Aurochs

Last updated

Aurochs
Temporal range: Middle Pleistocene–Holocene
O
S
D
C
P
T
J
K
Pg
N
Copenhagen Aurochse.jpg
Mounted skeleton of an aurochs bull at the National Museum of Denmark
Status iucn3.1 EX.svg
Extinct  (1627)  (IUCN 3.1) [1]
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Artiodactyla
Family: Bovidae
Subfamily: Bovinae
Genus: Bos
Species:
B. primigenius
Binomial name
Bos primigenius
Bojanus, 1825 [2]
Subspecies

See text

Aurochs distribution.png
Former distribution of the aurochs

The aurochs (Bos primigenius) ( /ˈɔːrɒks/ or /ˈrɒks/ , plural aurochs or aurochsen) is an extinct species of bovine, considered to be the wild ancestor of modern domestic cattle. With a shoulder height of up to 180 cm (71 in) in bulls and 155 cm (61 in) in cows, it was one of the largest herbivores in the Holocene; it had massive elongated and broad horns that reached 80 cm (31 in) in length.

Contents

The aurochs was part of the Pleistocene megafauna. It probably evolved in Asia and migrated west and north during warm interglacial periods. The oldest-known aurochs fossils date to the Middle Pleistocene. The species had an expansive range spanning from Western Europe and North Africa to the Indian subcontinent and East Asia. The distribution of the aurochs progressively contracted during the Holocene due to habitat loss and hunting, with the last known individual dying in the Jaktorów forest in Poland in 1627.

There is a long history of interaction between aurochs and humans, including archaic humans like Neanderthals. The aurochs is depicted in Paleolithic cave paintings, Neolithic petroglyphs, Ancient Egyptian reliefs and Bronze Age figurines. It symbolised power, sexual potency and prowess in religions of the ancient Near East. Its horns were used in votive offerings, as trophies and drinking horns.

Two aurochs domestication events occurred during the Neolithic Revolution. One gave rise to the domestic taurine cattle (Bos taurus) in the Fertile Crescent in the Near East that was introduced to Europe via the Balkans and the coast of the Mediterranean Sea. Hybridisation between aurochs and early domestic cattle occurred during the early Holocene. Domestication of the Indian aurochs led to the zebu cattle (Bos indicus) that hybridised with early taurine cattle in the Near East about 4,000 years ago. Some modern cattle breeds exhibit features reminiscent of the aurochs, such as the dark colour and light eel stripe along the back of bulls, the lighter colour of cows, or an aurochs-like horn shape.

Etymology

Both "aur" and "ur" are Germanic or Celtic words meaning "wild ox". [3] [4] In Old High German, this word was compounded with ohso ('ox') to ūrohso, which became the early modern Aurochs. [5] The Latin word "urus" was used for wild ox from the Gallic Wars onwards. [4] [6]

The use of the plural form aurochsen in English is a direct parallel of the German plural Ochsen and recreates the same distinction by analogy as English singular ox and plural oxen, although aurochs may stand for both the singular and the plural term; both are attested. [7] [8]

Taxonomy and evolution

The scientific name Bos taurus was introduced by Carl Linnaeus in 1758 for feral cattle in Poland. [9] The scientific name Bos primigenius was proposed for the aurochs by Ludwig Heinrich Bojanus who described the skeletal differences between the aurochs and domestic cattle in 1825, published in 1827. [2] [10] The name Bos namadicus was used by Hugh Falconer in 1859 for cattle fossils found in Nerbudda deposits. [11] Bos primigenius mauritanicus was coined by Philippe Thomas in 1881 who described fossils found in deposits near Oued Seguen west of Constantine, Algeria. [12]

In 2003, the International Commission on Zoological Nomenclature placed Bos primigenius on the Official List of Specific Names in Zoology and thereby recognized the validity of this name for a wild species. [13] [14]

Subspecies

Three aurochs subspecies have traditionally been recognised to have existed in historical times:

In the 21st century, Chinese geneticists published mitochondrial DNA evidence supporting that Eurasian aurochs populations from northern China were genetically isolated for large stretches of the Pleistocene, and as a result distinctive enough to be considered a separate subspecies, the East Asian aurochs (B. p. sinensis), even if the animals were not morphologically distinct. [17]

At least two dwarf subspecies of aurochs developed in Mediterranean islands as a result of sea level changes during the Pleistocene:

Evolution

Calibrations using fossils of 16 Bovidae species indicate that the Bovini tribe evolved about 11.7  million years ago. [21] The Bos and Bison genetic lineages are estimated to have genetically diverged from the Bovini about 2.5 to 1.65 million years ago. [22] [23] The following cladogram shows the phylogenetic relationships of the aurochs based on analysis of nuclear and mitochondrial genomes in the Bovini tribe: [22] [24] [25]

Bovini

Bubalina (buffalo)

Bos

Bos primigenius (aurochs)

Bos mutus (wild yak)

Bison bison (American bison)

Bison bonasus (European bison/wisent)

Bos javanicus (banteng)

Bos gaurus (gaur)

Bos sauveli (kouprey)

The cold Pliocene climate caused an extension of open grassland, which enabled the evolution of large grazers. [5] The origin of the aurochs is unclear, with authors suggesting either an African or Asian origin for the species. Bos acutifrons is considered to be a possible ancestor of the aurochs, of which a fossil skull was excavated in the Sivalik Hills in India that dates to the Early Pleistocene about 2  million years ago. [26]

An aurochs skull excavated in Tunisia's Kef Governorate from early Middle Pleistocene strata dating about 0.78  million years ago is the oldest well-dated fossil specimen to date. The authors of the study proposed that Bos might have evolved in Africa and migrated to Eurasia during the Middle Pleistocene. [27] Middle Pleistocene aurochs fossils were also excavated in a Saharan erg in the Hoggar Mountains. [28]

Fossils of the Indian subspecies (Bos primigenius namadicus) were excavated in alluvial deposits in South India dating to the Middle Pleistocene. [29] Remains of aurochs are common in Late Pleistocene sites across the Indian subcontinent. [30]

The earliest fossils in Europe date to the Middle Pleistocene. One site widely historically suggested to represent the first appearance of aurochs in Europe was the Notarchirico site in southern Italy, dating around 600,000 years ago, [31] however a 2024 re-examination of the site found that presence of aurochs at the locality was unsupported, with the oldest records of aurochs now placed at the Ponte Molle site in central Italy, [32] dating to around 550-450,000 years ago. [33] Aurochs were present in Britain by Marine Isotope Stage 11 ~400,000 years ago. [34]

The earliest remains aurochs in East Asia are uncertain, but may date to the late Middle Pleistocene. [35]

Late Pleistocene aurochs fossils were found in Affad 23 in Sudan dating to 50,000 years ago when the climate in this region was more humid than during the African humid period. [36]

Following the most recent deglaciation, the range of the aurochs expanded into Denmark and southern Sweden at the beginning of the Holocene, around 12-11,000 years ago. [37]

Description

Tur ZHerberstein pol XVIw small.jpg
Illustration by Sigismund von Herberstein captioned: Urus sum, polonis Tur, germanis Aurox; ignari Bisontis nomen dederant; translated: "I am Urus, Tur in Polish, Aurox in German; the ignorant ones gave me the name Bison"
Copenhagen Zoological Museum Aurochs bull.jpg
Aurochs skeleton from Zealand island in Denmark on display in the Natural History Museum of Denmark

According to a 16th-century description by Sigismund von Herberstein, the aurochs was pitch-black with a grey streak along the back; his wood carving made in 1556 was based on a culled aurochs, which he had received in Mazovia. [38] In 1827, Charles Hamilton Smith published an image of an aurochs that was based on an oil painting that he had purchased from a merchant in Augsburg, which is thought to have been made in the early 16th century. [39] This painting is thought to have shown an aurochs, [5] [40] although some authors suggested it may have shown a hybrid between an aurochs and domestic cattle, or a Polish steer. [41] Contemporary reconstructions of the aurochs are based on skeletons and the information derived from contemporaneous artistic depictions and historic descriptions of the animal. [5]

Coat colour

Remains of aurochs hair were not known until the early 1980s. [42] Depictions show that the North African aurochs may have had a light saddle marking on its back. [40] Calves were probably born with a chestnut colour, and young bulls changed to black with a white eel stripe running down the spine, while cows retained a reddish-brown colour. Both sexes had a light-coloured muzzle, but evidence for variation in coat colour does not exist. Egyptian grave paintings show cattle with a reddish-brown coat colour in both sexes, with a light saddle, but the horn shape of these suggest that they may depict domesticated cattle. [5] Many primitive cattle breeds, particularly those from Southern Europe, display similar coat colours to the aurochs, including the black colour in bulls with a light eel stripe, a pale mouth, and similar sexual dimorphism in colour. [5] [40] A feature often attributed to the aurochs is blond forehead hairs. According to historical descriptions of the aurochs, it had long and curly forehead hair, but none mentions a certain colour. Although the colour is present in a variety of primitive cattle breeds, it is probably a discolouration that appeared after domestication. [5]

Body shape

Aurochsfeatures.jpg
Drawing based on an aurochs bull skeleton from Lund and a cow skeleton from Cambridge, with characteristic features of the aurochs
Indian Aurochs B p namadicus 3.jpg
Speculative profile of an Indian aurochs

The proportions and body shape of the aurochs were strikingly different from many modern cattle breeds. For example, the legs were considerably longer and more slender, resulting in a shoulder height that nearly equalled the trunk length. The skull, carrying the large horns, was substantially larger and more elongated than in most cattle breeds. As in other wild bovines, the body shape of the aurochs was athletic, and especially in bulls, showed a strongly expressed neck and shoulder musculature. Therefore, the fore hand was larger than the rear, similar to the wisent, but unlike many domesticated cattle. Even in carrying cows, the udder was small and hardly visible from the side; this feature is equal to that of other wild bovines. [5]

Size

The aurochs was one of the largest herbivores in Holocene Europe. The size of an aurochs appears to have varied by region, with larger specimens in northern Europe than farther south. Aurochs in Denmark and Germany ranged in height at the shoulders between 155–180 cm (61–71 in) in bulls and 135–155 cm (53–61 in) in cows, while aurochs bulls in Hungary reached 160 cm (63 in). [43]

The African aurochs was similar in size to the European aurochs in the Pleistocene, but declined in size during the transition to the Holocene; it may have also varied in size geographically. [44]

