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.     

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.     

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.     

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.     

Utilization of offal and discards from "finfish" trawlers around the Falkland Islands by the Black-browed Albatross Diomedea melanophris

Multinational fisheries operating in the vicinity of the Falkland Islands currently take c. 90,000 tonnes of true fish ("finfish" as opposed to squid) per annum, including hakes Merluccius spp., Southern Blue Whiting Micromesistius australis, Hoki Macruronus magel-lanicus and Red Cod Salilota australis, and generate substantial quantities of fisheries waste in the form of discards and offal. This paper examines the use made of this waste by scavenging Black-browed Albatrosses Diomedea melanophris which breed in the Falklands. The various types of waste produced are described and their consumption by scavenging albatrosses is quantified. The results indicate that Black-browed Albatrosses obtain c. 8000 tonnes of food per annum from this source, of which two-thirds is offal and the remainder whole discards. The energy content of this waste is equivalent to 4.4% of the estimated total annual energy requirements of the Falklands Black-browed Albatross population. However, as the fishery is a greater predator of finfish stocks than are the albatrosses, its long-term impact may be detrimental to these birds.     

Interannual variation in the diets of two albatross species breeding at South Georgia: implications for breeding performance

The diet and breeding performance of Grey‐headed Albatrosses Thalassarche chrysostoma and Black‐browed Albatrosses Diomedea melanophris breeding at Bird Island, South Georgia, were studied simultaneously during the chick‐rearing period between 1996 and 2000. When samples for all years were combined, cephalopods and crustaceans were the main components in the diet of Grey‐headed and Black‐browed Albatrosses, respectively. However, their diets exhibited interannual variations. Cephalopods were the most important component in the diet of Grey‐headed Albatrosses between 1996 and 1999 (60–75% by mass) but decreased significantly in 2000 (17%), when crustaceans dominated (61%). The Black‐browed Albatross diet varied greatly, with cephalopods being the most important component in 1996 (49% by mass) and 1997 (48%), fish in 1998 (32%) and 1999 (40%), and crustaceans in 2000 (63%). In 1998 and 2000 there was a significant change in the cephalopod species present in the diet of both albatross species, when their breeding success was low. The consumption of the ommastrephid Martialia hyadesi was significantly and positively correlated with Grey‐headed Albatross breeding success. For Black‐browed Albatrosses significant correlations were found between its consumption of the Icefish Champsocephalus gunnari and breeding success, and between its consumption of M. hyadesi and M. hyadesi CPUE (Catch per Unit Effort). These findings suggest that Grey‐headed Albatrosses are more reliant on Antarctic Polar Frontal Zone prey (M. hyadesi and Lamprey Geotria australis) whereas Black‐browed Albatrosses are more dependent on Antarctic prey (Icefish and Antarctic Krill Euphausia superba). The differences between diets of Grey‐headed and Black‐browed Albatrosses breeding on different islands of the Southern Ocean showed that Grey‐headed Albatrosses feed more on oceanic cephalopods (e.g. M. hyadesi) whereas Black‐browed Albatrosses feed primarily on shelf fish (e.g. Blue Whiting Micromesistius australis), suggesting that albatross diets are likely to be influenced by the geographical position of those islands, albatross foraging preference and prey availability.     

Dietary segregation of krill-eating South Georgia seabirds

The diets of six of the main seabird species (two petrels, two albatrosses, two penguins) breeding at Bird Island, South Georgia were studied simultaneously during the chick-rearing period in 1986. For five species, Antarctic krill Euphausia superba was the main food (39–98% by mass); grey-headed albatrosses took mainly the ommastrephid squid Martialia hyadesi (71%) and only 16% krill. The size of the krill taken was similar between seabird species, although there were small but significant differences between penguins and the other species. Sex and reproductive status of krill, however, was different between all seabird species, reflecting some combination of differences in foraging ranges, selectivity by predators, or differences in escape responses of krill. For the krill-eating species, the rest of the diet varied substantially between species, comprising Martialia and nototheniid fish (blackbrowed albatross and, along with lanternfish, white-chinned petrel), lanternfish and amphipods (Antarctic prion and macaroni penguin), and icefish (gentoo penguin). Long-term data on breeding success and information on diet in 5–10 other years suggest that in 1986 seabird diet and reproductive performance was indicative of a year of good availability of krill around South Georgia. In such circumstances, ecological segregation between krill-eating species appears to be maintained chiefly by differences in foraging range and feeding methods, which are reviewed. This situation is rather different from the few studies of seabird communities elsewhere, where prey type and size are believed to be the main mechanisms of dietary segregation.     

