Susceptibility of the predatory stinkbug <Emphasis Type="Italic">Picromerus bidens</Emphasis> to selected insecticides

The Palaearctic stinkbug Picromerus bidens L. (Heteroptera: Pentatomidae) has been considered as a potential biocontrol agent of several defoliator pests in various agricultural and forest ecosystems. It may therefore be a valuable alternative for the Nearctic pentatomid Podisus maculiventris (Say) (Heteroptera: Pentatomidae), the augmentative use of which has largely been abandoned in Europe given its possible environmental impact as an exotic polyphagous predator. However, no study has yet documented the impact of insecticides on P. bidens, which is essential to evaluate the possible combination of this predatory pentatomid with current insecticide applications in integrated pest management (IPM) programmes. This study reports on laboratory experiments investigating the susceptibility of P. bidens to five insecticides with different modes of action: the pyrethroid deltamethrin, the diacylhydrazine methoxyfenozide, the juvenile hormone mimic pyriproxyfen, the spinosyn spinosad, and the neonicotinoid imidacloprid, all of which are used to control defoliator pests. Fourth-instar nymphs and female adults of the predator were exposed to formulated materials of the insecticides by residual contact. Methoxyfenozide and spinosad did not cause significant mortality to 4th instars and female adults of P. bidens. In contrast, deltamethrin and imidacloprid were harmful to nymphs and adults of the predator, with LC₅₀ values ranging between 1.5 and 9.9 mg a.i./l. Pyriproxyfen was toxic to 4th instars with an LC₅₀ value of 13.9 mg a.i./l but did not affect female adults. Reproduction and longevity of P. bidens were not adversely affected when the predator was exposed to field concentrations of spinosad, methoxyfenozide, or pyriproxyfen, or sublethal concentrations (around LC₁₀) of deltamethrin and imidacloprid. The results from residual contact experiments suggest that methoxyfenozide, spinosad, and to a lesser extent, pyriproxyfen may be compatible with P. bidens in an IPM programme. Further experiments assessing food chain toxicity of these compounds should offer a more complete picture of their selectivity.     

Toxicity of diflubenzuron and pyriproxyfen to the predatory bugPodisus maculiventris

The susceptibility of the predatory pentatomidPodisus maculiventris (Say) to the insect growth regulators (IGRs) diflubenzuron and pyriproxyfen was investigated in the laboratory. Fifth-instar nymphs were exposed to formulated materials of each compound via direct contact, residual contact and ingestion. Diflubenzuron was harmless toP. maculiventris by direct and residual contact, but was highly toxic when ingested via drinking water. Pyriproxyfen caused severe deformities at ecdysis whatever the method of exposure. Exposure of fifth instars to sublethal concentrations (around LC₁₀) of both compounds had no adverse effects on reproduction of emerging adults. The data suggest that the use of these IGRs in the integrated management of insect pests should be evaluated with caution.     

Feeding response of the cotton aphid,Aphis gossypii,to sublethal rates of flonicamid and imidacloprid

The cotton aphid, Aphis gossypii Glover (Hemiptera: Aphididae), is an important sap‐sucking pest of many plants, including melons and peppers. This study was conducted to determine the effects of sublethal exposure to flonicamid and imidacloprid and the mechanisms by which these insecticides affect the feeding behavior of A. gossypii. The median lethal concentrations (LC₅₀) of flonicamid and imidacloprid for adult A. gossypii were 2.40 and 1.92 mg l^?1, respectively. The lower lethal concentrations of flonicamid were 1.01 mg l^?1 (LC₃₀) and 0.29 mg l^?1 (LC₁₀), and those of imidacloprid were 0.82 mg l^?1 (LC₃₀) and 0.24 mg l^?1 (LC₁₀). The developmental period of A. gossypii nymphs at LC₃₀ was 3.6 days for both insecticides, which was shorter than that of the untreated controls (4.2 days). Longevity and total fecundity of A. gossypii adults were decreased at the sublethal concentrations of both insecticides. The lowest net reproductive rate was observed in A. gossypii treated with the LC₃₀ of flonicamid. Feeding behavior analyses using an electrical penetration graph showed that sublethal concentrations of flonicamid and imidacloprid had significant effects on the duration of phloem ingestion. Higher doses of flonicamid induced starvation by inhibiting phloem ingestion, whereas imidacloprid acted as a contact toxin rather than an inhibitor of feeding behavior.     

