Sunday, September 1, 2019

THE MARBLED CAT

The marbled cat (Pardofelis marmorata) is a small wild cat native from the eastern Himalayas to Southeast Asia, where it inhabits forests up to 2,500 m (8,200 ft) altitude. As it is present in a large range, it has been listed as Near Threatened on the IUCN Red List since 2015.[2]
The marbled cat was once considered to belong to the pantherine lineage of cats.[3] It is closely related to the Asian golden cat (Catopuma temminckii) and the bay cat (C. badia), all of which diverged from other felids about 9.4 million years ago.[4]

Marbled cat borneo.jpg

Characteristics

The marbled cat is similar in size to a domestic cat, but has rounded ears and a very long tail that is as long as the cat's head and body. The ground colour of its long fur varies from brownish-grey to ochreous brown above and greyish to buff below. It is patterned with black stripes on the short and round head, on the neck and back. On the tail, limbs and underbelly it has solid spots. On the flanks it has irregular dark-edged blotches that fuse to dark areas and look like a 'marbled' pattern. Its paws are webbed between the digits and are completely sheathed.[5] Its coat is thick and soft. Spots on the forehead and crown merge into narrow longitudinal stripes on the neck, and irregular stripes on the back. The legs and underparts are patterned with black dots, and the tail is marked with black spots proximally and rings distally. It has large feet and unusually large canine teeth, resembling those of the big cats, although these appear to be the result of parallel evolution. Marbled cats range from 45 to 62 cm (18 to 24 in) in head-body length with a 35 to 55 cm (14 to 22 in) long and thickly furred tail that indicates the cat's adaptation to an arboreal lifestyle, where the tail is used as a counterbalance. Recorded weights vary between 2 and 5 kg (4.4 and 11.0 lb).[6]

Distribution and habitat

The marbled cat occurs along the eastern Himalayan foothills and in tropical Indomalaya eastward into southwest China, and on the islands of Sumatra and Borneo. It is primarily associated with moist and mixed deciduous-evergreen tropical forests. Its distribution in India is confined to the north-eastern forests.[2]
In eastern Nepal, a marbled cat was recorded for the first time in January 2018, outside a protected area in the Kangchenjunga landscape at an altitude of 2,750 m (9,020 ft).[7]
In northeast India, marbled cats were recorded in Eaglenest Wildlife Sanctuary, Dampa and Pakke Tiger Reserves, Balpakram-Baghmara landscape and Singchung-Bugun Village Community Reserve in Arunachal Pradesh between January 2013 and March 2018.[8]
In Bhutan, it has been recorded in Royal Manas National Park, and in broadleaved and mixed conifer forests at elevations up to 3,810 m (12,500 ft) in Jigme Dorji National Park and Wangchuck Centennial National Park.[9][10][11]
In Thailand, it was recorded in a hill evergreen bamboo mixed forest in Phu Khieu Wildlife Sanctuary.[12]
In Borneo, it has also been recorded in peat swamp forest.[13] The population size of the marbled cat is not well understood. Few records were obtained during camera-trapping surveys throughout much of its range. In three areas in Sabah, the population density was estimated at 7.1 to 19.6 individuals per 100 km2 (39 sq mi), an estimate that may be higher than elsewhere in the cat's range.[14] In Kalimantan, marbled cats were recorded in mixed swamp forest and tall interior forest at altitudes below 20 m (66 ft) in the vicinity of Sabangau National Park between 2008 and 2018.[15]

Behaviour and ecology

Marbled cats recorded in northeastern India and Kalimantan on Borneo were active by day.[8][15]
The first-ever radio-tracked marbled cat had an overall home range of 5.8 km2 (2.2 sq mi) at an elevation of 1,000 to 1,200 m (3,300 to 3,900 ft) and was active primarily during nocturnal and crepuscular times.[12] Marbled cats recorded in northeast India were active during the day with activity peaks around noon.[8]
Forest canopies probably provide the marbled cat with much of its prey: birds, squirrels and other rodents, and reptiles.[6] In the Bukit Barisan Selatan National Park, a marbled cat was observed in a dense forest patch in an area also used by siamang.[16] In Thailand, one individual has been observed in Phu Khieo Wildlife Sanctuary preying on a Phayre's leaf monkey.[17]
A few marbled cats have been bred in captivity, with gestation estimated to be 66 to 82 days. In the few recorded instances, two kittens were born in each litter, and weighed from 61 to 85 g (2.2 to 3.0 oz). Their eyes open at around 12 days, and the kittens begin to take solid food at two months, around the time that they begin actively climbing. Marbled cats reach sexual maturity at 21 or 22 months of age, and have lived for up to 12 years in captivity.[6]