The body mass of aurochs appears to have shown some variability. Some individuals reached around 700 kg (1,540 lb), whereas those from the late Middle Pleistocene are estimated to have weighed up to 1,500 kg (3,310 lb). [5] The aurochs exhibited considerable sexual dimorphism in the size of males and females. [45]

Horns

The horns were massive, reaching 80 cm (31 in) in length and between 10 and 20 cm (3.9 and 7.9 in) in diameter. [40] Its horns grew from the skull at a 60-degree angle to the muzzle facing forwards and were curved in three directions, namely upwards and outwards at the base, then swinging forwards and inwards, then inwards and upwards. The curvature of bull horns was more strongly expressed than horns of cows. [5] The basal circumference of horn cores reached 44.5 cm (17.5 in) in the largest Chinese specimen and 48 cm (19 in) in a French specimen. [46] Some cattle breeds still show horn shapes similar to that of the aurochs, such as the Spanish fighting bull, and occasionally also individuals of derived breeds. [5]

Genetics

A well-preserved aurochs bone yielded sufficient mitochondrial DNA for a sequence analysis in 2010, which showed that its genome consists of 16,338 base pairs. [47] Further studies using the aurochs whole genome sequence have identified candidate microRNA-regulated domestication genes. [48] A comprehensive sequence analysis of Late Pleistocene and Holocene aurochs published in 2024 suggested that Indian aurochs (represented by modern zebu cattle) were the most genetically divergent aurochs population, having diverged from other aurochs around 300–166,000 years ago, with other aurochs populations spanning Europe and the Middle East to East Asia sharing much more recent common ancestry within the last 100,000 years. Late Pleistocene European aurochs were found to have a small (~3%) ancestry component from a divergent lineage that split prior to the divergence of Indian and other aurochs, suggested to be residual from earlier European aurochs populations. Towards the end of the Late Pleistocene, European aurochs experienced considerable gene flow from Middle Eastern aurochs. European Holocene aurochs primarily descend from those that were present in the Iberian Peninsula during the Last Glacial Maximum, with the Holocene also seeing mixing between previously isolated aurochs populations. [49]

Distribution and habitat

Life restoration of aurochs in a temperate forested landscape in Europe during the Eemian interglacial (130-115,000 years ago). Aurochs Eemian landscape.jpg
Life restoration of aurochs in a temperate forested landscape in Europe during the Eemian interglacial (130–115,000 years ago).

The aurochs was widely distributed in North Africa, Mesopotamia, and throughout Europe to the Pontic–Caspian steppe, Caucasus and Western Siberia in the west and to the Gulf of Finland and Lake Ladoga in the north. [50]

Fossil horns attributed to the aurochs were found in Late Pleistocene deposits at an elevation of 3,400 m (11,200 ft) on the eastern margin of the Tibetan plateau close to the Heihe River in Zoigê County that date to about 26,620±600 years BP. Most fossils in China were found in plains below 1,000 m (3,300 ft) in Heilongjiang, Yushu, Jilin, northeastern Manchuria, Inner Mongolia, near Beijing, Yangyuan County in Hebei province, Datong and Dingcun in Shanxi province, Huan County in Gansu and in Guizhou provinces. [46] Ancient DNA in aurochs fossils found in Northeast China indicate that the aurochs survived in the region until at least 5,000 years BP. [51] Fossils were also excavated on the Korean Peninsula, [52] and in the Japanese archipelago. [53] [54]

During warm interglacial periods the aurochs was widespread across Europe, [55] but during glacial periods retreated into southern refugia in the Iberian, Italian and Balkan peninsulas. [49]

Landscapes in Europe probably consisted of dense forests throughout much of the last few thousand years. The aurochs is likely to have used riparian forests and wetlands along lakes. [45] Analysis of specimens found in Britain suggests that aurochs preferred inhabiting low lying relatively flat landscapes. [56] Pollen of mostly small shrubs found in fossiliferous sediments with aurochs remains in China indicate that it preferred temperate grassy plains or grasslands bordering woodlands. [46] It may have also lived in open grasslands. [57] In the warm Atlantic period of the Holocene, it was restricted to remaining open country and forest margins, where competition with livestock and humans gradually increased leading to a successive decline of the aurochs. [58]

Behaviour and ecology

A Middle Pleistocene landscape in Spain, including aurochs (background right), as well as the extinct fallow deer Dama celiae (foreground) wild horse (left), the straight-tusked elephant (background centre-left), bison, (background centre) and the narrow-nosed rhinoceros (far right) Middle Pleistocene landscape in Manzanares valley.png
A Middle Pleistocene landscape in Spain, including aurochs (background right), as well as the extinct fallow deer Dama celiae (foreground) wild horse (left), the straight-tusked elephant (background centre-left), bison, (background centre) and the narrow-nosed rhinoceros (far right)

Aurochs formed small herds mainly in winter, but typically lived singly or in smaller groups during the summer. [50] If aurochs had social behaviour similar to their descendants, social status would have been gained through displays and fights, in which both cows and bulls engaged. [40] Since it has a hypsodont jaw, it has been suggested to have been a grazer, with a food selection very similar to domesticated cattle [5] feeding on grass, twigs and acorns. [50] Mesowear analysis of Holocene Danish aurochs premolar teeth indicates that it changed from an abrasion-dominated grazer in the Danish Preboreal to a mixed feeder in the Boreal, Atlantic and Subboreal periods. [58] Dental microwear and mesowear analysis of specimens from the Pleistocene of Britain has found these aurochs had mixed feeding to browsing diets, rather than being strict grazers. [59]

Mating season was in September, and calves were born in spring. [50] Rutting bulls had violent fights, and evidence from the Jaktorów forest shows that they were fully capable of mortally wounding one another. In autumn, aurochs fed for the winter, gaining weight and possessing a shinier coat than during the rest of the year. Calves stayed with their mothers until they were strong enough to join and keep up with the herd on the feeding grounds. Aurochs calves would have been vulnerable to predation by grey wolves (Canis lupus) and brown bears (Ursus arctos), while the immense size and strength of healthy adult aurochs meant they likely did not need to fear most predators. [5] According to historical descriptions, the aurochs was swift despite its build, could be very aggressive if provoked, and was not generally fearful of humans. [5] In Middle Pleistocene Europe, aurochs were likely predated upon by the "European jaguar" Panthera gombaszoegensis and the scimitar toothed-cat (Homotherium latidens), [60] with evidence for the consumption of aurochs by cave hyenas (Crocuta (Crocuta) spelaea) having been found from Late Pleistocene Italy. [61] The lion (Panthera leo), tiger (Panthera tigris) and wolf are thought to have been the aurochs main predators during the Holocene. [45]

During interglacial periods in the Middle Pleistocene and early Late Pleistocene in Europe, the aurochs occurred alongside other large temperate adapted megafauna species, including the straight-tusked elephant (Palaeoloxodon antiquus), Merck's rhinoceros (Stephanorhinus kirchbergensis), the narrow-nosed rhinoceros, (Stephanorhinus hemitoechus) and the Irish elk/giant deer (Megaloceros giganteus). [55]

Relationship with humans

In Asia

Unicorn with object. Mohenjo-daro.jpg
Seal from Mohenjo-daro
Berlin - Pergamon - Porta d'Ishtar - Ur.JPG
Relief on the Ishtar Gate on display at the Pergamon Museum

Acheulean layers in Hunasagi on India's southern Deccan Plateau yielded aurochs bones with cut marks. [62] An aurochs bone with cut marks induced with flint was found in a Middle Paleolithic layer at the Nesher Ramla Homo site in Israel; it was dated to Marine Isotope Stage 5 about 120,000 years ago. [63] An archaeological excavation in Israel found traces of a feast held by the Natufian culture around 12,000 years BP, in which three aurochs were eaten. This appears to be an uncommon occurrence in the culture and was held in conjunction with the burial of an older woman, presumably of some social status. [64] Petroglyphs depicting aurochs in Gobustan Rock Art in Azerbaijan date to the Upper Paleolithic to Neolithic periods. [65] Aurochs bones and skulls found at the settlements of Mureybet, Hallan Çemi and Çayönü indicate that people stored and shared food in the Pre-Pottery Neolithic B culture. [66] Remains of an aurochs were also found in a necropolis in Sidon, Lebanon, dating to around 3,700 years BP; the aurochs was buried together with numerous animals, a few human bones and foods. [67]

Seals dating to the Indus Valley civilisation found in Harappa and Mohenjo-daro show an animal with curved horns like an aurochs. [68] [69] Aurochs figurines were made by the Maykop culture in the Western Caucasus. [70]

The aurochs is denoted in the Akkadian words rīmu and rēmu, both used in the context of hunts by rulers such as Naram-Sin of Akkad, Tiglath-Pileser I and Shalmaneser III; in Mesopotamia, it symbolised power and sexual potency, was an epithet of the gods Enlil and Shamash, denoted prowess as an epithet of the king Sennacherib and the hero Gilgamesh. Wild bulls are frequently referred to in Ugaritic texts as hunted by and sacrificed to the god Baal. [71] An aurochs is depicted on Babylon's Ishtar Gate, constructed in the 6th century BC. [72]

In Africa

Petroglyphs depicting aurochs found in Qurta in the upper Nile valley were dated to the Late Pleistocene about 19–15,000 years BP using luminescence dating and are the oldest engravings found to date in Africa. [73] Aurochs are part of hunting scenes in reliefs in a tomb at Thebes, Egypt dating to the 20th century BC, and in the mortuary temple of Ramesses III at Medinet Habu dating to around 1175 BC. The latter is the youngest depiction of aurochs in Ancient Egyptian art to date. [74]

In Europe

Lascaux painting.jpg
Aurochs in a cave painting in Lascaux
Gold cup Vafio 1500 to 1450 BC, NAMA 1758 080866.jpg
A cup from Vaphio showing an aurochs hunt, 15th century BC
Moldavia's coat of Arms of 1481.jpg
Coat of arms of Moldavia from 1481 at Putna Monastery

Evidence has been found for the butchery of aurochs by archaic humans in Europe during the Middle Palaeolithic, such as the Biache-Saint-Vaast site in northern France dating to around 240,000 years ago, where bones of aurochs have been found burnt by fire and with cut marks, thought to have been created by Neanderthals. [75] [76] At the late Middle Palaeolithic Cueva Des-Cubierta site in Spain, Neanderthals are proposed to have kept the skulls of aurochs as hunting trophies. [77]

