Activity Time Budget during Foraging Trips of Emperor Penguins

We developed an automated method using depth and one axis of body acceleration data recorded by animal-borne data loggers to identify activities of penguins over long-term deployments. Using this technique, we evaluated the activity time budget of emperor penguins (n = 10) both in water and on sea ice during foraging trips in chick-rearing season. During the foraging trips, emperor penguins alternated dive bouts (4.8±4.5 h) and rest periods on sea ice (2.5±2.3 h). After recorder deployment and release near the colony, the birds spent 17.9±8.4% of their time traveling until they reached the ice edge. Once at the ice edge, they stayed there more than 4 hours before the first dive. After the first dive, the mean proportions of time spent on the ice and in water were 30.8±7.4% and 69.2±7.4%, respectively. When in the water, they spent 67.9±3.1% of time making dives deeper than 5 m. Dive activity had no typical diurnal pattern for individual birds. While in the water between dives, the birds had short resting periods (1.2±1.7 min) and periods of swimming at depths shallower than 5 m (0.25±0.38 min). When the birds were on the ice, they primarily used time for resting (90.3±4.1% of time) and spent only 9.7±4.1% of time traveling. Thus, it appears that, during foraging trips at sea, emperor penguins traveled during dives >5 m depth, and that sea ice was primarily used for resting. Sea ice probably provides refuge from natural predators such as leopard seals. We also suggest that 24 hours of sunlight and the cycling of dive bouts with short rest periods on sea ice allow emperor penguins to dive continuously throughout the day during foraging trips to sea.     

Short-term responses of king penguins Aptenodytes patagonicus to helicopter disturbance at South Georgia

The short-term behavioural effects of helicopter overflights on breeding king penguins Aptenodytes patagonicus at South Georgia were examined. Seventeen helicopter overflights were made at altitudes between 230 and 1,768 m (750–5,800 ft) above ground level. Noise from the aircraft engines and helicopter blades increased sound levels in the colony from a background level of 65–69 dB(A) to a maximum mean peak level of 80 dB(A) during overflights. Penguin behaviour changed significantly during all overflights at all altitudes compared to the pre- and post-flight periods. Pre-overflight behaviour resumed within 15 min of the aircraft passing overhead and no chicks or eggs were observed to be taken by predators during overflights. Non-incubating birds showed an increased response with reduced overflight altitude, but this was not observed in incubating birds. Variability in overflight noise levels did not affect significantly the behaviour of incubating or non-incubating birds. Penguins exhibited a reduced response to overflights as the study progressed (despite later flights generally being flown at lower altitudes) suggesting some degree of habituation to aircraft. To minimise disturbance to king penguins we recommend a precautionary approach such that overflights are undertaken at the maximum altitude that is operationally practical, or preferably are avoided altogether.     

Effect of fog on the arrival time of little penguins Eudyptula minor: a clue for visual orientation?

We report a dramatic change in the arrival time of little penguins Eudyptula minor at their breeding colony when a heavy low-level fog was present on the southern beaches of Phillip Island, Australia. On the evening of 21 December 2002, only 5% of penguins arrived at the expected time, and the peak time at arrival that night was 2 h behind the peak arrival times of previous and subsequent days. It appears that little penguins were unable or unwilling to return to the colony under the low visibility caused by the fog. Only half (52%) of the average number of penguins returned to the colony on the evening of the fog. We propose two explanations for our observation. First, penguins could have been close to the colony but did not come ashore in conditions of poor visibility to avoid predation. Secondly, the extensive fog may have affected the orientation of the penguins and they were unable to find their way back home. Our results could serve as indirect evidence for both hypotheses.     

A method to assess population changes in king penguins: the use of a Geographical Information System to estimate area-population relationships

During the last decades, king penguin (Aptenodytes patagonicus) populations have been reported to increase throughout most of their breeding range. In this study, we compared the results obtained from direct counts of incubating king penguins with the results yielded by the estimation of the change in area occupied by breeding birds at the Ratmanoff king penguin colony at the Kerguelen Islands. The area of the colony was determined using a Geographical Information System with a georeferencing extension on aerial pictures taken in 1963, 1985 and 1998. Individual king penguin were counted on the same pictures or pictures taken on the same day. The overall population increase between 1963 and 1998 was 733% while the colony area increased by 677%. This study indicates that monitoring change in colony size is a good indicator for detecting and monitoring large population changes in king penguins, in particular for remote colonies. The discrepancy between the two results may be from two different kinds of bias. Firstly, there could be a possible error in the estimation of the area occupied by the colony resulting from the georeferencing of oblique pictures, and secondly, the density of king penguins may also change with population number. This method, which only requires high-altitude pictures, also reduces the possible disturbance to breeding made by low- to medium-altitude flights. Accepted: 7 February 2000     