Threats

Indiscriminate snaring is prevalent throughout much of its range, and likely poses a major threat. It is valued for its skin, meat, and bones, but infrequently observed in the illegal Asian wildlife trade.[2] During a survey in the Lower Subansiri District of Arunachal Pradesh, a marbled cat was encountered that had been killed by a local hunter for a festival celebrated by the indigenous Apatani community in March and April every year. The dead cat was used in a ceremony, and its blood was sacrificed to the deity for goodwill of their family and for ensuring a good harvest, protection from wildlife, disease and pest.[18] Deforestation is a further threat to the marbled cat.[2]

Conservation

Pardofelis marmorata is included in CITES Appendix I and protected over parts of its range. Hunting is prohibited in Bangladesh, Cambodia, Yunnan, India, Indonesia, Malaysia, Myanmar, Nepal, and Thailand. Hunting is regulated in Laos and Singapore. In Bhutan and Brunei, the marbled cat is not legally protected outside protected areas. No information about protection status is available from Cambodia and Vietnam.[19]

Taxonomy

Felis marmorata was the scientific name proposed by William Charles Linnaeus Martin in 1836 for a skin of a male marbled cat from Java or Sumatra.[20] Felis longicaudata proposed by Henri Marie Ducrotay de Blainville in 1843 was a zoological specimen from India or Cochinchina.[21] Felis charltoni proposed by John Edward Gray in 1846 was a specimen from Darjeeling.[22] The generic name Pardofelis was proposed by Nikolai Severtzov in 1858.[23]
At present, two subspecies are recognized as valid:[24]
  • P. marmorata marmorata (Martin, 1836) – from the Malay Peninsula to Sumatra and Borneo
  • P. marmorata longicaudata (Blainville, 1843) – from Nepal to north of the Isthmus of Kra

Phylogeny

Results of a phylogenetic analysis indicate that the marbled cat diverged between 8.42 and 4.27 million years ago. Together with the Asian golden cat (Catopuma temminckii) and the bay cat (C. badia), it forms an evolutionary lineage that diverged between 12.77 and 7.36 million years ago.[4][25]





Pardofelis marmorata[1]
(Martin, 1836)


MarbledCat distribution.jpg 




 Distribution of Marbled cat, 2016[2]



















 

THE COMMON BLACKBIRD

The common blackbird (Turdus merula) is a species of true thrush. It is also called Eurasian blackbird (especially in North America, to distinguish it from the unrelated New World blackbirds),[2] or simply blackbird where this does not lead to confusion with a similar-looking local species. It breeds in Europe, Asia, and North Africa, and has been introduced to Australia and New Zealand.[3] It has a number of subspecies across its large range; a few of the Asian subspecies are sometimes considered to be full species. Depending on latitude, the common blackbird may be resident, partially migratory, or fully migratory.
The adult male of the nominate subspecies, which is found throughout most of Europe, is all black except for a yellow eye-ring and bill and has a rich, melodious song; the adult female and juvenile have mainly dark brown plumage. This species breeds in woods and gardens, building a neat, mud-lined, cup-shaped nest. It is omnivorous, eating a wide range of insects, earthworms, berries, and fruits.
Both sexes are territorial on the breeding grounds, with distinctive threat displays, but are more gregarious during migration and in wintering areas. Pairs stay in their territory throughout the year where the climate is sufficiently temperate. This common and conspicuous species has given rise to a number of literary and cultural references, frequently related to its song.
Common Blackbird.jpg
 Male T. m. merula

Taxonomy and systematics


 Common blackbird (Turdus merula mauretanicus) female.jpg
 Female T. m. mauretanicus


