New Guinea singing dog | |||||||||
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Other names | New Guinea Highland dog, Hallstrom's dog | ||||||||
Common nicknames | Singers | ||||||||
Origin | New Guinea | ||||||||
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Dog ( domestic dog ) |
The New Guinea singing dog or New Guinea Highland dog [1] (Canis lupus hallstromi) is an ancient (basal) [lower-alpha 1] lineage of dog [3] [4] [5] found in the New Guinea Highlands, on the island of New Guinea. Once considered to be a separate species in its own right, under the name Canis hallstromi, it is closely related to the Australian dingo. The dog is relatively unusual among canines; it is one of the few to be considered "barkless", and is known for the unusual "yodel"-like style of vocalizing that gives it its name.
In 1989, the Australian mammalogist Tim Flannery took a photo of a black-and-tan dog in Telefomin District. He noted that these dogs lived with local tribal peoples in the mountains, and that feral populations lived in the alpine and sub-alpine grasslands of the Star Mountains and the Wharton Range. The photo was published in his book, Mammals of New Guinea. [6] In 2012, Australian wilderness-adventure guide Tom Hewett took a photo of a tawny, thick-coated dog in the Puncak Mandala region of West Papua, Indonesia. [7] In 2016, a literature review found no definitive evidence that the earliest possible dogs, within captive populations of New Guinea singing dogs, were wild animals; successive generations of puppies were raised as members of village populations, thus being domestic dogs. [8]
In 2020, a genetic study found that the New Guinea Highland wild dogs were genetically basal to the dingo and the New Guinea singing dog, and therefore the potential originator of both. [9]
In 1999, a study of mitochondrial DNA (mtDNA) indicated that the domestic dog may have originated from multiple grey wolf populations, with the dingo and New Guinea singing dog "breeds" having developed at a time when human populations were more isolated from each other. [10] In the third edition of Mammal Species of the World published in 2005, the mammalogist W. Christopher Wozencraft listed under the wolf Canis lupus its wild subspecies, and proposed two additional subspecies: "familiaris Linnaeus, 1758 [domestic dog]" and "dingo Meyer, 1793 [domestic dog]". Wozencraft included hallstromi – the New Guinea singing dog – as a taxonomic synonym for the dingo. Wozencraft referred to the mtDNA study as one of the guides in forming his decision. [11] The inclusion of familiaris and dingo under a "domestic dog" clade has been noted by other mammalogists. [12] This classification by Wozencraft is debated among zoologists. [13]
The New Guinea singing dog's taxonomic status is debated, with proposals that include treating it within the species concept (range of variation) of the domestic dog Canis familiaris, [14] [15] [12] [6] a distinct species Canis hallstromi, [1] [16] and Canis lupus dingo when considered a subspecies of the wolf. [11] In 2019, a workshop hosted by the IUCN/SSC Canid Specialist Group considered the New Guinea singing dog and the dingo to be feral dogs Canis familiaris, and therefore should not be assessed for the IUCN Red List. [14]
During the Torres expedition to the south coast of New Guinea and the Torres Strait in 1606, small dogs were recorded by Captain Don Diego de Prado y Tovar:
We found small dumb dogs that neither bark nor howl, and do not cry out even if beaten with sticks [17]
On 26 October 1897, the Lieutenant-Governor of British New Guinea, Sir William MacGregor, was on Mount Scratchley, Central Province, Papua New Guinea. At an elevation of 7,000 ft (2,100 m) he recorded that "animals are rare," but listed "wild dog." MacGregor obtained the first specimen and later Charles Walter De Vis wrote a description of it in 1911. [18] [1] De Vis summarised from his description that:
... it is not a "truly a wild dog"; in other words that there was a time when its forebears were not wild. ...But if we decide that this dog is merely feral, of a domestic breed run wild, as dogs are apt to do, how are we to account for its habitat on Mount Scratchley? [18]
In 1954, collectors for the Australian Museum observed these dogs around villages situated at 8,000 ft (2,400 m) on Mount Giluwe in the Southern Highlands Province. [1] In 1956, Albert Speer and J. P. Sinclair obtained a pair of singing dogs in the Levani Valley that was situated in what is now Hela Province (formerly part of Southern Highlands Province). [19] [20] The two dogs had been obtained from natives. [1] The dogs were sent to Sir Edward Hallstrom, who had set up a native animal study center in Nondugi, and from there to the Taronga Zoo in Sydney, Australia. [20] In 1957, Ellis Troughton examined the two singing dog specimens from the Taronga Zoo and classified them as a distinct species Canis hallstromi in honour of Hallstrom. [21]
Troughton described the type specimen as follows:
Specimens. – Male holotype, female allotype, in possession of Sir Edward Hallstrom at Taronga Zoological Park, Sydney, for eventual lodgment in the collection of the Australian Museum.