Effects of a juvenile hormone analog, pyriproxyfen, on the apterous form of Lipaphis erysimi

Effects of a juvenile hormone analog, pyriproxyfen, on various developmental stadia of the apterous form of the turnip aphid, Lipaphis erysimi (Kaltenbach), were bioassayed at three concentrations (50, 100, and 150 mg [AI]/l) in the laboratory. Supernumerary-molted nymphs with 1-3 extra molts were found when the first three nymphal instars were treated, and all these nymphs died prematurely. In contrast, all treated fourth instar nymphs molted normally to adults. The longevity of all pyriproxyfen-treated L. erysimi nymphs and adults and the fecundity of treated adults were reduced by 50%. Higher concentrations of pyriproxyfen (100 and 150 mg [AI]/l) caused sterility in adults from treated fourth instars; whereas the lowest concentration (50 mg [AI]/l) did not cause any adult sterility. A majority of adults from treated fourth instars and treated adults produced normal nymphs, and some adults produced dead nymphs with normal appendages or dead and deformed nymphs without any appendages. Normal nymphs produced by the adults from treated adults or treated at fourth instars developed more slowly from first instar to adult than the water-treated nymphs, and all adults in the new generation apparently reproduced normally. The potential role of pyriproxyfen in a vegetable aphid IPM program was discussed.     

Effects of the ecdysteroid agonists RH 5849 an RH 5992, alone and in combination with a juvenile hormone analogue, pyriproxyfen, on larvae ofSpodoptera exigua

Biological activity assays with RH 5849 and RH 5992 indicated that both compounds affected growth and development of last-instar larvae ofSpodoptera exigua (Hübner) (Lepidoptera: Noctuidae) in a dose-dependent manner. Within the first 24 h after treatment by continuously offering leaves dipped in a water solution of ≥50 mg/l RH 5849 and ≥0.5 mg/l RH 5992, symptoms of a prematurely induced larval moult and head capsule apolysis were visible. Intoxicated larvae died shortly afterwards, showing signs of unsuccessful ecdysis. LC₅₀-values of RH 5849 and RH 5992 for fifth-instarS. exigua larvae were 110 and 2.5 mg/l, respectively. Pyriproxyfen alone affected the larval stage and disturbed normal metamorphosis. One supernumerary larval instar occurred occasionally. LC₅₀-value for pyriproxyfen was 1.7 mg/l. Larvae simultaneously treated with RH 5849 or RH 5992 and pyriproxyfen, continued to grow until they attained a size and weight about 2–3 times that of the controls. This growth was accompanied by at least one and sometimes two supernumerary moults. Concerning thein vivo imaginal wing disc growth and development, only in larvae treated with 10 and 50 mg/l RH 5849 or 0.5 mg/l RH 5992, tracheole migration was observed earlier than in the controls. When applying 300 mg/l RH 5849 or 3–7 mg/l RH 5992, the discs remained small and no signs of tracheole migration were observed. In larvae simultaneously treated with RH 5849 or RH 5992 and pyriproxyfen, tracheole migration was not prematurely induced and a pupal cuticle was produced in the discs of larvae, undergoing a supernumerary moult. No clear signs of evagination were observed.     

Effects of three modern insecticides, pyriproxyfen, spinosad and tebufenozide, on survival and reproduction of Chrysoperla carnea adults

Three novel insecticides, pyriproxyfen, spinosad and tebufenozide, were evaluated for their effect on survival and reproduction of Chrysoperla carnea adults using two methods of exposure: direct contact and ingestion. Pyriproxyfen and tebufenozide proved to be harmless to adult survival, whereas spinosad 72 h after treatment reduced the number of adults by 39.8% and 87.2% in topical and ingestion treatment at the maximum concentration recommended (800 mg a.i. litre^?1). Fecundity was not affected irrespective of the insecticide or time of application (before or after the onset of oviposition). Concerning fertility, only pyriproxyfen exerted a negative effect on hatching when the eggs were deposited by females treated by ingestion in the post‐oviposition period at the highest concentration tested (150 mg a.i. litre^?1).     