The common blackbird was described by Linnaeus in the 10th edition of his Systema Naturae in 1758 as Turdus merula (characterised as T. ater, rostro palpebrisque fulvis).[4] The binomial name derives from two Latin words, turdus, "thrush", and merula, "blackbird", the latter giving rise to its French name, merle,[5] and its Scots name, merl.[6]
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 blackbird is descended from ancestors that had colonised the Caribbean islands from Africa and subsequently reached Europe from there.[7] It is close in evolutionary terms to the island thrush (T. poliocephalus) of Southeast Asia and islands in the southwest Pacific, which probably diverged from T. merula stock fairly recently.[8]
It may not immediately be clear why the name "blackbird", first recorded in 1486, was applied to this species, but not to one of the various other common black English birds, such as the carrion crow, raven, rook, or jackdaw. However, in Old English, and in modern English up to about the 18th century, "bird" was used only for smaller or young birds, and larger ones such as crows were called "fowl". At that time, the blackbird was therefore the only widespread and conspicuous "black bird" in the British Isles.[9] Until about the 17th century, another name for the species was ouzel, ousel or wosel (from Old English osle, cf. German Amsel). Another variant occurs in Act 3 of Shakespeare's A Midsummer Night's Dream, where Bottom refers to "The Woosell cocke, so blacke of hew, With Orenge-tawny bill". The ouzel usage survived later in poetry, and still occurs as the name of the closely related ring ouzel (Turdus torquatus), and in water ouzel, an alternative name for the unrelated but superficially similar white-throated dipper (Cinclus cinclus).[10]
Juvenile T. m. merula in England
Young adult T. m. merula in Oxfordshire
A leucistic adult male in England with much white in the plumage
T. m. cabrerae on Gran Canaria, Canary Islands, Spain
Two related Asian Turdus thrushes, the white-collared blackbird (T. albocinctus) and the grey-winged blackbird (T. boulboul), are also named blackbirds,[8] and the Somali thrush (T. (olivaceus) ludoviciae) is alternatively known as the Somali blackbird.[11]
The icterid family of the New World is sometimes called the blackbird family because of some species' superficial resemblance to the common blackbird and other Old World thrushes, but they are not evolutionarily close, being related to the New World warblers and tanagers.[12] The term is often limited to smaller species with mostly or entirely black plumage, at least in the breeding male, notably the cowbirds,[13] the grackles,[14] and for around 20 species with "blackbird" in the name, such as the red-winged blackbird and the melodious blackbird.[12]

Subspecies

As would be expected for a widespread passerine bird species, several geographical subspecies are recognised. The treatment of subspecies in this article follows Clement et al. (2000).[8]
Female of subspecies merula
  • T. m. merula, the nominate subspecies, breeds commonly throughout much of Europe from Iceland, the Faroes and the British Isles east to the Ural Mountains and north to about 70 N, where it is fairly scarce. A small population breeds in the Nile Valley. Birds from the north of the range winter throughout Europe and around the Mediterranean including Cyprus and North Africa. The introduced birds in Australia and New Zealand are of the nominate race.[8]
  • T. m. azorensis is a small race which breeds in the Azores. The male is darker and glossier than merula.[15]
  • T. m. cabrerae, named for Ángel Cabrera, Spanish zoologist, resembles azorensis and breeds in Madeira and the western Canary Islands.[15]
  • T. m. mauretanicus, another small dark species with a glossy black male plumage, breeds in central and northern Morocco, coastal Algeria and northern Tunisia.[15]
  • First-summer male, probably subspecies aterrimus
  • T m. aterrimus breeds in Hungary, south and east to southern Greece, Crete northern Turkey and northern Iran. It winters in southern Turkey, northern Egypt, Iraq and southern Iran. It is smaller than merula with a duller male and paler female plumage.[15]
  • T. m. syriacus breeds on the Mediterranean coast of southern Turkey south to Jordan, Israel and the northern Sinai. It is mostly resident, but part of the population moves south west or west to winter in the Jordan Valley and in the Nile Delta of northern Egypt south to about Cairo. Both sexes of this subspecies are darker and greyer than the equivalent merula plumages.[8]
  • T. m. intermedius is an Asiatic race breeding from Central Russia to Tajikistan, western and north east Afghanistan, and eastern China. Many birds are resident but some are altitudinal migrants and occur in southern Afghanistan and southern Iraq in winter.[8] This is a large subspecies, with a sooty-black male and a blackish-brown female.[16]
The Asian subspecies, the relatively large intermedius also differs in structure and voice, and may represent a distinct species.[16] Alternatively, it has been suggested that they should be considered subspecies of T. maximus,[8] but they differ in structure, voice and the appearance of the eye-ring.[16][17]

Similar species

In Europe, the common blackbird can be confused with the paler-winged first-winter ring ouzel (Turdus torquatus) or the superficially similar European starling (Sturnus vulgaris).[18] A number of similar Turdus thrushes exist far outside the range of the common blackbird, for example the South American Chiguanco thrush (Turdus chiguanco).[19] The Indian blackbird, the Tibetan blackbird, and the Chinese blackbird were formerly considered subspecies.[20]

