Hostname: page-component-586b7cd67f-vdxz6 Total loading time: 0 Render date: 2024-11-21T23:23:08.209Z Has data issue: false hasContentIssue false

Incidental pinnipeds at high latitudes of the Vestfold Hills, Prydz Bay, East Antarctica

Published online by Cambridge University Press:  30 January 2024

John van den Hoff*
Affiliation:
Australian Antarctic Division, 203 Channel Highway, Kingston, 7050, Tasmania, Australia
Rights & Permissions [Opens in a new window]

Abstract

Species distributions are predicted to change with future climate-associated ecosystem changes such that so-called ‘vagrant’ individuals may become established or re-establish in areas currently thought to be beyond their principle ranges. Survey data were collated for occurrences of pinniped (seal) species at very high latitudes of the Vestfold Hills, East Antarctica. Aside from Weddell seals (Leptonychotes weddellii) and southern elephant seals (Mirounga leonina), which aggregate annually at the Vestfold Hills to breed and/or moult, three other pinniped species were observed with the recession of the fast-ice edge. Leopard seal (Hydrurga leptonyx) occurrences increased with an increase in a seasonally abundant prey resource, and crabeater seals (Lobodon carcinophaga) were seen at a time that coincides with their moult period. Occurrences of sub-adult male Antarctic fur seals (Arctocephalus gazella) increase the known southward range for this species and may reflect population increases at source populations in the Kerguelen Plateau area. Although there were no direct sightings of Ross seals (Ommatophoca rossii), their presence close to the Vestfold Hills was detected by underwater passive acoustic monitoring. Sightings of obligate drift-ice species and sub-Antarctic fur seals may change at the Vestfold Hills with climate-mediated changes in sea-ice conditions.

Type
Biological Sciences
Copyright
Copyright © The Author(s), 2024. Published by Cambridge University Press on behalf of Antarctic Science Ltd

Introduction

Five Phocidae (true seals) and one Otariidae (eared seals) species comprise the pinniped biodiversity of the Southern Ocean marine ecosystem south of 60° S; the phocids are Weddell seals (Leptonychotes weddellii), crabeater seals (Lobodon carcinophaga), leopard seals (Hydrurga leptonyx), Ross seals (Ommatophoca rossii) and southern elephant seals (Mirounga leonina), and the otariid is the Antarctic fur seal (Arctocephalus gazella). Ross, leopard and crabeater seals are found for most of the year within the drift-ice zone, whereas Weddell seals are primarily south of it within the fast-ice zone (Bengtson et al. Reference Bengtson, Laake, Boveng, Cameron, Hanson and Stewart2011). With the summer sea-ice recession, the habitat of the drift-ice species contracts south to remnant ice floes, the land-fast ice and the land at coastal ice-free areas (Bester et al. Reference Bester, Hofmeyr, Kirkman, Chauke, De Bruyn, Ferreira and et al2006, Bengtson et al. Reference Bengtson, Laake, Boveng, Cameron, Hanson and Stewart2011, Staniland et al. Reference Staniland, Ratcliffe, Trathan and Forcada2018). For the more sub-Antarctic species (the southern elephant seal and the Antarctic fur seal), the summer retreat of the drift-ice zone opens up high-latitude foraging areas and allows access to haul-out areas on the Antarctic coastline that are not usually occupied by those species (van den Hoff et al. Reference van den Hoff, Davies and Burton2003, Malpress et al. Reference Malpress, Bestley, Corney, Welsford, Labrousse, Sumner and Hindell2017, Salton et al. Reference Salton, Bestley, Gales and Harcourt2022). From long-term observations we know that each Antarctic pinniped species has a secondary distributional range that often extends north into low latitudes along the coasts of Southern Hemisphere continents and islands, and these individuals are often termed ‘vagrants’ (Acevedo et al. Reference Acevedo, Matus, Droguett, Vila, Aguayo-Lobo and Torres2011, Shaughnessy et al. Reference Shaughnessy, Kemper and Ling2012, Miskelly Reference Miskelly2015).

