Conservationists recognize the need to work beyond protected areas if they are to sustain viable populations of wildlife. But ambitious plans to extend wildlife corridors beyond protected areas must consider the economic and political implications when wildlife forage on crops, attack livestock, or otherwise threaten human security. Traditionally, humans respond by killing “problem” wildlife and transforming wild habitats to prevent further losses. This traditional response, however, is now illegal or socially unacceptable in many areas, changing a simple competitive relationship between people and wildlife into a political conflict. Here we draw from experience in Bolivia, Uganda, and Wisconsin to outline a strategy for mitigating human–wildlife conflict based on participatory methods and co-management with twin objectives of wildlife conservation and safeguarding human security. Incorporating local stakeholders as partners in planning and implementation can help to win space for wildlife beyond protected area boundaries. We also show why systematic study of local people's perceptions of risk and participant planning of interventions are irreplaceable components of such projects.
Summary: Primates dominate lists of pests that damage crops around African parks and reserves. Beyond creating management problems, crop foraging is integral to the ecology of primates inhabiting forest—agriculture ecotones. Twenty‐three months of data from four villages around Kibale National Park, Uganda, revealed that redtail monkeysCercopithecus ascanius, olive baboonsPapio cynocephalusand chimpanzeesPan troglodytesselected different crops or plant parts. Baboons took root and tuber crops ignored by other primates, and fed on the greatest variety of crops. All three species preferred maize and/or bananas. Redtails ate only banana fruit, baboons ate banana fruit more frequently than pith, and chimpanzees raided pith and fruit in equal proportions. Each primate showed a distinct monthly pattern of crop foraging, significantly non‐random for baboons and redtail monkeys, weakly for chimpanzees. Large inter‐monthly variation was observed for all three primates, but was least pronounced in redtails. Raiding frequency on maize peaked approximately 8 weeks after the onset of rains and was strongly correlated between the three primate species. Abundant forest fruit did not diminish primate appetite for maize. Raiding frequency on bananas varied considerably despite continuous availability of fruit and pith. Peaks in banana consumption were unrelated to rainfall or maize raiding, but were associated instead with forest fruit shortages, specificallyMimusops bagshawei. Chimpanzees consumed banana pith more frequently when forest fruits were scarce, whereas baboons targeted more banana fruits. The use of banana pith by chimpanzees supports the suggestion that energy‐rich pith is crucial to chimpanzees during fruit scarcity. Conservation ofMimusops bagshaweiand other key forest fruit trees may lessen primate raiding intensity on perennial crops, e.g. bananas. Maize raiding appears unaffected by forest fruit abundance. Such highly palatable crops are best planted > 500 m from the forest edge. Planting agroforestry buffers along park edges creates ideal habitat for crop‐raiders. This management strategy is appropriate where human population density is low and crop raiding species are legal game. When dangerous or destructive wildlife species forage amidst densely settled subsistence farmland, managers are challenged to separate forests from agriculture using non‐palatable plant barriers or electric fences.