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Leucistic Weddell seal (Leptonychotes weddellii) observations in Erebus Bay, Antarctica

Published online by Cambridge University Press:  25 February 2025

Morgan E. Anderson*
Affiliation:
Ecology Department, Montana State University, Bozeman, MT, USA
Parker M. Levinson
Affiliation:
Ecology Department, Montana State University, Bozeman, MT, USA
Jay J. Rotella
Affiliation:
Ecology Department, Montana State University, Bozeman, MT, USA
*
Corresponding author: Morgan E. Anderson; Email: morgan99anderson@gmail.com
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Abstract

Pigmentation and colouration are important to animal fitness. Colourations convey important information and impact predation risk, thermoregulation and mate selection. There are many cases of hypopigmentation across the animal kingdom, and leucism is a common form. We observed a Weddell seal (Leptonychotes weddellii) pup with cream-coloured fur, light skin and white nails multiple times in 2022 in Erebus Bay, Antarctica. The pup was observed 1 year later as a generally healthy yearling. This is the first documentation of a leucistic seal within this well-studied population and the second documentation of such colouration in this species. This seal offers a potential opportunity to observe the effects of hypopigmentation in Antarctic true seals.

Type
Short Note
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2025. Published by Cambridge University Press on behalf of Antarctic Science Ltd

Pigmentation is important to animal fitness. Colourations help convey important information in both interspecific and intraspecific interactions and can impact predation risk, thermoregulation and mate selection (Fertl & Rosel Reference Fertl, Rosel, Perrin, Wursig and Thewissen2002, Kratochwil & Mallarino Reference Kratochwil and Mallarino2023). The wide range of colours and patterns in animals is due to variation in the deposition of pigments in or from structural colours that interact with hair or feathers (Kratochwil & Mallarino Reference Kratochwil and Mallarino2023). Colouration and colour morphs are often genetically determined, and deviations from typical pigmentation can arise due to genetic mutations, diseases, diet or environmental conditions (van Grouw Reference van Grouw2021). While the effects of such atypical colourations on an individual’s fitness can be positive or negative, limited information on such fitness implications exists due to their rarity (Bried & Haubreux Reference Bried and Haubreux2000, Fertl & Rosel Reference Fertl, Rosel, Perrin, Wursig and Thewissen2002). Mutations in colour patterns may improve the population-level fitness as they can assist species in adapting to changing environments (Jones et al. Reference Jones, Mills, Alves, Callahan, Alves and Lafferty2018). Although most research suggests that such individuals have a higher predation risk, research by Chatellenaz & Zaracho (Reference Chatellenaz and Zaracho2021) suggests that individuals with atypical colourations may not have an increased risk of predation. Conversely, most research states that certain colour patterns may adversely affect an individual’s lifespan and reproductive success, hindering fitness (Bried & Haubreux Reference Bried and Haubreux2000, Fertl & Rosel Reference Fertl, Rosel, Perrin, Wursig and Thewissen2002).

Colouration is thought to be important to the survival of marine mammals, as many such species utilize countershading, with lighter ventral colouration and darker dorsal colouration, which is thought to help reduce their being detected (Hain & Leatherwood Reference Hain and Leatherwood1982). The potential importance of countershading for survival may help explain why atypical colourations in marine mammals are relatively rare (Rowland Reference Rowland, Vonk and Shackelford2022). Leucistic animals have reduced pigmentation caused by the hereditary absence of melanin-producing cells and frequently have white or light fur, skin or vibrissae but normal-coloured eyes (Acevedo et al. Reference Acevedo, Aguayo-Lobo and Torres2009a, van Grouw Reference van Grouw2021). Leucism is frequently misclassified as albinism (van Grouw Reference van Grouw2006). In contrast to leucism, albinism is a result of an inability to produce melanin, thus causing individuals to exhibit an anomalously white or light coat, pink skin and pink eyes. To classify the animal as albino, it must lack all pigmentation (Fertl & Rosel Reference Fertl, Rosel, Perrin, Wursig and Thewissen2002, van Grouw Reference van Grouw2021).

