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 - COMMON MYNA (Acridotheres tristis)

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 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.

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.

17-12-2015 LANGKAWI, MALAYSIA - PACIFIC SWALLOW (Hirundo tahitica)

The Pacific swallow (Hirundo tahitica ) is a small passerine bird in the swallow family. It breeds in tropical southern Asia and the islands of the south Pacific. It is resident apart from some local seasonal movements. This bird is associated with coasts, but is increasingly spreading to forested uplands. The hill swallow was formerly considered conspecific.

This species is a small swallow at 13 cm. It has a blue-black back and crown with browner wings and tail, a red face and throat, and dusky underparts. It differs from the barn swallow and the closely related welcome swallow in its shorter and less forked tail.

The Pacific swallow builds a neat cup-shaped nest, constructed with mud pellets collected in the beak, under a cliff ledge or on man-made structures such as a building, bridge or tunnel. The nest is lined with softer material, and the clutch is two to three eggs. It is similar in behaviour to other aerial insectivores, such as other swallows and the unrelated swifts. It is a fast flyer and feeds on insects, especially flies, while airborne.

The Pacific swallow (Hirundo tahitica) is a small passerine bird in the swallow family. It breeds in tropical southern Asia and the islands of the south Pacific. It is resident apart from some local seasonal movements. This bird is associated with coasts, but is increasingly spreading to forested uplands. The hill swallow and the welcome swallow were formerly considered conspecific.

The Pacific swallow was formally described in 1789 by the German naturalist Johann Friedrich Gmelin in his revised and expanded edition of Carl Linnaeus's Systema Naturae. He placed it with the swallows in the genus Hirundo and coined the binomial name Hirundo tahitica. Gmelin based his entry on the "Otaheite swallow" that had been described and illustrated in 1783 by the English ornithologist John Latham in his book A General Synopsis of Birds.

This species is a small swallow at 13 cm (5.1 in) in length. It has a blue-black back and crown with browner wings and tail, a red face and throat, and dusky underparts. It differs from the barn swallow and the closely related welcome swallow in its shorter and less forked tail.

The Pacific swallow builds a neat cup-shaped nest, constructed with mud pellets collected in the beak, under a cliff ledge or on man-made structures such as a building, bridge or tunnel. The nest is lined with softer material, and the clutch is two to three eggs. It is similar in behaviour to other aerial insectivores, such as other swallows and the unrelated swifts. It is a fast flyer and feeds on insects, especially flies, while airborne.

12-12-2015 JURONG, SINGAPORE - RADJAH SHELDUCK (Tadorna radjah)

The radjah shelduck (Radjah radjah ), is a species of shelduck found mostly in New Guinea and Australia, and also on some of the Moluccas. It is known alternatively as the raja shelduck, black-backed shelduck, or in Australia as the Burdekin duck.

Both the male and female of the species are mostly white, with dark wing-tips and a distinctive "collar" of dark feathers. Seen from above in flight the birds have green bands on the tops of their wings. The female has a harsh rattle and the male has a breathy, sore-throat whistle.

The radjah shelduck inhabits the mangrove forests and coastline of New Guinea (West Papua and Papua New Guinea) and Australia, and some of the Moluccas in eastern Indonesia. In Australia, its primary range is coastal tropical northern Australia, from central Queensland through northern Northern Territory (including Kakadu National Park) to the Kimberley in Western Australia. The radjah shelduck is listed as a protected bird in all states of Australia and penalties exist for harming or disturbing them.

The species prefers the brackish waters of mangrove flats and paperbark tree swamps, but will visit freshwater swamps, lagoons, and billabongs further inland during the wet season.

The radjah shelduck forms long-term pair-bonds, and is usually encountered in lone pairs or small flocks. During the wet season the males commonly become very irritable, and have been observed attacking their mates.

The diet consists mainly of mollusks, insects, sedge materials and algae. Pairs start searching for nesting sites during the months of January and February. They nest close to their primary food source, often in the hollow limbs of trees, which makes habitat destruction a particular issue.

The radjah shelduck does not use nesting materials except for some self-supplied down feathers. Egg-laying is usually done by May or June, but depends on the extent of the wet season. The clutches range from 6 to 12 eggs. Incubation time is about 30 days.

12-12-2015 BAGAN, MYANMAR - COMMON MYNA (Acridotheres tristis)

The common myna or Indian myna (Acridotheres tristis), sometimes spelled mynah, is a bird in the family Sturnidae, native to Asia. An omnivorous open woodland bird with a strong territorial instinct, the common myna has adapted extremely well to urban environments.

