The Antarctic Field Guides is a collaborative tool offering free access to information that can help you identify Antarctic organisms. Thanks to the initial efforts from Prof. Andrew Clarke, Dr David Barnes (British Antarctic Survey) and Dr Stefano Schiaparelli (University of Genoa and Italian National Antarctic Museum), it allows users to build a tailor-made, customized guide, to be taken in the field or simply browsed. The pages are generated on-the-fly from the contents of authoritative, quality controlled data resources (SCAR-MarBIN and ANTABIF, RAMS , GBIF), and ensures the user to access up-to-date information about the group of organisms he/she is interested in. Even if the primary focus is for scientists, the AFGs are open and free for all to enjoy.
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Scientific name
EG-BAMM, Jeroen CS Creuwels & Øystein Varpe
The global population size is assumed to be 10-20 million individuals, based on at-sea estimates. The total number of breeding pairs of known colonies is approximately 0.5 million, a mismatch with the numbers at sea. All colonies may not yet be known, and the numbers of birds in the colony vary greatly from year to year. Therefore, it is difficult to establish global population trends. The large number of birds justifies the current IUCN status of Least Concern.
The Antarctic petrel is a medium-sized petrel with a dark brown and white plumage. The dark brown parts may fade during the breeding season to pale brown. Head, neck and back are chocolate brown. Bill is very dark to black. The upperwing is dark brown with a large white bar over the secondary and first primary feathers, which is visible in flight. The underwing and belly are largely white. The sexes are alike, although males are slightly larger. The weight of adult birds fluctuates throughout the year between 550-800g, with peak weight around egg laying.
Antarctic Petrels have breeding colonies in the coastal zone of Antarctica and in inland Antarctica between 65° and 80°S. As of 1999, there are 35 known breeding colonies; all except one are situated in East Antarctica. The majority of the birds breeds in inland Antarctica (Dronning Maud Land) with colonies situated on nunataks hundreds of kilometres away from the sea-ice border. Colonies are found at altitudes up to 1600 m. At sea, Antarctic Petrels are generally associated with pack ice year-round: in summer normally south of 62°S and in wintertime they can be seen up to 48°S.
At sea, Antarctic Petrels are often found foraging together in large flocks or sitting on icebergs, regularly with other fulmarine petrels (often Snow Petrels). In summer, they are foraging in open waters, but can also be seen in areas with pack-ice. Breeding birds may have to forage far from the colony, hundreds to 1000 kilometres away, particularly early in the season when nearby waters tend to be ice covered. In winter, as the sea-ice grows, they move further north, but tend to remain in the vicinity of the sea ice.
The Antarctic Petrel colonies are located on snow-free areas such as cliffs, ridges, slopes, but also on relatively levelled areas. The colonies are often facing north to catch as much sunlight as possible and are relatively exposed to the wind preventing the snow to accumulate. Colonies can be large (>10.000 sites) and one inland colony (Svarthamaren, Dronning Maud Land) consists of more than 200.000 breeding pairs, but also several smaller colonies (10s-100s of sites) exist. Normally the nests are densely packed, but sometimes they are located more scattered. The nest consists of a shallow depression and is lined with some gravel or feathers, if material is available. Some nests are well sheltered by boulders and rocks, creating cave like conditions for some birds, whereas other nests have no or limited shelter. There is some risk of melt water accumulating in the nests, a problematic situation for the chick, and a risk that seems to be highest in the well sheltered nests.
In poor visibility conditions, Antarctic Petrels could be confused with the somewhat smaller Cape Petrels. Seen from below both species look similar, although Antarctic Petrels have less black. Both are mostly white with a dark head, but the black bands along the leading edge of the wing and on the end of the tail are smaller in Antarctic Petrels. When the upper parts are clearly visible, there should be little doubt between the two species. Cape Petrels are more black and white, and have a clearly chequered pattern on the wings and back, whereas in Antarctic Petrels the colour is uniform dark brown. Later in season, this colour is getting paler to lighter brown. Antarctic Petrels have the typical gliding flight of petrels with little flapping.
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The breeding biology of the Antarctic petrel is extremely synchronous; during laying, hatching and fledging most individuals are synchronized within a one week period. Antarctic Petrels lay one egg and do not relay. Individual birds return to the same nest each year, but occasionally they skip a breeding season. Birds generally return to the same partner and pair bonds are long-lasting, but divorces do occur. Antarctic Petrels are philopatric, which means that many return as a (sub)adult to their own native colony. Their age upon return or when they start breeding is not known. Longevity has not been estimated, due to lack of data, but it is expected that individuals may live up to 50 years old. In the colonies, adults are rarely taken by giant petrels or skuas. Abandoned eggs and young chicks, however, are vulnerable and heavily predated by skuas. Older chicks and adults are able to defend themselves against predators by spitting stomach oil. In addition, snow storms during the incubation or chick period may cause high mortality of eggs and chicks.
6
Scientific name
antarcticconnection.com
85 to 100 ft long
Largest of Earth's animals, the majestic Blue whale can be found in all the world's oceans. In summer, they frequent the fringes of the polar ice shelves, moving to tropical and subtropical waters during the winter months. They travel alone or occasionally in pairs, with the larger individuals occuring the farthest south. Once numbering close to 200,000 individuals, Blue whales were heavily exploited for their oil, meat, and baleen during the early to mid 1900's, severely reducing the species' population to near the point of extinction. Since the International Whaling Commission (IWC) imposed a hunting ban in 1966, Blues have returned to several areas of their former range, but recovery is slow (current populations are only 1% of their former numbers).
Blue whales are so named because their skin has a light-gray-and-white mottled pattern, which appears light blue when the whale is just below the surface of the water on a sunny day. Researchers use these skin patterns, which are unique to each animal, as a means of individual whale identification. Aside from the animal's massive size, distinguishing characteristics include its habit of showing its flukes when diving (other rorqual whales do not). Also, they have an unusually small dorsal fin which is set far back on the body.
Blue whales produce reverberating, low-frequency moans that can be heard in deep ocean waters up to 100 miles away. These moans enable the whales to remain in contact across a vast expanse of ocean.
Despite their enormous size, the Blue Whale's diet consists almost entirely of krill, tiny shrimplike crustaceans occurring in all oceans of the world. Feeding by lunging open-mouthed into dense groups of such creatures, they can consume as much as 4.5 tons in a day. Water and food rushing into the whale's pleated, expandable mouth is forced past hundreds of wide, black fringed baleen plates that hang from the roof of the mouth. The plates act like a sieve or comb, trapping the solid food inside the fringes and expelling the excess water. Occasionally working in pairs, Blue whales have been observed weave through schools of krill, apparently using each other's bodies to block the escape of their prey.
Female Blue whales reach sexual maturity at approximately 5 years of age. They may give birth once every two or three years. Mating occurs during the summer season, and the gestation period lasts about 11 months. A single calf is usually born the following spring; twins are rare. The calves nurse for seven or eight months, gaining as much as 200 pounds per day in the nutrient-rich Antarctic or Arctic waters.
7
Scientific name
EG-BAMM, Meagan Dewar
Humpback whales are generally dark on the dorsal side of the body, whilst on the ventral side; they have substantial areas of white pigmentation. The flippers are white on the ventral side, and vary from mostly black to white on the dorsal side. The flukes are dark on the dorsal side of the body and vary from all white to mostly black on the ventral side with distinct patterns. Researchers can use the distinct colouration patterns on the flukes to distinguish individual humpbacks as well as using other individually variable features such as serrations on the trailing edges of the flukes. Humpback whales grow between 11-18m in length, with males being around 1-1.5m shorter than females and weigh between 24-45 tons. Humpback whales live for around 50 years, becoming sexually mature at around 5-10 years of age.
A worldwide population size of more than 60,000 individuals has been estimated but this is considered to be an underestimate of the total abundance as abundance data is not available for all areas, whilst the population size for the Southern Hemisphere is estimated to be around 36,000. Based on recent population increases and the limited availability of information on the global population size prior to 1940, it is unlikely that humpback whales are below the threshold (50% of the 1940 level) that would qualify the species for inclusion in the Vulnerable category under criterion A. In addition, as the current population estimates total more than 60,000 individuals, and the range of the humpback is not restricted, excludes the species from being classified under criterion B, C and D. Therefore the humpback whale is classified as Least Concern by the IUCN red list. The IUCN states, that although the encouraging global status of the humpback whales, concerns still remain about discrete and small subpopulations of humpbacks for which data is not available.
The population estimate of the Antarctic feeding grounds is estimated to be between 34,000 – 52,000 individuals. During the breeding season, Southern Hemisphere humpback whales migrate to one of breeding grounds (A – G). The population abundance for breeding stock A (Brazil) is estimated to be 6,500 individuals, breeding stock B (south east Atlantic) is estimated to be 9,800, breeding stock C (south western Indian Ocean) is estimated to be 7,000, breeding stock D (south eastern Indian Ocean, Western Australia) is estimated to be 33,800 individuals, breeding stock E (south west Pacific, north eastern Australia) is estimated to be 14,522 individuals and breeding stock G is estimated to be 4,000 individuals. Unfortunately for breeding stock F, there is no abundance available.
The humpback whale (Megaptera novaeangliae) is a species of baleen whale and is one of the larger rorqual species, ranging in length from 11 to18 metres and can weigh up to 45 tons. Humpback whales belong to the family of rorqual whales, which are characterised by their flat heads, pointed snouts, round bodies and having their dorsal fins set well back on the body. In humpback whales, the most distinctive feature is their long pectoral fins. Humpback whales not only have the largest pectoral fins of any cetacean species, but also the largest appendage of any living animal with their fins measuring over 15 feet in length or almost one third of the whale’s body. The size of these exceptionally large pectoral fins is also reflected in their Latin name, Megaptera novaeangliae, meaning “long winged from New England.”
Humpback whales perform some of the longest migrations of any mammals, with humpback whales migrating annually from their feeding grounds in the North and South Pole, to their winter breeding grounds in the tropics near the equator. During the breeding season, humpback whales are known for their remarkable surface displays and vocal songs sang by the males during their annual migration.
The humpback whale is a cosmopolitan species found in all the major ocean basins and all but one of the subpopulations migrate between mating and calving grounds in tropical waters, usually near the continental coastlines and productive colder waters in temperate and high latitudes. In the Southern Ocean humpbacks are abundant throughout the Antarctic during the summer months and can be found south of the ice edge but not within the pack ice. In the winter, humpbacks in the Southern Ocean migrate from their polar feeding grounds to their sub-tropical winter breeding grounds in the Atlantic, Indian Ocean and Pacific. The Southern Hemisphere humpbacks are known feed in areas I-V of the management areas in Antarctic. Currently the International Whaling Commission recognises seven major breeding stocks (A-G). These include;
Breeding Stock A - Southwest Atlantic, (Brazil),
Breeding Stock B - Southeast Atlantic, (West Africa from the Gulf of Guinea down to South Africa),
Breeding Stock C – South western Indian Ocean (coasts of eastern South Africa, Mozambique, Madagascar (southern, western and eastern coasts), Mayotte, the Comoros and other western Indian Ocean island groups),
Breeding Stock D – South eastern Indian Ocean (North Western Australia),
Breeding Stock E – South west Pacific/North eastern Australia, New Caledonia, Tonga and Fiji,
Breeding Stock F - Central South Pacific (Cook Islands and French Polynesia),
Breeding Stock G – South east Pacific (Ecuador, Galápagos, Colombia, Panama and Costa Rica).
Although not much is known about the summer feeding areas for each breeding stock, the use of photo-identification, genetics data and satellite tracking has provided some information on the potential feeding grounds for each breeding stock. Breeding stock A feeds in the South Georgia/South Sandwich Islands in Area II, Breeding stock D feeds in Antarctic area IV and perhaps eastern area III, breeding stock G feeds along the Antarctic Peninsula and the South Shetlands; whilst breeding stock E feeds in Antarctic areas V. At this stage information on the feeding grounds of breeding stock B, C and F is not available.
Humpback whales can dive to a depth of 150m, with dives lasting anywhere from 3-40 minutes.
Humpback whales are found worldwide in all major oceans. They occur primarily in coastal and continental shelf waters, although they are also known to feed around some seamounts and migrating whales often pass through deep waters.
Humpback whales are distinguished from other whales in the same Family (Balaenopteridae) by extraordinary long flippers (up to 5 m or about 1P total body length), a more robust body, fewer throat grooves (14-35), more variable dorsal fin and their use of long (up to 30 min.), complex, repetitive songs during courtship. Humpback whales are black or dark grey dorsally and white ventrally. Their flippers are black on top and white underneath.
In humpback whales, the most distinctive feature is their long oar like pectoral fins. Humpback whales not only have the largest pectoral fins of any cetacean species, but also the largest appendage of any living animal with their fins measuring over 15 feet in length or almost one third of the whale’s body. In most other whale species their flippers are short and paddle shaped and used for steering or maintaining stability in the water. Whilst in humpbacks the flippers are thought to be used to row the animal through the water. Another distinguishing feature of the humpback is the presences of knobs along the leading edges of their flippers, whilst the head and lower jaw bear numerous tubercles and barnacles.
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Humpback whales grow between 11-18m long, with males being around 1-1.5m shorter than females, and weighing between 24-40 tons. Humpback whales live for around 50 years, becoming sexually mature at around 5 – 10 years of age. At birth calves are around 4-4.6m long and weigh around 1-2 tons. Humpback whales only give birth to one calf, with gestation ranging from 11.5 months, although multiple foetuses have been recorded in dead pregnant whales. Calves remain with their months for approximately 12 months.
9
Scientific name
EG-BAMM, Matthias Kopp
The general appearance of the Brown Skua is gull-like but they are more bulky, have a hooked bill and sharp claws like a bird of prey; overall looking more powerful and aggressive (than what they actually are). They are strong flyers and can easily outrace similar sized or even much larger birds, performing strong direct flights with constant shallow wing beets. They have a complete brownish colour whereas some white feather tips give the bird a flecked appearance. At the end of the breeding season the body feathers look more and more used and more feather tips become white. Both sexes emit at least three call types depending on the behavioral context: alarm, contact and long call (Janicke et al. 2007).
Brown Skua has an average wing span of 147 cm (64 cm long) and a mean mass of 1730 gram (range: 1420 – 2310 gram, n = 178, dataset originates from adult skuas from King George Island/ South Shetland Islands. The sexes in the Brown Skuas are similar in appearance, though in some (41% at Fildes Peninsula) cases males are darker than females (Peter et al. 1990). However, they differ in their size, with females being larger and heavier than males, known as reverse sexual dimorphism.
In its breeding range there is, beside in the zone of sympatric occurrence with south polar skuas, no species to mistake for the Brown Skua. South Polar Skuas are overall smaller and more gracile. In that area, most South Polar Skuas are dark morphes with dark brown feathers on the back and the prominent golden hackles on the neck. The body feathers are uniformly a lighter brown than the feathers on the back. However, even though there are size and colour differences between the two species it is not always possible to distinguish them exactly.
The Brown Skua Catharacta antarctica lonnbergi is evaluated in the Red List of Threatened Species as Least Concern. That is based on: firstly the huge range of occurrence, which is circumpolar, mostly on remote, isolated Sub-Antarctic islands; secondly, the population trend appears to be stable. According to BirdLife International the population is placed in the band 10 000 – 20 000 individuals.
The Brown Skua is the biggest of all southern hemisphere skua species. The current phylogenetic classification identifies three families in the order Lariformes in the high latitudes of the southern hemisphere: gulls, terns and skuas. Herein the skuas (Stercorariidae) for their part occur with three species: S. maccormicki, S. chilensis and S. antarcticus. The latter of which is subdivided into three sub-species: S. a. antarcticus, S. a. lonnbergi and S. a. hamiltoni (Ritz et al. 2008).
Brown Skuas have a huge area of distribution, which is circumpolar at high latitudes of the southern hemisphere. Their prevailing breeding sites are at Sub-Antarctic Islands within the Antarctic Convergence. But they also breed at islands near New Zealand, representing the northernmost breeding areas. On the other extreme side, Brown Skuas are breeding on islands near the Antarctic Peninsula (not further south than Anvers Island archipelago 64°46′ S 64°03′ W) (Ritz et al. 2006). An outlying, but however constant, breeding record (the only published one) is a single Brown Skua female which breeds at the western edge of the Ross sea (Port Martin) at the Antarctic Continent/ East Antarctic. That female breeds in a mixed pair constellation with a south polar skua (Barbraud et al. 1999).
The zone of sympatric occurrence with C. maccormicki: In the breeding range of the Brown Skua, there is a zone characterized by an alongside occurrence with another skua species, the South Polar Skua S. maccormicki. A 500km wide hybrid zone is located in the West Antarctic, in the area of the Antarctic Peninsula representing the southern and northern extremes of the breeding ranges of Brown- and South Polar Skuas, respectively. The zone ranges from the South Orkney Islands (60°45’S) in the north to the Anvers Island archipelago (about 65°S) in the south. Pairs formed by S. maccormicki x S. maccormicki and S. a. lonnbergi x S. a. lonnbergi are dominating the numbers and are occurring side by side. The characteristic feature of the hybrid zone is the occurrence of mixed species pairs, formed by S. maccormicki and S. a. lonnbergi. The percentage of such mixed species pairs varies within that zone and is highest in the northern part; like on Fildes Peninsula/ King George Island were 12 % of all breeding pairs are mixed pairs. These pairs are always formed by a South Polar Skua male and a Brown Skua female. The offspring of mixed species pairs is fertile (Ritz et al. 2006).
The hybrid zone has been intensively studied; amongst others in terms of species foraging ecology. In the area of sympatric occurrence, a foraging pattern different from the pattern of circumpolar allopatric occurrence has evolved which is due to species competition. However, Brown Skuas are dominating all terrestrial resources over South Polar Skuas by outcompeting them – so a change in the foraging behavior can be observed only in the South Polar Skua, which is forced to prey on marine resources.
Nests are built at places which are free of snow in early spring compared to the surrounding facilitated by landscape features e.g. small hills or moraines. As nest material they use lichens, grasses and/or mosses depending on the local availability. Like other skua species, the Brown Skua also occupies a territory around the nest which is defended against each intruder by the territory owners, and most vigorously against conspecifics (but also against scientists and unsuspecting tourists) (Trivelpiece et al. 1980). Herein, the size of the territory varies a lot and depends amongst others factors on the breeding location and landscape features. The territory may firstly be: a pure nest territory, defended to protect the brood or secondly an all-purpose territory which includes beneath the nest as well prey organisms (like a penguin rookery). It is a brood defense but also for all feeding needs within the whole breeding season (Hahn and Peter 2003).
The most conspicuous feature is a white patch in the middle of the under wing which is formed generally by the basal parts of eight primary feathers. They show this ornament when warning by lifting the wings (e.g. in case of entering the territory; happens in combination with emitting a call, in that case a long call).
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Within their huge breeding range, Brown Skuas experience a wide variety of climatic conditions, having consequences for the non-breeding period distribution. Brown Skuas do not necessarily migrate big distances but, typically for pelagic birds, they usually do leave the breeding grounds and return to land only for breeding. How far they move depends on the breeding area, whereas the northern breeding populations stay close to the breeding ground and the southern populations migrate further north. Herein the migration pattern and wintering areas are largely unknown (Olsen and Larsson 1997). Museum skins and colour slights of C. a. lonnbergi-specimens found/sighted at the northern hemisphere appeared to be misidentified being rather South Polar Skuas (Devillers 1977). Phillips et al. (2007) firstly used tracking devices for getting insight into migration patterns and wintering areas of that species. The study showed that Brown Skuas breeding at Bird Island/ South Georgia are leaving the breeding area and wintering over deep oceanic water in the Argentine basin between the Antarctic Polar Front and the northern sub-tropical-front.
11
Scientific name








