Italian wolf | |
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C. l. italicus | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Mammalia |
Order: | Carnivora |
Family: | Canidae |
Genus: | Canis |
Species: | |
Subspecies: | C. l. italicus |
Trinomial name | |
Canis lupus italicus Altobello, 1921 [2] | |
Italian wolf range: red means stable presence; yellow means irregular presence |
The Italian wolf (Canis lupus italicus [3] [4] or Canis lupus lupus [5] ), also known as the Apennine wolf, [6] [7] is a subspecies of the grey wolf native to the Italian Peninsula. It inhabits the Apennine Mountains and the Western Alps, though it is undergoing expansion towards the north and east. As of 2022 the wolf population within Italy is estimated to be 3,307 individuals. [8] Although not universally recognised as a distinct subspecies, [5] it nonetheless possesses a unique mtDNA haplotype [9] [10] [11] and a distinct skull morphology. [12]
It has been strictly protected in Italy since the 1970s, when the population reached a low of 70–100 individuals. The population is increasing in number, though illegal hunting and persecution still constitute a threat. Since the 1990s, the Italian wolf's range has expanded into southeastern France [13] and Switzerland. [14]
The Italian wolf features prominently in Latin and Italian cultures, such as the she-wolf in the legendary founding of Rome. [15] For this reason it is unofficially considered the national animal of Italy. [16] [17]
The modern Italian wolf was first recognised as a distinct subspecies in 1921 by zoologist Giuseppe Altobello, [2] who noted that its colour and skull differed from that of the common European wolf. He described the Italian population's skull as being rounder in form than that of the typical European wolf, with smaller teeth closely approaching those of dogs and golden jackals in appearance. [18] Altobello's classification was later rejected by several authors, including Reginald Innes Pocock, who synonymised C. l. italicus with C. l. lupus. [12] In 2002, the noted paleontologist R.M. Nowak reaffirmed the morphological distinctiveness of the Italian wolf in a study on grey wolf skulls from Italy, other Eurasian localities, and dog skulls. The results of this assessment showed no overlap in the skull morphology of Italian wolves and other grey wolves and dogs. Among the discovered characteristics distinguishing the Italian wolf were its relatively narrow palate between the first premolars, a broad frontal shield, and shallow jugal bone. The study recommended the recognition of Canis lupus italicus. [12]
As of 2005 [update] , [5] it is classed by the third edition of Mammal Species of the World as synonymous with C. l. lupus. Nevertheless, the National Center for Biotechnology Information does list and publish research papers recognising its distinctiveness. [19] [20] [21]
The last specimen of the Mosbach wolf Canis mosbachensis in Europe dates to 456–416 thousand years ago, when it gave rise to the wolf Canis lupus. The earliest remains of a wolf in Europe were found in the Middle Pleistocene site of La Polledrara di Cecanibbio, 20 km (12 mi) north-west of Rome in deposits dated 406 thousand years ago. [22] [23] The genetic analysis of Apennine wolves indicates that they went through a population decline of 100–1,000 fold between the past 4,700–23,800 years, which indicates genetic isolation south of the alps from other wolf populations for many thousands of years. [24]
In 1992, an examination of the mitochondrial DNA (mDNA) of 26 grey wolf populations worldwide revealed that the Italian wolf has a unique mitochondrial haplotype (a mutation) not shared by any other grey wolf population. [9] Further tests on grey wolf mDNA revealed that, unlike several European grey wolf populations, Italian wolves do not share haplotypes with either other grey wolves or domestic dogs. [10] [24] In 2010, a study compared the mDNA haplotypes of 24 ancient wolf specimens from Western Europe dated between 44,000 and 1,200 YBP with those of modern gray wolves. The phylogenetic tree indicated that the haplotypes represented two haplogroups that were separated by five mutational steps. The ancient wolf samples from Western Europe all belonged to haplogroup 2, indicating haplogroup 2 predominance in this region for over 40,000 years before and after the last glacial maximum. A comparison of current and past frequencies indicated that in Europe, haplogroup 2 became outnumbered by haplogroup 1 over the past several thousand years, but in North America, haplogroup 2 became extinct and was replaced by haplogroup 1 after the last glacial maximum. The Italian wolf is the only remaining grey wolf subspecies included in this ancient haplogroup [25] since the extinction of the Honshu wolf. [26]
In 2016, a study of mDNA sequences of both modern and ancient wolves indicated that in Europe, the two most genetically distinct haplotypes form the Iberian wolf and separately the Italian wolf. The phylogenetic tree generated from the sequences showed the Italian wolf positioned close to the ancient wolves of the Late Pleistocene. [27] In 2017, a study found a second mDNA haplotype that belonged to the Italian wolf, and called for the morphologically and genetically distinct Italian wolf to be considered as a subspecies. [28]
