21-7-2024 VIGUR ISLAND, ICELAND - BLACK GUILLEMOT (Cepphus grylle)

The black guillemot is a circumpolar species distributed in the boreal, low arctic and high arctic regions of the north Atlantic and arctic oceans and breeding between 43° and 82°N. The 5 listed subspecies inhabit different parts of this range. In North America, they can be found as far south as the Gulf of Maine and New England and across parts of the northern coast of North America as far as Alaska, where they are replaced by the pigeon guillemot in the North Pacific. In Europe and Asia, they are found from the British Isles and Northward across the northern coast of Asia. They are one of the few birds to breed on Surtsey, Iceland, a new volcanic island. It is a fairly common breeding bird in western and northern Scotland and Ireland. In Great Britain, they only breed at St. Bees Head in Cumbria, the Isle of Man and on east Anglesey in north Wales. Approximately 40% of the population breeds in the high arctic where the largest colonies are found, 30% in the low arctic, and 30% in boreal waters. In the winter, some of the birds in the high arctic waters are forced south by the winter ice making them seasonal migrants, but in more temperate zones the species is essentially resident.

Typically restricted to rocky shores, black guillemots utilize the cliffs, crevices and boulders for their nests, hunting the inshore waters for benthic prey. Compared to other auks, they forage fairly close to the colony, in the breeding season mostly in inshore waters more than 50m in depth, farther afield in the winter months.

One of the early ornithologists that described aspects of the behaviour of the black guillemot was Edmund Selous (1857–1934) in his book The Bird Watcher in the Shetlands (1905). In the chapter titled 'From the Edge of a Precipice he writes for instance that sometimes the black guillemots carry a fish they have caught in their beak for hours. He also gives further details about the behaviour.

Black guillemots are coastal foragers with diets typically associated with benthic and kelp-forest prey. They dive between 15-20m to catch their prey, but can dive to a depth of at least 43m. They use their wings to propel themselves forward and their feet to steer.  Small prey are swallowed underwater whole. Guillemots bring larger prey to the surface to soften in their bill before swallowing whole.  Guillemots are single-prey loaders, meaning they bring single prey items back to their chicks during the chick-rearing period. This limits the spatial range that parents can forage for food, as chicks must receive a high number of energy-rich prey items throughout each day.  Black guillemot diets include sculpins, butterfish, rock gunnel, northern sandlance, herring, jellyfish, mollusks, and other small crustaceans. 

A number of threats face Black guillemots. Black guillemots have been shown to be vulnerable to several species of predators including American Mink, Great Skua, gulls, and Otter Lutra Lutra, as well as introduced species like the Brown Rat and feral cats.  One large colony on an island in the Baltic Sea (approximately 2600 individuals) was wiped out by American Mink in the early 2000s.  Because Black guillemots forage close to shore, they tend to be exposed to more pollution than further oceangoing seabirds. Additional sources of pressure include fisheries bycatch, habitat destruction, and climate change. 

21-7-2024 VIGUR ISLAND, ICELAND - PURPLE SANDPIPER (Calidris maritima)

The purple sandpiper (Calidris maritima) is a small shorebird in the sandpiper family Scolopacidae. This is a hardy sandpiper that breeds in the arctic and subarctic regions of Eurasia and North America and winters further south on the Atlantic coast.

Adults have short yellow legs and a medium thin dark bill with a yellow base. The body is dark on top with a slight purplish gloss and mainly white underneath. The breast is smeared with grey and the rump is black. They measure 20–22 cm (7.9–8.7 in) in length and 42–46 cm (17–18 in) across the wings, and weight is from 50–105 g (1.8–3.7 oz).

Standard Measurements[10][11]

Total Body Length 210–240 mm (8.1–9.5 in)

Weight 70 g (2.5 oz)

Wingspan 430 mm (17 in)

Wing 117.9–130 mm (4.64–5.12 in)

Tail 55.9–63 mm (2.20–2.48 in)

Culmen 27.2–32 mm (1.07–1.26 in)

Tarsus 22–23.8 mm (0.87–0.94 in)

The purple sandpiper's breeding range extends from the arctic islands of northern Canada, eastwards to Greenland, Iceland, Svalbard and northern Scandinavia across to Western Siberia and the Taymyr Peninsula. In the high arctic the sandpiper breeds at low altitude on the tundra, sometimes far from the coastline, but in the subarctic regions of Sweden and Norway it breeds on barren mountain sides near the limit of the frozen ground. Birds breeding at high latitudes migrate south and spend the winter on rocky shores on both sides of the north Atlantic. They winter along the North America coast as far south as South Carolina and on the eastern Atlantic coast as far south as France and northern Iberia.

Birds wintering in northern Scotland and southwest Ireland migrate to Canada (Baffin Island and Devon Island) to breed.

In Britain, these birds occur in winter in good numbers principally along the east and south coasts, where they favour rocky shorelines adjacent to the sea. It is much rarer as a breeding bird, found only in a localised area of the Cairngorms National Park, where 1–3 pairs have bred since 1978. Records of breeding by this species in the UK are monitored and archived by the Rare Breeding Birds Panel.

They are late migrants and move to rocky, ice-free Atlantic coasts in winter.[citation needed] Most go no further south than North Carolina and northern Portugal. They are fairly gregarious, forming small flocks, often with ruddy turnstones. This species is tame and approachable.