The characteristic posture of the icefish is “sitting” on the botton kept by its elongate pelvic fins (Montgomery & Macdonald, 1998).
Chionodraco hamatus shows a circumantarctic distribution, although it is mainly recorded on the continental shelf of East Antarctica down to 600 m depth (Iwami & Kock 1990). The lack of haemoglobin in the blood, which characterises these fishes, has probably played a key role in determining their distribution within the cold and highly oxygenated waters of the Antarctic, where metabolic requirements dependent on temperature are low (Eastman 1993). Consequently, several studies on these species have focussed on their blood physiology, as well as on the structure and function of antifreeze components (Kunzmann 1989, 1991; Wells et al. 1990; Egginton 1996; Wöhrmann 1996, 1997).
The study of the morphology and composition of the three otoliths (sagitta, lapillus and asteriscus) of the Chionodraco hamatus by scanning electron microscopy and X-ray diffraction was carried out by Motta et al. (2009). It possessed a completely vateritic asteriscus, whereas its sagitta and lapillus were made mostly of aragonite. Parallel analysis of protein patterns in C. hamatus revealed that the sagitta significantly differed from the lapillus and asteriscus. The sagitta did not contain the S-100 protein and showed calmodulin and calbindin located in discontinuous or incremental zones, respectively.
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The channichthyid Chionodraco hamatus is a common icefish within the cold waters of the high-Antarctic zone. It is an endemic species to the Antarctic region. Off Terra Nova Bay, as well as in the Ross Sea, Chionodraco hamatus is by far the most abundant and eurybathic icefish, both in terms of biomass and frequency of occurrence (Eastman & Hubold 1999; Vacchi et al., 1999).
Chionodraco hamatus spawns in spring (September-October) in the Mawson Sea and throughout summer (December-March) in the Ross Sea, Davis Sea and Weddell Sea (Shandikov & Faleeva 1992; Duhamel et al., 1993; Vacchi et al., 1996). As in other high-Antarctic channichthyids, C. hamatus females are characterised by having low fecundity and they produce only a few thousand but large (3.5-5 mm) eggs (Vacchi et al. 1996). C. hamatus probably spawns a single batch of oocytes once a year (La Mesa et al., 2003).
13
Scientific name
British Antarctic Survey
Small (a few cm) and usually orange or red with a stalk. The test is covered in fine hairs.
Found below about 10m around the Antarctic Peninsula and Continent.
Ecology: This is an uncommon ascidian and very little is known about it. It has been found growing on other, larger species of ascidians, such as Ascidia challengeri.
14
Scientific name
British Antarctic Survey
As its name suggests Molgula pedunculata usually has a long stalk or peduncle, which may have fine hairs on it. It is large and fairly translucent and is typically 10-20cm.
10 to 437m [shallow depths all from Dave-check ok#], but generally below 100m, from Sub-Antarctica to the Antarctic Peninsula and Continent. Molgula pedunculata has a holdfast which allows it to attach to both hard and soft substrates [??#], and it often grows in patches or dense clumps.
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Antarctic ascidians grow relatively fast, appearing to be an exception to the Antarctic tendency towards large, slow-growing invertebrates. Molgula pedunculata has been shown to grow fast at first (up to 16.8cm in two years), but grows slower as it gets older. It is a suspension feeder, feeding mostly on resuspended benthic material, and it spawns between August and November.
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Scientific name
EG-BAMM, Ian Staniland
Fur seals, unlike phocid seals, are able to turn in their hind quarters and walk on all four flippers, enabling them to run and achieve considerable speed on land. They also have short pointed external ears and adult males have external testes.
Both sexes have thick bodies and relatively long necks, which make the head look small. The shape of the snout is smooth and pointy and appears flat from the forehead to the nose, especially in males.
Colour varies with sex, age and time ashore but generally the fur is grey to brownish usually lighter creamier on the throat and chest. Adult males have a heavier mane around the thickened neck that has a more grizzled appearance due to white tipped guard hairs.
In pups, the fur is black until the first molt although lighter colouration is often visible especially around the face. 1 – 2 ‰ of pups are born blonde/white with lack of pigmentation in the guard hairs and retain this coloration for life. These are not true albinos as the skin and eyes are pigmented. Intermediate colorations of mottled black, brown and white also occur but are rarer still.
There is large sexual dimorphism with males being up to 1.5 times longer and four times heavier than females. Bulls’ standard length is 180 cm (170-200 cm) weighing 130 kg (90-200). Adult females are on average 130 cm (115 – 140) in length and around 35 kg (20 – 50) in weight. Mean weights for new born pups are 5.4 kg for females and 5.9 kg for males with lengths ranging from 58 -66 cm.
Antarctic fur seals are one of the most numerous mammalian predators in the Antarctic. The population was hunted to near extinction at the start of the 20th Century for its pelt. It has subsequently recovered with the current population estimated to be in the region of 3-4 million. Around breeding beaches small groups or individuals can often be seen porpoising through the water and will often stop to investigate ships or small boats. On land they are often aggressive and, during the breeding season, large aggregations can make access to beaches difficult.
Wide distribution, primarily breeding on sub-Antarctic and Antarctic Islands in the South Atlantic and Indian Ocean regions of the Southern Ocean. 95% of the world population breeds on South Georgia. Non- breeding individuals are more widely dispersed.
Antarctic fur seals are shallow divers confined to surface waters. Females generally dive to 30 - 40 m and rarely exceed 200m. Larger males dive deeper ~100m with a maximum recorded of 350 m.
Fur seals preferentially breed on shale or pebble beaches close to areas of high marine productivity, but in areas of high density they can be found on almost all sea-shore environments. As the breeding season progresses mother-pup pairs usually move into tussock grass areas behind the breeding beaches.
Away from the mating season males appear to move southwards foraging around, and hauling out on, the ice edge or Antarctic islands. During winter females disperse at sea ranging from the ice edge to areas far north of the polar front.
Antarctic fur seals can easily be confused with most of the other fur seal species, their size, coloration and head shape are the easiest characteristics with which to identify them.
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Antarctic fur seals are highly polygynous with territorial bulls defending harems of, on average, nine females. Territories are established on breeding grounds in October to early November, when the musty-smelling males are extremely aggressive in defence of their patch of beach. Females arrive a few weeks later giving birth a few days after coming ashore. Lactating females then alternate between short trips to sea (2-10 days) and periods ashore (1-2 days) suckling their pups. Pups are weaned at about four months old. Mating takes place a few days after the pup is born and the female gestates for just over a year, so that she is pregnant whilst suckling.
They feed mostly on krill, Euphausia superba, in the South Atlantic part of their range with myctophids and nototheniids dominating elsewhere. The predation of squid or penguins may also be locally or seasonally significant. They have few predators although leopard seals and killer whales are known to take smaller individuals particularly juveniles.
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Scientific name
British Antarctic Survey
Yellowish and translucent, but often covered in sediment so that its appearance is obscured, however the siphons are distinct. The main body lies flat along the substrate, growing to a length of 17cm.
15 to 637m, found on a wide range of substrates from Sub-Antarctica to the Antarctic Peninsula and Continent.
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Ascidia challengeri has been shown to grow fast at first (up to 7.5cm in two years), but growth slows as it gets older. It is a suspension feeder, mostly sifting out detritus that has been re-stirred up from the sea floor. Ascidians have a low energy content and appear to be generally unattractive to potential predators, although they have occasionally been found in the stomachs of fish and brittle stars. Ascidia challengeri spawns during the Antarctic summer.
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Scientific name
British Antarctic Survey
Colour is ivory or grey. Corella eumyota sometimes has a short stalk, and grows up to 24cm long.
0 to 842m, but not usually found shallower than 20m. Corella eumyota occurs on a variety of substrates around Antarctica and the Sub-Antarctic and in temperate waters such as New Zealand, South Africa and southern Australia. It has also been recently (July 2002) found off northern France where it has probably newly invaded from southern waters. This is the first record of it in the northern hemisphere.
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Corella eumyota has been shown to grow fast at first (up to 14.4cm in two years), but growth slows as it gets older. It is a suspension feeder, mostly on material stirred up from the substrate. It broods its young until they are well developed and they settle a few minutes after release, so Corella eumyota is often found in clumps. Spawning occurs in the Antarctic summer.
22
Scientific name
Up to 25cm in diameter and 40cm in height
Cnemidocarpa verrucosa is probably the most common ascidian (sea squirt) in shallow waters and is fairly featureless – essentially resembling a translucent bag. It varies in colour from brown, through yellow to white and translucent. This species can be highly abundant and can dominate patches many metres in size. It is one of the best known of the Antarctic ascidians. It feeds during summer months and (like most of the benthos) has strongly seasonal reproduction, but unusually larvae are released in winter. Being almost just a ‘bag’ it has very low metabolic rates, even for Antarctic animals
5m to deep waters
occurs in most shallow coastal situations from sediment to hard rock
large, translucent ‘bag-like’
23
Scientific name
EG-BAMM, Maud Poisbleau & Laurent Demongin