The aurochs is widely represented in Upper Paleolithic cave paintings in the Chauvet and Lascaux caves in southern France dating to 36,000 and 21,000 years BP, respectively. [78] Two Paleolithic rock engravings in the Calabrian Romito Cave depict an aurochs. [79] Palaeolithic engravings showing aurochs were also found in the Grotta del Genovese on the Italian island of Levanzo. [80] Upper Paleolithic rock engravings and paintings depicting the aurochs were also found in caves on the Iberian Peninsula dating from the Gravettian to the Magdalenian cultures. [81] [82] [83] Aurochs bones with chop and cut marks were found at various Mesolithic hunting and butchering sites in France, Luxemburg, Germany, the Netherlands, England and Denmark. [84] Aurochs bones were also found in Mesolithic settlements by the Narva and Emajõgi rivers in Estonia. [85] Aurochs and human bones were uncovered from pits and burnt mounds at several Neolithic sites in England. [86] A cup found in the Greek site of Vaphio shows a hunting scene, in which people try to capture an aurochs. [87] One of the bulls throws one hunter on the ground while attacking the second with its horns. The cup seems to date to Mycenaean Greece. [88] [89] Greeks and Paeonians hunted aurochs and used their huge horns as trophies, cups for wine, and offerings to the gods and heroes. The ox mentioned by Samus, Philippus of Thessalonica and Antipater as killed by Philip V of Macedon on the foothills of mountain Orvilos, was actually an aurochs; Philip offered the horns, which were 105 cm (41 in) long and the skin to a temple of Hercules. [90] The aurochs was described in Julius Caesar's Commentarii de Bello Gallico . [6] Aurochs were occasionally captured and exhibited in venatio shows in Roman amphitheatres such as the Colosseum. [91] Aurochs horns were often used by Romans as hunting horns. [5]

In the Nibelungenlied , Sigurd kills four aurochs. [92] During the Middle Ages, aurochs horns were used as drinking horns including the horn of the last bull; many aurochs horn sheaths are preserved today. [93] The aurochs drinking horn at Corpus Christi College, Cambridge was engraved with the college's coat of arms in the 17th century. [94] An aurochs head with a star between its horns and Christian iconographic elements represents the official coat of arms of Moldavia perpetuated for centuries. [95]

Aurochs were hunted with arrows, nets and hunting dogs, and its hair on the forehead was cut from the living animal; belts were made out of this hair and believed to increase the fertility of women. When the aurochs was slaughtered, the os cordis was extracted from the heart; this bone contributed to the mystique and magical powers that were attributed to it. [5] In eastern Europe, the aurochs has left traces in expressions like "behaving like an aurochs" for a drunken person behaving badly, and "a bloke like an aurochs" for big and strong people. [45]

Domestication

The earliest-known domestication of the aurochs dates to the Neolithic Revolution in the Fertile Crescent, where cattle hunted and kept by Neolithic farmers gradually decreased in size between 9800 and 7500 BC. Aurochs bones found at Mureybet and Göbekli Tepe are larger in size than cattle bones from later Neolithic settlements in northern Syria like Dja'de el-Mughara and Tell Halula. [96] In Late Neolithic sites of northern Iraq and western Iran dating to the sixth millennium BC, cattle remains are also smaller but more frequent, indicating that domesticated cattle were imported during the Halaf culture from the central Fertile Crescent region. [97] Results of genetic research indicate that the modern taurine cattle (Bos taurus) arose from 80 aurochs tamed in southeastern Anatolia and northern Syria about 10,500 years ago. [15] Taurine cattle spread into the Balkans and northern Italy along the Danube River and the coast of the Mediterranean Sea. [98] Hybridisation between male aurochs and early domestic cattle occurred in central Europe between 9500 and 1000 BC. [99] Analyses of mitochondrial DNA sequences of Italian aurochs specimens dated to 17–7,000 years ago and 51 modern cattle breeds revealed some degree of introgression of aurochs genes into south European cattle, indicating that female aurochs had contact with free-ranging domestic cattle. [100] Cattle bones of various sizes found at a Chalcolithic settlement in the Kutná Hora District provide further evidence for hybridisation of aurochs and domestic cattle between 3000 and 2800 BC in the Bohemian region. [43] Whole genome sequencing of a 6,750-year-old aurochs bone found in England was compared with genome sequence data of 81 cattle and single-nucleotide polymorphism data of 1,225 cattle. Results revealed that British and Irish cattle breeds share some genetic variants with the aurochs specimen; early herders in Britain might have been responsible for the local gene flow from aurochs into the ancestors of British and Irish cattle. [101] The Murboden cattle breed also exhibits sporadic introgression of female European aurochs into domestic cattle in the Alps. [102] Domestic cattle continued to diminish in both body and horn size until the Middle Ages. [87]

Comparative analysis of single-nucleotide polymorphisms and shared alleles revealed admixture between East Asian aurochs and introduced taurine cattle in ancient China, for example at Shimao. This suggested the incorporation of local aurochs into domestic cattle as far back as 4,000 years BP, either through spontaneous introgression, or the capture of different aurochs groups to supplement domestic stocks. The same study detected derived alleles shared by aurochs and modern taurine cattle in East Asia, especially among Tibetan breeds. Introgression with local aurochs could have facilitated rapid adaptation to new environments. [17]

The Indian aurochs is thought to have been domesticated 10,000–8,000 years ago. [103] Aurochs fossils found at the Neolithic site of Mehrgarh in Pakistan are dated to around 8,000 years BP and represent some of the earliest evidence for its domestication on the Indian subcontinent. [30] Female Indian aurochs contributed to the gene pool of zebu (Bos indicus) between 5,500 and 4,000 years BP during the expansion of pastoralism in northern India. The zebu initially spread eastwards to Southeast Asia. [104] Hybridisation between zebu and early taurine cattle occurred in the Near East after 4,000 years BP coinciding with the drought period during the 4.2-kiloyear event. [105] The zebu was introduced to East Africa about 3,500–2,500 years ago, [98] and reached Mongolia in the 13th and 14th centuries. [106]

A third domestication event thought to have occurred in Egypt's Western Desert is not supported by results of an analysis of genetic admixture, introgression and migration patterns of 3,196 domestic cattle representing 180 populations. However, the same study supported extensive hybridization between taurine cattle in Africa, arrived from the Near East after domestication, and local wild African aurochs prior to the entry of the zebu in Africa. [98] The zebu was introduced through Ancient Egypt and started to spread comprehensively through West Africa in the last 1,400 years, along with Arabic cultural influences. Most modern African cattle breeds are hybridized to a variable extent with Indicine cattle, with introgression being most reduced in areas of West Africa where the tse-tse fly is present. [107]

Extinction

Scene from the tomb TT60 in Thebes, Egypt, depicting a North African aurochs bull, cow and calf being hunted with dogs and javelins. Intefiquer Tomb's aurochs.png
Scene from the tomb TT60 in Thebes, Egypt, depicting a North African aurochs bull, cow and calf being hunted with dogs and javelins.

The Indian aurochs (B. p. namadicus) became extinct sometime during the Holocene period, likely due to habitat loss caused by expanding pastoralism and interbreeding with the domestic zebu. [104] [108] The timing of extinction of aurochs in the Indian subcontinent is unclear, due to difficulty distinguishing aurochs remains from those of domestic cattle, with a 2021 review suggesting remains from Mehrgarh, Pakistan, dating to around 8,000 years ago "might constitute the only dated and reliably identified evidence" of Holocene Indian aurochs. [30] The extinction probably predates the historical period, due to a lack of references to the aurochs in Indian texts. [109]

A 2014 review suggested that the youngest remains of African aurochs (B. p. mauritanicus) dated to around 6,000 years Before Present (BP), [110] though some authors suggest that it may have survived until at least to the Roman period, as indicated by remains found in Buto and Faiyum in the Nile Delta. [44]

In China, aurochs persisted until at least 3,600 BP. [111]

The Eurasian aurochs (B. p. primigenius) was present in southern Sweden during the Holocene climatic optimum until at least 7,800 years BP. [112] In Denmark, the first-known local extinction of the aurochs occurred after the sea level rise on the newly formed Danish islands about 8,000–7,500 years BP, and the last documented aurochs lived in southern Jutland around 3,000 years BP. [37] The latest-known aurochs fossil in Great Britain dates to 3,245 years BP, and it was probably extinct by 3,000 years ago. [113]

Excessive hunting began and continued until the aurochs was nearly extinct. The gradual extinction of the aurochs in Central Europe was concurrent with the clearcutting of large forest tracts between the 9th and 12th centuries. [50]

By the 13th century, the aurochs existed only in small numbers in Eastern Europe, and hunting it became a privilege of nobles and later royals. [5] The population in Hungary was declining from at least the 9th century and was extinct in the 13th century. [114] [115]

Findings from subfossil records indicate that wild aurochs might have survived in northwestern Transylvania until the 14th to 16th century, in western Moldavia until probably the early 17th century. [116] [117]

The last-known aurochs herd lived in a marshy woodland in Poland's Jaktorów Forest. It decreased from around 50 individuals in the mid 16th century to four individuals by 1601. The last aurochs cow died in 1627 from natural causes. [118]

A 2021 study argued that the aurochs possibly survived in northeastern Bulgaria until at least the 17th century. [119] A horn-core excavated in 2020 in Sofia was identified as being from an aurochs; the archaeological layer in which it was found was dated to the second half of the 17th or first half of the 18th century, suggesting that aurochs may have survived in Bulgaria until that date. [120]

Breeding of aurochs-like cattle

Hausrindlainz.jpg
Heck cattle in Lainzer Tiergarten

In the early 1920s, Heinz Heck initiated a selective breeding program in Hellabrunn Zoo attempting to breed back the aurochs using several cattle breeds; the result is called Heck cattle. [121] Herds of these cattle were released to Oostvaardersplassen, a polder in the Netherlands in the 1980s as aurochs surrogates for naturalistic grazing with the aim to restore prehistorical landscapes. [122] Large numbers of them died of starvation during the cold winters of 2005 and 2010, and the project of no interference ended in 2018. [123]

Starting in 1996, Heck cattle were crossed with southern European cattle breeds such as Sayaguesa Cattle, Chianina and to a lesser extent Spanish Fighting Bulls in the hope of creating a more aurochs-like animal. The resulting crossbreeds are called Taurus cattle. [124] Other breeding-back projects are the Tauros Programme and the Uruz Project. [122] However, approaches aiming at breeding an aurochs-like phenotype do not equate to an aurochs-like genotype. [125]

See also

Related Research Articles

<span class="mw-page-title-main">Holocene</span> Current geological epoch

The Holocene is the current geological epoch, beginning approximately 11,700 years ago. It follows the Last Glacial Period, which concluded with the Holocene glacial retreat. The Holocene and the preceding Pleistocene together form the Quaternary period. The Holocene is an interglacial period within the ongoing glacial cycles of the Quaternary, and is equivalent to Marine Isotope Stage 1.

