A number of insect species infest human households and stored foods and products, leading to their designation as pests. Until recently, little was known about the factors driving the evolution of pests that feed on stored dry foods. Here, I review the effects of changes in climate and species interactions on the evolution and ecology of beetles that feed on dried seeds/grains. My review focuses on evidence that the host utilization by part of the species in the subfamily Bruchinae (Chrysomelidae) is a preadaptation for utilizing stored dry seeds and grains, thus leading to their status as a pest. These and other stored product pest beetles retain a higher percentage of water in their body, relative to the water content of their diet, than beetles that feed on fresh crops. I review the studies that have documented adaptation, acclimation and polyphenetic response to high temperatures and desiccation and/or made direct comparisons between these traits between developmental stages, populations and among higher taxonomic groups. Finally, I review evidence for the effects of environmental change on insect host-parasitoid and competitor assemblages.

The agouti (Dasyprocta punctata) meticulously defleshes Astrocaryum standleyanum palm seeds before scatter hoarding. On Barro Colorado Island, Panama, we experimentally tested three hypotheses on how this behaviour could reduce seed predation to the mutual benefit of the tree and the rodent. The first and established hypothesis – that defleshing reduces seed predation by bruchid beetles by intercepting larvae – was rejected. Experiments in which manually defleshed seeds or entire fruits were incubated at different times showed that defleshing reduced bruchid infestation before fruit fall but not after fruit fall. The second hypothesis – that defleshing reduces cache pilferage by making seeds less conspicuous – was supported. An experiment in which intact fruits and manually defleshed seeds were placed in mimicked agouti caches and followed showed that seeds with flesh were pilfered at higher rates than defleshed seeds. The third hypothesis – that defleshing reduces post-dispersal infestation of cached seeds – was rejected. An experiment in which intact fruits and manually defleshed seeds were placed in mammal exclosures and later collected to assess infestation showed that burial reduced seed infestation but defleshing did not. Thus, seed defleshing reduced palm seed predation, but in a different way than previously believed. We also found that (1) bruchid beetles can be pre-dispersal rather than post-dispersal seed predators, (2) seed infestation by scolytid beetles may control bruchid larvae, and (3) scolytids rather than bruchids are the main invertebrate seed predators of this palm.

Development and reproductive success of the solitary egg parasitoid Uscana lariophaga Steffan were examined after development in eggs of the bruchid storage pest Callosobruchus maculatus Fabricius reared at either low or high densities on cowpea seeds and laid at day 1 and 4 of maternal life. Both bruchid larval competition and maternal age negatively affected egg size, but the latter more than the former. Uscana lariophaga reared in small hosts developed slower, were smaller and produced fewer eggs compared to parasitoids reared in large hosts. Fecundity of the parasitoid was heavily influenced by host egg size. This was reflected in the values for the intrinsic rate of increase of U. lariophaga, which differed for wasps that developed in host eggs laid by bruchid females of different age. Wasps allocated marginally more female offspring to larger hosts.

Fruiting phenology, habitat types and proximity to conspecific fruiting adults may influence the degree of escape from pre- and post-dispersal seed predators. Successful predator escape by means of satiation is considered to be especially important for selection of masting and monocarpic reproduction in trees, such as exhibited by Tachigali versicolor, a tropical canopy tree. How pre- and post-dispersal predation rates varied with dispersal timing and among trees in T. versicolor was examined in young and old forests on Barro Colorado Island in Panama during a 4-mo period. Seeds were collected from above-ground traps to assess predispersal predation by bruchid beetles, and from quadrats on the ground to record predation and removal by terrestrial mammals. Proportion of seeds aborted varied greatly among trees (range 6–30 %, mean 16 %), and was especially high for trees on the edge of the island with fruiting conspecifics nearby during the early part of fruiting season. The proportion of seeds killed by bruchid beetles varied less among trees (14–25 %, mean 20 %), and remained constant throughout the fruiting season. Seeds on the ground were attacked mostly by rodents, and possibly by deer (26 % of all seeds and 43 % of intact dispersed seeds). The post-dispersal predation level was higher in the young forest than in the old forest (61 and 26 % of intact dispersed seeds, respectively), and was unaffected by the proximity of fruiting conspecifics. Temporal satiation of seed predators was evident only for post-dispersal mammalian predators in the old forest.

Bruchid beetles cause high losses of stored legumes in the tropics. Chemical control is inappropriate for the small scale farmer and the use of alternative measures should be encouraged. Different biological methods of control such as cultural, physical, varietal, biological, biorational and genetic control are reviewed. Cultural control techniques such as timely and frequent harvesting, legumes planted away from granaries, crop hygiene and storage in pods, are within the technical and financial means of the small scale farmer. The use of inert substances, vegetable oils and repellent plants may be cheap and effective if properly managed. The use of controlled atmosphere, vacuum, heating, cooling and sterilizing, requires relatively advanced techniques. Growth regulators and pheromones are currently not available for control. Varieties resistant to bruchids have been identified, but incorporation of resistance into suitable varieties has proven to be difficult. Biological control of bruchids should receive more attention in particular research on the introduction and conservation of natural enemies. To effectively implement control measures at farmer's level socio-economic and cultural aspects should be taken into account. Proven appropriate techniques should be combined in an overall integrated pest management strategy.

