Toxicity of spiromesifen to the developmental stages of Bemisia tabaci biotype B.

BACKGROUND: Spiromesifen is a novel insecticidal/acaricidal compound derived from spirocyclic tetronic acids that acts effectively against whiteflies and mites via inhibition of acetyl-CoA-carboxylase, a lipid metabolism enzyme. The effects of spiromesifen on the developmental stages of the whitefly Bemisia tabaci (Gennadius) were studied under laboratory conditions to generate baseline action thresholds for field evaluations of the compound. RESULTS: Adult B. tabaci mortality rate after spiromesifen treatment (5 mg L(-1)) was 40%. Treatment with 0.5 mg L(-1) reduced fecundity per female by more than 80%, and fertility was almost nil. LC(50) for eggs was 2.6 mg L(-1), and for first instar 0.5 mg L(-1). Scanning electron microscopy revealed that eggs laid by treated adult females had an abnormally perforated chorion, and females were unable to complete oviposition. Light and fluorescent microscopy showed significantly smaller eggs following treatment, and smaller, abnormally formed and improperly localized bacteriomes in eggs and nymphs. The number of ovarioles counted in females treated with 5 mg L(-1) was significantly reduced. Spiromesifen showed no cross-resistance with other commonly used insecticides from different chemical groups, and resistance monitoring in Israel showed no development of field resistance to this insecticide after 1 year of use. CONCLUSION: The strong effect on juvenile stages of B. tabaci with a unique mode of action and the absence of cross-resistance with major commonly used insecticides from different chemical groups suggest the use of spiromesifen in pest and resistance management programmes.

Effect of pyriproxyfen on developing stages and embryogenesis of California red scale (CRS), Aonidiella aurantii.

During the past decade, the insect growth regulator pyriproxyfen has been the most used insecticide for controlling the California red scale (CRS), Aonidiella aurantii (Maskell), an important pest in citrus groves worldwide. The aim of the present research was to develop bioassays for determining the effect of pyriproxyfen on developing stages and embryogenesis of CRS that can serve as baselines for monitoring resistance. Pyriproxyfen was very effective against first- and second-instar nymphs of a susceptible strain of CRS; 0.1 and 0.2 mg AI L(-1), resulting in 80 and 100% mortality of first-instar nymphs, and in 62.5 and 91.7% mortality of second-instar nymphs respectively. According to probit analysis, the LC(50) and LC(90) values of pyriproxyfen for first-instar nymphs were 0.03 and 0.15 mg AI L(-1), and for second-instar nymphs they were 0.05 and 0.25 mg AI L(-1) respectively. Pyriproxyfen was quite effective on first-instar nymphs of a CRS field strain originating from a citrus grove where two successive applications of the compound had been applied. Mortality rates were 86 and 100% at concentrations of 0.2 and 0.4 mg AI L(-1) respectively. Pyriproxyfen suppressed embryogenesis when CRS females were treated with pyriproxyfen. Young CRS females treated with 1.0 and 5.0 mg AI L(-1) pyriproxyfen produced 6.6 N(1)/F and 2.4 N(1)/F as compared with 10.9 N(1)/F in untreated control.

Emamectin, a novel insecticide for controlling field crop pests.

Emamectin is a macrocyclic lactone insecticide with low toxicity to non-target organisms and the environment, and is considered an important component in pest-management programmes for controlling field crop pests. It is a powerful compound for controlling the cotton bollworm Helicoverpa armigera (Hübner). A spray concentration of 25 mg AI litre-1 in a cotton field resulted in over 90% suppression of H armigera larvae up to day 28 after treatment, while similar mortality of the Egyptian cotton leafworm Spodoptera littoralis Boisduval, under the same conditions, was maintained for 3 days only. Emamectin is a potent compound for controlling the western flower thrips Frankliniella occidentalis (Pergande) under both laboratory and field conditions and its activity on adults was over 10-fold greater than that of abamectin. Spray concentrations of 10 and 50 mg AI litre-1 in Ageratum houstonianum Mill flowers resulted in total suppression of adults up to day 11 and of larvae up to day 20 after treatment. Under standard laboratory conditions, emamectin exhibits a considerable activity on the whitefly Bemisia tabaci (Gennadius) and the leafminer Liriomyza huidobrensis (Blanchard). Further studies are required to evaluate its potential activity on the latter pests under field conditions.

