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The addition of a novel host plant to a phytophagous insect's diet may result in subsequent host-plant specialisation, and is believed to be a key cause for speciation in this trophic group. In northern Britain, the tephritid fly Tephritis conura has experienced a unique host-plant expansion, from the melancholy thistle Cirsium heterophyllum to the marsh thistle C. palustre. Here, we examine whether the incorporation of C. palustre in the repertoire of British T. conura flies has caused genetic divergence between populations infesting the old host and the novel host, and how British populations differ from populations infesting C. heterophyllum in continental Europe where C. palustre is not infested. No evidence for restricted gene flow among British C. palustre and C. heterophyllum flies was found. Significant differentiation between British and continental T. conura was found at only one allozyme locus, hexokinase, and caused by a new allele, Hex_95. Hexokinase is related to host-race formation in continental European flies infesting C. heterophyllum and C. oleraceum, and might be linked to loci determining host choice. Based on morphological and phenological data from previous studies, we suggest that T. conura in Britain has adapted to the novel host but that host-race formation is impeded by similar plant phenologies.

The thistle-infesting fruit fly Tephritis conura Loew (Diptera: Tephritidae) forms host races on the melancholy thistle, Cirsium hetewphyllum (L.) Hill (Asterales: Asteraceae) and the cabbage thistle, Cirsium olemceum (L.). Scop. Previous research indicates that the host shift occurred from C. hetewphyllum to C. oleraceum. In this paper we address whether the host shift involved physiological adaptations by studying oviposition acceptance and survival of the two host races on the derived host C. oleraceum. Performance differed significantly between host races. T. conura originating from C. oleraceum produced adults in 75% of all egg-laying trials in contrast to only 6.6% in T. conura originating from C. hetewphyllum. Population fitness components measured as a function of life-stage was linear decreasing for T. conura on C. oleraceum but stepwise for T. conura on C. heterophyllum. Low performance of T. conura on C. hetewphyllum was determined by low plant acceptance and high mortality during the larval stage, whereas hatching (at least one larva per batch) and pupae survival were not affected.

The present study investigates morphological differentiation among host races of the fruit fly Te phritis conura Loew (Diptera: Tephritidae) for two fitness-related traits and whether these traits are host induced or genetically determined. Flies were analyzed from independent sympatric regions, and from one syntopic site where parental host plants [ Cirsium heterophyllum (L.) Hill. and Cirsium oleraceum (L.) Scop. (Cardueae)] and hybrid plants ( C. heterophyllum × C. oleraceum ) co-occur. As both host races may oviposit on hybrid plants and hybrid plants provide an identical environment for larvae of both host races, flies emerging from C. heterophyllum × C. oleraceum hybrids were used to assess whether host-race morphological differences are genetically determined or due to phenotypic plasticity. No significant size (wing length) differences were found among host races, whereas flies emerging from C. heterophyllum had on average 8.4% longer ovipositors than flies emerging from C. oleraceum. The mean size-corrected ovipositor length (i.e., the ratio ovipositor/wing length) was 10.3% longer. These proportions were repeated among host races emerging from hybrid plants. Although flies of the C. heterophyllum host race from hybrid plants were smaller than on parental host plants, the ratio ovipositor/wing length was constant. Hybrid flies (which emerged only on hybrid plants) were intermediate in relative and absolute ovipositor length. Thus, ovipositor-length differences among T. conura host races most likely have a genetic basis. This suggests that host-related differences in ovipositor length reflect adaptations to the respective host-plant species, most likely to the host’s flower-head size, whereas both host races experience similar selection regimes on body size.

The fruit fly Tephritis bardanae infests flower heads of two burdock hosts, Arctium tomentosum and A. minus. Observations suggest host-associated mating and behavioural differences at oviposition indicating host-race status. Previously, flies from each host plant were found to differ slightly in allozyme allele frequencies, but these differences could as well be explained by geographical separation of host plants. In the present study, we explicitly test whether genetic and morphological variance among T. bardanae are explained best by host-plant association or by geographical location, and if this pattern is stable over a 10-year period. Populations of A. tomentosum flies differed significantly from those of A. minus flies in (i) allozyme allele frequencies at the loci Pep-A and Pgd, (ii) mtDNA haplotype frequencies and (iii) wing size. In contrast, geographical location had no significant influence on the variance estimates. While it remains uncertain whether morphometric differentiation reflects genotypic variability or phenotypic plasticity, allozyme and mtDNA differentiation is genetically determined. This provides strong evidence for host-race formation in T. bardanae. However, the levels of differentiation are relatively low indicating that the system is in an early stage of divergence. This might be due to a lack of time (i.e. the host shift occurred recently) or due to relatively high gene flow preventing much differentiation at loci not experiencing selection.