Foraging strategy of the little auk Alle alle throughout breeding season – switch from unimodal to bimodal pattern

Energy and time allocation differs between incubation and chick‐rearing periods, which may lead to an adjustment in the foraging behaviour of parent birds. Here, we investigated the foraging behaviour of a small alcid, the little auk Alle alle during incubation and compared it with the chick‐rearing period in West Spitsbergen, using the miniature GPS (in Hornsund) and temperature loggers (in Magdalenefjorden). GPS‐tracking of 11 individuals revealed that during incubation little auks foraged 8–55 (median 46) km from the colony covering 19–239 (median 120) km during one foraging trip. Distance from the colony to foraging areas was similar during incubation and chick‐rearing period. During incubation 89% of foraging positions were located in the zone over shallower parts of the shelf (isobaths up to 200–300 m) with sea surface temperature below 2.5°C. Those environmental conditions are preferred by Arctic zooplankton community. Thus, little auks in the Hornsund area restrict their foraging (both during the incubation and chick‐rearing period) to the area under influence of cold, Arctic‐origin water masses where its most preferred prey, copepod Calanus glacialis is most abundant. The temperature logger data (from 4 individuals) indicate that in contrast to the chick‐rearing period, when parent birds alternated short and long trips, during the incubation they performed only long trips. Adopting such a flexible foraging strategy allows little auks to alter their foraging strategy to meet different energy and time demands during the two main stages of the breeding.     

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     

Inter-annual variation in provisioning behaviour of Southern Rockhopper Penguins Eudyptes chrysocome chrysocome at Staten Island, Argentina

Understanding the relationship between reproductive performance and food availability requires knowledge about many different variables, including such factors as the length of incubation shifts, provisioning rates and patterns, as well as how variability in these factors affects reproductive output. To examine some of the most important aspects of parental investment, we studied the provisioning behaviour and patterns of adult Southern Rockhopper Penguins Eudyptes chrysocome chrysocome breeding at Staten Island, Argentina. We investigated foraging trip duration, provisioning rates and chick survival using adult foraging patterns. Our results show that Rockhopper Penguins had clear sex-specific differences in their provisioning behaviour. Females provision chicks throughout chick rearing. By contrast, males provision chicks only during the crèche stage and at a slightly lower rate than females during this period. Foraging trips increased in length as the breeding season progressed. Rockhopper Penguins from Staten Island performed longer trips throughout the breeding season than do other species of Eudyptes at several other locations. Our results also show differences in parental investment between years that were related to differences in chick survival. We suggest that this was most likely to be related to female rather than male foraging behaviour as only females showed inter-annual differences in their provisioning rates.     

Nest attendance and foraging movements of northern fulmars rearing chicks at Bjørnøya Barents Sea

We studied several aspects of the foraging ecology of fulmars rearing young chicks on Bjørnøya. To determine precisely the duration of foraging trips during the brooding period, we used an automated logging system that recorded the presence of fulmars fitted with transponders. We also tracked, with satellite transmitters, four parent fulmars during the brooding period, and two after the chick had been left alone. When brooding the chick, fulmars appeared to alternate very rapidly on the nest, with foraging trips lasting on average 8?h. This period appeared constraining for the birds since parents lost mass. The growth of chicks was dependent on the ability of the female (and not the male) to do short foraging trips. At this time birds are foraging at an average distance of 60?km from the colony, with birds concentrating on the shelf around Bjørnøya. They did not return from one trip to the next to the same foraging area. As the season progressed and the chicks were left alone on the nest, parents increased the duration and maximum range of foraging trips as well as the distance covered. However, they still perform a succession of relatively short foraging trips to the east of the Bjørnøya shelf but they interspersed these short trips with longer foraging trips. One bird returned twice to the same site along the Norwegian coast 570?km from Bjørnøya, the other foraged at 580?km in the mid-Barents Sea. Average flight speed including time spent on the water was 28?km/h and reached 70?km/h during bouts of more than 1?h when the bird was probably continuously in flight.     

