An assessment of methacrifos as a grain protectant and its efficacy against oryzaephilus surinamensis L., Tribolium castaneum herbst,Sitophilus granarius L., Sitophilus oryzae L., Acarus siro L., Glycyphagus destructor schrank and Tyrophagus longior gervais

A trial was carried out to investigate the efficacy of methacrifos against susceptible and multi-resistant strains of four species of insect and three species of mite. Methacrifos was applied to two separate 20-tonne loads of English wheat which were then stored under ambient conditions for 24 weeks. The efficacy of methacrifos was assessed using established bioassay techniques which showed complete control for 24 weeks of all susceptible insects except S. oryzae, where there were survivors at week 24. Methacrifos also gave 100% mortality of resistant O. surinamensis for 24 weeks. There was >95% mortality for 16 weeks of resistant strains of T. castaneum and of resistant S. granarius and S. oryzae for 20 weeks. After S. granarius and S. oryzae were removed, the grain was incubated for 10 weeks. Subsequent F₁ emergence was considerably less from the treatments than from the controls. Methacrifos produced 100% mortality for T. longior for 24 weeks, but control of G. destructor fluctuated and was <100% at week 24. There were survivors of A. siro from week 4.     

Genetically engineered viral insecticides–A progress report 1986 1989

Among the viruses that are pathogenic for insect species, baculoviruses have been shown to be useful as insecticides for pest control. In some cases they have been used as cost-effective and environmentally acceptable alternatives to chemical insecticides. However, because viruses need to be ingested and replicate extensively in their host before they kill it, baculovirus insecticides are much slower than chemicals or other reagents that kill insects either on contact or shortly after ingestion. The objective of the programme of genetic engineering of baculovirus insecticides is to improve their speed of action while maintaining their host specificity and other attributes that make them desirable alternatives to chemical pesticides. Since 1986 four field releases have been undertaken involving genetically engineered baculovirus insecticides. The first release used a genetically marked Autographa californica nuclear polyhedrosis virus (AcNPV). The study began in 1986 and was terminated in 1987. The results demonstrated that an innocuous piece of DNA, appropriately positioned in the AcNPV genome, was an effective means to tag the virus without affecting its phenotype, allowing it to be identified in bioassays of plant and soil samples. The second release, in 1987, involved a genetically marked virus from which the gene coding for the protective polyhedrin protein of the virus had been removed. The field data obtained with this virus showed that it did not persist in the environment, neither in soil, nor on vegetation, nor in the corpses of caterpillars. The third and fourth releases were undertaken in 1988. For one of these studies the marked, polyhedrin-negative virus was again used. In the other study a polyhedrin-negative virus that contained a junk' (/?-galactosidase) gene was employed.     

Use of insect antifeedants against aphid vectors of plant virus disease

The probing and feeding behaviour of aphids can result in uptake of viruses from infected plants and subsequent transmission to healthy plants. It is possible to interfere with virus acquisition and transmission by influencing aphid host-selection and feeding behaviour with antifeedant chemicals. Published work is reviewed and new work is presented in this paper. The two most successful classes of antifeedants against aphids are (a) compounds derived from the aphid alarm pheromone and (b) plant-derived antifeedants such as the sesquiterpene (-)-polygodial. Results with these and other compounds are discussed in terms of antifeedant activity against Myzus persicae, their effects on resistant aphids and the evidence for dec?ease in virus spread by aphids in laboratory and field.     

Baculoviruses as vectors for foreign gene expression in insect cells

Recombinant DNA technology has enabled the expression of a large number of eukaryotic genes in vitro. There has been growing interest in recent years in the development of baculovirus expression vectors as an easily manipulated gene expression system. Both virus and insect cell culture are relatively easy to handle, and biologically active proteins have been produced abundantly from a variety of eukaryotic, prokaryotic and viral genes. This review describes the molecular biology of baculoviruses and some of the current applications of the baculovirus expression system in insect cells. Specific emphasis is placed on those features relevant to the use of this system in pesticide research.     