Side-effects of pesticides on the predatory bug Orius laevigatus (Heteroptera: Anthocoridae) in the laboratory

Laboratory trials were carried out in order to test the effects of 29 pesticides on the predatory bug, Orius laevigatus. To evaluate residual contact activity, newly moulted fourth instar nymphs of O. laevigatus were placed on treated Petri dishes and their mortality was checked after 7 days. The fecundity of surviving females was tested for 14 days. Young O. laevigatus adults were fed with eggs of Ephestia kuehniella, treated with the (above-mentioned) pesticides, to assess the effect of pesticides by ingestion. Adult mortality, female fecundity and egg hatching were recorded. Azadirachtin, granulosis virus products, mineral oil, pirimicarb, tebufenozide, clofentezine, hexythiazox and copper oxychloride had no significant effect on the survival and fecundity of O. laevigatus when predators were exposed to pesticide residues by contact or by ingestion. Triflumuron and diflubenzuron appeared to be harmless by contact, but diflubenzuron was slightly toxic when ingested. Buprofezin and teflubenzuron were slightly to moderately toxic, while hexaflumuron, flufenoxuron, and lufenuron showed a marked toxicity by contact as well as by ingestion. A number of organophosphates, endosulfan and deltamethrin were detrimental especially by contact. Imidacloprid was very toxic by contact but only slightly toxic when ingested. Indoxacarb and methoxyfenozide were less toxic than imidacloprid. These findings should be considered when releases of O. laevigatus are used in greenhouses or on outdoor crops.     

Toxic effects of pyriproxyfen,neemarin, acetamiprid and Ferula assafoetida essential oil on the common pistachio psylla,Agonoscena pistaciae

The common pistachio psylla, Agonoscena pistaciae, Burckhardt and Lauterer (Hemiptera: Psyllidae) is the key pest of pistachio orchards in Iran. Chemical control is the common method for the control of this pest. In this study, the effects of pyriproxyfen (an insect growth regulator), neemarin (a botanical insecticide), acetamiprid (a neonicotinoid) and Ferula assafoetida essential oil were investigated on the fifth instar nymphs of A. pistaciae. Probit analysis of concentration-mortality data was conducted to estimate the LC₅₀ values. The LC₅₀ values for neemarin, pyriproxyfen, acetamiprid and F. assafoetida essential oil were estimated to be 0.22, 0.52, 290 and 5.62 ppm, respectively. Our results showed that the fifth instar nymphs of A. pistaciae are very sensitive to neemarin and pyriproxyfen.     

Insecticidal activity of Artemisia sieberi,Eucalyptus camaldulensis,Thymus persicus and Eruca sativa oils against German cockroach,Blattella germanica (L.)

The German cockroach, Blattella germanica (L.) (Blattodea: Blattellidae), has been recognized as a serious health problem because of its potential to harbor and transmit human disease-causing pathogens. The development of new and environmentally friendly control agents is essential as alternative tool to conventional chemical insecticides. The aim of the current study was to determine the fumigant and contact toxicity of essential oils (EOs), Artemisia sieberi Besser, Eucalyptus camaldulensis Dehn. and Thymus persicus (Ronniger ex Rech. f.) and cold press oil of Eruca sativa (Miller) (ESO) against first instar nymphs and adults. According to results, the LC₅₀ values of EOs were between 15.01 and 28.80 μl/l air for fumigant toxicity, 2202.8 and 5600.2 mg/l for dipping toxicity and 9484.2 and 34,421.1 mg/l for applied surface toxicity. Fumigant activity of the oils were significantly more toxic than other methods. In general, the toxicity of A. sieberi was higher than other EOs. Also, the first instar nymphs were more susceptible than adults. Additionally, the results showed that the EOs were significantly more toxic than ESO in both fumigant and dipping methods. In addition to contact effects, the fumigant activity of ESO was proved, although the toxicity was lower than the EOs. Hence, it is important to consider the production cost benefit of ESO in comparison with the EOs. So, the ESO could be considered as a good candidate in control of the cockroach but in enclosed spaces such as inaccessible cockroach hiding places, the EO of A. sieberi can be useful.     

Effects on German cockroach nymphs of contact exposure to IGRs, singly and in combination

Late instar German cockroach male and female nymphs were exposed continuously for two weeks to surfaces treated with fenoxycarb, diflubenzuron, and pyriproxyfen, singly and in combination. Concentrations were determined that eliminated or nearly eliminated reproduction in matings with untreated mates, either through mortality, effects on reproduction, or a combination of mortality and sterility (no hatch). The major effect of fenoxycarb, pyriproxyfen, and pyriproxyfen plus fenoxycarb was on reproduction. The major effect of diflubenzuron was mortality. No hatch occurred in matings of females that were exposed to low concentrations of pyriproxyfen and fenoxycarb (2 ng/cm² and 6 ng/cm², respectively); sterility was incomplete when females were exposed to 600 ng/cm² of diflubenzuron. Mortality and sterility acted together to eliminate productive matings (matings that produced nymphs) when relatively high concentrations of diflubenzuron were combined with one or both of the other insect growth regulators (IGRs). In the triple combination, very small amounts of fenoxycarb and pyriproxyfen (total 1.1 ng/cm²) combined with 200 ng/cm² of diflubenzuron eliminated productive matings of treated females, but similar results with treated males were found only at higher concentrations of each IGR.     

