THE FOOD AND FEEDING ECOLOGY OF GREY-HEADED ALBATROSS DIOMEDEA CHRYSOSTOMA AND BLACK-BROWED ALBATROSS D. MELANOPHRIS

The food and feeding ecology of Black-browed Albatrosses and Grey-headed Albatrosses was studied from 1975 to 1978 at Bird Island, South Georgia. Two hundred and seventy food samples (averaging 75–85 % by weight of the mean chick feed) were collected from adults of each species in February and March. Chicks of both species received meals of the same size, of which half consisted of liquid. The three major components of the solid diet (krill, squid and fish) were similar for both albatrosses. By weight, fish represented about 35 % of the diet of both species; squid predominated (50 %) in the diet of Grey-headed Albatross, and krill (40 %) in the diet of Black-browed Albatross. Lampreys were confined to the Grey-headed Albatross and, although squid of similar sizes were taken by both species, Black-browed Albatrosses took a much greater diversity of squid. Each major prey type was associated with a characteristic amount of liquid in the complete samples and only in the case of krill and lamprey was this lipid-rich.
As these two albatrosses are of similar size, breed over the same period and feed meals of equivalent weight to their chicks at similar intervals, the difference in the composition of the diet is possibly the most significant mechanism of ecological segregation (in the breeding season).
Evidence of the effect of krill shortage in drastically reducing Black-browed Albatross breeding success is presented to support this. The two species have largely non-overlapping winter oceanic ranges which are probably also correlated with the distribution of preferred prey.     

Population dynamics of Black-browed and Grey-headed Albatrosses Diomedea melanophrys and D. chrysostoma at Campbell Island, New Zealand, 1942–96

The numbers of Black-browed Albatrosses Diomedea melanophrys and Grey-headed Albatrosses D. chrysostoma at Campbell Island, New Zealand, have declined dramatically since the 1940s. Black-browed Albatross numbers went into a steep decline in the 1970s and, since at least 1984, have been increasing slightly at average rates of 1.1% and 2.1% per annum at two colonies. The long-term downward trend in numbers of the Grey-headed Albatross has continued into the 1990s, averaging annually between 3.0% and 4.8% per annum at different colonies. A demographic study carried out between 1984 and 1996 indicates that Black-browed and Grey-headed Albatrosses have similarly high annual adult survival rates (0.945 and 0.953, respectively). Black-browed Albatrosses breed for the first time at a younger average age than do Grey-headed Albatrosses (10 years and 13.5 years, respectively), have a higher average breeding success (0.663 compared with 0.397 for the latter species) and are annual breeders whereas Greyheaded Albatross show a typical biennial pattern of breeding. Both show low survival from fledging to first breeding; averaging 0.186 and 0.162 for Black-browed and Grey-headed Albatrosses, respectively. Both species are accidentally killed in the Japanese long-line fishery for tuna Thunnus sp. in the Australasian region. The steep decline of Black-browed Albatross numbers in the 1970s was concomitant with the development of this fishery in the foraging region of the Campbell Island birds. Currently, the slight increase in numbers is due to high adult survival rates and breeding success, and is coincident with a great reduction in long-line fishing. With stable and high adult survival rates, it is expected that future population trends will be mainly influenced by the recruitment rates. The continuous decline in Grey-headed Albatross numbers since the 1940s, before long-line fishing developed in this region, indicates that natural environmental processes contributed to the downward trend in breeding numbers. Modelling indicates that Grey-headed Albatross numbers will continue to decrease with the present demographic parameters. A comparison between the species breeding at different sites shows that differing environmental conditions influence demographic characteristics.     

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.     