The range of the common myna is increasing at such a rapid rate that in 2000 the IUCN Species Survival Commission declared it one of the world's most invasive species and one of only three birds listed among "100 of the World's Worst Invasive Species" that pose a threat to biodiversity, agriculture and human interests. In particular, the species poses a serious threat to the ecosystems of Australia, where it was named "The Most Important Pest/Problem" in 2008.

The common myna is readily identified by the brown body, black hooded head and the bare yellow patch behind the eye. The bill and legs are bright yellow. There is a white patch on the outer primaries and the wing lining on the underside is white. The sexes are similar and birds are usually seen in pairs.

The common myna obeys Gloger's rule in that the birds from northwestern India tend to be paler than their darker counterparts in southern India.

The common myna is native to Asia, with its initial home range spanning Iran, Pakistan, India, Nepal, Bhutan, Bangladesh and Sri Lanka, Afghanistan, Uzbekistan, Tajikistan, Turkmenistan, Myanmar, Malaysia, Singapore, peninsular Thailand, Indochina, Japan (both mainland Japan and the Ryukyu Islands) and China.

The common myna has been introduced to many other parts of the world such as Canada, Australia, Israel, New Zealand, New Caledonia, Fiji, the United States (South Florida only, South Africa, Kazakhstan, Kyrgyzstan Uzbekistan, the Cayman Islands, islands in the Indian Ocean (the Seychelles – from which it was subsequently eradicated at great expense, Mauritius, Réunion, Madagascar, the Maldives, the Andaman and Nicobar Islands and the Lakshadweep archipelago) and also in islands of the Atlantic (such as Ascension and Saint Helena, Pacific Ocean and Cyprus February 2022.

11-12-2015 BAGAN, MYANMAR - HOUSE SPARROW (MALE) (Passer domesticus)

17-12-2015 LANGKAWI, MALAYSIA - BRAHMINY KITE EAGLE (Haliastur indus)

15-12-2015 PHUKET,THAILAND - EURASIAN TREE SPARROW (MALE) (Passer montanus)

8-12-2015 KUALA LUMPUR, MALAYSIA - YELLOW BILLED STORK (Mycteria ibis)

The yellow-billed stork (Mycteria ibis), sometimes also called the wood stork or wood ibis, is a large African wading stork species in the family Ciconiidae. It is widespread in regions south of the Sahara and also occurs in Madagascar.

The yellow-billed stork (Mycteria ibis ), sometimes also called the wood stork or wood ibis, is a large African wading stork species in the family Ciconiidae. It is widespread in regions south of the Sahara and also occurs in Madagascar.

The yellow-billed stork has appeared on postage stamps in several African countries.

The yellow-billed stork is closely related to three other species in the genus Mycteria: the American woodstork (Mycteria americana), the milky stork (Mycteria cinerea) and the painted stork (Mycteria leucocephala). It is classified as belonging to one clade with these three other species because they all display remarkable homologies in behavior and morphology. In one analytical study of feeding and courtship behaviours of the wood-stork family, M.P. Kahl attributed the same general ethology to all members of the genus Mycteria, with relatively few species-specific variations. These four species are collectively referred to as the wood-storks, which should not be confused with one alternative common name (wood-stork) for the yellow-billed stork.

Before it was established that the yellow-billed stork was closely related to the American wood stork, the former was assigned to the genus Ibis, together with the milky stork and painted stork. However, the yellow-billed stork has actually long been recognised as a true stork and along with the other 3 related stork species, it should not strictly be called an ibis.

This medium-sized stork stands 90–105 cm (35–41 in) tall. Its body is white with a short black tail that is glossed green and purple when freshly moulted. The bill is deep yellow, slightly decurved at the end and with a rounder cross-section than in other stork species outside the Mycteria. Feathers extend onto the head and neck just behind the eyes, with the face and forehead being covered by deep red skin. Both sexes are similar in appearance, but the male is larger and has a slightly longer heavier bill. Males and females weigh approximately 2.3 kg (5.1 lb) and 1.9 kg (4.2 lb) respectively.

Colouration becomes more vivid during the breeding season. In the breeding season, the plumage is coloured pink on the upperwings and back; the ordinarily brown legs also turn bright pink; the bill becomes a deeper yellow and the face becomes a deeper red.

Juveniles are greyish-brown with a dull, partially bare orange face and a dull yellowish bill. The legs and feet are brown and feathers are blackish-brown all over. At fledging, salmon-pink colouration in the underwings begins to develop and after about one year, the plumage is greyish-white. Flight feathers on the tail and wing also become black. Later, the pink colouration typical of adult plumage appears.

