This Blog contains Wildlife and Bird Photos from Walks, Safaris, Birding Trips and Vacations. Most of the pictures have been taken with my Nikon P900 and P950X cameras. On the right of the page are labels for each species of Bird/Animal etc. Click on a label and it will show all of the photos taken for that species. I am adding information for each species from sources like Wikipedia. To see any pictures at a large size just click on the image.
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Wednesday 6 January 2016
27-12-2015 SAIGON, VIETNAM - GREY HEADED SWAMPHEN (Porphyrio poliocephalus)
The grey-headed swamphen (Porphyrio poliocephalus ) is a species of swamphen occurring from the Middle East and the Indian subcontinent to southern China and northern Thailand. It used to be considered a subspecies of the purple swamphen, but was elevated to full species status in 2015; today the purple swamphen is considered a superspecies and each of its six subspecies groups are designated full species.
The male has an elaborate courtship display, holding water weeds in his bill and bowing to the female with loud chuckles.
The grey-headed swamphen was introduced to North America in the late 1990s due to avicultural escapes in the Pembroke Pines, Florida area. State wildlife biologists attempted to eradicate the birds, but they have multiplied and can now be found in many areas of southern Florida. Ornithological authorities consider it likely that the swamphen will become an established part of Florida's avifauna. It was added to the American Birding Association checklist in February 2013.
Looking like an oversized version of a Purple Gallinule with a massive red bill, the Gray-headed Swamphen is an impressive bird and the largest rail in North America. Originally from southern Asia, it became established in southern Florida in the mid-1990s when birds escaped from captivity and began breeding. Like gallinules, this species forages in marshes by wading, swimming, and even climbing to reach aquatic vegetation, insects, and animal prey. Swamphens are aggressive competitors and may dominate or displace our native North American rails.
27-12-2015 SAIGON, VIETNAM - MARABOU STORK (Leptoptilos crumenifer)
The Marabou stork (Leptoptilos crumenifer) is a large wading bird that breeds in Africa often near human habitation, especially landfill sites. It is sometimes called the "undertaker bird" due to its shape from behind: cloak-like wings and back, skinny white legs, and sometimes a large white mass of "hair".
Marabou storks are scavengers and feed mainly on carrion. However, they occasionally eat other birds including pigeons, doves, pelican and cormorant chicks, and even flamingos. During the breeding season, adult marabous take mostly small, live prey since nestlings need this kind of food to survive. Common prey at this time may consist of fish, frogs, insects, eggs, small mammals, and reptiles such as crocodile hatchlings and eggs, and lizards and snakes.
The Marabou stork is a massive bird. This bird is unmistakable due to its size, bare head, and neck, huge bill, pink gular sac at its throat (crumenifer(us) - means "carrier of a pouch for money"), and neck ruff. The male and the female are alike, but the young bird is browner and has a smaller bill.
Marabou storks breed in Africa south of the Sahara. They live in both wet and arid habitats and can be found in open dry savannas, grasslands, riverbanks, lakeshores, and swamps. These birds are also frequent visitors to landfills and fishing villages.
Marabou storks are monogamous and form strong pair bonds that last for life. They breed in colonies, starting during the dry season when food is more readily available as the pools shrink. Males attract a female with bill-rattling courtship displays and their throat sac is also used to make various noises at that time. Marabous build a small nest in a tree made of sticks and line it with twigs and green leaves. The female lays 2-3 eggs which hatch after an incubation period of 30 days. At hatching, the chicks are fed by both parents and fledge between 13 and 15 weeks of age. They remain with their parents for about another 4 months and reach reproductive maturity at 4 years of age.
Marabous will also forage by wading in shallow water using their sensitive bills. When prey touches the bill it snaps shut and the bird swallows its catch. Increasingly, marabous have become dependent on human garbage and hundreds of these huge birds are seen around African dumps or waiting for a handout in urban areas. Marabous eating human garbage have been seen to devour virtually anything that they can swallow, including even shoes and pieces of metal.
27-12-2015 SAIGON, VIETNAM - EURASIAN TREE SPARROW (MALE) (Passer montanus)
The Eurasian tree sparrow (Passer montanus) is asmall passerine bird that breeds over most of temperate Eurasia and Southeast Asia, where it is known as the Tree sparrow. It has been introduced elsewhere including the United States, where it is known as the Eurasian tree sparrow or German sparrow to differentiate it from the native unrelated American tree sparrow.