Reproductive endocrinology of the Black-browed albatross Diomedea melanophris and the Grey-headed albatross D. chrysostoma

Gonadal size and the circulating concentrations of two pituitary hormones (luteinizing hormone and prolactin) and three gonadal steroids (testosterone, progesterone and oestradiol-17β) were measured in two closely related Diomedea albatrosses at South Georgia. The Grey-headed albatross D. chrysostoma , if successful in rearing a chick, usually breeds biennially, whilst the Black-browed albatross D. melanophris normally breeds annually. Direct examination (by laparoscopy) of the gonads showed that the testes of both species underwent annual cycles, whilst endocrine data confirmed that those male Grey-headed albatrosses at the colony in the pre-laying period but not breeding in that year (having bred successfully the previous year) were apparently in full reproductive condition with elevated testosterone levels typical of breeding birds. However, the females of the two species differed markedly. Grey-headed albatrosses, in a year following successful breeding, had undeveloped ovaries with low levels of circulating oestradiol but high levels of progesterone, whereas the Black-browed albatrosses showed a pattern consistent with annual ovarian development. The profiles of gonadal steroids through the breeding season were similar for the males of both species but differences existed between the females. In the female Grey-headed albatrosses, transient peaks of progesterone were present throughout chick rearing but these were absent from Black-browed albatrosses. Prolactin had a similar profile in both species, with uniformly high levels throughout incubation and a rapid fall near the end of the brood-guard period. It is suggested that Grey-headed, like Black-browed, albatrosses are intrinsically annual breeders. However, if a female Grey-headed albatross breeds successfully in one year, then nutritional factors operate to ensure that in the following year the female does not show ovarian development, although the ovary is active in terms of progesterone secretion.     

Quantitative analysis of the use of discards from squid trawlers by Black-browed Albatrosses Diomedea melanophris in the vicinity of the Falkland Islands

In the past decade, a major trawl fishery for the squid Loligo gahi has developed in the vicinity of Beauchêne Island, an internationally important breeding site for the Black-browed Albatross Diomedea melanophris. The breeding season diet of this albatross in the Falklands and its use of discards generated by the Loligo fishery were investigated. Albatross chicks are fed extensively on commercially exploited species of squid and fish including Loligo gahi and southern blue whiting Micromesistius australis. The quantity of waste generated by the Loligo fishery amounts to c. 5% of the reported catch and just over 50% of this waste, mainly Loligo and nototheniid fish, is scavenged by adult Black-browed Albatrosses. The total quantity scavenged during the chick rearing period amounts to 1000–2000 tonnes per year. This is equivalent to 10–15% of the total food requirement of the breeding Black-browed Albatross population on Beauchene Island during the period when the fishery is operating. Although the Loligo fishery currently provides a significant quantity of food to these albatrosses, its net effect may be detrimental to them, as it is a much greater predator of Loligo stocks than the albatrosses are estimated to have been prior to the fishery's development.     

Fly or die: the role of fat stores in the growth and development of Grey-headed Albatross Diomedea chrysostoma chicks

Chicks of albatrosses, like other Procellariiformes, become independent at a mass similar to their parents but during growth attain a peak mass some 30% or more greater, before losing mass prior to fledging. The current views are that this high peak mass represents chicks storing fat reserves as an energy sink, or as an insurance against periodic food scarcity, or as a Consequence of natural stochastic variation in provisioning rate. We analysed growth and body composition of Grey‐headed Albatross Diomedea chrysostoma chicks at Bird Island, South Georgia in 1984 and 1986, two years of very different food availability. In 1984 when overall breeding success was only 28% (the lowest in 20 years and less than halt that in 1986), chicks were significantly smaller in terms of peak mass (by 37%), primary length (by 25%), liver, lung, heart and kidney size (by 18–34%) and fat (by 75–80%) but not significantly different in terms of skeletal (tarsus, culmen, ulna, sternum) or muscle (pectoral, leg) size. Despite these differences, there were some important similarities in the patterns of growth in both years. Up to the attainment of peak mass, most of the growth of organs and of skeletal structures was completed and little fat was deposited. In the remaining part of the chick‐rearing period, feather growth and acquisition of fat stores were undertaken. Thus Grey‐headed Albatross chicks begin to acquire substantial fat stores only during the later part of the development period; this is contrary to the predictions of any of the existing hypotheses concerning provisioning patterns and the role of fat stores in Procellariiformes. We propose that the deposition of fat in the later stages of chick growth is an adaptation to: (a) ensure against energy demands and/or nutritional stress affecting the quality of flight feathers (many of which are not renewed for up to three years after fledging); and (b) provide an energy reserve for chicks to use in the critical period immediately after independence.     

