Impact of predation on king penguin Aptenodytes patagonicus in Crozet Archipelago

Predation can have major effects on population dynamics, but predator–prey interactions in marine ecosystems have rarely been studied. While the king penguin is one of the most studied seabirds, little is known about the impact of predation on its population dynamics. Here, we determine the impact of the main predators (giant petrels and skuas) on king penguin breeding success taking into account the nocturnal predation of petrels. We found that predation is the most important source of breeding failure for king penguins. The smallest chicks within crèches are the most hunted. The periphery of the colony suffers the highest risk of predation during summer. Our study shows the unequal quality of some areas inside the colony in terms of predation risk and breeding success, and points out the importance of timing in successful breeding.     

Estimating the critical body mass of king penguins

King penguins (Aptenodytes patagonicus) can fast for over a month. However, they return to sea to forage before their body mass reaches a critical value (cMb), beyond which there is an increase in rate of mass loss and in protein catabolism, termed phase III of fasting. Thus when studying king penguins onshore, accurate estimation of their cMb and, in turn, the date at which that body mass would be reached, will be informative to behavioural and physiological data being collected. For penguins being studied during fasts in captivity, knowing cMb is particularly important because of the need to release the birds back into their colony while they are still in good nutritional condition. The present study investigates the validity of using measures of beak, flipper and foot length together to estimate cMb in king penguins and provides a simple and effective prediction equation for researchers. The three morphometric measurements, along with body mass just prior to going to sea after the moult fast (taken to represent cMb), were obtained for nine king penguins in a colony at the Crozet Archipelago. A multiple linear regression of the three morphometric measurements against cMb provided an R ² of 71.2%. Mean absolute percentage error of the estimate of cMb over the nine birds was 8.82 ± 1.20%. The described technique could probably be employed for estimating cMb in other long-fasting seabirds.     

Summer diet of king penguins (Aptenodytes patagonicus) at the Falkland Islands, southern Atlantic Ocean

The diet of king penguins (Aptenodytes patagonicus) brooding chicks was investigated during February 2001 at the Falkland Islands, where a small but increasing population is located at the limit of the breeding range of this species. Fish was the most important food source by number (98.0%) and reconstituted mass (97.8%), squids accounting for the remainder. Myctophid fishes represented the main part of the diet (97.7% by number and 96.6% by reconstituted mass), Protomyctophum choriodon being by far the main prey item (84.2% and 88.1%, respectively). Four other myctophids and one squid species each contributed to more than 1% of the diet by number: Krefftichthys anderssoni (4.8%), Electrona carlsbergi (4.6%), Gymnoscopelus nicholsi (2.2%) and Protomyctophum tenisoni (1.8%), together with small juveniles of Gonatus antarcticus (1.8%). Twelve squid species were identified from accumulated lower beaks, including the ommastrephid Martialia hyadesi (48.3% by number), the onychoteuthids Moroteuthis ingens (15.6%), Kondakovia longimana (10.5%) and Moroteuthis knipovitchi (7.3%), and Gonatus antarcticus (9.2%). The stable-carbon and stable-nitrogen isotopic composition of chick food and adult blood differed in a way that suggests that, during the same trip, adult birds fed for themselves in distant foraging grounds, and fed for their chicks on their way back to the colony. The study emphasizes that king penguins are specialist myctophid eaters throughout their breeding range in summer, and highlights the importance of Protomyctophum choriodon as a link between zooplankton and top predators in the pelagic ecosystem of the southwestern Atlantic Ocean.     

Projected poleward shift of king penguins' (Aptenodytes patagonicus) foraging range at the Crozet Islands, southern Indian Ocean

Seabird populations of the Southern Ocean have been responding to climate change for the last three decades and demographic models suggest that projected warming will cause dramatic population changes over the next century. Shift in species distribution is likely to be one of the major possible adaptations to changing environmental conditions. Habitat models based on a unique long-term tracking dataset of king penguin (Aptenodytes patagonicus) breeding on the Crozet Islands (southern Indian Ocean) revealed that despite a significant influence of primary productivity and mesoscale activity, sea surface temperature consistently drove penguins' foraging distribution. According to climate models of the Intergovernmental Panel on Climate Change (IPCC), the projected warming of surface waters would lead to a gradual southward shift of the more profitable foraging zones, ranging from 25 km per decade for the B1 IPCC scenario to 40 km per decade for the A1B and A2 scenarios. As a consequence, distances travelled by incubating and brooding birds to reach optimal foraging zones associated with the polar front would double by 2100. Such a shift is far beyond the usual foraging range of king penguins breeding and would negatively affect the Crozet population on the long term, unless penguins develop alternative foraging strategies.     