General characters:
Muzzle or rostral region short and narrow in contrast with the remarkable facial or bi-zygomatic width, imparting the strikingly vulpine or fox-like appearance. This comparison is sustained in the narrow body and very short bushy tail which measures little more than one third of the combined head-and-body length, with the width of the brush a fraction under 4 in (10 cm). The fleshy, softly furred, triangulate ears remain erect, though rounded and curved forward in conch-like fashion.
Colour (Ridgway [lower-alpha 2] ) of the head a clear tawny brown; the back a darker russet-brown owing to the admixture of blackish-brown hairs, the darker hairs enclosing a yellowish "saddlemark" somewhat more conspicuous in the female. Outer shoulders and hips clear ochraceous-tawny; tail about tawny-olive brindled above with blackish-brown, tip white; four paws whitish. Underparts a light buffy, a dark mark across the jaw separating the light chin-spot from the pale undersurface.
Dimensions of Holotype:
Head and body approximately 650 mm (26 in); tail exactly 245 mm (9.6 in), less brush; heel to longest toe, less nail, 145 mm (5.7 in); dew-claw from base to ground, 25 mm (0.98 in); ear, length from outer base to tip 75 mm (3.0 in), midwidth 40 mm (1.6 in); longest vibrissa 52 mm (2.0 in); length of head to extremity of sagittal crest 180 mm (7.1 in) (approx.) and bi-zygomatic width 100 mm (3.9 in); rear molar to incisor 90 mm (3.5 in); width across incisors 23 mm (0.91 in); height of upper canine 16 mm (0.63 in). [21]
By the close of the last glacial period 11,700 years ago, five ancestral lineages had diversified from each other and were expressed in ancient dog samples found in the Levant (7,000 YBP), Karelia (10,900 YBP), Lake Baikal (7,000 YBP), ancient America (4,000 YBP), and in the New Guinea singing dog (present day). [5]
Mitochondrial genome sequences indicates that the dingo falls within the domestic dog clade, [25] and that the New Guinea singing dog is genetically closer to those dingoes that live in southeastern Australia than to those that live in the northwest. [23] The dingo and New Guinea singing dog lineage can be traced back through the Malay Archipelago to Asia. [26]
In 2016, a literature review found that:
there is no convincing evidence that New Guinea wild-living dogs and some, or all, pre-colonization New Guinea village dogs were distinct forms. Further, there is no definitive evidence that either high altitude wild-living dogs were formerly isolated from other New Guinea canids or that the animals that were the founding members of captive populations of New Guinea Singing Dogs were wild-living animals or the progeny of wild-living animals rather than being born and raised as members of village populations of domestic dogs. We conclude that:
- (1) at the time of European colonization, wild dogs and most, if not all, village dogs of New Guinea comprised a single though heterogeneous gene pool
- (2) eventual resolution of the phylogenetic relationships of New Guinea wild dogs will apply equally to all or most of the earliest New Guinea village-based, domesticated, dogs; and
- (3) there remain places in New Guinea, such as Suabi and neighbouring communities, where the local village-based population of domestic dogs continues to be dominated by individuals whose genetic inheritance can be traced to pre-colonization canid forebears. [8]
In 2020, the first whole genome analysis of the dingo and the New Guinea singing dog was undertaken. The study indicates that the ancestors of these two dogs arose in southern East Asia, migrated through Island Southeast Asia 9,900 YBP, and reached Australia 8,300 YBP. The study rejects earlier suggestions that these dogs arrived from southern Asia 4,300 YBP or as part of the Austronesian expansion into Island Southeast Asia, which arrived in New Guinea about 3,600 YBP. The genetic evidence is that dingoes arrived in Australia 8,300 YBP and brought by an unknown human population. [27]
In 2024, a study found that the Dingo and New Guinea singing dog show 5.5% genome introgression from the ancestor of the recently extinct Japanese wolf, with Japanese dogs showing 4% genome introgression. This introgression occurred before the ancestor of the Japanese wolf arrived in Japan. [28]