The adult's crown and nape are rich chestnut, and there is a kidney-shaped black ear patch on each pure white cheek; the chin, throat, and the area between the bill and throat are black. The upperparts are light brown, streaked with black, and the brown wings have two distinct narrow white bars. The legs are pale brown, and the bill is lead-blue in summer, becoming almost black in winter. This sparrow is distinctive even within its genus in that it has no plumage differences between the sexes; the juvenile also resembles the adult, although the colors tend to be duller. Its contrasting face pattern makes this species easily identifiable in all plumages; the smaller size and brown, not grey, crown are additional differences from the male house sparrow. Adult and juvenile Eurasian tree sparrows undergo a slow complete molt in the autumn and show an increase in body mass despite a reduction in stored fat. The change in mass is due to an increase in blood volume to support active feather growth and generally higher water content in the body.
19-12-2015 MALACCA, MALAYA - MALAYAN NIGHT HERON (Gorsachius melanolophus)
The Malayan night heron (Gorsachius melanolophus), also known as Malaysian night heron and tiger bittern, is a medium-sized heron. It is distributed in southern and eastern Asia.
The Malayan night heron has been found in India, Sri Lanka, Brunei, Nepal, Bangladesh, Myanmar, Cambodia, Laos, Vietnam, Thailand, Malaysia, Singapore, China, Indonesia, the Philippines, Taiwan and Japan. It is a vagrant in Palau and Korea. Its range size is estimated at 1,240,000 km2. One roadkilled bird was discovered on Christmas Island, Australia where it is likely a vagrant. This bird occurs in forests, streams, and marshes. In Japan, population densities of the herons increased as undisturbed forest cover on islands increased.
The Malayan night heron is about 48 cm (19 in) long. The wingspan is about 86 cm (34 in). It is stocky, with a short beak. Its neck and breast are rufous. There are streaks going down the centre of the neck to the breast. The upperparts are chestnut and vermiculated. The flight feathers are blackish. The crown is black, the chin is white, and the eyes are yellow. The beak is black and the legs are greenish. The juvenile is greyish to rufous and is spotted and vermiculated. Males have been reported to have deeper blue lores and a longer crest compared to females during the breeding season. Males develop the dark blue lores 30-60 days prior to pair-bonding, while females had bluish-green lores when they first appeared in the breeding areas. Colours of the lores of both sexes faded as incubation progressed, with colours changing to bluish-green to green to greyish-green. If pairs laid a second clutch, the colouration of their lores were duller than the colouration during the first clutch.
The Malayan night heron is usually solitary. It roosts in trees and feeds in open areas. It seems to nest singly and not colonially in association with other waterbirds. In Taiwan, nests are sometimes close to urban buildings and feed on earthworms and frogs in open areas amid buildings. Birds with immature plumage attempt to disrupt pair bonding of adults, and sometimes immature birds are seen bonded with adults though their ability to build nests seemed poor. In one observed instance, people assisted an immature-adult pair by building a base for a poorly constructed nest. Of six breeding pairs observed in Taiwan, four were immature-adult pairs suggesting that the species in Taiwan has few breeding adults. Birds in immature plumage appeared to be sexually mature
Its territorial call is deep oo notes. It also produces hoarse croaks and arh, arh, arh.
The most common food items are earthworms and frogs, and it will sometimes eat fish. A study of its pellets found reptiles, snails, chilopods, arachnids, crabs and insects. Pellets of breeding birds in Korea had earthworms, snails and cicadas. An instance of predation of the Brown Anole Anolis sagrei has been observed.
The bird has a large range and its global population is between 2,000 and 20,000 individuals. Its population trend is not known, but it does not meet the criteria for a vulnerable species status.
20-12-2015 JURONG, SINGAPORE - BLUE CROWNED HANGING PARROT (Loriculus galgulus)
The blue-crowned hanging parrot (Loriculus galgulus) is a parrot species endemic to southern Burma and Thailand, Malaya, Singapore, and Indonesia (Sumatra, Java, Borneo). These parrots are 12cm in height and weight 28g and have a longevity of 14 years. They are recognized by their green plumage, black beak and characteristic blue feathers arranged like a crown on their head.