Description

The common blackbird of the nominate subspecies T. m. merula is 23.5 to 29 centimetres (9.25 to 11.4 in) in length, has a long tail, and weighs 80–125 grams (2.8 to 4.4 oz). The adult male has glossy black plumage, blackish-brown legs, a yellow eye-ring and an orange-yellow bill. The bill darkens somewhat in winter.[18] The adult female is sooty-brown with a dull yellowish-brownish bill, a brownish-white throat and some weak mottling on the breast. The juvenile is similar to the female, but has pale spots on the upperparts, and the very young juvenile also has a speckled breast. Young birds vary in the shade of brown, with darker birds presumably males.[18] The first year male resembles the adult male, but has a dark bill and weaker eye ring, and its folded wing is brown, rather than black like the body plumage.[8]

Distribution and habitat

The common blackbird breeds in temperate Eurasia, North Africa, the Canary Islands, and South Asia. It has been introduced to Australia and New Zealand.[8] Populations are sedentary in the south and west of the range, although northern birds migrate south as far as northern Africa and tropical Asia in winter.[8] Urban males are more likely to overwinter in cooler climes than rural males, an adaptation made feasible by the warmer microclimate and relatively abundant food that allow the birds to establish territories and start reproducing earlier in the year.[21] Recoveries of blackbirds ringed on the Isle of May show that these birds commonly migrate from southern Norway ( or from as far north as Trondheim) to Scotland, and some onwards to Ireland. Scottish-ringed birds have also been recovered in England, Belgium, Holland, Denmark, and Sweden[22]. Female blackbirds in Scotland and the north of England migrate more (to Ireland) in winter than do the males[23]
Common over most of its range in woodland, the common blackbird has a preference for deciduous trees with dense undergrowth. However, gardens provide the best breeding habitat with up to 7.3 pairs per hectare (nearly three pairs per acre), with woodland typically holding about a tenth of that density, and open and very built-up habitats even less.[24] They are often replaced by the related ring ouzel in areas of higher altitude.[25] The common blackbird also lives in parks, gardens and hedgerows.[26]
The common blackbird occurs up to 1000 metres (3300 ft) in Europe, 2300 metres (7590 ft) in North Africa, and at 900–1820 metres (3000–6000 ft) in peninsular India and Sri Lanka, but the large Himalayan subspecies range much higher, with T. m. maximus breeding at 3200–4800 metres (10560–16000 ft) and remaining above 2100 metres (6930 ft) even in winter.[8]
This widespread species has occurred as a vagrant in many locations in Eurasia outside its normal range, but records from North America are normally considered to involve escapees, including, for example, the 1971 bird in Quebec.[27] However, a 1994 record from Bonavista, Newfoundland, has been accepted as a genuine wild bird,[8] and the species is therefore on the North American list.[28]

Behaviour and ecology

Eggs in a nest
Two chicks in their first hours as another egg begins to hatch
Two chicks in a nest
The male common blackbird defends its breeding territory, chasing away other males or utilising a "bow and run" threat display. This consists of a short run, the head first being raised and then bowed with the tail dipped simultaneously. If a fight between male blackbirds does occur, it is usually short and the intruder is soon chased away. The female blackbird is also aggressive in the spring when it competes with other females for a good nesting territory, and although fights are less frequent, they tend to be more violent.[24]
The bill's appearance is important in the interactions of the common blackbird. The territory-holding male responds more aggressively towards models with orange bills than to those with yellow bills, and reacts least to the brown bill colour typical of the first-year male. The female is, however, relatively indifferent to bill colour, but responds instead to shinier bills.[29]
As long as winter food is available, both the male and female will remain in the territory throughout the year, although occupying different areas. Migrants are more gregarious, travelling in small flocks and feeding in loose groups in the wintering grounds. The flight of migrating birds comprises bursts of rapid wing beats interspersed with level or diving movement, and differs from both the normal fast agile flight of this species and the more dipping action of larger thrushes.[15]

