Accumulation pattern and insecticidal effect of aldicarb in cotton following soil treatment for the control of the tobacco whitefly (Bemisia tabaci)

The accumulation pattern of the pesticide aldicarb [2-methyl-2-(methylthio) propionaldehyde O-(methylcarbamoyl)-oxime] and of its sulfoxide and sulfone metabolites was studied in field-grown cotton, following soil treatments at various intervals from planting. Control of the tobacco whitefly(Bemisia tabaci) was determined and correlated with the concentration of aldicarb and of its metabolites in cotton leaves. The main constituent found in the leaves was aldicarb sulfoxide, which reached its maximum concentration there at about 22 days post-treatment. Late application of the insecticide (mid-July) resulted in higher concentrations toward the end of the growing season and so gave improved control of the pest. Results are presented for residues in young and mature leaves and in the seeds.     

Distribution of the radioactivity in sugar beet plants treated with [14C]aldicarb

Sugar beet plants were grown in the field, after in-furrow application of [¹⁴C]aldicarb (3 kg of aldicarb ha^?1) at planting. Some plants (the growing plants) were harvested 99 days after sowing and the rest (the ripe plants) 196 days after sowing. The percentages of the weights of [¹⁴C]aldicarb equivalents (the total aldicarb plus aldicarb sulphoxide and sulphone, plus all the other metabolites of [¹⁴C]aldicarb which contain ¹⁴C, expressed as aldicarb equivalents) incorporated into the beet plants, relative to the weight applied to the soil, were 2.8 and 1.8, respectively for the growing and ripe plants. The concentrations of [¹⁴C]aldicarb equivalents (mg kg^?1 fresh weight) in the growing and ripe plants, respectively were: blades of the external leaves, 3.16 and 0.93; blades of the internal leaves, 0.63 and 0.68; petioles of the external leaves, 0.51 and 0.26; petioles of the internal leaves, 0.15 and 0.05; crowns, 0.14 and 0.15; roots, 0.16 and 0.13. The proportions of the extractable aldicarb plus aldicarb sulphoxide and aldicarb sulphone determined by gas-liquid chromatography (expressed as aldicarb equivalents) relative to [¹⁴C]aldicarb equivalents, in the external and internal leaf blades of the growing beets, were 56 and 60%, respectively; these values declined to 25 and 19%, respectively in the ripe plants. The proportion was 21 % or less in all other parts of the growing and ripe plants.     

Susceptibility of Aphelinus certus to foliar‐applied insecticides currently or potentially registered for soybean aphid control

BACKGROUND: Soybean aphid, a serious economic pest of soybean in North America, is currently managed by applying non‐selective foliar insecticides during outbreaks according to decision thresholds and crop maturity. Natural enemies, such as the parasitoid Aphelinus certus Yasnosh, potentially play an important role in suppressing soybean aphid. Using selective insecticides that preserve A. certus may enhance the biological control service they provide and thus prevent or reduce the severity of soybean aphid outbreaks. The toxicity of five insecticides (λ‐cyhalothrin, dimethoate, flonicamid, mineral oil, spirotetramat) and the biopesticide Beauveria bassiana to A. certus was assessed. RESULTS: The LD₅₀ values of λ‐cyhalothrin and dimethoate were similar; however, the hazard quotient of dimethoate was greater than that of λ‐cyhalothrin. In a screening bioassay, the descending order of toxicity for the recommended rates 48 h after application was dimethoate > λ‐cyhalothrin > flonicamid > mineral oil > Beauveria bassiana > spirotetramat. CONCLUSIONS: Overall, λ‐cyhalothrin and dimethoate were both harmful to A. certus. The other insecticides tested were harmless to A. certus and are potential candidates for inclusion in soybean aphid management programs. Copyright © 2011 Society of Chemical Industry     

Control of Aphis fabae on broad beans (Vicia faba) by the systemic action of gamma-bhc,thionazin and aldicarb