Adults have very dark bluish-grey head and upperparts, clearly demarcated from white underparts. The underside of the flippers is mainly white with a variable dark pattern. The head is ornamented with yellow eyebrows (superciliary crests), long yellow feathers falling behind the eyes and black crests on the rear crown. The bill is red-orange, quite strong and bulbous. The legs are pinkish. The irises are red.
Juveniles differ from adults by the absence of yellow and black crests, the very faint yellow eyebrows, the chin and throat mottled of greyish and white, the darker bill. After the first moult when they are one year old, immature birds can be distinguished by their shorter crests and usually by their not fully dark chin. They are also a bit smaller than adults.
Southern rockhopper penguins are the second smallest penguins after the little penguins Eudyptula minor. The body size from the tip of the feet to the tip of the bill is only about 50 cm. Males and females are similar but bill depth and length of females tend to be slightly smaller. Because breeding southern rockhopper penguins endure several long fasting periods, their mass varies strongly several times between October and April. They reach a maximum of 4 - 4.5 kg when they arrive at the colony to breed and prior to the moult, and a minimum of about 2 - 2.5 kg after the first fasting period of the incubation, and also at the end of the moult.
The global population is currently estimated at about 320,000 breeding pairs in the Falkland Islands (about 70% concentrated on three islands) and 564,000 breeding pairs in South America (174,000 in Argentina and 390,000 in Chile). The Falkland colonies have been regularly monitored since the 1980s. This population has shown major, long-term population changes, declining by 86%, from 1.5 million to 210,000 pairs from the 1930s to 2005. In 2010, the Falkland Islands population of rockhopper penguins was estimated to be 319,163 ± 18,503 breeding pairs, i.e. the second largest population (after Chile). The number of breeding pairs counted in 2010 was 50.6% higher than the number counted in 2005 which was the first count after a population crash in 2002-2003 (see below). The Falkland Islands rockhopper penguin population is best described as stable, but remains at less than 20% of the 1930s population estimate. The colonies of South America are much more difficult to monitor because of their difficult accessibility in remote uninhabited islands. Four islands hold 97% of the population that have slightly increased since the 1980s.
The causes for the decreases in southern rockhopper penguins have not been explained although some threats have been identified. At the Falkland Islands, a harmful algal bloom caused paralytic shellfish poisoning and death in a large number of seabirds in 2002-2003. That season, southern rockhopper penguins bred in low numbers and their breeding success was very low. For instance, the number of breeding pairs decreased by 30% from 2000 to 2005, a period during which a whole area census was made. In 1987, moulting birds were apparently starving (to death) possibly related to a food shortage caused by an unusually long period of hot weather conditions. Similarly, slight deviations from normal sea surface temperature (SST) had a negative impact on the survival rate of adults. Interactions with commercial fishing operations (competition and by-catch) are also suspected to be major threats for southern rockhopper penguins. Oil pollution frequently occurs along the coast of Argentina and may occur further south as well. Southern rockhopper penguins may be exposed to this threat. Egg collection was a common habit in the past but is now abandoned. Chick mortality can be high during long periods of hot weather or during strong rains.
Under the 2008 IUCN Red List Category, Birdlife International (2008) lists Eudyptes chrysocome chrysocome and E. c. filholi as Vulnerable. A re-evaluation is needed for the chrysocome (sub)-species only.
Southern rockhopper penguins belong to the crested penguins, the largest genus of the Spheniciforms including seven other species of Eudyptes: eastern rockhopper penguin Eudyptes filholi, northern rockhopper penguin Eudyptes moseleyi, macaroni penguin Eudyptes chrysolophus, royal penguin Eudyptes schlegeli, Fiordland penguin Eudyptes pachyrhynchus, Snares penguin Eudyptes robustus and erect-crested penguin Eudyptes sclateri. The three subspecies of rockhopper penguins have recently been elevated to species level although, to date, BirdLife International recognises only two species (the southern rockhopper penguin Eudyptes chrysocome with the two subspecies chrysocome and filholi, and the northern rockhopper penguin Eudyptes moseleyi).
The distribution of Southern rockhopper penguins is limited to the Falkland Islands/Malvinas (about 35 colonies) and the South American islands around Tierra del Fuego (7 islands in Chile, 2 in Argentina). Vagrant birds have been reported from the Antarctic Peninsula (64°8'S), Brazil (about 30°S), South Africa (about 33°S) and the Snares Islands, south of New Zealand.
Southern rockhopper penguins dive to 20 - 60 meters depth for 1 min on average with a maximum depth of 113 m and 4 min duration.
Southern rockhopper penguins breed on islands that were initially free of terrestrial predators, such as cats and rats, before humans introduced them. The breeding colonies range from sea level sites to cliff-tops, and are sometimes located inland. The birds are able to climb steep rocks by small jumps. Their claws leave striations in the rocks on their way to the colony. Nests are very basic and usually comprise only a small cup in the soil, between rocks or under tussock. Nesting material is limited to small stones and some vegetation. At the Falkland Islands, they can nest amongst black-browed albatrosses Thalassarche melanophrys and king shags Phalacrocorax atriceps and may use old nests of black-browed albatrosses that they are forced to abandon if an albatross returns. King shags are also able to chase away the adults and to destroy their nests.
The shape of the yellow eyebrow, the long yellow crest falling behind the eye and the black crest on the rear crown are characteristic of rockhopper penguins. Southern species can be distinguished by the black gape, which is pink in the eastern and northern species.
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The timing of the breeding cycle of the southern rockhopper penguin is remarkably constant between years, at least in the Falkland Islands where they are studied in detail. Here, they can breed for the first time when they are only three years old and adults breed every year, except in years of very poor environmental conditions. Nest site and mate fidelity are high. They tend to come back the colony to lay at the same date every year. The populations from South America, which are further from the Antarctic Polar Front than the ones from the Falklands, breed a few weeks earlier.
In the Falkland Islands, southern rockhopper penguins return from their winter migration at the beginning of October, the males arriving a few days before the females. The females start to lay in the last week of October. The laying period is highly synchronous, lasting about 10-14 days within a colony. The clutch size is always two eggs that are laid four days apart. With an average weight of 118 g, the second egg (B-egg) is about 20% bigger than the first one (A-egg) that averages 92 g. The incubation starts only when the B-egg is laid and lasts 32-34 days. The females take on the first incubation shift while the males forage at sea for about two weeks. By the time the males depart, the have fasted for six weeks and, their body mass is about half of their arrival mass. When males return, the females depart the colony (after around 7 weeks of fasting) and usually come back just before hatching. The length of this foraging trip varies individually; some females return every day to the colony. The eggs are always attended. Otherwise, they would be quickly predated. Eggs lost to predation or lost by accident are never replaced.
The males care for the chicks for about three weeks after hatching while the females provision offspring regularly, usually every day. After the chicks have entered the crèches, males make a short trip to regain condition after their second fasting period. Then both parents feed the chicks until they fledge. The chicks moult when they are about 40 days old and the moult lasts about two weeks. At the Falkland Islands, chicks normally fledge at the age of about ten weeks during the first half of February. The adults depart the colonies and go to sea to fatten up before returning to their breeding colonies to moult. Adults fast again during the 3-4 weeks of moult. Between mid-April and mid-May, they return to sea for five months for their winter migration.
Breeding success is highly variable among colonies and between years, ranging from 0.35 to 0.69 in the Falkland but being only 0.23 - 0.31 at Staten Island (Argentina) during two seasons. In the Falklands, the annual survival rate of adults can reach up to 96% and the return rate of juveniles three years after hatching averages 80% during years with good conditions. These rates are almost the highest of any penguin species, which is exceptional for such a small species. However, these rates can be much lower if conditions are bad, especially in case of food shortage prior to moult or during harmful algal blooms.
The main predators of eggs and chicks are brown skuas Catharacta antarctica antarctica and striated caracaras Phalcoboenus australis, and additionally kelp gulls Larus dominicanus. Other scavengers are dolphin gulls Larus scoresbii, turkey vultures Cathartes aura, southern giant petrels Macronectes giganteus, Chilean skuas Catharacta chilensis, crested caracaras Caracara plancus or even cats that take mainly abandoned eggs and dead chicks and adults. At sea, birds can be killed by sea lions, fur seals and maybe by southern giant petrels.
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Scientific name
EG-BAMM, Barbara Wienecke
Royal penguins are the largest among the crested penguins. Their white faces and throats are the most distinguishing feature although some individuals have grey and even black faces and throats. For a long time, Royal penguins were considered a subspecies of Macaroni penguins. However, currently they are considered a separate species.
In 1984/85, the population of Royal penguins was estimated to comprise about 850,000 breeding pairs. Although the population is sizeable, the International Union for the Conservation of Nature has listed Royal penguins as Vulnerable to extinction. This is because of their limited distribution range.
The penguins live in 57 colonies, most of which occur along the east and west coast of the island. Colonies vary in size from less than a thousand pairs to over 20,000 pairs. The largest colony with around half a million breeding pairs is located at Hurd Point at the southern coast of the island. This colony covers approximately 65,000 square metres and is close to sea level. Other colonies, like those at Sandy Bay and the Nuggets, are about 200 metres above sea level.
Although the population is thought to be stable, good long-term data on the population trend are not available.
Royal penguins belong to the eudyptid or crested penguins that also include Erect-crested, Fiordland, Macaroni, Rockhopper and Snares penguins. Like in all penguins, males and females look very much alike but males are noticeably larger and have chunkier beaks than females.
Royal penguins are most easily confused with Macaroni penguins because of the similarities in their colourations. While the faces and throats of Macaroni penguins are all black, among the Royal penguins there is a range of colours from all black to all white. Royal penguins are the only penguin with pale gray to white facial colourings. Interestingly, females have more frequently darker faces than males. The colouration of the rest of the body is identical in males and females. The top and back of the head, back are dark bluish-black while the chest, belly are white. The flippers are mainly black but have a thin white trailing edge; their underside is white. The black and white body parts are clearly separated. Long dark yellow and black plumes (superciliary feathers) arise from a patch on the forehead and extend backwards.
The beaks are large and heavy set and dark orange-brown. At the base of the beaks are triangular pink patches of bare skin. The feet and legs are pink but the sole of the feet is black. The irises are reddish-brown.
Juveniles can be distinguished from adults only in their first year when they still lack the long superciliary feathers, which take about 3 years to develop fully. Juveniles are also often smaller than fully grown adults and have a greyish rather than white face and throat.
Royal penguins stand about 65-75 cm tall with both feet on the ground. Their body mass varies throughout the year. At the beginning of their breeding cycle, these penguins weigh usually 4.2 – 7.0 kilogram; males tend to be heavier than females. Post-breeding and prior to the moult they can reach a body mass of more than 8 kilogram.
Like Chinstrap and Adélie penguins, their tail feathers are much longer compared to other penguin species.
This penguin species has a highly restricted breeding range and colonies are found exclusively on Macquarie Island and the nearby Bishop and Clerk Islets.
During the breeding season, Royal penguins forage offshore in waters more than 2000 metres deep and up to 600 kilometres from their colonies. They are most active during day light hours and although capable of diving to more than 100 metres (the deepest dive recorded is 226 metres) they mainly forage at depths of less than 60 metres. They usually perform up to 18 dives per hour and dives last on average about 2.5 minutes.
The seas surrounding Macquarie Island are the foraging ground of Royal penguins. Their breeding colonies are found mainly in the coastal areas around the island but some colonies are located inland. These inland colonies are often connected to the beaches by small creeks that also serve as access path to the colonies. Royal penguins build nests on sandy, level ground but also on rocky substrate when the pebbles are small and on scree slopes.
The most distinguishing characteristics are their often lightly coloured faces and throats and the fact that they only occur at Macquarie Island.
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Royal penguins spend the winter months at sea. They usually return to nesting sites of the previous season from late September to mid-October. Royal penguins also often have the same partner as in the previous season. The breeding colonies vary in size (see below). Many are located along the east and west coasts of the island. But some colonies are located nearly 1.5 km inland and more than 100 m above sea level.
The main land-based predators of Royal penguins are skuas and possibly Southern giant petrels. Until they were eradicated, Wekas (a land bird introduced from New Zealand by the sealers) probably took eggs. Rats also used to take some eggs and introduced cats preyed on chicks. Cats were eliminated from the island and an eradication program targeting rodents is currently underway.
Royal penguins sometimes ingest plastic rubbish floating in the ocean. Plastic pollution can kill the birds. Disturbance caused by people is generally managed by personnel in place. The biggest threats the penguins are facing are changes to their food supply due to climate change.
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Scientific name
EG-BAMM, Jean-Baptiste Thiebot