Body mass changes in Brünnich's guillemots Uria lomvia with age and breeding stage

Body mass of Brünnich's guillemots Uria lomvia breeding at Coats Island, Canada, was measured during incubation and chick‐rearing in 1988–2001. In most years, mass increased during incubation and fell after hatching, leveling off by the time chicks were 18 d old, close to the age at which chicks departed. Mass during incubation increased with age up to about 12 yr, but the mass of birds brooding chicks was not related to age. The trend towards increasing mass during incubation was mainly a consequence of mass increases of young breeders as older birds maintained a constant mass. The variation in adult mass with age during incubation seems likely to reflect age‐related variation in foraging ability, but the loss of mass after hatching, being greater for older birds, appears best explained as a response to the demands of provisioning chicks, with older birds transferring their accumulated reserves to their chicks via higher provisioning rates.     

Investigator disturbance reduces reproductive success in Short‐tailed Shearwaters Puffinus tenuirostris

Research procedures can have a detrimental effect on the reproductive success of the study species. In this study, the frequency of investigator disturbance on Short‐tailed Shearwaters Puffinus tenuirostris was examined experimentally throughout the incubation period to assess whether disturbance influences hatching success, pre‐fledging chick survival and chick body size. Handling of incubating birds every day, every 3 days and once a week reduced hatching success by 100, 61 and 39%, respectively, compared with pairs that were not disturbed. Most failures resulted from egg abandonment by the parents, particularly during the early stage of incubation. Chick survival did not differ between treatment groups, but control chicks were significantly heavier and had larger bill depths and longer wings. The difference in chick body mass and size observed between the control and disturbed chicks might be due to physiological or behavioural mechanisms in adults or carry‐over effects from the incubation stage to the next life‐history stage. Reduced offspring quality has the potential to affect post‐fledging survival and recruitment. These findings are significant in broader terms because any investigator disturbance that reduces reproductive success, survival and offspring fitness could interfere with the accurate assessment of demographic parameters and exacerbate population declines.     

Experimental increase of flying costs in a pelagic seabird: effects on foraging strategies,nutritional state and chick condition

A central point in life history theory is that parental investment in current reproduction should be balanced by the costs in terms of residual reproductive value. Long-lived seabirds are considered fixed investors, that is, parents fix a specific level of investment in their current reproduction independent to the breeding requirements. We tested this hypothesis analysing the consequences of an experimental increase in flying costs on the foraging ecology, body condition and chick condition in Cory’s shearwaters Calonectris diomedea. We treated 28 pairs by reducing the wing surface in one partner and compared them with 14 control pairs. We monitored mass changes and incubation shifts and tracked 19 foraging trips per group using geolocators. Furthermore, we took blood samples at laying, hatching and chick-rearing to analyse the nutritional condition, haematology, muscle damage and stable isotopes. Eighty-day-old chicks were measured, blood sampled and challenged with PHA immune assay. In addition, we analysed the effects of handicap on the adults at the subsequent breeding season. During incubation, handicapped birds showed a greater foraging effort than control birds, as indicated by greater foraging distances and longer periods of foraging, covering larger areas. Eighty-day-old chicks reared by treated pairs were smaller and lighter and showed a lower immunity than those reared by control pairs. However, oxygen demands, nutritional condition and stable isotopes did not differ between control and handicapped birds. Although handicapped birds had to increase their foraging effort, they maintained physical condition by reducing parental investment and transferred the experimentally increased costs to their partners and the chick. This result supports the fixed investment hypothesis and is consistent with life history theory.     

Benefits of mass reduction for commuting flight with heavy food load in Leach’s storm-petrel,Oceanodroma leucorhoa

When rearing chicks, Leach’s storm-petrels (Oceanodroma leucorhoa) commute between foraging areas and breeding colonies with heavy food loads. At this time they should maximize the size of energy-supplying organs in response to increased energy expenditure but minimize total body mass to decrease the energetic cost of flight. Nineteen storm-petrels were killed to examine the changes in body composition and the masses of energy-supplying organs in birds that were incubating and rearing chicks. Parents lost a mean of 7.95 g in body mass between the stages of incubation and chick-rearing mainly via a loss of skin including subcutaneous adipose tissue, and a small fraction of heart and digestive organs, which are considered energy-supplying organs. This mass loss actually enables them to decrease flight cost by 14.4%. The benefits of decreasing flight costs by reducing total body mass are greater than if the energy-supplying organs of birds are enlarged only.