The in-row application of aldicarb granules at 2 lb active ingredient (a.i.)/acre (2·24 kg/ha) at sowing gave complete control of Aphis fabae Scop. on broad beans (Vicia faba L. cv. Seville) up to 7 days before harvest and resulted in a three-fold increase in yield compared with a similar thionazin treatment. Bean plants grown from seeds which were soaked in a gamma-BHC solution at 20 ppm for 24 h prior to planting were protected from this aphid for most of the growing season almost as effectively as with the thionazin treatment. A thin-layer chromatography method was developed for the determination in plants and soil of aldicarb and its two major toxic metabolites, the sulphoxide and sulphone. Gas-liquid chromatography was used to monitor the declining levels of gamma-BHC and thionazin, and simultaneous bioassays were made with Aphis fabae on excised leaf discs from the crop. Analysis of the bean seeds and pods at harvest 90 days after sowing indicated no detectable gamma-BHC, less than 0·01 ppm of thionazin and approximately 0·09 ppm total residue of aldicarb sulphone and sulphoxide. Approximately 22% and 13% of the applied aldicarb, in the form of sulphone and sulphoxide but not the parent compound, remained in the top 6 in (152 mm) of soil at the end of 2 and 4 months respectively. Toxicity studies with Aphis fabae, Acyrthosiphon pisum Harris, and Megoura viciae Buck showed an increasing sensitivity in that order to gamma-BHC at 1 ppm in bean plants. Acute toxicity investigations with feeding Aphis fabae indicated an increasing sensitivity in the order of gamma-BHC < aldicarb sulphone < aldicarb sulphoxide < thionazin < aldicarb. Despite the high acute toxicity of thionazin to Aphis fabae it gave low protection against aphids, possibly owing to its relatively short persistence in both plants and soil when compared with aldicarb.     

The use of insecticides to control potato leafroll virus in seed-potato crops on the Golan Heights

Experiments were carried out in the laboratory and in the field for 3 years, in an attempt to protect seed-potato crops on the Golan Heights from potato leafroll virus (PLRV) by means of insecticides. The best results with spray compounds were obtained with pirimicarb (Pirimor), methamidophos (Tamaron) and ethiofencarb (Croneton); the commonly used and recommended aphicides oxydemetonmethyl (Metasystox R) and endosulfan (Thionex) were less efficient. The best results with granular insecticides were obtained with aldicarb (Temik) and ethiofencarb, while phorate (Thimet), carbofuran (CURATERR) and oxamyl (Vydate) were much less efficient. Dimethoate (Rogor) gave good results in the laboratory test, but was less efficient in the field trials. The flight of aphids in the Golan Heights is characterized by two close peaks: in May-June, and from late July to September. Potatoes are planted in early May, and hence crops need to be protected throughout almost the entire season. Weekly sprays using, in turn, pirimicarb, methamidophos and ethiofencarb, reduced PLRV incidence in seed-potato plots in 1977 from 33.4% (in the untreated controls) to 2.8%, thus ensuring their certification. A single pre-emergence treatment with aldicarb reduced PLRV incidence from 12.6% (in the untreated controls) to 1.8%; however, the best results (no infection) were obtained by the addition of weekly sprays, starting at the end of July, to a pre-emergence treatment with a granular insecticide.     

The distribution of aldicarb and its metabolites between Lumbricus terrestris,water and soil

Aldicarb is taken up by earthworms from aqueous solution to give concentrations in the worms comparable to that in the external aqueous solutions. Uptake from waterlogged soils is similar, but much less aldicarb is taken up from drier soils. Aldicarb sulphoxide [2-methyl-2-(methylsulphinylpropionaldehyde O-methylcar-bamoyloxime], aldoxycarb and oxamyl are poorly taken up, giving concentrations in the worm of about 5% of the external aqueous concentration. In worms, aldicarb is rapidly converted to the sulphoxide which has a half-life in worms of 19 h at 15°C, and 50 h at 5°C.     

Foliar residues and toxicity to green leafhoppers of the systemic insecticides aldicarb and its isomer butocarboxim in young peach and plum groves

The isomeric systemic carbamoyloximes aldicarb and butocarboxim were applied at two dose rates to the soil in young peach and plum groves to control the green leafhopper Asymmetrasca decedens Paoli. The effectiveness of the treatments was assessed indirectly by measuring the growth rate of shoots, and by determining the adult mortality of leafhoppers that were collected in the field and kept for 24 h on detached peach leaves in the laboratory. Residues of the insecticides and of their sulphoxide and sulphone metabolites, in the leaves of the peach trees, were determined 18 and 31 days after treatment. Only the sulphoxides and sulphones were found; the sulphoxides amounted to 70–80% of the toxic residues after 18 days, and to 50–70% after 31 days. At an identical rate of application, the leaves from aldicarb-treated peach trees contained higher concentrations of the toxic metabolites and were more toxic to leafhoppers than those of trees treated with butocarboxim.     