In 2019, an mDNA study of 19 Late Pleistocene-Holocene wolf samples from northern Italy found that these fell within mitochondrial haplogroup 2 except for one sample. Four out of the six detected haplotypes matched ancient Beringian wolves, ancient wolves from northern Europe, some modern European and Chinese wolf populations, and are closely related to the two haplotypes currently found in the Italian wolves. The Italian wolf haplotypes were only one or two mutations away from those of the Pleistocene wolves, indicating mutation in their Italian glacial refuge. The Italian wolf population represents genetic uniqueness highlighted in several mitochondrial and nuclear DNA studies. It is the only remaining wolf population in Europe which belongs exclusively to an mDNA haplogroup that was once widespread in central and western Europe for over 40,000 years, and in North America until the Last Glacial Maximum. Additionally, one canid specimen from the Cava Filo archaeological site of San Lazzaro di Savena, Bologna fell within the domestic dog clade A haplotype — it was radio-carbon dated to be 24,700 years old. [29]
In 2020, a genomic study of Eurasian wolves found that the populations of the Dinaric Alps-Balkan Mountains region, the Iberian peninsula, and Italy diverged from each other 10,500 years ago followed by negligible gene flow between them. Their long-term isolation may explain the morphological and genetic differences between them.
Tooth variable | 90 | 55 | 50 | 45 | 40 | 30 | 20 | Today |
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lower m1 length | 24.5 | 24.0 | 28.0 | 28.5 | 27.5 | 28.0 | 29.0 | 27.0 |
lower m1 width | 10.0 | 9.5 | 11.25 | 11.75 | 11.25 | 11.5 | 12.0 | 11.0 |
upper P4 length | 22.0 | 25.0 | 24.75 | 26.0 | 24.5 | 24.0 | 25.5 | 24.0 |
Upper P4 width | 8.75 | 8.9 | 9.5 | 10.0 | 10.5 | 9.5 | 10.0 | 9.75 |
Canis |
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Canis lupus maximus (Boudadi-Maligne, 2012) was a species larger than all other known fossil and extant wolves from Western Europe. The fossilized remains of this Late Pleistocene subspecies were found across a wide area of south-western France at Jaurens cave, Nespouls, Corrèze dated 31,000 YBP; Maldidier cave, La Roque-Gageac, Dordogne dated 22,500 YBP; and Gral pit-fall, Sauliac-sur-Célé, Lot dated 16,000 YBP. The wolf's long bones are 10% longer than those of extant European wolves and 20% longer than its probable ancestor, C. l. lunellensis. The teeth are robust, the posterior denticules on the lower premolars p2, p3, p4 and upper P2 and P3 are highly developed, and the diameter of the lower carnassial (m1) were larger than any known European wolf. Wolf body size in Europe has followed a steady increase from their first appearance up to the peak of the last glacial maximum. The size of these wolves is thought to be an adaptation to a cold environment (Bergmann's rule) and plentiful game, as their remains have been found in association with reindeer fossils. [34]
In a 2017 study, the dimensions of the upper and lower carnassial teeth of the Italian wolf are close to those of C. l. maximus. Fluctuations in the size of C. lupus carnassial teeth correlate with the spread of megafauna. The Italian wolf underwent a reduction in body size with the loss of the red deer during the Italian Renaissance only centuries ago. [6]
The Italian wolf typically weighs 25–35 kg (55–77 lb), though some big males have been weighed at 40–45 kg (88–99 lb). It measures 110–148 cm (43–58 in) in body length and 50–70 cm (20–28 in) in shoulder height. [35] The pelt is generally of a grey-fulvous colour, which reddens in summer. The belly and cheeks are more lightly coloured, and dark bands are present on the back and tail tip, and occasionally along the fore limbs. Black wolves have been reported in the north-central Apennines, though their origin is unknown, as some melanistic individuals show no sign of wolf-dog hybridisation. It typically lives in packs of two to seven individuals. [36]
Wolf populations strongly declined across Europe during the 18th and 19th centuries largely due to human persecution, and by the end of the Second World War they had been eradicated from all of Central Europe and almost all of Northern Europe. Their population decline continued until the 1960s, with isolated populations surviving in Italy, Spain, Portugal, Greece, and Finland. Wolf populations have commenced recovering naturally since then. [24]
The Italian wolf was widespread in the Italian Peninsula, including Sicily, until the mid-1800s. The extermination of the grey wolf in Italy was not as complete as in Northern Europe, due to greater cultural tolerance of the species. [37] It was largely extirpated in the Alps during the 1920s, and disappeared from Sicily in the 1940s. Its range along the south-central Apennines was still relatively continuous by the 1950s, though this population was reduced in the decades after World War II because of widespread poisoning campaigns. At least 400 wolves were killed between 1960 and 1970, with the population reaching an all-time low in the early 1970s. The last documented wolf in the northern Apennines was killed in Santo Stefano d'Aveto, Genoa, in 1946, though this was an isolated individual, as the local wolf population had long been extinct. [38]