These storks walk with a high-stepped stalking gait on the ground of shallow water. Their approximate walking rate has been recorded as 70 steps per minute. They fly with alternating flaps and glides, with the speed of their flaps averaging 177–205 beats per minute. They usually flap only for short journeys and often fly in a soaring and gliding motion over several kilometres for locomotion between breeding colonies or roosts and feeding sites. By soaring on thermals and gliding by turns, they can cover large distances without wasting much energy. On descending from high altitudes, this stork has been observed to dive deeply at high speeds and flip over and over from side to side, hence showing impressive aerobatics. It even appears to enjoy these aerial stunts.

This species is generally non-vocal, but will utter hissing falsetto screams during social displays in the breeding season. These storks also engage in bill clattering and an audible “woofing” wing beat at breeding colonies Nestlings make a loud continual monotonous braying call to beg parental adults for food.

The yellow-billed stork occurs primarily in Eastern Africa,but is widely distributed in areas extending from Senegal and Somalia down to South Africa and in some regions of western Madagascar. During one observation of a mixed species bird colony on the Tana River in Kenya, it was found to be the commonest species there, with 2000 individuals being counted at once.

The species does not generally migrate far, at least not outside its breeding range; but does usually make short migratory movements which are influenced by rainfall. It makes local movements in Kenya and has also been found to migrate from North to South Sudan with the rainy season. It may also migrate regularly to and from South Africa. However, little is actually known about this bird's general migratory movements. Due to apparent observed variation in migratory patterns throughout Africa, the yellow-billed stork has been termed a facultative nomad. It may migrate simply to avoid areas where water or rainfall conditions are unfavourable for feeding on prey. Some populations migrate considerable distances between feeding or breeding sites; usually by using thermals to soar and glide. Other local populations have been found to be sedentary and remain in their respective habitats all year round.

Preferred habitats include wetlands, shallow lakes and mudflats, usually 10–40 cm deep[4] but it usually avoids heavily forested regions in central Africa. It also avoids flooded regions and deep expansive bodies of water because feeding conditions there are unsuitable for their typical grope and stir feeding techniques.

This species breeds especially in Kenya and Tanzania. Although it is known to breed in Uganda, breeding sites have not been recorded there. It has been found to breed also in Malakol in Sudan and often inside walled cities in West Africa from Gambia down to northern Nigeria. Still other breeding sites include Zululand in South Africa and northern Botswana, but are rarer below northern Botswana and Zimbabwe where sites are well-watered. Although there is no direct evidence of current breeding in Madagascar, young birds unable to fly have been observed near Lake Kinkony during October.

This stork's diet mainly comprises small, freshwater fish of about 60-100mm length and maximally 150g, which they swallow whole. They also feed on crustaceans, worms, aquatic insects, frogs and occasionally small mammals and birds.

This species appears to rely principally on sense of touch to detect and capture prey, rather than by vision. They feed patiently by wading through the water with partially open bills, probing for prey at intervals. Contact of the bill with a prey item prompts a rapid snap-bill reflex, whereby the bird snaps shut its mandibles, raises its head and swallows the prey whole. The speed of this reflex in the closely related American woodstork (Mycteria americana) has been recorded as 25 milliseconds and although the corresponding reflex in the yellow-billed stork has not been quantitatively measured, the yellow-billed stork's feeding mechanism appears to be at least qualitatively identical to that of the American wood stork.

In addition to the snap-bill reflex, the yellow-billed stork also uses a systematic foot stirring technique to sound out evasive prey. It prods and churns up the bottom of the water as part of a “herding mechanism” to force prey out of the bottom vegetation and into the bird's bill. The bird does this several times with one foot before bringing it forwards and repeating with the other foot. Although they are normally active predators, they have also been observed to scavenge fish regurgitated by cormorants.

The yellow-billed stork has been observed to follow moving crocodiles or hippopotami through the water and feed behind them, appearing to take advantage of organisms churned up by their quarry. Feeding lasts for only a short time before the bird obtains its requirements and proceeds to rest again.

Parents feed their young by regurgitating fish onto the nest floor, whereupon it is picked up and consumed by the nestlings. The young eat voraciously and an individual nestling increases its body weight from 50 grams to 600 grams during the first ten days of its life. Hence, this species has earned the German colloquial common name “Nimmersatt”; meaning “never full”.

8-12-2015 KUALA LUMPUR, MALAYSIA - YELLOW BILLED STORK (JUVENILE) (Mycteria ibis)

They can snap their beaks shut in just 0.025 seconds. Storks will nest in groups in trees, sometimes with other species. Storks regurgitate water over their babies to keep them cool, and to encourage water intake.