Their breeding habitat is the northern tundra on Arctic islands in Canada and coastal areas in Greenland and northwestern Europe. They can breed at one year of age. The male makes several scrapes on the ground; the female chooses one and lays 3 or 4 eggs. These are olive with brown blotches and are approximately 37 mm × 26 mm (1.5 in × 1.0 in) in size. The male takes the major responsibility for incubation of the eggs which hatch in 21–22 days. The chicks are covered with dense down. The upperparts have black and cinnamon patches with white specks; the underparts are mainly white. Usually only the male tends the chicks which can feed themselves. The maximum age recorded from ring-recovery data in Europe is 20 years and 9 months for a bird recovered in Sweden.

These birds forage on rocky coasts, picking up food by sight. They mainly eat arthropods and molluscs, mainly littorinids and mussels, also some plant material. One of the main staples are seaweed flies of the Coelopa genera (C. frigida).

The purple sandpiper has an extremely large range and although the population appears to be decreasing, the population is very large. 

21-7-2024 VIGUR ISLAND, ICELAND - ATLANTIC PUFFIN (Fratercula arctica)

The Atlantic puffin (Fratercula arctica), also known as the common puffin, is a species of seabird in the auk family. It is the only puffin native to the Atlantic Ocean; two related species, the tufted puffin and the horned puffin are found in the northeastern Pacific. The Atlantic puffin breeds in Russia, Iceland, Ireland, Britain, Norway, Greenland, Newfoundland and Labrador, Nova Scotia, and the Faroe Islands, and as far south as Maine in the west and France in the east. It is most commonly found in the Westman Islands, Iceland. Although it has a large population and a wide range, the species has declined rapidly, at least in parts of its range, resulting in it being rated as vulnerable by the IUCN. On land, it has the typical upright stance of an auk. At sea, it swims on the surface and feeds on zooplankton, small fish, and crabs, which it catches by diving underwater, using its wings for propulsion.

This puffin has a black crown and back, pale grey cheek patches, and a white body and underparts. Its broad, boldly marked red-and-black beak and orange legs contrast with its plumage. It moults while at sea in the winter, and some of the brightly coloured facial characteristics are lost, with colour returning during the spring. The external appearances of the adult male and female are identical, though the male is usually slightly larger. The juvenile has similar plumage, but its cheek patches are dark grey. The juvenile does not have brightly coloured head ornamentation, its bill is narrower and is dark grey with a yellowish-brown tip, and its legs and feet are also dark. Puffins from northern populations are typically larger than in the south and these populations are generally considered a different subspecies.

Spending the autumn and winter in the open ocean of the cold northern seas, the Atlantic puffin returns to coastal areas at the start of the breeding season in late spring. It nests in clifftop colonies, digging a burrow in which a single white egg is laid. Chicks mostly feed on whole fish and grow rapidly. After about 6 weeks, they are fully fledged and make their way at night to the sea. They swim away from the shore and do not return to land for several years.

Colonies are mostly on islands with no terrestrial predators, but adult birds and newly fledged chicks are at risk of attacks from the air by gulls and skuas. Sometimes, a bird such as an Arctic skua or blackback gull can cause a puffin arriving with a beak full of fish to drop all the fish the puffin was holding in its mouth. The puffin's striking appearance, large, colourful bill, waddling gait, and behaviour have given rise to nicknames such as "clown of the sea" or "sea parrot". It is the official bird of the Canadian province of Newfoundland and Labrador. 

The Atlantic puffin is a bird of the colder waters of the North Atlantic Ocean. It breeds on the coasts of northwest Europe, the Arctic fringes, and eastern North America. More than 90% of the global population is found in Europe (4,770,000–5,780,000 pairs, equalling 9,550,000–11,600,000 adults) and colonies in Iceland alone are home to 60% of the world's Atlantic puffins. The largest colony in the western Atlantic (estimated at more than 260,000 pairs) can be found at the Witless Bay Ecological Reserve, south of St. John's, Newfoundland and Labrador. Other major breeding locations include the north and west coasts of Norway, the Faroe Islands, Shetland and Orkney, the west coast of Greenland, and the coasts of Newfoundland. Smaller-sized colonies are also found elsewhere in the British Isles, the Murmansk area of Russia, Novaya Zemlya, Spitzbergen, Labrador, Nova Scotia, and Maine. Islands seem particularly attractive to the birds for breeding as compared to mainland sites, likely to avoid predators.

20-7-2024 HUSAVIK, ICELAND - NOOTKA LUPINE (Lupinus nootkatensis)

In Iceland, the Nootka lupine has been designated an invasive species. The plant was introduced in the first half of the 20th century to combat erosion, speed up land reclamation and help with reforestation. Dense lupine cover and soil fertility can be gained within a relatively short time span, where the growth of the lupine is not limited by droughts. The plant has spread from the loose, eroded soil in which it was originally planted and is now found throughout the lowlands of Iceland.