Documented observations of leucism in marine mammals are predominantly in cetacean species (e.g. whales, dolphins and porpoises) and infrequently in pinniped species (e.g. seals; Acevedo et al. Reference Acevedo, Aguayo-Lobo and Torres2009a,Reference Acevedo, Torres and Aguayo-Lobob). Most documented instances of leucistic pinnipeds have occurred in the Otariidae (eared seals) family, including a South American sea lion (Arctocephalus australis Zimmermann) in Chile (Acevedo & Aguayo Reference Acevedo and Aguayo2008) and an Antarctic fur seal (Arctocephalus gazella Peters) on Marion Island, South Africa (De Bruyn et al. Reference De Bruyn, Pistorius, Tosh and Bester2007). However, occurrences within Phocidae (true seals) remain relatively scarce, with only a handful of such observations having been published to date (Aguayo-Lobo et al. Reference Aguayo-Lobo, Ibáñez, Rauch and Vallejos1995, Bried & Haubreux Reference Bried and Haubreux2000, Acevedo & Aguayo Reference Acevedo and Aguayo2008, Bester et al. Reference Bester, De Clercq, Hofmeyr and De Bruyn2008, Reisinger et al. Reference Reisinger, Mufanadzo, De Bruyn and Bester2009, Romero & Tirira Reference Romero and Tirira2017, Jones et al. Reference Jones, Risi, Osborne and Bester2019).

Weddell seals are a true seal species found circum-Antarctica and a high-level predator in the ecosystem (LaRue et al. Reference LaRue, Salas, Nur, Ainley, Stammerjohn and Pennycook2021). The usual colouration for adult Weddell seals is a darker grey or brown dorsal side, a lighter grey to white ventral side and light spots extending across the body. Like other marine mammals, this countershading helps camouflage Weddell seals in the water column (Hain & Leatherwood Reference Hain and Leatherwood1982). Pups are born covered in lanugo, a soft and long fur that is similar in colour to adult plumage and helps keep the pups warm in the cold Antarctic environment (Fig. 1; Ray & Smith Reference Ray and Smith1968, Thomas & Terhune Reference Thomas, Terhune, Perrin, Wursig and Thewissen2009). Shedding their lanugo at ~6 weeks of age, pups transition to their adult coat, featuring shorter, more structured hair (Thomas & Terhune Reference Thomas, Terhune, Perrin, Wursig and Thewissen2009).

Figure 1. A pup with typical-coloured lanugo and its mother at rest on the ice. Photo credit: Morgan E. Anderson.

The largest population of Weddell seals is found in Erebus Bay, Antarctica (77.7°S, 166.5°E; Fig. 2) and has been the focus of intensive research through a long-term capture-mark-recapture project spanning over 50 years (Stirling Reference Stirling1969, Siniff et al. Reference Siniff, DeMaster, Hofman and Eberhardt1977, Cameron & Siniff Reference Cameron and Siniff2004, Hadley et al. Reference Hadley, Rotella, Garrott and Nichols2006, Rotella Reference Rotella2023). During each field season from October to December, hundreds of adults and pups are observed daily as part of the tagging work associated with the long-term project, and since 1982 every single pup in the study area has been tagged with a uniquely identifiable plastic livestock tag (various makes and models). Over 29 000 seals have been tagged throughout the history of this project, and thousands more have been observed but not tagged. This Short Note documents the first observation of a leucistic animal in this population.

Figure 2. a. Erebus Bay study area location relative to b. Antarctic continent study area boundary (dashed line) and major pupping colonies. Hutton Cliffs, located along the peninsula, is where the pup described in this paper was born and resided for the entirety of our study period. It is one of the biggest colonies in the study area. Turtle Rock, located north of Hutton Cliffs, is the location of her re-sighting.