Prydz Bay (73.5° E, 69° S) is a large embayment of the Lars Christensen and Ingrid Christensen coasts that not only extends the East Antarctic continental shelf southward from a typically narrow latitudinal range of 62–65° S to ~70° S (O'Brien et al. Reference O'Brien, Harris, Post and Young2014), it also extends the limits of the drift-ice zone southward by ~300 km. From observations beginning during the 1950s and continuing to date, we know Weddell, crabeater, leopard and southern elephant seals were seasonally present in the Prydz Bay area (Ingham Reference Ingham1960, Johnstone et al. Reference Johnstone, Lugg and Brown1973, Rogers & Bryden Reference Rogers and Bryden1997, Southwell et al. Reference Southwell, Paxton, Borchers, Boveng and de la Mare2008a,Reference Southwell, Paxton, Borchers, Boveng, Rogers and Williamb,Reference Southwell, Paxton, Borchers, Boveng, Nordøy, Blix and Williamc, Kumar & Johnston Reference Kumar and Johnson2014, Heerah et al. Reference Heerah, Hindell, Andrew-Goff, Field, McMahon and Charrassin2017, Malpress et al. Reference Malpress, Bestley, Corney, Welsford, Labrousse, Sumner and Hindell2017), suggesting high-latitude habitats are part of their primary ranges. Both the Ross seal and the Antarctic fur seal have not yet been directly observed at very high latitudes in ice-free areas such as the Vestfold Hills.

From December 2017 to March 2022, observers surveyed the Vestfold Hills for presences of pinniped species. I collated those observations with previous studies, compared species occurrences and re-assessed the status of those species within the survey area.

Materials and methods

The survey area for this study was the coastline of the Vestfold Hills, including the adjoining fast ice, the fjords and the nearshore islands from the Wyatt Earp Islands to the north to Sørsdal Glacier at the southern extent (Fig. 1). Changes in the sea-ice conditions dictated choice of survey platform. Over-ice vehicles were preferred for surveying the broader area when conditions were favourable. When ice conditions were not suited to over-ice travel, aerial surveys were conducted from helicopters flying at speeds between 40 and 60 knots at an altitude of 750 m often, but not always, between 14h00 and 15h00 local time (Lake et al. Reference Lake, Burton and Hindell1997, Rogers & Bryden Reference Rogers and Bryden1997). Flight paths were monitored by GPS, each seal sighting was plotted onto a 1:50 000 map and, where possible, an image of the sighting was captured using a variety of film and digital cameras fitted with telephoto lenses. In-flight estimates of seal numbers and species identifications were verified from those images.

Figure 1. Map of the Vestfold Hills, East Antarctica, showing the locations of leopard seal (Hydrurga leptonyx; triangles), crabeater seal (Lobodon carcinophaga; diamonds) and Antarctic fur seal (Arctocephalus gazella; dots) sightings between 2017 and 2022. Light brown shading = ice-free land. AMAR = approximate location of an autonomous multichannel acoustic recorder.

Localized shore-based searches of the coast between Powell Point and Ellis Fjord (Fig. 1) were done on foot. During periods of open water, boat transport was used to access offshore islands and the coastline south of Ellis Fjord to Sørsdal Glacier. Those terrestrial areas were then surveyed on foot. As a minimum, the date, a count by species and the location were recorded for each sighting.

The term ‘pseudo-vagrant’ is applied here to describe species that occur repeatedly but whose migratory routes are not well understood (Gilroy & Lees Reference Gilroy and Lees2003).

Results

Twenty-seven individuals of three pinniped species, not including Weddell and southern elephant seals, were reported during surveys of the Vestfold Hills between December 2017 and March 2022. Three sightings were of an otariid (the Antarctic fur seal), and the remainder were of two phocid species (the crabeater and leopard seals).

The crabeater seal Lobodon carcinophaga (Hombron and Jacquinot, 1842)

Five crabeater seals were observed: four were seen during January and one was seen in February. Two individuals were on land, whereas the remainder were on the fast ice within Long Fjord (Fig. 1). An individual seen in Heidemann Bay had extensive healed bite wounds to its flanks and tail region (Fig. 2a).