The lupine is well suited for reclamation of large, barren areas because of its nitrogen fixation and rapid growth. Furthermore, it has an ability to extract phosphorus from compounds in poor soils. In spite of these good qualities, it has a tendency to become dominant and to colonize already vegetated areas such as dwarf shrub-highlands, where it overtakes the natural flora and threatens biodiversity. The growth of the Nootka lupine has led to public debate about its presence in Iceland, with some praising its improvement of soil through nitrogen fixation and the vibrant colour it brings to Iceland's landscape, and others concerned that it will eradicate native flora, particularly the favoured native crowberry and blueberry patches.

The initial expectation was for the Nootka lupine to retreat gradually along with increased fertility of the soil and give way for other species. This is evident on sites in Iceland where the lupine was introduced early, such as in Heiðmörk near Reykjavík. However, plant succession is towards a forb-rich grassland, often dominated by the invasive species Anthriscus sylvestris, meaning that careful management of lupine is necessary to prevent it from colonizing areas where its presence is not desirable.

20-7-2024 AKUREYRI, ICELAND - LESSER BLACK BACKED GULL (Larus fuscus)

The lesser black-backed gull (Larus fuscus) is a large gull that breeds on the Atlantic coasts of Europe. It is migratory, wintering from the British Isles south to West Africa. However, it has increased dramatically in North America, especially along the east coast. Formerly just a winter visitor to North America, it has increased and occurs in large numbers some winters and birds are now recorded year-round. However, there is serious concern about decline in many parts of its range. The species is on the UK Amber List because the UK is home to 40 per cent of the European population and more than half of these are found at fewer than ten breeding sites.

The lesser black-backed gull was one of the many species originally described by Carl Linnaeus in his 1758 10th edition of Systema Naturae, and it still bears its original name Larus fuscus. The scientific name is from Latin. Larus appears to have referred to a gull or other large seabird, and fuscus meant black or brown.

20-7-2024 HUSAVIK, ICELAND - REDWING (Turdus iliacus)

The redwing (Turdus iliacus) is a bird in the thrush family, Turdidae, native to Europe and the Palearctic, slightly smaller than the related song thrush.

This species was first described by Carl Linnaeus in his 1758 10th edition of Systema Naturae under its current scientific name.

The English name derives from the bird's red underwing. It is not closely related to the red-winged blackbird, a North American species sometimes nicknamed "redwing", which is an icterid, not a thrush. The binomial name derives from the Latin words turdus, "thrush", and ile "flank".

About 65 species of medium to large thrushes are in the genus Turdus, characterised by rounded heads, longish, pointed wings, and usually melodious songs. Although two European thrushes, the song thrush and mistle thrush, are early offshoots from the Eurasian lineage of Turdus thrushes after they spread north from Africa, the redwing is descended from ancestors that had colonised the Caribbean islands from Africa and subsequently reached Europe from there.

The redwing has two subspecies:

T. i. iliacus, the nominate subspecies described by Linnaeus, which breeds in mainland Eurasia.

T. i. coburni described by Richard Bowdler Sharpe in 1901, which breeds in Iceland and the Faroe Islands and winters from western Scotland and Ireland south to northern Spain. It is darker overall, and marginally larger than the nominate form.

It is 20–24 cm long with a wingspan of 33–34.5 cm and a weight of 50–75 g. The sexes are similar, with plain brown backs and with dark brown spots on the white underparts. The most striking identification features are the red flanks and underwing, and the creamy white stripe above the eye. Adults moult between June and September, which means that some start to replace their flight feathers while still feeding young.

The male has a varied short song, and a whistling flight call. Redwings show a distinct dialectic variation in song, having a considerable similarity in song patterns among birds within a local population.

The Redwing song consists of a number of introductory elements of descending or ascending frequency. These elements may be of pure tonal quality, or of a more harsh quality (varying degrees of frequency modulations or "trills"). After the introductory elements, a fast and more complex song pattern often follows. It is the introductory elements which show a geographic variation. The boundaries of any given dialect may vary but in a rural and forested environment in Norway the average size of these dialect areas is around 41.5 km2.

It breeds in northern regions of Europe and the Palearctic, from Iceland south to northernmost Scotland, and east through Scandinavia, the Baltic States, northern Poland and Belarus, and through most of Russia to about 165°E in Chukotka Autonomous Okrug. In recent years it has expanded its range slightly, both in eastern Europe where it now breeds south into northern Ukraine, and in southern Greenland, where the Qaqortoq area was colonised in 1990–1991.

It is often replaced by the related ring ouzel in areas of higher altitude.

It is migratory, wintering in western, central and southern Europe, north-west Africa, and south-west Asia east to northern Iran. Birds in some parts of the west of the breeding range (particularly south-western Norway) may be resident, not migrating at all, while those in the far east of the range migrate at least 6,500–7,000 km to reach their wintering grounds.

There are multiple records of vagrants from the north-east coast of North America, as well as two sightings on the north-west coast (one in Washington in 2005, and one in Seward, Alaska in November 2011).

Migrating and wintering birds often form loose flocks of 10 to 200 or more birds, often feeding together with fieldfares, common blackbirds and starlings, sometimes also with mistle thrushes, song thrushes, and ring ouzels. Unlike the song thrush, the more nomadic redwing does not tend to return regularly to the same wintering areas.

The movement occurs in the Autumn to early Winter and they often move at night making a "Tseep" contact call that can carry a long distance.

Nests are often constructed on the ground.