In 2017, the New Guinea Highland Wild Dog Foundation (NGHWDF) announced to the media that in 2016, it and the University of Papua had located and photographed a group of 15 of what it referred to as "highland wild dogs." [29] DNA analysis of scats indicate that these dogs have a genetic relationship with other dogs found in Oceania, including the dingo and the New Guinea singing dog. [30]
In 2020, a nuclear genome study indicates that the highland wild dogs from the base of Puncak Jaya, within the Tembagapura district in the Mimika Regency of Papua, Indonesia, were the population from which captive New Guinea singing dogs were derived. The study revealed that the wild dogs show much more genetic diversity than the captive animals, which are severely inbred. This indicates the wild population is healthy. The size and distribution of the wild population is not known. Mitochondrial DNA indicates that the highland wild dogs possess the A29 haplotype, rather than the A79 haplotype which is found in the New Guinea singing dog. The A29 haplotype is found in dingoes, some New Guinea singing dogs, and some Asian, Arctic, and village dogs. A phylogenetic tree shows the highland wild dogs to be basal to the dingo and New Guinea singing dog, and therefore the potential originator of both. [9]
These dogs live wildly in a harsh and remote environment between 3,900–4,170 metres (12,800–13,680 ft) in elevation, which suggests they are a lineage of proto-dog that is related to the dingo and are not feral village dogs. This has led to some researchers to suggest that the taxon Canis dingo is appropriate for the only truly wild-living dog populations – the dingo, the New Guinea Highland wild dog, and the New Guinea singing dog. [3]
Australian mammalogist Tim Flannery in his book the Mammals of New Guinea describes the "New Guinea Wild Dog" as looking similar to the dingo, only smaller. Most of these dogs in New Guinea are domesticated with large numbers being kept by widows and bachelors, with hunters keeping at least two for assisting them with hunting. These dogs do not bark, and their chorused howling makes a haunting and extraordinary sound, which has led to their alternative name of "New Guinea Singing Dog." Flannery published in his book a photo of a black-and-tan dog in the Telefomin District. He wrote that these dogs live with native people in the mountains, and that there were feral populations living in the alpine and sub-alpine grasslands of the Star Mountains and the Wharton Range. [6]
Compared with other forms of dog, the New Guinea singing dog is described as relatively short-legged and broad-headed. These dogs have an average shoulder height of 31–46 cm (12–18 in) and weigh 9–14 kg (20–31 lb). They do not have rear dewclaws. [16]
The limbs and spine of the New Guinea singing dog are very flexible and they can spread their legs sideways to 90°, comparable to the Norwegian Lundehund. They can also rotate their front and hind paws more than domestic dogs, which enables them to climb trees with thick bark or branches that can be reached from the ground; however, their climbing skills do not reach the same level as those of the gray fox, [31] and are closely related to those of a cat. [32]
The eyes, which are highly reflective, are triangular (or almond-shaped) and are angled upwards from the inner to outer corners with dark eye rims. Eye color ranges from dark amber to dark brown. Their eyes exhibit a bright green glow when lights are shone on them in low light conditions. There are two features which researchers believe allow New Guinea singing dogs to see more clearly in low light. [31] One is that of their pupils, which open wider and allow in more light than in other dog varieties. The other is that they possess a higher concentration of cells in the tapetum.
New Guinea singing dogs have erect, pointed, fur-lined ears. As with other wild dogs, the ears 'perk,' or lay forward, which is suspected to be an important survival feature for the form. The ears can be rotated like a directional receiver to pick up faint sounds. Their tails are bushy, long enough to reach the hock, free of kinks, and have a white tip.