Food, feeding ecology and ecological segregation of seabirds at South Georgia

At the sub-Antarctic island of South Georgia 25 of the 29 breeding species are seabirds. Fifteen of these have recently been studied in some detail. By examining the timing of their breeding seasons and their diet and feeding ecology (especially feeding techniques and potential foraging ranges), the nature of their ecological isolating mechanisms, and in particular the way in which they partition the resources of the marine environment, are reviewed.
Although breeding season adaptations occur (winter breeding in Wandering Albatross and King Penguin; out of phase breeding in two species-pairs of small petrels) these are less important than dillerences in food and feeding ecology. There is a fundamental distinction between the niche of pursuit-diving species (mainly penguins) and the remainder which are basically surface-feeders. The two abundant krill-eating penguins show clear differences in feeding zones. Three albatrosses and a petrel feed mainly on squid and there are differences in both the species and size of the prey of each. The remaining seabirds chiefly take krill (although the giant petrels are extensive scavengers and some smaller petrels specialize on copepods) and utilize different feeding methods and areas to do so.
Various adaptations related to inshore and offshore feeding zones are discussed. Although most species possess a combination of ecological isolating mechanisms additional evidence for the particular importance of dietary differences is presented.     

The fish diet of black-browed albatrossDiomedea melanophris and grey-headed albatrossD. Chrysostoma at South Georgia

 The fish component of the diet of black-browed and grey-headed albatrosses at South Georgia was investigated by intercepting 155 meals from adults arriving to feed chicks during February 1986 and 1994. Fish represented 30% and 72% by mass of the diet of black-browed albatrosses and 14% and 60% by mass of the diet of grey-headed albatrosses in 1986 and 1994 respectively. We determined the identity and quantified the contribution (by numbers, size and mass) of fish species mainly by using otoliths (54 representing 9 taxa and 57 representing 17 taxa in black-browed and grey-headed albatross samples respectively). For black-browed albatrosses in 1986 the main fish prey was Patagonotothen guntheri (77% of otoliths, 51% of estimated fish biomass) and a single large specimen of Icichthys australis (40% estimated biomass), whereas in 1994 Pseudochaenichthys georgianus was the main fish prey (57% of estimated biomass) with Magnisudis prionosa (30%) and Champsocephalus gunnari (12%) also making substantial contributions. Grey-headed albatross samples from 1986 were dominated by southern lampreys (40% by number, 79% of estimated biomass), lanternfish (32% of numbers, 9% by mass) and Patagonotothen guntheri (11% by mass); in 1994 Champsocephalus gunnari (42% by numbers, 24% by mass), Magnisudis prionosa (13% by number, 36% by mass), Muraenolepis microps (90% by number), Pseudochaenichthys georgianus (15% by mass) and lanternfish (18% by number but only 1% by mass) were the main prey. The importance of Patagonotothen guntheri to both species in 1986 and its absence in 1994 probably reflect albatrosses obtaining it from the commercial fishery, which was active in 1986 but closed in 1994. Otherwise the fish diet of black-browed albatrosses is dominated by krill-feeding fish, characteristic of the waters of the South Georgia shelf. In contrast, the grey-headed albatross diet comprises deeper water mesopelagic species, especially lanternfish, which reflect its affinity for the Antarctic Polar Frontal Zone and associated oceanic upwellings. Received: 28 June 1995 / Accepted: 8 October 1995     

Chick growth in albatrosses: curve fitting with a twist

We present a new type of equation to describe the growth patterns of procellariiform seabirds and other species whose chicks characteristically lose mass towards the end of the rearing period. Our equation is based on the Gompertz curve; our principles are also applicable to logistic and von Bertalanffy curves. From our model, five coefficients can be derived to characterise the patterns of growth. These are: growth rate, peak mass and age at which it is attained, loss rate and an index describing the overall shape of the curve. We illustrate the use of this new equation with data collected, using automated weighing platforms, on six years of chick growth of Black-browed Diomedea melanophris and Grey-headed D. chrysostoma albatrosses at Bird Island, South Georgia. In comparison with Grey-headed Albatross, Black-browed Albatross chicks grow at a faster rate and to a higher peak mass; they also reach their peak mass at an earlier age, and lose mass at a faster rate in the mass recession period. However, in both species, chicks reached peak mass when 72% of the rearing period had elapsed; within species, only this did not vary between years. This new equation not only enables the period of mass recession to be incorporated into growth analysis, but, because it does not require assumptions about asymptotic mass, greatly facilitates inter-species comparisons.     