Figure 2. Incidental pinnipeds at the Vestfold Hills, East Antarctica. a. Crabeater seal (Lobodon carcinophaga) ashore at Heidemann Bay, 8 February 2019 (photograph: Kris Carlyon and Erica Adamson). Note the healed tooth rake marks indicating that this individual had escaped the jaws of a killer whale (Orcinus orca). b. Leopard seal (Hydrurga leptonyx) observed on an ice floe from an altitude of ~750 m on 18 February 2020 (photograph: Andrew Irvine). c. Sub-adult male Antarctic fur seal (Arctocephalus gazella) in Heidemann Bay on 23 February 2019 (photograph: Erica Adamson and Kris Carlyon). d. Another A. gazella ashore at Riviera Point on 7 March 2020 (photograph: Rachel McInerney).

The leopard seal Hydrurga leptonyx (Gistel, 1848)

Eighteen leopard seals were recorded on ice floes north of Long Fjord during aerial surveys (Figs 1 & 2b). As many as nine individuals were sighted during a single survey, and all were on separate floes. Leopard seals were seen hunting Adélie penguins (Pygoscelis adeliae) close to shore at their breeding colonies on Gardner and other islands (author's personal observation 2001).

The Ross seal Ommatophoca rossii (Gray, 1844)

No Ross seals were seen ashore or on the sea ice at the Vestfold Hills during the study period. However, their under-ice presence was betrayed when siren calls were recorded by passive acoustic monitoring (AMAR G4) between 16 December 2021 and 3 January 2022 (Fig. 1; Australian Antarctic Division, unpublished data 2022).

The Antarctic fur seal Arctocephalus gazella (Peters, 1857)

Three sub-adult male Antarctic fur seals were seen. The first was in Heidemann Bay on 21 February 2016 and the second on 23 February 2019 (Fig. 2c), and the third (Fig. 2d) was seen 1 year later on 7 March 2020 at Riviera Point, just 2 km from the location of the previous sighting.

Status

Crabeater seals and leopard seals were seen during two observational periods (1957–1973 and 2017–2022), Antarctic fur seals were seen only during the second survey period and Ross seals have not been seen during either period, but their vocalizations were recorded in the later period. Changes in the status of those species are given in Table I. Since little is known of the migratory behaviours of Antarctic fur seals from the Kerguelen Plateau area, this species was given a pseudo-vagrant status (Table I).

Table I. Change in status of three pinniped species at the Vestfold Hills between two study periods.

b Vocalizations recorded in the area.

NR = not reported.

Discussion

For the first time in 65 years of written biological history has the presence of an Antarctic fur seal been reported at the Vestfold Hills (Fig. 2c,d). The three individuals observed there represent the most southerly occurrences for this species to date. All individuals appeared to be in reasonable body condition, suggesting that they had foraged successfully over the course of their ~1700 km ocean transit between Heard Island (53° S, 73.5° E), the nearest breeding location for the species, and the Vestfold Hills. Antarctic fur seals on the East Antarctic coast appear to be exceptional because they had travelled south of their primary range rather than north of it (Shaughnessy & Burton Reference Shaughnessy and Burton1986, Bester & Reisinger Reference Bester and Reisinger2010, Acevedo et al. Reference Acevedo, Matus, Droguett, Vila, Aguayo-Lobo and Torres2011). Limited southward dispersal for male Antarctic fur seals from natal colonies is known, and it is thought to be representative of reduced overlap with female foraging grounds and increased population size at natal locations (Boyd et al. Reference Boyd, McCafferty, Reid, Taylor and Walker1998, Convey & Hughes Reference Convey and Hughes2022, Salton et al. Reference Salton, Bestley, Gales and Harcourt2022). Perhaps the same logic may be applied to the individuals seen in East Antarctica but on a larger scale of dispersal. The Antarctic fur seal populations at Heard Island and Îles Kerguelen were increasing when last surveyed (Page et al. Reference Page, Welling, Chambellant, Goldsworthy, Dorr and van Veen2003, Jeanniard-du-Dot Reference Jeanniard-du-Dot2015), and some tracked juvenile males moved south from those islands (Raymond et al. Reference Raymond, Lea, Patterson, Andrews-Goff, Sharples and Charrassin2015, Salton et al. Reference Salton, Bestley, Gales and Harcourt2022). The appearances of Antarctic fur seals at the Vestfold Hills therefore represent a consequence of population increases and avoidance of competition between the sexes. Our (human) current level of understanding of Antarctic fur seal migrations places that species firmly within the definition of a pseudo-vagrant (Gilroy & Lees Reference Gilroy and Lees2003) to the Vestfold Hills.