It breeds in conifer and birch forest and tundra. Redwings nest in shrubs or on the ground, laying four to six eggs in a neat nest. The eggs are typically 2.6 x 1.9 centimetres in size and weigh 4.6 grammes, of which 5% is shell, and which hatch after 12–13 days. The chicks fledge at 12–15 days, but the young remain dependent on their parents for a further 14 days.

It is omnivorous, eating a wide range of insects and earthworms all year, supplemented by berries in autumn and winter, particularly of rowan Sorbus aucuparia and hawthorn Crataegus monogyna.

A Russian study of blood parasites showed that all the fieldfares, redwings and song thrushes sampled carried haematozoans, particularly Haemoproteus and Trypanosoma.

The redwing has an extensive range, estimated at 10 million square kilometres (3.8 million square miles), and an estimated population of 26 to 40 million individuals in Europe alone. The European population forms approximately 40% of the global population, thus the very preliminary estimate of the global population is 98 to 151 million individuals. The species is believed to approach the thresholds for the population decline criterion of the IUCN Red List (i.e., declining more than 30% in ten years or three generations), and is therefore precautionarily uplisted to near threatened. Numbers can be adversely affected by severe winters, which may cause heavy mortality, and cold wet summers, which reduce breeding success.

20-7-2024 HUSAVIK, ICELAND - COMMON RINGED PLOVER (Charadrius hiaticula)

The common ringed plover or ringed plover (Charadrius hiaticula) is a small plover that breeds across much of northern Eurasia, as well as Greenland. The genus name Charadrius is a Late Latin word for a yellowish bird mentioned in the fourth-century Vulgate. It derives from Ancient Greek kharadrios a bird found in ravines and river valleys (kharadra, "ravine"). The specific hiaticula is Latin and has a similar meaning to the Greek term, coming from hiatus, "cleft" and -cola, "dweller" (colere, "to dwell").

Adults are 17–19.5 cm (6.7–7.7 in) in length with a 35–41 cm (14–16 in) wingspan. They have a grey-brown back and wings, a white belly, and a white breast with one black neckband. They have a brown cap, a white forehead, a black mask around the eyes and a short orange and black bill. The legs are orange and only the outer two toes are slightly webbed, unlike the slightly smaller but otherwise very similar semipalmated plover, which has all three toes slightly webbed, and also a marginally narrower breast band; it was in former times included in the present species. Juvenile ringed plovers are duller than the adults in colour, with an often incomplete grey-brown breast band, a dark bill and dull yellowish-grey legs.

This species differs from the smaller little ringed plover in leg colour, the head pattern, and the lack of an obvious yellow eye-ring.

The common ringed plover's breeding habitat is open ground on beaches or flats across northern Eurosiberia and in Arctic northeast Canada. Some birds breed inland, and in western Europe they nest as far south as northern France. They nest on the ground in an open area with little or no plant growth.

If a potential predator approaches the nest, the adult will walk away from the scrape, calling to attract the intruder and feigning a broken wing. Once the intruder is far enough from the nest, the plover flies off.

Common ringed plovers are migratory and winter in coastal areas south to Africa. In Norway, geolocators have revealed that adult breeding birds migrate to West Africa. Many birds in Great Britain and northern France are resident throughout the year.

These birds forage for food on beaches, tidal flats and fields, usually by sight. They eat insects, crustaceans and worms.

16-7-2024 ROTTERDAM ZOO, NETHERLANDS - EURASIAN OTTER (Lutra lutra)

The Eurasian otter (Lutra lutra), also known as the European otter, Eurasian river otter, European river otter, common otter, and Old World otter, is a semiaquatic mammal native to Eurasia and Maghreb. The most widely distributed member of the otter subfamily (Lutrinae) of the weasel family (Mustelidae), it is found in the waterways and coasts of Europe, many parts of Asia, and parts of northern Africa. The Eurasian otter has a diet mainly of fish, and is strongly territorial. It is endangered in some parts of its range, but is recovering in others.

The Eurasian otter is the most widely distributed otter species, its range including parts of Asia and northern Africa, as well as being spread across Europe, south to Palestine. Though currently thought to be extinct in Liechtenstein and Switzerland, it is now common in Latvia, along the coast of Norway, in the western regions of Spain and Portugal and across Great Britain and Ireland. In Italy, it lives in southern parts of the peninsula. It inhabits unpolluted bodies of fresh water such as lakes, streams, rivers, canals and ponds, as long as the food supply is adequate. In Andalusia, it uses artificial lakes on golf courses.[8] It prefers the open areas of the streams and also lives along the coast in salt water, but requires regular access to fresh water to clean its fur.

The Eurasian otter is a typical species of the otter subfamily. Brown above and cream below, these long, slender creatures are well-equipped for their aquatic habits. Their bones show osteosclerosis, increasing their density to reduce buoyancy. This otter differs from the North American river otter by its shorter neck, broader visage, the greater space between the ears and its longer tail. However, the Eurasian otter is the only otter in much of its range, so it is rarely confused for any other animal. Normally, this species is 57 to 95 cm (22.5 to 37.5 in) long, not counting a tail of 35–45 cm (14–17.5 in). The female is shorter than the male.[4] The otter's average body weight is 7 to 12 kg (15 to 26 lb), although occasionally a large old male may reach up to 17 kg (37 lb). The record-sized specimen, reported by a reliable source but not verified, weighed over 24 kg (53 lb).

