Governing evolution: A socioecological comparison of resistance management for insecticidal transgenic Bt crops among four countries.

Cooperative management of pest susceptibility to transgenic Bacillus thuringiensis (Bt) crops is pursued worldwide in a variety of forms and to varying degrees of success depending on context. We examine this context using a comparative socioecological analysis of resistance management in Australia, Brazil, India, and the United States. We find that a shared understanding of resistance risks among government regulators, growers, and other actors is critical for effective governance. Furthermore, monitoring of grower compliance with resistance management requirements, surveillance of resistance, and mechanisms to support rapid implementation of remedial actions are essential to achieve desirable outcomes. Mandated resistance management measures, strong coordination between actors, and direct linkages between the group that appraises resistance risks and growers also appear to enhance prospects for effective governance. Our analysis highlights factors that could improve current governance systems and inform other initiatives to conserve susceptibility as a contribution to the cause of public good.

Toxicity and Cross-Resistance of Insecticides to Cry2Ab-Resistant and Cry2Ab-Susceptible Helicoverpa armigera and Helicoverpa punctigera (Lepidoptera: Noctuidae).

Since 2004-2005 cotton expressing Cry1Ac and Cry2Ab insecticidal proteins from the bacterium Bacillus thuringiensis has been commercially available in Australia to manage the target pests Helicoverpa armigera (Hübner) and Helicoverpa punctigera (Wallengren). In both target species, the frequency of alleles conferring resistance to Cry2Ab is unexpectedly high in field populations. A significant challenge for managing these pests would occur if resistance to Cry2Ab toxins inadvertently selected for resistance to other insecticides used to control them. Dose-response bioassays were performed to measure the toxicity of currently registered insecticide sprays on isogenic strains of Cry2Ab-resistant and Cry2Ab-susceptible H. armigera and H. punctigera. Within-species comparisons of Cry2Ab-resistant and Cry2Ab-susceptible strains of H. armigera and H. punctigera indicate no cross-resistance with pyrethroid insecticides. Additionally, Cry2Ab-resistant strains were not cross-resistant to the following selective insecticides: indoxacarb, chlorantraniliprole, and avermectins. In both H. armigera and H. punctigera, Cry2Ab-resistant colonies exhibited a small, but significant, degree of enhanced susceptibility in response to chlorpyrifos and methomyl. We report higher tolerance to conventional insecticides in H. armigera compared with H. punctigera. Our results indicate that there is no significant interplay between Cry2Ab resistance frequencies in H. armigera and H. punctigera and frequencies of resistance to a range of insecticide sprays currently registered for cotton. Therefore, we conclude that any increases in frequencies of the common Cry2Ab resistance phenotypes identified in Australian populations of Helicoverpa spp. are unlikely to increase resistance risk for the indoxacarb, chlorantraniliprole, or avermectin classes of insecticide.

Vip3A resistance alleles exist at high levels in Australian targets before release of cotton expressing this toxin.

Crops engineered to produce insecticidal crystal (Cry) proteins from the soil bacterium Bacillus thuringiensis (Bt) have revolutionised pest control in agriculture. However field-level resistance to Bt has developed in some targets. Utilising novel vegetative insecticidal proteins (Vips), also derived from Bt but genetically distinct from Cry toxins, is a possible solution that biotechnical companies intend to employ. Using data collected over two seasons we determined that, before deployment of Vip-expressing plants in Australia, resistance alleles exist in key targets as polymorphisms at frequencies of 0.027 (n = 273 lines, 95% CI = 0.019-0.038) in H. armigera and 0.008 (n = 248 lines, 0.004-0.015) in H. punctigera. These frequencies are above mutation rates normally encountered. Homozygous resistant neonates survived doses of Vip3A higher than those estimated in field-grown plants. Fortunately the resistance is largely, if not completely, recessive and does not confer resistance to the Bt toxins Cry1Ac or Cry2Ab already deployed in cotton crops. These later characteristics are favourable for resistance management; however the robustness of Vip3A inclusive varieties will depend on resistance frequencies to the Cry toxins when it is released (anticipated 2016) and the efficacy of Vip3A throughout the season. It is appropriate to pre-emptively screen key targets of Bt crops elsewhere, especially those such as H. zea in the USA, which is not only closely related to H. armigera but also will be exposed to Vip in several varieties of cotton and corn.

Do incubation-induced changes in a lizard's phenotype influence its vulnerability to predators?

Strong evidence affirms that incubation temperatures can influence the phenotype of hatchling reptiles, but few studies have examined the fitness consequences of such modifications. Vulnerability to predation is one plausible way that phenotypic shifts could affect an organism's fitness. We incubated the eggs of three sympatric lizard species at temperatures similar to the thermal extremes of natural nests, and measured several traits that are likely to influence a hatchling's susceptibility to a natural (snake) predator. We also examined the lizards' actual vulnerability to snake predators in direct encounters in the laboratory. Our results show that incubation temperature can affect an individual's date of hatching, morphology, locomotor performance, chemosensory responses to snake scent, and ability to avoid a snake predator during staged laboratory encounters. Incubation temperature did not modify the hatchling's `attractiveness' to snakes (as measured via chemical cues) or its antipredator tactics (propensity to escape predation through fleeing or caudal autotomy). The magnitude and direction of incubation- induced phenotypic shifts varied among the three species (even those with similar life histories, thermoregulatory preferences, and microhabitat requirements), and depended on body temperatures and hatchling age. We conclude that incubation-induced modifications to a lizard's phenotype affect a suite of traits that are likely to influence its vulnerability, and also its actual ability to escape from a predator. This result suggests that incubation regimes can influence organismal fitness via their effects on predator-prey interactions.

Can pregnant lizards adjust their offspring phenotypes to environmental conditions?

We exposed females of a highly placentotrophic viviparous scincid lizard (Pseudemoia pagenstecheri) to various environmental factors during pregnancy, and quantified the effects of these treatments on their offspring. The clear result was that the phenotypes of neonatal lizards can be substantially modified by the environment that their mother experiences during gestation. Restricting prey availability to the females reduced the size of their offspring. Limiting the females' basking opportunities delayed their seasonal timing of parturition, and modified body proportions (tail length relative to snout-vent length) of the neonates. More surprisingly, female lizards that were regularly exposed to the scent of sympatric lizard-eating snakes gave birth to offspring that were heavier, had unusually long tails relative to body length, and were highly sensitive to the odour of those snakes (as measured by tongue-flick responses). The neonates' antipredator responses were also modified by the experimental treatment to which their mother was exposed. The modifications in body mass, tail length and response to snake scent plausibly reduce the offspring's vulnerability to predatory snakes, and hence may constitute adaptive maternal manipulations of the neonatal phenotype.