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BACKGROUND: The green peach aphid, Myzus persicae (Sulzer), is one of the most economically important crop pests worldwide. Insecticide resistance in this pest was first detected over 60 years ago, with resistance in M. persicae now spanning over 80 active ingredients. Sulfoxaflor is a relatively new insecticide that is primarily used to control sap‐feeding insects. In 2018 resistance to sulfoxaflor was discovered in field populations of M. persicae in Australia. This study aimed to determine the current distribution and phenotypic levels of sulfoxaflor resistance in Australian clones of M. persicae and to investigate how these patterns relate to clonal type. RESULTS: For the first time, we show there is low‐level resistance (8–26‐fold) distributed across Australia, with resistance being detected in aphids collected from approximately 20% of all M. persicae collected and screened. Furthermore, this study shows sulfoxaflor resistance is found in two M. persicae haplotypes, providing evidence that there have been multiple independent evolutionary events which have given rise to sulfoxaflor resistance in this species. CONCLUSION: These findings have important implications for the chemical control of M. persicae in Australia, especially when considering the broader genetic background of these aphids which are known to harbour a number of other insecticide resistance mechanisms. We recommend continuous monitoring of sulfoxaflor resistance in field populations of M. persicae (in Australia and elsewhere) and further research into the underlying genetic mechanisms conferring resistance to sulfoxaflor in both clonal haplotypes. © 2023 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Context. Invasive mammalian predators are a threat to biodiversity and agriculture globally, yet management outcomes for lethal predator control remain difficult to monitor and evaluate. Understanding whether changes in activity indices correspond to true changes in population density will help inform effective monitoring and management programs. Aims. The aim of this study was to evaluate the effect of poison baiting on invasive red fox (Vulpes vulpes) populations using two alternative population metrics: fox activity from camera trap surveys and density estimation from scat genetic analysis. Methods. We conducted before–after control–impact studies in two regions of semi-arid Australia (Wimmera and Mallee) by monitoring paired nontreatment and treatment sites during unbaited and baited periods. We estimated the effects of poison baiting on: (1) a monthly fox activity index, derived from an array of 10 off-road camera traps per site; and (2) fox density. To estimate density, we collected fox scats along 14-km transects, identified individuals using polymorphic microsatellite DNA markers and fitted spatially explicit capture–recapture models. Key results. Fox activity remained consistently low at all sites except the Mallee non-treatment. The top-ranked models of fox activity and density contained an interaction between treatment and period, with an interactive and additive effect of region, respectively. However, there was little evidence that baiting reduced fox activity or density. In the unbaited period, fox densitiesranged from 0.69 (95% CI: 0.47–1.0) to 1.06 (95% CI: 0.74–1.51) foxes km−2 and were similar across regions. Conclusions. Camera traps have the potential to provide continuous index-based measures of fox populations but may not record sufficient observations to detect change. Indices can also be confounded by variations in animal behaviour. Scat genetic analysis is a viable option for providing direct estimates of population change at specific snapshots in time; however, this approach is considerably more expensive, and large sample sizes may be required if genotyping successislow. Implications. Ourstudy presents a rare example of multiple concurrent – and non-invasive – monitoring techniques to evaluate the effectiveness of predator control. We highlight the value of rigorous study designs and high-quality density information for designing predator management and monitoring programs. [ABSTRACT FROM AUTHOR]

Biological invasions are increasing globally in number and extent despite efforts to restrict their spread. Knowledge of incursion pathways is necessary to prevent new invasions and to design effective biosecurity protocols at source and recipient locations. This study uses genome‐wide single nucleotide polymorphisms (SNPs) to determine the origin of 115 incursive Aedes aegypti(yellow fever mosquito) detected at international ports in Australia and New Zealand. We also genotyped mosquitoes at three point mutations in the voltage‐sensitive sodium channel (Vssc) gene: V1016G, F1534C and S989P. These mutations confer knockdown resistance to synthetic pyrethroid insecticides, widely used for controlling invertebrate pests. We first delineated reference populations using Ae. aegypti sampled from 15 locations in Asia, South America, Australia and the Pacific Islands. Incursives were assigned to these populations using discriminant analysis of principal components (DAPC) and an assignment test with a support vector machine predictive model. Bali, Indonesia, was the most common origin of Ae. aegypti detected in Australia, while Ae. aegypti detected in New Zealand originated from Pacific Islands such as Fiji. Most incursives had the same allelic genotype across the three Vsscgene point mutations, which confers strong resistance to synthetic pyrethroids, the only insecticide class used in current, widely implemented aircraft disinsection protocols endorsed by the World Health Organization (WHO). Additionally, all internationally assigned Ae. aegypti had Vssc point mutations linked to pyrethroid resistance that are not found in Australian populations. These findings demonstrate that protocols for preventing introductions of invertebrates must consider insecticide resistance, and highlight the usefulness of genomic data sets for managing global biosecurity objectives. [ABSTRACT FROM AUTHOR]

Abstract: Environmental DNA (eDNA) sampling is a promising tool for monitoring cryptic species. Numerous studies have demonstrated that eDNA sampling can achieve higher detection rates than traditional monitoring techniques, such as trapping; however, the consequences of that sensitivity for survey design requirements and resulting survey costs have not been investigated. We demonstrate how site occupancy detection models and optimal survey design methods can be used to evaluate the cost‐efficiency of eDNA sampling vs. traditional survey methods. We apply these approaches to two datasets—one in which eDNA sampling and trapping were conducted simultaneously (paired dataset), and another in which sampling methods were independently deployed (unpaired dataset)—to assess the cost‐efficiency of eDNA sampling for detecting a freshwater mammal: the platypus Ornithorhynchus anatinus. Conditional probabilities of platypus eDNA being captured in a single water sample (paired dataset: 0.838, unpaired: 0.879), and detected in a single water sample by qPCR (paired: 0.892, unpaired: 0.858), were higher than the conditional probability of detecting a platypus with a single trapping visit (paired: 0.470, unpaired: 0.219). eDNA sampling was more cost‐efficient than trapping, regardless of whether the management objective was to (1) minimize the survey budget needed to achieve a particular asymptotic variance of the occupancy estimator, or (2) minimize the survey budget needed to detect a change in occupancy over time. Site occupancy detection models coupled with optimal survey design methods provide a powerful means with which to compare the sensitivity and cost‐efficiency of eDNA sampling vs. traditional sampling methods. [ABSTRACT FROM AUTHOR]

Abstract: Parthenogenetic reproduction is taxonomically widespread and occurs through various cytological mechanisms, which have different impact on the genetic variation of the offspring. Extatosoma tiaratum is a facultatively parthenogenetic Australian insect (Phasmatodea), in which females oviposit continuously throughout their adult lifespan irrespective of mating. Fertilized eggs produce sons and daughters through sexual reproduction and unfertilized eggs produce female offspring via parthenogenesis. Here, we developed novel microsatellite markers for E. tiaratum and characterized them by genotyping individuals from a natural population. We then used the microsatellite markers to infer the cytological mechanism of parthenogenesis in this species. We found evidence suggesting parthenogenesis in E. tiaratum occurs through automixis with terminal fusion, resulting in substantial loss of microsatellite heterozygosity in the offspring. Loss of microsatellite heterozygosity may be associated with loss of heterozygosity in fitness related loci. The mechanism of parthenogenetic reproduction can therefore affect fitness outcomes and needs to be considered when comparing costs and benefits of sex versus parthenogenesis. [ABSTRACT FROM AUTHOR]