Pups are born with a dark chocolate brown pelt with gold flecks and reddish tinges, which changes to light brown by the age of six weeks. Adult coloration occurs around four months of age. For adult dogs, the colors brown, black, and tan have been reported, all with white points. The sides of the neck and zonal stripes behind the scapula are golden. Black and very dark guard hair is generally lightly allocated over the hair of the spine, concentrating on the back of the ears and the surface of the tail over the white tip. The muzzle is always black on young dogs. Generally, all colors have white markings underneath the chin, on the paws, chest and tail tip. About one third also have white markings on the muzzle, face and neck. By 7 years of age, the black muzzle begins to turn grey. [16]
All sightings in the wild were of single dogs or pairs, therefore it can be inferred that wild New Guinea singing dogs do not form permanent packs. [16] Tim Flannery's short 1989 report on dogs in the mountains of Papua New Guinea described them as "extraordinarily shy" and "almost preternaturally canny." [33] According to Robert Bino (1996), [lower-alpha 3] these dogs only use their resting places under roots and ledges in New Guinea sporadically. Bino conjectured that these dogs are highly mobile and forage alone and concluded that they therefore might use several hiding places in their home range. [34]
During research observations, the examined dogs generally showed a lower threshold of behaviour (e.g., scent rolling) than other domestic dogs, as well as an earlier developmental onset than other domestic dogs or grey wolves (e.g., hackle biting at two weeks compared to other domestic dogs/grey wolves at 6 weeks) and a quantitative difference (e.g., reduced expression of intraspecific affiliate behaviours). The dogs observed did not show the typical canid play bow; however, Imke Voth found this behaviour during examinations in the 1980s. [35]
Several behaviours unique to New Guinea singing dogs have been noted: [16]
Additionally, New Guinea singing dogs have an unusual form of auto-erotic stimulation, which includes a strong tendency to target the genitals for both playful and aggressive bites, a cheek-rub that may be a marking behaviour and a tooth-gnashing threat.
During estrus, when potential partners are present, same-sex New Guinea singing dogs often fight to the point of severe injury. Furthermore, adults also display a high degree of aggression towards unfamiliar dogs, which would indicate that they are strongly territorial. [16] Their distinctive aggression could not be observed to that extent among Australian dingoes (who live without human contact). [36] [ page needed ]
Researchers have noted rough play behaviour by the mothers towards their pups, which often switched over to agonistic behaviour as well as "handling." The mothers did not adequately react to the pups' shouts of pain but rather interpreted it as further "invitation" for "playing." The researchers stated that this behaviour was noted in their subjects only and does not necessarily apply to all singing dogs. [36] [ page needed ]
New Guinea singing dogs are named for their distinctive and melodious howl, which is characterized by a sharp increase in pitch at the start and very high frequencies at the end. [37] The howling of these dogs can be clearly differentiated from that of Australian dingoes, and differs significantly from that of grey wolves and coyotes. [38] [ better source needed ]
An individual howl lasts an average of 3 seconds, but can last as long as 5 seconds. At the start, the frequency rises and stabilizes for the rest of the howling, but normally shows abrupt changes in frequency. Modulations can change quickly every 300–500 milliseconds or every second. Five to eight overtones can generally be distinguished in a spectrographic analysis of the howling. [16]
New Guinea singing dogs sometimes howl together, which is commonly referred to as chorus howling. During chorus howling, one dog starts and others join in shortly afterward. In most cases, chorus howling is well synchronized, and the howls of the group end nearly simultaneously. Spontaneous howling is most common during the morning and evening hours. [36] [ page needed ] A trill, with a distinctly "bird-like" character, is emitted during high arousal. It is a high-frequency pulsed signal whose spectral appearance suggests a continuous source that is periodically interrupted, and might last as long as 800 milliseconds. Such a sound is not known for any other canid; however, a similar sound (with lower frequency) has been described for a dhole at the Moscow Zoo. [16] When they are kept with dogs that bark, New Guinea singing dogs may mimic the other dogs. [36] [ page needed ]