Killer whale predation on penguins in Antarctica

We report here the first published observations of killer whales (Orcinus orca) feeding on penguins in Antarctica. The sightings took place in the Gerlache Strait off the western Antarctic Peninsula during February 2010. Two species of pygoscelid penguins were taken—gentoo (Pygoscelis papua, at least four individuals) and chinstrap (P. antarctica, 2). From remains left at the surface, it was clear that the killer whales fed mainly on the breast muscles, although some penguins may have been swallowed whole. The killer whales were ecotype B, which are purported seal specialists, but we also saw ecotype A, prey specialists on Antarctic minke whales Balaenoptera bonaerensis, chase, but not catch penguins. Because of their small relative size, if penguins are regularly targeted by killer whales in Antarctica, the impact on their populations could be significant.     

Gastrointestinal helminths of King penguins (Aptenodytes patagonicus) at Crozet Archipelago

Communities of helminths are known to be related to feeding behaviors of hosts. While climate change and overfishing can impact food availability for Antarctic piscivorous predators, knowledge about infectious and parasitic diseases among Antarctic species is scarce or fragmentary. We studied the helminth community of King penguins (Aptenodytes patagonicus) from the Crozet Archipelago, the main breeding area of the species. Based on a sample of 41 individuals found freshly dead from predation or starvation, the gastrointestinal helminth community in King penguins was composed of 1 species of cestode (Tetrabothrius wrighti) and 2 species of nematodes (Tetrameres wetzeli and Contracaecum heardi). Cestodes formed the core of the helminth community (97.5% of worms collected) with a prevalence of infestation of 100% and a mean intensity of 178.6 worms per host. Sources of infestation and pathologies caused by these worms are also discussed.     

Speciation and phylogeography of giant petrels Macronectes

We examine global phylogeography of the two forms of giant petrel Macronectes spp. Although previously considered to be a single taxon, and despite debate over the status of some populations and the existence of minimal genetic data (one mitochondrial cytochrome b sequence per form), the current consensus based on morphology is that there are two species, Northern Giant Petrel M. halli and Southern Giant Petrel M. giganteus. This study examined genetic variation at cytochrome b as well as six microsatellite loci in giant petrels from 22 islands, representing most island groups at which the two species breed. Both markers support separate species status, although sequence divergence in cytochrome b was only 0.42% (corrected). Divergence was estimated to have occurred approximately 0.2 mya, but with some colonies apparently separated for longer (up to 0.5 my). Three clades were found within giant petrels, which separated approximately 0.7 mya, with the Southern Giant Petrel paraphyletic to a monophyletic Northern Giant Petrel. There was evidence of past fragmentation during the Pleistocene, with subsequent secondary contact within Southern Giant Petrels. The analysis also suggested a period of past population expansion that corresponded roughly to the timing of speciation and the separation of an ancestral giant petrel population from the fulmar Fulmarus clade.     

Comparative ecology of the six albatross species breeding on the Crozet Islands

Six species of albatrosses breed sympatrically at the Crozet Islands. The population size, masses and measurements of adults, nesting habitats and coloniality, laying, hatching and fledging dates, duration of incubation and brooding shifts are compared. The growth of chicks, diets and feeding methods of the six species are reviewed. Their distribution in the south Indian Ocean is described in relation to the feeding frequency of chicks. Various aspects of ecological isolation among the species are analysed. Overlaps exist in the timing of breeding in the small albatrosses and to a lesser extent in their diet. Differences in the foraging zones at sea appear to be the most important factor in reducing interspecific competition. It is shown that the effective division of resources results from a relative scarcity of resources around the Crozet Islands. Finally the close interrelationship between foraging strategy, breeding biology, diet, chick growth and breeding frequency in the small albatrosses is demonstrated.     

Subantarctic krill, Euphausia vallentini Stebbing, preyed upon by penguins around Crozet Islands (Southern Indian Ocean): population structure and annual cycle

Dietary studies performed on three planktivorous penguins, Eudypteschrysolophus, E.chrysocome and Pygoscelis papua, provided alarge collection of well-preserved Euphausia vallentiru at differentperiods of the year. The change of carapace-length distributions,gut fullness and sexual maturity stages of E.vallentini aredescnbed. and a scheme for the life history of this speciesis proposed from this set of data. Its main characteristicsare as follows: mating peak in October-November; recruitmentof post-larval individuals from December-January onwards; fastgrowth until May; zero winter growth between June and mid-Augustdue to a minimum feeding activity Feeding activity reaches itshighest level from August to early October and is coincidentwith maturation, growth recovery, enhancement of sexual dimorphismand beginning of breeding season. Assuming that juveniles are1 year old when they begin to be recruited in penguin stomachs,E.vallentini is supposed to have a 2-year-life span in Crozetwaters. Two-year-old individuals are supposed to die in summeror autumn Juveniles can reach sexual maturity as early as November-Decemberwhen they are 1 year old and 16 mm body length: however, theyare unlikely to mate in significant numbers at this age. Inspite of specific limitations, the present sampling method iswell suited to routine surveys of local euphausiid populations.     