In Syria, the Eurasian otter was recorded in montane creeks in Latakia and Raqqa Governorates and in the lower Euphrates valley in Deir ez-Zor Governorate. In western Nepal, its presence was documented at elevations of around 1,600 m (5,200 ft) in Barekot river in Jajarkot District and at 1,337 m (4,386 ft) in Tubang river in Eastern Rukum District. In India, it is distributed in the Himalayan foothills, southern Western Ghats and the central Indian landscape.

16-7-2024 ROTTERDAM ZOO, NETHERLANDS - MARBLED TEAL (Marmaronetta angustirostris)

The marbled duck or marbled teal (Marmaronetta angustirostris) is a medium-sized species of duck from southern Europe, northern Africa, and western and central Asia. The scientific name, Marmaronetta angustirostris, comes from the Greek marmaros, marbled and netta, a duck, and Latin angustus, narrow or small and -rostris billed.

This duck formerly bred in large numbers in the Mediterranean region, but is now restricted to a few sites in southern Spain, southern Italy, northwest Africa and the broader Levant. Further east it survives in the Mesopotamian marshland in southern Iraq and in Iran (Shadegan Marshes - the world's most important site), as well as isolated pockets in Armenia, Azerbaijan, South European Russia, western India and western China. In general the species has nomadic tendencies. In some areas birds disperse from the breeding grounds, and have been encountered in the winter period in the Sahel zone, south of the Sahara.

Its preferred breeding habitat is temporary and shallow fresh, brackish or alkaline waters with densely vegetated shores in regions that otherwise are fairly dry. It may also breed in coastal lagoons, along slow rivers or man-made waters like reservoirs. The on average c. 12 eggs are placed in a nest covered by dense vegetation at the waters edge. It is usually on the ground, but occasionally higher among reeds or on huts made from reeds. They are common in captive collections but are a nervous and flighty bird.

These are gregarious birds, at times even when nesting. Outside the breeding season flocks are often small, although large wintering flocks have been reported in some areas. The largest winter concentration known is in Khuzestan, Iran.

In 2011, a group of Iraqi ornithologists counted a single flock of the rare marbled teal on the lakes of the Iraqi marshes, numbering at least 40,000 birds.

16-7-2024 ROTTERDAM ZOO, NETHERLANDS - NORTH AFRICAN SPINY TAILED LIZARD [Uromastyx acanthinura]

 

Uromastyx acanthinura, the North African mastigure or North African spiny-tailed lizard, is a species of agamid lizard. It is found in Morocco, Algeria, Tunisia, Libya, Egypt, Western Sahara, Chad, Mali, Niger, and Sudan.

16-7-2024 ROTTERDAM ZOO, NETHERLANDS - FALL PHLOX [Phlox paniculata]

Phlox paniculata is a species of flowering plant in the phlox family (Polemoniaceae). It is native to parts of the eastern and central United States. It is extensively cultivated in temperate regions as an ornamental plant and has become established in the wild in scattered locales in other regions. Common names include fall phlox, garden phlox, perennial phlox, summer phlox, and panicled phlox.

Phlox paniculata is an erect herbaceous perennial growing to 120 cm (47 in) tall by 100 cm (39 in) wide, with opposite, simple leaves on slender green stems. The flowers are 1.5–2.5 cm (0.6–1.0 in) in diameter, often strongly fragrant and borne in summer through fall (autumn). The flowers are grouped in panicles (with many branching stems), hence the specific epithet paniculata. Typical flower colors in wild populations are pink or purple (rarely white).

Fall phlox is native to parts of the central and eastern United States. It occurs as an introduced species in other parts of the United States, Canada, Europe, and Asia. In the Chicago Region it is questionably native, or native populations may have all been destroyed: "populations in our area appear to be escapes from gardens to nearby woods and waste ground, which no doubt accounts for all collections since 1945".

In its natural range, it grows along streambanks and in moist wooded areas.

16-7-2024 ROTTERDAM ZOO, NETHERLANDS - GREAT WHITE PELICAN (Pelecanus onocrotalus)

The great white pelican is a huge bird—only the Dalmatian pelican is, on average, larger among pelicans. It measures 140 to 180 cm (55 to 71 in) in length with a 28.9 to 47.1 cm (11.4 to 18.5 in) enormous pink and yellow bill, and a dull pale-yellow gular pouch. The wingspan measures 226 to 360 cm (7 ft 5 in to 11 ft 10 in), the latter measurement being the highest among extant flying animals outside of the great albatross. The adult male measures about 175 cm (69 in) in length; it weighs from 9 to 15 kg (20 to 33 lb)  and larger races from the Palaearctic are usually around 11 kg (24 lb), with few exceeding 13 kg (29 lb). It has a bill measuring 34.7 to 47.1 cm (13.7 to 18.5 in). The female measures about 148 cm (58 in) in length, and is considerably less bulky, weighing 5.4 to 9 kg (12 to 20 lb), and has a bill that measures 28.9 to 40.0 cm (11.4 to 15.7 in) in length.[8] In Lake Edward, Uganda, the average weight of 52 males was found to 11.45 kg (25.2 lb) and in 22 females it was 7.59 kg (16.7 lb). In South Africa, the average weight of males was 9.6 kg (21 lb) and of females was 6.9 kg (15 lb). Thus the sexual dimorphism is especially pronounced in this species (perhaps the greatest known in any extant pelican), as at times the male can average more than 30% more massive than the female. The great white pelican rivals the kori bustard, which has even more pronounced sexual dimorphism, as the heaviest flying bird to reside in Africa (both averaging perhaps slightly heavier than the cape vulture and the wattled crane). 