The New Guinea singing dog possesses an annual seasonality, and if not impregnated will have a second estrus within a few weeks after the end of the first. Sometimes they will have a third. [39] Males in captivity often participate in raising the pups, including the regurgitation of food. Female New Guinea singing dogs are protective of their young and will aggressively attack their male counterpart if they suspect he poses a danger to the pups. During the first breeding season following their birth, especially if there is a potential mate present, pups are often aggressively attacked by the same-sex parent. [16]
Reports from local sources in Papua New Guinea from the 1970s and the mid-1990s indicate that New Guinea singing dogs—like wild dogs found in New Guinea, whether they were pure New Guinea singing dogs or hybrids—fed on small to middle-sized marsupials, rodents, birds, and fruits. Robert Bino stated that their prey consisted of cuscuses, wallabies, and possibly dwarf cassowaries. [39] [16] New Guinea singing dogs in captivity do not require a specialized diet, but they seem to thrive on lean raw meat diets based on poultry, beef, elk, deer, or bison. [40]
Natives interviewed in the highlands state that these dogs steal the kills of Papuan eagles. [41]
Since 1956, New Guinea singing dogs have been obtained or sighted in the wild chiefly in mountainous terrain around the central segment of the New Guinea Highlands, a major island-extensive east–west running mountain range formation. The 1956 dogs obtained by Papua New Guinea District Officer J.P. Sinclair and his medical assistant Albert Speer (see 'Taxonomic history' section above) were obtained from the Levani Valley, located in what is now North Koroba Rural LLG, Hela Province, Papua New Guinea, and were sent to Taronga Zoo in Sydney, Australia. In 1976, the German explorer Wolfgang Nelke captured five dogs in the Eipomek River Valley and sent them to Germany. Today, the captive population in the United States descends from individuals obtained from Taronga Zoo. There are also captive dog populations in Germany, Canada, and the United Kingdom. [19]
Reports of the Kalam people capturing New Guinea singing dogs in the mid-1970s imply the human tribe's range just off center east on the northeastern mainland coast (see 'Relationship with humans' section below). A 2007 sighting in the Kaijende Highlands was east of the center. The 2012 sighting was near Puncak Mandala slightly to the west, all in the highlands around the range's spine.
The reported habitat of the New Guinea singing dog consists of mountains and swampy mountain regions of Papua New Guinea at an altitude of 2,500 to 4,700 meters. The main vegetation zones are the mixed forest, beech and mossy forest, sub-alpine coniferous forest and alpine grassland. Based on archaeological, ethnographic, and circumstantial evidence, it can be assumed that New Guinea singing dogs were once distributed over the whole of New Guinea and later restricted to the upper mountains. [16] Since there have been no verified sightings of these dogs in Papua New Guinea since the 1970s until an August 2012 photograph in the wild, these dogs are now apparently rare. [37] [42]
There were reports of New Guinea singing dogs in the Star Mountains until 1976, and in the mid-1970s reports of capture and training, but not breeding by the Kalam people (see § Relationship with humans).
In his 1998 book Throwim Way Leg , Tim Flannery states that the dokfuma (which he describes as sub-alpine grassland with the ground being sodden moss, lichens and herbs growing atop a swamp) at 3,200 meters elevation had plenty of New Guinea singing dogs, which could usually be heard at the beginning and end of each day. When alone in his campsite one day, a group of canines came within several hundred meters of him. Flannery apparently did not have his camera along or ready, since he reported no pictures taken.