Leopard seals are known to move south as the extent of their primary habitat - the drifting ice - recedes to the Antarctic coast during the summer (references in Hupman et al. Reference Hupman, Visser, Fyfe, Cawthorn, Forbes and Grabham2020). Their regular occurrences at the Vestfold Hills appears to be a confluence of this seasonal recession in sea-ice extent, seasonal food availability in the form of Adélie penguins and the presence of remnant ice floes upon which individuals can haul out to rest (Johnstone et al. Reference Johnstone, Lugg and Brown1973). Adélie penguin remains were the most common prey items found in the diet of leopard seals at the ice edge in Prydz Bay (Rogers & Bryden Reference Rogers and Bryden1995, McFarlane Reference McFarlane1996, Hall-Aspland & Rogers Reference Hall-Aspland and Rogers2004), and the individuals observed during this study were most often on remnant ice floes (Fig. 1b) at a time when Adélie penguins had aggregated in nearby areas for breeding. Although living leopard seals have not yet been reported ashore at the Vestfold Hills, their frozen carcasses have been found far inland in the Vestfold Hills and on the adjoining ice sheet (Johnstone et al. Reference Johnstone, Lugg and Brown1973), suggesting misadventure.

The progressive southward summer recession of the drift-ice zone probably also contributed to occurrences of crabeater seals close to the Larsemann Hills’ coast (Kumar & Johnson Reference Kumar and Johnson2014) and at the Vestfold Hills (Johnstone et al. Reference Johnstone, Lugg and Brown1973). Their occurrences at ice-free areas coincided with the moult period for this species (Kooyman Reference Kooyman, Ridgway and Harrison1981), and so it is plausible that the individuals seen at the Vestfold Hills were there to moult, but so far none have been reported doing so. Unfortunately for Southern Ocean ice-inhabiting marine mammal species, the retreating ice edge is a favoured hunting habitat for large-form type B killer whales (Orcinus orca), and crabeater seals are on their list of vittles (Pitman & Ensor Reference Pitman and Ensor2003). The tooth rake marks on the flank and tail regions of the crabeater seal seen in Heidemann Bay (Fig. 2a) are reminiscent of killer whale bite wounds observed on southern elephant seals (van den Hoff & Morrice Reference van den Hoff and Morrice2008), and they suggest that this individual was fortunate to have escaped a ‘butchering’ by the killer whale (Pitman & Durban Reference Pitman and Durban2012).

The primary distribution of the Ross seal differs somewhat from other ice-inhabiting Southern Ocean pinnipeds. Studies suggest Ross seals typically forage north of the Antarctic drift ice for most of the year but return to it in October and January for breeding and moulting, respectively (Blix & Nordøy Reference Blix and Nordøy2007, Southwell et al. Reference Southwell, Paxton, Borchers, Boveng, Nordøy, Blix and William2008c, Arcalís-Planas et al. Reference Arcalís-Planas, Sveegaard, Karlsson, Harding, Wåhlin, Harkonen and Teilmann2015). Indeed, more Ross seals have been seen ashore in Australia and New Zealand (Shaughnessy et al. Reference Shaughnessy, Kemper and Ling2012, Miskelly Reference Miskelly2015) than have ever been seen at the Vestfold Hills. Although Ross seals were not observed in the study area, their distinct siren call vocalizations were recorded by autonomous acoustic monitoring (Fig. 1; Australian Antarctic Division, unpublished data 2022). Such an outcome serves to reiterate that no single survey method can be expected to provide all of the information required for a comprehensive survey of an area's biodiversity.

The literature contains numerous reports of living or indisposed individuals (or species) thought to have occurred beyond their natural ranges. Those individuals have been variously termed ‘vagrants', ‘biosecurity risks', ‘accidental strays', ‘transient visitors’ and ‘duds’ (Davis & Watson Reference Davis and Watson2018). However, they are also representative of increasing source populations, and in a dynamic world we might expect a change in the status of those purported climate refugees (Table I; Veit Reference Veit2000, Lees & Gilroy Reference Lees and Gilroy2014, Hupman et al. Reference Hupman, Visser, Fyfe, Cawthorn, Forbes and Grabham2020). In this case, the regular or increasing occurrences of drift-ice seals at the Vestfold Hills suggest that the high latitudes have some secondary ecological importance to those species. None of the seals seen at the Vestfold Hills between 2017 and 2020 were individually marked, and no diet-related information was collected (e.g. scats). Therefore, at this stage, we can make no statements about potential new migratory patterns for those species, and we do not know how those individuals might interact with an ecosystem that is outside of their primary ranges.