During the 2022 field season, a female leucistic Weddell seal pup (unique identifying number: 28324) was documented in Erebus Bay, Antarctica. The leucistic pup was born with cream-coloured lanugo, white nails and pink skin; however, her pupils were pigmented (Fig. 3a). Her coat colour was visibly lighter than that of other pups both while on the ice and while swimming (Supplemental Video 1). She was first documented at Hutton Cliffs, one of the largest colonies in Erebus Bay (Fig. 2b), on 22 October 2022, when she was fewer than 2 days old. As part of the ongoing capture-mark-recapture project, she was tagged on 26 October 2022. She was regularly seen and photographed (Fig. 3) throughout the season, with the final recorded observation occurring on 28 November 2022, when she was seen alone on the sea ice. She was denoted as a generally healthy-looking pup who displayed typical behaviours for a pup of her age, including nursing, steadily gaining weight and swimming with her mother (Petch et al. Reference Petch, Rotella, Link, Paterson and Garrott2023). As the pup got older and began to shed her lanugo, she grew in a darker-coloured coat, similar in colouration to that of a typical adult Weddell seal; however, her skin, nails and vibrissae showed no signs of darkening (Fig. 3c). Her mother (unique identifying number: 21607) was 10 years old, had typical coat colouration and had given birth to four previous pups. None of the previous pups were observed with leucistic traits.

Figure 3. a. A leucistic female Weddell seal pup and her mother at the Hutton Cliffs colony in Erebus Bay, Antarctica. Note the light skin, lanugo, whiskers and nails. Photo credit: John Hobgood. b. Leucistic female pup on 18 November 2022 with her extremely light lanugo coat at ~3 weeks of age. Photo credit: Parker M. Levinson. c. Leucistic female at ~1 month of age on 27 November 2022, having shed her lanugo to reveal a darker-coloured coat. Note the pink eye rings and light whiskers. Photo credit: Parker M. Levinson.

During the subsequent field season, the leucistic female was spotted and recorded on 23 October 2023 as a yearling ~1 km from where she was born in 2022. Her coat appeared noticeably paler, and her white whiskers and pink eye rings persisted (Fig. 4). She was observed to be healthy and inquisitive. She was last observed on 14 November 2023 during a census of the study area, ~5 km west of the Turtle Rock colony (Fig. 2b) and closer to the open ocean. On this observation, the leucistic female had some small lacerations, probably from intraspecies fighting that occurs within the colonies (Smith Reference Smith1966). Weddell seals have just under a 50% chance of surviving the first year of life and are typically not re-sighted in the Erebus Bay study area until at least 4 years old (Hastings et al. Reference Hastings, Testa and Rexstad1999, Stauffer et al. Reference Stauffer, Rotella and Garrott2013). Given the moderate survival and re-sight probabilities for juveniles with normal pelage, it is notable that we observed this leucistic individual as a yearling in 2023.

Figure 4. Leucistic yearling female near Turtle Rock on 23 October 2023. Note the pink eye rings, pale coat colour and white whiskers. Photo credit: Parker M. Levinson.

Based on the observed characteristics (e.g. notably lighter fur but pigmented eyes), it is highly probable that the female is leucistic rather than an albino. Her light pigmentation was present within the first 48 hours of her life and has remained with her for over 1 year, making it probable that this was not a result of diet. Additionally, no other seals in the vicinity or in the history of the study have been documented with this colouration, suggesting that the colouration was not a result of environmental causes. As such, we are reasonably confident that her light colouration is a result of a genetic mutation causing leucism, and, based on her pigmented eyes, it is improbable that she has albinism. More extensive genetic or physiological testing would be required for this to be confirmed.