Breeding

Eggs, Collection Museum Wiesbaden
The male common blackbird attracts the female with a courtship display which consists of oblique runs combined with head-bowing movements, an open beak, and a "strangled" low song. The female remains motionless until she raises her head and tail to permit copulation.[24] This species is monogamous, and the established pair will usually stay together as long as they both survive.[15] Pair separation rates of up to 20% have been noted following poor breeding.[30] Although the species is socially monogamous, there have been studies showing as much as 17% extra-pair paternity.[31]
Nominate T. merula may commence breeding in March, but eastern and Indian races are a month or more later, and the introduced New Zealand birds start nesting in August (late winter).[8][25] The breeding pair prospect for a suitable nest site in a creeper or bush, favouring evergreen or thorny species such as ivy, holly, hawthorn, honeysuckle or pyracantha.[32] Sometimes the birds will nest in sheds or outbuildings where a ledge or cavity is used. The cup-shaped nest is made with grasses, leaves and other vegetation, bound together with mud. It is built by the female alone. She lays three to five (usually four) bluish-green eggs marked with reddish-brown blotches,[24] heaviest at the larger end;[25] the eggs of nominate T. merula are 2.9×2.1 centimetres (1.14×0.93 in) in size and weigh 7.2 grammes (0.25 oz), of which 6% is shell.[33] Eggs of birds of the southern Indian races are paler than those from the northern subcontinent and Europe.[8] The female incubates for 12–14 days before the altricial chicks are hatched naked and blind. Fledging takes another 10–19 (average 13.6) days, with both parents feeding the young and removing faecal sacs.[15] The nest is often ill-concealed compared with those of other species, and many breeding attempts fail due to predation.[34] The young are fed by the parents for up to three weeks after leaving the nest, and will follow the adults begging for food. If the female starts another nest, the male alone will feed the fledged young.[24] Second broods are common, with the female reusing the same nest if the brood was successful, and three broods may be raised in the south of the common blackbird's range.[8]
A common blackbird has an average life expectancy of 2.4 years,[35] and, based on data from bird ringing, the oldest recorded age is 21 years and 10 months.[36]

Songs and calls

Blackbird tree.jpg
A male singing
Song 1
Song 2
Alarm calls
In its native Northern Hemisphere range, the first-year male common blackbird of the nominate race may start singing as early as late January in fine weather in order to establish a territory, followed in late March by the adult male. The male's song is a varied and melodious low-pitched fluted warble, given from trees, rooftops or other elevated perches mainly in the period from March to June, sometimes into the beginning of July. It has a number of other calls, including an aggressive seee, a pook-pook-pook alarm for terrestrial predators like cats, and various chink and chook, chook vocalisations. The territorial male invariably gives chink-chink calls in the evening in an (usually unsuccessful) attempt to deter other blackbirds from roosting in its territory overnight.[24] During the northern winter, blackbirds can be heard quietly singing to themselves, so much so that September and October are the only months in which the song cannot be heard.[37] Like other passerine birds, it has a thin high seee alarm call for threats from birds of prey since the sound is rapidly attenuated in vegetation, making the source difficult to locate.[38]
At least two subspecies, T. m. merula and T. m. nigropileus, will mimic other species of birds, cats, humans or alarms, but this is usually quiet and hard to detect.

Feeding

Adult male feeding on berries in Lausanne, Switzerland
The common blackbird is omnivorous, eating a wide range of insects, earthworms, seeds and berries. It feeds mainly on the ground, running and hopping with a start-stop-start progress. It pulls earthworms from the soil, usually finding them by sight, but sometimes by hearing, and roots through leaf litter for other invertebrates. Small amphibians and lizards are occasionally hunted. This species will also perch in bushes to take berries and collect caterpillars and other active insects.[24] Animal prey predominates, and is particularly important during the breeding season, with windfall apples and berries taken more in the autumn and winter. The nature of the fruit taken depends on what is locally available, and frequently includes exotics in gardens.

