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Aim  The use of host‐specific biological control agents is widely considered an effective option for the management of invasive alien plant species. However, the formation of novel associations between released biological control agents and indigenous species poses risks. Here, we investigate whether native food webs associated with two galling biological control agents on Acacia longifolia and A. saligna are similar to those found in their introduced range. Location  Gall inhabitants recorded from South Africa and Australia. Methods  Non‐targeted insects were collected from galls in introduced ranges for comparisons to that of the agents’ native ranges. Results  We find that two host plant‐specific galling biological control agents accumulate food web links with higher trophic levels in their introduced range that are similar in number, taxonomic/phylogenetic pattern and guild composition to those in their native range. Bray‐Curtis percentage similarity between native (Australia) and novel (South Africa) food webs was 30–50% and 50–75% at the family and superfamily taxonomic level, respectively, and 45–50% if considering shared phylogenetic diversity. Main conclusions  Trichilogaster acaciaelongifoliae and Uromycladium tepperianum accumulated food webs in South Africa that are strikingly similar in complexity and structure to those that occur in their native ranges. This indicates that the structure of food webs in the introduced range could be predicted by studying food webs in the native range of a biological control agent, potentially paving the way for more effective risk assessment of weed biological control.

The woolly apple aphid Eriosoma lanigerum (Hausmann) is one of the most damaging apple pests in South Africa. Information on its genetic diversity is lacking and this study, in which the genetic structure of parthenogenetic E. lanigerum populations was characterized in the Western Cape Province of South Africa, represents the first local study of its kind. A total of 192 individuals from four different regions were collected and analysed using amplified fragment length polymorphism (AFLP). Using five selective AFLP primer pairs, 250 fragments were scored for analysis. Results indicated that a low level of genetic variation was apparent in E. lanigerum populations in the Western Cape (H = 0.0192). Furthermore, populations collected from geographically distant regions were very closely related, which can partly be explained by the fact that agricultural practices were responsible for dissemination of populations from a common ancestor to geographically distant areas. The low level of variation found indicated that the possibility of controlling E. lanigerum in the Western Cape using host plant resistance is favourable. This is the first report of AFLP being used to characterize the genetic structure of an aphid species. Results indicate that this marker may be useful for analysis of other aphid species.

Correct species identification is critical when dipteran larvae are used for inference of the postmortem interval. To facilitate DNA-based identification of forensically important flies of the genus Lucilia in the continental United States, we develop a vouchered reference collection and DNA sequence database. A total of 122 specimens were collected for nine of the 10 species of Lucilia reported to occur in the continental United States. Using the polymerase chain reaction and DNA sequencing, data were obtained for an 1100-bp region of the mitochondrial gene encoding cytochrome oxidase I (COI). We consider a species suitable for DNA-based identification if it is exclusively monophyletic in >95% of bootstrap pseudoreplicate phylogenetic analyses. Seven of the nine species meet that criterion. Two species (Lucilia coeruleiviridis and Lucilia mexicana) share COI sequence and cannot be distinguished using our reference database. We conclude that DNA-based identification is likely to be successful for the other seven species.