Some aspects of the biology of Callosobruchus subinnotatus (Pic) were investigated at controlled conditions. Temperature and relative humidity were found to have effect on oviposition, development and longevity of adults. The best condition for oviposition was 30°C, 80% r.h. at which the mean number of eggs laid was 135.8 and the worst condition was 35°C, 50% r.h. at which 61.1 eggs were laid per female. Oviposition lasted very long at 25°C and was too short at 35°C. Relative humidity favoured oviposition at 30 and 35 but not at 25°C. The beetles were found to be positively phototactic as more eggs were laid at 12 hr light and 12 hr dark (105.1 eggs) and continuous light (98.6) than at continuous darkness (43.0).

Duration of development was shorter at 35°C than at other temperatures investigated. The shortest developmental period was at 35°C, 80 % r.h. (23.2 days) while longest was at 25°C, 50 % r.h. (42.6 days). While development was shorter at 35°C, more progenies were produced at 30°C and the rate of increase was better enhanced at 30°C. Adults were heavier when reared at lower temperatures and high humidities than at high temperatures and low humidities. Adults lived longer at lower temperatures and high humidities than at higher temperatures and lower humidities. The females were heavier and lived longer than the males.

Females of Bruchidius atrolineatus (Pic) lay their eggs in the fields on maturing or dry pods of their host plant, Vigna unguiculata. Under experimental conditions in the presence of maturing and dry pods connected with the plant, 80% of eggs are laid on maturing pods. The preference for maturing pods is observed in two generations of B. atrolineatus and varies with the age of females. In the presence of pods separated from the plant, 69% of eggs are laid on dry pods. These results show the importance of methodology during insect behavioural studies. In the absence of choice, reproduction of B. atrolineatus females is more stimulated with dry pods than with maturing ones. These experiments show that factors which influence the choice of the pods are probably different from those stimulating oviposition.

Bruchidius atrolineatus (Pic) is present in crops of Vigna unguiculata towards the end of the dry season at the beginning of September when pods start to form. Females lay many eggs on most available green pods. However, this oviposition behaviour results in an important egg mortality. During September, pods gradually reach maturity whilst new pods are formed. Females therefore have at their disposal a growing number of differently mature pods. Confronted with such a situation, B. atrolineatus females show an opportunist behaviour and lay most of their eggs on the most abundant stage, i.e. the most easily discovered stage (ripening green pods in mid-September or dry pods towards the end of September). However, they also lay eggs on other phenological stages no matter how abundant they are. B. atrolineatus females therefore show a certain behavioural plasticity enabling them to reproduce on all stages of pods whose maturity, chemistry and texture may differ. Larvae can develop either in maturing or dry seeds. The number of eggs laid from mid September is lower and lower whatever the phenological stage attacked. This decrease would be due to a reduction of the first generation adult bruchids and of the reproductive potential of females.

Callosobruchus maculatus appears in crops at the same time as B. atrolineatus, but oviposits preferentially on dry pods. Eggs are observed during the whole period of study, but the numbers laid are always low. With the increase in pod number, eggs are dispersed among the different substrates available. However, the average number of eggs laid on the pods remains constant. Despite the high mortality due to the oviposition behaviour of B. atrolineatus and to other factors (impact of hymenopterous parasitoids), these two bruchids cause important losses to seeds of V. unguiculata. Control methods against these pests should be envisaged in the field before harvesting.

In Acanthoscelides obtectus (Say) (Coleoptera, Bruchidae) several first instar larvae can use a hole made in the seed coat by a conspecific to enter the seed. The present study tests whether there exists different seed-coat piercing abilities related to the hatching rank. The hatching rhythm was found to be well synchronized with the periodic conditions. The hatching rank had no influence on the piercing behaviour. On the basis of these observations the hypothesis of a behavioural dimorphism as has been suggested in the literature may be rejected.

Bruchidius atrolineatus appears at the end of the rainy season when pods of its host plant Vigna unguiculata begin to mature. The eggs are deposited along the ventral suture of pods in the vicinity of the seeds. When the eggs are not attacked by Trichogrammatidae their larvae penetrate the seeds and mortality is low during the post-embryonic development. Most of the adults emerging at pod maturity have functional reproductive organs. In that case the females laid on the same mature pods and larvae develop inside the seeds during the first part of the drying season characterised by high diurnal temperature and low relative humity. If the first emerged adults have functional reproductive organs, the following (60% of the population) are in reproductive diapause. Such diapausing insects have been found during the dry season in shelters near the cultivated fields of Vigna unguiculata. Induction or termination of this reproductive diapause are not yet studied. This diapause probably allows the maintenance of populations during the dry season in absence of host plant.