Global relationships amongst black-browed and grey-headed albatrosses: analysis of population structure using mitochondrial DNA and microsatellites

The population structure of black-browed (Thalassarche melanophris and T. impavida) and grey-headed (T. chrysostoma) albatrosses was examined using both mitochondrial DNA (mtDNA) and microsatellite analyses. mtDNA sequences from 73 black-browed and 50 grey-headed albatrosses were obtained from five island groups in the Southern Ocean. High levels of sequence divergence were found in both taxa (0.55-7.20% in black-browed albatrosses and 2.10-3.90% in grey-headed albatrosses). Black-browed albatrosses form three distinct groups: Falklands, Diego Ramirez/South Georgia/Kerguelen, and Campbell Island (T. impavida). T. melanophris from Campbell Island contain birds from each of the three groups, indicating high levels of mixture and hybridization. In contrast, grey-headed albatrosses form one globally panmictic population. Microsatellite analyses on a larger number of samples using seven highly variable markers found similar population structure to the mtDNA analyses in both black-browed and grey-headed albatrosses. Differences in population structure between these two very similar and closely related species could be the result of differences in foraging and dispersal patterns. Breeding black-browed albatrosses forage mainly over continental shelves and migrate to similar areas when not breeding. Grey-headed albatrosses forage mainly at frontal systems, travelling widely across oceanic habitats outside the breeding season. Genetic analyses support the current classification of T. impavida as being distinct from T. melanophris, but would also suggest splitting T. melanophris into two groups: Falkland Islands, and Diego Ramirez/South Georgia/Kerguelen.     

Predator–prey interactions: why do larger albatrosses eat bigger squid?

The relationship between predator sizes and prey sizes is well documented for terrestrial but rarely for marine ecosystems. We show that wandering albatrosses, the biggest albatross species, feed on larger cephalopod prey than those consumed by smaller albatrosses (grey-headed and black-browed albatrosses). This reflects differences in timing of breeding, foraging ecology and their feeding methods. Wandering albatrosses breed later in the year, during the austral winter, than smaller albatrosses (therefore catching older squid) and forage most of the year in Antarctic open waters, sub-Antarctic, subtropical and tropical waters, overlapping minimally with the smaller albatrosses' foraging range while breeding. Also, wandering albatrosses mostly scavenge whereas smaller albatrosses feed more on live prey. Prey ecology may also play a key role because many squid species might experience post-spawning mortality during the austral winter, becoming easily available to wandering albatrosses. Spawning in winter can be linked to predator avoidance (i.e. reduction in mortality in winter by avoiding pelagic predators) and would allow squid larvae to develop and take advantage of the high productivity (i.e. Antarctic phytoplankton bloom) in spring and at the beginning of summer. Thus, aspects of prey and predator ecology may combine to generate observed differences in prey size.     

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.     

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.     

Associations among Antarctic seabirds in mixed-species feeding flocks

We studied ten mixed-species feeding flocks of seabirds and seals off South Georgia (55̀S, 35̀W) to assess the factors that influenced the species composition of the flocks. The ten flocks were distributed between two oceanographic regions; four flocks were observed off the northwestern end of South Georgia, and six off the island's southeastern end. The flocks differed dramatically in size and species composition. The northwestern flocks were ten to 20 times larger and contained more seals and penguins. We tested whether these differences were a consequence of location, because the two regions were populated by different assemblages of species, and determined that this was not the case. Differences in flock size and species composition reflected differences in the depth distribution of the birds' and seals' prey. The northwestern flocks were associated with deep swarms of Antarctic krill Euphausia superba with a significant quantity of krill also present at the surface. We also tested for differential flock participation by the species found in the surrounding waters and classified species by their proclivity to participate in the flocks. Our results indicate that Black-browed Albatross Diomedea melanophris have a strong tendency to join, and diving-petrels Pelecanoides spp. to avoid, mixed-species feeding flocks. We postulate that Black-browed Albatrosses serve as visual cues to the presence of food for one another and for other species, and that diving-petrels avoid mixed-species flocks in part because of the risk of predation.     

