DNA-based techniques are providing valuable new approaches to tracking predator-prey interactions. The gut contents of invertebrate predators can be analysed using species-specific primers to amplify prey DNA to confirm trophic links. The problem is that each predator needs to be analysed with primers for the tens of potential prey available at a field site, even though the mean number of species detected in each gut may be as few as one or two. Conducting all these PCRs (polymerase chain reactions) is a lengthy process, and effectively precludes the analysis of the hundreds of predators that might be required for a meaningful ecological study. We report a rapid, more sensitive and practical approach. Multiplex PCRs, incorporating fluorescent markers, were found to be effective at amplifying degraded DNA from predators' guts and could amplify mitochondrial DNA fragments from 10+ species simultaneously without 'drop outs'. The combined PCR products were then separated by size on polyacrylamide gels on an ABI377 sequencer. New primers to detect the remains of aphids, earthworms, weevils and molluscs in the guts of carabid predators were developed and characterized. The multiplex-sequencer approach was then applied to field-caught beetles, some of which contained DNA from as many as four different prey at once. The main prey detected in the beetles proved to be earthworms and molluscs, although aphids and weevils were also consumed. The potential of this system for use in food-web research is discussed.

Summary1. An explicitly spatial sampling approach was employed to test the null hypothesis that the predation on slugs by the carabid beetle Pterostichus melanarius (Illiger) was opportunistic. 2. The beetles and slugs were sampled across a nested series of grids of sampling points, in a ®eld of winter wheat during June and July 1997. 3. The spatial distribution of all slugs in June was found to change with the scale of the sampling grid, from random on the 0.25 m scale, through aggregation at 1 m, to random at 4 m. At the highest scale of 16 m, the slugs were signi®cantly spatially aggregated. 4. The distribution of beetles in June was also spatially dynamic, with randomness observed at the 4 m and 8 m scales. At 16 m, signi®cant aggregation was observed. 5. The dynamic distributions of slugs and beetles, at 16 m, were found not to be associated with, and thus were not determined by, soil or crop factors. 6. Comparison of slug and beetle populations showed, however, that the distributions at 16 m were dynamically associated with each other. In June where there were many slugs there were also many carabids, whilst in July where there were many carabids there were few slugs. 7. Approximately 11% of the beetles sampled across the 16 m grid in June and July were found to have ingested slug protein, following intensive enzyme-linked immunosorbent assay (ELISA) testing. 8. The spatial distribution of these slug-positive beetles was signi®cantly associated with the distribution of the larger slug classes, over 25 mg. Where there were many large slugs in June there were many slug-positive beetles. Conversely, in July few large slugs were found where there were many slug-positive beetles. 9. Parametric analysis revealed that these changes in the large slug class, at each sampling point between June and July (growth), were negatively related to the local numbers of slug-positive beetles, and that growth declined as the local numbers of beetles increased. 10. These ®ndings suggest that predation was not opportunistic, but direct and dynamic, falsifying the null hypothesis. Moreover, this predation elicited signi®cant changes in the spatial distribution and local density of the slugs, in a manner that may be termed spatially density dependent.

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SUMMARYBoth crowding and poor nutrition induce the appearance of emigrants in Rhopalosiphum padi L. No emigrants developed when the aphid was reared in isolation for six successive generations on actively growing leaves of bird cherry. However, emigrants developed as soon as the leaves ceased to grow or when the aphids became crowded.Crowding of mothers and postnatal crowding of the nymphs of apterous exules both influenced the induction of alate exules. The highest proportion of alate exules developed when both mother and offspring were crowded.Short day‐length induced the appearance of gynoparae and males. For 50% production of gynoparae and males, over the range of temperature 10–18d̀C, a 1.75 h reduction in day‐length is required for every 4d̀ increase in temperature. At 18 d̀C, even at day‐lengths as short as 6 h, exposure for three generations is required before all offspring become gynoparae or males. Low temperature and short day‐length was ineffective in inducing the development of gynoparae or males in the first three generations developing from the fundatrix.

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