Moult in Black-browed and Grey-headed Albatrosses Diomedea melanophris and D. chrysostoma

We recorded the age of individual wing and tail feathers of Black-browed and Grey-headed Albatrosses Diomedea melanophris and D. chrysostoma of known age and breeding status at Bird Island, South Georgia. Breeders and non-breeders of both species moult their rectrices annually. Non-breeders moult primaries biennially. In the first year of a cycle, the outer three and some inner primaries are moulted descendantly; in the next year the inner primaries are moulted ascendantly, starting from primary seven. There is a general progression to moulting equal numbers of primaries in each half of the cycle by the time breeding starts at about 10 years of age. Grey-headed Albatrosses usually moult fewer primaries than Black-browed Albatrosses, particularly as 3-year-olds, when they undertake substantial plumage change in body moult. Most secondaries in Black-browed Albatrosses have been replaced once by age 4 years. Breeding Black-browed Albatrosses continue the moult pattern established as immatures whether they fail or not, as do failed Grey-headed Albatrosses. Successful Grey-headed Albatrosses, which breed again 16 months later, moult their three innermost primaries after breeding in the remainder of the current year and, after a period when moult is interrupted, renew the remaining primaries the following year. Comparisons between species and between failed and successful birds within species indicate that moult rate is not closely linked to the length of the interval between breeding attempts. Interspecies differences are better explained by breeding latitude, with tropical albatrosses moulting twice as fast as sub-Antarctic species, possibly reflecting food availability outside the breeding season.     

Growth and energy expenditure of Wandering Albatross Diomedea exulans chicks

Wandering Albatross Diomedea exulans chicks require 9–10 months to achieve adult body size at fledging, at which time they are also sexually size dimorphic. Because the developmental period spans the winter season, chicks must endure severe winter conditions and variability in provisioning effort by their parents. Thus chicks may adjust their rate of energy utilization to accommodate variations in provisioning, but this has not previously been studied. We followed longitudinally the changes in growth, body composition and oxygen consumption of 10 chicks from the end of the brooding period until fledging on the Crozet Islands. Body mass, culmen length and wing length were measured every 10 days and total body water (TBW) and resting metabolic rate (RMR) were measured monthly. Overall growth followed a logistic curve for all chicks, and sexual dimorphism in body mass appeared as early as the second month of measurements (males being heavier than females). Absolute TBW followed a logistic increase like that of body mass and was significantly higher in males owing to the difference in body mass. Conversely, mass-specific TBW (i.e. the proportion of body mass made up of water) did not differ significantly between male and female chicks. Absolute RMR peaked at 1.5 × adult basal metabolism in midwinter when chicks achieved maximum body mass, but decreased to adult levels by the time chicks fledged. The decrease in absolute RMR following attainment of peak mass is atypical of most seabird chicks (Procellariiformes) and may be explained partly by a reduction in size of the gut when parents reduce provisioning effort. The changes in mass-specific RMR did not differ between sexes but male chicks, being heavier, had higher absolute oxygen consumption and therefore greater energy requirements.     

Timing of fledging is influenced by glucocorticoid physiology in Laysan Albatross chicks

Fledging is a major life transition for birds, when juveniles move from the safety of a nest into an environment where they must find food and avoid predators. The timing of fledging within a season can have significant effects on future survival and breeding success. Proximate triggers of fledging are unknown: though wing development is likely a primary factor, other physiological changes, such as elevated plasma corticosterone (CORT), may affect fledging behavior. Laysan Albatross (Phoebastria immutabilis) chicks have an extended post−hatching period during which they reach 150% of adult mass. However, approaching fledging, chicks fast for days to weeks and lose mass while still putting energy into feather growth. We evaluated chick morphology and physiology to elucidate proximate triggers of fledging. As in some other species, CORT increased as chicks fasted and lost body mass. At the same time, corticosteroid binding globulin (CBG) declined, thus amplifying free CORT prior to fledging. Once chicks reached a morphological threshold, free CORT levels predicted how long they stayed at the colony: chicks with higher free CORT fledged sooner. To perturb the relationship between body condition, endocrine physiology, and fledging behavior, we supplementally fed chicks for the month before fledging. Fed birds had a slower decrease in body mass, slower decrease in CBG, slower increase in free CORT, and stayed at the colony longer after reaching a morphological threshold. Our study suggests that as chicks lose mass, free CORT acts as a signal of energetic or nutritional state to adjust the timing of fledging.     

