) residual period of systemic activity of spinosad in leaves and fruit after drenching; and (iv) effect of spinosad drenching on tomato plant growth parameters.

RESULTS

The estimated LC₅₀ value (Lethal Concentration at which 50% of the larvae died) differed between instars. The LC₅₀ for second-instar larvae (0.41 ppm) to spinosad was significantly lower than that for third- (0.64 ppm) and fourth-instar (0.63 ppm) larvae. The LC₈₀ value (Concentration at which 80% of the larvae died) for fourth-instar larvae (2.48 ppm) was 2.6- and 1.7-fold higher than that for the second- and third-instar larvae, respectively. The spinosad concentration recorded in leaves at 25 days after treatment (DAT; 0.26 μg g⁻¹) was significantly lower than that in leaves sampled at 3, 10 and 15 DAT. High larval mortalities were, however, recorded for the duration of the experiment, which lasted 25 days (equivalent to one T. absoluta generation).

CONCLUSION

Systemic spinosad effectively controlled T. absoluta larvae over a prolonged period. However, drenching this insecticide violates the recommendation of the Insecticide Resistance Action Committee to avoid treating consecutive insect generations with the same mode of action and can therefore result in the evolution of insecticide resistance. © 2023 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.     

Insecticidal activity and mode of action of 2,4‐diaminopyrimidines

Three 2,4‐diaminopyrimidines were tested against several insect species. They were active against lepidopteran pests with LC₅₀ values <3 mg liter⁻¹ for most species tested. They were also active against two‐spotted spider mite, Tetranychus urticae, (LC₅₀ 10–40 mg liter⁻¹). Folinate, but not hypoxanthine or thymidine was found to be an effective rescue agent, requiring a concentration of 100 mg liter⁻¹ diet to rescue half of the intoxicated larvae. The results confirm dihydrofolate reductase to be the site of action for these insecticides and are consistent with the mode of action of folinate rescue in mammals. © 2000 Society of Chemical Industry     

Paradoxical effects of sublethal exposure to the naturally derived insecticide spinosad in the dengue vector mosquito,Aedes aegypti

BACKGROUND: Recent studies have indicated that spinosad, a mixture of two tetracyclic macrolide compounds produced during the fermentation of a soil actinomycete, may be suitable for controlling a number of medically important mosquito species, including the dengue vector, Aedes aegypti L. The authors determined the effects of a 1 h exposure to a 50% lethal concentration (LC₅₀) of spinosad in the larval stage on the wing length, longevity and reproductive capacity of the adult survivors. RESULTS: The LC₅₀ of spinosad for a wild‐caught population of Ae. aegypti from Chiapas, southern Mexico, was estimated to be 0.06 mg AI L^?1 in late third instars. Paradoxically, the female survivors of exposure to this concentration were significantly larger (as determined by wing length) laid more eggs, but were slightly less fertile than control females. This was probably due to elimination of the smaller and more susceptible fraction of mosquito larvae from the experimental population following spinosad treatment. Male survivors, in contrast, were significantly smaller than controls. No significant differences were detected in the adult longevity of treated and control insects of either sex. CONCLUSIONS: The increase in reproductive capacity of spinosad‐treated females did not compensate for mortality in the larval stage and would be unlikely to result in population increase in this mosquito under the conditions that were employed. Sustained‐release formulations would likely assist in minimizing the occurrence of sublethal concentrations of this naturally derived product in mosquito breeding sites. Copyright © 2008 Society of Chemical Industry     

The toxicity of cyromazine to Chironomus zealandicus (chironomidae) and Deleatidium sp. (leptophlebiidae)

The toxicity of cyromazine and a commercial formulation, ‘Vetrazin’®, to Chironomus zealandicus (thummi) Hudson and Deleatidium sp. was investigated. Under acute test conditions, the LC₅₀ values for each species were quite comparable. For C. zealandicus, the value varied according to instar, 100–400 mg litre^?1 for second- and third-instar to 1000–10000 mg litre^?1 for older fourth-instars. For the one size class of Deleatidium tested (c.10 mm long), the value was 300–400 mg litre^?1. High control mortalities of C. zealandicus limit that species' usefulness as an acute bioassay candidate. Under chronic test conditions, cyromazine showed a high toxicity to eggs or early-instar larvae of C. zealandicus. The maximum acceptable toxicant concentration for cyromazine against C. zealandicus was approximately 17.5 μg litre^?1. The possibility of water contamination at this level is discussed. Whole-of-life chronic tests with C. zealandicus indicated that the most susceptible stage was in the egg or soon after larval emergence. These results highlight the dangers of using short-term acute toxicity results to formulate environmental exposure limits for modern pesticides that do not have dysfunction of the nervous system as their mode of action.     