<span class="mw-page-title-main">Zebu</span> South Asian domestic cattle

The zebu, sometimes known in the plural as indicine cattle, Camel cow or humped cattle, is a species or subspecies of domestic cattle originating in South Asia. Zebu, like many Sanga cattle breeds, differs from taurine cattle by a fatty hump on their shoulders, a large dewlap, and sometimes drooping ears. They are well adapted to withstanding high temperatures and are farmed throughout the tropics.

<span class="mw-page-title-main">Bovinae</span> Subfamily of mammals

Bovines comprise a diverse group of 10 genera of medium to large-sized ungulates, including cattle, bison, African buffalo, water buffalos, and the four-horned and spiral-horned antelopes. The members of this group are classified into loose tribes rather than formal subgroups, as the evolutionary relationships within the groups are still uncertain. General characteristics include cloven hooves and usually at least one of the sexes of a species having true horns. The largest extant bovine is the gaur.

<i>Bos</i> Genus of wild and domestic cattle

Bos is a genus of bovines, which includes, among others, wild and domestic cattle.

<span class="mw-page-title-main">Yak</span> Long-haired domesticated bovid

The yak, also known as the Tartary ox, grunting ox, hairy cattle, or domestic yak, is a species of long-haired domesticated cattle found throughout the Himalayan region of Gilgit-Baltistan, Nepal, Sikkim (India), the Tibetan Plateau (China), Tajikistan Pamir mountains Afghanistan and as far north as Mongolia and Siberia. It is descended from the wild yak.

<span class="mw-page-title-main">Banteng</span> Species of wild bovine

The banteng, also known as tembadau, is a species of wild bovine found in Southeast Asia.

<span class="mw-page-title-main">Steppe bison</span> Extinct species of mammal

The steppe bison or steppe wisent is an extinct species of bison. It was widely distributed across the mammoth steppe, ranging from Western Europe to eastern Beringia in North America during the Late Pleistocene. It is ancestral to all North American bison, including ultimately modern American bison. Three chronological subspecies, Bison priscus priscus, Bison priscus mediator, and Bison priscus gigas, have been suggested.

<span class="mw-page-title-main">Late Pleistocene</span> Third division (unofficial) of the Pleistocene Epoch

The Late Pleistocene is an unofficial age in the international geologic timescale in chronostratigraphy, also known as the Upper Pleistocene from a stratigraphic perspective. It is intended to be the fourth division of the Pleistocene Epoch within the ongoing Quaternary Period. It is currently defined as the time between c. 129,000 and c. 11,700 years ago. The late Pleistocene equates to the proposed Tarantian Age of the geologic time scale, preceded by the officially ratified Chibanian. The beginning of the Late Pleistocene is the transition between the end of the Penultimate Glacial Period and the beginning of the Last Interglacial around 130,000 years ago. The Late Pleistocene ends with the termination of the Younger Dryas, some 11,700 years ago when the Holocene Epoch began.

<i>Pelorovis</i> Extinct genus of cattle

Pelorovis is an extinct genus of African wild cattle which existed during the Pleistocene epoch. Originally believed to be a giant member of Caprinae, related to modern sheep, it is now known to be a relative of cattle and buffalos. The best known and type species is Pelorovis oldowayensis, from the Early Pleistocene of Olduvai Gorge, Tanzania, though several others have been named. "Pelorovis" antiquus from the Late Pleistocene-Holocene, and "P." kaisensis, have since been moved into Syncerus, the same genus as living African buffalo.

Bos acutifrons is the most ancient representative of the genus Bos cattle. Fossils of an individual of B. acutifrons were found in middle Pleistocene-aged strata of Siwalik Hills of Kashmir, in either modern Pakistan or India, in the 19th century. The prehistoric species was described, along with Bos planifrons, by Richard Lydekker in 1877. In 1898 Lydekker synonymised B. planifrons with B. acutifrons, reconsidering the skull found to be that of a female individual of the same species.

<span class="mw-page-title-main">Bovini</span> Tribe of cattle

The tribe Bovini or wild cattle are medium to massive bovines that are native to Eurasia, North America, and Africa. These include the enigmatic, antelope-like saola, the African and Asiatic buffalos, and a clade that consists of bison and the wild cattle of the genus Bos. Not only are they the largest members of the subfamily Bovinae, they are the largest species of their family Bovidae. The largest species is the gaur, weighing up to 1,500 kg (3,300 lb).

<span class="mw-page-title-main">Sanga cattle</span> Breed of cattle

Sanga cattle is the collective name for indigenous cattle of some regions in Africa. They are sometimes identified as a subspecies with the scientific name Bos taurus africanus. Their history of domestication and their origins in relation to taurine cattle, zebu cattle (indicine), and native African varieties of the ancestral aurochs are a matter of debate. "African taurine", "sanga", "zenga", "sheko", "African indicine" are all sub-groups of Sanga cattle.

<span class="mw-page-title-main">Indian aurochs</span> Subspecies of mammals

The Indian aurochs is an extinct subspecies of aurochs that inhabited West Asia and the Indian subcontinent from the Late Pleistocene until its eventual extinction during the South Asian Stone Age. With no remains younger than 3,800 YBP ever recovered, the Indian aurochs was the first of the three aurochs subspecies to become extinct; the Eurasian aurochs and the North African aurochs persevered longer, with the latter being known to the Roman Empire, and the former surviving until the mid-17th century in Central Europe.

<span class="mw-page-title-main">Cattle</span> Large, domesticated, cloven-hooved herbivores

Cattle are large, domesticated, bovid ungulates widely kept as livestock. They are prominent modern members of the subfamily Bovinae and the most widespread species of the genus Bos. Mature female cattle are called cows and mature male cattle are bulls. Young female cattle are called heifers, young male cattle are oxen or bullocks, and castrated male cattle are known as steers.

<span class="mw-page-title-main">Uruz Project</span> Project having the goal of breeding back the extinct cattle species of aurochs

The Uruz Project had the goal of breeding back the extinct aurochs. Uruz is the old Germanic word for aurochs. The Uruz Project was initiated in 2013 by the True Nature Foundation and presented at TEDx DeExtinction, a day-long conference organised by the Long Now Foundation with the support of TED and in partnership with National Geographic Society, to showcase the prospects of bringing extinct species back to life. The de-extinction movement itself is spearheaded by the Long Now Foundation.

<i>Bubalus murrensis</i> Extinct species of mammal

Bubalus murrensis, also known as European water buffalo, is an extinct water buffalo species native to Europe during the Pleistocene epoch, possibly persisting into the Holocene.

<span class="mw-page-title-main">Bovina (subtribe)</span> Subtribe of cattle

Bovina is a subtribe of the Bovini tribe that generally includes the two living genera, Bison and Bos. However, this dichotomy has been challenged recently by molecular work that suggests that Bison should be regarded as a subgenus of Bos. Wild bovinans can be found naturally in North America and Eurasia.

<span class="mw-page-title-main">Pastoral period</span> Most Common Type of Central Saharan rock art

Pastoral rock art is the most common form of Central Saharan rock art, created in painted and engraved styles depicting pastoralists and bow-wielding hunters in scenes of animal husbandry, along with various animals, spanning from 6300 BCE to 700 BCE. The Pastoral Period is preceded by the Round Head Period and followed by the Caballine Period. The Early Pastoral Period spanned from 6300 BCE to 5400 BCE. Domesticated cattle were brought to the Central Sahara, and given the opportunity for becoming socially distinguished, to develop food surplus, as well as to acquire and aggregate wealth, led to the adoption of a cattle pastoral economy by some Central Saharan hunter-gatherers of the Late Acacus. In exchange, cultural information regarding utilization of vegetation in the Central Sahara was shared by Late Acacus hunter-gatherers with incoming Early Pastoral peoples.

<i>Bubalus mephistopheles</i> Extinct species of bovid

Bubalus mephistopheles, also known as the short-horned water buffalo, is an extinct species of bovine that lived in China during the Pleistocene and Holocene. It survived into historic times, perhaps as recently as 1200 BC.

Bos buiaensis is an extinct species of cattle. The species is known from a million year old skull fossil found at the archaeological site of Buya, Eritrea in 2003. It was reassembled by excavators from over one hundred shards.