Influence of block and cell size,growing medium and insecticide dose on the behaviour and uptake of phorate by lettuce and uptake of carbofuran and chlorfenvinphos by calabrese

Phorate residues in peat blocks and lettuce were determined following incorporation of the insecticide into different block and ‘Speedling’ cell sizes. Between-block variability was influenced little by block size. Phorate oxidation was most extensive in the largest blocks containing the smallest dose. Total residue concentrations in the lettuce declined from the time of planting to harvest, although accumulation of insecticide continued and was related more to dose than to block or cell size. Residues in the lettuce at harvest exceeded the proposed maximum limit of 0.2 mg kg^?1 in some treatments. Residues at planting comprised mainly the parent sulphoxide and sulphone, but by harvest, the oxygen analogue sulphoxide and sulphone predominated. Lettuce weight was not influenced by dose but was related directly to block size. Carbofuran and chlorfenvinphos residues were determined in calabrese sown into two sizes of blocks. At planting time, carbofuran residue concentrations were 100 times greater than those of chlorfenvinphos but residues of both insecticides in the mature heads were < 0.01 mg kg^?1. Seedling weights in both sowings declined with increasing concentrations of the insecticides. It was concluded that manipulations of block size and the dose of insecticide need to be evaluated for individual insecticide/crop combinations to exploit the technique fully.     

Comparative ester hydrolysis of carbaryl and ethiofencarb in four mammalian species

The comparative ester hydrolysis and selective toxicity of carbamate insecticides were studied in four mammalian species. Hydrolysis rates of carbaryl and ethiofencarb (Croneton) were examined in the rat, mouse, guinea pig, and gerbil. Respiratory ¹⁴CO₂ resulting from the hydrolysis of orally administered [carbonyl-¹⁴C]carbamates (0.2 mg/kg) was taken as measure of in vivo hydrolytic capabilities. Ester hydrolysis was found to be greater for ethiofencarb than for carbaryl in all species tested, although the relative order of hydrolysis among species was the same with both compounds. After 24 hr, gerbils had hydrolyzed 91% of the ethiofencarb and 65% of the carbaryl. Guinea pigs hydrolyzed somewhat less of the compounds, 65 and 58%, but considerably more than rats and mice, about 40 and 25%. Comparing hydrolysis capabilities to acute toxicity data revealed that those species exhibiting the greatest hydrolysis were equally or more susceptible to carbamate poisoning than those having lesser hydrolytic capabilities. While ester hydrolysis destroys the anticholinesterase activity of carbamates, it is clear from these findings that factors other than hydrolysis are largely responsible for the variation in toxicity of the carbamates to different mammalian species.     

拟除虫菊酯类杀虫剂在烟叶烘烤过程中的消解动态与最终残留

采用气相色谱-质谱联用技术,测定了良好农业规范(GAP)条件下3种常用拟除虫菊酯类杀虫剂高效氯氟氰菊酯、高效氯氰菊酯及溴氰菊酯在山东、四川、云南、辽宁和江西5地烟叶中的消解动态及最终残留。样品经乙腈提取,SPE-PSA柱净化,气-质联用、选择离子监测模式(GC-MS/SIM)下测定,外标法定量。结果表明:在0.01 ~1 mg/kg添加水平下,3种农药在鲜烟叶和干烟叶中的平均回收率分别在82.9% ~ 110.9%和85.2%~108.3%之间,相对标准偏差(RSD)分别为1.7% ~4.4%和2.3% ~5.7%;3种农药在鲜烟叶和干烟叶中的定量限(LOQ)均为0.01mg/kg;方法的准确度和精密度均符合农药残留检测要求。烘烤过程中残留农药消解明显,高效氯氟氰菊酯、高效氯氰菊酯和溴氰菊酯的消解率分别高达78%、89%和91%。高效氯氟氰菊酯、高效氯氰菊酯和溴氰菊酯乳油分别按有效成分450~675 g/hm2、600~900 g/hm2及450~675 g/hm2于烟叶采 烤初期喷雾施药2次,距末次施药后14d,干烟叶中3种农药的残留量分别为0.022~ 0.50、0.14~0.82和0.046~0.21 mg/kg,均低于国际烟草合作研究中心(CORESTA)提出的指导性农药残留限量标准(GRL)值(0.5、1和1mg/kg),因此建议其安全间隔期可定为14d。     

Residue analysis of butocarboxim and aldicarb applied in a drip-irrigated peach grove by the HPLC post-column fluorogenic labeling technique