Diurnal sleep depth changes in the king penguin (<Emphasis Type="Italic">Aptenodytes patagonicus</Emphasis>)

Avian sleep quality depends on its depth (deeper sleep being of better quality). In king penguins (Aptenodytes patagonica), sleep may be disturbed by congeners passing in the sleeper's vicinity. As king penguin activity is increased in the morning, sleep disturbances are more likely to occur during this time period. One might therefore assume that afternoon sleepers (AS) sleep more profoundly than morning sleepers (MS). To test this hypothesis, we examined the diurnal variations in sleep depth of king penguins sleeping in resting sites adjacent to the colony of 'La Baie du Marin' (Crozet Archipelago). We measured the bodily tactile arousal threshold at the upper back level. The arousal threshold in AS was twice as high as in MS. This study demonstrates for the first time that sleep depth changes according to time of day in a diurnal wild bird. We postulate that diurnal sleep depth is increased due to decreased congener movements close to the sleeping penguin.     

Contribution of alien and indigenous species to plant-community assemblages near penguin rookeries at Crozet archipelago

The influence of seabird colonies on a remote insular flora was investigated through the analysis of plant community patterns at the boundaries of three colonies of king penguins (Aptenodytes patagonicus) on the subantarctic Île de la Possession. This study revealed that the physical and chemical impacts of these seabirds greatly influence plant assemblages (community composition, alien and native species abundance and richness). Plant richness appears to be maximum for a moderate disturbance intensity, on areas slightly influenced by penguin activities. The abundance of alien species near penguin rookeries may be due to their ability to withstand animal-induced disturbances and to efficiently colonise the stripped areas. In addition, the diversity and abundance of alien species recorded in study plots depend on the location of the colony. The closer the colony is to the permanent scientific station, the higher the number and abundance of aliens recorded.     

Effect of Approaching Boats on Nesting Black Skimmers: Using Response Distances to Establish Protective Buffer Zones

ABSTRACT Understanding how birds respond to the activities of people is an important component of conserving wildlife. We measured responses of nesting black skimmers (Rynchops niger) to an approaching boat in Barnegat Bay, New Jersey, USA, by examining distance to first respond, distance to flush, and time to return to the colony. Our objective was to determine if response distances of skimmers changed as a function of year, reproductive stage, direction of approach (direct or tangential), or number of birds nesting in the colony. Generally, reproductive stage had the greatest effect on all responses, followed by direction of approach, number of adults present at the colony, number of nests, and year, which also explained variation in behavioral responses. The distance at which skimmers first flew when a boat approached decreased from the pre-egg-laying period to hatching, and then increased slightly later in the season. Time (x̄± SE) for skimmers to return to the nesting colony varied seasonally, with birds taking longer to return during the pre-egg period (9.5 ± min) than during hatching (0.7 ± 0.1 min). The decision process for determining set-back distances to protect nesting skimmers should involve selecting 1) behavioral response of highest concern, 2) reproductive stage of highest concern, and 3) an appropriate level of response at which to establish the buffer area. We recommend that managers use a set-back distance of ± 118 m from the perimeter of the colony for black skimmers, which is the 95% percentile of the distance that skimmers first flew in response to approaching boats. Managers can use these data to set buffer distances for skimmers and other colonial birds.     

Changes in size of the Hope Bay Adélie penguin rookery as inferred from Lake Boeckella sediment

Concentrations of phosphorus and copper in the sediments of Lake Boeckella (Antarctic peninsula) were used to provide an estimate of the size of the Adélie penguin rookery Pygocetis adeliae Based on dated subsamples from a sediment core, I conclude that penguins have been present in Hope Bay since 5550 BP, with the exception of a short penod around 5300 BP Their influence on the lake sediment reached a maximum at c 40 BP and has drastically declined since then The rookery started to grow between 850 and 1250 BP due to a climate deterioration The increased amount of food (mainly krill), caused by extensive fur seal hunting in the nineteenth century was probably not enough to affect rookery growth However, the drastic decline m whale stock in the 1930's and 1940's and the subsequent increase m krill abundance may have enhanced rookery growth The increasing disturbance by man in Hope Bay seems only to have changed the shape of the rookery and the penguins paths to the sea, but not to have stopped the growth of the rookery     