Sublethal effects of buprofezin on development,reproduction, and chitin synthase 1 gene (SfCHS1) expression in the white-backed planthopper,Sogatella furcifera (Hemiptera: Delphacidae)

The white-backed planthopper, Sogatella furcifera (Horváth) (Hemiptera: Delphacidae), is a major rice pest in some Asia-Pacific countries. Buprofezin is an insect growth regulator with relatively low mammalian toxicity but high efficacy to many rice pests. In this study, we estimated the toxicity of buprofezin against 3rd-instar nymphs of S. furcifera using the rice-stem dipping method. The results showed that the LC₅₀ of buprofezin to 3rd-instar nymphs were 0.89?mg/L. When 3rd-instar nymphs were exposed to the LC₁₀ and LC₂₅ (0.10 and 0.28?mg/L) of buprofezin, the duration of juvenile development was significantly prolonged in the F₀ and F₁ generations. The fecundity (eggs per female) of the F₁ females was reduced by 5.29% and 12.34%, respectively, in addition to the survival rate, emergence rate, copulation rate, and hatchability were decreased by treatment with buprofezin at LC₁₀ and LC₂₅, compared with the control group. The relative fitness of S. furcifera in LC₁₀ and LC₂₅ treatments was reduced by 47% and 63%, respectively. Furthermore, real-time quantitative PCR analyses revealed increased the expressions of SfCHS1 and its two variants following the exposure of nymphs to buprofezin. Increased these genes mRNA levels associated with reduced chitin biosynthesis may result from the inhibition of chitin synthase activity, and thereby leading to a higher mortality of S. furcifera. Overall, sublethal concentrations of buprofezin suppressed the population growth of S. furcifera.     

Variation in susceptibility and selection for resistance to imidacloprid and thiamethoxam in Mediterranean populations of Orius laevigatus

Imidacloprid and thiamethoxam are neonicotinoids that have been tested in several Orius species, including Orius laevigatus (Fieber) (Hemiptera: Anthocoridae), but not the variability in their effect among Orius populations of a single species. In this study, the variation in susceptibility to imidacloprid and thiamethoxam in 30 Mediterranean wild populations and four commercial populations of O. laevigatus was investigated in the laboratory using a standard dip bioassay method. Lethal concentration values (LC₅₀) and the mortality of adults at the maximum field rate (MFR) were calculated. The range of LC₅₀ of thiamethoxam was from 0.7 to 5.9 mg l^?1, an 8.4‐fold variability, obtaining mortality at MFR (100 mg l^?1) of >89.1% in all populations. The baseline obtained a value of 2.1 mg l^?1, which is very low compared to the MFR. For imidacloprid, the LC₅₀ varied from 7.7 to 94.7 mg l^?1 (12.3‐fold variability). Mortalities at the MFR (150 mg l^?1) were 57.7–99.2%, that is, more variable than for thiamethoxam. The LC₅₀ value of the baseline was 48.7 mg l^?1, also low compared to the MFR. This variation was exploited to select two populations resistant to thiamethoxam and imidacloprid, respectively. Artificial selection for on average 40 cycles significantly increased the resistance to thiamethoxam (LC₅₀ = 149.1 mg l^?1) and imidacloprid (LC₅₀ = 309.9 mg l^?1). Mortalities at the MFR in the thiamethoxam‐ and imidacloprid‐resistant populations were 44.5 and 36.9%, respectively. These results demonstrate that resistance can be enhanced in biocontrol agents by artificial selection under laboratory conditions, starting with populations showing no or very low tolerance. Our neonicotinoid‐resistant populations might enhance the wider adoption of biological control by allowing punctual or hotspot applications of neonicotinoids to control several main and secondary pests.     