The Italian wolf was first given legal protection on 23 July 1971, with a nationwide population census being taken in 1973. This census was funded by the Italian branch of the World Wide Fund for Nature as part of a conservation plan dubbed "Operazione San Francesco” (Operation Saint Francis, linked to the traditional legend of peace set by the saint between wolf and men of Gubbio in Umbria region). The census revealed that the Italian wolf population consisted of 100–110 individuals distributed throughout a fragmented range in the main mountainous areas of south-central Italy, from the Sibillini to La Sila. In 1983, the population had reached 200–220 individuals inhabiting two unconnected areas in central and southern Italy. By the late 1990s, the Italian wolf population had increased to an estimated 400–500 individuals with a continuous distribution along the entire Apennines, from Aspromonte to the Maritime Alps, with some isolated populations in Tuscany and Lazio. In 2008, a wolf carcass was discovered in the Fiemme Valley in Trentino, and by 2010, 45–55 wolves were estimated to have recolonised Piedmont.
IUCN assessment information about peninsular population is as follows: “The Italian wolf population is estimated to be 500-800 individuals distributed along the Apennines. The shape of the range is narrow and elongated, restricted to the Apennines. The population has limited exchanges with the population of the Western Alps and recent genetic evidence indicates a flux of genes only in the direction toward the Alps. In spite of the recent increase in numbers and range, the Italian wolf population is still highly vulnerable to local extermination from human pressures (poison, shooting, car accidents) and the stochastic nature of these events suggest to maintain a cautionary assessment. The population does not qualify for the category Endangered, but it may easily reverse its current favorable status.”
In the early 1990s Italian wolves began to cross from Italy into France, where they have become established in approximately one third of its contintental territories, particularly in the French Alps and Provence, but also throughout the Massif Central. [39] [40] Even before the presence of wolves was publicly reported in France, some farmers around the Mercantour National Park had reported unusual stock depredation which was at the time attributed by authorities to uncontrolled domestic dogs. [40] Wolves are protected in France; [note 1] in order to protect the livelihoods of farmers from wolf predation, from the late 1990s the French government has subsidised various methods of protecting flocks from depredation, including electrified pasture fencing, secured electrified night pens, hiring of additional farm hands, and the purchase, training and upkeep of livestock guardian dogs. [40]
The Italian wolf was first sighted in southwestern France in 1992. In the two decades following its initial recolonisation, the wolf has expanded its range at the west of the Rhône, in the Massif Central, the eastern Pyrenees, and the Jura and Vosges Mountains. [13]
At least 13 transient Italian wolves (12 males and a female) were counted in Catalonia between 2000 and 2011, a century after the local Iberian wolf (C. l. signatus) was extirpated from the area. [41] One of these was reported in the media to have been killed on the road and identified in Baix Empordà, Catalonia in 2018. Technicians and veterinarians of the Torreferrussa Wildlife Center identified the body as being of the subspecies Canis lupus italicus. [42]
The first evidence of grey wolf expansion into Switzerland occurred in 1995–1996 in the southern Canton of Valais, where around 100 sheep were killed. In 1998–1999, 40 sheep were killed and two wolves were found dead from poaching and car collisions. [14] The first wolf pack formed 17 years after the return of the first wolves, in 2012 in the canton of Grisons. The reproducing female F07 of this first pack was confirmed to be still alive in 2023, making it 13–14 years old. [43] Since the formation of the first pack, the Swiss population is growing rapidly. [44] In 2023, there were 240 wolves, 18 wolf packs entirely in Switzerland and five on the border to France or Italy. [44] Most of these wolf packs roam in the cantons of Grisons, Valais and Ticino. [45]
Italian, French and Swiss wolves share the same mtDNA haplotype, [46] a haplotype that has never been found in any other wolf population worldwide, [47] which corroborate the scenario of a natural expansion of wolves from the Italian source population. [46] Although the Italian and Dinaric wolf populations have remained distinct for a long time, their ranges are beginning to overlap as they expand. In the canton of Glarus, Switzerland, the first hybrid offspring has been documented, born to parent wolves originating from both of these populations. [48]
