Foraging locations of female New Zealand sea lions (

Figure of Eight Island is located in the southern end of the Auckland Islands and hosts the smallest breeding colony of New Zealand (NZ) sea lions (Phocarctos hookeri). Between 1995/96 and 2005/06, pup production in this colony decreased by 57% (from 144 to 62 pups). In contrast, there was a 30% decrease in pup production in the largest colony in the north-east of the Auckland Islands over the same period. NZ sea lions in the Auckland Islands area are subject to by-catch deaths and resource competition from subantarctic trawl fisheries. The present study investigated where four lactating females from Figure of Eight Island foraged during the austral summer of 2007/08 and compared their foraging areas with female NZ sea lions from the northern Auckland Islands breeding locations (Enderby and Dundas islands) and with fisheries activities. Females foraged south of Adams Island (the southernmost Auckland Island), predominantly at the edge of the Auckland Islands shelf, but those from Figure of Eight Island made shorter foraging trips within more concentrated areas than females from Enderby or Dundas islands. The 59 female NZ sea lions satellite-tracked to date from Figure of Eight, Enderby and Dundas islands foraged over the entire area of the Auckland Islands shelf and many (including three of the four females from Figure of Eight Island) had extensive overlap with subantarctic trawl fisheries. Further research is needed to determine whether the foraging behaviour of females from Figure of Eight Island is linked to their greater decline in pup production.     

On‐land habitat preferences of female New Zealand sea lions at Sandy Bay,Auckland Islands

Terrestrial habitat is important for breeding in most pinnipeds. On land, most species remain near the shore, but New Zealand (NZ) sea lions, Phocarctos hookeri, often rest inland up to 1.5 km from the sea. Only three breeding areas of NZ sea lions exist today after the species was extirpated from its historical range (NZ mainland). The study was conducted at the Sandy Bay breeding colony, Auckland Islands, between December 2002 and March 2003. We used daily Global Positioning System locations of breeding females with pups and mapping in a Geographic Information System to determine terrestrial habitat use and preferences. Slopes less than 20° were preferred throughout the study. Females chose nursing sites with a seasonal change, preferentially based on the distance from the sea and habitat type. Comparisons with the other breeding colonies of NZ sea lions are presented and data are discussed in the context of the recolonization of the NZ mainland. Overall, the most suitable terrestrial habitat configuration for a breeding aggregation of NZ sea lions appears to be a sandy beach, with a wide area above high tide and moderate intertidal zone (for breeding), backed with vegetated sand dunes and forest on primarily flat terrain (for later dispersion).     

Growth and survival of New Zealand sea lions, <Emphasis Type="Italic">Phocarctos hookeri:</Emphasis> birth to 3 months

Offspring birth mass and growth rate represent important life history traits, which influence many vital population and individual characteristics, while offspring survival is a key factor in variation in female reproductive success. For a threatened population of pinnipeds, such as New Zealand sea lions, Phocarctos hookeri, (Grey, 1844, NZ sea lions), understanding individual life history parameters and population dynamics is vital for their management and conservation. This is the first study of the behaviour of females during parturition, pup birth mass and growth, and pre-weaning survival of NZ sea lions, Enderby Island, Auckland Islands during austral summer breeding seasons, 2001/2002 to 2003/2004. Pregnant females arrived ashore 2.1 ± 0.16 days prior to giving birth. After parturition, mothers suckled their pups for 8.6 ± 0.16 days before leaving on their first foraging trip. Male pups were born significantly heavier than female (males 10.6 ± 1.4 kg, females 9.7 ± 0.9 kg). Pups lost on average 48 ± 0.14 g per day mass during the early postpartum period (between birth and mothers first foraging trip). Pup mortality did not vary by pup sex, birth mass, date of birth or any maternal characteristics however it varied significantly between years due to a bacterial infection epidemic (Pup mortality at 60 days: 2001 32%; 2002 21%; 2003 12%). The absolute growth rate per day for pups was 151 g/day over all years. Pup growth rate measured as the slope of linear line fitted to pup mass by age was consistently higher for pups with heavier birth mass, male pups and during the 2002 season. High offspring mortality and slow growth rates coupled with maternal foraging behaviour at their physiological limits may reflect a threatened species which has limited ability for population growth in an environment which is at the extreme of their historical range and impacted upon by fisheries.     