Extreme dives by free-ranging emperor penguins

We examined the incidence of extreme diving in a 3-year overwintering study of emperor penguins Aptenodytes forsteri in East Antarctica. We defined extreme dives as very deep (> 400 m) and/or very long (> 12 min). Of 137364 dives recorded by 93 penguins 264 dives reached depths > 400 m and 48 lasted > 12 min. Most (65%) very long dives occurred in winter (May–August) while 83% of the very deep dives took place in spring (September–November). The two most extreme dives (564 m depth, 21.8 min duration) were separate dives and were performed by different individual penguins. Penguins diving extremely deeply may have done so as part of their foraging strategy whereas penguins diving for very long times may have been forced to do so by changes in the sea-ice conditions.     

Diving pattern and performance in the macaroni penguin Eudptes chrysolophus

The pattern and characteristics of diving in two female macaroni penguins Eudyptes chrysolophus was studied, during the brooding period, using continuous-recording time-depth recorders, for a total of I8 days (15 consecutive days) during which the depth, duration and timing of 4876 dives were recorded. Diving in the first 11 days was exclusively diurnal, averaging 244 dives on trips lasting 12 hours. Near the end of the brooding period trips were longer and included diving at night. About half of all trips (except those involving continuous night-time diving) was spent in diving and dive rate averaged 14–25 dives per hour (42 per hour at night). The duration of day time dives varied between trips, and averaged 1.4–1.7 min, with a subsequent surface interval of 0.5–0.9 min. Dive duration was significantly directly related to depth, the latter accounting for 53% of the variation. The average depths of daytime dives were 20–35 m (maximum depth 11 5 m). Dives at night were shorter (average duration 0.9 min) and much shallower (maximum 11 m); depth accounted for only 6% of the variation in duration. Estimates of potential prey capture rates (3–5 krill per dive; one krill every 17–20 s) are made. Daily weight changes in chicks were directly related to number of dives, but not to foraging trip duration nor time spent diving. Of the other species at the same site which live by diving to catch krill, gentoo penguins forage exclusively diurnally, making longer. deeper dives; Antarctic fur seals, which dive to similar depths as macaroni penguins, do so mainly at night.     

At‐sea distribution and habitat use in king penguins at sub‐Antarctic Marion Island

King penguins make up the bulk of avian biomass on a number of sub‐Antarctic islands where they have a large functional effect on terrestrial and marine ecosystems. The same applies at Marion Island where a substantial proportion of the world population breeds. In spite of their obvious ecological importance, the at‐sea distribution and behavior of this population has until recently remained entirely unknown. In addressing this information deficiency, we deployed satellite‐linked tracking instruments on 15 adult king penguins over 2 years, April 2008 and 2013, to study their post‐guard foraging distribution and habitat preferences. Uniquely among adult king penguins, individuals by and large headed out against the prevailing Antarctic Circumpolar Current, foraging to the west and southwest of the island. On average, individuals ventured a maximum distance of 1,600 km from the colony, with three individuals foraging close to, or beyond, 3,500 km west of the colony. Birds were mostly foraging south of the Antarctic Polar Front and north of the southern boundary of the Antarctic Circumpolar Current. Habitat preferences were assessed using boosted regression tree models which indicated sea surface temperate, depth, and chorophyll a concentration to be the most important predictors of habitat selection. Interestingly, king penguins rapidly transited the eddy‐rich area to the west of Marion Island, associated with the Southwest Indian Ocean Ridge, which has been shown to be important for foraging in other marine top predators. In accordance with this, the king penguins generally avoided areas with high eddy kinetic energy. The results from this first study into the behavioral ecology and at‐sea distribution of king penguins at Marion Island contribute to our broader understanding of this species.     