     

Taking a trip to the shelf: Behavioral decisions are mediated by the proximity to foraging habitats in the black‐legged kittiwake

For marine top predators like seabirds, the oceans represent a multitude of habitats regarding oceanographic conditions and food availability. Worldwide, these marine habitats are being altered by changes in climate and increased anthropogenic impact. This is causing a growing concern on how seabird populations might adapt to these changes. Understanding how seabird populations respond to fluctuating environmental conditions and to what extent behavioral flexibility can buffer variations in food availability can help predict how seabirds may cope with changes in the marine environment. Such knowledge is important to implement proper long‐term conservation measures intended to protect marine predators. We explored behavioral flexibility in choice of foraging habitat of chick‐rearing black‐legged kittiwakes Rissa tridactyla during multiple years. By comparing foraging behavior of individuals from two colonies with large differences in oceanographic conditions and distances to predictable feeding areas at the Norwegian shelf break, we investigated how foraging decisions are related to intrinsic and extrinsic factors. We found that proximity to the shelf break determined which factors drove the decision to forage there. At the colony near the shelf break, time of departure from the colony and wind speed were most important in driving the choice of habitat. At the colony farther from the shelf break, the decision to forage there was driven by adult body condition. Birds furthermore adjusted foraging behavior metrics according to time of the day, weather conditions, body condition, and the age of the chicks. The study shows that kittiwakes have high degree of flexibility in their behavioral response to a variable marine environment, which might help them buffer changes in prey distribution around the colonies. The flexibility is, however, dependent on the availability of foraging habitats near the colony.     

Partitioning of foraging effort in Adélie penguins provisioning chicks at Béchervaise Island, Antarctica

Analyses of the body masses of Adélie penguins (Pygoscelis adeliae) departing on foraging trips of long and short duration (> and<40 h, respectively) during chick rearing showed that the departure weights of birds prior to long trips were significantly lighter than were those prior to short trips. Penguins, particularly males, were significantly heavier at the start of the guard stage than at the end and both sexes gained similar amounts of body mass during the crèche period. Results support the hypothesis that the foraging effort of Adélie penguins at Béchervaise Island is partitioned between the sexes, with males accepting a net rate of negative energy gain to provide regular meals for their offspring during the guard stage. Adélie penguin foraging behaviour may be driven by a trade-off between the allocation of food to chicks and the storage of parental body reserves, similar to that previously postulated for some species of flying seabirds. The relevance of such a foraging strategy to the breeding success of penguins in the Mawson region of eastern Antarctica is discussed in relation to micronekton distribution in the area. Accepted: 3 June 2000     

Effects of geolocation archival tags on reproduction and adult body mass of sooty shearwaters (Puffinus griseus)

Abstract

We attached 11 g (1.4% body‐mass equivalent) global location sensing (GLS) archival tag packages to tarsi of 25 breeding sooty shearwaters (Puffinus griseus, titi) on Whenua Hou (Codfish Island), New Zealand during the chick‐rearing period in 2005. Compared with chicks reared by non‐handled adults that did not carry tags, deployment of tags on one or both adult parents ultimately resulted in 35% reduction in chick body mass and significantly reduced chick skeletal size preceding fledging (19 April). However, body mass between chick groups was not significantly different after controlling for skeletal size. Effects on chicks were more pronounced in six pairs where both parents carried tags. Chick mass was negatively related to the duration that adults carried tags. In this study, none of the chicks reared by pairs where both parents were tagged, 54% of chicks reared by pairs where one parent was tagged, and 83% of chicks reared by non‐handled and non‐tagged parents achieved a previously determined pre‐fiedging mass threshold (564 g; Sagar & Horning 1998). Body mass of adults carrying tags and returning from trans‐equatorial migration the following year were 4% lighter on average than non‐tagged birds, but this difference was not statistically significant. Reduced mass among chicks reared by adults carrying tags during the chick‐provisioning period indicated that adults altered “normal” provisioning behaviours to maintain their own body condition at the expense of their chicks. Population‐level information derived from telemetry studies can reveal important habitat‐linked behaviours, unique aspects of sea‐bird foraging behaviours, and migration ecology. Information for some species (e.g., overlap with fisheries) can aid conservation and marine ecosystem management. We advise caution, however, when interpreting certain data related to adult provisioning behaviours (e.g., time spent foraging, provisioning rates, etc.). If effects on individuals are of concern, we suggest shorter‐term deployments, smaller and lighter tags, and alternative attachment techniques, especially when investigating threatened or endangered species.     