The wandering albatross is a gigantic seabird (115 cm length, wingspan from 2.5 to 3.5 m) with plumage of variable coloration, whitening with age. The juvenile is chocolate-brown with a white face mask and underwing, while underwing tips and trailing margin are black. Underparts (breast, belly) become pure white with age. Back whitens first on upperparts, and a white wedge forms in centre upperwing, extending outwards to coverts. Even at whitest stage, black tips remain on outer tail feathers. The bill is pink and legs flesh-coloured. Confusion possible in identification at-sea with Southern Royal D. epomophora, Northern Royal D. sanfordi, Tristan D. dabbenena and Antipodean D. antipodensis albatrosses.
Most recent comprehensive estimates give a total global population of ~6,100 pairs breeding in any given year (approximately 20,100 mature individuals). The relative contribution by locality is as follows: South Georgia (Georgias del Sur, ~25% of the global breeding population), Prince Edward Islands (South Africa, ~40%), Crozet and Kerguelen Islands (French Southern Territories, ~10%) and Macquarie Island (Australia, approximately four pairs breeding per year).
All populations have shown a decrease at some stage over the last 25 years. At South Georgia, the population has declined by almost 2% per year for the last 20 years, worsening to 4% decrease per year since 1997. The population on Crozet declined by 54% between 1970 and 1986 (by 1986, the population has been reduced by 53.8% from c. 500 pairs observed in the late 1960s). From the mid 1980s to late 1990s, populations from the southern Indian Ocean appeared to be stable or increasing. The slow upward trend for Crozet and Kerguelen Islands is thought to reflect improved adult survival and recruitment attributed to the Japanese long-line southern bluefin tuna fishery in the Indian Ocean moving away from the islands. However recent trends in these populations are less clear. On Macquarie Island numbers of breeding pairs have fluctuated considerably since the 1960s, with a maximum of 28 in 1968 and minimum of 2 in 1985. Over 70 years, it is estimated that global population decreases exceeded 30%.
The wandering albatross (also referred to as 'Snowy albatross') is an iconic seabird of the Southern Ocean. This large, almost totally white, seabird is unmistakable as it glides effortlessly for hours around ships.
Diomedea exulans breeds on remote islands of the southern oceans and roams vast expenses of the Southern Ocean. This wide ranging species has a circumpolar distribution, and both breeding and non-breeding birds have very large foraging ranges (as such, their at-sea distribution overlaps with 10 Regional Fisheries Management Organisations). Satellite tracking data indicate that breeding birds forage at very long distances from colonies (up to 4,000 km), with cases of double circumpolar navigation during the non-breeding period. Satellite tracking has also revealed that juvenile birds tend to forage further north than adults, and so do the breeding females compared to the males, in general. Foraging strategies change throughout the breeding season: during incubation stage, breeding birds forage over pelagic waters between the Antarctic continent and subtropical latitudes. During the brooding period however, adults concentrate their foraging activity in the vicinity of their breeding site, in shorter at-sea trips. During later stages of chick-rearing, D. exulans forage in short trips close to the colony in neritic waters, or in long trips far from the colony in oceanic waters to the north.
Outside the breeding season, recoveries and satellite tracking data indicate initial dispersal of the birds from South Georgia across the South Atlantic Ocean to areas off South Africa, followed by migration across the Indian Ocean to winter in south-eastern Australian waters. Non-breeding and juvenile birds from the southern Indian Ocean remain north of 50°S between subantarctic and subtropical waters, with a significant proportion of them crossing the Indian Ocean to wintering grounds around the southern and eastern coasts of Australia, and eastward to the Pacific and the western coast of South America. A single adult tracked from Macquarie Island during the non breeding dispersal showed a circumpolar distribution.
Although their body is not designed for underwater locomotion, wandering albatrosses have been recorded to dive to 60 cm under the surface to seize prey (Prince et al. 1984).
Wandering albatrosses nest in open or patchy vegetation near exposed ridges or hillocks. This habitat selection is ideal for birds with such a large wingspan that needs an open space to land and also need to jump from cliffs to take off. Yet, the downside of nesting in an open habitat is that the chicks and adults are exposed to native (giant petrels) or introduced (mice, cats) predators (e.g. Dilley et al. 2013).
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The species is listed as Vulnerable in IUCN Red List, because of continuous rapid decline over three generations (70 years) at South Georgia, and strong decreases of Crozet and Kerguelen Islands populations between 1970 and 1986. Main cause of decline in this species (as with many other albatross and petrel species) is incidental mortality at sea in long-line fishing operations, because the birds may grab the baited hooks on the lines before they sink, or get entangled in the lines, generally resulting in drowning of the individuals. The consequences are reductions in not only adult survival but also juvenile recruitment. Because of its vast distribution range at sea, this species may encounter many different longline fleets indeed while foraging. The growth of the southern bluefin tuna long-line fishery in the Southern Ocean until the mid 1980s and subsequent development of the Patagonian toothfish long-line fishery coincided with the steady decline of D. exulans populations at Crozet, Kerguelen and Marion Island. Adult females are more likely to interact with the subtropical tuna fisheries as they generally distribute more northerly than males during the breeding season. The South Georgia population may be most at risk from recently developed longline fisheries operating in the south-west Atlantic throughout the year, whereas the Crozet and Prince Edward Island populations are most vulnerable to pelagic longline fishing in the Indian Ocean and Australian region. Juvenile birds forage mainly in subtropical waters where the tuna long-line fishery has expanded in recent times. Chicks are also impacted by the fisheries, as fishing hooks were found to have been ingested in half the number of chicks surveyed at Bird Island. Facing this situation, the Commission for the Conservation of Antarctic Marine Living Resources (CCAMLR) has implemented measures which have reduced bycatch of albatrosses around South Georgia by over 99%. Recently, other Regional Fisheries Management Organisations, including the tuna commissions in the subtropical areas, have taken initial steps to reduce seabird bycatch.
On land, all breeding sites of wandering albatrosses are currently legally protected and access is restricted. However, some populations show severe reductions in breeding success owing to predation of the nestlings by alien species (such as cats on Kerguelen).
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British Antarctic Survey
Barrukia cristata has a scale-covered, flattened body, up to 6.5cm long.
5 to 1,120m, found commonly in mud from Sub-Antarctica to the Antarctic Peninsula and Continent.
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Barrukia cristata is an ambush predator whose diet is reported to include crustaceans. It is known to be eaten by Trematomus fish. Individuals probably live for not much longer than a year and a half, and population studies indicate that three generations are produced per year.
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Scientific name
British Antarctic Survey
Pale to black and up to 20cm long (and 1.5cm wide)
from low tide to 970m in soft substrates throughout Antarctica and north to southern Argentina.
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Scientific name
Myriam Schuller
Two of these specimens are gigantic Polynoids. That from Sta. 30 is the largest, and measures 148 mm. by 31 mm. (without the feet) for 37 chaetigers. The other large specimen is from Sta. 107, and measures 110 mm. by 20 mm. (without the feet) for 37 chaetigers. The third specimen is much smaller, and measures only 60 mm. by 12 mm. (without the feet), also for 37 chaetigers. There are 15 pairs of elytra arranged as in Harmothoë. Except for traces of brown transverse hands upon the hack there is little colour in spirit. The bristles are conspicuously golden. Purplish-brown markings are discernible on the head except in the largest specimen. The head (fig. 4a) is roughly cordiform, and there are two pairs of almost contiguous eyes at the outermost edges of the prostomium. The lateral tentacles are inserted terminally, and there are no peaks. Most of the tentacles, etc., are lost, and the following account is a reconstruction from the three speci mens.
The palps are very long, reaching back to the tenth chaetiger. They are papillated, but the papillae, instead of being diffuse, are arranged in six rows of two or three lines of papillae. The median tentacle is lost. Below the median tentaculophore there is a subtentacular cirrus about half the length of the head. The lateral tentacles are about half as long as the tentacular cirri, which they otherwise resemble. They are papillated, and have a subterminal enlargement and a filiform tip. At the base of the tentacular cirri there are an aciculum and a few bristles. At the back of the head there is a conical fleshy nuchal pad extending almost to the level of the hinder pair of eyes. Behind this pad there is an occipital flap or gibbosity.
The elytra have become detached, and those belonging to the smallest specimen are lost. Those belonging to the largest example (fig. 4b) are huge, leathery, reniform structures, meas uring about 30 mm. by 21 mm. at the widest part. They are flesh-coloured, with the border op posite the hilum pigmented dark brown. Near the hilum they are thickly covered with small tubercles, but the rest of the scale has a dense covering of longer and shorter spines (fig. 4e) resembling those of Harmothoë crosetensis, interspersed with rather soft ovate vesicles. Both spines and vesicles are largest near the border opposite the hilum (fig. 4d). The elytra of the second of the large specimens are relatively considerably smaller, and are splashed with brown markings. They differ from those of the largest specimen in that the ovate vesicles are absent and are replaced by a relatively small number of gigantic tubercles surmounted by clusters of long spines (fig. 4e).
The elytrophores are prominent, and pseudo-elytrophores are present. The dorsal cirri are set low down on the feet, and the cirrophores have a prominent lateral expansion. The dorsal cirri are lost in all except the smallest specimen, and in this they are hirsute, and reach to the end of the ventral bristles. The ventral cirri reach to the end of the foot.
The feet (fig. 4f) resemble those of Eulagisca corrientis (see Monro, 1930, fig. 11b). The dorsal ramus sends out a long sheathed aciculum behind and below the dorsal bristle bundle. The ventral ramus has a longer sheather aciculum in front of the ventral bristle bundle.
The dorsal bristles (fig. 4g) are very numerous, almost as long as the ventral, rather slender and pectinated. The ventral bristles (fig. 4h) are more numerous and finer than the dorsal. They have frills extending over about a quarter of their length, and a rather long and delicate uni-dentate naked tip. The anus is terminal.
This species is close to the type-species, E. corrientis McIntosh, but differs chiefly in the ornamentation of the elytra. The elytra of E. corrientis are smooth. McIntosh described them as comparatively smooth over the greater part of the area, and having a few clavate cilia at the pos terior border. Of the Discovery Committee's material a specimen from the Palmer Archipelago has a few elytra, and these agree with McIntosh's account, except that I see no cilia. Moreover. I suspect that the specimens attributed to McIntosh's species by Benham (1921, 43) may belong to the present species. Benham, in describing one of the second pair of scales, writes, "there are three large, broad, round-tipped conical tubercles near the external margin, and springing from the surface of the scale between them, but nearer to the margin are a few long, fine, cylindrical hair-like papillae. The concealed portion of the elytron bears numerous small, rounded, low, and highly refringent tubercles, only visible under a high magnification. There is no fringe."
At any rate the elytra in Benham's specimens were not smooth as in E. corrientis. Benham's account of the elytra is not in close agreement with those of my specimens, but that the ornamen tation is variable is shown by the differences between the elytra of the two larger specimens already noted.”
(Monro, 1939)
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Scientific name
Brigitte Hilbig
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British Antarctic Survey
Large for an amphipod, reaching up to 4cm, and with an overall roundish shape.
80 to 550m, from Sub-Antarctica to the Antarctic Peninsula and Continent. It is found on the substrate or on benthic organisms such as sponges.
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Epimeria robusta is an ambush predator and feeds on a variety of small invertebrates including plankton, sponges, worms, echinoderms and other crustaceans. In its turn it is preyed on by fish and squid
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Large and yellow or orange with red eyes and hairs on its antennae. Reaches up to 5.5 cm in length
Oediceroides emarginatus generally lives with its back legs burrowed into sand and head out in the open. It is found from Sub-Antarctica to the Antarctic Peninsula
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Little is know about its feeding habits but it is probably an opportunistic predator and scavenger
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Scientific name
British Antarctic Survey
Pale and translucent, with long feather-like hairs or spines on its forelimbs. Grows up to 1cm long.
0 to 250m from Sub-Antarctica and South Georgia to the Antarctic Peninsula and Continent
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Haplocheira plumosa is a filter feeder, using the feathery net of hairs on its forelimbs to sift food from the water column.*
Antarctic amphipods are generally preyed on by fish and squid.
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British Antarctic Survey