The new high-performance liquid chromatography (HPLC) post-column fluorogenic labeling technique was used for the analysis of residues of butocarboxim, aldicarb and their sulfoxide and sulfone metabolites in peach leaves and fruits. In order to simplify the procedure, the different metabolites were separated by column chromatography during the cleanup process and the residues were determined by HPLC employing an aqueous methanol solvent in the isocratic mode. The limit of detection for the two insecticides was 0.1 μg/g in the leaves and 0.02 μg/g in the fruit. Aldicarb (10% granular formulation) and butocarboxim (50% E.C. diluted 1:5 with water) were applied to the soil in a drip-irrigated peach grove, by placement under one dripper on one side of each tree. The insecticides were taken up by the tree and distributed almost equally on both sides of the tree. The concentration of the insecticides was somewhat lower in the younger leaves. Residue levels of 0.4 to 0.9 μg/g were detected in the fruits at harvest, 10 and 18 days after the last treatment. Based on the results from the field experiment it was concluded that one of the advantages of drip irrigation was that it enabled adequate control of the green leafhopper (Asymmetrasca decedens) throughout the summer with relatively low dosages of systemic insecticides.     

一些农药对温室白粉虱的毒力及其抗药性测定

用11种农药对温室自粉虱(Trialeurodes vaporariorum Westw.)进行了室内毒力测定。结果表明:拟除虫菊酯类杀虫剂、灭螨猛对温室白粉虱各虫态毒力均高,并且随虫龄的增加,白粉虱的抗药性增强。稻丰散、乐果、氧化乐果对温室白粉虱若虫毒力尚可,但对其它虫态效果差。马拉硫磷、二嗪农、敌敌畏、洗衣粉除对一龄若虫有一定效果外,对其它虫态毒力极低。北京地区温室白粉虱对某些药剂已出现明显的抗药性。     

Synergistic and antagonistic effects of atrazine on the toxicity of organophosphorodithioate and organophosphorothioate insecticides to Chironomus tentans (Diptera: Chironomidae)

The acute toxicities of two organophosphorodithioate (dimethoate and disulfoton) and two organophosphorothioate (omethoate and demeton-S-methyl) insecticides were evaluated individually and in binary combination with the herbicide atrazine using fourth-instar larvae of the aquatic midge, Chironomus tentans. Atrazine alone up to 1000 μg/L did not show significant toxicity to the midges in a 48-h bioassay. However, atrazine concentrations as low as 1 μg/L in combination with dimethoate at EC₂₅ (concentration to affect 25% of tested midges), 100 μg/L in combination with disulfoton (EC₂₅), and 10 μg/L in combination with demeton-S-methyl (EC₂₅) significantly enhanced the toxicity of each organophosphate insecticide. In contrast, atrazine concentrations of 10 μg/L and above in combination with omethoate (EC₂₅) significantly decreased the toxicity of the insecticide. Biochemical analysis indicated that increased toxicity of dimethoate, disulfoton, and demeton-S-methyl in binary combination with atrazine correlated to the increased inhibition of acetylcholinesterase. Furthermore, cytochrome P450-dependent O-deethylation activity in the midges exposed to atrazine at 1000 μg/L was 1.5-fold higher than that in the control midges. Thus, atrazine appeared to induce cytochrome P450 monooxygenases in the midges. Elevated cytochrome P450 monooxygenase activity may increase the toxicities of dimethoate, disulfoton, and demeton-S-methyl by enhancing the oxidative activation of dimethoate into omethoate, and disulfoton and demeton-S-methyl into their sulfoxide analogs with increased anticholinesterase activity. In contrast, atrazine reduced the toxicity of omethoate possibly by enhancing the oxidative metabolic detoxification since omethoate does not require oxidative activation.     

Rate, placement and timing of aldicarb applications to control Asian citrus psyllid, Diaphorina citri Kuwayama (Hemiptera: Psyllidae), in oranges

BACKGROUND: The Asian citrus psyllid (ACP), Diaphorina citri Kuwayama (Hemiptera: Psyllidae), is a cosmopolitan insect pest of citrus and vectors the bacterium Candidatus Liberibacter asiaticus, a suspected causal organism of citrus greening or ‘huanglongbing’ disease. Aldicarb 150 g kg^?1 GR (Temik^® 15 G) was evaluated at three rates, two placements and three timings for ACP control in orange trees. RESULTS: Application of aldicarb at 5.6, 2.8 and 1.4 kg AI ha^?1 in March 2006 reduced adults by 58–66%, 45–46% and 25–37% respectively compared with untreated controls in two separate trials. No difference was observed in placement (one versus two sides of the tree) or tree size (8 years old versus 12 years old). Application at 5.6 kg ha^?1 in January 2007 reduced adults by 86% and shoot infestation by 77% in spring, and was generally better than the November and especially February applications. Even more striking results were evident on adults caged on treated plants for 25 days in March. Spiders and ladybeetles were equally abundant in treated and untreated trees. CONCLUSION: Aldicarb application at 5.6 kg ha^?1 to the bed side of mature citrus trees 2–3 months before spring growth can suppress ACP through spring without a direct effect on principal psyllid natural enemies. Copyright © 2008 Society of Chemical Industry     