Population viability analysis of New Zealand sea lions, Auckland Islands, New Zealand’s sub-Antarctics: assessing relative impacts and uncertainty

A common issue faced in wildlife management is how to assess the uncertainty of potential impacts on the viability of a species or population. The pup production of New Zealand (NZ) sea lions (Phocarctos hookeri) has declined 50% in the last 12?years at their main breeding area, the Auckland Islands. The two major known atypical impacts on NZ sea lions are as follows: (1) the direct mortality as bycatch of trawling and (2) bacterial epizootics, which can affect reproduction and mortality. Both of these impacts include high levels of uncertainty, with fisheries data being variable due to percentage observer coverage and the effect of sea lion exclusion devises, while the timing and severity of bacterial epizootics are not predictable. In this paper, an age-structured model of the NZ sea lion population at the Auckland Islands was built to examine the predicted effects of fisheries mortality and catastrophes (bacterial epizootics), both separately and then combined, on population viability over a 100-year period using the VORTEX population viability analysis programme. These models are then compared against 15?years of empirical field data to determine the actual level of impacts being observed. Model results indicate that although naturally occurring epizootics reduce the growth rate of the population, it does not cause a decline in the Auckland Island population. However, sustained fisheries bycatch at current estimated levels, particularly considering its potential impact on adult female survival, could result in a population decline and possible functional extinction over the modelled time period.     

Variability in the diet of New Zealand sea lion (Phocarctos hookeri) at the Auckland Islands, New Zealand

We examined the stomach contents of 121 New Zealand (NZ) sea lions ( Phocarctos hookeri ) caught by the squid fishery during the summer/autumn 1997–2006 around the Auckland Islands (51°S, 166°E). Dietary variation was assessed among juveniles, lactating females, nonlactating females and males, and between areas on the Auckland Islands shelf. The digested fraction of the contents consisted mostly of opalfish ( Hemerocoetes spp.) (50.1% by number [ N ], 4.7% by mass [ M ]), rattail ( Coelorinchus spp.) (12.0% N , 2.4% M ), arrow squid ( Nototodarus sloani ) (14.1% N , 17.9% M ), octopus ( Enteroctopus zealandicus ) (2.1% N , 27.8% M ), and red cod ( Pseudophycis bachus ) (3.8% N , 4.3% M ). Opalfish was found in greater proportions in the stomachs of females (lactating: 58.1% N , nonlactating: 62.4% N ) and juveniles (56.9% N ) than males (14.5% N ). Juveniles caught smaller opalfish and rattail than adults did. Over all classes, sea lions ate larger prey in the east than in the north of the Auckland Islands shelf. The common prey—arrow squid and rattail—constitute an abundant resource at the edges of the Auckland Islands shelf, where lactating NZ sea lions forage. Although these key areas are far from the rookeries and impacted by the squid fishery, they may provide the only reliable resource able to support the cost of benthic foraging behavior in the deepest diver of all otariids.     

The population decline of the New Zealand sea lion Phocarctos hookeri: a review of possible causes

• 1 The New Zealand (NZ) sea lion Phocarctos hookeri is NZ's only endemic pinniped and is listed as ‘nationally critical’. The species breeds in the NZ sub‐Antarctic: 71% of the population at the Auckland Islands (2010 pup production: 1814 ± 39) and the remaining 29% on Campbell Island (726 pups in 2010).
• 2 Pup production at the Auckland Islands has declined by 40% since 1998 (1998: 3021 pups produced): only 1501 pups were born in 2009. This decline is directly linked to philopatric females not returning to breeding areas. While the Auckland Island population has declined, the Campbell Island population appears to be increasing slowly.
• 3 Potential reasons for the decline in the Auckland Island population, but not in the Campbell Island population, include non‐anthropogenic factors: (i) disease epizootics, (ii) predation, (iii) permanent dispersal or migration, (iv) environmental change; and anthropogenic impacts: (v) population ‘overshoot’, (vi) genetic effects, (vii) effects of contaminants, (viii) indirect effects of fisheries (i.e. resource competition) and (ix) direct effects of fisheries (i.e. by‐catch deaths). Of the nine potential reasons examined here, six can be discounted (ii–vii). Bacterial epizootics (i) occur in the NZ sea lion population, but their impact has predominantly increased pup mortality, which is unlikely to cause the severe decline observed, as pup mortality throughout the species is naturally high and variable.
• 4 The most plausible hypotheses, based on available evidence, are that the observed decline, in particular, the decreasing number of breeding females in the Auckland Island population, is caused by (viii) fisheries‐induced resource competition and (ix) fisheries‐related by‐catch. By‐catch is the main known anthropogenic cause of mortality in the species. Competition with fisheries resulting in resource competition, nutrient stress and decreased reproductive ability in NZ sea lions should be a priority area for future research.