There are a small few slightly heavier flying birds in the Eurasian portions of the range. Among standard measurements, the wing chord is 60 to 73 cm (24 to 29 in), the tail 16 to 21 cm (6.3 to 8.3 in), and the tarsus 13 to 14.9 cm (5.1 to 5.9 in) long. Standard measurements from different areas indicate that pelicans from the Western Palaearctic are somewhat larger than those from Asia and Africa.

The male has a downward bend in the neck and the female has a shorter, straighter beak. The plumage is predominantly white except on remiges, with a faint pink tinge on the neck and a yellowish base on the foreneck. The primary feathers are black, with white shafts at the bases, occasionally with paler tips and narrow fringes. The secondary feathers are also black, but with a whitish fringe. The upperwing coverts, underwing coverts, and tertials are white. The forehead is swollen and pinkish skin surrounds the bare, dark eyes having brown-red to dark brown irides It has fleshy-yellow legs and pointed forehead-feathers where meeting the culmen. In breeding season, the male has pinkish skin while the female has orangey skin on its face. The bill is mostly bluish grey, with a red tip, reddish maxilla edges, and a cream-yellow to yolk-yellow gular pouch. The white plumage becomes tinged-pink with a yellow patch on the breast, and the body is tinged yellowish-rosy. It also has a short, shaggy crest on the nape. The white covert feathers contrast with the solid black primary and secondary feathers. The legs are yellow-flesh to pinkish orange. Both male and female are similar, but the female is smaller and has brighter orange facial skin in the breeding season.

The juvenile has darker, brownish underparts that are palest at the rump, center of the belly, and uppertail coverts. The underwing coverts are mostly dull-white, but the greater coverts are dark and there is a dark brownish bar over the lesser coverts. The rear tertials upperwing coverts mostly have paler tips with a silvery-grey tinge on the greater secondary coverts and tertials. It has dark flight feathers, and brow-edged wings. The head, neck, and upperparts, including the upperwing coverts, are mostly brown—this is the darkest part of the neck. The facial skin and the bill, including its gular pouch, are greyish to dusky greyish. The forehead, rump, and abdomen are white, and its legs and feet are grey. Its blackish tail occasionally has a silvery-grey tinge. Its underparts and back are initially browner and darker than those of the Dalmatian pelican, and the underwing is strongly patterned, similar to the juvenile brown pelican.

The great white pelican is distinguished from all other pelicans by its plumage. Its face is naked and the feathering on its forehead tapers to a fine point, whereas other species are completely feathered. In flight, the white underwing with black remiges of the adult are similar only to those of the American white pelican (P. erythrorhynchos), but the latter has white inner secondary feathers. It differs from the Dalmatian pelican in its pure white – rather than greyish-white – plumage, a bare pink facial patch around the eye, and pinkish legs. The spot-billed pelican (P. philippensis) of Asia is slightly smaller than the great white pelican, with greyish tinged white plumage, and a paler, duller-colored bill. Similarly, the pink-backed pelican (P. rufescens) is smaller, with brownish-grey plumage, a light pink to off-grey bill, and a pinkish wash on the back.

The bird is mostly silent but has a variety of low-pitched lowing, grunting, and growling calls. The flight call is a deep, quiet croak., while at breeding colonies, it gives deep moooo calls.

16-7-2024 ROTTERDAM ZOO, NETHERLANDS - YELLOW MONGOOSE (Cynictis penicillata)

 

The social structure of the yellow mongoose is hierarchical, based around a central breeding pair and their most recent offspring. There are also subadults, the elderly, or adult relatives of the central pair. Male ranges tend to overlap, while females from other dens have contiguous non-overlapping ranges. Every day, the alpha male will mark members of his group with anal gland secretions, and his boundaries with facial and anal secretions, as well as urine. The alpha male also rubs his back against raised objects, leaving behind hair as a visual marker of territory. Other members of the group mark their dens with cheek secretions. A colony can have 20-40 members.

Predators of the yellow mongoose are birds of prey, snakes and jackals. When frightened, the yellow mongoose will growl and secrete from its anal glands. It can also scream, bark, and purr, though these are exceptions, as the yellow mongoose is usually silent, and communicates mood and status through tail movements.

The yellow mongoose (Cynictis penicillata), sometimes referred to as the red meerkat, is a member of the mongoose family. It averages about 0.45 kg (1 lb) in weight and about 510 mm (20 in) in length. It lives in open country, semi-desert scrubland and grasslands in Angola, Botswana, South Africa, Namibia, and Zimbabwe. It is the only species in the genus Cynictis.