References

  1. Mallon, D.P. (2023). "Bos primigenius". IUCN Red List of Threatened Species . 2023: e.T136721A237471616. Retrieved 27 September 2024.
  2. 1 2 Bojanus, L.H. (1827). "De Uro nostrate eiusque sceleto commentation". Nova Acta Physico-medica Academiae Caesareae Leopoldino-Carolinae Naturae Curiosum (in Latin). 13 (5): 53–478.
  3. Partridge, E. (1983). "Urus, Uri gallica". Origins: A Short Etymological Dictionary of Modern English. New York: Greenwich House. p. 523. ISBN   978-0-517-41425-5.
  4. 1 2 Lewis, C. T. & Short, C. (1879). "ūrus". A Latin Dictionary. Oxford: Clarendon Press. p. 1936.
  5. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Van Vuure, C. (2005). Retracing the Aurochs: History, Morphology and Ecology of an extinct wild Ox. Sofia: Pensoft Publishers. ISBN   954-642-235-5.
  6. 1 2 McDevitte, W. A. (1869). "Book 6, Chapter 28". The Gallic Wars by Julius Caesar. Harper's New Classical Library. Translated by Bohn, W. S. (First ed.). New York: Harper & Brothers.
  7. Crystal, David (2003). The Cambridge Encyclopedia of the English Language (Third ed.). Cambridge: Cambridge University Press. p. 213. ISBN   9781108437738.
  8. Campbell, D.I. & Whittle, P.M. (2017). "Three Case Studies: Aurochs, Mammoths and Passenger Pigeons". Resurrecting Extinct Species. Cham: Palgrave Macmillan. p. 30. doi:10.1007/978-3-319-69578-5_2. ISBN   978-3-319-69578-5.
  9. Linnaeus, C. (1758). "Bos Taurus". Systema naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis (in Latin). Vol. 1 (Tenth reformed ed.). Holmiae: Laurentii Salvii. p. 71.
  10. Daszkiewicz, P. & Samojlik, T. (2019). "Corrected date of the first description of aurochs Bos primigenius (Bojanus, 1827) and steppe bison Bison priscus (Bojanus, 1827)". Mammal Research. 64 (2): 299–300. doi: 10.1007/s13364-018-0389-6 .
  11. Falconer, H. (1859). "Notice of the various species of bovine animals". The Zoologist. 17: 6414–6429.
  12. Thomas, P. (1881). "Recherches sur les bovidés fossiles de l'Algérie". Bulletin de la Société Zoologique de France. 6 (Avril): 92–136.
  13. International Commission on Zoological Nomenclature (2003). "Opinion 2027 (Case 3010). Usage of 17 specific names based on wild species which are pre-dated by or contemporary with those based on domestic animals (Lepidoptera, Osteichthyes, Mammalia)". The Bulletin of Zoological Nomenclature. 60 (1): 81–84.
  14. Gentry, A.; Clutton-Brock, J. & Groves, C.P. (2004). "The naming of wild animal species and their domestic derivatives". Journal of Archaeological Science. 31 (5): 645–651. Bibcode:2004JArSc..31..645G. doi:10.1016/j.jas.2003.10.006.
  15. 1 2 Bollongino, R.; Burger, J.; Powell, A.; Mashkour, M.; Vigne, J.-D. & Thomas, M. G. (2012). "Modern Taurine Cattle descended from small number of Near-Eastern founders". Molecular Biology and Evolution . 29 (9): 2101–2104. doi: 10.1093/molbev/mss092 . PMID   22422765.
  16. Avise, J.C. & Ayala, F.J. (2009). In the Light of Evolution. Vol. 106. pp. 9933–9938. doi: 10.17226/12692 . ISBN   978-0-309-13986-1. PMID   25032348.
  17. 1 2 3 Hou, Jiawen; Guan, Xiwen; Xia, Xiaoting; Lyu, Yang; Liu, Xin; et al. (15 November 2024). "Evolution and legacy of East Asian aurochs". Science Bulletin. 69 (21): 3425–3433. Bibcode:2024SciBu..69.3425H. doi: 10.1016/j.scib.2024.09.016 . ISSN   2095-9273. PMID   39322456. Creative Commons by small.svg  This article incorporates textfrom this source, which is available under the CC BY 4.0 license.
  18. Mangano, G., Bonfiglio, L., & Petruso, D. (2005). Excavations of 2003 at the S. Teodoro cave (North-Eastern Sicily, Italy): preliminary faunistic and stratigraphic data. Geo. Alp, 2, 71-76.
  19. Petruso, D., Sara, M., Surdi, G., & Masini, F. (2011). Le faune a mammiferi della Sicilia tra il Tardiglaciale e l'Olocene. Biogeographia–The Journal of Integrative Biogeography, 30(1).
  20. Siarabi, S.; Kostopoulos, D. S.; Bartsiokas, A.; Rozzi, R. (2023). "Insular aurochs (Mammalia, Bovidae) from the Pleistocene of Kythera Island, Greece". Quaternary Science Reviews. 319. 108342. Bibcode:2023QSRv..31908342S. doi:10.1016/j.quascirev.2023.108342. S2CID   263817925.
  21. Bibi, F. (2013). "A multi-calibrated mitochondrial phylogeny of extant Bovidae (Artiodactyla, Ruminantia) and the importance of the fossil record to systematics". BMC Evolutionary Biology. 13 (1): 166. Bibcode:2013BMCEE..13..166B. doi: 10.1186/1471-2148-13-166 . PMC   3751017 . PMID   23927069.
  22. 1 2 Wang, K.; Lenstra, J.A.; Liu, L.; Hu, Q.; Ma, T.; Qiu, Q. & Liu, J. (2018). "Incomplete lineage sorting rather than hybridization explains the inconsistent phylogeny of the wisent". Communications Biology. 1 (1): 169. doi: 10.1038/s42003-018-0176-6 . PMC   6195592 . PMID   30374461.
  23. Zeyland, J.; Wolko, Ł.; Lipiński, D.; Woźniak, A.; Nowak, A.; Szalata, M.; Bocianowski, J. & Słomski, R. (2012). "Tracking of wisent–bison–yak mitochondrial evolution". Journal of Applied Genetics. 53 (3): 317–322. doi: 10.1007/s13353-012-0090-4 . PMC   3402669 . PMID   22415349.
  24. Bibi, F. (2013). "A multi-calibrated mitochondrial phylogeny of extant Bovidae (Artiodactyla, Ruminantia) and the importance of the fossil record to systematics". BMC Evolutionary Biology. 13 (1): 166. Bibcode:2013BMCEE..13..166B. doi: 10.1186/1471-2148-13-166 . PMC   3751017 . PMID   23927069.
  25. Sinding, M.-H. S.; Ciucani, M. M.; Ramos-Madrigal, J.; Carmagnini, A.; Rasmussen, J. A.; Feng, S.; Chen, G.; Vieira, F. G.; Mattiangeli, V.; Ganjoo, R. K.; Larson, G.; Sicheritz-Pontén, T.; Petersen, B.; Frantz, L.; Gilbert, M. T. P. (2021). "Kouprey (Bos sauveli) genomes unveil polytomic origin of wild Asian Bos". iScience. 24 (11): 103226. Bibcode:2021iSci...24j3226S. doi:10.1016/j.isci.2021.103226. PMC   8531564 . PMID   34712923.
  26. Samartzidou, E.; Pandolfi, L.; Tsoukala, E.; Maniatis, Y. & Stoulos, S. (2021). "Bos primigenius Bojanus, 1827 (Mammalia, Bovidae) in Greece: new finds and a revision of the species, with a comparison with body-size variations of aurochs from the Italian Peninsula". Acta Zoologica Bulgarica. 74: 119–139.
  27. Martínez-Navarro, B.; Karoui-Yaakoub, N.; Oms, O.; Amri, L.; López-García, J.M.; Zerai, K.; Blain, H.A.; Mtimet, M.S.; Espigares, M.P.; Ali, N.B.H.; Ros-Montoya, S.; Boughdiri, M.; Agustí J.; Khayati-Ammar, H.; Maalaoui K.; El Khir, M.O.; Sala, R.; Othmani, A.; Hawas, R.; Gómez-Merino, G.; Solè, À.; Carbonell, E. & Palmqvist, P. (2014). "The early Middle Pleistocene archeopaleontological site of Wadi Sarrat (Tunisia) and the earliest record of Bos primigenius". Quaternary Science Reviews. 90: 37–46. Bibcode:2014QSRv...90...37M. doi:10.1016/j.quascirev.2014.02.016.
  28. Thomas, H. (1977). Géologie et paléontologie du gisement acheuléen de l'erg Tihodaïne, Ahaggar Sahara Algérien. Paris: Memoires du centre de recherches anthlropologiques, prehistoriques et ethnographiques.
  29. Pilgrim, G.E. (1947). "The evolution of the buffaloes, oxen, sheep and goats". Zoological Journal of the Linnean Society. 41 (279): 272–286. doi:10.1111/j.1096-3642.1940.tb02077.x.
  30. 1 2 3 Turvey, S.T.; Sathe, V.; Crees, J.J.; Jukar, A.M.; Chakraborty, P. & Lister, A.M. (2021). "Late Quaternary megafaunal extinctions in India: How much do we know?" (PDF). Quaternary Science Reviews. 252: 106740. Bibcode:2021QSRv..25206740T. doi:10.1016/j.quascirev.2020.106740. S2CID   234265221.
  31. Gómez-Olivencia, Asier; Sala, Nohemi; Arceredillo, D.; García, N.; Martínez-Pillado, V.; Rios-Garaizar, J.; Garate, D.; Solar, G.; Libano, I. (2015). "The Punta Lucero Quarry site (Zierbena, Bizkaia): a window into the Middle Pleistocene in the Northern Iberian Peninsula". Quaternary Science Reviews. 121: 52–74. Bibcode:2015QSRv..121...52G. doi:10.1016/j.quascirev.2015.05.001.
  32. Mecozzi, B.; Iannucci, A.; Carpentieri, M.; Pineda, A.; Rabinovich, R.; Sardella, R.; Moncel, M.-H. (2024). "Climatic and environmental changes of ~100 thousand years: The mammals from the early Middle Pleistocene sequence of Notarchirico (southern Italy)". PLOS ONE. 19 (10): e0311623. Bibcode:2024PLoSO..1911623M. doi: 10.1371/journal.pone.0311623 . PMC   11498728 . PMID   39441829.
  33. Mecozzi, B.; Iannucci, A.; Mancini, M.; Sardella, R. (2021). "Redefining Ponte Molle (Rome, central Italy): an important locality for Middle Pleistocene mammal assemblages of Europe". Alpine and Mediterranean Quaternary. 34 (1): 131–154. doi:10.26382/AMQ.2021.09.