A large amphipod, up to 8cm long.
20 to 2,000m, found on the seafloor or on other benthic invertebrates from Sub-Antarctica to the Antarctic Peninsula and Continent
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Eusirus perdentatus is a carnivorous predator with occasional scavenging behaviour. It mainly eats other small crustaceans and its diet also includes polychaete worms. It is preyed on by Trematomus fish.
Studies suggest that this animal only breeds once in its lifetime, and the juveniles hatch out at the end of the austral summer.
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Scientific name
British Antarctic Survey
Reaches up to 1cm long
2 to 457m, from southern Argentina to Continental Antarctica. Heterophoxus videns lives buried in soft sediments. It often occurs in dense groups.
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Heterophoxus videns is a voracious predator and eats animals at the sediment surface such as settling larvae, small or young worms, other crustaceans, sponges and diatoms. It and other predatory under-surface crustaceans probably play a major role in the composition and size of polychaete populations. Its predators include Trematomus fish
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Scientific name
British Antarctic Survey
This species is very distinctive, being red and fairly squat, with a spiky outline. It is large for an amphipod and reaches up to 7cm in length
Found as shallow as intertidal depth, but more usually deeper, between 80 to 550m. It occurs from Sub-Antarctica to the Antarctic Peninsula and Continent
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Epimeria rubrieques is an ambush predator with a variety of prey. It can swim, but only rarely does so.
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Scientific name
British Antarctic Survey