Movements of foraging king penguins through marine mesoscale eddies

Despite increasing evidence that marine predators associate with mesoscale eddies, how these marine features influence foraging movements is still unclear. This study investigates the relationship of at-sea movements of king penguins to mesoscale eddies using oceanographic remote sensing and movement data from 43 individual trips over 4 years. Simultaneous satellite measurements provided information on gradients of sea surface temperature and currents associated with eddies determined from altimetry. Penguins tended to swim rapidly with currents as they travelled towards foraging zones. Swimming speed indicative of foraging occurred within mesoscale fronts and strong currents associated with eddies at the Polar Front. These results demonstrate the importance of mesoscale eddies in directing foraging efforts to allow predators to rapidly get to rich areas where high concentrations of prey are likely to be encountered. When returning to the colony to relieve the incubating partner or to feed the chick, the birds followed a direct and rapid path, seemingly ignoring currents.     

Foraging strategies of incubating and brooding king penguins Aptenodytes patagonicus

For oceanic birds like king penguins, a major constraint is the separation of foraging areas from the breeding colony, largely because swimming increases foraging costs. However, the relationship between foraging strategy and breeding stage has been poorly investigated. Using time-depth recorders, we studied the diving behaviour of two groups of king penguins that were either incubating or brooding chicks at Crozet Islands (Southern Indian Ocean) at the same period of the year. Although birds with chicks had the highest predicted energy demand, they made foraging trips half as long as incubating birds (6 vs. 14 days) and modified their time and depth utilisation. Birds with chicks dived deeper during daylight (mean maximum depth of 280 m vs. 205 m for those incubating). At night, birds with chicks spent twice as much time diving as those incubating, but birds at both stages never dived beyond 30 m. Movements to greater depths by brooding birds are consistent with the vertical distribution of myctophid fish which are the main prey. As chick provisioning limits trip duration, it is suggested that it is more efficient for parents to change their diving patterns rather than to restrict their foraging range. Received: 23 June 1997 / Accepted: 3 November 1997     

Estimates of population size of white-chinned petrels and grey petrels at Kerguelen Islands and sensitivity to fisheries

White-chinned petrels Procellaria aequinoctialis and grey petrels Procellaria cinerea are among the most frequently killed seabird species by accidental bycatch, and both species have received strong conservation concern. Data on population size are required to evaluate the impact of bycatch and to establish management plans. We estimated the population size of both species at Kerguelen, Southern Indian Ocean, from 2004 to 2006 by explicitly taking into account detection probability of burrows using distance sampling and burrow occupancy. A total of 31 line-transects were distributed across the eastern part of Kerguelen, representing a total length of 566 km. Detectability was low (from 0.19 to 0.54 for white-chinned petrels, 0.58 for grey petrels). Burrow densities varied from 1.37±0.67 to 25.77±5.23 burrows ha⁻¹ for white-chinned petrels and was 2.78±0.79 burrows ha⁻¹ for grey petrels. For white-chinned petrels, these densities were extrapolated to the entire surface area of vegetation and there were 234 000 (186 000–297 000) active burrows on Kerguelen. For grey petrels, the number of active burrows for the eastern part of Kerguelen was 3400 (1900–5600). Based on these estimates, the potential biological removal method suggests that the additional mortality on birds caused by the fisheries operating around Kerguelen can be considered a serious threat for the species at least at the regional scale of the Southern Indian Ocean, especially for grey petrels.     

Effect of fasting on the VO2-fh relationship in king penguins, Aptenodytes patagonicus

King penguins (Aptenodytes patagonicus) may fast for up to 30 days during their breeding period. As such extended fasting may affect the relationship between the rate of O(2) consumption (Vo(2)) and heart rate (f(H)), five male king penguins were exercised at various speeds on repeated occasions during a fasting period of 24-31 days. In addition, Vo(2) and f(H) were measured in the same animals during rest in cold air and water (4 degrees C). Vo(2) and f(H) at rest and Vo(2) during exercise decreased with fasting. There was a significant relation between Vo(2) and f(H) (r(2) = 0.56) that was improved by including speed, body mass (M(b)), number of days fasting (t), and a cross term between f(H) and t (r(2) = 0.92). It was concluded that there was a significant change in the Vo(2)-f(H) relationship with fasting during exercise. As t is measurable in the field and was shown to be significant and, therefore, a practical covariate, a regression equation for use when birds are ashore was obtained by removing speed and M(b). When this equation was used, predicted Vo(2) was in good agreement with the observed data, with an overall error of 3.0%. There was no change in the Vo(2)-f(H) relationship in penguins at rest in water.     