In general, the yellow mongoose has lighter highlights on the underbelly and chin, a bushy tail, and a complete lack of sexual dimorphism. Southern yellow mongooses are larger, have yellow or reddish fur, longer fur, and a longer tail with a characteristic white tip. Northern subspecies tend towards smaller size, grey colouration, a grey or darker grey tip to the tail, and shorter hair more appropriate to the hotter climate.

The yellow mongoose is primarily diurnal, though nocturnal activity has been observed. Living in colonies of up to 20 individuals in a permanent burrow complex, the yellow mongoose will often co-exist with Cape ground squirrels or suricates and share maintenance of the warren, adding new tunnels and burrows as necessary. The tunnel system has many entrances, nearby which the yellow mongoose makes its latrines.

The yellow mongoose is a carnivore, feeding mostly on beetles, termites, grasshoppers, crickets, caterpillars, and ants, but also on rodents, small birds, reptiles, amphibians, carrion, eggs, grass, and seeds. In urban environments in South Africa, it also forages among human food garbage.

The yellow mongoose's mating season is between July and September, and it gives birth underground between October and December, with no bedding material, in a clean chamber of the burrow system. Usually, two offspring are produced per pregnancy, and they are weaned at 10 weeks, reaching adult size after 10 months.

19-7-2024 AT SEA, ICELAND - NORTHERN GANNET (Morus bassanus)

The northern gannet (Morus bassanus) is a seabird, the largest species of the gannet family, Sulidae. It is native to the coasts of the Atlantic Ocean, breeding in Western Europe and Northeastern North America. It is the largest seabird in the northern Atlantic. The sexes are similar in appearance. The adult northern gannet has a mainly white streamlined body with a long neck, and long and slender wings. It is 87–100 cm (34+1⁄2–39+1⁄2 in) long with a 170–180 cm (67–71 in) wingspan. The head and nape have a buff tinge that is more prominent in breeding season, and the wings are edged with dark brown-black feathers. 

The long, pointed bill is blue-grey, contrasting with black, bare skin around the mouth and eyes. Juveniles are mostly grey-brown, becoming increasingly white in the five years it takes them to reach maturity.

Nesting takes place in colonies on both sides of the North Atlantic, the largest of which are at Bass Rock (75,000 pairs as of 2014), St. Kilda (60,000 pairs as of 2013) and Ailsa Craig (33,000 pairs as of 2014) in Scotland, Grassholm in Wales, and Bonaventure Island (60,000 pairs in 2009) off the coast of Quebec. 

Its breeding range has extended northward and eastward, with colonies being established on Russia's Kola Peninsula in 1995 and Bear Island (the southernmost island of Svalbard), in 2011. Colonies are mostly located on offshore islands with cliffs, from which the birds can more easily launch into the air. The northern gannet undertakes seasonal migrations and catches fish (which are the mainstay of its diet) by making high-speed dives into the sea.

The northern gannet was previously hunted for food in certain parts of its range, and although that practice still continues in the Outer Hebrides of Scotland and the Faroe Islands, the bird faces few other natural or man-made threats.

16-7-2024 ROTTERDAM ZOO, NETHERLANDS - BLACK TAILED PRAIRIE DOG (Cynomys ludovicianus)

 

The black-tailed prairie dog (Cynomys ludovicianus) is a rodent of the family Sciuridae (the squirrels) found in the Great Plains of North America from about the United States–Canada border to the United States–Mexico border.[3] Unlike some other prairie dogs, these animals do not truly hibernate. The black-tailed prairie dog can be seen above ground in midwinter. A black-tailed prairie dog town in Texas was reported to cover 25,000 sq mi (64,000 km2) and included 400,000,000 individuals. Prior to habitat destruction, the species may have been the most abundant prairie dog in central North America. It was one of two prairie dogs described by the Lewis and Clark Expedition in the journals and diaries of their expedition.

Black-tailed prairie dogs are generally tan in color, with lighter-colored bellies. They may have color variation in their pelt, such as dark fur on their back in black and brown tones. Their tails have black tips, from which their name is derived. Adults can weigh from 1.5 to 3.0 lb (0.68 to 1.36 kg), males are typically heavier than females. Body length is normally from 14 to 17 in (36 to 43 cm), with a 3-to-4-inch (7.6 to 10.2 cm) tail. The black-tailed have black long claws used for digging in the ground. The body of the black-tailed prairie dog is compact, and the ears are quite small and close to the head.

The historic range of the black-tailed prairie dog was from southern Saskatchewan and Alberta to Chihuahua, Mexico, and included portions of Montana, North Dakota, South Dakota, Wyoming, Colorado, Nebraska, Kansas, Oklahoma, Texas, Arizona, and New Mexico. As of 2007, black-tailed prairie dogs occur across most of their historic range, excluding Arizona; however, their occupied acreage and populations are well below historic levels.

Black-tailed prairie dogs are diurnal. Above-ground activity is reduced when rain or snow is falling and during days when the temperature exceeds 100 °F (38 °C). During the winter months, black-tailed prairie dogs do not fully hibernate. They continue to leave the burrow to forage, but will enter a state of torpor at night to conserve energy. Torpor is categorized by a drop in metabolism, heart rate and respiration similar to hibernation, but is involuntary and shorter in duration. On average, black-tailed prairie dogs will lose twenty percent of their body weight during the fall and winter seasons when they go through bouts of torpor. As winter progressed, the amount of time spent in torpor increases. Between different colonies the overall time spent in torpor varies, independent of prairie dog body mass. This may be due to weather during the previous growing season. As black-tailed prairie dogs receive most of their water from their diet, in years with poor rainfall, the black-tailed prairie dogs spend more time in torpor.