Yellow or brown in colour and roundish and squat in outline. Reaches up to 3.5cm long
Found down to 660m, but most abundantly in shallow algae, from Sub-Antarctica to the Antarctic Peninsula and Continent
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Waldeckia obesa is a necrophage. It eats carrion, usually in a highly decomposed state. Although it lives in sub-tidal waters one of its predators is known to be the Antarctic tern (Sterna vittata). Possibly in this instance predation occurs when carcasses containing amphipods get washed ashore, bringing them within easy reach of the birds.
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British Antarctic Survey
Orange in colour
Found amongst algae in shallow water, along the Antarctic Peninsula and Continent.
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This is a motile free-living species. Little is known of its ecology but it is opportunistic and has been reported feeding on decaying algae.
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British Antarctic Survey
Reaches up to 2.5cm in size
0 to 800m, but most common in deeper waters (below 50m). Found from Sub-Antarctica to the Antarctic Peninsula and Continent.
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Abyssorchomene plebs is an omnivorous scavenger and predator, and feeds in swarms on carrion, fecal matter and sometimes on live animals in a mass assault. It is preyed on by fish and the Antarctic tern (Sterna vittata) which probably eats it when carcasses containing amphipods get washed ashore. Abyssorchomene plebs reaches maturity after 18 months and reproduces and develops eggs in winter so that the young hatch out in spring. Experiments on this species have shown that the optimum temperature for its lifestyle is below freezing and it cannot tolerate temperatures much above 8 oC. This is probably the case for most Antarctic animals.
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British Antarctic Survey
Yellow, growing up to around 1cm in size
0 to 800m from Sub-Antarctica and South Georgia to the Antarctic Peninsula and Continent.
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Orchomenella pinguides mostly eats carrion and fecal matter, feeding in swarms. It is preyed on by octopus and by the emerald rockcod Trematomus bernacchii.
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Original description by Kirkpatrick (1907):
Sponge dome-shaped or spheroidal, attached or free. Surface beset with a dense short pile of cortical microtyles; with several usually elongated papillae with or without a large terminal orifice. Dermal pores distributed over the cortex, each pore opening into a single tubular canal in the cortex; the mouth or pore of the pore-canal is guarded with a ring of radiating cortical tyles. Flagellated chambers diplodal.
Skeleton formed mainly of radiating fibres composed of styles, with diverging brushes of spherostyles near the surface. Cortex with a surface-layer of densely packed tufts of small vertical tyles, and a subcortical layer of tangential styles and tyles.
Spicules.- Spherostyles 8 mm in length by 30 μm in diameter in the middle, and 14 μm in the region below the distal knob; distal knob 28 μm in diameter, hemispherical, with granular surface and with a few square teeth or serrations on the edge.
Styles straight, fusiform, blunt-pointed, 2.8 mm in length, 41 μm in diameter in the middle, 23 μm in diameter at the rounded end.
Cortical tyles curved, 146 μm long, head 3.25 μm in diameter; neck slender, 2.75 μm thick, with broad oar-blade-like shaft, but circular in section, 7 μm thick.
Styles of lower cortical tangential layer, also in choanosome, 900x20 μm. Tyles of the same layer nearly straight, 270 μm long, with head 7 μm in diameter and relatively thick neck 6.8 μm in diameter.
Slender, curved tyles, 460x10 μm scattered in choanosome.
Young specimens are oval, with one long closed papilla; the bundles of divergent exotyles are more or less separate and distinct, and the distal knobs retained and not broken off.
Circumantarctic distribution (Vacelet & Arnaud, 1972), Chile (Desqueyroux-Faundez, 1989).
S. antarcticus inhabit on hard bottoms as rocks and stones, but it was collected also in soft-bottoms such as mud (Burton 1932) at 17-450 m depth (Hooper & Wiedenmayer, 1994).
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British Antarctic Survey






White or orange head, either spherical or oblong, on a smooth, long, slender stalk. The head is up to 2.5 cm diameter and the entire sponge grows up to 20cm high.
13 to 2,900m. Stylocordyla borealis is an example of a bipolar sponge, found in both Arctic and Antarctic seas. This is, unsurprisingly, a rare situation in Antarctic species. It has been found as far south as Canada and Norway and as far north as New Zealand, with occurrences in the tropics near Brazil and Granada.
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Stylocordyla borealis is a suspension feeder. It occurs in patches, probably due to its mode of reproduction, in which eggs are incubated inside the mother sponge and released as fully complete young sponges to settle nearby. Stylocordyla borealis has a system of rooting spicules which enables it to attach and grow in soft bottomed areas.
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British Antarctic Survey













Greenish grey to yellow. Hemispherical and bristly with one or two large conical papillae which contract when disturbed. The sponge reaches a diameter of up to 11cm.
18 to 1,266m from Sub-Antarctica and South Georgia to the Antarctic Peninsula and Continent. Polymastia invaginata is commonly found on cliffs. It grows on hard surfaces, but can also grow in muddy areas by settling on small stones and then extending out onto the mud. It appears to be able to remove sediment build-up, possibly by contracting and relaxing.
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Suspension feeder, preyed upon by seastars such as Perknaster fuscus (when juvenile) and Odontaster meridionalis, and by the dorid nudibranch Austrodoris kerguelenensis. Its larvae have been observed in aquaria to disperse by crawling
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White and club shaped or branching, with a smooth surface. Homaxinella balfourensis is attached to the substrate by stolons or a root system and grows up to 1m high, with 10cm long branches
Found on hard substrates? down to 550m from Sub-Antarctica to Continental Antarctica.
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Homaxinella balfourensis grows relatively rapidly in comparison to other Antarctic sponges (although still very slowly by tropical sponge standards). It contains substances with antifreeze properties, and can defend itself to some extent against diatom fouling which might otherwise interfere with respiration and feeding. It is a suspension feeder and is preyed on by seastars.
Homaxinella balfourensis contains diatoms living within its cells, but their role is unclear.
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British Antarctic Survey
Yellow, orange, pink or white in colour. This brittle, foliaceous species is typically 4-20cm high and wide. It differs from most other bryozoans and animals by being ‘fenestrate’; that is, having lots of pores or windows in its walls. It is endemic to Antarctica and is the largest species in a highly speciose genus, at least 8 of which also occur in the Southern Ocean.
20m to deep water, on hard substrates from the Scotia Arc islands to the Antarctic Peninsula and Ross Sea.
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In shallow water R. frigida tends to occur in ice-sheltered ledges, cliffs and overhangs but also occurs as small colonies on other animals such as ascidians. The foliose colonies it builds are frequently home to many species, such as worms (particularly polychaetes), amphipods, isopods and sea cucumbers. R. frigida, like all bryozoans, is a suspension feeder eating smaller phytoplankton. It feeds for about half the year when phytoplankton is most abundant.
The main predators of R. frigida are probably nudibranch sea slugs, though seastars and echinoids probably eat it incidentally.
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Colossendeis specimens are beautiful creatures highly admired in collections due to their larger size compared to other pycnogonid species. The bizarre morphology of pycnogonids is in full display in this genus in which most of the species have a proboscis longer than the trunk. Colossendeis australis is known as a circumpolar and eurybathic (15-3935 m) species and can be recognized by a unique combination of characters that include a downcurved swollen proboscis, subchelate oviger strigilis and short propodal claws. The biology of Colossendeidae in general is poorly known, there is no information about their reproductive biology as no eggs or larvae have ever been found. On the other hand this lineage of pycnogonids could be one of the most ancient according to the phylogeny proposed (Arango pers. comm.).
Although Colossendeis has representatives in all oceans around the world, the deep waters of the Southern Ocean appear as a centre of species radiation for these fascinating animals (Arango pers. comm.).
C. australis is present in a wide bathymetric range from 143 to 3931 m depth (Cano & López-González, 2007). It has a circumpolar distribution and some sites in the Southern Atlantic and Southern Pacific basins, and is found in the Falkland Islands, South Sandwich Islands, Orcadas Islands, South Giorgia, Kerguelen Islands, Antarctic Peninsula, Ross Sea, Adelie Coast and off the coast of Chile and Argentina (Child, 1995).
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N. australe has a circumpolar distribution, but it is found also in more temperate zones as New Zealand, Falkland Islands, off the coast of Chile and Argentina, and Southern Indian Ocean (Child, 1995).
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Nymphon australe is the most frequently collected of all pycnogonid species in Antarctic area (Munilla & Soler-Membrives, 2009) and in the highest numbers (Arango et al, 2010). It is considered circumpolar and eurybathic, found in most Antarctic and subantarctic benthic collections. As most of pycnogonids Nymphon australe lacks a planktonic stage (Arnaud & Bamber, 1987).
Thus, it is of interest to understand how these marine organisms with an apparent limited dispersal capacity have achieved such wide geographical and bathymetric distributions. N. australe is classified within a group of Southern Ocean species of Nymphon sharing few morphological characters such as inflated ovigers, a robust body and setae present on trunk and legs. This group of species or 'australe-complex', is to be tested in a phylogenetic context using both morphology and molecular data to understand the diversification of the group, their relationships to other Antarctic (~60 spp.) species and also the evolutionary history of the cosmopolitan Nymphon (~270 spp.) (Arango et al., 2010).
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British Antarctic Survey












Vivid red and thickly branching, reaching a size of up to 30cm high
18 to 640m. Found in patchy assemblages from Sub-Antarctica and South Georgia to the Antarctic Peninsula and Continent.
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Kirkpatrickia variolosa is a suspension feeder and preyed on by seastars, particularly Perknaster fuscus when juvenile, and Acodontaster conspicuus. Derivatives from Kirkpatrickia variolosa have been found to have antitumour and antiviral properties, and are being trialled as potential anti-cancer drugs.
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British Antarctic Survey
Pale with distinctive flattened fronds and a hard stalk. Slow-growing, reaching a height of up to 50cm
16 to 900m, from Sub-Antarctica to the Antarctic Peninsula and Continent
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Calyx arcuarius is a suspension feeder. Its predators include the seastars Odontaster meridionalis and Acodontaster hodgsoni, and the dorid nudibranch Austrodoris kerguelenensis, although extracts from it have been shown to have antipredator and antibacterial effects.
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British Antarctic Survey
Identification is very difficult without expert knowledge. Microxina benedeni is usually white, orange or pink and irregularly shaped, growing up to 18cm high.
30 to 1,266m, from southern Argentina to Continental Antarctica
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Microxina benedeni is a suspension feeder and contains diatoms living within its cells, but their role is unclear. Its predators include the dorid nudibranch Austrodoris kerguelenensis.
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British Antarctic Survey
Orange/green to white in colour. This species forms long thin, branching fronds. These curl lengthwise so the colony seems to ‘flop’ a bit. The branches are just a few zooids wide
25m to deep water, on hard and soft substrates inside the Polar Frontal zone (so not Subantarctic islands) from South Georgia and Bouvet Island through to Antarctic continental waters. Has not been reported from East Antarctica.
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H. antarcticum is an endemic Antarctic species, which can be very abundant but is probably ignored by zoologists mistaking it for a clump of algae. It (suspension) feeds for just over half the year and probably grows quickly (for a polar species). Its rear surface is often colonised by spirorbid worms.
The main observed predators of H. antarcticum are pycnogonans, though it seems likely other animals might eat it too.
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British Antarctic Survey
Yellow to orange in colour. This species is encrusting and has a membranous front to each zooid. The individuals can be seen clearly with the naked eye – they look shiny when they dry out. This is not an easy species to separate from a number of other encrusting bryozoans.
5m to deep water, common in shallows, particularly on boulders (unusually on the upper surfaces rather than the under as other species) and on the ascidian Cnemidocarpa verrucosa. The species has a patchy distribution, being described from the Chatham Is (NZ), Chilean Patagonia and west Antarctica, including the Ross Sea.
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The species is common in the shallows, particularly in highly disturbed areas and places with high water flow. It is a highly aggressive species and fights all other colonies it meets of the same species, unlike most other encrusting species. # It is a suspension feeder, eating phytoplankton. It is probably grazed by limpets and echinoids.
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British Antarctic Survey
Forms colonies of small, eight-tentacled polyps which are usually white and up to 1cm high.
12 to around 600m, on hard substrates from Sub-Antarctica to the Antarctic Peninsula and Continent.
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Clavularia frankliniana is a suspension feeder, mostly on matter resuspended from the sea-floor, and is preyed on by sea spiders and nudibranchs such as Tritoniella belli. It contains compounds which deter most potential predators. Despite this T. belli not only feeds on it but appears to store and re-use these deterrent compounds in it's own defense.
Clavularia frankliniana reproduces throughout the year, both by releasing larvae and by asexual fission.
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British Antarctic Survey
Small, individual, pale yellow to orange# cups, up to 5cm in diameter.
A deep water coral found below 200m. It attaches to hard substrates, often other corals and occurs worldwide, a rarity amongst stony corals.
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Desmophyllum dianthus is a suspension feeder. Stony corals, particularly in the tropics, often have symbiotic algae living within their tissue whose by-products greatly supplement the corals food supply, but Desmophyllum dianthus lives too deep for these algae to grow, as they require light.
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British Antarctic Survey
White with a dark tough cuticle and 96 tentacles of which the inner tentacles are longer. It grows to 5cm in diameter and around 10cm high
15 to 3,020m, from southern Argentina to Continental Antarctica.
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British Antarctic Survey
up to nearly 30cm in height and 15 cm wide
PanAntarctic
40m to deep waters
sediment or stones amongst sediment
Bright orange, rooted, plate-like bryozoan
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Colonies of Cellarinella watersi generally occur in groups of tens to hundreds on continental shelf waters. The Cellarinellids are, all but one, endemic to Antarctica and form great ‘forests’ over parts of the seabed, particularly deeper than 100m. The colonies are thin plates a few mm thick with growth lines obvious representing each years growth. If pieces break off in currents they grow rootlets and re-erect themselves to form new colonies, growing from the fragment. They feed on phytoplankton for about 4/5 months over the summer period when they appear ‘hairy’ underwater from all the tentacles protracting.
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British Antarctic Survey
Orange/brown to translucent yellow in colour. This species is encrusting but the zooids stand upright connected by little ‘rootlets’ at the base. Many species of Beania occur in the Subantarctic and Magellanic regions but none in the Antarctic.
5m to deep water, patchily very common in shallows, particularly on boulder undersurfaces. B. erecta is very widespread and occurs at most localities within the Polar Frontal Zone right round Antarctica.
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This species is typically found under very large rocks, on cliff faces or particularly on shallow overhangs. It is an extremely good competitor, overgrowing nearly all other encrusters and many other animal types – it is also a common epibiont on, for example, brachiopods. It is a suspension feeder and eats phytoplankton. It is specifically eaten by the nudibranch Charcotia granulosa but probably also incidentally grazed by limpets and echinoids.
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British Antarctic Survey
Grey/ yellow to white in colour but translucent when young. The apertures (from which the tentacles emerge) of each zooid are hemispherical with a characteristic notch in.
5m to deep water. The species occurs in Patagonia, Kerguelen Island and throughout west Antarctica. Two other Antarctic species occur in southern polar waters, L. hosteensis and L. watersi. Further Lacerna species occur in the Subantarctic.
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This species is uncommon on boulder undersurfaces but quite common on other organisms such as ascidians, other bryozoans (particularly I. tenuis), brachiopods, or molluscs. Little is known about its ecology. It is a suspension feeder, eating phytoplankton during spring and summer months. It is probably grazed by limpets and echinoids.
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Census of Antarctic Marine Life