Blue-crowned hanging parrots have green plumage and adults have black beaks. There is sexual dimorphism between males and females of the species. Adult males have a characteristic blue "crown" patch on their head and a red mark on their throat as well as a red rump bordered by a yellow lower back. Adult females plumage is duller green in color compared to the males, they do not have the red throat mark and have a less apparent or absent blue crown on the head and lack yellow feathers on their lower back. Juveniles' plumage is dull green, they also have little to no blue crown patch, they have a little to no blue crown visible and their bills are light in color.
The calls these birds make when flying are shrill and squeaky. When flying in flocks, the calls can be described as rapid and ringing. As they forage, they utter shrill two-syllable calls.
Tuesday 5 January 2016
6-1-2016 HONG KONG AVIARY - WHITE NAPED YUHINA (Yuhina bakeri)
The white-naped yuhina (Yuhina bakeri ) is a bird species in the white-eye family Zosteropidae.
It is found from the Himalayas to northern Myanmar. Its natural habitats are temperate forests and subtropical or tropical moist lowland forests.
Exquisite yuhina with an orange head and crest with white ears and throat. Nape is not obviously pale, but the white “trim” to the back edge of the crest is noticeable. Forages in broadleaf forests from lower foothills up to montane areas. Social and often seen in large flocks, occasionally with other species. Vocal; gives a range of calls, including fluid-sounding twitters and a nasal bleating.
27-12-2015 SAIGON, VIETNAM - CHINESE POND HERON (Ardeola bacchus)
The Chinese pond heron (Ardeola bacchus ) is an East Asian freshwater bird of the heron family, (Ardeidae).
It is one of six species of birds known as "pond herons" (genus Ardeola ). It is parapatric (or nearly so) with the Indian pond heron (A. grayii ) to the west and the Javan pond heron (A. speciosa ) to the south, and these three are presumed to form a superspecies. As a group they are variously affiliated with the squacco heron (A. ralloides ) or the Malagasy pond heron (A. idae ). As of mid-2011 there are no published molecular analyses of pond heron interrelationships and osteological data is likewise not analyzed for all relevant comparison taxa.
The Chinese pond heron is typically 47 cm (19 in) long with white wings, a yellow bill with a black tip, yellow eyes and legs. Its overall colour is red, blue and white during breeding season, and greyish-brown and flecked with white at other times.
It is found in shallow fresh and salt water wetlands and ponds in China and adjacent temperate and subtropical East Asia. Essentially a lowland bird, its range is delimited by the subarctic regions in the north, and by the mountain ranges in the west and south.
The species is prone to some vagrancy. One individual in breeding plumage was seen by the river at Bonzon near Gangaw – just inside the Chin State of Burma – west of the species' usual range, on April 8, 1995. A stray bird stopping over on Saint Paul Island, Alaska on August 4–9, 1997 was the first recorded occurrence of this species in North America.
Its food consists of insects, fish, and crustaceans. The Chinese pond heron often nests in mixed-species heronries. It lays a clutch of 3–6 blue-green eggs.
19-12-2015 MALACCA, MALAYA - EURASIAN TREE SPARROW (MALE) (Passer montanus)
The Eurasian tree sparrow (Passer montanus) is asmall passerine bird that breeds over most of temperate Eurasia and Southeast Asia, where it is known as the Tree sparrow. It has been introduced elsewhere including the United States, where it is known as the Eurasian tree sparrow or German sparrow to differentiate it from the native unrelated American tree sparrow.
The adult's crown and nape are rich chestnut, and there is a kidney-shaped black ear patch on each pure white cheek; the chin, throat, and the area between the bill and throat are black. The upperparts are light brown, streaked with black, and the brown wings have two distinct narrow white bars. The legs are pale brown, and the bill is lead-blue in summer, becoming almost black in winter. This sparrow is distinctive even within its genus in that it has no plumage differences between the sexes; the juvenile also resembles the adult, although the colors tend to be duller. Its contrasting face pattern makes this species easily identifiable in all plumages; the smaller size and brown, not grey, crown are additional differences from the male house sparrow. Adult and juvenile Eurasian tree sparrows undergo a slow complete molt in the autumn and show an increase in body mass despite a reduction in stored fat. The change in mass is due to an increase in blood volume to support active feather growth and generally higher water content in the body.
