King penguins Aptenodytes patagonicus are known to change their diving behaviour in response to changes in both prey location and their breeding status through the early stages of the breeding cycle (austral summer and autumn). However, little information exists on whether and how these changes affect the energy expenditure of such behaviour. By deploying heart rate and hydrostatic pressure data loggers, we investigated detailed changes in the dive time budgeting of king penguins during foraging dives across the breeding season, in the same individuals, and the associated changes in estimated oxygen consumption during those dives. Maximum dive depth, duration, bottom duration, feeding events (indicated by wiggles) per dive and post-dive duration increased through the study period. While a foraging dive later in the breeding season was energetically more costly than a dive earlier in the season, the overall rate of energy expenditure did not change, nor did energy cost per unit prey capture. These findings indicate an ability of king penguins to adjust their foraging dive behaviours through the summer and autumn without affecting the energetic costs of diving to capture prey. Such plasticity may be necessary to compensate for changes both in prey location and abundance, and in the energy requirements of the chick over time.
KEY WORDS: Behavioural plasticity · Diving · Energy costs · Heart rate · Aptenodytes patagonicus · Seabirds
Resale or republication not permitted without written consent of the publisherMar Ecol Prog Ser 401: [279][280][281][282][283][284][285][286][287][288][289] 2010 about late January onwards, the foraging parent must obtain sufficient food not only to sustain itself while brooding the chick (and hence fasting) but also to feed to the chick (Gauthier-Clerc et al. 2000). When foraging, during both the incubating stage and at the chickrearing stage, the parents travel to the polar frontal zone to feed in summer (Charrassin & Bost 2001), but chick-rearing birds dive deeper than incubating birds (Charrassin et al. 1998). The suggested reason for this is that deeper dives are undertaken to reach denser patches of myctophid fish (Zasel'sliy et al. 1985, Charrassin et al. 1998, the most common prey of king penguins , Pütz & Bost 1994, so that a greater amount of food energy is obtained per dive (Charrassin et al. 1998). While such dives may use more energy (Tremblay & Cherel 2003, Halsey et al. 2006a, it is assumed that net energy gain is higher, which is necessary to meet overall energetic requirements during brooding.During foraging trips towards the end of summer and the beginning of autumn (March), king penguins tend to undertake foraging dives at a particularly high frequency (Charrassin et al. 1999). At this stage of breeding, the now thermally emancipated chick needs to grow rapidly and build fat stores in preparation for the ensuing winter fast (Stonehouse 1960, Weimerskirch et al. 1992. The chick requires large quantities of food at a high rate , van Heezik et al. 1993, Chere...