Black-tailed prairie dogs are native to grassland habitats in North America. They inhabit shortgrass prairie, mixed-grass prairie, sagebrush steppe, and desert grassland.

Habitat preferences for the black-tailed prairie dog are influenced by vegetative cover type, slope, soil type, and amount of rainfall. Their foraging and burrowing activities influence environmental heterogeneity, hydrology, nutrient cycling, biodiversity, landscape architecture, and plant succession in grassland habitats.

Black-tailed prairie dogs inhabit grasslands, including short- and mixed-grass prairie, sagebrush steppe, and desert grasslands. Shortgrass prairies dominated by buffalo grass (Buchloe dactyloides), blue grama (Bouteloua gracilis), and western wheatgrass (Pascopyron smithii), and mixed-grass prairies  that have been grazed by native and non-native herbivores are their preferred habitat. Slopes of 2% to 5% and vegetation heights between 3 and 5 in (8 and 13 cm) are optimal for detecting predators and facilitating communication.

In the Great Plains region, black-tailed prairie dog colonies commonly occur near rivers and creeks. Of 86 colonies located in Mellette County, South Dakota, 30 were located on benches or terraces adjacent to a creek or floodplain, 30 occurred in rolling hills with a slope more than 5°, 20 were in flat areas, and six were in badland areas. The slopes of playa lakes in the Texas Panhandle and surrounding regions are used as habitat for the black-tailed prairie dog. Colonies in Phillips County, Montana, were often associated with reservoirs, cattle salting grounds, and other areas affected by humans.

Black-tailed prairie dogs tolerate "high degrees" of disturbance over long periods of time. New colonies are rarely created on rangeland in "good" to "excellent" condition; however, continuously, long-term, heavily grazed land reduces habitat quality due to soil erosion. Black-tailed prairie dogs may colonize heavily grazed sites, but do not necessarily specialize in colonizing overgrazed areas. Overgrazing may occur subsequent to their colonization. Black-tailed prairie dogs were associated with areas intensively grazed by livestock and/or areas where topsoil had been disturbed by human activities in sagebrush-grassland habitat on the Charles M. Russell National Wildlife Refuge and Fort Belknap Agency, Montana. Roads and cattle trails were found in 150 of 154 black-tailed prairie dog colonies, and colonies were located significantly closer to livestock water developments and homestead sites than randomly located points.

16-7-2024 ROTTERDAM ZOO, NETHERLANDS - COTTON HEADED TAMARIN (Saguinus oedipus)

The cotton-top tamarin (Saguinus oedipus) is a small New World monkey weighing less than 0.5 kg (1.1 lb). This New World monkey can live up to 24 years, but most of them die by 13 years. One of the smallest primates, the cotton-top tamarin is easily recognized by the long, white sagittal crest extending from its forehead to its shoulders. The species is found in tropical forest edges and secondary forests in northwestern Colombia, where it is arboreal and diurnal. Its diet includes insects and plant exudates, and it is an important seed disperser in the tropical ecosystem.

The cotton-top tamarin displays a wide variety of social behaviors. In particular, groups form a clear dominance hierarchy where only dominant pairs breed. The female normally gives birth to twins and uses pheromones to prevent other females in the group from breeding. These tamarins have been extensively studied for their high level of cooperative care, as well as altruistic and spiteful behaviors. Communication between cotton-top tamarins is sophisticated and shows evidence of simple grammatical structure.

Up to 40,000 cotton-top tamarins are thought to have been caught and exported for use in biomedical research before 1976, when CITES gave them the highest level of protection and all international commercial trade was prohibited. Now, the species is at risk due to large-scale habitat destruction, as the lowland forest in northwestern Colombia where the cotton-top tamarin is found has been reduced to 5% of its previous area. It is currently classified as critically endangered and is one of the rarest primates in the world, with only 6,000 individuals left in the wild.

The cotton-top tamarin is restricted to a small area of northwest Colombia, between the Cauca and Magdalena Rivers to the south and east, the Atlantic coast to the north, and the Atrato River to the west. They are found exclusively in Colombia; 98% of their habitat has been destroyed. Historically, the entire area was suitable for the cotton-top tamarin, but due to habitat loss through deforestation, it survives in fragmented parks and reserves. One of the most important areas for the cotton-top is the Paramillo National Park, which consists of 460,000 hectares (1,800 sq mi) of primary and secondary forests.

The cotton-top tamarin is found in both primary and secondary forests, from humid tropical forests in the south of its range to tropical dry forests in the north. It is seldom found at altitudes above 400 m (1,300 ft), but has been encountered up to 1,500 m (4,900 ft). It prefers the lower levels of the tropical forests, but may also be found foraging on the ground and between the understory and the canopy. It can adapt to forest fragments and can survive in relatively disturbed habitats. In the dry forests are pronounced seasons. Between December and April, it is dry, while heavy rainfall occurs between August and November which can flood the forest floor. Across its range, annual rainfall varies between 500 and 1,300 mm (20 and 51 in).