18-12-2015 LOMUT, MALAYSIA - CRAB EATING MACAQUE MONKEY (Macaca fascicularis)
The crab-eating macaque (Macaca fascicularis), also known as the long-tailed macaque and referred to as the cynomolgus monkey in laboratories, is a cercopithecine primate native to Southeast Asia. A species of macaque, the crab-eating macaque has a long history alongside humans. The species has been variously seen as an agricultural pest, a sacred animal, and, more recently, the subject of medical experiments.
The crab-eating macaque lives in matrilineal social groups of up to eight individuals dominated by females.they reach puberty. It is an opportunistic omnivore and has been documented using tools to obtain food in Thailand and Myanmar. The crab-eating macaque is a known invasive species and a threat to biodiversity in several locations, including Hong Kong and western New Guinea. The significant overlap in macaque and human living space has resulted in greater habitat loss, synanthropic living, and inter- and intraspecies conflicts over resources.
Macaca comes from the Portuguese word macaco, which was derived from makaku, a word in Ibinda, a language of Central Africa (kaku means monkey in Ibinda). The specific epithet fascicularis is Latin for a small band or stripe. Sir Thomas Raffles, who gave the animal its scientific name in 1821, did not specify what he meant by the use of this word.
In Indonesia and Malaysia, the crab-eating macaque and other macaque species are known generically as kera, possibly because of their high-pitched cries.
The crab-eating macaque has several common names. It is often referred to as the long-tailed macaque due to its tail, which is often longer than its body. The name crab-eating macaque refers to its being often seen foraging beaches for crabs. Another common name for M. fascicularis is the cynomolgus monkey, from the name of a race of humans with long hair and handsome beards who used dogs for hunting according to Aristophanes of Byzantium, who seemingly derived the etymology of the word cynomolgus from the Greek κύων, cyon 'dog' (gen. cyno-s) and the verb ἀμέλγειν, amelgein 'to milk' (adj. amolg-os), by claiming that they milked female dogs. This name is commonly used in laboratory settings.
The body length of the adult, which varies among subspecies, is 38–55 cm (15–22 in) with relatively short arms and legs. Males are considerably larger than females, weighing 5–9 kg (11–20 lb) compared to the 3–6 kg (6.6–13.2 lb) of females. The tail is longer than the body, typically 40–65 cm (16–26 in), which is used for balance when they jump distances up to 5 m (16 ft). The upper parts of the body are dark brown with light golden brown tips. The under parts are light grey with a dark grey/brown tail. Crab-eating macaques have backwards-directed crown hairs which sometimes form short crests on the midline. Their skin is black on their feet and ears, whereas the skin on the muzzle is a light grayish pink color. The eyelids often have prominent white markings and sometimes there are white spots on the ears. Males have a characteristic mustache and cheek whiskers, while females have only cheek whiskers. Crab-eating macaques have a cheek pouch which they use to store food while foraging. Females show no perineal swelling.
The crab-eating macaque's native range encompasses most of mainland Southeast Asia, from extreme southeastern Bangladesh south through the Malay Peninsula and Singapore, the Maritime Southeast Asia islands of Sumatra, Java, and Borneo, offshore islands, the islands of the Philippines, and the Nicobar Islands in the Bay of Bengal. This primate is a rare example of a terrestrial mammal that violates the Wallace line, being found out across the Lesser Sunda Islands. It lives in a wide variety of habitats, including primary lowland rainforests, disturbed and secondary rainforests, shrubland, and riverine and coastal forests of nipa palm and mangrove. It also easily adjusts to human settlements and is considered sacred at some Hindu temples and on some small islands, but as a pest around farms and villages. Typically, it prefers disturbed habitats and forest periphery.
The crab-eating macaque is an introduced alien species in several countries, including Hong Kong, Taiwan, West Papua, Papua New Guinea, New Britain, New Ireland, New Caledonia, Solomon Islands, Fiji, Tonga, Samoa, Nauru, Vanuatu, Pohnpei, Anggaur Island in Palau, and Mauritius. This has led the Invasive Species Specialist Group of the International Union for Conservation of Nature to list the crab-eating macaque as one of the "100 of the World's Worst Invasive Alien Species". In Mauritius, it is a threat for the endemic and endangered Roussea simplex, as it destroys its flowers. It also hinders germination of some endemic trees by destroying most of their fruits when unripe and competes with the endemic endangered Mauritian flying fox for native fruits.