Acknowledgements

The author thanks the Davis Station expeditioners who contributed sightings information. Dr Louise McMahon was the first person on Earth to report an occurrence of a fur seal in the Vestfold Hills. Shavawn Donoghue and Toby Travers are thanked for producing Figs 1 & 2, respectively.

References

Acevedo, J., Matus, R., Droguett, D., Vila, A., Aguayo-Lobo, A. & Torres, D. 2011. Vagrant Antarctic fur seals, Arctocephalus gazella, in southern Chile. Polar Biology, 34, 939943.CrossRefGoogle Scholar
Arcalís-Planas, A., Sveegaard, S., Karlsson, O., Harding, K.C., Wåhlin, A., Harkonen, T. & Teilmann, J. 2015. Limited use of sea ice by the Ross seal (Ommatophoca rossii), in Amundsen Sea, Antarctica, using telemetry and remote sensing data. Polar Biology, 38, 445461.CrossRefGoogle Scholar
Bengtson, J.L., Laake, J.L., Boveng, P.L., Cameron, M.F., Hanson, M.B. & Stewart, B.S. 2011. Distribution, density, and abundance of pack-ice seals in the Amundsen and Ross Seas, Antarctica. Deep Sea Research II - Topical Studies in Oceanography, 58, 12611276.CrossRefGoogle Scholar
Bester, M.N. & Reisinger, R.R. 2010. Vagrant Antarctic fur seals at Gough Island in 2009. Polar Biology, 33, 709711.CrossRefGoogle Scholar
Bester, M.N., Hofmeyr, G.J.G., Kirkman, S.P., Chauke, L.F., De Bruyn, P.J.N., Ferreira, S.M., et al, . 2006. The leopard seal at Marion Island, vagrant or seasonal transient? South African Journal of Wildlife Research, 36, 195198.Google Scholar
Blix, A.S. & Nordøy, E.S. 2007. Ross seal (Ommatophoca rossii) annual distribution, diving behaviour, breeding and moulting, off Queen Maud Land, Antarctica. Polar Biology, 30, 14491458.CrossRefGoogle Scholar
Boyd, I.L., McCafferty, D.J., Reid, K., Taylor, R. & Walker, T.R. 1998. Dispersal of male and female Antarctic fur seals (Arctocephalus gazella). Canadian Journal of Fisheries and Aquatic Sciences, 55, 845852.CrossRefGoogle Scholar
Convey, P. & Hughes, K.A. 2022. Untangling unexpected terrestrial conservation challenges arising from the historical human exploitation of marine mammals in the Atlantic sector of the Southern Ocean. Ambio, 52, 10.1007/s13280-022-01782-4.Google ScholarPubMed
Davis, R.A. & Watson, D.M. 2018. Vagrants as vanguards of range shifts in a dynamic world. Biological Conservation, 224, 238241.CrossRefGoogle Scholar
Gilroy, J.J. & Lees, A.C. 2003. Vagrancy theories: are autumn vagrants really reverse migrants? British Birds, 96, 427438.Google Scholar
Hall-Aspland, S.A. & Rogers, T.L. 2004. Summer diet of leopard seals (Hydrurga leptonyx) in Prydz Bay, Eastern Antarctica. Polar Biology, 27, 729734.CrossRefGoogle Scholar
Heerah, K., Hindell, M., Andrew-Goff, V., Field, I., McMahon, C.R. & Charrassin, J.B. 2017. Contrasting behavior between two populations of an ice-obligate predator in East Antarctica. Ecology and Evolution, 7, 606618.CrossRefGoogle ScholarPubMed
Hupman, K., Visser, I.N., Fyfe, J., Cawthorn, M., Forbes, G., Grabham, A.A., et al. 2020. From vagrant to resident: occurrence, residency and births of leopard seals (Hydrurga leptonyx) in New Zealand waters. New Zealand Journal of Marine and Freshwater Research, 54, 123.CrossRefGoogle Scholar
Ingham, S.E. 1960. The status of seals (Pinnipedia) at Australian Antarctic stations. Mammalia, 24, 422430.Google Scholar
Jeanniard-du-Dot, T. 2015. Foraging strategies and efficiencies of lactating northern and Antarctic fur seals: implications for reproductive success. PhD thesis. University of British Columbia, 201 pp.Google Scholar
Johnstone, G.W., Lugg, D.J. & Brown, D.A. 1973. The biology of the Vestfold Hills, Antarctica. Australian National Antarctic Research Expeditions Scientific Reports, Series B (I) Zoology, 123, 4449.Google Scholar
Kooyman, G.L. 1981. Crabeater seal, Lobodon carcinophagus (Hombron and Jacquinot, 1842). In Ridgway, S.H. & Harrison, R.J., eds, Handbook of marine mammals, vol. 2. London: Academic Press, 221235.Google Scholar
Kumar, R.S. & Johnson, J.A. 2014. Aerial surveys for pack-ice seals along the Ingrid Christensen and Princess Astrid coasts, East Antarctica. Journal of Threatened Taxa, 6, 62306238.CrossRefGoogle Scholar
Lake, S.E., Burton, H.R. & Hindell, M.A. 1997. Influence of time of day and month on Weddell seal haul-out patterns at the Vestfold Hills, Antarctica. Polar Biology, 18, 319324.CrossRefGoogle Scholar
Lees, A.C. & Gilroy, J.J. 2014. Vagrancy fails to predict colonization of oceanic islands. Global Ecology and Biogeography, 23, 405413.CrossRefGoogle Scholar