A biochemical mechanism of resistance to pirimicarb in two glasshouse clones of Aphis gossypii

The susceptibility of three clones of Aphis gossypii Glover to 15 insecticides was established by bioassay. A high level of resistance towards pirimicarb was confirmed for a clone from Holland (Dutch R) and a clone from Japan (Jap R), while the susceptible clone (S) was killed by very low doses of the insecticide. However, only limited cross-resistance was shown towards other carbamates and organophosphates, and no marked resistance to the pyrethroids tested. The acetylcholinesterase (AChE) of both resistant clones hydrolysed acetyl-choline faster than that of susceptible aphids, with greatest enzyme activity shown by the Dutch R clone. Inter-clone differences in these rates were consistent with differences in catalytic centre activities. Inhibition (I₅₀) of AChE by pirimicarb was approximately 900-fold higher for the resistant clones than for the S clone. First-order kinetics revealed that resistance to pirimicarb in Dutch R and Jap R involved a modified AChE which had a reduced (approximately 350-fold) affinity (K_d) for pirimicarb. The marked change in AChE affinity for pirimicarb was not repeated with the other carbamates tested, ethiofencarb and aldicarb. It was considered that the resistant aphids would not require mechanisms in addition to insensitive AChE in order to show the high level of resistance to pirimicarb shown in the bioassay.     

Response of susceptible and resistant peach-potato aphids Myzus persicae (Sulz.) to insecticides in leaf-dip bioassays

The response of susceptible (S), moderately resistant (R₁) and strongly resistant (R₂) peach-potato aphids, Myzus persicae (Sulz.) to organophosphorus, carbamate and pyrethroid insecticides was tested by a leaf-dip bioassay. The aphids were placed on potato leaves (dipped in insecticide solutions 1–2 or 24 h before infestation) and their mortality examined 48 h later. R₁ aphids were virtually susceptible to most of the carbamates, demephion and acephate, but were slightly to moderately resistant (2.1–9.4 times) to permethrin, cypermethrin and (S)-α-cyano-3-phenoxybenzyl (1R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate (I), (NRDC 161), to 5,6,7,8-tetrahydro-2-methylquinolin-4-yl dimethylcarbamate (II), (Hoechst 25 682) and demeton-S-methyl. R₂ aphids resisted more strongly or very strongly (between 65 and 1280 times) the pyrethroids, demeton-S-methyl (×94), II (×83) and demephion (×9), and were slightly to moderately (2–5 times) resistant to acephate, pirimicarb, ethiofencarb and 2-(dimethylcarbamoyloxyimino)-3-methoxyimino-N,N- dimethylbutyramide (III), (DPX 3853). Both resistant strains were susceptible to nitrilacarb [4,4-dimethyl-5-(methylcarbamoyloxyimino)pentanenitrile] complex (1:1) with zinc chloride (IV), (AC 85 258). The implications of these results in terms of practical aphid control are discussed.     

Factors affecting the sequential acquisition by Danish houseflies (musca domestica L.) of resistance to organophosphorus insecticides

The prolonged use of dimethoate, introduced into Denmark to control houseflies (Musca domestica L.) that had become resistant to parathion and diazinon, resulted ultimately in dimethoate resistance. Selection with dimethoate led to the disappearance of the hydrolytic phosphatase, a major mechanism of resistance to parathion and diazinon, and its replacement by the acetylcholinesterase AChER with somewhat decreased sensitivity to inhibition by organophosphorus (OP) insecticides. The hydrolytic phosphatase probably disappeared because low substrate turn-over made it ineffective against dimethoxon (O, O-dimethyl S-methylcarbamoylmethyl phosphorothioate, also known as omethoate). which accumulates at higher concentrations than paraoxon (diethyl4-nitrophenyl phosphate) in the haemolymph. Dimethoate selected AChER preferentially because it improved the chances of houseflies surviving against the relatively poor AChE inhibitor dimethoxon, whereas its relatively small insensitivity to OP insecticides, unimportant against good inhibitors such as paraoxon, prevented its selection by parathion.     