In 1996 Robert Bino undertook a field study of these dogs, but was not able to observe any wild New Guinea singing dogs and instead used signs, such as scats, paw prints, urine markings and prey remnants, to make conclusions about their behaviour. No DNA sampling was conducted. There have been reports from local residents that wild dogs have been seen or heard in higher reaches of the mountains. [31]
In a 2007 report, a more recent sighting was the fleeting glimpse of a dog at Lake Tawa in the Kaijende Highlands. Local assistants assured the researchers that the dogs at Lake Tawa were wild-living dogs, since there were no villages near that location. It needs to be made clear, however, that "wild-living" does not necessarily mean that canines observed by natives are New Guinea singing dogs. It is possible that they are simply feral domestic dogs or New Guinea singing dog hybrids. [43]
On 24 August 2012, the second known photograph of a New Guinea singing dog in the wild was taken by Tom Hewitt, Director of Adventure Alternative Borneo, in the Jayawijaya Mountains or Star Mountains of Papua Province, Indonesia, Western New Guinea by a trek party returning from Puncak Mandala, at approximately 4,760 m high the highest peak in the Jayawijaya range and second highest freestanding mountain of Oceania, Australasia, New Guinea and Indonesia (though Hewitt himself seems to erroneously say this peak is in the Star Mountains, which are adjacent to the Jayawijaya range, and also casually calls the region 'West Papua' rather than Indonesia's Papua Province in the Western geopolitical 'half' of the New Guinea landmasses, while his identification of the peak is quite clear, including its estimated elevation which is distinctive among New Guinea's peaks). In a valley flanked by waterfalls on both sides among approximately 4 km (13,000 ft) high limestone peaks, replete with such flora and fauna as cycads, grasses and blooms of the highlands, cuscuses, possums, tree kangaroos, unidentified ground-nesting birds in swamp grass, and a bird-of-paradise species heard but not seen, Hewitt relates that his veteran trek guide called out "dog" four times and pointed to fetch Hewitt and his trek client from their explorations behind large boulders and have them realize that ahead and above the guide and camp cook on a rocky outcrop was a dog, in Hewitt's words "not scared, but...genuinely curious...as we were of it, and it certainly felt like a rare meeting for both sides. The guides and cook were also surprised". While the guide had at first approached "quite close", the dog retreated as the party came toward it, though it stayed on the hillside while being photographed for a mutual observation session of about 15 minutes. Hewitt only became fully aware of the importance of his party's sighting and photograph of this dog when he contacted Tom Wendt, New Guinea Singing Dog International (NGSDI)'s founder upon returning home, then regretting that he did not videorecord the encounter. Hewitt and Wendt observe that West Papuan locals report that sightings are rare, and that New Guinea singing dogs have not been domesticated by current human inhabitants of their area. [42] [44]
In 2016, a literature review found that "there is no definitive evidence that...the founding members of captive populations of New Guinea Singing Dogs were wild-living animals or the progeny of wild-living animals rather than being born and raised as members of village populations of domestic dogs." [8] In the same year, the New Guinea Highland Wild Dog Foundation announced to the media that it and the University of Papua had located and photographed a group of 15 of what it referred to as "highland wild dogs". [29] DNA analysis of scats indicate that these dogs have a genetic relationship with other dogs found in Oceania, including the dingo and the New Guinea singing dog. [30]
According to reports from the late 1950s and mid-1970s, wild dogs believed to be New Guinea singing dogs were shy and avoided contact with humans. It was reported in the mid-1970s that the Kalam in the highlands of Papua caught young New Guinea singing dogs and raised them as hunting aids, but did not breed them. Some of these dogs probably stayed with the Kalam and reproduced. The Eipo tribe kept and bred wild dogs as playmates for their children. Although the majority of the highland tribes never used village dogs as a food source, it is known that even today they attempt to catch, kill and eat wild dogs. Tribes such as the Malakomofip Villagers hunt them for trophy hunting and are revered alongside wild pigs and cassowaries as a challenging quarry. [45]
Dog-findings in archaeological sites of New Guinea are rare, mostly consisting of teeth (used as ornaments) and trophy-skulls. Since the beginning of the 20th century, the inhabitants of the highlands started to keep chickens, and New Guinea singing dogs had a penchant for poultry. To add to the problem, natives kept other domestic dogs. The crossbred dogs were generally larger in size, as well as less of a challenge to train, so they tended to be of more value than New Guinea singing dogs. One might conclude that the relationship between the contemporary New Guineans and their dogs will give information about how they treated the New Guinea singing dogs, but modern "village dogs" are not genetically representative of pure New Guinea singing dogs. [39] [16] [31]