Natural threats

A male attempting to distract a male kestrel close to its nest
Near human habitation the main predator of the common blackbird is the domestic cat, with newly fledged young especially vulnerable. Foxes and predatory birds, such as the sparrowhawk and other accipiters, also take this species when the opportunity arises.[39][40] However, there is little direct evidence to show that either predation of the adult blackbirds or loss of the eggs and chicks to corvids, such as the European magpie or Eurasian jay, decrease population numbers.[32]
This species is occasionally a host of parasitic cuckoos, such as the common cuckoo (Cuculus canorus), but this is minimal because the common blackbird recognizes the adult of the parasitic species and its non-mimetic eggs.[41] In the UK, only three nests of 59,770 examined (0.005%) contained cuckoo eggs.[42] The introduced merula blackbird in New Zealand, where the cuckoo does not occur, has, over the past 130 years, lost the ability to recognize the adult common cuckoo but still rejects non-mimetic eggs.[43]
As with other passerine birds, parasites are common. 88% of common blackbirds were found to have intestinal parasites, most frequently Isospora and Capillaria species.[44] and more than 80% had haematozoan parasites (Leucocytozoon, Plasmodium, Haemoproteus and Trypanosoma species).[45]
Common blackbirds spend much of their time looking for food on the ground where they can become infested with ticks, which are external parasites that most commonly attach to the head of a blackbird.[46] In France, 74% of rural blackbirds were found to be infested with Ixodes ticks, whereas, only 2% of blackbirds living in urban habitats were infested.[46] This is partly because it is more difficult for ticks to find another host on lawns and gardens in urban areas than in uncultivated rural areas, and partly because ticks are likely to be commoner in rural areas, where a variety of tick hosts, such as foxes, deer and boar, are more numerous.[46] Although ixodid ticks can transmit pathogenic viruses and bacteria, and are known to transmit Borrelia bacteria to birds,[47] there is no evidence that this affects the fitness of blackbirds except when they are exhausted and run down after migration.[46]
The common blackbird is one of a number of species which has unihemispheric slow-wave sleep. One hemisphere of the brain is effectively asleep, while a low-voltage EEG, characteristic of wakefulness, is present in the other. The benefit of this is that the bird can rest in areas of high predation or during long migratory flights, but still retain a degree of alertness.[48]
Historic image of blackbird
in Nederlandsche Vogelen
(1770)

Status and conservation

The common blackbird has an extensive range, estimated at 10 million square kilometres (3.8 million square miles), and a large population, including an estimated 79 to 160 million individuals in Europe alone. The species is not 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 evaluated as Least Concern.[49] In the western Palaearctic, populations are generally stable or increasing,[15] but there have been local declines, especially on farmland, which may be due to agricultural policies that encouraged farmers to remove hedgerows (which provide nesting places), and to drain damp grassland and increase the use of pesticides, both of which could have reduced the availability of invertebrate food.[39]
The common blackbird was introduced to Australia by a bird dealer visiting Melbourne in early 1857,[50] and its range has expanded from its initial foothold in Melbourne and Adelaide to include all of south-eastern Australia, including Tasmania and the Bass Strait islands.[51] The introduced population in Australia is considered a pest because it damages a variety of soft fruits in orchards, parks and gardens including berries, cherries, stone fruit and grapes.[50] It is thought to spread weeds, such as blackberry, and may compete with native birds for food and nesting sites.[50][52]
The introduced common blackbird is, together with the native silvereye (Zosterops lateralis), the most widely distributed avian seed disperser in New Zealand. Introduced there along with the song thrush (Turdus philomelos) in 1862, it has spread throughout the country up to an elevation of 1,500 metres (4,921 ft), as well as outlying islands such as the Campbell and Kermadecs.[53] It eats a wide range of native and exotic fruit, and makes a major contribution to the development of communities of naturalised woody weeds. These communities provide fruit more suited to non-endemic native birds and naturalised birds, than to endemic birds.[54]

In culture

Sing a Song for Sixpence cover illustration
The common blackbird was seen as a sacred though destructive bird in Classical Greek folklore, and was said to die if it consumed pomegranate.[55] Like many other small birds, it has in the past been trapped in rural areas at its night roosts as an easily available addition to the diet,[56] and in medieval times the practice of placing live birds under a pie crust just before serving may have been the origin of the familiar nursery rhyme:[56]
Sing a song of sixpence,
A pocket full of rye;
Four and twenty blackbirds baked in a pie!
When the pie was opened the birds began to sing,

Oh wasn't that a dainty dish to set before the king?[57]
The common blackbird's melodious, distinctive song is mentioned in the poem Adlestrop by Edward Thomas;
And for that minute a blackbird sang