Where it is not a native species, particularly on island ecosystems whose species often evolved in isolation from large predators, it is a documented threat to many native species. The immunovaccine porcine zona pellucida (PZP), which causes infertility in females, is currently being tested in Hong Kong to investigate its use as potential population control.
Macaques live in social groups that contain three to 20 females, their offspring, and one or many males. The groups usually have fewer males than females. In social groups of macaques, a clear dominance hierarchy is seen among females. These ranks remain stable throughout the female's lifetime and also can be sustained through generations of matrilines. Females have their highest birth rates around 10 years of age and completely stop bearing young by age 24.
The social groups of macaques are female-bonded, meaning the males will disperse at the time of puberty. Thus, group relatedness on average appears to be lower than compared to matrilines. More difference in relatedness occurs when comparing high-ranking lineages to lower ranking lineages, with higher-ranking individuals being more closely related to one another. Additionally, groups of dispersing males born into the same social groups display a range of relatedness, at times appearing to be brothers, while at other times appearing to be unrelated.
In addition to the matrilineal dominance hierarchy, male dominance rankings also exist. Alpha males have a higher frequency of mating compared to their lower-ranking conspecifics. The increased success is due partially to his increased access to females and also due to female preference of an alpha male during periods of maximum fertility. Though females have a preference for alpha males, they do display promiscuous behavior. Through this behavior, females risk helping to rear a non-alpha offspring, yet benefit in two specific ways, both in regard to aggressive behavior. First, a decreased value is placed on one single copulation. Moreover, the risk of infanticide is decreased due to the uncertainty of paternity.
Increasing group size leads to increased competition and energy spent trying to forage for resources, and in particular, food. Further, social tensions build and the prevalence of tension-reducing interactions like social grooming fall with larger groups. Thus, group living appears to be maintained solely due to the safety against predation.
Crab-eating macaques sometimes form mixed species groups with other primate species, including the southern pig-tailed macaque, dusky langur and white-thighed surili. They have been observed engaging in grooming with other primate species, including the southern pig-tailed macaque and leaf monkeys such as Raffles' banded langur and the dusty langur.
Group living in all species is dependent on the tolerance of other group members. In crab-eating macaques, successful social group living requires postconflict resolution. Usually, less dominant individuals lose to a higher-ranking individual when conflict arises. After the conflict has taken place, lower-ranking individuals tend to fear the winner of the conflict to a greater degree. In one study, this was seen in the ability to drink water together. Postconflict observations showed a staggered time between when the dominant individual begins to drink and the subordinate. Long-term studies reveal the gap in drinking time closes as the conflict moves further into the past.
Grooming and support in conflict among primates is considered to be an act of reciprocal altruism. In crab-eating macaques, an experiment was performed in which individuals were given the opportunity to groom one another under three conditions: after being groomed by the other, after grooming the other, and without prior grooming. After grooming took place, the individual that received the grooming was much more likely to support their groomer than one that had not previously groomed that individual. These results support the reciprocal altruism theory of grooming in long-tailed macaques.
Crab-eating macaques demonstrate two of the three forms of suggested postconflict behavior. In both captive and wild studies, the monkeys demonstrated reconciliation, or an affiliative interaction between former opponents, and redirection, or acting aggressively towards a third individual. Consolation was not seen in any study performed.
Postconflict anxiety has been reported in crab-eating macaques that have acted as the aggressor. After a conflict within a group, the aggressor appears to scratch itself at a higher rate than before the conflict. Though the scratching behavior cannot definitely be termed as an anxious behavior, evidence suggests this is the case. An aggressor's scratching decreases significantly after reconciliation. This suggests reconciliation rather than a property of the conflict is the cause of the reduction in scratching behavior. Though these results seem counterintuitive, the anxiety of the aggressor appears to have a basis in the risks of ruining cooperative relationships with the opponent.
18-12-2015 LOMUT, MALAYSIA - BROWN SHRIKE (Lanius cristatus)
The brown shrike (Lanius cristatus ) is a bird in the shrike family that is found mainly in Asia. It is closely related to the red-backed shrike (L. collurio ) and isabelline shrike (L. isabellinus ). The genus name, Lanius, is derived from the Latin word for "butcher", and some shrikes are also known as "butcher birds" because of their feeding habits. The specific cristatus is Latin for "crested", used in a broader sense than in English. The common English name "shrike" is from Old English scríc, "shriek", referring to the shrill call.