The animal features prominently in pre-Roman, Roman, and later Italian cultures. In Roman mythology, the wolf played a role in the founding of Rome by suckling the twins Romulus and Remus. According to Terry Jones, "The Romans did not see [the tale of Romulus, Remus and the she-wolf] as a charming story; they meant to show that they had imbibed wolfish appetites and ferocity with their mother's milk". [49] The wolf was also considered sacred to Mars, and to see a wolf before going into battle was considered a good omen. [50] The origin of the myth can be traced back to a wolf cult among the neighbouring Sabines. The Sabines had two words for wolf: hirpus (used in religious contexts) and lupus, the latter of which was incorporated into Latin. [51]
Although the Romans did not worship wolves, killing them was likely considered taboo; unlike the Etruscans, the Romans very rarely sacrificed wolves in rituals, and no records have been found of wolves being used in the amphitheatres, despite being more numerous and easily accessible compared to other, more exotic animals used. The use of wolves in Roman folk medicine, while attested by Pliny the Elder, was minimal compared to other animals such as snakes or bears and, contrary to popular imagery, Roman standard bearers did not wear wolf skins, with the only units attested to have worn them being the velites, who were the poorest and youngest warriors using the wolf skins to distinguish themselves. Wolves entering cities or temples were usually only killed when the animal had no means of escape, unlike the case with wasps, oxen, and owls, which were quickly eliminated if they entered sacred areas. [52] Negative attitudes towards wolves in Italy largely began with the invasion of the Lombards, who zoomorphically described their raids and invasions as wolf raids, bringing wolves into disrepute. [51] The belief in werewolves was still widespread in Italy during the early 1920s, and covering their faces when resting outside at night was once traditional among rural people, as sleeping whilst facing the full moon was thought to transform the sleeper into a wolf. The wolf also featured prominently in Italian folk medicine. Baby colic was treated by tying a sack filled with a piece of wolf gut around the child's neck, while miscarriages were prevented by tying a wolf's intestine around the mother's abdomen. Rheumatism and tonsillitis were treated with wolf fat, while a tooth or tuft of fur was worn as a talisman against the evil eye. [2]
The Romans apparently did not consider wolves overly dangerous to people, with the only references to them attacking people being proverbial or mythological. [52] Although Italy has no records of wolf attacks on humans after World War II and the eradication of rabies in the 1960s, [53] historians examining church and administrative records from northern Italy's central Po Valley region (which includes a part of modern-day Switzerland) found 440 cases of wolves attacking people between the 15th and 19th centuries. The 19th-century records show that from 1801 to 1825, 112 attacks occurred, 77 of which resulted in death. Of these cases, only five were attributed to rabid animals. [54]
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 wolf, also known as the gray wolf or grey wolf, is a large canine native to Eurasia and North America. More than thirty subspecies of Canis lupus have been recognized, including the dog and dingo, though gray wolves, as popularly understood, only comprise naturally-occurring wild subspecies. The wolf is the largest extant member of the family Canidae, and is further distinguished from other Canis species by its less pointed ears and muzzle, as well as a shorter torso and a longer tail. The wolf is nonetheless related closely enough to smaller Canis species, such as the coyote and the golden jackal, to produce fertile hybrids with them. The wolf's fur is usually mottled white, brown, gray, and black, although subspecies in the arctic region may be nearly all white.
The eastern wolf, also known as the timber wolf, Algonquin wolf and eastern timber wolf, is a canine of debated taxonomy native to the Great Lakes region and southeastern Canada. It is considered to be either a unique subspecies of gray wolf or red wolf or a separate species from both. Many studies have found the eastern wolf to be the product of ancient and recent genetic admixture between the gray wolf and the coyote, while other studies have found some or all populations of the eastern wolf, as well as coyotes, originally separated from a common ancestor with the wolf over 1 million years ago and that these populations of the eastern wolf may be the same species as or a closely related species to the red wolf of the Southeastern United States. Regardless of its status, it is regarded as unique and therefore worthy of conservation with Canada citing the population in eastern Canada as being the eastern wolf population subject to protection.