Organized Cell Swimming Motions in Bacillus subtilis Colonies: Patterns of Short-Lived Whirls and Jets

The swimming motions of cells within Bacillus subtilis colonies, as well as the associated fluid flows, were analyzed from video films produced during colony growth and expansion on wet agar surfaces. Individual cells in very wet dense populations moved at rates between 76 and 116 μm/s. Swimming cells were organized into patterns of whirls, each approximately 1,000 μm², and jets of about 95 by 12 μm. Whirls and jets were short-lived, lasting only about 0.25 s. Patterns within given areas constantly repeated with a periodicity of approximately 1 s. Whirls of a given direction became disorganized and then re-formed, usually into whirls moving in the opposite direction. Pattern elements were also organized with respect to one another in the colony. Neighboring whirls usually turned in opposite directions. This correlation decreased as a function of distance between whirls. Fluid flows associated with whirls and jets were measured by observing the movement of marker latex spheres added to colonies. The average velocity of markers traveling in whirls was 19 μm/s, whereas those traveling in jets moved at 27 μm/s. The paths followed by markers were aligned with the direction of cell motion, suggesting that cells create flows moving with them into whirls and along jets. When colonies became dry, swimming motions ceased except in regions close to the periphery and in isolated islands where cells traveled in slow whirls at about 4 μm/s. The addition of water resulted in immediate though transient rapid swimming (> 80 μm/s) in characteristic whirl and jet patterns. The rate of swimming decreased to 13 μm/s within 2 min, however, as the water diffused into the agar. Organized swimming patterns were nevertheless preserved throughout this period. These findings show that cell swimming in colonies is highly organized.     

Pond Use by Captive African Penguins (Spheniscus demersus) in an Immersive Exhibit Adjacent to Human Bathers

Nonhuman animals in zoos are exposed to a continuous human presence, which affects their behaviors and welfare. However, little is known about what role the “visitor effect” has on penguins in captivity. The African penguin (Spheniscus demersus) is an endangered species commonly housed in zoos worldwide. The aim of this study was to evaluate whether the abundance of human bathers could reduce the average time spent in the water of a colony of African penguins housed in an exhibit where their pond habitat was adjacent to a swimming pool. Observations were carried out on 7 penguins in the summer of 2009. Data were collected during 3 time periods (Time 1 [T1] = opening of the swimming season, Time 2 [T2] = core of the season, Time 3 [T3] = late season) of 14 days each. The human disturbance caused by bathers strongly reduced the pond use by penguins at T1 and T2, especially when there were large numbers of visitors. However, at T3, we observed that the overall use of the pond by penguins increased, and the average duration of their diving was no longer dependent on the number of visitors.     

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.     

The long engagement of the emperor penguin

In birds, courtship is generally short relative to the whole breeding cycle. Emperor penguins (Aptenodytes forsteri), however, are an exception as their courtship period is much longer (ca. 6 weeks) than the courtship of other penguin species. This strategy may appear surprising, as it is especially costly to fast and endure drastic climatic conditions for long periods at the colony (1.5 and up to 4 months for females and males, respectively). We examined here the reasons of this extended courtship period and found that emperor penguins returned earlier to the colony when primary oceanic production before breeding was high. This suggests that emperor penguins return to the colony as soon as primary oceanic production in summer allows them to replenish their body reserves. The extended period of time spent at the colony during courtship may therefore result from an evolutionary process that confers advantages to emperor penguins that arrive earlier at the colony by reducing predation risks and offering better chances of securing a partner.     

Responses of king penguin Aptenodytes patagonicus adults and chicks to two food‐related odours

Increasing evidence suggests that penguins are sensitive to dimethyl sulphide (DMS), a scented airborne compound that a variety of marine animals use to find productive areas of the ocean where prey is likely to be found. Here we present data showing that king penguins Aptenodytes patagonicus are also sensitive to DMS. We deployed DMS on a lake near a king penguin colony at Ratmanoff beach in the Kerguelen archipelago. We also presented DMS to ‘sleeping’ adults on the beach. On the lake, penguins responded to the DMS deployments by swimming more, while on the beach, penguins twitched their heads and woke up more for the DMS than for the control presentations. Interestingly, penguins did not respond to cod liver oil deployments on the lake; mirroring at‐sea studies of other penguins. Although at‐sea studies are needed to confirm that king penguins use DMS as a surface cue that informs them of productivity under the water, this study is an important first step in understanding how these birds locate prey over significant distances.     

