A significant reduction in age of mating occurred during the first four generations (G1-G4) of laboratory adaptation of wild Bactrocera tryoni (Froggatt) and this was associated with the earlier attainment of peak egg load although no significant differences were detected in the peak egg load itself. A long term laboratory (LTL) strain had a significantly earlier mating age and higher peak egg load than flies of wild origin or those from the first four laboratory generations. The amount of protein consumed by females in the first week of adult life was significantly higher in the LTL strain than in flies of wild origin or G1-G4 but there were no significant changes (or only slight changes) with laboratory adaptation in the amounts of protein consumed up to the ages of mating and peak egg load. Laboratory adaptation resulted in no significant changes in egg size, egg dry weight, puparial fresh weight and the dry weight of newly emerged females. The large increase in fecundity with laboratory adaptation is associated with a 4- to 5-fold increase in the rate of conversion of dietary protein to eggs (i.e. eggs produced per mg of protein consumed).

No abstract

Many insects have coevolved with certain angiosperm taxa to act as pollinators. However, the nectar and pollen from such flowers is also widely fed upon by other insects, including entomophagous species. Conservation biological control seeks to maximise the impact of these natural enemies on crop pests by enhancing availability of nectar and pollen-rich plants in agroecosystems. A risk with this approach is that pests may also benefit from the food resource. We show that the flowers of some plants (viz., buckwheat, Fagopyron esculentum Moench and dill, Anethum graveolens L.), and the extrafloral nectaries of faba bean (Vicia faba L.) benefit both Copidosoma koehleri Blanchard (Hymenoptera: Encyrtidae) and its host, the potato pest, Phthorimaea operculella Zeller (Lepidoptera: Gelechiidae). In contrast, phacelia (Phacelia tanacetifolia Benth) and nasturtium (Tropaeoleum majus L.) benefited only the parasitoid. When adult moths of P. operculella were caged with flowers of phacelia or nasturtium, longevity of males and females, egg laying life, fecundity, average oviposition rate, and number of eggs in ovaries at death were no greater than in the control treatment with access to shoots without flowers plus water. All the foregoing measures were increased compared to the control when the moths were allowed access to dill, buckwheat or faba bean extrafloral nectaries. Such 'selectivity' has the potential to make the use of floral resources in conservation biological control more strategic. We present morphometric and observational evidence to illustrate how such mechanisms may operate.

Data were obtained from mark recapture trials pertaining to the dispersal of medfly, Ceratitis capitata (Dipt., Tephritidae), over both short (10-160 m) and very long distances (0.5-9.5 km) within the surveillance trapping array in Adelaide, Australia. They could be related to previously reported data sets by expressing the capture rates of each set in common terms that corrected for differences in recapture rate resulting from type of trap, season or climate. The mean capture rate at each distance from the point of release in each data set was expressed as a percentage of the real or inferred rate of that set at a distance of 100 m. The resulting distribution of dispersal distances conformed to both an inverse power model and a modified Cauchy model regardless of whether the present and previous data were combined or not. The modified Cauchy model inferred that the median distance flown was extremely short and 90% of flies displaced only 400-700 m despite the fact that a consistent trend in declining catch rates was obtained up to 9.5 km. The spread of invading propagules in quarantined zones in the first generation is likely to be limited by a decline to nonviable density within 1 km or less of the incursion point and the spread of larger infestations could be limited by the longevity of the dispersers. The results also have significance to the ability of surveillance trapping arrays to detect infestations and also to methods of distributing insects for the Ôsterile insect techniqueÕ.