Astrotoma agassizii, the large brittle star belonging to the suborder Euryalina, has long, flexible, and mobile arms that use to capture the prey from the water column.
Astrotoma agassizii is found throughout the Southern Ocean in depths of 70-1000 m (Bernasconi & D’Agostino, 1977) and occurs irregularly on the shelves of sub-Antarctic islands and the Antarctic continent (Ferrari & Dearborn, 1989). Along the Chilean margin between Chiloe (42° S) and the Strait of Magellan. On the South Atlantic to North (39°) off Argentina Coast; Tierra del Fuego; Falklands, South Georgia and Shag Rocks Islands; Antarctic region (Tierra de Graham, Ross Sea, Haakon VII Sea; Tierra Adelia, Reina María, Mac Robertson and Enderby) (Castro Manso, 2010).
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The analysis of the stomach contents showed that the diet consisted of members of only two major taxa, Crustacea and Chaetognatha. Copepods occurred in 75.6% of brittle stars containing food and were the dominant prey group, followed by mysids (34.6%), chaetognaths (10.2%), and euphausiids (8.9%). Other prey included unidentified crustacean and organic remains, ostracodes, and amphipods. Euchaeta antarctica and Calanoides acutus constituted about 80% of the stomach content copepods (Dearborn et al. 1986).
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British Antarctic Survey
Orangey brown or yellowish brown in colour, with a knobbly disc up to 2cm in diameter, and arms up to 6cm long.
40 to 2,725m on various substrates but mostly mud and soft sediments. Found from Sub-Antarctica and South Georgia to the Antarctic Peninsula and Continent.
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Ophiurolepis gelida is an active predator, capturing and feeding on a wide variety of invertebrates and in particular polychaete worms. It also feeds on detritus by gathering surface sediment into small mounds, which it then engulfs, consuming any food within the mud. It is preyed on by another brittle star, Ophiosparte gigas, and by the giant isopod Glyptonotus antarcticus, and possibly by fish and seastars. Ophiurolepis gelida is frequently parasitised by a brown sponge, Iophon radiatus, which grows over the disc and arms of the brittle star and may obscure its colour.
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British Antarctic Survey
5 arms. Colour is variable from brown to bluish grey or white. The disc can be up to 4cm diameter while the arms are up to 9cm long.
5 to 1,266m on a variety of substrates (sometimes in very high densities) from Sub-Antarctica to the Antarctic Peninsula and Continent.
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Ophionotus victoriae is an opportunistic predator on a wide variety of invertebrates, particularly krill which it captures from the water column, although it does not appear to suspension or filter feed. It is also a scavenger of dead matter and detritus, and will cannibalise juveniles of its own species. Its predators include fish and the large brittle star Ophiosparte gigas, which it will try to flee from upon contact. Ophionotus victoriae spawns annually in the Antarctic summer.
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British Antarctic Survey
Up to 25cm height
Colonies of Isosecuriflustra rubefacta occur in groups of hundreds to thousands in continental shelf waters. The species is generally found with two others: Nematoflustra flagellata and Himantozoum antarcticum. It is common and abundant but often only below 20m. It is typically brown to purple with striking bands across the frond, but these are not growth lines as described in Cellarinella watersi. The bands are formed by the brood chambers which are dark when containing embryos and translucent when these are released in January. Also unlike C. watersi the flustrid species are just unilaminar, that is active zooids are only on one surface of the frond not both. There are few Antarctic bryozoans for which more is known than this species. They feed for about 10 months of the year on small phytoplankton and grow nearly continuously. The fronds are colonised by a rich variety of tiny animals, a single frond may contain representatives of >8 major groups of animals and are a good place to look for marine mites.
PanAntarctica
10m to deep waters
hard rock ledges, cliffs and boulder fields
Thin banded frond, resembles ‘hornwrack’ or algae
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British Antarctic Survey
Mainly transparent but the thin skeleton is white in colour. This species forms thin sheet-like fronds up to 6cm high (almost like onion skin). Curls up if dried out. Although the genus is speciose, only one other species (C. curva) is common in Antarctic waters, and this is dark brown and barely transparent.
5m to deep water, on hard substrates from Magellanic to some Subantarctic islands (Prince Edward, Kerguelen, Heard) to the Scotia Arc, Antarctic Peninsula and Ross Sea.
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This species is the shallowest occurring frond-like bryozoan. Unusually it is an annual species, growing new fronds each year from a base. These suspension feeders eat phytoplankton during the summer periods. Disjointed growth of zooids can be seen where it repairs damage to fronds. It is very lightly calcified and one of the faster growing bryozoans. Its main predators are probably nudibranchs, pycnogonans and seastars, though none have ever been seen to eat it.
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British Antarctic Survey
Orange/brown in colour. This species forms long (up to 20cm) and branching sheet-like fronds. These are curled and have very distinctive long ‘hairs’ called vibracula over its entire inside surface. These move up and down to clear debris and possibly small predators away from its feeding tentacles. Deep-water specimens (100m+) are stringier and less branched.
35m to deep water, on hard and soft substrates inside the Polar Frontal zone (so not Subantarctic islands) from South Georgia through to Antarctic continental waters.
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N. flagellata is an extremely distinctive endemic Antarctic species. It (suspension) feeds most of the year round, pausing for just three months mid-winter, and may live decades. The banding seen sometimes are areas of reproductive activity, not growth lines. The non-active surface is frequently covered with encrusting animals such as other bryozoans or polychaete worms.
The main observed predators of N. flagellata are nudibranch sea slugs, some small grazing gastropods and pycnogonans.
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British Antarctic Survey
White to translucent in colour. This species is encrusting and is often so transparent that the tentacles and body can be seen inside the zooids when retracted. This species is the most common of its genus in shallows, though F. antarctica, F. cervicornis, F. crystallina, F. exigua, F. parvipora and F. proxima also occur.
5m to deep water, patchily very common in shallows, particularly on boulders undersurfaces. F. rugula occurs in the Scotia Arc and Antarctic Peninsula.
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In places this species represents more than 90% of the bryozoan colonies and is sometimes more abundant than the tiny white spirorbid worms. Typically growth in previous years contrasts in appearance from that in the present year, and when dry, faint annual rings can even be seen, enabling colonies to be aged. It is a fast growing pioneer species overgrown by almost all other encrusters. It is a suspension feeder and eats phytoplankton. It is probably grazed by limpets and echinoids.
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British Antarctic Survey


Diplasterias brucei normally has five arms, but there is a 6-armed form common at South Georgia. Colour is very variable, from pale blue-green to yellow or orange and it grows to a size of around 25cm across.
0 to 725m on a variety of substrates from Sub-Antarctica and South Georgia to the Antarctic Peninsula and Continent.
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Unlike many seastars, Diplasterias brucei does not appear to eat sponges. Its primary food source is molluscs, and in particular the bivalve Limatula hodgsoni, but it will also scavenge on dead matter. It is eaten by the anemone Urticinopsis antarctica. Diplasterias brucei broods its young until they are fully developed into juvenile seastars.
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British Antarctic Survey
Has around 20-40 arms. The number of arms is very variable but increases with age, more arms being added as the sunstar grows. Labidiaster radiosus is large and reaches up to around 40cm across.
Found below 20m or so from southern South America to Sub-Antarctica and the Antarctic Peninsula.
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Often seen with some of its arms raised in a feeding posture. Sunstars are primarily suspension feeders and catch food such as small crustaceans, plankton and sometimes fish from the water column, using their raised arms. Labidiaster radiosus has been considered to be the same animal as Labidiaster annulatus, consequently a lot of the literature for L. annulatus may actually apply to L. radiosus, however they are in fact two distinct species (they can be distinguished by close examination of the pedicellaria in the central disc).
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British Antarctic Survey
Pale in colour with 5 relatively flexible arms.
Found as shallow as the intertidal zone, but its full depth range is not known
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Little is known about this seastar. Its diet has been noted as including the bivalve Laternula elliptica, which lives burrowed into soft sediments. Other name: Diplasterias turqueti
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British Antarctic Survey