A study published in 2021 surveyed owners of New Guinea singing dogs living in North America as companion animals. The study found that New Guinea singing dogs behave like other ancient/primitive domestic dog breeds, and demonstrated less aggression than many of the breeds included in the study. They were also found to be similarly trainable to Basenjis and Canaan Dogs. Owners reported that owning a singing dog is similar to owning a Shiba Inu or Akita. Owners of New Guinea singing dogs also reported participating in dog sports and working as therapy and service dogs. [46]
In the past, the New Guinea singing dog was considered "unworthy" of scientific study, as it was regarded as an insignificant variety of feral domestic dog. However, due to its potential value as a resource for the determination of the process of domestication, particularly in relation to the dingo, as well as several of its unique genetic, behavioural, ecological, reproductive and morphological characteristics, limited research has been undertaken. [16] The New Guinea Department of Environment and Conservation has announced protection measures. [37]
Hybridization is one of the most serious threats facing the New Guinea singing dog. New Guinea singing dogs are handicapped, as are many canids such as the Australian dingo, by their susceptibility to being bred by canines other than those of their own kind. This vulnerability has, and is still, causing a "watering down" of dingo genes needed to maintain purity.[ citation needed ]
There are two organizations formed for conserving and preserving New Guinea singing dogs. They are the New Guinea Singing Dog Conservation Society, founded in 1997, [47] and New Guinea Singing Dog Club of America, a national breed club, rescue, and pet education group. [48] Both of these organizations are based in the United States.
There are 38 subspecies of Canis lupus listed in the taxonomic authority Mammal Species of the World. These subspecies were named over the past 250 years, and since their naming, a number of them have gone extinct. The nominate subspecies is the Eurasian wolf.
The dingo is an ancient (basal) lineage of dog found in Australia. Its taxonomic classification is debated as indicated by the variety of scientific names presently applied in different publications. It is variously considered a form of domestic dog not warranting recognition as a subspecies, a subspecies of dog or wolf, or a full species in its own right.
A feral animal or plant is one that lives in the wild but is descended from domesticated individuals. As with an introduced species, the introduction of feral animals or plants to non-native regions may disrupt ecosystems and has, in some cases, contributed to extinction of indigenous species. The removal of feral species is a major focus of island restoration.
Canis is a genus of the Caninae which includes multiple extant species, such as wolves, dogs, coyotes, and golden jackals. Species of this genus are distinguished by their moderate to large size, their massive, well-developed skulls and dentition, long legs, and comparatively short ears and tails.
A wolfdog is a canine produced by the mating of a domestic dog with a gray wolf, eastern wolf, red wolf, or Ethiopian wolf to produce a hybrid.
The Ethiopian wolf, also called the red jackal, the Simien jackal or Simien fox, is a canine native to the Ethiopian Highlands. In southeastern Ethiopia, it is also known as the horse jackal. It is similar to the coyote in size and build, and is distinguished by its long and narrow skull, and its red and white fur. Unlike most large canids, which are widespread, generalist feeders, the Ethiopian wolf is a highly specialised feeder of Afroalpine rodents with very specific habitat requirements. It is one of the world's rarest canids, and Africa's most endangered carnivore.
A bark is a sound most often produced by dogs. Other animals that make this noise include, but are not limited to, wolves, coyotes, foxes, seals, frogs, and barking owls. "Bark" is also a verb that describes the sound of many canids.
Canid hybrids are the result of interbreeding between the species of the subfamily Caninae.
The domestication of the dog was the process which led to the domestic dog. This included the dog's genetic divergence from the wolf, its domestication, and the emergence of the first dogs. Genetic studies suggest that all ancient and modern dogs share a common ancestry and descended from an ancient, now-extinct wolf population – or closely related wolf populations – which was distinct from the modern wolf lineage. The dog's similarity to the grey wolf is the result of substantial dog-into-wolf gene flow, with the modern grey wolf being the dog's nearest living relative. An extinct Late Pleistocene wolf may have been the ancestor of the dog.
The fauna of New Guinea comprises a large number of species of mammals, reptiles, birds, fish, invertebrates and amphibians.
Dog behavior is the internally coordinated responses of individuals or groups of domestic dogs to internal and external stimuli. It has been shaped by millennia of contact with humans and their lifestyles. As a result of this physical and social evolution, dogs have acquired the ability to understand and communicate with humans. Behavioral scientists have uncovered a wide range of social-cognitive abilities in domestic dogs.