     

Foraging site fidelity of lactating New Zealand sea lions

Ecologists often describe the foraging ecology of a species as a whole, treating conspecific individuals as ecologically equal. However, individual specialization has potentially important ecological, evolutionary and conservation implications. Foraging studies are usually based on the foraging behaviours of individuals sampled in only 1 year. In this study, the site fidelity of foraging locations of nine female New Zealand sea lions (NZ sea lions Phocarctos hookeri ) from Enderby Island, Auckland Islands, were investigated by repeating their satellite tracking between 1 and 4 years after they were first tracked. Females were monitored during early lactation in the austral summers of 2001–2005. The kernel ranges of females' foraging satellite location concentrations overlapped consistently within and between years. As predicted for benthic foragers, NZ sea lions show low individual variability in foraging behaviour and greater specialization. It is important to understand the spatial and temporal limitations on an individual's foraging-site fidelity, because they can affect a species' ability to cope with environmental changes and anthropogenic impacts. This has significant implications for NZ sea lions management and conservation.     

Size and experience matter: diving behaviour of juvenile New Zealand sea lions (Phocarctos hookeri)

The diving ability of juvenile animals is constrained by their physiology, morphology and lack of experience, compared to adults. We studied the influences of age and mass on the diving behaviour of juvenile (2–3-year-old females, n = 12; 3–5-year-old males, n = 7) New Zealand (NZ) sea lions (Phocarctos hookeri) using time–depth recorders (TDRs) from 2008 to 2010 in the NZ subantarctic Auckland Islands. Diving ability (e.g. dive depth, duration and bottom time per dive) improved with age and mass. However, the percentage of each dive spent at the bottom, along with percentage time at sea spent diving, was comparable between younger and lighter juveniles and older and heavier juveniles. These suggest that younger and older juveniles expend similar foraging effort in terms of the amount of time spent underwater. Only, 5-year-old male juveniles dove to adult female depths and durations and had the highest foraging efficiency at depths >250 m. It appears that juvenile NZ sea lions attain adult female diving ability at around 5 years of age (at least in males), but prior to this, their performance is limited. Overall, the restricted diving capabilities of juvenile NZ sea lions may limit their available foraging habitat and ability to acquire food at deeper depths. The lower diving ability of juvenile NZ sea lions compared to adults, along with juvenile-specific constraints, should be taken into consideration for the effective management of this declining, nationally critical species.     

Sexual Segregation in Juvenile New Zealand Sea Lion Foraging Ranges: Implications for Intraspecific Competition,Population Dynamics and Conservation

Sexual segregation (sex differences in spatial organisation and resource use) is observed in a large range of taxa. Investigating causes for sexual segregation is vital for understanding population dynamics and has important conservation implications, as sex differences in foraging ecology may affect vulnerability to area-specific human activities. Although behavioural ecologists have proposed numerous hypotheses for this phenomenon, the underlying causes of sexual segregation are poorly understood. We examined the size-dimorphism and niche divergence hypotheses as potential explanations for sexual segregation in the New Zealand (NZ) sea lion (Phocarctos hookeri), a nationally critical, declining species impacted by trawl fisheries. We used satellite telemetry and linear mixed effects models to investigate sex differences in the foraging ranges of juvenile NZ sea lions. Male trip distances and durations were almost twice as long as female trips, with males foraging over the Auckland Island shelf and in further locations than females. Sex was the most important variable in trip distance, maximum distance travelled from study site, foraging cycle duration and percent time at sea whereas mass and age had small effects on these characteristics. Our findings support the predictions of the niche divergence hypothesis, which suggests that sexual segregation acts to decrease intraspecific resource competition. As a consequence of sexual segregation in foraging ranges, female foraging grounds had proportionally double the overlap with fisheries operations than males. This distribution exposes female juvenile NZ sea lions to a greater risk of resource competition and bycatch from fisheries than males, which can result in higher female mortality. Such sex-biased mortality could impact population dynamics, because female population decline can lead to decreased population fecundity. Thus, effective conservation and management strategies must take into account sex differences in foraging behaviour, as well as differential threat-risk to external impacts such as fisheries bycatch.     