McFarlane, R.A. 1996. Some observations on Adelie penguin (Pygoscelis adeliae) mortality in East Antarctica. Avian Pathology, 25, 187190.CrossRefGoogle ScholarPubMed
Malpress, V., Bestley, S., Corney, S., Welsford, D., Labrousse, S., Sumner, M. & Hindell, M. 2017. Bio-physical characterisation of polynyas as a key foraging habitat for juvenile male southern elephant seals (Mirounga leonina) in Prydz Bay, East Antarctica. PLoS ONE, 12, e0184536.CrossRefGoogle ScholarPubMed
Miskelly, C.M. 2015. Records of three vagrant Antarctic seal species (family Phocidae) from New Zealand: crabeater seal (Lobodon carcinophaga), Weddell seal (Leptonychotes weddellii) and Ross seal (Ommatophoca rossii). New Zealand Journal of Marine and Freshwater Research, 49, 448461.CrossRefGoogle Scholar
O'Brien, P.E., Harris, P.T., Post, A.L. & Young, N. 2014. East Antarctic continental shelf: Prydz Bay and the Mac. Robertson Land Shelf. Geological Society, London, Memoirs, 41, 241254.CrossRefGoogle Scholar
Page, B., Welling, A., Chambellant, M., Goldsworthy, S.D., Dorr, T. & van Veen, R. 2003. Population status and breeding season chronology of Heard Island fur seals. Polar Biology, 26, 219224.CrossRefGoogle Scholar
Pitman, R.L. & Durban, J.W. 2012. Cooperative hunting behavior, prey selectivity and prey handling by pack ice killer whales (Orcinus orca), type B, in Antarctic Peninsula waters. Marine Mammal Science, 28, 1636.CrossRefGoogle Scholar
Pitman, R.L. & Ensor, P. 2003. Three forms of killer whales (Orcinus orca) in Antarctic waters. Journal of Cetacean Research and Management, 5, 131140.Google Scholar
Raymond, B., Lea, M.A., Patterson, T., Andrews-Goff, V., Sharples, R., Charrassin, J.B., et al. 2015. Important marine habitat off east Antarctica revealed by two decades of multi-species predator tracking. Ecography, 38, 121129.CrossRefGoogle Scholar
Rogers, T.L. & Bryden, M.M. 1995. Predation of Adélie penguins (Pygoscelis adeliae) by leopard seals (Hydrurga leptonyx) in Prydz Bay, Antarctica. Canadian Journal of Zoology, 73, 10011004.CrossRefGoogle Scholar
Rogers, T.L. & Bryden, M.M. 1997. Density and haul-out behavior of leopard seals (Hydrurga leptonyx) in Prydz Bay, Antarctica. Marine Mammal Science, 13, 293302.CrossRefGoogle Scholar
Salton, M., Bestley, S., Gales, N. & Harcourt, R. 2022. Environmental drivers of foraging behaviour during long-distance foraging trips of male Antarctic fur seals. Animal Behaviour, 183, 103116.CrossRefGoogle Scholar
Shaughnessy, P.D. & Burton, H.R. 1986. Fur seals Arctocephalus spp. at Mawson Station, Antarctica, and in the Southern Ocean. Polar Record, 23, 7981.CrossRefGoogle Scholar
Shaughnessy, P.D., Kemper, C.M. & Ling, J.K. 2012. Records of vagrant phocid seals (family Phocidae) in South Australia. Australian Mammalogy, 34, 155169.CrossRefGoogle Scholar
Southwell, C., Paxton, C.G., Borchers, D., Boveng, P. & de la Mare, W. 2008a. Taking account of dependent species in management of the Southern Ocean krill fishery: estimating crabeater seal abundance off east Antarctica. Journal of Applied Ecology, 45, 622631.CrossRefGoogle Scholar
Southwell, C., Paxton, C.G., Borchers, D., Boveng, P., Rogers, T. & William, K. 2008b. Uncommon or cryptic? Challenges in estimating leopard seal abundance by conventional but state-of-the-art methods. Deep Sea Research I - Oceanographic Research Papers, 55, 519531.CrossRefGoogle Scholar
Southwell, C.J., Paxton, C.G., Borchers, D.L., Boveng, P.L., Nordøy, E.S., Blix, A.S. & William, K. 2008c. Estimating population status under conditions of uncertainty: the Ross seal in East Antarctica. Antarctic Science, 20, 123133.CrossRefGoogle Scholar
Staniland, I.J., Ratcliffe, N., Trathan, P.N. & Forcada, J. 2018. Long term movements and activity patterns of an Antarctic marine apex predator: the leopard seal. PLoS ONE, 13, e0197767.CrossRefGoogle ScholarPubMed
van den Hoff, J. & Morrice, M.G. 2008. Sleeper shark (Somniosus antarcticus) and other bite wounds observed on southern elephant seals (Mirounga leonina) at Macquarie Island. Marine Mammal Science, 24, 239247.CrossRefGoogle Scholar
van den Hoff, J., Davies, R. & Burton, H. 2003. Origins, age composition and change in numbers of moulting southern elephant seals (Mirounga leonina L.) in the Windmill Islands, Vincennes Bay, East Antarctica, 1988–2001. Wildlife Research, 30, 275280.CrossRefGoogle Scholar
Veit, R.R. 2000. Vagrants as the expanding fringe of a growing population. The Auk, 117, 242246.CrossRefGoogle Scholar
Figure 0