Dynamics of insecticide resistance in Bemisia tabaci: a case study with the insect growth regulator pyriproxyfen.

The dynamics of pyriproxyfen resistance in Bemisia tabaci (Gennadius) have been studied intensively in cotton fields and greenhouses in Israel. High resistance to pyriproxyfen evolved one year after its introduction for use on flowers in greenhouses, after three successive applications. After ten years of pyriproxyfen use in cotton fields, with only one application per season, a high level of resistance was observed, but its rate of development differed among localities. It is hypothesized that these differences reflect temporal and spatial variations in the availability of alternative host plants for B tabaci, and that pyriproxyfen resistance evolved most readily in geographically isolated areas. It is also likely that the occurrence and development of resistance is partially biotype-related. Pyriproxyfen use has ceased in high-resistance localities, but in areas with low frequencies of resistance, cotton growers have continued to achieve acceptable control of B tabaci with pyriproxyfen. Due to the absence of applications of pyriproxyfen in some cotton fields, resistance levels tended to decline between 1998 and 2001. Laboratory experiments support the hypothesis that this decline reflects, in part, fitness costs associated with pyriproxyfen resistance.

Dynamics of resistance to the neonicotinoids acetamiprid and thiamethoxam in Bemisia tabaci (Homoptera: Aleyrodidae).

The dynamics of resistance in the sweetpotato whitefly, Bemisia tabaci (Gennadius), to the neonicotinoids acetamiprid and thiamethoxam was studied extensively in cotton fields in Israel during the cotton-growing seasons 1999-2003. Whitefly strains were collected in early and late seasons mainly in three locations in northern, central, and southern Israel. The whiteflies were assayed under laboratory conditions for susceptibility to neonicotinoids, as part of the Israeli cotton insecticide resistance management strategy. Selections to both acetamiprid and thiamethoxam and cross-resistance between them also were conducted in the laboratory. Although no appreciable resistance to acetamiprid was observed up to 2001, a slight increase of approximately five-fold resistance was detected during 2002 and 2003. However, from 2001 to 2003 thiamethoxam resistance increased >100-fold in the Ayalon Valley and Carmel Coast cotton fields. In cross-resistance assays with both neonicotinoids, the strain that had been selected with thiamethoxam for 12 generations demonstrated almost no cross-resistance to acetamiprid, whereas the acetamiprid-selected strain exhibited high cross-resistance of >500-fold to thiamethoxam.

Dynamics of biotypes B and Q of the whitefly Bemisia tabaci and its impact on insecticide resistance.

BACKGROUND: The whitefly Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) is a key pest in many agricultural crops, including vegetables, ornamentals and field crops. B. tabaci is known for its genetic diversity, which is expressed in a complex of biotypes or, as recently suggested, a complex of distinct cryptic species. The biotypes are largely differentiated on the basis of biochemical or molecular polymorphism and differ in characteristics such as host plant range, attraction by natural enemies, secondary symbionts and expression of insecticide resistance. An extensive survey of B. tabaci biotypes and their impact on insecticide resistance was conducted from 2003 to 2012 in cotton fields and other crops from several locations in Israel. RESULTS: Two biotypes of B. tabaci, B and Q, were identified, and some differences in the biotype dynamics were recorded from different areas. In northern Israel from 2003 to 2007, a higher proportion of the B biotype was consistently found in early season. However, by the end of the season a definite rise of the Q biotype was sampled, ranging from 60 to 100%, along with high resistance to the insect growth regulator (IGR) pyriproxyfen and to a lesser extent to the neonicotinoid insecticides. In fields located in the central part of Israel, the Q biotype was predominant throughout the seasons, with high resistance to pyriproxyfen. Since 2009, a significant shift in the biotype ratios has been observed: the B biotype has come to predominate over the Q biotype ranging up to 90% or more in most fields. At the same time, resistance to the IGR pyriproxyfen was reduced considerably. CONCLUSION: The possible reasons for the change in the dynamics of B. tabaci biotypes, and its implications for resistance management, are discussed. Strong B. tabaci resistance to pyriproxyfen in Israel has been associated with the Q rather than with the B biotype. The B biotype is more competitive than the Q biotype under untreated conditions. Reduction in the acreage of cotton fields during recent years, along with a decrease in insecticide use, especially pyriproxyfen, has resulted in the expansion of the B biotype.