Egg formation and the pre-laying period of Black-browed and Grey-headed Albatrosses Diomedea melanophris and D. chrysostoma at Bird Island, South Georgia

Egg composition and factors influencing egg formation were studied in Black-browed and Grey-headed Albatrosses Diomedea melanophris and D. chrysostoma at Bird Island, South Georgia. At nests where eggs were laid, females arrived 6–7 days after males, stayed one day during which 96% of observed copulations occurred, then departed to sea for c. 16 days in D. chrysostoma, c. 10 days in D. melanophris , returning c. two days before laying. Yolk deposition, however, lasted 21 and 20 days, and started 32 and 29 days before laying, in D. chrysostoma and D. melanophris respectively. Therefore, it is probably initiated by environmental factors not by copulation. Egg, albumen and yolk mass are significantly greater in D. chrysostoma but the proportionate composition of the species' eggs is nearly identical. Reduced differences in chick mass at hatching may reflect the longer incubation period in D. chrysostoma or relate to subsequent differences in chick growth rate.     

Individual quality and reproductive performance in the Grey-headed Albatross Diomedea chrysostoma

The reproductive performances of Grey-headed Albatrosses Diomedea chrysostoma with a previous record (≤5 years) of consistent success (≤70% chicks fledged from eggs laid—"top" birds) or failure (≤ 70% of attempts failed—"bottom" birds) were compared during 1993 -1995. In 1995, top birds arrived back at the colony significantly earlier, had significantly shorter first and second incubation shifts and hatched larger chicks which grew significantly faster than bottom birds. In 1994, top birds also had larger hatchlings with higher rates of growth than bottom birds. In 1994, top birds had significantly higher hatching, fledging and therefore overall breeding success than bottom birds; very similar trends were evident in 1993 and 1995. Chick-rearing success and all indices of chick growth suggested that food availability was high in 1995 (and 1993) and low in 1994. Therefore the superior performance of top birds was maintained in years of very different conditions, with the chick-rearing period particularly critical. A simple model (using published demographic parameters for Grey-headed Albatrosses on South Georgia) suggests that top birds would produce 2.5 more chicks over their lifetime than bottom birds. With the currently declining population numbers, the relative contribution of top birds to the next generation may be even greater than this.     

Male chicks are more costly to rear than females in a monogamous seabird, the Common Murre

Feeding rates and mass loss during chick rearing were comparedfor individually marked parents of male and female Common Murre(Uria aalge) chicks at Great Island, Newfoundland, Canada, from1997–2001. Both parents in this socially monogamous seabirdspecies share parental care duties until colony departure, afterwhich the single chick is fed only by its father. Because murresprovision their single chicks with one clearly visible fishper trip, it is possible to accurately determine whether parentsdifferentially feed male and female chicks. Based on slightlygreater mass of males in adulthood, possibly favored by sexdifferences in breeding roles, we predicted that male nestlingswould be fed more than females. Fathers' feeding rate to sons,but not daughters, increased with chick age, whereas maternalfeeding rate increased with chick age for both sexes. When year-correctedfeeding rates of pairs rearing both sexes were compared, bothmothers and fathers fed their sons significantly more than theirdaughters in the later part of the chick-rearing period. Moreover,parents rearing male chicks lost mass at a significantly higherrate than those rearing females. There was no difference infledging age for sons and daughters. These results indicatethat differential parental allocation occurs and has measurablecosts even in a species with only slight adult sexual dimorphism.     