Yellow-billed Stork - Birds of South Africa

They nest in colonies in trees, often along with other species of birds such as cormorants or African Spoonbills. The location of the nest site is normally chosen by the male and can the nest can take up to 10 days to build. Up to 3 eggs may be laid. In captivity the Yellow-billed Stork can live for up to 30 years.

Yellow-billed storks live in much of sub-Saharan Africa. They prefer wetland habitats such as swamps, estuaries, riverbanks, rice paddies, lagoons, and mudflats. They are sometimes also found in savanna woodland.

Yellow-billed storks are adaptive and intelligent. They have a fishing technique of using one foot to stir up the water to flush out prey. A quick muscular reflex in the neck enables yellow-billed storks to catch almost all of their food in the water. These storks do not socialize much with one another and tend to isolate themselves in swamps, muddy rivers and marshes. They breed nearly year round. The male chooses the location of the nest and works with the female to build it in 7-10 days. Two or three eggs are laid one at a time, two days apart, so the chicks hatch on different days about a month later.

8-12-2015 KUALA LUMPUR, MALAYSIA - BLACK CROWNED NIGHT HERON (Nycticorax nycticorax)

The black-crowned night-heron (Nycticorax nycticorax), or black-capped night-heron, commonly shortened to just night-heron in Eurasia, is a medium-sized heron found throughout a large part of the world, including parts of Europe, Asia, and North and South America. In Australasia it is replaced by the closely related nankeen night-heron (N. caledonicus), with which it has hybridized in the area of contact.

The black-crowned night-heron was formally described by the Swedish naturalist Carl Linnaeus in 1758 in the tenth edition of his Systema Naturae. He placed it with herons, cranes and egrets in the genus Ardea and coined the binomial name Ardea nicticorax. It is now placed in the genus Nycticorax that was introduced in 1817 by the English naturalist Thomas Forster for this species. The epithet nycticorax is from Ancient Greek and combines nux, nuktos meaning "night" and korax meaning "raven". The word was used by authors such as Aristotle and Hesychius of Miletus for a "bird of ill omen", perhaps an owl. The word was used by the Swiss naturalist Conrad Gessner in 1555 and then by subsequent authors for a black-crowned night-heron.

Adults have a black crown and back with the remainder of the body white or grey, red eyes, and short yellow legs. They have pale grey wings and white under parts. Two or three long white plumes, erected in greeting and courtship displays, extend from the back of the head. The sexes are similar in appearance although the males are slightly larger. Black-crowned night-herons do not fit the typical body form of the heron family. They are relatively stocky with shorter bills, legs, and necks than their more familiar cousins, the egrets and "day" herons. Their resting posture is normally somewhat hunched but when hunting they extend their necks and look more like other wading birds.

Immature birds have dull grey-brown plumage on their heads, wings, and backs, with numerous pale spots. Their underparts are paler and streaked with brown. The young birds have orange eyes and duller yellowish-green legs. They are very noisy birds in their nesting colonies, with calls that are commonly transcribed as quok or woc.

Measurements:

Length: 22.8–26 in (58–66 cm)

Weight: 25.6–35.8 oz (726–1,015 g)

Wingspan: 45.3–46.5 in (115–118 cm)

The breeding habitat is fresh and salt-water wetlands throughout much of the world. The subspecies N. n. hoactli breeds in North and South America from Canada as far south as northern Argentina and Chile, N. n. obscurus in southernmost South America, N. n. falklandicus in the Falkland Islands, and the nominate race N. n. nycticorax in Europe, Asia and Africa. Black-crowned night-herons nest in colonies on platforms of sticks in a group of trees, or on the ground in protected locations such as islands or reedbeds. Three to eight eggs are laid.

This heron is migratory in the northernmost part of its range, but otherwise resident (even in the cold Patagonia). The North American population winters in Mexico, the southern United States, Central America, and the West Indies, and the Old World birds winter in tropical Africa and southern Asia.

A colony of the herons has regularly summered at the National Zoo in Washington, D.C. for more than a century. The birds also prominently live year-round in the shores around the San Francisco Bay, with the largest rookery in Oakland. Their ever presence at Oakland's Lake Merritt and throughout the city's downtown area, as well as their resilience to the urban environment and displacement efforts, have led to them being named Oakland's official city bird.

8-12-2015 KUALA LUMPUR, MALAYSIA - SPOTTED WOOD OWL (Strix seloputo)

The spotted wood owl (Strix seloputo) is an owl of the earless owl genus, Strix. Its range is disjunct; it occurs in many regions surrounding Borneo, but not on that island itself.