This sighting marks the first documented instance of leucism in the Erebus Bay Weddell seal population. Although it is possible that other occurrences of leucism and albinism might have gone unrecorded, the intensive nature (visits to each pupping colony typically occur every 2–3 days and all pups are approached within 1–15 m on each visit) of the multi-decadal population study makes such oversights improbable (Rotella Reference Rotella2023). Prior documentation of leucism in Weddell seals is limited to a single juvenile seal found on Livingston Island, Antarctica (Acevedo et al. Reference Acevedo, Aguayo-Lobo and Torres2009a). Because both leucistic Weddell seals were observed as subadults, it is unknown whether whatever causes leucism in Weddell seals only impacts juveniles or persists into adulthood. However, given the pink pigmentation of her eye rings, it appears that this seal’s skin is also impacted by this mutation, and she will probably carry some, if not all, of the leucistic traits with her throughout her life.

Due to the infrequency of observations, there has been little research on the fitness cost of leucism in marine mammals. Leucism could be a rare and deleterious mutation that drastically decreases an individual’s fitness so that few, if any, survive to adulthood. It is possible that these individuals are more susceptible to predation due to increased visibility (Acevedo & Aguayo Reference Acevedo and Aguayo2008). Negative impacts could also involve reduced viability due to sensory or nervous system defects, low fertility, increased susceptibility to disease, a decrease in heat absorption and a decrease in ultraviolet protection (Hain & Leatherwood Reference Hain and Leatherwood1982, Fertl & Rosel Reference Fertl, Rosel, Perrin, Wursig and Thewissen2002, Acevedo & Aguayo Reference Acevedo and Aguayo2008). As such, it is probable that there could be a fitness cost for this individual due to her pelage colour, and researchers will continue to keep watch for her in future years, which may aid in answering some questions about how leucism affects an individual’s fitness.

However, genetic mutations are important for evolution and population persistence because rare phenotypes can hold some fitness benefit in rapidly changing environments (Acevedo & Aguayo Reference Acevedo and Aguayo2008, Jones et al. Reference Jones, Mills, Alves, Callahan, Alves and Lafferty2018). Additionally, these colour mutations may be associated with different genes that control traits other than pigmentation, increasing an individual’s fitness in other ways (Brazill-Boast et al. Reference Brazill-Boast, Griffith and Pryke2013, Lehnert et al. Reference Lehnert, Garver, Richard, Devlin, Lajoie, Pitcher and Heath2018). Documentation of mature individuals with leucism shows that leucistic individuals can reach adulthood and potentially pass on their genes (Hain & Leatherwood Reference Hain and Leatherwood1982, Fertl et al. Reference Fertl, Pusser and Long1999, Acevedo et al. Reference Acevedo, Aguayo-Lobo and Torres2009a, Romero & Tirira Reference Romero and Tirira2017, Grebieniow et al. Reference Grebieniow, Korczak-Abshire, Gasek and Górecka-Bruzda2020). As such, despite the potential for decreased fitness of leucistic individuals, the mutation may hold some evolutionary benefit to the population in the rapidly changing Antarctic environment (Convey et al. Reference Convey, Bindschadler, di Prisco, Fahrbach, Gutt and Hodgson2009). Without having a large sample size or genetic samples, it is impossible to determine any answers to these questions, but such a mutation does pose interesting evolutionary possibilities.

Supplementary material

To view supplementary material for this article, please visit http://doi.org/10.1017/S095410202500001X.

Acknowledgements

The authors wish to thank Mairan Smith, Avalon Conklin, Brandon Davis and John Hobgood for aiding in the data collection required to record this sighting. We appreciate all of the logistical field support provided by the United States Antarctic Program, Leidos Antarctic Support Contract and the United States Navy and Air Force. All work and photography were completed under the National Marines Fisheries Service permit No. 26375.

Financial support

The research was supported by the Office of Polar Programs (Grant No 2147553) and the United States Antarctic Program.

Competing interests

The authors declare none.