The role of ferrous ions in the rapid degradation of oxamyl,methomyl and aldicarb in anaerobic soils

The carbamoyloxime pesticides methomyl, oxamyl and aldicarb, together with the oxidation products of aldicarb, are known to break down much more rapidly in certain anaerobic subsoils than in the aerobic topsoils from the same site. Ferrous ions have now been shown to be involved in this reaction. Oxamyl was degraded in aqueous solutions at 30°C containing 250 μg ml^?1 Fe²⁺ with a half-life of about 10 h, independent of pH in the range of 5.65–7.66; the observed products of this reaction were N,N-dimethyl-l-cyanoformamide and methanethiol. These same products, rather than the oximino hydrolysis product observed from degradation in aerobic soils, were rapidly and quantitatively formed from oxamyl in suspensions of anaerobic reduced subsoils (Fe²⁺ concentration 27–41 μg ml^?1 soil water), but oxamyl was rather stable in water-saturated Vredepeel subsoil (Fe²⁺ concentration 0.65 μg ml^?1) in which the redox potential was much higher. Methomyl behaved similarly. The rates of reaction in the suspensions of anaerobic subsoils were greater than expected from the concentrations of Fe²⁺ in the soil water, but most of the Fe²⁺ present in soil was bound to the soil particles by cation exchange and this bound Fe²⁺ may have participated. Breakdown of aldicarb was accelerated both in solutions of Fe²⁺ and in the suspensions of anaerobic reduced subsoils, though the rate enhancement was less than observed with methomyl and oxamyl; 2-methyl-2-methylthiopropionitrile and 2-methyl-2-methylthiopropionaldehyde were the observed products from aldicarb in anaerobic soil but only the former was produced in Fe²⁺ solutions; the corresponding nitriles and aldehydes were also yielded by aldicarb sulphoxide and aldicarb sulphone in the anaerobic, reduced subsoils.     

Sublethal effects of nine insecticides on Drosophila suzukii and its major pupal parasitoid Trichopria drosophilae

Background

Although the pupal parasitoid Trichopria drosophilae is used in conservative and augmentative biocontrol of Drosophila suzukii infestations, current pest management strategies mostly rely on multiple insecticide applications. In this context, the aim of the study was to investigate the baseline toxicity of nine insecticides on D. suzukii larvae and their multiple sublethal effects (LC₁₀) on immature stages of the pest feeding on contaminated diet and T. drosophilae developing within the intoxicated host.

Results

Chlorpyriphos and azadirachtin showed the lowest and the highest LC₁₀, the values of which were 9.78 × 10¹³ and 1.46 × 10³ times lower than their recommended label field rate, respectively. Among tested insecticides, imidacloprid, malathion and dimethoate were the only treatments that did not affect the juvenile development time of D. suzukii, while spinosad and the organophosphates chlorpyriphos and dimethoate did not influence fly pupal size. No sublethal effects were recorded on T. drosophilae degree of infestation (DI) and juvenile development time. On the contrary, cyazypyr and dimethoate negatively affected the success of parasitism (SP) and the number of progeny of the pupal parasitoid, in association with malathion for the first parameter and spinosad for the fertility. Compared to the untreated control, more female progeny emerged following azadirachtin exposure, while dimethoate caused the opposite effect. Imidacloprid, lambda-cyhalothrin and spinetoram decreased hind tibia length of emerged parasitoids.

Conclusion

This study provides new insights on the (eco)toxicological profile of nine insecticides and new information needed to support the deployment of T. drosophilae in the field within the sustainable management techniques against D. suzukii. © 2023 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.     

The metabolism of [14C]aldicarb in the leaves of sugar beet plants

Sugar beet plants were grown in the field, after in-furrow application of [¹⁴C]aldicarb (3 kg of aldicarb ha^?1) at planting. The ripe sugar beet plants were harvested, and the blades and petioles of the leaves were analysed separately. In the whole leaves, 15% of the ¹⁴C (all the percentages of ¹⁴C are relative to the total ¹⁴C incorporated into the whole leaves) was insoluble in ethanol+ water (1+1 by volume), 31% was organo-soluble (and thus unconjugated in the leaves), and 54% was water-soluble (mainly conjugated to plant constituents). The weights and concentrations (as aldicarb equivalents) of various identified metabolites of aldicarb, incorporated into the leaves, were determined; no aldicarb, as such, was detected.