B型与浙江非B型烟粉虱药剂敏感性的比较

比较了新入侵我国的B型烟粉虱Bemisiatabaci(Gennadius)与非B型烟粉虱ZHJ-1种群对5%吡虫啉乳油和5%吡丙醚乳油2种杀虫剂的敏感性。ZHJ-1种群卵、若虫和成虫对这2种药剂的敏感性均比B型的明显或显著要高。吡丙醚具有高杀卵活性,在有效成分为0.25mg/L时,2个烟粉虱种群卵的死亡率高于90%。药剂敏感性的差异可能是B型竞争取代本地非B型烟粉虱的一个重要原因。     

Identification and virulence characterization of entomopathogenic fungus <Emphasis Type="BoldItalic">Lecanicillium attenuatum</Emphasis> against the pea aphid <Emphasis Type="BoldItalic">Acyrthosiphon pisum</Emphasis> (Hemiptera: Aphididae)

An entomopathogenic fungal strain was originally isolated on artificial medium from the corpse of a pea aphid (Acyrthosiphon pisum Harris) collected at Jingzhou, China (N30°21′18.15″, E112°08′41.63″). Based on tests of the morphological, physiological and biochemical characteristics and analysis of internal transcribed spacer (ITS) sequences, it was considered to be a strain of Lecanicillium attenuatum Zare & W. Gams. Therefore, the strain was designated L. attenuatum YZU 151121. The activity of the biological agents under study was determined at 26 °C and 90% relative humidity. The number of A. pisum killed was increased by increasing the concentration of L. attenuatum. The results demonstrated that L. attenuatum YZU 151121 showed a high efficacy against 3rd-instar nymphs (LC₅₀ = 2.91 ± 0.365 × 10⁵ conidia/ml) and adults (LC₅₀ = 3.12 ± 0.398 × 10⁶ conidia/ml) after 6 days of exposure. Crude extract from this strain was tested for contact toxicity and showed high activity in 3rd-instar nymphs and adults, with LC₅₀ values of 251.34 ± 49.54 and 315.46 ± 87.66 mg/l, respectively. In addition, crude extract at a concentration of 200 mg/l could significantly reduce fecundity in adults. These results revealed that the strain YZU 151121 may be useful in biopesticides for controlling pea aphid.     

Effects of triflumezopyrim on the reproduction of brown planthopper,Nilaparvata lugens

The brown planthopper, Nilaparvata lugens Stål (Hemiptera: Delphacidae), is a notorious pest on rice in Asia and has evolved serious resistance to traditional chemical insecticides in recent years. Triflumezopyrim, a newly commercialized mesoionic insecticide, exhibited an excellent control effect on sucking insects, including N. lugens. However, the effects of triflumezopyrim on the reproduction of N. lugens have not yet been fully elucidated. In this study, we investigated the impacts of different concentrations of triflumezopyrim (LC₁₀, LC₅₀ and LC₉₀) on the reproduction and the reproduction related genes of N. lugens exposure to the insecticide via systemic and contact route. The results indicated that the preoviposition periods of N. lugens females in the LC₅₀ and LC₉₀ triflumezopyrim-treated groups (♀ t × ♂ t) were prolonged in contact toxicity treatment, compared with control (acetone treatment). The fecundities for three pair combinations (♀ c ×♂ t, ♀ t ×♂ c and ♀ t ×♂ t) treated with LC₅₀ and LC₉₀ concentrations of triflumezopyrim showed a significant decrease compared to water/acetone-treated control via contact and systemic route. No significant effects of LC₁₀ triflumezopyrim on preoviposition period and fecundity were found in contact and systemic toxicity treatments. However, the triflumezopyrim did not influence the egg hatchability. By microscope observation, the LC₅₀ and LC₉₀ triflumezopyrim impended the ovarian development in females. qRT-PCR analysis showed that the vitellogenin (NlVg) relative expression level of female adults exposed to LC₅₀ and LC₉₀ triflumezopyrim decreased by 30.3 – 39.5% in two toxicity treatments. The titers of another reproduction related hormones juvenile hormone III (JH III) in LC₅₀ and LC₉₀ triflumezopyrim-treatments were 27.4% and 25.8% lower than control in contact toxicity treatment and 27.08% and 37.18% lower than control in systemic toxicity treatment. In summary, these results suggested that the median lethal and high lethal concentrations of triflumezopyrim inhibited the reproduction and reduced the expression of NlVg and JH III in N. lugens. This study provided a reference for the efficient and scientific utilization of triflumezopyrim in the field.     