Author contributions

All authors contributed to data collection and fieldwork. MEA and PML contributed to the writing of the paper, with crucial editing and review conducted by PML and JJR.

Data availability statement

The capture-mark-recapture database for the Erebus Bay Weddell seal population can be found on the US Antarctica Data Center website (https://www.usap-dc.org/; filed under ’Rotella’) and includes unique Weddell seal identifying numbers, seal ages and the number of pups produced by each female seal. The database through 2017 is available at https://www.usap-dc.org/view/dataset/601125, and up-to-date databases are published on the US Antarctica Data Center website every 5–7 years. If data are required in the interim, they can be obtained from Dr Jay Rotella ().

References

Acevedo, J. & Aguayo, M. 2008. Leucistic South American sea lion in Chile, with a review of anomalously color in otariids. Revista de Biologia Marina y Oceanografia, 43, 10.4067/S0718-19572008000200017.Google Scholar
Acevedo, J., Aguayo-Lobo, A. & Torres, D. 2009a. Albino Weddell seal at Cape Shirreff, Livingston Island, Antarctica. Polar Biology, 32, 10.1007/s00300-009-0680-8.Google Scholar
Acevedo, J., Torres, D. & Aguayo-Lobo, A. 2009b. Rare piebald and partially leucistic Antarctic fur seals, Arctocephalus gazella, at Cape Shirreff, Livingston Island, Antarctica. Polar Biology, 32, 10.1007/s00300-008-0500-6.Google Scholar
Aguayo-Lobo, A., Ibáñez, P., Rauch, M. & Vallejos, V. 1995. Primer registro del elefante marino del sur, Mirounga leonina, en la Isla de Pascua, Chile. Serie Científica INACH, 45, 123129.Google Scholar
Bester, M.N., De Clercq, H., Hofmeyr, G.J.G. & De Bruyn, P.J.N. 2008. Leucistic southern elephant seal at Marion Island? Polar Biology, 31, 10.1007/s00300-007-0380-1.CrossRefGoogle Scholar
Brazill-Boast, J., Griffith, S.C. & Pryke, S.R. 2013. Morph-dependent resource acquisition and fitness in a polymorphic bird. Evolutionary Ecology, 27, 10.1007/s10682-013-9651-1.CrossRefGoogle Scholar
Bried, J. & Haubreux, D. 2000. An aberrantly pigmented southern elephant seal (Mirounga leonina) at Iles Kerguelen, southern Indian Ocean. Marine Mammal Science, 16, 10.1111/j.1748-7692.2000.tb00964.x.CrossRefGoogle Scholar
Cameron, M.F. & Siniff, D.B. 2004. Age-specific survival, abundance, and immigration rates of a Weddell seal (Leptonychotes weddellii) population in McMurdo Sound, Antarctica. Canadian Journal of Zoology, 82, 10.1139/z04-025.CrossRefGoogle Scholar
Chatellenaz, M.L. & Zaracho, E.M. 2021. Record of a leucistic pampas fox Lycalopex gymnocercus (Carnivora: Canidae) in northeastern of Argentina. Oecologia Australis, 25, 10.4257/oeco.2021.2504.10.CrossRefGoogle Scholar
Convey, P., Bindschadler, R., di Prisco, G., Fahrbach, E., Gutt, J., Hodgson, D.A., et al. 2009. Antarctic climate change and the environment. Antarctic Science, 21, 10.1017/S0954102009990642.CrossRefGoogle Scholar
De Bruyn, P.J.N., Pistorius, P.A., Tosh, C.A. & Bester, M.N. 2007. Leucistic Antarctic fur seal Arctocephalus gazella at Marion Island. Polar Biology, 30, 10.1007/s00300-007-0320-0.CrossRefGoogle Scholar
Fertl, D. & Rosel, P.E. 2002. Albinism. In Perrin, W.F., Wursig, B. & Thewissen, J.G.M., eds, Encyclopedia of marine mammals. Cambridge, MA: Academic Press, 10.1016/B978-0-12-373553-9.00006-7.Google Scholar