Spatial and temporal variation in the provisioning behaviour of female rockhopper penguins Eudyptes chrysocome filholi

As seabirds are central place foragers during breeding, their provisioning behaviour and their ability to face variable energy demand from the chicks is expected to vary with environmental conditions. The provisioning behaviour of female rockhopper penguins Eudyptes chrysocome filholi was recorded over the chick‐rearing period at Kerguelen (KER) and Crozet (CRO) archipelagoes (two very distinct marine environments), using time‐depth recorders, or VHF transmitters coupled with an automatic recording station. No influences of the method have been found on the average foraging trip durations. Some previously undescribed short and multiple trips within a day were recorded using the automatic recording system. These multiple trips (6.8 h) were mostly performed with <5 days old chicks, a period during which feeding rates were the highest (1.1 meals per day), at both sites. During the brooding period, both KER and CRO females mainly performed daily trips of increasing duration (2 h longer at CRO) and at decreasing frequency. During the crèche compared to the brooding period, females from KER performed slightly fewer daily trips (0.6 per day) and more (<3 days) overnight trips, while females from CRO performed very few daily trips (0.1 per day) and more overnight trips, some of them being long trips lasting 5 to 29 days, mostly initiated during the transition between the brooding and the crèche periods. The result fit the hypothesis that long trips permit females to restore and/or maintain their body condition at more distant foraging places. It seemed that chick developement during the brooding period and environmental factors during the crèche period conditioned trip duration of females. Due to more long trips at CRO, the female feeding frequency was twice as high at KER than at CRO during the crèche period, while males participated in the feeding duties. Based on differences in female behaviour, we hypothesize that the male's contribution is likely to differ strongly from one site to another, and may buffer the possible decrease in female feeding frequency by feeding the chicks if food is less abundant.     

Foraging location and range of White-chinned Petrels Procellaria aequinoctialis breeding in the South Atlantic

The foraging range and principal feeding areas of White‐chinned Petrels breeding at South Georgia were determined using satellite telemetry. Foraging trips during incubation lasted 12–15 days and covered 3000–8000 km and 2–11 days and 1100–5900 km during chick‐rearing. Adults covered less distance per day during chick‐rearing (71 km) than during incubation (91 km) but the proportion covered at night (47%) was the same. Mean (31–34 km/h) and maximum (80 km/h) flight velocities were similar during both periods of the breeding season and during day and night. Between incubation shifts, White‐chinned Petrels travelled to the Patagonian shelf; during chick‐rearing they foraged more extensively. Most locations were between 30° to 55°W and 52° to 60°W around South Georgia/Shag Rocks and south to the South Orkney Islands. Diet samples from known foraging locations suggested birds fed mainly on krill and squid. They caught the squid Brachioteuthis? picta and Galiteuthis glacialis around Shag Rocks/South Georgia and also at sites close to the South Orkney Islands; Illex argentinus on the Patagonian shelf. Dispersal of adults after breeding failure was south to the South Orkney Islands then west to the Falkland Islands. This study confirms that breeding White‐chinned Petrels are amongst the widest‐ranging of seabirds; they may minimise competition with other Procellariiformes in the South Atlantic by their more extensive foraging range. The nature and extent of their range also brings substantial risk of high mortality rate in South Atlantic long‐line fisheries.     

Foraging trip decisions by the streaked shearwater Calonectris leucomelas depend on both parental and chick state

Parents of albatross and shearwater species employ a dual foraging strategy, feeding their chicks quickly in repeated short trips and then restoring their own fuel reserves during longer trips. A decline in parental body condition is believed to trigger longer trips, but chick body condition and age may also play a role. To investigate these factors in the little-studied streaked shearwater Calonectris leucomelas, we monitored the nest attendance of 17 pairs on Mikura Island in 2005 using an automated identification system. We also monitored body mass changes and meal masses of 5 of the 17 pairs using an automated weighing system. Although the birds did not show a clear dual foraging pattern, trip duration varied widely from 1 to 15 days. On average, the birds fed chicks 67.6 g during nighttime meals at 2.74-day intervals. Since meal mass did not depend on trip duration, feeding efficiency (meal mass delivered per unit trip duration) decreased as trip duration increased. Parents accumulated more energy reserves when they took longer trips. Parents appeared likely to initiate longer trips when their body condition declined or chick body condition recovered.     