Usually yellow or orange in colour, with arms that are thick at the base but taper suddenly near the tip. This rarely seen seastar is very large, reaching up to 50cm across.
0 to 655m. Found mostly on fine sediments from Sub-Antarctica and South Georgia to the Antarctic Peninsula and Continent
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Macroptychaster accrescens is an active predator on a variety of invertebrates such as gastropod and bivalve molluscs and brittle stars. It is also known to eat the seastars Odontaster validus and Odontaster meridionalis, and the sea urchin Sterechinus neumayeri
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British Antarctic Survey


Very variable in colour, from pink, red or purple to pale yellow or white. Reaches up to around 30cm across.
on a variety of substrates, but most commonly found on mud. Occurs from Sub-Antarctica to the Antarctic Peninsula and Continent.
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Psilaster charcoti employs a variety of feeding strategies: actively preying on some invertebrate species, scavenging on dead material and faeces and ingesting mud to utilise any food in it. It produces large amounts of mucous, which indicates that it probably is also sometimes a ciliary-mucous feeder, collecting falling detritus with the mucous, which is then passed along to the mouth and ingested.
Other names: Ripaster charcoti
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The endemic Antarctic scallop Adamussium colbecki is reported on a wide variety of substrates: in shallow waters it was found byssally attached to rocks (Stockton, 1984), while, deeper it was found free-living on sandy, gravelly and also silt-sandy bottoms, at the surface or recessed within the sediments (Berkman, 1990). Juveniles, were found byssally attached to adults valves and the remain attached during the swimming bout (Cattaneo-Vietti et al., 1997; Ansell et al., 1998; Chiantore et al., 2000)
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Up to 80mm
Yellow to orange (Antarctic Peninsula) or milky white to transparent (Weddell sea). Some have white pigmentation on tips and ridges.
Antarctica and South Georgia
18 to 710m
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mounds typically between 20cm to exceptionally >1m in height
Mounds of Mycale acerata and the starfish that eat them are a common feature of hard bottom communities. Although it has no programmed shape (like many sponges) it tends to form mounds like those made by termites with many smooth rounded lobes protruding. Sometimes M acerata is the most common sponge and one of the most important contributors of biomass. This sponge is particularly notable for being one of the few sponges, or even any Antarctic invertebrates, that grows quickly. Despite this it still grows somewhat slower than the fastest growing temperate or tropical sponges. In periods of food shortage this species and some others may actually shrink over considerable periods of time. It is not known how long this sponge lives but it could probably be many decades.
Patagonia to Circum subantarctic and Antarctic waters
10m to deep waters
grows on hard rock ledges and cliffs
dull yellow, a common lobed sponge of shallow waters. Lined texture on surface quite distinctive. Slimy.
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EG-BAMM, Anne-Mathilde Thierry


Adélie penguins have a very distinctive black and white robe, and a white ring around the eyes. The beak is dark reddish in colour with a black tip. They measure 60-70 cm in height. Depending on the timing of the year, they can weigh between 3 and 8 kg. Average weight during the chick-rearing period (when penguins regularly forage at sea) is typically 4.5-6 kg. Sexes are alike, but males are slightly larger and heavier than females. Fledglings and yearlings have white chins and throats.
The total number of breeding pairs is about 2.5 million (range: 1.8 - 2.9 million). Numbers are increasing in the Ross Sea region and decreasing in the Antarctic Peninsula, with an overall increase of the net global population (Ainley et al. 2010). However, the species is expected to undergo a 30 % population decline over the next three generations due to the effects of projected climate change, in particular in relation with a decrease in sea-ice concentration. Consequently, the species is listed as Near Threatened by IUCN since 2012.
Adélie penguin is one of the most common penguin species along the Antarctic coast, and it is probably also the most studied species. They are obligate inhabitants of the pack ice that surrounds the Antarctic continent. They breed from late October to early March in colonies that are found on ice-free coastal areas. During this time, they alternate between foraging trips at sea and sojourns on land to incubate the egg or rear their two chicks. After breeding and moulting, they spend the winter in the pack ice.
Jacques Hombron and Honoré Jacquinot published the first scientific description of Adélie penguins in 1841. These two surgeons and naturalists were part of an expedition led by French explorer Jules Sébastien César Dumont d’Urville, which was the first to reach the Antarctic continent. The section of the Antarctic coast discovered in January 1840 was named Terre Adélie after the explorer’s wife, Adèle. The first specimens of Adélie penguins were collected at this site, and named after it.
Adélie penguins are found along the entire Antarctic coast and some of its nearby islands, including the Balleny and South Shetland island groups, the South Orkney and the South Sandwich islands.
Adélie penguins are torpedo-like swimmers. They hunt their prey at depths of up to 175 m, but most of their diving activity occurs in the first 50 m of the water column.
Adélie penguins nest on ice-free coastal areas, but spend most of their time, including winter, in the pack ice surrounding the Antarctic continent. Adélie penguins are not found north of the pack ice during winter. Changes in sea-ice extent and the timing of its retreat can have major consequences on the breeding success of Adélie penguins.
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Adélie penguins face predation by leopard seals and occasionally killer whales at sea, as well as giant petrels and skuas on land. Today the threats of global environmental change, and competition from commercial fishing, threaten the future of Adélie penguins, which rely on sea-ice and krill to breed.
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Odontaster validus is the commonest and most abundant sea star inhabiting the shallow environment around the Antarctic continent (Dearborn, 1977; McClintock et al., 1988).
O. validus is distributed throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, South Orkney Islands, South Sandwich Islands, South Georgia Island, Shag Rocks, Marion and Prince Edward Islands, and Bouvet Island at depths from 0 to 914 meters (Clark, 1962; Clark, 1963; Bernasconi, 1970)
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Odontaster validus has a late sexual maturity and slow rate of growth. This starfish may grow only 1-2 g year-1, takes 3-6 years to reach sexual maturity (Pearse, 1969). O. validus may live for about 100 years (Pearse, 1969). The starfish O. validus has a demersal feeding larva with a brief pelagic phase to allow the dispersion without exposing the larvae to the hazardous surface waters. The larval development of Odontaster is extremely slow; it remains in the bipinnaria larval stage for about 2 months in the laboratory condition (Chia, 1970). In McMurdo Sound the period of spawning is from June to mid October (Pearse et al., 1986; Bosch & Pearse, 1990). O. validus is an omnivorous. Its diet includes the bivalves Limatula hodgsoni and Laternula elliptica, the sponges Rossella racovitzae, Rossella nuda, Scolymastra joubini, Tetilla leptoderma, and Homaxinella balfourensis, the hydroid Halecium arboreum, the sea star Acodontaster conspicuus, the sea urchin Sterechinus neumayeri, the isopod Glyptonotus antarcticus, bryozoans, suspended matter, animal dtritus, red algae, amphipods, crustacean nauplii larvae, ostracods, shrimp, ectoprocts, diatoms, and seal feces (Conlan et al., 2006). O. validus is prey of the sea anemone Urticinopsis antarcticus and the sea star Macroptycaster accrescens (Conlan et al., 2006).
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British Antarctic Survey
5 arms. Porania antarctica is very variable in colour and has a domed appearance, with short arms. It usually grows to a size of around 10cm across.
Intertidal to 3,200m, on various substrates from as far north as central Argentina and south to Continental Antarctica
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British Antarctic Survey


Colour variable depending on circumstances and diet; generally yellow to red, and blotchy. It reaches up to around 30cm across.
0 to 457m, generally on mud or amongst sponges, from Sub-Antarctica to the Antarctic Peninsula and Continent
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Perknaster fuscus mainly eats sponges and specialises in particular on the slimy sponge, Mycale acerata, which is relatively fast growing and which, without predation, would potentially dominate sponge communities. Mycale acerata is one of the most toxic of Antarctic sponges and consequently avoided by most other sponge eaters. Perknaster fuscus also has chemicals in its body wall to defend it against predators, but is eaten by the anemone Urticinopsis antarcticus. It probably spawns once a year.
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5 arms. Colour varies but is generally pale orange to brownish, and fairly large (up to 30cm across)
0 to 761m (mostly below 30m) from Sub-Antarctica and South Georgia to the Antarctic Peninsula and Continent.
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Feeds on various sponges including glass sponges and the slimy sponge Mycale acerata; a relatively fast growing sponge which could dominate sponge communities if not regulated by predation from Acodontaster conspicuous and from another seastar, Perknaster fuscus. Acodontaster conspicuous is itself known to be preyed upon by the worm Parbolasia corrugatus, the anemone Urticinopsis antarcticus and the much smaller seastar Odontaster validus, which will attack as a gang, after the initial solo assault. Predation by O. validus probably keeps Acodontaster populations under control.
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British Antarctic Survey
Large and variable in colour, with red blotches. Reaches up to around 40cm across
Known from between 18 and 310m in depth, from Sub-Antarctica and South Georgia to the Antarctic Peninsula and Continent.
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AntarcticConnection.com

The Blue-eyed Shag, or Cormorant, is found on the western side of the Antarctic Peninsula, the Scotia Arc, South Georgia and the western coast of South America. They are the only member of the Cormorants to venture down into the Antarctic proper, with colonies found as far as 68 degrees south. They are unique among Antarctic and sub-antarctic birds in that they will maintain a nest year-round where the sea is open and they actively avoid pack ice. They were welcomed by the early explorers and sealers because they never ventured far from their nest site out to sea, and thus, were a sure sign of approaching land.
Blue-eyed shags are characterized by a vivid blue eye color and an orange/yellow growth at the base of their beaks that becomes particularly large and bright during the breeding season. They have a white-breast, a black back and largely white cheeks and neck. The bill is dark brown and the feet pink.
Blue-eyed shags feed mainly on fish and invertebrates, often forming dense "rafts" at sea of hundreds of birds that continuously dive down onto the shoals below looking for fish. By fishing in such large groups they help each other by panicking the fish into having nowhere to go except into the beak of the next bird. They are excellent divers with a recorded maximum dive of 400 feet. Once underwater they are able use their powerful webbed feet to propel themselves rapidly in search of food.
The nests of these gregarious birds are built on cliff tops close to the ocean. The colonies can become quite raucous and lively affairs, especially during the breeding season. Courtship activities begin in late August to early October. Up to three eggs are laid in October through to early January and these hatch in November to February. Unlike other Antarctic birds, Shag chicks are born "naked", meaning without any down feathers. This makes them susceptible to extreme weather and especially dependent on their parents when very young. Fledging occurs in January to March, and the adults leave the colonies in April.
The main predators of Blue-eyed shags are the sheathbill, which steals eggs from the nest, and leopard seals, which attack the birds at sea.
Cormorants do not seem to be under any current threat, however, but some populations are so small (a few hundred pairs) that their status needs monitoring.
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In 1981, the first Georg von Neumayer Station in the Antarctic was established on the Ekstrom Ice Shelf as a research observatory for geophysical, meteorological and atmospheric chemistry measurements, as well as a logistics base for summer expeditions. Georg von Neumayer, whom the station is named after, was an important patron of Germany's research activities in Antarctica. Ice movements and heavy snow deposits demanded the construction of a new station building in the early 1990s. In March 1992, the new Neumayer station was completed only ten kilometres from the original site. The station's research and observation programme has steadily expanded ever since and now includes monitoring of atmospheric ozone. After 17 years of operation, the old Neumayer Station has already sunk fourteen meters deep into the ice. Thus, the construction of a new station was necessary.
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Picture by Stephen Roberts (BAS)