Fertl, D., Pusser, L.T. & Long, J.J. 1999. First record of an albino bottlenose dolphin (Tursiops truncatus) in the Gulf of Mexico, with a review of anomalously white cetaceans. Marine Mammal Science, 15, 10.1111/J.1748-7692.1999.TB00794.X.CrossRefGoogle Scholar
Grebieniow, A., Korczak-Abshire, M., Gasek, A. & Górecka-Bruzda, A. 2020. Antarctic fur seal (Arctocephalus gazella) annual migration and temporal patterns of on-shore occurrence of leucistic individuals on King George Island. 43, 10.1007/s00300-020-02694-3.CrossRefGoogle Scholar
Hadley, G.L., Rotella, J.J., Garrott, R.A. & Nichols, J.D. 2006. Variation in probability of first reproduction of Weddell seals. Journal of Animal Ecology, 75, 10.1111/j.1365-2656.2006.01118.x.CrossRefGoogle ScholarPubMed
Hain, J.H.W. & Leatherwood, S. 1982. Two sightings of white pilot whales, Globicephala melaena, and summarized records of anomalously white cetaceans. Journal of Mammalogy, 63, 338343.CrossRefGoogle Scholar
Hastings, K.K., Testa, J.W. & Rexstad, E.A. 1999. Interannual variation in survival of juvenile Weddell seals (Leptonychotes Weddellii) from McMurdo Sound, Antarctica: effects of cohort, sex and age. Journal of Zoology, 248, 307323.CrossRefGoogle Scholar
Jones, C.W., Risi, M.M., Osborne, A. & Bester, M.N. 2019. First record of a leucistic sub-Antarctic fur seal. Polar Biology, 42, 10.1007/S00300-019-02506-3/FIGURES/2.CrossRefGoogle Scholar
Jones, M.R., Mills, L.S., Alves, P.C., Callahan, C.M., Alves, J.M., Lafferty, D.J.R., et al. 2018. Adaptive introgression underlies polymorphic seasonal camouflage in Snowshoe Hares. Science, 1358, 13551358.CrossRefGoogle Scholar
Kratochwil, C.F. & Mallarino, R. 2023. Mechanisms underlying the formation and evolution of vertebrate color patterns. Annual Review of Genetics, 57, 10.1146/annurev-genet-031423-120918.CrossRefGoogle ScholarPubMed
LaRue, M., Salas, L., Nur, N., Ainley, D., Stammerjohn, S., Pennycook, J., et al. 2021. Insights from the first global population estimate of Weddell seals in Antarctica. Science Advances, 7, 10.1126/sciadv.abh3674.CrossRefGoogle ScholarPubMed
Lehnert, S.J., Garver, K.A., Richard, J., Devlin, R.H., Lajoie, C., Pitcher, T.E. & Heath, D.D. 2018. Significant differences in maternal carotenoid provisioning and effects on offspring fitness in Chinook salmon colour morphs. Journal of Evolutionary Biology, 31, 10.1111/jeb.13383.CrossRefGoogle ScholarPubMed
Petch, S.M., Rotella, J.J., Link, W.A., Paterson, J.T. & Garrott, R.A. 2023. Investigating diverse sources of variation in the amount of time Weddell seal (Leptonychotes weddellii) pups spend in the water during the lactation period. Marine Mammal Science, 39, 10.1111/mms.12955.CrossRefGoogle Scholar
Ray, C. & Smith, M.S.R. 1968. Thermoregulation of the pup and adult Weddell seal, Leptonychotes weddelli (Lesson), in Antarctica. Zoologica: Scientific Contributions of the New York Zoological Society. , 53, 10.5962/p.203262.Google Scholar
Reisinger, R.R., Mufanadzo, N.T., De Bruyn, P.J.N. & Bester, M.N. 2009. Leucistic southern elephant seal at Marion Island. Polar Biology, 32, 10.1007/s00300-008-0572-3.CrossRefGoogle Scholar