  34. Preece, R.C.; Parfitt, S.A.; Bridgland, D.R.; Lewis, S.G.; Rowe, P.J.; Atkinson, T.C.; Candy, I.; Debenham, N.C.; Penkman, K.E.H.; Rhodes, E.J.; Schwenninger, J.-L.; Griffiths, H.I.; Whittaker, J.E.; Gleed-Owen, C. (2007). "Terrestrial environments during MIS 11: evidence from the Palaeolithic site at West Stow, Suffolk, UK". Quaternary Science Reviews. 26 (9–10): 1236–1300. Bibcode:2007QSRv...26.1236P. doi:10.1016/j.quascirev.2006.11.016.
  35. Tong, H.; Chen, X.; Zhang, B. & Wang, F. (2018). "New fossils of Bos primigenius (Artiodactyla, Mammalia) from Nihewan and Longhua of Hebei, China". Vertebrata PalAsiatica. 56 (1): 69–92.
  36. Osypinska, M.; Osypinski, P.; Belka, Z.; Chlodnicki, M.; Wiktorowicz, P.; Ryndziewicz, R. & Kubiak, M. (2021). "Wild and Domestic Cattle in the Ancient Nile Valley: Marks of ecological change". Journal of Field Archaeology. 46 (7): 429–447. doi:10.1080/00934690.2021.1924491. S2CID   236373843.
  37. 1 2 Gravlund, P.; Aaris-Sørensen, K.; Hofreiter, M.; Meyer, M.; Bollback, J.P. & Noe-Nygaard, N (2012). "Ancient DNA extracted from Danish aurochs (Bos primigenius): genetic diversity and preservation". Annals of Anatomy. 194 (1): 103–111. CiteSeerX   10.1.1.392.4989 . doi:10.1016/j.aanat.2011.10.011. PMID   22188739.
  38. Senglaub, K. (2002). "Sigmund von Herberstein (1486–1566) und die historischen Konfusionen um Ur und Wisent" (PDF). Säugetierkundliche Informationen. 5 (26): 253–266. Archived (PDF) from the original on 9 October 2022.
  39. Lydekker, R. (1912). "The wild Ox and its extermination". The ox and its kindred. London: Methuen &Co. Ltd. pp. 37–67.
  40. 1 2 3 4 5 Frisch, W. (2010). Der Auerochs: Das europäische Rind. Starnberg: Lipp Graphische Betriebe. ISBN   978-3-00-026764-2.
  41. Pyle, C.M. (1995). "Update to: "Some late sixteenth-century depictions of the aurochs (Bos primigenius Bojanus, extinct 1627): New evidence from Vatican MS Urb. Lat. 276". Archives of Natural History. 22 (3): 437–438. doi:10.3366/anh.1995.22.3.437.
  42. Ryder, M.L. (1984). "The first hair remains from an aurochs (Bos primigenius) and some medieval domestic cattle hair". Journal of Archaeological Science. 11 (1): 99–101. Bibcode:1984JArSc..11...99R. doi:10.1016/0305-4403(84)90045-1.
  43. 1 2 Kysely, R. (2008). "Aurochs and potential crossbreeding with domestic cattle in Central Europe in the Eneolithic period. A metric analysis of bones from the archaeological site of Kutná Hora-Denemark (Czech Republic)". Anthropozoologica. 43 (2): 7–37.
  44. 1 2 Linseele, V. (2004). "Size and size change of the African aurochs during the Pleistocene and Holocene". Journal of African Archaeology. 2 (2): 165–185. doi:10.3213/1612-1651-10026.
  45. 1 2 3 4 Van Vuure, T. (2002). "History, morphology and ecology of the Aurochs (Bos primigenius)". Lutra. 45 (1): 1–16. CiteSeerX   10.1.1.534.6285 .
  46. 1 2 3 Zong, G. (1984). "A record of Bos primigenius from the Quaternary of the Aba Tibetan Autonomous Region" (PDF). Vertebrata PalAsiatica. 22 (3). Translated by Dehut, J.: 239–245. Archived from the original (PDF) on 27 September 2007.
  47. Edwards, C.J.; Magee, D.A.; Park, S.D.E.; McGettigan, P.A. & Lohan, A.J. (2010). "A complete mitochondrial genome sequence from a mesolithic wild Aurochs (Bos primigenius)". PLOS ONE. 5 (2): e9255. Bibcode:2010PLoSO...5.9255E. doi: 10.1371/journal.pone.0009255 . PMC   2822870 . PMID   20174668.
  48. Braud, M.; Magee, D.A.; Park, S.D.E.; Sonstegard, T.S.; Waters, S.M.; MacHugh, D.E. & Spillane, C. (2017). "Genome-wide microRNA binding site variation between extinct wild Aurochs and modern cattle identifies candidate microRNA-regulated domestication genes". Frontiers in Genetics. 8: 3. doi: 10.3389/fgene.2017.00003 . PMC   5281612 . PMID   28197171.
  49. 1 2 Rossi, C.; Sinding, M.-H.S.; Mullin, V.E.; Scheu, A.; Erven, J.A.M.; Verdugo, M.P.; Daly, K.G.; Ciucani, M.M.; Mattiangeli, V.; Teasdale, M.D.; Diquelou, D.; Manin, A.; Bangsgaard, P.; Collins, M.; Lord, T.C. (2024). "The genomic natural history of the aurochs". Nature. 635 (8037): 136–141. Bibcode:2024Natur.635..136R. doi:10.1038/s41586-024-08112-6. PMID   39478219.
  50. 1 2 3 4 5 Heptner, V.G.; Nasimovich, A.A. & Bannikov, A.G. (1988) [1961]. "Aurochs, primitive cattle". Mlekopitajuščie Sovetskogo Soiuza. Moskva: Vysšaia Škola[Mammals of the Soviet Union]. Vol. Volume I. Artiodactyla and Perissodactyla. Washington DC: Smithsonian Institution and the National Science Foundation. pp. 539–549.
  51. Cai, D.; Zhang, N.; Zhu, S.; Chen, Q.; Wang, L.; Zhao, X.; Ma, X.; Royle, T.C.; Zhou, H. & Yang, D.Y. (2018). "Ancient DNA reveals evidence of abundant aurochs (Bos primigenius) in Neolithic Northeast China" (PDF). Journal of Archaeological Science. 98: 72–80. Bibcode:2018JArSc..98...72C. doi:10.1016/j.jas.2018.08.003. S2CID   135295723. Archived (PDF) from the original on 9 October 2022.
  52. Jo, Y.-S.; Baccus, J.T. & Koprowski, J. (2018). Mammals of Korea. Seoul: Magnolia Press. ISBN   978-89-6811-369-7.
  53. Kurosawa, Y. "モノが語る牛と人間の文化 - ② 岩手の牛たち" (PDF). LIAJ (109): 29–31. Archived (PDF) from the original on 9 October 2022. Retrieved 6 April 2016.
  54. Hasegawa, Y.; Okumura, Y. & Tatsukawa, H. (2009). "First record of Late Pleistocene Bison from the fissure deposits of the Kuzuu Limestone, Yamasuge, Sano-shi, Tochigi Prefecture, Japan" (PDF). Bulletin of Gunma Museum of Natural History (13): 47–52. Archived from the original (PDF) on 24 September 2015. Retrieved 6 April 2016.
  55. 1 2 Pushkina, D. (2007). "The Pleistocene easternmost distribution in Eurasia of the species associated with the Eemian Palaeoloxodon antiquus assemblage". Mammal Review. 37 (3): 224–245. doi:10.1111/j.1365-2907.2007.00109.x.
  56. Hall, S.J.G. (2008). "A comparative analysis of the habitat of the extinct aurochs and other prehistoric mammals in Britain". Ecography. 31 (2): 187–190. Bibcode:2008Ecogr..31..187H. doi:10.1111/j.0906-7590.2008.5193.x.
  57. Beutler, A. (1996). "Die Großtierfauna Europas und ihr Einfluss auf Vegetation und Landschaft". Natur und Kulturlandschaft. 1: 51–106.
  58. 1 2 Schulz, E. & Kaiser, T.M. (2007). "Feeding strategy of the Urus Bos primigenius Bojanus, 1827 from the Holocene of Denmark". Courier Forschungsinstitut Senckenberg. 259: 155–164.
  59. Rivals, F.; Lister, A.M. (2016). "Dietary flexibility and niche partitioning of large herbivores through the Pleistocene of Britain". Quaternary Science Reviews. 146: 116–133. Bibcode:2016QSRv..146..116R. doi:10.1016/j.quascirev.2016.06.007.
  60. Domingo, L.; Rodríguez-Gómez, G.; Libano, I.; Gómez-Olivencia, A. (2017). "New insights into the Middle Pleistocene paleoecology and paleoenvironment of the Northern Iberian Peninsula (Punta Lucero Quarry site, Biscay): A combined approach using mammalian stable isotope analysis and trophic resource availability modeling". Quaternary Science Reviews. 169: 243–262. Bibcode:2017QSRv..169..243D. doi:10.1016/j.quascirev.2017.06.008.
  61. Crezzini, J.; Boscato, P.; Ricci, S.; Ronchitelli, A.; Spagnolo, V.; Boschin, F. (2016). "A spotted hyaena den in the Middle Palaeolithic of Grotta Paglicci (Gargano promontory, Apulia, Southern Italy)". Archaeological and Anthropological Sciences. 8 (2): 227–240. Bibcode:2016ArAnS...8..227C. doi:10.1007/s12520-015-0273-0.
  62. Sathe, V. & Paddayya, K. (2012). "The faunal background of the stone age cultures of Hunsgi and Baichbal Valleys, Southern Deccan". Bulletin of the Deccan College Research Institute. 72: 79–97. JSTOR   43610690.
  63. Prévost, M.; Groman-Yaroslavski, I.; Gershtein, K.M.C.; Tejero, J.M. & Zaidner, Y. (2021). "Early evidence for symbolic behavior in the Levantine Middle Paleolithic: A 120 ka old engraved aurochs bone shaft from the open-air site of Nesher Ramla, Israel". Quaternary International. early view: 80–93. doi:10.1016/j.quaint.2021.01.002. S2CID   234236699.
  64. Munro, N.D. & Grosman, L. (2010). "Early evidence (ca. 12,000 B.P.) for feasting at a burial cave in Israel". Proceedings of the National Academy of Sciences of the United States of America. 107 (35): 15362–15366. Bibcode:2010PNAS..10715362M. doi: 10.1073/pnas.1001809107 . PMC   2932561 . PMID   20805510.
  65. Farajova, M. (2011). "Gobustan: Rock Art Cultural Landscape" (PDF). Adoranten. 11: 41–66. Archived (PDF) from the original on 9 October 2022.