INVESTIGATING THE BIASES IN THE USE OF HARD PREY REMAINS TO IDENTIFY DIET COMPOSITION USING ANTARCTIC FUR SEALS (ARCTOCEPHALUS GAZELLA) IN CAPTIVE FEEDING TRIALS

The analysis of pinniped scats has been used to quantify their diet, using prey remains to identify species and to estimate the numbers and sizes of prey consumed. There are, however, potential biases involved with scat analysis and, for this method to be used successfully, these biases need to be quantified. Thirty-six Antarctic fur seals ( Arctocephalus gazella ) were fed meals of exclusively either fish, squid, or krill and their scats were collected and analyzed. The major sources of error in the analysis of prey remains from scats were the differential erosion and passage rate of items in relation to their size. However, using simple correction functions, such as those which model otolith erosion, it is possible to reduce these errors. Using plastic beads as dietary markers showed recovery rates were negatively related to their size. Larger squid beaks had lower recovery rates than smaller beaks, but there was no size-related bias in the recovery rates of krill carapaces. Only 33% of the squid beaks and 27% of the otoliths originally fed were recovered from the scats. Recovery rates were greater for squid (77%) and fish (50%) eye lenses and these structures gave a better estimate of numbers eaten. Differences found between experimentally derived and published regression equations (used to calculate prey sizes eaten from prey remains) highlights the need for regression equations based on local prey characteristics, if these are to be used with any success to describe the prey eaten.     

The diet of the Imperial Shag Phalacrocorax atriceps at a colony on New Island, Falkland/Malvinas Islands combining different sampling techniques

The diet of the Imperial Shag Phalacrocorax atriceps was studied on New Island, Falkland/Malvinas Islands during the 2008/2009 breeding season, with some additional data from 2007/2008. The diet comprised a large variety of prey, mainly fish, crustaceans and squid. In contrast to other species of the blue-eyed shag complex, prey not only consisted of benthic organisms but also included pelagic prey. Different sampling techniques were combined in order to obtain a comprehensive overview of the diet. Pellets, regurgitations and stomach contents yielded different results. We discuss the causes for these variations including different sample availability over time. In particular, the stomach analyses seem to overestimate the importance of squid based on the occurrence of squid beaks. For the pellet analyses, lobster krill accounted for the majority of the prey remains except during the second half of December (i.e. when young chicks were being attended), when fish was more important.     

Intraspecific differences in the diet of Antarctic fur seals at Nyrøysa, Bouvetøya

Intraspecific differences in the diets of many species of pinnipeds are to be expected in view of the great differences in morphology, life history and foraging behaviour between the sexes of many species. We examined the diet of the Antarctic fur seal population at Bouvetøya, Southern Ocean, to assess intersexual differences. This was made possible by the analysis of prey remains extracted from scats and regurgitations collected in areas used primarily by one or the other sex. The results indicate that both males and females feed primarily on Antarctic krill Euphausia superba with several species of fish and squid being taken, likely opportunistically given their prevalence. Significant differences were identified in the frequency of occurrence of otoliths in scats and the percentage numerical abundance of the major fish prey species in the diet. Adult males ate a smaller quantity of fish overall, but ate significantly more of the larger fish species. The greater diving capabilities of males and the fact that they are not limited in the extent of their foraging area by having to return regularly to feed dependant offspring may play a role in the differences found between the diets of males and females. Additionally, females might be more selective, favouring myctophids because they are richer in energy than krill. The absence of major differences in the diet between the sexes at this location is likely due to the high overall abundance of prey at Bouvetøya.     

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.     

Fish prey of the Wandering Albatross Diomedea exulans at South Georgia

Summary The fish diet (45% of total diet by weight) of Wandering Albatrosses rearing chicks at South Georgia during the austral winters of 1983 and 1984 was investigated using otoliths retrieved from regurgitations. These provide the first quantitative data for this species and for any albatross. By number of identified otoliths (32% could be identified only as ?Macrouridae and ?Moridae), Pseudochaenichthys georgianus (35%), Muraenolepis microps (33%) and Chaenocephalus aceratus (20%) predominated, with Notothenia gibberifrons, Pagothenia hansoni and Champsocephalus gunnari (together 12%) also present. Composition by weight (estimated from otolith length) of the main species was Pseudochaenichthys 51%, Muraenolepis 14%, Chaenocephalus 27%; if digestion and wear had reduced otoliths by 10% the values would be Pseudochaenichthys 54%, Chaenocephalus 25%, Muraenolepis 13%. Composition by weight (actual or corrected values) was almost identical between years but epipelagic fish were significantly more abundant in 1983 than 1984. All identified fish eaten by Wandering Albatrosses are common on the South Georgia continental shelf and most of them are caught in the commercial fishery there. However, two of the three main target species of this fishery in 1983–1984, Notothenia rossii and Champsocephalus were not, or rarely, caught by Wandering Albatrosses. It seems unlikely, therefore, that the albatrosses depend greatly on the fishery for acquisition of fish prey but how they catch several species, including Muraenolepis, which are mainly benthic in habit is unknown.