Romero, V. & Tirira, D.G. 2017. Leucistic Antarctic fur seal (Arctocephalus gazella) at Robert Island, South Shetland Islands, Antarctica, with a note on colour morph nomenclature. Polar Biology, 40, 10.1007/s00300-016-2069-9.CrossRefGoogle Scholar
Rotella, J.J. 2023. Patterns, sources, and consequences of variation in age-specific vital rates: Insights from a long-term study of Weddell seals. Journal of Animal Ecology, 92, 10.1111/1365-2656.13870.CrossRefGoogle ScholarPubMed
Rowland, H.M. 2022. Countershading. In Vonk, J. & Shackelford, T.K., eds, Encyclopedia of animal cognition and behavior. Cham: Springer International Publishing, 10.1007/978-3-319-55065-7_684.Google Scholar
Siniff, D.B., DeMaster, D.P., Hofman, R.J. & Eberhardt, L.L. 1977. An analysis of the dynamics of a Weddell seal population. Ecological Monographs, 47, 10.2307/1942520.CrossRefGoogle Scholar
Smith, M.S.R. 1966. Injuries as an indication of social behaviour in the Weddell seal (Leptonychotes weddelli). Mammalia, 30, 10.1515/mamm.1966.30.2.241.CrossRefGoogle Scholar
Stauffer, G.E., Rotella, J.J. & Garrott, R.A. 2013. Variability in temporary emigration rates of individually marked female Weddell seals prior to first reproduction. Oecologia, 172, 10.1007/s00442-012-2472-z.CrossRefGoogle ScholarPubMed
Stirling, I. 1969. Ecology of the Weddell seal in McMurdo Sound, Antarctica. Ecology, 50, 10.2307/1936247.CrossRefGoogle Scholar
Thomas, J.A. & Terhune, J. 2009. Weddell seal: Leptonychotes weddellii . In Perrin, W.F., Wursig, B. & Thewissen, J.G.M., eds, Encyclopedia of marine mammals. Cambridge, MA: Academic Press, 10.1016/B978-0-12-373553-9.00278-9.Google Scholar
van Grouw, H. 2006. Not every white bird is an albino: sense and nonsense about colour aberrations in birds. Dutch Birding, 28, 7989.Google Scholar
van Grouw, H. 2021. What’s in a name? Nomenclature for colour aberrations in birds. Bulletin of the British Ornithologists’ Club, 141, 276299.CrossRefGoogle Scholar
Figure 0

Figure 1. A pup with typical-coloured lanugo and its mother at rest on the ice. Photo credit: Morgan E. Anderson.

Figure 1

Figure 2. a. Erebus Bay study area location relative to b. Antarctic continent study area boundary (dashed line) and major pupping colonies. Hutton Cliffs, located along the peninsula, is where the pup described in this paper was born and resided for the entirety of our study period. It is one of the biggest colonies in the study area. Turtle Rock, located north of Hutton Cliffs, is the location of her re-sighting.

Figure 2

Figure 3. a. A leucistic female Weddell seal pup and her mother at the Hutton Cliffs colony in Erebus Bay, Antarctica. Note the light skin, lanugo, whiskers and nails. Photo credit: John Hobgood. b. Leucistic female pup on 18 November 2022 with her extremely light lanugo coat at ~3 weeks of age. Photo credit: Parker M. Levinson. c. Leucistic female at ~1 month of age on 27 November 2022, having shed her lanugo to reveal a darker-coloured coat. Note the pink eye rings and light whiskers. Photo credit: Parker M. Levinson.

Figure 3

Figure 4. Leucistic yearling female near Turtle Rock on 23 October 2023. Note the pink eye rings, pale coat colour and white whiskers. Photo credit: Parker M. Levinson.

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