The absorption of cypermethrin in the grasshopper Melanoplus sanguinipes (Fab.): Effects of volatilisation,temperature, age,sex and parasitisation by Malameba locustae (King and Taylor)

The residues from metered doses of cypermethrin were recovered from excised portions of grasshopper cuticle to determine losses by volatilisation. Residues from similar doses were also recovered from the cuticles of intact grasshoppers and from whole body homogenates after rinsing the cuticle, to determine rates of absorption and losses from metabolism. Residues were recovered from males and females one week and three weeks after fledging in grasshoppers infected with Malameba locustae and in uninfected ones. They were maintained at 15 or 30°C and sampled from each combination of factors at 4, 8, 16, 24, 30 and 48 h after treatment. There was no measurable loss of cypermethrin by volatilisation up to 72 h after application to excised portions of cuticle at either 15 or 30°C. In all combinations of factors, more cypermethrin was recovered externally (P <0.05) from grasshoppers held at 15°C than those held at 30°C and more from infected grasshoppers than from those that were uninfected. Significantly more cypermethrin was also recovered externally from males than from females (P <0.05) and more from infected one-week-old grasshoppers than those that were three weeks old. At 15°C there was a gradual trend towards accumulation of cypermethrin internally, but at 30°C an initial trend towards accumulation was followed by one of decline. Residual cypermethrin recovered could in general be related to the negative temperature coefficient of toxicity, to a decreased sensitivity to cypermethrin in infected grasshoppers and to an increased sensitivity in older grasshoppers.     

Sulfur in pesticide action and metabolism: Edited by J. D. Rosen,P. S. Magee,and J. E. Casida,American Chemical Society,Washington, D.C., 1981. 172 pp., $33.00

The distribution of ¹⁴C-acid-, ¹⁴C-alcohol-, and ¹⁴C-cyano-labeled deltamethrin and selected metabolites were followed in the liver, blood, cerebrum, cerebellum, and spinal cord after iv administration of a toxic, but nonlethal dose (1.75 mg/kg) to rats. Approximately 50% of the dose was cleared from the blood within 0.7–0.8 min, after which the rate of clearance decreased. 3-Phenoxybenzoic acid (PBacid) was isolated from the blood in vivo, and was also the major metabolite when ¹⁴C-alcohol-labeled deltamethrin was incubated with blood in vitro. Deltamethrin levels in the liver peaked at 7–10 nmol/g at 5 min and then decreased to 1 nmol/g by 30 min. In contrast, peak central nervous system levels of deltamethrin were achieved within 1 min (0.5 nmol/g), decreasing to 0.2 nmol/g at 15 min, and remaining stable until 60 min. peak levels of deltamethrin did not correspond to the severity of toxicity, although the levels of non-pentane-soluble radiolabel did appear to correlate with motor signs of toxicity. Experiments with brain homogenates, using in vivo concentrations of deltamethrin, failed to reproduce the pentane-unextractable radioactivity in vitro nor was any metabolism demonstrated.     

M. Ichinari,M. Masuko,H. Takenaka,R. Hasegawa,T. Ichiba,Y. Hayase and R. Takeda, ‘Structure and fungicidal activities of methoxyiminophenylacetamide derivatives’. Pesticide Science 55(3) 1999, 347–349

The original article to which this Correction refers was published in Pesticide Science 55 (3) 1999, 347–349. © 1999 Society of Chemical Industry     

Genetic Relatedness among Pseudomonas avellanae, P. Syringae pv. Theae and P.s. pv. Actinidiae, and their Identification

A total of 37 strains of Pseudomonas avellanae, P. syringae pv. theae and P.s. pv. actinidiae, including pathotype and reference strains, obtained from all the countries where these pathogens have been reported, were compared by means of ARDRA, repetitive PCR using ERIC, BOX and REP primer sets, whole-cell protein analysis, biochemical and nutritional tests, and pathogenicity tests. P. syringae pathovar type strains representing six genomospecies sensu Gardan et al. (1999), were also included for comparison in UPGMA cluster analysis of repetitive PCR data and SDS-PAGE of protein extracts. Among the 12 endonucleases used in ARDRA, only Tru 9I differentiated P. avellanae from P.s. pv. theae and P.s. pv. actinidiae. UPGMA cluster analysis of repetitive PCR genomic fingerprints showed 65% similarity between P.s. pv. theae and P. avellanae and 50% between the latter species and P.s. pv. actinidiae. Strains of P.s. pv. actinidiae could be grouped according to their geographic origin. Similar results were obtained with SDS-PAGE cluster analysis. PCR amplification using primers PAV 1 and PAV 22 that were developed to detect P. avellanae in apparently healthy and visibly infected hazelnut specimens yielded a band of 762bp from all strains of P. avellanae, P.s. pv. theae and P.s. pv. actinidiae. All strains lacked the syrB gene. Based on these data, we suggest that P.s. pv. actinidiae should be included in the genomospecies 8 together with P. avellanae and P.s. pv. theae. Selected biochemical and nutritional tests could differentiate these groups of strains. Pathogenicity tests clearly indicated that each group is specifically pathogenic only on the host plant species from which it was originally isolated.The author is staff member of the Istituto Sperimentale per la Patologia Vegetale, Roma, Italy temporarily assigned to ISF.