Many insects have coevolved with certain angiosperm taxa to act as pollinators. However, the nectar and pollen from such flowers is also widely fed upon by other insects, including entomophagous species. Conservation biological control seeks to maximise the impact of these natural enemies on crop pests by enhancing availability of nectar and pollen-rich plants in agroecosystems. A risk with this approach is that pests may also benefit from the food resource. We show that the flowers of some plants (viz., buckwheat, Fagopyron esculentum Moench and dill, Anethum graveolens L.), and the extrafloral nectaries of faba bean (Vicia faba L.) benefit both Copidosoma koehleri Blanchard (Hymenoptera: Encyrtidae) and its host, the potato pest, Phthorimaea operculella Zeller (Lepidoptera: Gelechiidae). In contrast, phacelia (Phacelia tanacetifolia Benth) and nasturtium (Tropaeoleum majus L.) benefited only the parasitoid. When adult moths of P. operculella were caged with flowers of phacelia or nasturtium, longevity of males and females, egg laying life, fecundity, average oviposition rate, and number of eggs in ovaries at death were no greater than in the control treatment with access to shoots without flowers plus water. All the foregoing measures were increased compared to the control when the moths were allowed access to dill, buckwheat or faba bean extrafloral nectaries. Such 'selectivity' has the potential to make the use of floral resources in conservation biological control more strategic. We present morphometric and observational evidence to illustrate how such mechanisms may operate.

Previous authors have used simple models to investigate the relative importance to population increase of variations in the total and age-specific reproductive rates. But while acknowledging that the latter were the product of the age specific birth and death rates, they have used their models only to investigate changes in total or age-specific birth rates and have not been concerned with variations in death rates. This paper extends the use of Lewontin's (1965) model, to a wide range of values of r, the exponential rate of population increase. It shows how the relative importance of changes in certain life-history features can change with r and be reversed when r is near to zero. It is also shown that variations in mortality rate are not necessarily best expressed in analogous terms to variations in birth rate. If more suitable terms are used it is seen that changes in mortality rate can be of varying importance depending on the existing mortality rate. They can be overwhelmingly important when the mortality rate is high.

Dispersal of immature and sexually mature Queensland fruit fly, Bactrocera tryoni (Froggatt) from releases made at a single point was assessed from recapture rates obtained by using arrays of traps. The recapture data (pertaining to distances up to 480 m) fitted both logarithmic and Cauchy models although the fits for the releases of immature flies were inferior because of high variability in catches at certain distances. When combined with data previously published for longer distances, a Cauchy model fitted data for releases of immature flies well and indicated that the median distance dispersed after emerging from the puparium was ~120 m and that 90% of flies would displace less than 800 m despite the fact that a consistent trend in declining catch rates can be obtained up to at least 85 km. This is consistent with the tail of the Cauchy distribution having a slope congruent with a negative power curve and thus being scale invariant for longer distances. The distribution of recaptured flies that were released as adults also fitted a Cauchy model with a tail of the same slope, suggesting that the spatial distribution of long-distance dispersers is not only scale invariant but also age invariant. This has significance to the ability of surveillance trapping arrays to detect infestations and also to methods of distributing insects for the sterile insect technique. Whereas the spread of invading propagules in the first generation is likely to be limited by a decline to non-viable density within 1 km or less of the incursion point, the influence of larger infestations on nearby uninfested regions would be limited by the longevity of the dispersers.

We examined data from 75 infestations of the Mediterranean fruit fly (Medfly) and 286 of the Queensland fruit fly (Qfly) that have occurred in quarantined and normally fly-free zones in Australia from 1974 to 2000. The radius of occurrence of both adult male flies and infested fruit was almost always less than 1 km. The rare cases where there was an isolated occurrence beyond 1 km of an epicentre were most likely due to (and can be treated as) separate introductions. Our analysis shows that effective quarantine radii for suspension of fly-free status should be related to the number of flies trapped around the epicentre and the density of the trap array (if the appropriate code of practice is applied). Most detections of fruit flies involve the trapping of very few flies and 18% of Medfly infestations and 71% of Qfly infestations that are detected are not classified as outbreaks and are left to die out without any treatment. For each species, we have used 3 alternative methods to calculate confidence limits for infestation radii. The upper limits could also serve as quarantine radii. These limits increase with the rate of trapping of male flies and have a theoretical probability of 3/100 000 (i.e. probit 9) of being exceeded. The quarantine radii for most declared outbreaks, when calculated with any of our methods, would be small because the number of flies detected is usually only just above the threshold for such a declaration. If our methods were used for beneficial species or for re-introductions of endangered species, the lower confidence limits could be used to calculate the size of inoculum required for a high probability of initial establishment.