Residual toxicity and sublethal effects of chlorantraniliprole on Plutella xylostella (lepidoptera: plutellidae)

BACKGROUND: The diamondback moth (DBM), Plutella xylostella (L.), is the most important pest of cruciferous vegetables in the world. Chlorantraniliprole is a novel anthranilic diamide insecticide registered for the control of lepidopteran pests. The dose response, residual toxicity and sublethal effects of chlorantraniliprole applied for 48 h at LC₁₀ (0.02 mg L^?1) and LC₂₅ (0.06 mg L^?1) on P. xylostella were investigated. RESULTS: Leaf‐dip bioassays showed that chlorantraniliprole had a high level of toxicity against larvae of P. xylostella, and the 48 h LC₅₀ values were 0.23 and 0.25 mg L^?1 for a susceptible and field strain respectively. Chlorantraniliprole also had a long‐lasting effect when the larvae were exposed to chlorantraniliprole field sprayed on radish seedlings. Sublethal effects of chlorantraniliprole were indicated by reduced pupation, pupal weight and adult emergence rates. There was also an increase in the duration of female preoviposition period, decreased fecundity and egg hatch and decreased survival rates of the offspring. The mean values of the net reproductive rate (R₀), intrinsic rate of increase (r_m), finite rate of increase (λ) were significantly lower in the treatment than in control groups. CONCLUSIONS: These results indicate that chlorantraniliprole is effective against P. xylostella. The sublethal concentrations of chlorantraniliprole may reduce the population growth of P. xylostella by decreasing its survival and reproduction, and by delaying its development. Copyright © 2012 Society of Chemical Industry     

Effect of ABT on the activity and rate of degradation of isoproturon in susceptible and resistant biotypes of Phalaris minor and in wheat

The effect of the monooxygenase inhibitor, 1-aminobenzotriazole (ABT) on isoproturon phytotoxicity and metabolism was studied in resistant (R) and susceptible (S) biotypes of Phalaris minor and in wheat (Triticum aestivum). Addition of ABT (2·5, 5 and 10 mg litre^-1) to isoproturon (0·25, 0·5, 1, 2 and 4 mg litre^-1) in the nutrient solution significantly enhanced the phytotoxicity of isoproturon against the R biotype. Isoproturon at 0·25 mg litre^-1 reduced the dry weight (DW) of the S biotype by 77%, whereas the R biotype required 4·0 mg litre^-1 for similar reduction. Addition of 10 mg litre^-1 of ABT to the 0·25 mg litre^-1 isoproturon caused 71 and 82% reduction in DW of R and S biotypes, respectively. Wheat was more sensitive to the mixture of isoproturon and ABT than the R biotype of P. minor. Reduced concentrations of ABT in the mixture from 10 to 2·5 mg litre^-1 increased the DW of the R biotype more than that of the S biotype. The R biotype metabolised [¹⁴C]isoproturon at a faster rate than the S biotype. ABT (5 mg litre^-1) inhibited the degradation of [¹⁴C]isoproturon in both biotypes of P. minor and in wheat. In the presence of ABT, about half of the applied [¹⁴C]isoproturon remained as parent herbicide in all the three species after two days. The metabolites were similar in the R and S biotypes and wheat as determined by co-chromatography with reference standards and mass spectroscopy (MS). ABT inhibited the appearance of the hydroxy and monomethyl metabolites and their conjugates in all the test plants. These results suggest that the activity of the enzymes responsible for the degradation of isoproturon is greater in the R than in the S biotype of P. minor, resulting in its rapid detoxification. Incorporation of the monooxygenase inhibitor ABT into the nutrient solution greatly inhibited the degradation of [¹⁴C]isoproturon in the R biotype and increased its phytotoxicity. Both hydroxylation and N-dealkylation reactions were found to be sensitive to ABT; inhibition of hydroxylation was greater than that of demethylation. Since ABT could not completely suppress isoproturon degradation, it is possible that more than one monooxygenase is involved. © 1998 SCI     

Correction: Pestic. Sci. 53, 201–208 (1998)

In the paper ‘Proinsecticides effective against insecticide-resistant peach-potato aphid (Myzus persicae (Sulzer)),’ by D. Hedley et al., in Table 3 the units of both columns headed LC₅₀ should be (mg litre⁻¹)     

Synthesis and Evaluation of New Ethyl 2,3- Dihydro-3-oxoisothiazolo[5,4-b]pyridine- 2-alkanoate Derivatives as Potential Herbicides