Like most other shrikes, it has a distinctive black "bandit-mask" through the eye and is found mainly in open scrub habitats, where it perches on the tops of thorny bushes in search of prey. Several populations of this widespread species form distinctive subspecies which breed in temperate Asia and migrate to their winter quarters in tropical Asia. They are sometimes found as vagrants in Europe and North America.
This shrike is mainly brown on the upper parts and the tail is rounded. The black mask can be paler in winter and has a white brow over it. The underside is creamy with rufous flanks and belly. The wings are brown and lack any white "mirror" patches. Females tend to have fine scalloping on the underside and the mask is dark brown and not as well marked as in the male. The distinction is not easy to use in the field but has been tested with breeding birds in Japan where the female can be identified from the presence of a brood patch. The use of multiple measurements allows discrimination of the sex of about 90% of the birds. Subspecies lucionensis has a grey crown shading into the brown upperparts and the rump appears more rufous than the rest of the upper back. The tail is more brownish and not as reddish as in the red-backed shrike. Younger birds of lucionensis have a brown crown and lack the grey on the head. Subspecies superciliosus has a broad white supercilium and a richer reddish crown. The tail is redder and tipped in white.
A number of confusing forms are known from central Asia where the populations of cristatus, isabellinus and collurio overlap. The taxonomy has been in a state of flux and some forms such as phoenicuroides formerly considered as subspecies of L. cristatus have been moved to the species L. isabellinus. Subspecies lucionensis has been recorded interbreeding with superciliosus in Ishikawa, Japan while superciliosus has interbred with Lanius tigrinus in central Japan.
18-12-2015 LOMUT, MALAYSIA - BRAHMINY KITE EAGLE (Haliastur indus)
Brahminy Kites have weak feet so, although they have long, sharp curved claws, they cannot take large prey. However they are expert at snatching prey in flight.
The Brahminy Kite is one of the medium-sized raptors (birds of prey), with a white head and breast. The rest of its body is a striking chestnut brown. The very tip of its tail is white. The wings are broad, with dark 'fingered' wing tips and the tail is short. The legs are short and not feathered, the eye is dark and the lemon yellow coloured bill is strongly hooked. It sails on level wings along shorelines and mudflats.
The Brahminy Kite is a bird of the coast, particularly mangrove swamps and estuaries. It is sometimes seen over forests and along rivers.
The Brahminy Kite is widespread across northern Australia, mainly along the coastline from Western Australia to northern New South Wales, and is more common in the north of its range. It is widespread throughout tropical Asia.
17-12-2015 LANGKAWI, MALAYSIA - WHITE BELLIED SEA EAGLE (Haliaeetus leucogaster)
The White-bellied sea eagle (Haliaeetus leucogaster) is a large diurnal bird of prey. Originally described by Johann Friedrich Gmelin in 1788, it is closely related to Sanford's sea eagle of the Solomon Islands, and the two are considered superspecies. The White-bellied sea eagle is revered by indigenous people in many parts of Australia, and is the subject of various folk tales throughout its range.
The White-bellied sea eagle has a white head, rump and underparts, and dark or slate-grey back and wings. In flight, the black flight feathers on the wings are easily seen when the bird is viewed from below. The large, hooked bill is a leaden blue-grey with a darker tip, and the irides are dark brown. The cere is also lead grey. The legs and feet are yellow or grey, with long black talons (claws). Unlike those of eagles of the genus Aquila, the legs are not feathered. The sexes are similar but like many raptors, the female is larger than the male. A young White-bellied sea eagle in its first year is predominantly brown, with pale cream-streaked plumage on their head, neck, nape, and rump areas. The plumage becomes more infiltrated with white until it acquires the complete adult plumage by the fourth or fifth year.
White-bellied sea eagles are found regularly from Mumbai eastwards in India, Bangladesh, and Sri Lanka in southern Asia, through all of coastal Southeast Asia including Burma, Thailand, Malaysia, Indonesia, Indochina, the main and offshore islands of the Philippines, and southern China including Hong Kong, Hainan, and Fuzhou, eastwards through New Guinea and the Bismarck Archipelago, and Australia. In the northern Solomons, they are restricted to Nissan Island. These birds occur mainly in coastal areas, islands, and estuaries but also in large inland water bodies, lakes, rivers, and wetlands. They usually breed near the water with some forest cover or in rocky areas.
