The spatio‐temporal dynamics of two aphid species (Metopolophium dirhodum and Sitobion avenae) and a generalist predator (Pterostichus melanarius) were observed in a field‐scale study using a grid of 256 sampling locations with a 12‐m spacing. Using Spatial Analysis by Distance Indices we demonstrate that populations show ephemeral spatial pattern at the field scale. We observed a positive, lagged beetle response to this aphid pattern; conversely, the aphids displayed a negative, lagged response to beetle spatial pattern. Examination of the local structure of the spatio‐temporal dynamics revealed a strong response by the beetle population to aphid patches. The temporal structure of spatial associations between the species shows a strong correspondence with those from a conceptual model of predator–prey spatial interaction. The spatially coupled dynamics were sufficiently strong for the predator to have a negative effect on the intrinsic rate of increase of their prey.

Background: Dispersal plays a key role in shaping biological and ecological processes such as the distribution of spatially-structured populations or the pace and scale of invasion. Here we have studied the relationship between long-distance dispersal behaviour of a pest-controlling money spider, Erigone atra, and the distribution of maternally acquired endosymbionts within the wider meta-population. This spider persists in heterogeneous environments because of its ability to recolonise areas through active long-distance airborne dispersal using silk as a sail, in a process termed 'ballooning'.

Summary1. The spatial distribution of cereal aphids infesting a field of winter wheat during the population establishment, development and decline phases were studied using a field-scale grid of sampling locations. 2. The distribution of two generalist predators, Pterostichus melanarius and P. madidus , were sampled contemporaneously. 3. Using spatial analysis by distance indices (SADIE), spatial pattern in the aphid population, predator activity-density, predator hunger and aphid predation was detected and mapped. 4. We tested the hypothesis that carabids and aphids were spatially associated with one another through predation. Aphid predation by individual beetles was detected using enzyme-linked immunosorbent assays (ELISA) and hunger was assessed by measurement of foregut weights. 5. Initially, there was a strong spatial dissociation between aphids and P. melanarius activity-density. While the aphid population was increasing there was a strong spatial association between aphids and both P. melanarius and P. madidus activity-density. During aphid population decline there was no measurable association between aphids and predatory activity-density. 6. Predation of aphids was strongly locally associated with predator activity-density on all sample dates for both predator species, regardless of the association with aphid spatial pattern. 7. Areas within the field most isolated from P. melanarius predation had the highest rates of aphid population increase. 8. Although the proportion of P. melanarius individuals consuming aphids was much lower compared to P. madidus , it was concluded that it was a more effective biological control agent due to its comparative abundance.

In crop protection and ecology accurate and precise estimates of insect populations are required for many purposes. The spatial pattern of the organism sampled, in relation to the sampling scheme adopted, affects the difference between the actual and estimated population density, the bias, and the variability of that estimate, the precision. Field monitoring schemes usually adopt time-effi cient sampling regimes involving contiguous units rather than the most effi cient for estimation, the completely random sample. This paper uses spatially-explicit ecological fi eld data on aphids and beetles to compare common sampling regimes. The random sample was the most accurate method and often the most precise; of the contiguous schemes the line transect was superior to more compact arrangements such as a square block. Bias depended on the relationship between the size and shape of the group of units comprising the sample and the dominant cluster size underlying the spatial pattern. Existing knowledge of spatial pattern to inform the choice of sampling scheme may provide considerable improvements in accuracy. It is recommended to use line transects longer than the grain of the spatial pattern, where grain is defi ned as the average dimension of clusters over both patches and gaps, and with length at least twice the dominant cluster size.

The distribution of aphid predators within arable fields has been previously examined using pitfall traps. With this technique predominantly larger invertebrate species are captured, especially Carabidae, but the technique provides no estimate of density unless mark-recapture is used. However, many other numerically important aphid predators occur in arable fields and relatively little is known about their distribution patterns nor whether they exhibit a density-dependent response to patches of cereal aphids. Identification of the most effective predators can allow management practices to be developed accordingly. In this study, the distribution of cereal aphids and their predators was examined by suction sampling within a field of winter wheat in Devon, UK, along with visual estimates of weed patchiness. Sampling was conducted on four occasions in 1999 across a grid of 128 sample locations. The distribution of 11 predatory taxa from the Carabidae, Staphylinidae and Linyphiidae was examined. Additionally, the total number of aphid predators and a predation index were used in these analyses. Carabid adults and larvae, along with staphylinid larvae showed the strongest aggregation into patches and the most temporal stability in their distribution. Other taxa had more ephemeral distributions as did the cereal aphids. The distribution of carabid larvae was disassociated from the distribution of cereal aphids for the first two sampling occasions indicating biocontrol was occurring. Other predatory groups showed both association and disassociation. Carabid larvae, Bathyphantes and total numbers of Linyphiidae showed a strong correlation with weed cover for two of the sample dates. Cereal aphids were disassociated from weed cover on three sampling occasions.