Unique and isolated: population structure has implications for management of the endangered New Zealand sea lion

Female otariids (eared seals) frequently display strong levels of philopatry, a behaviour that has the potential to influence population structure, particularly at the mitochondrial level. Conversely, male otariids often move between breeding colonies, likely facilitating nuclear gene flow between colonies. Such gender-specific movements have the potential to influence species population structure. Here we investigate the genetic population structure of the endangered New Zealand (NZ) sea lion, using nuclear (microsatellite) and mitochondrial molecular markers, with the intention to better inform conservation through identification of management units for the species. The strong levels of female philopatry in this species have potential to lead to population structure at the mitochondrial loci. In contrast, weak or no population structure is expected across nuclear loci. NZ sea lions were sampled from the main breeding areas across the species’ current distribution (three Auckland Islands sites, two Campbell Island sites, one Stewart Island site and one Otago Peninsula site). Individuals were screened for microsatellite (n?=?271; 16 loci) and mitochondrial (n?=?56; 1027 bp D-loop and 1189 bp cytb). Despite a small (c. 9880 individuals) population size, moderate levels of microsatellite variation are observed in the NZ sea lions, in contrast to low levels of mitochondrial genetic variation. Results from mitochondrial DNA analyses revealed no population structure, suggesting that the strong level of female philopatry in NZ sea lions alone is not sufficient to maintain genetic population structure. Due to the frequent male movements between breeding colonies, no population structure was detected across the nuclear loci either. The absence of genetic structure suggests that, from a genetic perspective, NZ sea lions can be considered to be a single population. Despite this, the differing impacts of threats (e.g. fisheries by-catch) to each individual breeding colony must also be taken into consideration when defining management units for this endangered species.     

Habitat use and spatial fidelity of male South American sea lions during the nonbreeding period

Conditions experienced during the nonbreeding period have profound long‐term effects on individual fitness and survival. Therefore, knowledge of habitat use during the nonbreeding period can provide insights into processes that regulate populations. At the Falkland Islands, the habitat use of South American sea lions (Otaria flavescens) during the nonbreeding period is of particular interest because the population is yet to recover from a catastrophic decline between the mid‐1930s and 1965, and nonbreeding movements are poorly understood. Here, we assessed the habitat use of adult male (n = 13) and juvenile male (n = 6) South American sea lions at the Falkland Islands using satellite tags and stable isotope analysis of vibrissae. Male South American sea lions behaved like central place foragers. Foraging trips were restricted to the Patagonian Shelf and were typically short in distance and duration (127 ± 66 km and 4.1 ± 2.0 days, respectively). Individual male foraging trips were also typically characterized by a high degree of foraging site fidelity. However, the isotopic niche of adult males was smaller than juvenile males, which suggested that adult males were more consistent in their use of foraging habitats and prey over time. Our findings differ from male South American sea lions in Chile and Argentina, which undertake extended movements during the nonbreeding period. Hence, throughout their breeding range, male South American sea lions have diverse movement patterns during the nonbreeding period that intuitively reflects differences in the predictability or accessibility of preferred prey. Our findings challenge the long‐standing notion that South American sea lions undertake a winter migration away from the Falkland Islands. Therefore, impediments to South American sea lion population recovery likely originate locally and conservation measures at a national level are likely to be effective in addressing the decline and the failure of the population to recover.     

ONTOGENY OF MOVEMENTS AND FORAGING RANGES IN THE AUSTRALIAN SEA LION

This study tracked the movements of Australian sea lion ( Neophoca cinerea ) pups, juveniles, and adult females to identify home ranges and determine if young sea lions accompanied their mothers at sea. Satellite tags were deployed on nine 15-mo-old pups, nine 23-mo-old juveniles, and twenty-nine adult female Australian sea lions at Seal Bay Conservation Park, Kangaroo Island, South Australia. Females did not travel with their offspring at sea, suggesting young Australian sea lions learn foraging behaviors independently. Although home ranges increased with age, 23-mo-old juveniles had not developed adult movement capacity and their range was only 40.6% of the adult range. Juveniles traveled shorter distances (34.8 ± 5.5 km) at slower speeds (2.0 ± 0.3 km/h) than adults (67.9 ± 3.5 km and 3.9 ± 0.3 km/h). Young sea lions also stayed in shallower waters; sea floor depths of mean locations were 48 ± 7 m for juveniles and 74 ± 2 m for females. Restricted to shallow coastal waters, pups and juveniles are more likely to be disproportionately impacted by human activities. With limited available foraging habitat, young Australian sea lions appear particularly vulnerable to environmental alterations resulting from fisheries or climate change.     

