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.     

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.     

Foraging interactions between Wandering Albatrosses Diomedea exulans breeding on Marion Island and long-line fisheries in the southern Indian Ocean

Wandering Albatrosses Diomedea exulans are frequently killed when they attempt to scavenge baited hooks deployed by long-line fishing vessels. We studied the foraging ecology of Wandering Albatrosses breeding on Marion Island in order to assess the scale of interactions with known long-line fishing fleets. During incubation and late chick-rearing, birds foraged further away from the island, in warmer waters, and showed high spatial overlap with areas of intense tuna Thunnus spp. long-line fishing. During early chick-rearing, birds made shorter foraging trips and showed higher spatial overlap with the local Patagonian Toothfish Dissostichus eleginoides long-line fishery. Tracks of birds returning with offal from the Toothfish fishery showed a strong association with positions at which Toothfish long-lines were set and most diet samples taken during this stage contained fishery-related items. Independent of these seasonal differences, females foraged further from the islands and in warmer waters than males. Consequently, female distribution overlapped more with tuna long-line fisheries, whereas males interacted more with the Toothfish long-line fishery. These factors could lead to differences in the survival probabilities of males and females. Non-breeding birds foraged in warmer waters and showed the highest spatial overlap with tuna long-line fishing areas. The foraging distribution of Marion Island birds showed most spatial overlap with birds from the neighbouring Crozet Islands during the late chick-rearing and non-breeding periods. These areas of foraging overlap also coincided with areas of intense tuna long-line fishing south of Africa. As the population trends of Wandering Albatrosses at these two localities are very similar, it is possible that incidental mortality during the periods when these two populations show the highest spatial overlap could be driving these trends.     

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.     

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.     

Distribution, abundance and behaviour of Buller's, Chatham Island and Salvin's Albatrosses off Chile and Peru

During 15 cruises between 1980 and 1995, we studied three species of albatross that nest in New Zealand but occur as non‐breeders along the Pacific coast of South America: Buller's Thalassarche bulleri, Chatham Island T. eremita, and Salvin's Albatross T. salvini. We logged 547 h of observation, surveying 7638 km² of ocean surface, and recorded 86, 27, and 475 individuals, respectively, of the three species. Chatham Island and Salvin's Albatrosses occurred throughout the Humboldt Current, but habitats differed. Buller's and Salvin's Albatrosses preferred the continental slope, while Chatham Island Albatrosses frequented mostly pelagic waters. On a latitudinal basis, Salvin's Albatross distribution was skewed northward in the austral autumn and southward in spring; Chatham Island Albatross occurred southward during autumn, but was everywhere scarce in spring; and Buller's Albatross occurred almost exclusively in the south (30°S to 40°S) in both seasons. Upwelling and wind speed were positively correlated with densities of Buller's and Salvin's Albatrosses. Densities of Chatham Island Albatrosses also were positively correlated with wind speed, but they occurred further offshore in more stratified waters (with less mixing/upwelling) than did the other two. Pelagic population estimates for the Humboldt Current system, analysed using generalized additive models, peaked at 26 700 individuals for Buller's Albatross (95% confidence interval (CI) 13 100–37 100); 6790 for Chatham Island Albatross (CI 3900–11 100); and 133 100 for Salvin's Albatross (CI 82 800–183 600). Based on adult:subadult ratios observed in the study area, our best estimates for the number of wintering adults were 9100, 5800 and 114 400 birds, respectively, or 20%, 73% and 75% of the numbers estimated (44 500, 8000 and 153 300 birds) for the breeding populations at respective colonies. If we subtract from the autumn count the number of adult‐plumaged birds seen in spring (assumed to be non‐breeders), then respective percentages were 0%, 73% and 65%. Foraging locations and attraction by these birds to commercial fishing operations makes them susceptible to mortality as a result of the recent development of a long‐line fishery on the continental slope of Chile.     

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.     

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.     

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.     

Foraging movements of the Shy Albatross Diomedea cauta breeding in Australia; implications for interactions with longline fisheries

Satellite telemetry was used to identify the foraging zones of Shy Albatrosses Diomedea cauta breeding at two sites off Tasmania, Australia (Albatross Island in western Bass Strait and Pedra Branca to the south) to assess their level of interaction with longline fisheries. Adult birds from both colonies fed locally both in and outside the breeding season. Breeding birds from Albatross Island foraged over the Australian continental shelf or slope waters off northwest Tasmania, while those from Pedra Branca foraged between the colony and the southeastern edge of the continental shelf. The distances travelled by the birds and the duration of their foraging trips varied during the breeding cycle and tended to decrease as eggs approached hatching. Adults which were tracked near the end of the breeding season (March-April, n = 7 birds) deserted their chicks prematurely, and while dispersing further than incubating or brooding birds, they remained over the continental shelf and slope waters off southeast Australia. Home range analyses indicated 41% overlap between foraging zones of birds during successive breeding stages. Dispersal during the postbreeding period extended the foraging zones with less overlap between individuals (10% for Albatross Island and 19% for Pedra Branca). The recent contraction of the Japanese Southern Bluefin Tuna longline fishery to the south and east coasts of Tasmania has resulted in extensive overlap with adult Shy Albatrosses from Pedra Branca, but appears to pose a minimal threat to adult birds from Albatross Island. Coupled with the concomitant increase in the Australian domestic tuna longlining industry, adult Shy Albatrosses from southern Tasmania (Pedra Branca and the Mewstone) are vulnerable to incidental capture through out their annual cycle.     