The kinetics of insecticide action. Part IV: the in-vivo distribution of pyrethroid insecticides during insect poisoning

The distribution of pyrethroids in insects has been studied using a combination of mathematical modelling and experimental observation. This approach has resulted in the formulation of a physiological model of the pharmaco-kinetics of cypermethrin applied topically to larvae of Spodoptera littoralis. Development of this model from simpler two- and three-compartment models is described. Simple models, whilst capable of complex behaviour, consider only the average rates and magnitudes of pharmaco-kinetic processes over whole animals, and cannot account for differences in concentration of insecticide between individual tissues. This can be achieved by using physiological models, but these require more experimental information for their validation. Moreover, unless simplifying assumptions are made, analytical solutions are not feasible for the large number of equations necessary to define such models. The modelling studies prompted an investigation of (1) in-vivo binding of insecticide to insect tissues, (2) the sizes of body compartments, and (3) the factors which affect the distribution of toxicant between these compartments. Binding has a marked effect on pharmacokinetic profiles and may result in oscillatory behaviour. During poisoning, the total bound cypermethrin increases proportionally to the cube root of the elapsed time. This results in a rapid rate of increase over early elapsed times (< 3h) which slows to approach a more linear form thereafter. Average sizes for the body compartments of larvae of Spodoptera littoralis Boisd, and the steady-state distribution of cypermethrin in these compartments are described. Although the haemolymph, which acts as the main distributive phase during poisoning, forms the largest compartment by volume, it has a low affinity for cypermethrin and distribution reaches steady state within 5 min after topical application. The nerve cord (the target tissue), which is the smallest compartment, has the highest steady-state concentration of cypermethrin. The distribution of cypermethrin in larval tissues is related to the ratios of tissue dry matter to water content.     

Review—mechanism of action of herbicidal and fungicidal compounds on cell membranes

The eukaryotic cell membrane is thought to consist of a mobile bilayer of phospholipid, sometimes intercalated with sterols, in which peripheral and transmembrane proteins are embedded. This provides a model whereby the mode of action of many fungicidal and herbicidal compounds can be rationalised and understood. Some compounds, such as the polyene antibiotics, steroidal saponins and certain phytoalexins, induce membrane malfunction by direct insertion, often complexing with vital components. Others, such as paraquat and the nitrodiphenyl ether herbicides, cause membrane damage by inducing lipid peroxidations. Furthermore, there are many compounds, including the sterol-biosynthesis-inhibiting fungicides and the aryloxyphenoxypropionate and cyclohexanedione herbicides, which interfere with the biosynthesis of membrane components. Because membrane structure is fundamentally similar in eukaryotes, it is important to discover the reasons for any differential toxicity displayed by these compounds and, if necessary, to find ways of optimising desirable patterns of selectivity.     

Studies into the action of the diphenyl ether herbicides acifluorfen and oxyfluorfen. Part I: Activation by light and oxygen in leaf tissue

The effect of acifluorfen and oxyfluorfen on chlorophyll bleaching, lipid peroxidation and photosynthesis in pea leaf discs was studied. Both her- bicides induced light-dependent bleaching and lipid peroxidation, the level of damage being greater at higher light intensities. Photosynthetic carbon dioxide fixation was only partially inhibited in treated leaf discs incubated in darkness, thus indicating that these herbicides did not inhibit photo- synthesis as a primary mode of action. Leaf discs maintained in darkness showed no visible signs of injury, and light-dependent herbicide-induced damage was reduced by incubating discs under nitrogen, orpre-incubating them with the electron-transport inhibitor monuron. It is suggested that acifluorfen and oxyfluorfen are activated by a light-dependent process, which requires photosynthetic electron transport.     

Permethrin treatments in canadian forests. Part 1: Impact on stream fish

The effects of permethrin on native and caged fish when aerially applied directly to forest streams at dosages between 8.8 and 70 g ha^?1 were studied between 1976 and 1981. None of the applications caused mortality of caged or native fish in streams. Trout and salmon diets were altered by the treatments due to effects on fish food organisms. The duration of the effects varied from several months to over a year with increasing dosage. Reductions in salmonid growth rates and reductions in fish densities in treated areas, presumably due to emigration, were documented following severe impacts on aquatic invertebrates in salmon nursery streams. Growth rates and population densities both recovered within four months after treatment.