White-bellied sea eagles are generally territorial; some birds form permanent pairs that inhabit territories throughout the year, while others are nomadic. Immature birds are generally dispersive, with many moving over 50 km (31 mi) away from the area they were raised. These birds are diurnal and often seen perched high in a tree or soaring over waterways and adjacent land. They spend time singly or in pairs. Small groups of White-bellied sea eagles sometimes gather if there is a plentiful source of food such as a carcass or fish offal on a ship. A pair may cooperate to hunt. During hunting the bird prepares for the strike by holding its feet far forward (almost under its chin) and then strikes backward while simultaneously beating its wings to lift upwards. They often catch a fish by flying low over the water and grasping it in its talons. Generally, only one foot is used to seize prey. White-bellied sea eagles may also dive at a 45-degree angle from their perch and briefly submerge to catch fish near the water's surface. These large birds of prey have a loud goose-like honking call which is heard particularly during the breeding season; pairs often honk in unison and often carry on for some time when perched. The male's call is higher-pitched and more rapid than that of the female.
17-12-2015 LANGKAWI, MALAYSIA - SOUTHEAST ASIAN WATER MONITOR (Varanus salvator ssp. macromaculatus)
The Asian water monitor (Varanus salvator) is a large varanid lizard native to South and Southeast Asia. It is one of the most common monitor lizards in Asia, ranging from coastal northeast India, Bangladesh, Sri Lanka, mainland Southeast Asia, and southern China to Indonesian islands where it lives close to water. It is listed as Least Concern on the IUCN Red List. It was described by Laurenti in 1768 and is among the largest squamates in the world.
Some common names for the species are Malayan water monitor, common water monitor, two-banded monitor, rice lizard, ring lizard, plain lizard, no-mark lizard and water monitor etc.
They are the world's second-heaviest lizard, after the Komodo dragon. Their bodies are muscular, with long, powerful, laterally compressed tails. The scales in this species are keeled; scales found on top of the head have been noted to be larger than those located on the back. Water monitors are often defined by their dark brown or blackish coloration with yellow spots found on their underside - these yellow markings have a tendency to disappear gradually with age. This species is also denoted by the blackish band with yellow edges extending back from each eye. These monitors have very long necks and an elongated snout. They use their powerful jaws, serrated teeth and sharp claws for both predation and defense.
In captivity, Asian water monitors' life expectancy has been determined to be anywhere between 11 and 25 years depending on conditions, in the wild it is considerably shorter.
The Asian water monitor is semiaquatic and opportunistic; it inhabits a variety of natural habitats though predominantly resides in primary forests and mangrove swamps. It has been noted that it is not deterred from living in areas near human civilization. In fact, it has been known to adapt and thrive in agricultural areas as well as cities with canal systems, such as in Sri Lanka, where they are not hunted or persecuted. Habitats that are considered to be most important are mangrove vegetation, swamps, wetlands, and elevations below 1,000 m (3,300 ft). It does not thrive in habitats with extensive loss of natural vegetation and aquatic resources.
The Asian water monitor is widely distributed from India, Bangladesh, Sri Lanka, Myanmar and Thailand, Cambodia, Laos, Vietnam, the Chinese Guangxi and Hainan provinces, Malaysia, Singapore to the Sunda islands Sumatra, Java, Bali, Borneo and Sulawesi. It inhabits primarily lowland freshwater and brackish wetlands. It has been recorded up to an elevation of 1,800 m (5,900 ft).
The Asian water monitor is semiaquatic and opportunistic; it inhabits a variety of natural habitats though predominantly resides in primary forests and mangrove swamps. It has been noted that it is not deterred from living in areas near human civilization. In fact, it has been known to adapt and thrive in agricultural areas as well as cities with canal systems, such as in Sri Lanka, where they are not hunted or persecuted. Habitats that are considered to be most important are mangrove vegetation, swamps, wetlands, and elevations below 1,000 m (3,300 ft). It does not thrive in habitats with extensive loss of natural vegetation and aquatic resources.
Water monitors defend themselves using their tails, claws, and jaws. They are excellent swimmers, using the raised fin on their tails to steer through water. When encountering smaller prey items, the water monitor will subdue it in its jaws and proceed to violently thrash its neck, destroying the prey's organs and spine which leaves it dead or incapacitated. The lizard will then swallow it whole.
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