11种不同类型杀虫剂对卷蛾分索赤眼蜂繁殖的亚致死效应

在实验室条件下通过药膜法研究了11种不同类型的杀虫剂对卷蛾分索赤眼蜂Trichogrammatoidea bactrae Nagaraja成蜂的毒性, 并研究了杀虫剂对其繁殖的亚致死效应, 旨在评估各药剂对卷蛾分索赤眼蜂成蜂的安全性, 为小菜蛾Plutella xylostella防治过程中杀虫剂的合理施用提供科学依据。研究结果表明, 卷蛾分索赤眼蜂成蜂对阿维菌素最敏感, 致死中浓度LC₅₀和亚致死浓度LC₃₀分别为0.1984和0.1660 mg/L, 其次为氟虫腈（0.2027和0.1903 mg/L）、溴虫腈（0.3069和0.2038 mg/L）、多杀霉素（1.3630和1.0481 mg/L）、杀螟丹（8.1042 和6.7891 mg/L）、高效氯氰菊酯（10.3647和5.8035 mg/L）和丁醚脲（11.5318 和9.9212 mg/L）。经亚致死浓度LC₃₀的阿维菌素、溴虫腈、杀螟丹、丁醚脲、多杀霉素和氟虫腈处理后, 卷蛾分索赤眼蜂的寿命（1.00~1.67 d）显著缩短, 寄生卵量（0~21.70粒/雌）明显降低, 种群参数（净生殖力R₀、内禀增长率r_m、周限增长率λ和世代平均历期T）明显低于对照（P<0.05）。田间推荐浓度的茚虫威、氟啶脲、苏云金杆菌Bacillus thuringiensis、虫酰肼对卷蛾分索赤眼蜂寿命及产卵量均没有不利影响, 但能通过缩短其世代平均历期T, 从而使净生殖力R₀、内禀增长率r_m和周限增长率λ增加。而经亚致死浓度LC₃₀的高效氯氰菊酯处理后, 卷蛾分索赤眼蜂的寿命（3.77 d）显著延长, 寄生卵量（55.47粒/雌）明显提高, 种群参数明显高于对照(P<0.05)。结果说明, 氟啶脲、茚虫威、苏云金杆菌和虫酰肼对卷蛾分索赤眼蜂较安全; 丁醚脲对卷蛾分索赤眼蜂成蜂的寄生能力影响极大, 在田间施用时应当尽量避开卷蛾分索赤眼蜂成蜂的盛发期。     

Insecticidal activities of monoterpenes and phenylpropenes against <Emphasis Type="Italic">Sitophilus oryzae</Emphasis> and their inhibitory effects on acetylcholinesterase and adenosine triphosphatases

In the present study, six monoterpenes [(?)-citronellal, p-cymene, (?)-menthone, α-pinene, α-terpinene, and (?)-terpinen-4-ol] and two phenylpropenes [trans-cinnamaldehyde and eugenol] were evaluated for their contact and fumigant toxicities against Sitophilus oryzae adults. The effects of these compounds on the mortality of S. oryzae adults in stored wheat and their inhibitory effects on acetylcholinesterase (AChE) and adenosine triphosphatases (ATPases) were examined. The tested compounds showed varying degrees of contact toxicity, with trans-cinnamaldehyde (LC₅₀ = 0.01 mg/cm²) being the most potent compound, followed by (?)-menthone (LC₅₀ = 0.013 mg/cm²) and eugenol (LC₅₀ = 0.015 mg/cm²). In a fumigant toxicity assay, the monoterpenes α-terpinene, p-cymene, and (?)-menthone showed the highest toxicities (LC₅₀ = 50.79, 52.37, and 54.08 μl/L air, respectively). Trans-cinnamaldehyde, (?)-citronellal, and eugenol were the least toxic (LC₅₀ > 100 μl/L air). In general, the oxygenated compounds exhibited high contact toxicities while the hydrocarbon compounds exhibited high fumigant toxicities. When tested for their insecticidal activities against S. oryzae in stored wheat, trans-cinnamaldehyde was found to be the most potent compound, with 73.9% mortality at an application rate of 0.5 g/kg and complete mortality (100%) at 1 and 5 g/kg after 1 week of treatment. All of the tested compounds showed AChE inhibition, although (?)-citronellal and trans-cinnamaldehyde presented the strongest enzyme inhibition, with IC₅₀ values of 18.40 and 18.93 mM, respectively. On the other hand, (?)-terpinene-4-ol exhibited the highest inhibition of ATPases, followed by α-pinene and α-terpinene.     