The Japanese wolf, also known as the Honshū wolf, is an extinct subspecies of the gray wolf that was once endemic to the islands of Honshū, Shikoku and Kyūshū in the Japanese archipelago.
The Himalayan wolf is a canine of debated taxonomy. It is distinguished by its genetic markers, with mitochondrial DNA indicating that it is genetically basal to the Holarctic grey wolf, genetically the same wolf as the Tibetan and Mongolian wolf, and has an association with the African wolf. No striking morphological differences are seen between the wolves from the Himalayas and those from Tibet. The Himalayan wolf lineage can be found living in Ladakh in the Himalayas, the Tibetan Plateau, and the mountains of Central Asia predominantly above 4,000 m (13,000 ft) in elevation because it has adapted to a low-oxygen environment, compared with other wolves that are found only at lower elevations.
A Red Dingo is a large dingo species cross between a dingo and a domestic dog. The current population of free ranging domestic dogs in Australia is probably higher than in the past. However, the proportion of the so-called "pure" dingoes has been on the decrease over the last few decades due to hybridisation and is regarded as further decreasing.
In the taxonomic treatment presented in the third (2005) edition of Mammal Species of the World, Canis lupus dingo is a taxonomic rank that includes both the dingo that is native to Australia and the New Guinea singing dog that is native to the New Guinea Highlands. It also includes some extinct dogs that were once found in coastal Papua New Guinea and the island of Java in the Indonesian Archipelago. In this treatment it is a subspecies of Canis lupus, the wolf, although other treatments consider the dog as a full species, with the dingo and its relatives either as a subspecies of the dog, a species in its own right, or simply as an unnamed variant or genetic clade within the larger population of dogs. The genetic evidence indicates that the dingo clade originated from East Asian domestic dogs and was introduced through the Malay Archipelago into Australia, with a common ancestry between the Australian dingo and the New Guinea singing dog. The New Guinea singing dog is genetically closer to those dingoes that live in southeastern Australia than to those that live in the northwest.
A free-ranging dog is a dog that is not confined to a yard or house. Free-ranging dogs include street dogs, village dogs, stray dogs, feral dogs, etc., and may be owned or unowned. The global dog population is estimated to be 900 million, of which around 20% are regarded as owned pets and therefore restrained.
Purported remains of "Paleolithic dogs" have been reported from several European archaeological sites dating to over 30,000 years ago. Their status as domesticated is highly controversial, with some authors suggesting them to be the ancestors of the domestic dog or an extinct, morphologically and genetically divergent wolf population.
It is widely agreed that the evolutionary lineage of the grey wolf can be traced back 2 million years to the Early Pleistocene species Canis etruscus, and its successor the Middle Pleistocene Canis mosbachensis. The grey wolf Canis lupus is a highly adaptable species that is able to exist in a range of environments and which possesses a wide distribution across the Holarctic. Studies of modern grey wolves have identified distinct sub-populations that live in close proximity to each other. This variation in sub-populations is closely linked to differences in habitat – precipitation, temperature, vegetation, and prey specialization – which affect cranio-dental plasticity.
The Polynesian Dog refers to a few extinct varieties of domesticated dogs from the islands of Polynesia. These dogs were used for both companionship and food and were introduced alongside poultry and pigs to various islands. They became extinct as a result of the crossbreeding that occurred after European breeds of dogs were introduced. Modern studies done on the DNA of the Polynesian dogs indicate that they descended from the domesticated dogs of Southeast Asia and may have shared a remote ancestor with the dingo.
Canis mosbachensis is an extinct wolf that inhabited Europe from the late Early Pleistocene to the Middle Pleistocene, around 1.4 million to 400,000 years ago. Canis mosbachensis is widely considered to have descended from the earlier Canis etruscus, and to be the ancestor of the living grey wolf with some considering it as a subspecies of the wolf as Canis lupus mosbachensis. The morphological distinction between C. mosbachensis and C. lupus has historically been vague, and attribution of fossils to C. mosbachensis or to C. lupus around the transition time between the two species is ambiguous.
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