Winter distribution and behaviour of gentoo penguins<Emphasis Type="Italic"> Pygoscelis papua</Emphasis> at South Georgia

Knowledge of the spatial and temporal dynamics of foraging penguins is important to our understanding of the Southern Ocean marine ecosystem. We use satellite tracking to provide the first data on the distribution and behaviour of gentoo penguins (Pygoscelis papua) during the winter at South Georgia. Five penguins tracked from Bird Island remained close inshore, and although they did not return to the initial tagging site, they did appear to return to land each evening. They made diurnal trips to sea of similar distance from land as those during the breeding season, even though the constraints of chick rearing were absent. Despite potential greater flexibility in their responses to variations in prey availability in winter, the penguins still returned to land each night. This may reflect benefits from conserving energy by resting on land, possibly facilitating information exchange and avoiding predation. The distribution and behaviour of gentoo penguins during the winter enables efficient exploitation of a dynamic, patchy prey resource and may ultimately determine the timing of return to the colony, and onset of breeding in the following season.     

Sex differences in Adélie penguin foraging strategies

Consistent sex differences in foraging trip duration, feeding locality and diet of breeding Adélie penguins (Pygoscelis adeliae) were demonstrated at two widely separated locations over several breeding seasons. Differences in foraging behaviour were most pronounced during the guard stage of chick rearing. Female penguins made on average longer foraging trips than males, ranged greater distances more frequently and consumed larger quantities of krill. In contrast, males made shorter journeys to closer foraging grounds during the guard period and fed more extensively on fish throughout chick rearing. Mean guard stage foraging trip durations over four seasons at Béchervaise Island, Eastern Antarctica and over two seasons at Edmonson Point, Ross Sea ranged between 31 and 73 h for females and 25 and 36 h for males. Ninety percent of males tracked from Béchervaise Island by satellite during the first 3 weeks post-hatch foraged within 20 km of the colony, while the majority (60%) of females travelled to the edge of the continental shelf (80–120 km from the colony) to feed during this period. Received: 10 December 1997 / Accepted: 10 April 1998     

Penguins from space: faecal stains reveal the location of emperor penguin colonies

Aim  To map and assess the breeding distribution of emperor penguins ( Aptenodytes forsteri ) using remote sensing.
Location  Pan-Antarctic.
Methods  Using Landsat ETM satellite images downloaded from the Landsat Image Mosaic of Antarctica (LIMA), we detect faecal staining of ice by emperor penguins associated with their colony locations. Emperor penguins breed on sea ice, and their colonies exist in situ between May and December each year. Faecal staining at these colony locations shows on Landsat imagery as brown patches, the only staining of this colour on sea ice. This staining can therefore be used as an analogue for colony locations. The whole continental coastline has been analysed, and each possible signal has been identified visually and checked by spectral analysis. In areas where LIMA data are unsuitable, freely available Landsat imagery has been supplemented.
Results  We have identified colony locations of emperor penguins at a total of 38 sites. Of these, 10 are new locations, and six previously known colony locations have been repositioned (by over 10 km) due to poor geographical information in old records. Six colony locations, all from old or unconfirmed records, were not found or have disappeared.
Main conclusions  We present a new pan-Antarctic species distribution of emperor penguins mapped from space. In one synoptic survey we locate extant emperor penguin colonies, a species previously poorly mapped due to its unique breeding habits, and provide a vital geographical resource for future studies of an iconic species believed to be vulnerable to future climate change.     

Seasonal change in foraging areas and dive depths of breeding king penguins at Heard Island

The seasonal variation in the foraging behaviour of king penguins (Aptenodytes patagonicus) was studied at Heard Island (53°05′S, 73°30′E) during 1992/1993. On seven occasions throughout the breeding cycle, time-depth-light recorders were deployed on breeding adults to record the dive activities and foraging. Foraging locations changed with season: in autumn and spring 1992, adults foraged between 48–52°S and 74–78°E, about 370 km NNE of Heard Island close to the Polar Front. Two penguins tracked in winter travelled 2220 km east of Heard Island (95°E) along the northern ice limit, and 1220 km south of Heard Island to approximately 65°S, respectively. In spring (October), the penguins again foraged further north than during winter. The foraging area utilised in October overlapped the area where the penguins foraged in March/April. The penguins' diving behaviour also varied seasonally: the modal depth of deep dives (>50 m) increased from about 100 m in February to 220 m in October. Mean dive depths increased from 70 ± 52 m in March 1992 to 160 ± 68 m in August 1992. Penguins dived deep (>50 m) only during daylight hours (16 h in February, 9 h in July). Mean dive durations ranged from 2.9 ± 1.1 min in March 1992 to 5.1 ± 1.2 min in August 1992. Associated with changes in foraging location and dive behaviour was a change in diet composition: during summer the penguins ingested mainly myctophid fish (>90%) while in winter the most important diet item was squid. Accepted: 19 October 1998