Several ethyl 2,3-dihydro-3-oxoisothiazolo[5,4-b]pyridine-2-alkanoate derivatives were synthesized as herbicides. Only 5-methyl derivatives inhibited both hypocotyl and root growth in the lettuce (Lactuca sativa L.) seedling test at 100 mg litre^-1. Only ethyl propionate and valerate derivatives showed significant inhibition at 0·1 mg litre^-1, whereas ethyl acetate or butyrate derivatives were inactive. Contrary to unoxidized derivatives, the inhibitory effect of 1-oxide and 1,1-dioxide derivatives was strongly dependent on concentration; ethyl 2,3-dihydro-5-methyl-3-oxoisothiazolo[5,4-b]pyridine-2-propionate 1,1-dioxide inhibited 100% of germination at 100 mg litre^-1 and 45% of lettuce seedling growth at 0·1 mg litre^-1. Quantitative structure–inhibition of growth relationship analysis carried out by adaptive least-squares (ALS) method gave a good correlation with small and hydrophobic 5-substituents as well as with odd carbon-chain ethyl alkanoates in position 2. Active compounds did not show auxin-like activity from 0·1 to 100 mg litre^-1. © 1997 SCI.     

Effect of Hydrogen Cyanide and Carbonyl Sulphide on the Germination and Plumule Vigour of Wheat

Several factors which may influence the germination of wheat fumigated with hydrogen cyanide or carbonyl sulphide were investigated. Dosages of hydrogen cyanide ranged from 10 mg litre⁻¹ for 24-h exposure up to 150 mg litre⁻¹ for 96-h exposure. Dosages of carbonyl sulphide ranged from 25 mg litre⁻¹ for 24-h exposure up to 500 mg litre⁻¹ for 72-h exposure. The experiments were conducted on wheat of 11·4, 13·8 and 15·7% moisture content. The higher levels of these fumigants exceed those needed for control of insects in wheat. Germination was not diminished and may have been slightly enhanced with hydrogen cyanide, but was diminished by high levels of carbonyl sulphide in the drier wheat. The plumule length was reduced following all dosages of hydrogen cyanide, but only after high dosages of carbonyl sulphide, especially on the driest wheat. It is concluded that hydrogen cyanide and carbonyl sulphide could be used to control insects in wheat without affecting seed viability, provided that concentrations are carefully controlled.     

Post-harvest disinfestation of lightbrown apple moth,Epiphyas postvittana Walker (Lepidoptera: Tortricidae), with an alkane

Lightbrown apple moth (LBAM), Epiphyas postvittana Walker was used as a test insect to evaluate a post-harvest oil, C15 Ampol CPD, and a spray oil, C23 Ampol DC-Tron NR, both applied as dips. CPD was much more efficacious than C23 DC-Tron NR against exposed third-instar larvae. Higher oil concentrations were required to penetrate and kill larvae sheltering under the calyx of oranges. LBAM eggs were more susceptible to CPD oil than larval stages. LBAM larvae dipped in sub-lethal doses of oil continued to develop, but the fecundity of both males and females was reduced. DC-Tron had a significant effect on egglaying. CPD and C23 DC-Tron NR affected the fertility of eggs laid. CPD oil sprayed at 50 ml litre⁻¹ on adult LBAM moths reduced their fertility. Factors contributing to the higher efficacy of CPD and its potential use as a post-harvest treatment are discussed. © 1999 Society of Chemical Industry     

Toxicity,persistence and efficacy of indoxacarb and two other insecticides on Plutella xylostella (Lepidoptera: Plutellidae) immatures in cabbage

Toxicities of indoxacarb on eggs and 5-day-old larvae of diamondback moth, Plutella xylostella L., on cabbage and those of field-aged leaf residues on 5-day-old larvae were determined in the laboratory. The persistence and efficacies of indoxacarb and two other newer insecticides (spinosad and emamectin benzoate) to P. xylostella were tested under field conditions. Results from laboratory bioassays indicate that indoxacarb was highly toxic to P. xylostella larvae through food ingestion, with LC₅₀ and LC₉₀ values of 24.1 and 90.1 mg AI l ^{- 1}, respectively. However, indoxacarb had no significant effects on eggs and larvae through direct contact compared with water control. The toxicity of field-aged leaf residues of indoxacarb (0-, 3-, 5-, 7-, 10-, 14-, 17- and 21-day-old residues) declined slowly and gradually under the field conditions in South Texas. Almost all larvae died on day 5 after feeding on the leaves with 0 - 14-day residue, and the mortalities were as high as 94 and 78% for the 14- and 17-day-old leaf residues. With one application, indoxacarb suppressed P. xylostella larvae below the economic threshold for 14 - 21 days. Two field trials showed that indoxacarb at 0.05 - 0.07 kg AI ha ^{- 1} was effective against P. xylostella, providing marketable cabbage with three applications per season. In addition, indoxacarb was as effective as spinosad, and significantly more effective than emamectin benzoate.