Body mass patterns of Little Stints at different latitudes during incubation and chick-rearing

Due to the ‘double‐clutch’ mating system found in the arctic‐breeding Little Stint Calidris minuta, each parent cares for a clutch and brood alone. The resulting constraint on feeding time, combined with the cold climate and a small body size, may cause energetic bottlenecks. Based on the notion that mass stores in birds serve as an ‘insurance’ for transient periods of negative energy balance, but entail certain costs as well, body mass may vary in relation to climatic conditions and stage of the breeding cycle. We studied body mass in Little Stints in relation to breeding stage and geographical location, during 17 expeditions to 12 sites in the Eurasian Arctic, ranging from north Norway to north‐east Taimyr. Body mass was higher during incubation than during chick‐rearing. Structural size, as estimated by wing length, increased with latitude. This was probably caused by relatively more females (the larger sex) incubating further north, possibly after leaving a first clutch to be incubated by a male further south. Before and after correction for structural size, body mass was strongly related to latitude during both incubation and chick‐rearing. In analogy to a similar geographical pattern in overwintering shorebirds, we interpret the large energy stores of breeding Little Stints as an insurance against periods of cold weather which are a regular feature of arctic summers. Climate data showed that the risk of encountering cold spells lasting several days increases with latitude over the species’ breeding range, and is larger in June than in July. Maintaining these stores is therefore less necessary at southern sites and during the chick‐rearing period than in the incubation period. When guarding chicks, feeding time is less constrained than during incubation, temperatures tend to be higher than in the incubation period, reducing energy expenditure, and the availability of insect prey reaches a seasonal maximum. However, the alternative interpretation that the chick‐tending period is more energetically stressful than the incubation period, resulting in a negative energy balance for the parent, could not be rejected on the present evidence.     

Chick provisioning rates and growth in Blacklbrowed Albatross Diomedea melanophris and Grey-headed Albatross D. chrysostoma at Bird Island, South Georgia

We compared the parental division of labour and the pattern and rate of parental provisioning by two sympatric species of albatross of similar mass and breeding timetable but differing in diet and in the duration of chick‐rearing. Using electronic weighing platforms inside artificial nests, we recorded chick mass of Black‐browed Albatross and Grey‐headed Albatross at Bird Island, South Georgia every 10 minutes for both species in 1993 and 1994 and for each species in two other years between 1990 and 1996. The chick mass data (nearly one million weighings) were used to calculate meal mass (over 5000 meals) and intervals between meals. Adult birds were fitted with radio‐transmitters which allowed each meal to be allocated to the appropriate parent. The combination of meal mass and foraging trip duration were used to calculate provisioning rates for chicks and individual adults. Overall, Black‐browed Albatrosses delivered significantly lighter meals (569 g) than Grey‐headed Albatrosses (616 g) but more frequently (every 2.07 days and 2.50 days respectively). Thus combining foraging trip data for both parents, Black‐browed Albatross chicks received a meal every 1.22 days compared with 1.26 days for Greyheaded Albatross. These rates did not differ significantly. The contribution of each sex of each species in chick provisioning fluctuated between years, being similar in some years or biased towards males in others. Chicks of both species that failed to fledge received smaller, less frequent meals than successful chicks. In 1990 and 1994, Black‐browed Albatross chick provisioning rates were lower than in 1992 and 1993. In 1990, both meal mass and trip duration were affected, but only in 1994 was trip duration longer. Greyheaded Albatross chick provisioning rate was lower in 1994 than in other years but trip duration was longer. In each species, significant changes in meal mass and trip duration occurred within the chick‐rearing period. Chick provisioning rates invariably declined before chicks attained their peak mass. For both species, chick growth rates and peak and fledging mass, but not fledging age, were affected by differences in provisioning rate.     

