Solanum tarnii, a wild diploid, tuber-bearing Mexican species belonging to the series Pinnatisecta is highly resistant to Potato virus Y (PVY) and Colorado potato beetle and shows a strong hypersensitive reaction to Phytophthora infestans. Therefore, it could be a potential source of resistance to pathogens for potato breeders. S. tarnii (2n=2x=24) is reproductively isolated from tetraploid Solanum tuberosum and hence difficult to include in potato breeding programmes. In this study, interspecific somatic hybrids were produced for the first time by protoplast electrofusion of the cells of potato cv. Delikat (Solanum tuberosum L.) and Solanum tarnii. The hybrid nature of the regenerants was confirmed by simple sequence repeat (SSR) and amplified fragment length polymorphism (AFLP) markers and by morphological analysis and flow cytometry. Selected somatic hybrids were successfully backcrossed with cv. Delikat. Parental lines, primary somatic hybrids and BC1 progeny were assessed for resistance to PVY by mechanical inoculation, grafting and exposure to viruliferous aphid vectors in the field, and resistance to late blight (P. infestans) by detached leaflet and whole tuber tests. The somatic hybrids showed no symptoms of viral infection and most of them displayed high levels of resistance to foliage blight. The BC1 progenies were highly resistant to PVY and a few were resistant to foliage blight. Selected hybrids and BC1 clones were evaluated in the field for tuber quality and tuber yield. Some BC1 clones produced yields of good quality tubers. The results confirm that both the resistance to PVY and to late blight of S. tarnii is expressed in somatic hybrids, and PVY resistance is transferred to BC1 progeny, whereas blight resistance is harder to transfer. Somatic hybridization again proved to be a valuable tool for producing pre-breeding material with increased genetic diversity.

The two subspecies of the host‐alternating black bean aphid, Aphis fabae Scopoli, used in this study have different secondary host plants but reproduce sexually in autumn on the same host plant, spindle, Euonymus europaea L. In both Aphis fabae fabae Scopoli and A. f. solanella Theobald the percentage of adult mating females (oviparae) calling (releasing sex pheromone) each day increased with age up to day 8. During the course of a day the mating females of A. f. solanella called most actively early in the morning and then showed a gradual decrease in calling activity. In contrast, few A. f. fabae called early in the day and were most active around midday, after which the incidence of calling decreased slightly, with 50% still calling in the evening. In both taxa the activity of the males in the absence of mating females paralleled the calling activity of their respective females. In an olfactometer, males showed a marked preference for the sex pheromone released by conspecific females over that of the other subspecies and did not respond to the odour of spindle. Thus, as in the other species of aphids there are specific mate recognition systems in A. f. fabae and A. f. solanella, which are likely to reduce the incidence of hybridisation.

The resistance of oilseed rape pollen beetles to lambda‐cyhalothrin has increased in Germany over the period 2002 to 2007. Oilseed rape pollen beetles are very good at dispersing, therefore field results should always be compared with those of laboratory experiments. The response of oilseed rape pollen beetles to active substances may not be the same as that to formulated products. Bioassays in which beetles are exposed to insecticides on either complete inflorescences or flower buds give different results. It is evident that samples of the genus Meligethes collected in the field can include several different species. Monitoring for insecticide resistance should be done using only the true oilseed rape pollen beetle.

From 2005 to 2015, Ostrinia nubilalis were collected in the most important maizegrowing areas in Europe where MON 810 was cultivated. The susceptibility of these O. nubilalis collections to the Cry1Ab protein was determined using overlay bioassays and compared to that of reference (control) strains. Larvae that died or did not moult K E Y W O R D SCry1Ab protein, diagnostic concentration, European corn borer, moulting inhibition concentration

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