Abstract

During migration, many species of birds rely on stored fat for fuel. The extra mass taken on for migration entails costs (Witter and Cuthill 1993). Time and energy must be devoted to foraging to build up fat loads, and increased feeding may increase the risk of being attacked by predators. An additional cost of increased fuel loads may be higher predation risk owing to reduced ability to take off, maneuver, and climb. Mass-dependent predation risk has been the focus of several recent theoretical studies (McNamara and Houston 1990, Hedenstrdm 1992, Witter and Cuthill 1993, Brodin 2000). In species that depend on flight to escape from predators, takeoff ability is crucial because once the prey are airborne, the success rate of predators diminishes (e.g. Rudebeck 1950, Kenward 1978, Lindstrdm 1989, Cresswell 1993). Within the natural range of body mass of nonmigratory birds (ca. 10% diurnal increase in mass), mass seems to have no measurable effect on takeoff ability (Kullberg 1998, Kullberg et al. 1998, Veasey et al. 1998, van der Veen and Lindstrdm 2000). In migratory birds, fuel loads of 20 to 30% of lean mass are common (Alerstam and Lindstrbm 1990), and fuel loads may exceed 100% of lean mass when passerines are about to cross wide barriers (e.g. Fry et al. 1970, Finlayson 1981). Although fat storage is the most common explanation for mass changes in birds, mass may change because of other reversible processes, e.g. by increases or decreases in muscle mass and in various internal organs (Piersma and Lindstrdm 1997). To date, only two species of migrants have been studied with respect to takeoff ability in a predatorescape situation. Kullberg et al. (1996) calculated that Blackcaps (Sylvia atricapilla) carrying 60% of lean body mass as fuel would have an angle of ascent that was 32% lower and a velocity that was 17% lower

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