The spotted wood owl grows to a length of about 44 to 48 cm (17 to 19 in) with a wing length of 30 to 36 cm (12 to 14 in). The head is chocolate brown with an orangish-buff facial disc and, in the nominate subspecies, a yellowish throat band, but there are no ear-tufts. The upper parts are coffee-coloured, with white bars and spots edged with black. The underparts are dull yellow with broad white and narrow black bars. The eye is dark brown and the beak greenish-black. The legs and toes are well-feathered, with the visible parts being olive. The call is a rolling "huhuhu" followed by a long "whoo".

There are three subspecies: Strix seloputo seloputo occurs in South Myanmar and central Thailand to Singapore as well as Jambi (Sumatra) and Java; Strix seloputo baweana is endemic to the island of Bawean off North Java; Strix seloputo wiepkini occurs in the Calamian Islands and Palawan (Philippines). Typical habitats include lowland forest, mangrove swamps, cleared woodland, plantations, and parks in towns and villages.

The diet of this owl consists mainly of mice and rats, supplemented by insects and small birds.

The spotted wood owl has a very wide range, and is described as being common in some areas. The population size has not been quantified but it seems to be stable, and the International Union for Conservation of Nature has assessed the bird's conservation status as being of "least concern".

8-12-2015 KUALA LUMPUR - ROSE RINGED PARAKEET (Psittacula krameri)

Since the 19th century, the rose-ringed parakeet has successfully colonised many other countries. It breeds further north than any other parrot species. It has established itself on a large scale in Germany, France, Belgium, the Netherlands, Italy, and the UK. 

The analyses show that the risk of parakeet establishment may rise further as a result of decreasing frost days due to global warming, rising urbanization, and rising human populations. Because of the significant separate parakeet imports in Europe, researchers are capable of investigating the widely held hypothesis of climate matching and human activity at the species level.

In the wild, rose-ringed parakeets usually feed on buds, fruits, vegetables, nuts, berries, and seeds. Wild flocks also fly several miles to forage in farmlands and orchards, causing extensive damage. Feral parakeets will regularly visit gardens and other locations near human habitation, taking food from bird feeders.

In India, they feed on cereal grains, and during winter also on pigeon peas. In Egypt during the spring, they feed on mulberry and in summer they feed on dates and nest inside palm trees and eat from sunflower and corn fields.

In captivity, rose-ringed parakeets will take a large variety of food and can be fed on a number of fruits, vegetables, pellets, seeds, and even small amounts of cooked meat for protein. Oils, salts, chocolate, alcohol, and other preservatives should be avoided.

In northwestern India, Indian rose-ringed parakeets form pairs from September to December. They do not have life mates and often breed with another partner during the following breeding season. During this cold season, they select and defend nest sites, thus avoiding competition for sites with other birds. Feeding on winter pea crops provides the female with nutrients necessary for egg production. From April to June, they care for their young. Fledglings are ready to leave the nest before monsoon.

Seasonal changes in testicular activity, plasma luteinizing hormone (LH), estradiol (E2), testosterone (T), and 5 α-dihydrotestosterone (5 α-DHT) were related to pair bond formation, nest building, nest defense, and parental behavior in free living Indian rose-ringed parakeets in northwest India. The parakeets are able to reproduce in the winter because it allows them to avoid competing with other birds for nesting places, postpone having young during the monsoon season, and take use of the winter pea harvest, which provides the female with extra nutrients for egg formation.

8-12-2015 KUALA LUMPUR, MALAYSIA - GREATER FLAMINGO (Phoenicopterus roseus)

The Greater flamingo (Phoenicopterus roseus) is the most widespread and largest species of the flamingo family. It was described by Peter Simon Pallas in 1811. The Greater flamingo was previously thought to be the same species as the American flamingo, but because of coloring differences of its head, neck, body, and bill, the two flamingos are now most commonly considered separate species.

Greater flamingos have an attractive coloration and appearance. Their feathers are pinkish/white, the wing coverts are red and the primary and secondary flight feathers are black. They have long pink bills with a black tip, yellow eyes and long pink legs. The male is bigger than the female, and juveniles have a gray-brown coloration, with some pink on their underparts, tail and wings, with the legs and beak being mainly brown.

The Greater flamingo inhabits Africa, the Middle East, southern Europe, and the Indian subcontinent. They occur in relatively shallow water bodies, such as saline lagoons, salt pans, large alkaline or saline lakes, and estuaries. Breeding takes place on sandbanks, mudflats, sandy or rocky islands, or open beaches.