Figure 1. Map of the Vestfold Hills, East Antarctica, showing the locations of leopard seal (Hydrurga leptonyx; triangles), crabeater seal (Lobodon carcinophaga; diamonds) and Antarctic fur seal (Arctocephalus gazella; dots) sightings between 2017 and 2022. Light brown shading = ice-free land. AMAR = approximate location of an autonomous multichannel acoustic recorder.

Figure 1

Figure 2. Incidental pinnipeds at the Vestfold Hills, East Antarctica. a. Crabeater seal (Lobodon carcinophaga) ashore at Heidemann Bay, 8 February 2019 (photograph: Kris Carlyon and Erica Adamson). Note the healed tooth rake marks indicating that this individual had escaped the jaws of a killer whale (Orcinus orca). b. Leopard seal (Hydrurga leptonyx) observed on an ice floe from an altitude of ~750 m on 18 February 2020 (photograph: Andrew Irvine). c. Sub-adult male Antarctic fur seal (Arctocephalus gazella) in Heidemann Bay on 23 February 2019 (photograph: Erica Adamson and Kris Carlyon). d. Another A. gazella ashore at Riviera Point on 7 March 2020 (photograph: Rachel McInerney).

Figure 2

Table I. Change in status of three pinniped species at the Vestfold Hills between two study periods.