Behavioural time budget of breeding king penguins (Aptenodytes patagonica)

As do so many other seabirds, penguins fast when ashore for breeding. For penguins in dense colonies, territory defence seems to imply conflicting energetic requirements because of its assumed high energy cost, when the birds need to limit energy expenditure to cope with their fast. In this context, behavioural time budget over 24 h was investigated during breeding in the king penguin, Aptenodytes putugonicu , by using a remote-controlled videocamera. The comparison of day-night activity was performed in relation to breeding status (incubation vs. brooding) and duration of fasting (beginning vs. end of incubation shift). Five categories of behaviours were quantified: territoly defence, comfort, resting, sleeping and chick-feeding. Breeding king penguins remain active by day as well as by night. Between incubation and brooding we found a three-fold increase in the energy consuming temtory defence, together with a drastic decrease in that posture which corresponds to deep sleep, is. when most energy is saved. These increases in aggressiveness and vigilance may be related to protection of the newly hatched chick. Between the onset and the end of an incubation shift, the time spent in sleep increases three-fold, whereas territory defence remains unchanged. These data for penguins under natural conditions accord with previous studies on captive birds which have shown that an increasing proportion of sleep during the course of fasting may contribute to energy saving. On the other hand, both resting (which is the main component of penguins'time budget; about 65%) and comfort (about 16% of time) show no change either between incubation and brooding or during the course of fasting.     

The breeding biology and population dynamics of King Penguins Aptenodytes patagonica on the Crozet Islands

Among King Penguins Aptenodytes patagonica at Possession Island, one of the Crozet Islands, the length of the moult period, pre-laying period, incubating and brooding shifts were highly variable according to the year and to the stage of the breeding season. The moulting period was shorter in late breeders than in early breeders. Only half of the birds which successfully reared a chick bred the following cycle, but late in the season. Almost all these late breeders were unsuccessful. The reasons for the high variability in the breeding pattern observed in this species between years, as well as between colonies and between individuals are discussed. Breeding success was on average 30.6% and survival during the first year at sea could reach 50%. The survival of adult birds has increased during the past 10 years from 90.7% to 95.2% per annum. Despite an almost biennial breeding frequency and a very high rate of chick loss during the winter fast, the King Penguin population of Possession Island has doubled between 1966 and 1985 due to a high survival rate of adult and immature birds. The increase during the last decade in adult survival and in adult and chick condition suggests that the population increase could be the result of an improvement in food availability.     

Foraging range of king penguins Aptenodytes patagonicm during summer at Marion Island

Foraging ranges of king penguins Aptenodytes patagonicus were estimated by combining information on the feeding rates to chicks and brood shift lengths of adults (assessed by daily weighings of large chicks and daily checks of marked birds brooding small chicks) with measurements of travelling speeds and activity budgets at sea (assessed using remote recording devices). Adults brooding small chicks were relieved on average every 13 days and large chicks were fed every four days. Adults with large chicks spent 36% of their time, between attachment of the device and recapture, travelling at an average speed of 8.7 km.h^-1. This gives an estimated mean maximum foraging range of about 300 km. Adults attending small chicks spent 19% of their time away swimming, giving an estimated mean maximum foraging range of 225 km. Extreme foraging ranges for all birds were 75 and 902 km for penguins returning between two and 24 days at sea, respectively. Total distance travelled was highly correlated with time away from the colony.     

Behavioral and physiological significance of minimum resting metabolic rate in king penguins

Because fasting king penguins (Aptenodytes patagonicus) need to conserve energy, it is possible that they exhibit particularly low metabolic rates during periods of rest. We investigated the behavioral and physiological aspects of periods of minimum metabolic rate in king penguins under different circumstances. Heart rate (f(H)) measurements were recorded to estimate rate of oxygen consumption during periods of rest. Furthermore, apparent respiratory sinus arrhythmia (RSA) was calculated from the f(H) data to determine probable breathing frequency in resting penguins. The most pertinent results were that minimum f(H) achieved (over 5 min) was higher during respirometry experiments in air than during periods ashore in the field; that minimum f(H) during respirometry experiments on water was similar to that while at sea; and that RSA was apparent in many of the f(H) traces during periods of minimum f(H) and provides accurate estimates of breathing rates of king penguins resting in specific situations in the field. Inferences made from the results include that king penguins do not have the capacity to reduce their metabolism to a particularly low level on land; that they can, however, achieve surprisingly low metabolic rates at sea while resting in cold water; and that during respirometry experiments king penguins are stressed to some degree, exhibiting an elevated metabolism even when resting.