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.     

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.     

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.     

Modelling the effect of fishing on southern Buller's albatross using a 60-year dataset

Abstract

Many albatross populations are declining and a major cause is believed to be incidental mortality from fishing. We investigated the effect of fishing on southern Buller's albatross Thalassarche bulleri bulleri, using a new approach to seabird population modelling that allows estimation of demographic parameters from multiple data types. Three types of data were used: a 60-year set of mark–recapture observations, four censuses of the breeding population, and estimates of fishing effort and bycatch. The fisheries risk to the viability of this population over the last 60 years appears to have been small, since the adult population is estimated to have increased about five-fold over that time. There is some cause for concern in recent changes (population growth has slowed, and perhaps reversed, and adult survival rates are falling). The most common age at first breeding was 12 years, and about 80% of adults breed each year. Annual survival was estimated to be 0.91 for juveniles, and varied between this value and 1 for adults. Though this population is not in immediate danger from fishing, there is a need for continued monitoring to see whether the recent fall in survival rates persists and causes a decline in abundance. Our analysis showed that when, as is common, mark–recapture data do not provide good estimates of all demographic rates, the assessment of seabird population trends can be improved by the use of other types of data, particularly abundance.     

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.     

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.     

Demographic parameters of black-browed albatrosses Thalassarche melanophris from the Falkland Islands

Black-browed albatrosses Thalassarche melanophris are currently classified as globally endangered. The most important populations of this species are believed to be declining due to, amongst other factors, unsustainable levels of incidental mortality in fishing gear. However, detailed demographic data are lacking for several critical populations, including the largest of all, nesting in the Falkland Islands. Here, we present data from the first Falkland Islands detailed demographic study (at New Island) and show that, from 2003 to 2009, the mean adult survival probability was 0.942 (95% CI: 0.930–0.952). Nesting frequency of adults is amongst the highest recorded for Thalassarche albatrosses and breeding success (0.564 chicks per egg) is within normal values. The nesting population in the intensively studied plots experienced an increase of 4% per year from 2004 to 2009. These results indicate that the Falklands population may not be as threatened as previously supposed, although studies from more sites and a longer time series are needed to confirm or refute this. The high survival rates may partly reflect recent efforts to mitigate bycatch made by the Falkland Islands and other fisheries in the region. The reinforcement of such initiatives may be critical to buffer the black-browed albatross population against ecosystem shifts and natural disasters (such as harmful algal blooms) that will likely become more frequent with ongoing global changes.     

Combined impacts of longline fisheries and climate on the persistence of the Amsterdam Albatross Diomedia amsterdamensis

Incidental capture of seabirds in longline fishing gear is a central issue in the conservation of many long-lived marine species. Despite growing evidence of climate-induced effects on population trends of long-lived species, climate change remains generally overlooked in most risk assessments of seabirds. Because variation in climate may interact with the detrimental effects of bycatch, considering climate is of great importance, especially in the context of ongoing global warming. This paper examines the combined effects of bycatch and climate change on the persistence of one of the world's rarest birds, the Amsterdam Albatross Diomedea amsterdamensis , which has a single population in the upland plateau of Amsterdam Island (Southeast Indian Ocean). Using continuous monitoring from 1983 onwards, we first estimated the relationship between climate and the species' demographic parameters. We then built a stochastic matrix population model to estimate the population growth rate and the probability that the population declines below the level recorded in 1983 of nine breeding pairs under different scenarios involving the joint effects of additional mortality caused by longline fisheries and climate change. The results suggest that the demography of the Amsterdam Albatross is influenced by climate in both breeding and wintering grounds and that these relationships may to some extent compensate for the impact of additive bycatch mortality. However, these compensatory effects would be negligible if the annual additional mortality exceeds around six individuals per year, suggesting that the resumption of longline fishery in the foraging range of the Amsterdam Albatross would rapidly put this species at risk of extinction.     

Size‐selective fishing affects sex ratios and the opportunity for sexual selection in Alaskan sockeye salmon Oncorhynchus nerka

Selective exploitation can cause adverse ecological and evolutionary changes in wild populations and also affect sex ratios but few studies have empirically documented skewed sex ratios in exploited fishes (other than species with extreme sexual size dimorphism, SSD). To investigate the possibility of sex‐selective fishing on Alaskan sockeye salmon Oncorhynchus nerka, we assessed sex ratios in fish at two spatial scales: within each of five fishing districts and among 13 breeding populations in one of these districts. We predicted that populations’ sex ratios would vary based on the average size of fish and SSD because size affects vulnerability to fishing. At the larger scale, we found a small but significant bias in fish returning to four of the five fishing districts (average = 52% females), and in four of the five districts males were caught at significantly higher rates than females. At the finer scale there was marked variation in sex ratio on the breeding grounds, ranging from 36% to 47% males. Populations with fish of intermediate sizes experienced the greatest sex ratio biases; the greater vulnerability of males than females to fishing resulted from a combination of larger SSD and different harvest rates between the sexes associated with the fishery size‐selectivity curve shape. Skewed sex ratios may change competition and behavior on the breeding grounds, relaxing selection on male traits associated with mate choice by females or intra‐sexual competition and altering demographic and evolutionary pressures on the fish. Assessment of the size selectivity of fishing gear and the population's SSD can help to illuminate if and how exploitation can affect sex ratios. Future studies examining size‐selective fishing should also evaluate the consequences for sex ratios, as this might help explain changes in harvested population structure and sustainability.