Specialized foraging habits of adult female California sea lions Zalophus californianus

Individual foraging specialization occurs when organisms use a small subset of the resources available to a population. This plays an important role in population dynamics since individuals may have different ecological functions within an ecosystem related to habitat use and prey preferences. The foraging habitat fidelity and degree of specialization of California sea lions (Zalophus californianus) were evaluated by analyzing the stable isotopes values of carbon and nitrogen in vibrissae collected from 16 adult females from the reproductive colony on Santa Margarita Island, Magdalena Bay, Mexico, in 2012 and 2013. Based on the degree of individual specialization in δ¹⁵N, 62.5% of the females assessed can be considered specialist consumers focusing on the same prey or different prey from the same trophic level. The degree of individual specialization in δ¹³C indicated that 100% of the individuals showed fidelity to their foraging habitat as some fed in the lagoon, others foraged along the coast, and a third group preferred prey from the pelagic environment during both the breeding and nonbreeding seasons, suggesting diversification of foraging areas. Foraging area fidelity persisted despite the 2°C increase in the sea surface temperature over the course of the study period.     

Interactions between killer whales (<Emphasis Type="Italic">Orcinus orca</Emphasis>) and Steller sea lions (<Emphasis Type="Italic">Eumetopias jubatus</Emphasis>) in the vicinity of Brat Chirpoev Island,Kuril Islands

The behaviors of breeding Steller sea lions in response to encounters with killer whales near the shore were observed on Brat Chirpoev Island, Kuril Islands between May and July 2002–2007. Approaches by killer whales and sea lion behavior was observed visually and recorded. Killer whales approached the rookery 104 times during the entire period of observations (289 days). In most cases (n = 95), beached sea lions did not show any apparent reactions to the presence of killer whales, and there were no observed interactions. Sea lions showed agitation during nine of the approaches; five of these events were considered to be predation attempts. The killer whales attacked the sea lions three times, however all the attacks were unsuccessful. We recorded two different types of responses towards the killer whales: (1) beaching on the shore (three times) and (2) mass exodus from the rookery with subsequent formation of a tight, actively swimming and vocalizing group (six times). The latter is the first recorded observation of this behavior for Steller sea lions. The observation suggests a low degree of interactions between these two species near the studied rookery. Despite the numerous observations of killer whales near the rookery, there were no observations of direct predation on sea lions. It is likely the killer whale predation has little or no direct impact on the Steller sea lion population on Brat Chirpoev Islands during the breeding period.     

Interannual variation in the at‐sea behavior of California sea lions (Zalophus californianus)

To be successful, marine predators must alter their foraging behavior in response to changes in their environment. To understand the impact and severity of environmental change on a population it is necessary to first describe typical foraging patterns and identify the underlying variability that exists in foraging behavior. Therefore, we characterized the at‐sea behavior of adult female California sea lions (n = 32) over three years (2003, 2004, and 2005) using satellite transmitters and time‐depth recorders and examined how foraging behavior varied among years. In all years, sea lions traveled on average 84.7 ± 11.1 km from the rookery during foraging trips that were 3.2 ± 0.3 d. Sea lions spent 42.7% ± 1.9% of their time at sea diving and displayed short (2.2 ± 0.2 min), shallow dives (58.5 ± 8.5 m). Among individuals, there was significant variation in both dive behavior and movement patterns, which was found in all years. Among years, differences were found in trip durations, distances traveled, and some dive variables (e.g., dive duration and bottom time) as sea lions faced moderate variability in their foraging habitat (increased sea‐surface temperatures, decreased upwelling, and potential decreased prey abundance). The flexibility we found in the foraging behavior of California sea lions may be a mechanism to cope with environmental variability among years and could be linked to the continuing growth of sea lion populations.     

Characterizing habitat suitability for a central‐place forager in a dynamic marine environment

Characterizing habitat suitability for a marine predator requires an understanding of the environmental heterogeneity and variability over the range in which a population moves during a particular life cycle. Female California sea lions (Zalophus californianus) are central‐place foragers and are particularly constrained while provisioning their young. During this time, habitat selection is a function of prey availability and proximity to the rookery, which has important implications for reproductive and population success. We explore how lactating females may select habitat and respond to environmental variability over broad spatial and temporal scales within the California Current System. We combine near‐real‐time remotely sensed satellite oceanography, animal tracking data (n = 72) from November to February over multiple years (2003–2009) and Generalized Additive Mixed Models (GAMMs) to determine the probability of sea lion occurrence based on environmental covariates. Results indicate that sea lion presence is associated with cool ( <14°C ), productive waters, shallow depths, increased eddy activity, and positive sea‐level anomalies. Predictive habitat maps generated from these biophysical associations suggest winter foraging areas are spatially consistent in the nearshore and offshore environments, except during the 2004–2005 winter, which coincided with an El Niño event. Here, we show how a species distribution model can provide broadscale information on the distribution of female California sea lions during an important life history stage and its implications for population dynamics and spatial management.     