The Great Plains wolf, also known as the buffalo wolf or loafer, is a subspecies of gray wolf that once extended throughout the Great Plains, from southern Manitoba and Saskatchewan in Canada southward to northern Texas in the United States. The subspecies was thought to be extinct in 1926, until studies declared that its descendants were found in Minnesota, Wisconsin and Michigan. They were described as a large, light-colored wolf but with black and white varying between individual wolves, with some all white or all black. The Native Americans of North Dakota told of how only three Great Plains wolves could bring down any sized bison.
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 Iberian wolf, is a subspecies of grey wolf. It inhabits the northwest of the Iberian Peninsula, which includes northwestern Spain and northern Portugal. It is home to 2,200-2,700 wolves which have been isolated from mixing with other wolf populations for over a century. They form the largest wolf population in Western Europe.
The Indian wolf is a subspecies of gray wolf that ranges from Southwest Asia to the Indian subcontinent. It is intermediate in size between the Himalayan wolf and the Arabian wolf, and lacks the former's luxuriant winter coat due to it living in warmer conditions. Within this subspecies, the "Indian plains wolf" is genetically basal to all other extant Canis lupus apart from the older-lineage Himalayan wolf, with both proposed as separate species. The Indian wolf travels in smaller packs and is less vocal than other variants of the gray wolf, and has a reputation for being cunning. The Indian wolf is one of the most endangered populations of gray wolf in the world.
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.
Armbruster's wolf is an extinct species that was endemic to North America and lived during the Irvingtonian stage of the Pleistocene epoch, spanning from 1.9 Mya—250,000 years BP. It is notable because it is proposed as the ancestor of one of the most famous prehistoric carnivores in North America, the dire wolf, which replaced it.
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.
The Kenai Peninsula wolf, also known as the Kenai Peninsula grey wolf, is an extinct subspecies of the gray wolf that lived on the Kenai Peninsula in southern Alaska.
The Greenland wolf is a subspecies of gray wolf that is native to Greenland. Historically, it was heavily persecuted, but today it is fully protected and about 90% of the wolf's range falls within the boundaries of the Northeast Greenland National Park.
The Beringian wolf is an extinct population of wolf that lived during the Ice Age. It inhabited what is now modern-day Alaska, Yukon, and northern British Columbia. Some of these wolves survived well into the Holocene. The Beringian wolf is an ecomorph of the gray wolf and has been comprehensively studied using a range of scientific techniques, yielding new information on their prey species and feeding behaviors. It has been determined that these wolves are morphologically distinct from modern North American wolves and genetically basal to most modern and extinct wolves. The Beringian wolf has not been assigned a subspecies classification and its relationship with the extinct European cave wolf is not clear.
During the Pleistocene, wolves were widely distributed across the Northern Hemisphere. Some Pleistocene wolves, such as Beringian wolves and those from Japan, exhibited large body size in comparison to modern gray wolf populations. Genetic analysis of the remains of Late Pleistocene wolves suggest that across their range populations of wolves maintained considerable gene flow between each other and thus there was limited genetic divergence between them. Modern wolves mostly draw their ancestry from some Siberian populations of Late Pleistocene gray wolves, which largely replaced other gray wolf populations after the Last Glacial Maximum.
The cave wolf is an extinct glacial mammoth steppe-adapted white wolf that lived during the Middle Pleistocene to the Late Pleistocene. It inhabited Europe, where its remains have been found in many caves. Its habitat included the mammoth steppe grasslands and boreal needle forests. This large wolf was short-legged compared to its body size, yet its leg size is comparable with that of the Arctic wolf C. l. arctos. Genetic evidence suggests that Late Pleistocene European wolves shared high genetic connectivity with contemporary wolves from Siberia, with continual gene flow from Siberian wolves into European wolves over the course of the Late Pleistocene. Modern European wolves derive most of their ancestry from Siberian wolf populations that expanded into Europe during and after the Last Glacial Maximum, but retain a minor fraction of their ancestry from earlier Late Pleistocene European wolves.
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.
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.
The Sicilian wolf is an extinct subspecies of the gray wolf that was endemic to Sicily. It was paler than the mainland Italian wolf and comparable in size to the extant Arabian wolf and extinct Japanese wolf. The subspecies reportedly went extinct due to human persecution in the 1920s, though there were several possible sightings up to the 1970s. It was identified as a distinct subspecies in 2018 through morphological examinations of the few remaining mounted specimens and skulls, as well as mtDNA analyses.
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