Close by, and round him, mistier,
Farther and farther, all the birds

Of Oxfordshire and Gloucestershire.[58]
In the English Christmas carol The Twelve Days of Christmas, the line commonly sung today as "four calling birds" is believed to have originally been written in the 18th century as "four colly birds", an archaism meaning "black as coal" that was a popular English nickname for the common blackbird.[59]
The common blackbird, unlike many black creatures, is not normally seen as a symbol of bad luck,[56] but R. S. Thomas wrote that there is "a suggestion of dark Places about it",[60] and it symbolised resignation in the 17th century tragic play The Duchess of Malfi;[61] an alternate connotation is vigilance, the bird's clear cry warning of danger.[61]
The common blackbird is the national bird of Sweden,[62] which has a breeding population of 1–2 million pairs,[15] and was featured on a 30 öre Christmas postage stamp in 1970;[63] it has also featured on a number of other stamps issued by European and Asian countries, including a 1966 4d British stamp and a 1998 Irish 30p stamp.[64] This bird—arguably—also gives rise to the Serbian name for Kosovo, which is the possessive adjectival form of Serbian kos ("blackbird") as in Kosovo Polje ("Blackbird Field").[65]
A Common blackbird can be heard singing on the Beatles song Blackbird.[66]
The famous Lebanese singer, Sabah, one of the biggest recording and movie stars of the twentieth century in the Arab World, was nicknamed the "blackbird of the valley" at the launch of her artistic career due to her beautiful voice.[67]






Turdus merula

Eurasian Blackbird.png


 Global range of the nominate subspecies based on reports to eBird     Year-round range     Summer range     Winter range




 

THE SUNDA CLOUDED LEOPARD

The Sunda clouded leopard (Neofelis diardi) is a medium-sized wild cat native to Borneo and Sumatra. It is listed as Vulnerable on the IUCN Red List since 2015, as the total effective population probably consists of fewer than 10,000 mature individuals, with a decreasing population trend. On both Sunda islands, it is threatened by deforestation.[1]
In 2006, it was classified as a species, distinct from the clouded leopard in mainland Southeast Asia.[2] Its fur is darker with a smaller cloud pattern.[3][4]
It is also known as the Sundaland clouded leopard, Enkuli clouded leopard,[1] Diard's clouded leopard,[5] and Diard's cat.[6]
 
Borneo clouded leopard.jpg

Characteristics

The Sunda clouded leopard is overall grayish yellow or gray hue. It has a double midline on the back and is marked with small irregular cloud-like patterns on shoulders. These cloud markings have frequent spots inside and form two or more rows that are arranged vertically from the back on the flanks.[3] It has a stocky build and weighs around 12 to 26 kg (26 to 57 lb). Its canine teeth are 2 in (5.1 cm) long, which, in proportion to the skull length, are longer than those of any other living cat. Its tail can grow to be as long as its body, aiding balance.[citation needed] It is the largest cat in Borneo.
It can purr as its hyoid bone is ossified. Its pupils contract to vertical slits.[7]

Distribution and habitat

The Sunda clouded leopard is restricted to the islands of Borneo and Sumatra. In Borneo, it occurs in lowland rainforest, and at lower density in logged forest below 1,500 m (4,900 ft). In Sumatra, it appears to be more abundant in hilly, montane areas. It is unknown if it still occurs on the Batu Islands close to Sumatra.[1]
Between March and August 2005, tracks of clouded leopards were recorded during field research in the Tabin Wildlife Reserve in Sabah. The population size in the 56 km2 (22 sq mi) research area was estimated to be five individuals, based on a capture-recapture analysis of four confirmed animals differentiated by their tracks. The density was estimated at eight to 17 individuals per 100 km2 (39 sq mi). The population in Sabah is roughly estimated at 1,500–3,200 individuals, with only 275–585 of them living in totally protected reserves that are large enough to hold a long-term viable population of more than 50 individuals.[8] Density outside protected areas in Sabah is probably much lower, estimated at one individual per 100 km2 (39 sq mi).[9]
In Sumatra, it was recorded in Kerinci Seblat, Gunung Leuser and Bukit Barisan Selatan National Parks.[10][11][12] It occurs most probably in much lower densities than on Borneo. One explanation for this lower density of about 1.29 individuals per 100 km2 (39 sq mi) might be that on Sumatra it is sympatric with the Sumatran tiger, whereas on Borneo it is the largest carnivore.[13]
Clouded leopard fossils were excavated on Java, where it perhaps became extinct in the Holocene.[14]

Ecology and behaviour

The habits of the Sunda clouded leopard are largely unknown because of the animal's secretive nature. It is assumed that it is generally solitary. It hunts mainly on the ground and uses its climbing skills to hide from dangers.[citation needed]