Stable Isotopes Reveal Long-Term Fidelity to Foraging Grounds in the Galapagos Sea Lion (Zalophus wollebaeki)

Most otariids have colony-specific foraging areas during the breeding season, when they behave as central place foragers. However, they may disperse over broad areas after the breeding season and individuals from different colonies may share foraging grounds at that time. Here, stable isotope ratios in the skull bone of adult Galapagos sea lions (Zalophus wollebaeki) were used to assess the long-term fidelity of both sexes to foraging grounds across the different regions of the Galapagos archipelago. Results indicated that the stable isotope ratios (δ¹³C and δ¹⁵N) of sea lion bone significantly differed among regions of the archipelago, without any significant difference between sexes and with a non significant interaction between sex and region. Moreover, standard ellipses, estimated by Bayesian inference and used as a measure of the isotopic resource use area at the population level, overlapped widely for the sea lions from the southern and central regions, whereas the overlap of the ellipses for sea lions from the central and western regions was small and non-existing for those from the western and southern regions. These results suggest that males and females from the same region within the archipelago use similar foraging grounds and have similar diets. Furthermore, they indicate that the exchange of adults between regions is limited, thus revealing a certain degree of foraging philopatry at a regional scale within the archipelago. The constraints imposed on males by an expanded reproductive season (~ 6 months), resulting from the weak reproductive synchrony among females, and those imposed on females by a very long lactation period (at least one year but up to three years), may explain the limited mobility of adult Galapagos sea lions of both sexes across the archipelago.     

Reestablishment of former wintering grounds by New Zealand southern right whales

Historically, the range of the southern right whale (SRW) included winter calving grounds around the North and South Islands (mainland) of New Zealand (NZ) and in the NZ subantarctic Auckland and Campbell Islands. Due to extensive whaling in the 19th and 20th centuries, no SRW was seen around mainland NZ for nearly four decades (1928–1963). Here we present evidence for the regular use of the mainland NZ wintering ground, presumably from a remnant population that persisted in the NZ subantarctic Auckland and Campbell Islands. SRWs have been sighted every year around mainland NZ since 1988, with 125 sightings during the focus of this work: from 2003 to 2010. There were 28 cow‐calf pairs sighted around mainland NZ from 2003 to 2010, compared with 11 sightings from 1991 to 2002. Furthermore, two females, identified by DNA profiles, were sighted with calves around mainland at 4 yr intervals: the first evidence of female site fidelity to the mainland NZ calving ground. Individual identification from photographs of natural markings and DNA profiles provided information on within‐year movements and residency around the mainland, and further evidence for exchange between the mainland and subantarctic wintering grounds. Despite these promising signs, the distribution of NZ SRWs remains primarily concentrated in the NZ subantarctic.     

Assessment of Competition between Fisheries and Steller Sea Lions in Alaska Based on Estimated Prey Biomass,Fisheries Removals and Predator Foraging Behaviour

A leading hypothesis to explain the dramatic decline of Steller sea lions (Eumetopias jubatus) in western Alaska during the latter part of the 20th century is a change in prey availability due to commercial fisheries. We tested this hypothesis by exploring the relationships between sea lion population trends, fishery catches, and the prey biomass accessible to sea lions around 33 rookeries between 2000 and 2008. We focused on three commercially important species that have dominated the sea lion diet during the population decline: walleye pollock, Pacific cod and Atka mackerel. We estimated available prey biomass by removing fishery catches from predicted prey biomass distributions in the Aleutian Islands, Bering Sea and Gulf of Alaska; and modelled the likelihood of sea lions foraging at different distances from rookeries (accessibility) using satellite telemetry locations of tracked animals. We combined this accessibility model with the prey distributions to estimate the prey biomass accessible to sea lions by rookery. For each rookery, we compared sea lion population change to accessible prey biomass. Of 304 comparisons, we found 3 statistically significant relationships, all suggesting that sea lion populations increased with increasing prey accessibility. Given that the majority of comparisons showed no significant effect, it seems unlikely that the availability of pollock, cod or Atka mackerel was limiting sea lion populations in the 2000s.