  66. Bogaard, A.; Charles, M.; Twiss, K.C.; Fairbairn, A.; Yalman, N.; Filipović, D.; Demirergi, G.A.; Ertuğ, F.; Russell, N. & Henecke, J. (2009). "Private pantries and celebrated surplus: storing and sharing food at Neolithic Çatalhöyük, Central Anatolia". Antiquity. 83 (321): 649–668. doi:10.1017/S0003598X00098896. S2CID   162522860.
  67. Makarem, M. (2012). "Et si Europe était sidonienne?". L'Orient Le Jour (in French). Beirut. Archived from the original on 25 May 2013. Retrieved 3 January 2020.
  68. Mackay, E.J.H. (1935). "Steatite pectoral, once mounted in metal and filled with inlay". The Indus civilization. London: Lovat Dickson & Thompson Ltd. p. Plate J.
  69. Geer, A.A.E. (2008). "Bos primigenius. The Aurochs". Animals in stone: Indian mammals sculptured through time. Leiden: Brill. pp. 111–114. ISBN   978-90-04-16819-0.
  70. Reinhold, S.; Gresky, J.; Berezina, N.; Kantorovich, A.R.; Knipper, C.; Maslov, V.E.; Petrenko, V.G.; Alt, K.W. & Belinsky, A.B. (2017). "Contextualising Innovation: Cattle Owners and Wagon Drivers in the North Caucasus and Beyond". In Maran, J. & Stockhammer, P. (eds.). Appropriating Innovations. Entangled Knowledge in Eurasia, 5000-150 BCE. Oxford: Oxbow Books. pp. 78–97. ISBN   9781785707247.
  71. Wyatt, S. & Wyatt, N. (2013). "The longue durée in the beef business". In Loretz, O.; Ribichini, S.; Watson, W.G.E. & Zamora, J.Á. (eds.). Ritual, Religion, and Reason. Studies in the Ancient World in Honour of Paolo Xella. Münster: Ugarit-Verlag. pp. 417–450. ISBN   9783868350876.
  72. Shugart, H.H. (2014). "Taming the Unicorn, Yoking the Aurochs: Animal and Plant Domestication and the Consequent Alteration of the Surface of the Earth". Foundations of the Earth. Columbia University Press. pp. 35–70. doi:10.7312/shug16908-003. ISBN   9780231537698.
  73. Huyge, D.; Vandenberghe, D.A.; De Dapper, M.; Mees, F.; Claes, W. & Darnell, J.C. (2011). "First evidence of Pleistocene rock art in North Africa: securing the age of the Qurta petroglyphs (Egypt) through OSL dating". Antiquity. 85 (330): 1184–1193. doi:10.1017/S0003598X00061998. S2CID   130471822.
  74. Beierkuhnlein, C. (2015). "Bos primigenius in Ancient Egyptian art – historical evidence for the continuity of occurrence and ecology of an extinct key species" (PDF). Frontiers of Biogeography. 7 (3): 107–118. doi:10.21425/F5FBG21527. S2CID   55643283. Archived (PDF) from the original on 9 October 2022.
  75. Bahain, J.-J.; Falguères, C.; Laurent, M.; Dolo, J.-M.; Shao, Q.; Auguste, P.; Tuffreau, A. (2015). "ESR/U-series dating of faunal remains from the paleoanthropological site of Biache-Saint-Vaast (Pas-de-Calais, France)". Quaternary Geochronology. 30: 541–546. Bibcode:2015QuGeo..30..541B. doi:10.1016/j.quageo.2015.02.020.
  76. Hérisson, D.; Locht, J.-L.; Auguste, P.; Tuffreau, A. (2013). "Néandertal et le feu au Paléolithique moyen ancien. Tour d'horizon des traces de son utilisation dans le Nord de la France" (PDF). L'Anthropologie (in French). 117 (5): 541–578. doi:10.1016/j.anthro.2013.10.002.
  77. Baquedano, E.; Arsuaga, J. L.; Pérez-González, A.; Laplana, C.; Márquez, B.; Huguet, R.; Gómez-Soler, S.; Villaescusa, L.; Galindo-Pellicena, M. Ángeles; Rodríguez, Laura; García-González, R.; Ortega, M.-C.; Martín-Perea, D. M.; Ortega, A. I.; Hernández-Vivanco, L. (2023). "A symbolic Neanderthal accumulation of large herbivore crania". Nature Human Behaviour. 7 (3): 342–352. doi:10.1038/s41562-022-01503-7. PMC   10038806 . PMID   36702939.
  78. Geneste, J.M. (2017). "From Chauvet to Lascaux: 15,000 years of cave art". Archaeology, Ethnology & Anthropology of Eurasia. 45 (3): 29–40. doi: 10.17746/1563-0110.2017.45.3.029-040 .
  79. Vacca, B.B. (2012). "The hunting of large mammals in the Upper Palaeolithic of southern Italy: A diachronic case study from Grotta del Romito". Quaternary International. 252: 155–164. Bibcode:2012QuInt.252..155V. doi:10.1016/j.quaint.2011.06.054.
  80. Di Maida, G.; García-Diez, M.; Pastoors, A. & Terberger, T. (2018). "Palaeolithic art at Grotta di Cala dei Genovesi, Sicily: a new chronology for mobiliary and parietal depictions". Antiquity. 92 (361): 38–55. doi:10.15184/aqy.2017.209. S2CID   166147585.
  81. Weniger, G.C. (1999). "Representations of the Aurochs in the Upper Palaeolithic and Epipalaeolithic on the Iberian Peninsula". In Weniger, G.C. (ed.). Archäologie und Biologie des Aurochsen. Bonn: Neanderthal Museum. pp. 133–140. ISBN   9783980583961.
  82. Fernandes, A.P.B. (2008). "Aesthetics, ethics, and rock art conservation: How far can we go? The case of recent conservation tests carried out in un-engraved outcrops in the Côa Valley, Portugal" (PDF). In Heyd, T.; Clegg, J. (eds.). Aesthetics and Rock Art III: Symposium. British Archaeological Reports. Vol. 1818. Oxford: Archaeopress. pp. 85–92. ISBN   9781407303048. Archived (PDF) from the original on 9 October 2022.
  83. Soares De Figueiredo, S.; Botica, N.; Bueno Ramirez, P.; Tsoupra, A. & Mirao, J. (2020). "Analysis of portable rock art from Foz do Medal (Northwest Iberia): Magdalenian images of horses and aurochs". Comptes Rendus Palevol. 19 (4): 63–77. doi: 10.5852/cr-palevol2020v19a4 .
  84. Prummel, W. & Niekus, M.J.L.T. (2011). "Late Mesolithic hunting of a small female aurochs in the valley of the River Tjonger (the Netherlands) in the light of Mesolithic aurochs hunting in NW Europe". Journal of Archaeological Science. 38 (7): 1456–1467. Bibcode:2011JArSc..38.1456P. doi:10.1016/j.jas.2011.02.009.
  85. Kriiska, A. (2000). "Settlements of coastal Estonia and maritime hunter-gatherer economy". Lietuvos Archeologija. 19: 153–166.
  86. Lynch, A.H.; Hamilton, J. & Hedges, R.E.M. (2008). "Where the wild things are: Aurochs and Cattle in England". Antiquity. 82 (318): 1025–1039. doi:10.1017/S0003598X00097751. S2CID   161079743.
  87. 1 2 Ajmone-Marsan, P.; Garcia, J.F. & Lenstra, J.A. (2010). "On the origin of cattle: How Aurochs became cattle and colonized the World". Evolutionary Anthropology. 19 (4): 148–157. doi:10.1002/evan.20267. S2CID   86035650.
  88. Davis, E.N. (1974). "The Vapheio Cups: One Minoan and One Mycenean?". The Art Bulletin. 56 (4): 472–487. doi:10.1080/00043079.1974.10789932.
  89. De Grummond, W.W. (1980). "Hands and Tails on the Vapheio Cups". American Journal of Archaeology. 84 (3): 335–337. doi:10.2307/504710. JSTOR   504710.
  90. Douglas, N. (1927). Birds and Beasts of the Greek Anthology. Florence: B. Blom. ISBN   9780405084614.
  91. Knight, C. (1847). "European bison, or Aurochs". The National Cyclopaedia of Useful Knowledge. Vol. (Volume III). London: Little, Brown and Co. pp. 367–371.
  92. Heinzle, J., ed. (2013). Das Nibelungenlied und die Klage: Nach der Handschrift 857 der Stiftsbibliothek St. Gallen. Deutscher Klassiker Verlag. p. 300. ISBN   9783618661207.
  93. Bro-Jørgensen, M.H.; Carøe, C.; Vieira, F.G.; Nestor, S.; Hallström, A.; Gregersen, K.M.; Etting, V.; Gilbert, M.T.P. & Sinding, M.H.S. (2018). "Ancient DNA analysis of Scandinavian medieval drinking horns and the horn of the last aurochs bull". Journal of Archaeological Science. 99: 47–54. Bibcode:2018JArSc..99...47B. doi:10.1016/j.jas.2018.09.001. S2CID   133684586.
  94. Oman, C. (1972). "Cambridge and Cornelimünster". Aachener Kunstblätter. 43: 305–307.
  95. Boutiuc, M.; Florescu, O.; Vasilache, V. & Sandu, I. (2020). "The comparative study of the state of conservation of two medieval documents on parchment from different historical periods". Materials. 13 (21): 4766. Bibcode:2020Mate...13.4766H. doi: 10.3390/ma13214766 . PMC   7662666 . PMID   33114524.
  96. Helmer, D.; Gourichon, L.; Monchot, H.; Peters, J. & Segui, M.S. (2005). "Identifying early domestic cattle from pre-pottery Neolithic sites on the Middle Euphrates using sexual dimorphism". In Vigne, J.D.; Peters, J. & Helmer, D. (eds.). The first steps of animal domestication: new archeological approaches. Oxford: Oxbow Books. pp. 86–95. ISBN   1-84217-121-6.
  97. Arbuckle, B.S.; Price, M.D.; Hongo, H. & Öksüz, B. (2016). "Documenting the initial appearance of domestic cattle in the Eastern Fertile Crescent (northern Iraq and western Iran)" (PDF). Journal of Archaeological Science. 72: 1–9. Bibcode:2016JArSc..72....1A. doi:10.1016/j.jas.2016.05.008. S2CID   85441215. Archived (PDF) from the original on 9 October 2022.