Flufenerim, a novel insecticide acting on diverse insect pests: biological mode of action and biochemical aspects.

A new chemical compound was tested for its insecticidal activity against several major insect pests. The compound, called "flufenerim", has a core pyrimidine structure and an unknown mode of action and showed potent activity against the sweet potato whitefly Bemisia tabaci (Gennadius), the green peach aphid Myzus persicae (Sulzer), and the African cotton leafworm Spodoptera littoralis (Boisduval); however, it did not show any activity against two thrips species: western flower thrips Frankliniella occidentalis (Pergande) and tobacco thrips Thrips tabaci (Lindeman). The compound was relatively potent against the three tested pests and caused mortality rates that reached up to 100% at concentrations under 10 mg of active ingredient (ai) L(-1). The action of the compound was very fast, and mortality was observed within 48 h after exposure of the insects to treated leaves. A unique characteristic of this compound is its very short residual activity, which approximates to 4 days after application under laboratory conditions and to 2 days under outdoor conditions for both B. tabaci and S. littoralis. Although this new compound's mode of action is yet unknown, its rapid and potent action against sap-sucking pests suggests that it acts on a very important target site in the insect body and possibly could be applied very close to harvesting.

Synthesis and insecticidal activity of heptafluoroisopropyl-containing benzoylphenylurea structures.

Fourteen novel heptafluoroisopropyl-containing benzoylphenylureas were designed and synthesized. Their insecticidal activities against armyworm ( Pseudaletia separata Walker) were examined and compared with the commercial product diflubenzuron. Three compounds (IIi, IIj, and IIk) showed excellent insecticidal effect, and their activity resembled that of diflubenzuron. Compound IIi also showed nearly the same insecticidal activity as novaluron on African cotton leafworm ( Spodoptera littoralis ). Furthermore, results from a field trial indicated that 5% EC IIi exhibited similar efficacy in comparison with chlorfluazuron and hexaflumuron against imported cabbage worm ( Pieris rapae L.) and diamondback moth ( Plutella xylostella ), respectively.

Biorational insecticides: mechanism and cross-resistance.

Potency and cross-resistance of various biorational insecticides, exemplified by the whitefly Bemisia tabaci, have been studied. Bemisia tabaci were exposed to the juvenile hormone mimic pyriproxyfen for the past 12 years resulting in an over 2,000-fold resistance, but there was no appreciable cross-resistance with the benzoylphenyl urea novaluron. Similarly, no cross-resistance was found between pyriproxyfen and the two neonicotinoids, acetamiprid and imidacloprid. On the other hand, a slight cross-resistance of 5-13-fold was observed with another neonicotinoid thiamethoxam. Among the neonicotinoids, a resistant strain of B. tabaci to thiamethoxam (approximately 100-fold) showed no appreciable cross-resistance to either acetamiprid or imidacloprid, while another strain 500-fold resistant to thiamethoxam resulted in a mild of 4-6-fold resistance to acetamiprid and imidacloprid. In other assays, B. tabaci strain resistant to thiamethoxam (approximately 100-fold) had no cross-resistance to pyriproxyfen. Our findings indicate that no appreciable cross-resistance was observed between the benzoylphenyl urea novaluron, the juvenile hormone mimic pyriproxyfen, and the neonicotinoids acetamiprid and imidacloprid. Hence, these compounds could be used as components in insecticide resistance management programs.