Seabirds attending bottom long-line fishing off southeastern Brazil

Flocks of seabirds attending commercial bottom long-line fishing operations on the coastal shelf off southeastern Brazil show a greater species diversity during the summer than the winter (16 v 9 species), although the number of birds per flock tended to be greater during the cold season. During the summer, the Spectacled Petrel Procellaria aequinoctialis conspi-cillata was the commonest species, followed by the Great Shearwater Puffinus gravis, Cory's Shearwater Calonectris diomedea, skuas Stercorarius spp. and the Yellow-nosed Albatross Diomedea chlororhynchus. During the winter, the White-chinned Petrel Procellaria aequin-octialis, Yellow-nosed Albatross and Black-browed Albatross Diomedea melanophrys were jointly the commonest species. Marked differences in the relative abundance of species were observed between the different sampling periods, probably because of migratory movements but also because of seasonal shifts of the sea currents and the influence of cold fronts. Waters off southeastern Brazil are important feeding areas for some seabird populations nesting in the Tristan da Cunha and Gough group, especially for nonbreeding Spectacled Petrels and post-breeding Yellow-nosed Albatrosses.     

Sex-Based Differences in Adélie Penguin (Pygoscelis adeliae) Chick Growth Rates and Diet

Sexually size-dimorphic species must show some difference between the sexes in growth rate and/or length of growing period. Such differences in growth parameters can cause the sexes to be impacted by environmental variability in different ways, and understanding these differences allows a better understanding of patterns in productivity between individuals and populations. We investigated differences in growth rate and diet between male and female Adélie Penguin (Pygoscelis adeliae) chicks during two breeding seasons at Cape Crozier, Ross Island, Antarctica. Adélie Penguins are a slightly dimorphic species, with adult males averaging larger than adult females in mass (~11%) as well as bill (~8%) and flipper length (~3%). We measured mass and length of flipper, bill, tibiotarsus, and foot at 5-day intervals for 45 male and 40 female individually-marked chicks. Chick sex was molecularly determined from feathers. We used linear mixed effects models to estimate daily growth rate as a function of chick sex, while controlling for hatching order, brood size, year, and potential variation in breeding quality between pairs of parents. Accounting for season and hatching order, male chicks gained mass an average of 15.6 g d^-1 faster than females. Similarly, growth in bill length was faster for males, and the calculated bill size difference at fledging was similar to that observed in adults. There was no evidence for sex-based differences in growth of other morphological features. Adélie diet at Ross Island is composed almost entirely of two species—one krill (Euphausia crystallorophias) and one fish (Pleuragramma antarctica), with fish having a higher caloric value. Using isotopic analyses of feather samples, we also determined that male chicks were fed a higher proportion of fish than female chicks. The related differences in provisioning and growth rates of male and female offspring provides a greater understanding of the ways in which ecological factors may impact the two sexes differently.     

Quantifying habitat use in satellite-tracked pelagic seabirds: application of kernel estimation to albatross locations

We develop a new approach to quantifying habitat use within the foraging ranges of satellite-tracked seabirds. We applied kernel estimation techniques to 167 days (3738 locations) of data from Black-browed and Grey-headed albatrosses Diomedea melanophris and D. chrysostoma during the chick-rearing period of the breeding cycle at South Georgia. At this time the activity range of these two species covers an estimated 440 000 and 640 000 km², respectively, with very substantial overlap. In contrast, kernel estimation reveals that the main foraging areas of these two sympatric, congeneric species are very distinct. Based on location density categories accounting for 50% of locations, the foraging areas cover c. 81 500 and c. 119 700 km², respectively, with 42% and 50% of the range of one species overlapping with that of the other.     

Avian pox in Magellanic Penguins (Spheniscus magellanicus)

Avian pox is an enveloped double-stranded DNA virus that is mechanically transmitted via arthropod vectors or mucosal membrane contact with infectious particles or birds. Magellanic Penguins (Spheniscus magellanicus) from two colonies (Punta Tombo and Cabo Dos Bahías) in Argentina showed sporadic, nonepidemic signs of avian pox during five and two of 29 breeding seasons (1982-2010), respectively. In Magellanic Penguins, avian pox expresses externally as wart-like lesions around the beak, flippers, cloaca, feet, and eyes. Fleas (Parapsyllus longicornis) are the most likely arthropod vectors at these colonies. Three chicks with cutaneous pox-like lesions were positive for Avipoxvirus and revealed phylogenetic proximity with an Avipoxvirus found in Black-browed Albatross (Thalassarche melanophrys) from the Falkland Islands in 1987. This proximity suggests a long-term circulation of seabird Avipoxviruses in the southwest Atlantic. Avian pox outbreaks in these colonies primarily affected chicks, often resulted in death, and were not associated with handling, rainfall, or temperature.     