The effects of food abundance on breeding performance and adult time budgets of Guillemots Uria aalge

The breeding performance, food fed to chicks and adult time budgets of Guillemots Uria aalge were examined in a year of high and a year of low food availabiIity. There was no difference between the 2 years in reproductive success, although the rate of chick feeding, chick weight and fledging success were greater in the year of high food availability. On average, chick prey items were larger in the poor food year, but this was insufficient to compensate for the lower feeding frequency. Chick feeding frequency did not differ between days in the good year but did increase later in the season in the poor food year. Compared with the high food availability year, adult Guillemots in the year of low food availability spent much less time resting at the breeding colony. and their foraging trips were twice as long. Foraging birds tended to make several successive trips before resuming brooding duties from their mates when food supplies were good, but in the low food availability year single trips were the norm. These results demonstrate that predators experiencing reduced food supply may mitigate the effects on their reproductive output by shifting their time allocation such that more time is available for foraging.     

Exploitation of distant Antarctic waters and close neritic waters by short‐tailed shearwaters breeding in South Australia

Identifying the primary foraging grounds of abundant top predators is of importance in marine management to identify areas of high biological significance, and to assess the extent of competition with fisheries. We studied the search effort and habitat selection of the highly abundant short‐tailed shearwater Puffinus tenuirostris to assess the search strategies employed by this wide‐ranging seabird. During the chick‐rearing period 52 individuals were tracked performing 39 short foraging trips (1–2 days), and 13 long trips (11–32 days). First‐passage time analysis revealed that 46% of birds performing short trips employed area‐restricted searches, concentrating search effort at an average scale of 14 ± 5 km. Foraging searches were more continuous for the other 54%, who travelled faster to cover greater distances, with little evidence of area‐restricted searches. The prey returned indicated that continuous searchers consumed similar prey mass, but greater prey diversity than area‐restricted search birds. On long trips 23% of birds travelled 500–1000 km to neritic (continental shelf) habitats, showing weak evidence of preference for areas of higher chlorophyll a concentration, and foraged at a similar spatial scale to short trips. The other 76% performed rapid outbound flights of 1000–3600 km across oceanic habitats commuting to regions with higher chlorophyll a. The spatial scale of search effort in oceanic habitat varied widely with some performing broad‐scale searches (260–560 km) followed by finer‐scale nested searches (16–170 km). This study demonstrates that a range of search strategies are employed when exploiting prey across ocean basins. The trade‐offs between different search strategies are discussed to identify the value of these contrasting behaviours to wide‐ranging seabirds.     

Overnight foraging trips by chick‐rearing Nazca Boobies Sula granti and the risk of attack by predatory fish

Most tropical booby species complete breeding foraging trips within daylight hours, thus avoiding nights at sea. Nazca Boobies Sula granti are unusual in this respect, frequently spending one or more nights away from the nest. We used GPS dataloggers, time‐depth recorders, and changes in body weight to characterize foraging trips and to evaluate potential influences on the decisions of 64 adult Nazca Boobies to spend a night at sea, or to return to their chicks on Isla Española, Galápagos, in daylight hours. The tagged birds foraged east of Isla Española, undertaking both single‐day (2–15 h, 67% of trips) and overnight trips (28 h–7.2 days, 33%), and executing 1–19 foraging plunge‐dives per single‐day trip. Birds might forage longer if they are in nutritional stress when they depart, but body weight at departure was not correlated with trip length. Birds might be expected to return from longer trips with more prey for young, but they returned from single‐day and overnight trips with similar body weights, consistent with previous indications that Nazca Boobies forage until accumulating a target value of prey weight. Birds with a lower dive frequency during the first 5 h of a trip were more likely to spend the night at sea, suggesting that they might choose to spend the night at sea if prey capture success was low. At night, birds almost never dived and spent most of their time resting on the water’s surface (11.8–12.1 h, > 99% of the time between civil sunset and civil dawn). Thus, the night is an unproductive time spent among subsurface predators under low illumination. The birds’ webbed feet provided evidence of this risk: 24% of birds were missing > 25% of their foot tissue, probably due to attacks by predatory fish, and the amount of foot tissue lost increased with age, consistent with a cumulative risk across the lifespan. In contrast, other tropical boobies (Blue‐footed Sula nebouxii and Brown Boobies Sula leucogaster), which do not spend the night on the water, showed no such damage. These results suggest that chick‐rearing Nazca Boobies accept nocturnal predation risk on occasions of low prey encounter during a foraging trip’s first day.