Biotypes B and Q of Bemisia tabaci and their relevance to neonicotinoid and pyriproxyfen resistance.

Resistance monitoring for Bemisia tabaci field populations to the juvenile hormone mimic, pyriproxyfen, was conducted from 1996 to 2003 in commercial cotton fields in two areas of Israel: the Ayalon Valley (central Israel) and the Carmel Coast (northwestern Israel). Although the use of pyriproxyfen ceased in these areas in 1996-1997 (because of the resistance), resistance levels to pyriproxyfen declined to some extent in the fields but remained quite stable, and the susceptibility has not been totally restored. Two strains of B. tabaci collected from the Ayalon Valley in the late 1999 and 2002 cotton seasons (AV99L, AV02L) were assayed for their susceptibility to pyriproxyfen at F1, and subsequently a line of each strain was kept under controlled conditions without exposure to insecticides. After maintenance of more than 20 generations under laboratory conditions, the resistance to pyriproxyfen in the untreated strains substantially declined. This decline was concurrent with a replacement of Q biotype by B-type under non-insecticidal regimes; apparently B biotype was more competitive than the pyriproxyfen-resistant Q-type. Selection under controlled conditions with neonicotinoids on these B. tabaci strains resulted in continued pyriproxyfen resistance, predominantly of Q biotype. Based on our data, applications of either pyriproxyfen or neonicotinoids may select for biotype Q, which would survive to a greater degree where these insecticides are applied.

Novaluron (Rimon), a novel IGR: potency and cross-resistance.

The potency of novaluron on laboratory susceptible and field strains of S. littoralis resembles that of chlorfluazuron and both compounds are about 20-fold more potent than teflubenzuron. No appreciable resistance to novaluron or chlorfluazuron was observed in a field strain of Spodoptera littoralis collected from cucumber field in the central part of Israel. On the other hand, the field strain showed a mild resistance of about 4-fold to teflubenzuron as compared to the laboratory susceptible strain. A very resistant colony of Bemisia tabaci to pyriproxyfen (1,200- to 2,000-fold) showed no appreciable cross-resistance to novaluron. Two field colonies of B. tabaci pressurized with acetamiprid or thiamethoxam for 22 generations, resulting in a 30- to 50-fold resistance to acetamiprid and thiamethoxam, has no cross-resistance to novaluron. The above results are of special interest, indicating a possible alternation between novaluron, pyriproxyfen, and neonicotinoids in insecticide-resistance management programs aiming at preventing resistance development to these novel groups of insecticides against important pests such as whitefly and lepidopteran species.

Novaluron (Rimon), a novel IGR--mechanism, selectivity and importance in IPM programs.

Novaluron (Rimon), a new IGR, acts by both ingestion and contact. It is a powerful toxicant for controlling lepidopteran larvae resulting in LC-90 values of 0.42 and 0.30 mg a.i./liter for Spodoptera littoralis and S. exigua, respectively. Its residual activity under field conditions ranges between 10 and 30 days depending on environmental conditions. The compound is a powerful toxicant against developing stages of whiteflies, resulting in LC-90 values of 0.68 and 8.56 mg a.i./liter for Bemisia tabaci and Trialeurodes vaporariorum, respectively. It has translaminar activity, enabling the control of the leaf miner Liriomyza huidobrensis at concentrations ranging between 5 and 45 mg a.i./liter. Novaluron has no cross-resistance with other leading compounds for controlling whiteflies such as buprofezin and pyriproxyfen. It is a rain fast compound suitable in the tropics and in rainy seasons. It has no appreciable effect on parasitoids and phytoseiids and a mild effect on other natural enemies and may be considered a potential component in IPM programs. The compound is in the process of commercialization worldwide by Makhteshim Chemical Works for controlling agricultural pests.