Lipid reserves,fasting capability and the evolution of nestling obesity in procellariiform seabirds

Several alternative explanations have been proposed to account for the evolution of nestling obesity in a variety of avian groups. These predict quite different patterns of fat accumulation, storage and use by chicks of different ages. Yet surprisingly few studies have measured changes in body composition during chick development. We tested the applicability of these hypotheses for fulmars, Fulmarus glacialis, by direct measurement of changes in water, lipid and lean dry mass in growing chicks. Lipid and lean dry mass increased until ca. 70% of the way through chick rearing, but then levelled off. Total body water also increased until the same stage, but gradually declined thereafter, and it was this change rather than fat metabolism that resulted in mass recession. The observed pattern of a continued increase in stored lipid, and most importantly, its maintenance all the way through the mass-recession phase until chicks reach fledging, is incompatible with many of the proposed hypotheses. We suggest that the most likely ultimate explanation for large fat deposits is to fuel chicks during the initial critical period away from the nest site while they learn to forage     

The diet of the Wandering Albatross Diomedea exulans at Subantarctic Marion Island

Summary The diet of the Wandering Albatross at Subantarctic Marion Island was studied by inducing recently fed chicks to regurgitate and by stomach flushing adults about to feed chicks. Liquid comprised 70.2% of stomach content mass recovered from chicks. Solid material comprised cephalopods (58.6% by mass), fish (36.5%) and crustacean, cetacean and seabird material as minor items. Twenty-three taxa of cephalopods were identified, the onychcteuthid squid Kondakovia longimana being the most important. Estimated average mass of squid was 694 g with a maximum of over 8 kg. Diet of the Wandering Albatross at Marion Island was broadly similar to that at other studied localities. The high proportion of cephalopods known to float after death in the diet, and the deep-water habits of the few fish identified, suggest that scavenging plays an important role in foraging behaviour.     

Use and exploitation of channel waters by the black-browed albatross

Black-browed albatrosses are the most abundant albatross species of the southern hemisphere, breeding on sub-Antarctic and Antarctic oceanic islands around the globe. Their foraging habitat during the breeding season is reasonably well known along its distributional range, indicating a preferred use of waters <500 m deep. The discovery of a colony inserted within the Admiralty Sound, Tierra del Fuego, poses an interesting challenge to the known precepts on foraging behavior for the species. In this study, we present the first record on the foraging distribution of the only known inner-channel colony of albatrosses in the world, using high-resolution GPS loggers. Black-browed albatrosses breeding at the Albatross Islet used exclusively inner-channel waters, at least during the chick-guard stage. Our results indicate a significant smaller foraging range during chick-guard compared with conspecifics from Diego Ramirez and Falklands/Malvinas Islands. Implications for the conservation of this colony are discussed.     

Growth and its relationship to fledging success of African black oystercatcher Haematopus moquini chicks

We investigated the growth of African black oystercatcher Haematopus moquini chicks on Robben Island, South Africa, over three austral summers, 2001-2004. Using a robust regression analysis to determine the growth parameters of chicks of known and unknown age we found that oystercatchers from our study population had a Gompertz growth rate coefficient that was 2% less than predicted for body mass based on the equation for waders. Leg growth lagged initially, then increased and slowed again as the chicks became older, whereas wing growth was slow initially but increased with age. Chicks with small growth rate coefficients for body mass exhibited retarded growth of all body measures except wing length. This enabled these chicks to fledge in a shorter period of time than their slow growth would otherwise allow. The growth rate of body mass was observed to vary greatly between chicks. Fast-growing African black oystercatchers had a shorter pre-fledging period; were larger at fledging and were more likely to fledge successfully. African black oystercatchers display sibling rivalry, and once a dominance relationship is established, the larger chick remains so during the pre-fledging period. Larger siblings fledged earlier and at a heavier mass than the smaller siblings and this may improve their chances of survival. Neither hatching date nor brood size influenced the growth rate coefficients.