  98. 1 2 3 Pitt, D.; Sevane, N.; Nicolazzi, E.L.; MacHugh, D.E.; Park, S.D.; Colli, L.; Martinez, R.; Bruford, M.W. & Orozco-terWengel, P. (2019). "Domestication of cattle: Two or three events?". Evolutionary Applications. 12 (1): 123–136. Bibcode:2019EvApp..12..123P. doi: 10.1111/eva.12674 . PMC   6304694 . PMID   30622640.
  99. Götherström, A.; Anderung, C.; Hellborg, L.; Elburg, R.; Smith, C.; Bradley, D.G. & Ellegren, H. (2005). "Cattle domestication in the Near East was followed by hybridization with aurochs bulls in Europe". Proceedings of the Royal Society B: Biological Sciences. 272 (1579): 2345–2351. doi: 10.1098/rspb.2005.3243 . PMC   1559968 . PMID   16243693.
  100. Beja-Pereira, A.; Caramelli, D.; Lalueza-Fox, C.; Vernesi, C.; Ferrand, N.; Casoli, A.; Goyache, F.; Royo, L.J.; Conti, S.; Lari, M.; Martini, A.; Ouragh, L.; Magid, A.; Atash, A.; Zsolnai, A.; Boscato, P.; Triantaphylidis, C.; Ploumi, K.; Sineo, L.; Mallegni, F.; Taberlet, P.; Erhardt, G.; Sampietro, L.; Bertranpetit, J.; Barbujani, G.; Luikart, G. & Bertorelle, G. (2006). "The origin of European cattle: Evidence from modern and ancient DNA". Proceedings of the National Academy of Sciences of the United States of America. 103 (21): 8113–8118. Bibcode:2006PNAS..103.8113B. doi: 10.1073/pnas.0509210103 . PMC   1472438 . PMID   16690747.
  101. Park, S.D.E.; Magee, D.A.; McGettigan, P.A.; Teasdale, M.D.; Edwards, C.J.; Lohan, A.J.; Murphy, A.; Braud, M.; Donoghue, M.T.; Liu, Y.; Chamberlain, A.T.; Rue-Albrecht, K.; Schroeder, S.; Spillane, C.; Tai, S.; Bradley, D.G.; Sonstegard, T.S.; Loftus, B.J. & MacHugh, D.E. (2015). "Genome sequencing of the extinct Eurasian wild aurochs, Bos primigenius, illuminates the phylogeography and evolution of cattle". Genome Biology. 16 (1): 234. doi: 10.1186/s13059-015-0790-2 . PMC   4620651 . PMID   26498365.
  102. Cubric-Curik, V.; Novosel, D.; Brajkovic, V.; Rota Stabelli, O.; Krebs, S.; Sölkner, J.; Šalamon, D.; Ristov, S.; Berger, B.; Trivizaki, S.; Bizelis, I.; Ferenčaković, M.; Rothammer, S.; Kunz, E.; Simčič, M.; Dovč, P.; Bunevski, G.; Bytyqi, H.; Marković, B.; Brka, M.; Kume, K.; Stojanović, S.; Nikolov, V.; Zinovieva, N.; Schönherz, A.A.; Guldbrandtsen, B.; Čačić, M.; Radović, S.; Miracle, P.; Vernesi, C.; Curik, I. & Medugorac, I. (2021). "Large-scale mitogenome sequencing reveals consecutive expansions of domestic taurine cattle and supports sporadic Aurochs introgression". Evolutionary Applications. 15 (4): 663–678. doi: 10.1111/eva.13315 . PMC   9046920 . PMID   35505892.
  103. Bradley, D.G.; MacHugh, D.E.; Cunningham, P. & Loftus, R.T. (1996). "Mitochondrial diversity and the origins of African and European cattle". Proceedings of the National Academy of Sciences of the United States of America. 93 (10): 5131–5135. Bibcode:1996PNAS...93.5131B. doi: 10.1073/pnas.93.10.5131 . PMC   39419 . PMID   8643540.
  104. 1 2 Chen, S.; Lin, B.-Z.; Baig, M.; Mitra, B.; Lopes, R. J.; Santos, A. M.; Magee, D. A.; Azevedo, M.; Tarroso, P.; Sasazaki, S.; Ostrowski, S.; Mahgoub, O.; Chaudhuri, T. K.; Zhang, Y.-p.; Costa, V.; Royo, L. J.; Goyache, F.; Luikart, G.; Boivin, N.; Fuller, D. Q.; Mannen, H.; Bradley, D. G.; Beja-Pereira, A. (2010). "Zebu Cattle are an exclusive legacy of the South Asia Neolithic". Molecular Biology and Evolution. 27 (1): 1–6. doi: 10.1093/molbev/msp213 . PMID   19770222.
  105. Verdugo, M.P.; Mullin, V.E.; Scheu, A.; Mattiangeli, V.; Daly, K.G.; Delser, P.M.; Hare, A.J.; Burger, J.; Collins, M.J.; Kehati, R. & Hesse, P. (2019). "Ancient cattle genomics, origins, and rapid turnover in the Fertile Crescent" (PDF). Science. 365 (6449): 173–176. Bibcode:2019Sci...365..173V. doi:10.1126/science.aav1002. PMID   31296769. S2CID   195894128. Archived (PDF) from the original on 9 October 2022.
  106. Mannen, H.; Kohno, M.; Nagata, Y.; Tsuji, S.; Bradley, D.G.; Yeo, J.S.; Nyamsamba, D.; Zagdsuren, Y.; Yokohama, M.; Nomura, K. & Amano, T. (2004). "Independent mitochondrial origin and historical genetic differentiation in North Eastern Asian cattle" (PDF). Molecular Phylogenetics and Evolution. 32 (2): 539–544. Bibcode:2004MolPE..32..539M. doi:10.1016/j.ympev.2004.01.010. PMID   15223036. Archived from the original (PDF) on 5 March 2023. Retrieved 22 December 2021.
  107. Meghen, C.; MacHugh, D.E.; Bradley, D.G. "Genetic characterization and West African cattle". fao.org. Archived from the original on 26 February 2019. Retrieved 20 September 2021.
  108. Rangarajan, M. (2001). India's Wildlife History. Delhi, India: Permanent Black. p. 4. ISBN   978-81-7824-140-1.
  109. van Vuure, T. (30 October 2014), Melletti, Mario; Burton, James (eds.), "Aurochs Bos primigenius Bojanus, 1827", Ecology, Evolution and Behaviour of Wild Cattle (1 ed.), Cambridge University Press, pp. 240–254, doi:10.1017/cbo9781139568098.017, ISBN   978-1-139-56809-8 , retrieved 2 November 2024
  110. Faith, J. Tyler (January 2014). "Late Pleistocene and Holocene mammal extinctions on continental Africa". Earth-Science Reviews. 128: 105–121. Bibcode:2014ESRv..128..105F. doi:10.1016/j.earscirev.2013.10.009.
  111. Hou, Jiawen; Guan, Xiwen; Xia, Xiaoting; Lyu, Yang; Liu, Xin; Mazei, Yuri; Xie, Ping; Chang, Fengqin; Zhang, Xiaonan; Chen, Jialei; Li, Xinyi; Zhang, Fengwei; Jin, Liangliang; Luo, Xiaoyu; Sinding, Mikkel-Holger S. (September 2024). "Evolution and legacy of East Asian aurochs". Science Bulletin. 69 (21): 3425–3433. Bibcode:2024SciBu..69.3425H. doi: 10.1016/j.scib.2024.09.016 . PMID   39322456.
  112. Magnell, O. (2017). "Climate Change at the Holocene Thermal Maximum and Its Impact on Wild Game Populations in South Scandinavia". In Monks, G.G. (ed.). Climate Change and Human Responses. Vertebrate Paleobiology and Paleoanthropology. Dordrecht: Springer. pp. 123–135. doi:10.1007/978-94-024-1106-5_7. ISBN   978-94-024-1105-8.
  113. Clutton-Brock, J. (1989). "Five thousand years of livestock in Britain". Biological Journal of the Linnean Society. 38 (1): 31–37. doi:10.1111/j.1095-8312.1989.tb01560.x.
  114. Bartosiewicz, L. (2006). "Interdisciplinary analysis of an Iron Age Aurochs horn core from Hungary: a case study". Acta Archaeologica Academiae Scientiarum Hungaricae. 57 (1–3): 153–163. doi:10.1556/AArch.57.2006.1-3.10.
  115. Bartosiewicz, L. (1997). "A horn worth blowing? A stray find of Aurochs from Hungary". Antiquity. 71 (274): 1007–1010. doi:10.1017/S0003598X00085902. S2CID   161722401.
  116. Bejenaru, L.; Stanc, S.; Popovici, M.; Balasescu, A. & Cotiuga, V. (2013). "Holocene subfossil records of the auroch (Bos primigenius) in Romania". The Holocene. 23 (4): 603–614. Bibcode:2013Holoc..23..603B. doi:10.1177/0959683612465448. S2CID   131580290.
  117. Németh, A.; Bárány, A.; Csorba, G.; Magyari, E.; Pazonyi, P.; Pálfy, J. (2017). "Holocene mammal extinctions in the Carpathian Basin: a review" (PDF). Mammal Review. 47 (1): 38–52. doi:10.1111/mam.12075. Archived (PDF) from the original on 9 October 2022.
  118. Rokosz, M. (1995). "History of the Aurochs (Bos taurus primigenius) in Poland" (PDF). Animal Genetics Resources Information. 16: 5–12. doi:10.1017/S1014233900004582. Archived from the original (PDF) on 14 January 2013.
  119. Boev, Z. (2016). "Subfossil vertebrate fauna from Forum Serdica (Sofia, Bulgaria), 16–18th Century AD". Acta Zoologica Bulgarica. 68 (3): 415–424.
  120. Boev, Z. (2021). "The last Bos primigenius survived in Bulgaria (Cetartiodactyla: Bovidae)". Lynx. New Series. 52: 139–142. doi: 10.37520/lynx.2021.010 . S2CID   246761121.
  121. Heck, H. (1951). "The breeding-back of the Aurochs". Oryx. 1 (3): 117–122. doi: 10.1017/S0030605300035286 .
  122. 1 2 Lorimer, J. & Driessen, C. (2016). "From "Nazi cows" to cosmopolitan "ecological engineers": specifying rewilding through a history of Heck cattle". Annals of the American Association of Geographers. 106 (3): 631–652. Bibcode:2016AAAG..106..631L. doi:10.1080/00045608.2015.1115332. S2CID   131547744.
  123. Theunissen, B. (2019). "The Oostvaardersplassen Fiasco". Isis. 110 (2): 341–345. doi: 10.1086/703338 .
  124. Bunzel-Drüke, M. (2001). "Ecological substitutes for Wild Horse (Equus ferus, Boddaert 1785 = E. przewalskii, Poljakov 1881) and Aurochs (Bos primigenius, Bojanus 1827)". Natur- und Kulturlandschaft. 4: 240–252. CiteSeerX   10.1.1.403.8349 .
  125. Sinding, M.-H.S. & Gilbert, M.T.P. (2016). "The draft genome of extinct European Aurochs and its implications for de-extinction". Open Quaternary. 2. doi: 10.5334/oq.25 .