Taxonomy and evolution

Illustration published 1834 in William Jardine's The Natural History of The Feline
Felis diardi was the scientific name proposed by Georges Cuvier in 1823 in honour of Pierre-Médard Diard, who sent a skin and a drawing from Java.[15] It was subordinated as a clouded leopard subspecies by Reginald Innes Pocock in 1917.[16]
Results of genetic analysis of hair samples from Neofelis nebulosa and Neofelis diardi showed that the two taxa diverged between 2 and 0.9 million years ago, after having used a now submerged land bridge to reach Borneo and Sumatra from mainland Asia.[2]
Results of a morphometric analysis of the pelages of 57 clouded leopards sampled throughout the genus' wide geographical range indicated that there are two distinct morphological groups, differing primarily in the size of their cloud markings.[3] DNA samples from the Bornean and mainland Asia populations were used in molecular genetic analyses, revealing differences in mtDNA, nuclear DNA sequences, microsatellite and cytogenetic variation. Thirty-six fixed mitochondrial and nuclear nucleotide differences, and 20 microsatellite loci with nonoverlapping allele-size ranges distinguished the populations — a degree of differentiation equivalent to, or greater than, comparable measures among the Panthera species — and strongly support a species-level distinction between Neofelis nebulosa and Neofelis diardi.[2][3]
In December 2006, the genus Neofelis was reclassified as comprising two distinct species:[2][3]
Molecular, craniomandibular and dental analysis indicates distinction of the Sunda clouded leopard in two subspecies with separate evolutionary histories:[17]
Both populations are estimated to have diverged from each other during the Middle to Late Pleistocene. The split of these two Sunda clouded leopard subspecies corresponds roughly with the catastrophic super-eruption of the Toba Volcano in Sumatra 69,000–77,000 years ago. A probable scenario is that Sunda clouded leopards from Borneo recolonized Sumatra during periods of low sea levels in the Pleistocene, and were later separated from their source population by rising sea levels.[17]

Threats

Deforestation in Sumatra
Sunda clouded leopards being strongly arboreal are forest-dependent, and are increasingly threatened by habitat destruction following deforestation in Indonesia as well as in Malaysia.[1]
Since the early 1970s, much of the forest cover has been cleared in southern Sumatra, in particular lowland tropical evergreen forest. Fragmentation of forest stands and agricultural encroachments have rendered wildlife particularly vulnerable to human pressure.[18] Borneo has one of the world's highest deforestation rates. While in the mid-1980s forests still covered nearly three quarters of the island, by 2005 only 52% of Borneo was still forested. Both forests and land make way for human settlement. Illegal trade in wildlife is a widely spread practice.[19]
The population status of Sunda clouded leopards in Sumatra and Borneo has been estimated to decrease due to forest loss, forest conversion, illegal logging, encroachment, and possibly hunting. In Borneo, forest fires pose an additional threat, particularly in Kaltim and in the Sebangau National Park.[20]
There have been reports of poaching of Sunda clouded leopards in Brunei's Belait District where locals are selling their pelts at a lucrative price.[21]

Conservation

Neofelis diardi is listed on CITES Appendix I, and is fully protected in Sumatra, Kalimantan, Sabah, Sarawak and Brunei. Sunda clouded leopards occur in most protected areas along the Sumatran mountain spine and in most protected areas on Borneo.[1]
Since November 2006, the Bornean Wild Cat and Clouded Leopard Project based in the Danum Valley Conservation Area and the Tabin Wildlife Reserve aims to study the behaviour and ecology of the five species of Bornean wild cat — bay cat, flat-headed cat, marbled cat, leopard cat, and Sunda clouded leopard — and their prey, with a focus on the clouded leopard; investigate the effects of habitat alteration; increase awareness of the Bornean wild cats and their conservation needs, using the clouded leopard as a flagship species; and investigate threats to the Bornean wild cats from hunting and trade in Sabah.[22]
The Sunda clouded leopard is one of the focal cats of the project Conservation of Carnivores in Sabah based in northeastern Borneo since July 2008. The project team evaluates the consequences of different forms of forest exploitation for the abundance and density of felids in three commercially used forest reserves. They intend to assess the conservation needs of these felids and develop species specific conservation action plans together with other researchers and all local stakeholders.[23]

Names

The scientific name of the genus Neofelis is a composite of the Greek word νεο- meaning "new, fresh, strange", and the Latin word feles meaning "cat", so it literally means "new cat."[24][25]
The Indonesian name for the clouded leopard rimau-dahan means "tree tiger" or "branch tiger".[26]



 Christiansen, Kitchener, Kemp, Ambu and Fickel, 2007

 Sunda-Clouded-leopard distribution.jpg



 Distribution of Sunda clouded leopard,