Effects of a juvenile hormone analogue, pyriproxyfen, on the apterous form of soybean aphid (Aphis glycines)

The soybean aphid, Aphis glycines Matsamura, is an eastern Asian soybean [Glycine max (L.) Merr.] pest which can reduce soybean yield. We determined the effects of pyriproxyfen, a juvenile hormone analogue, on development, mortality, longevity and fecundity of A. glycines under laboratory conditions. Distance Insect Growth Regulator, containing ∼11.2% pyriproxyfen, was applied at two concentrations, 50 and 150 mg/l, to first and fourth instar nymphs. When first or fourth instar A. glycines were treated with pyriproxyfen, some nymphs became supernumerary‐molted nymphs with 1–3 extra molts or were sterilized. Mortality of treated first instar nymphs was >68% greater than the control group and longevity was reduced by >40%. The higher concentration of pyriproxyfen reduced fecundity of first instar nymphs when they reached adulthood by ∼79%. Pyriproxyfen similarly affected fourth instar nymphs. Mortality of treated fourth instar nymphs was ≥15% greater than the control group and longevity was reduced by >24%. Both concentrations of pyriproxyfen lowered the fecundity of fourth instar nymphs by >27%. Pyriproxyfen also had other sublethal effects on fourth instar nymphs which became apparent when they molted to adulthood. In a few instances they developed wing pads and many produced dead, deformed or abnormal neonates that lacked appendages.     

Side effects of diflubenzuron on a pear psylla predator:Forficula auricularia

A series of laboratory, semi-field and field tests showed the high toxicity of diflubenzuron toForficula auricularia L. nymphs, at concentrations of 15 and 20 g a.i./hl registered in various European countries and the United States to controlCydia pomonella L. Diflubenzuron proved more selective using the 10 g/hl concentration registered in France, but several sublethal effects have been observed: morphological abnormalities, reduced weight increase and mobility. Unexpectedly for a chitin-deposit inhibitor, intake was reduced, which became apparent from the beginning of exposure to the insecticide, before the onset of the moulting process. In the semi-field tests, and despite diflubenzuron's slowing down effect on psylla nymphs, the earwig's reduced predatory activity due to the product resulted in greater growth of the psylla populations than without treatment. The field-test confirmed the efficacy ofF. auricularia as a psylla predator, and the relative selectivity of diflubenzuron at the lowest concentration.     

Transport and kinetics of diflubenzuron and pyriproxyfen in the beet armywormSpodoptera exigua and its predatorPodisus maculiventris

Transport and retention of the insect growth regulators (IGRs) diflubenzuron and pyriproxyfen in larvae of the beet armywormSpodoptera exigua (Hübner) and in nymphs of the predatory bugPodisus maculiventris (Say) were investigated. In a first experiment, the retention of orally administered [¹⁴C]radiolabeled isotopes of both compounds in fifth-instar larvae of the beet armyworm was studied. Rate of excretion of both IGRs inS. exigua caterpillars was high, with a 50% excretion time of approximately 6 h after intake. In a second experiment, the transport of the compounds from prey to predator and their retention inside the predator were studied. Fifthinstar nymphs ofP. maculiventris were allowed to feed on caterpillars that had been given contaminated food. For both diflubenzuron and pyriproxyfen, more than 80% of the amount of radiolabel applied was recovered in consumed prey. Low levels of radioactivity (c. 3% of the applied amount of radiolabel) were also found in the fluid regurgitated by the prey larvae when attacked by the predatory bugs. Relatively small amounts of radiolabel (c. 8 and 15% of the amount orally applied to the prey for diflubenzuron and pyriproxyfen, respectively) were ingested byP. maculiventris nymphs when feeding on beet armyworm caterpillars. The data suggest that the predators did not use gut content as food. The pattern of excretion in nymphs ofP. maculiventris differed between compounds. For diflubenzuron, there was a drastic decrease of radioactivity inside the predator body of around 40% within the first 6 h and then the level of retained radiolabel remained stable at 3–4% up to 72 h. For pyriproxyfen, a slow decrease of radioactivity inside the body was observed and at 72 h only 2% of the applied quantity was detected. Results of this study are discussed in relation to the findings from previous studies on the toxicity of both IGRs toP. maculiventris.