European fallow deer

European fallow deer
Male (buck)
A male (buck) bellowing, UK, October 1964
Female (doe)
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Artiodactyla
Family: Cervidae
Subfamily: Cervinae
Tribe: Cervini
Genus: Dama
Species:
D. dama
Binomial name
Dama dama
Range:
1: (Former) native, includes D. mesopotamica
2: Possibly native
3: Early human introductions
4: Modern human introductions
Synonyms

Cervus dama Linnaeus, 1758

The European fallow deer (Dama dama), also known as the common fallow deer or simply fallow deer, is a species of ruminant mammal belonging to the family Cervidae. It is historically native to Turkey and possibly the Italian Peninsula, Balkan Peninsula, and the island of Rhodes near Anatolia. Prehistorically native[2] to and introduced into a larger portion of Europe, it has also been introduced to other regions in the world. It is one of two living species of fallow deer (Dama) alongside the Persian fallow deer (Dama mesapotamica).

Taxonomy[edit]

Some taxonomists include the rarer Persian fallow deer as a subspecies (D. d. mesopotamica),[3] with both species being grouped together as the fallow deer, while others treat it as a different species (D. mesopotamica).[1] The white-tailed deer (Odocoileus virginianus) was once classified as Dama virginiana and the mule deer or black-tailed deer (Odocoileus hemionus) as Dama hemionus; they were given a separate genus in the 19th century.

Description[edit]

Male (buck)
Mature buck showing common darker colouring of a winter coat with lighter area around the tail

The male fallow deer is known as a buck, the female is a doe, and the young a fawn. Adult bucks are 140–160 cm (55–63 in) long, 85–95 cm (33–37 in) in shoulder height, and typically 60–100 kg (130–220 lb) in weight; does are 130–150 cm (51–59 in) long, 75–85 cm (30–33 in) in shoulder height, and 30–50 kg (66–110 lb) in weight. The largest bucks may measure 190 cm (75 in) long and weigh 150 kg (330 lb).[4] Fawns are born in spring around 30 cm (12 in) and weigh around 4.5 kg (10 lb). Their lifespan is around 12–16 years.

Much variation occurs in the coat colour of the species, with four main variants: common, menil, melanistic, and leucistic – a genuine colour variety, not albinistic.[5] White is the lightest coloured, almost white; common and menil are darker, and melanistic is very dark, sometimes even black (and is easily confused with the sika deer).

  • Common: Chestnut coat with white mottles, it is most pronounced in summer with a much darker, unspotted coat in the winter. The light-coloured area around the tail is edged with black. The tail is light with a black stripe.
  • Menil: Spots are more distinct than common in summer and no black is seen around the rump patch or on the tail. In winter, spots are still clear on a darker brown coat.
  • Melanistic (black): All year the coat is black, shading to greyish-brown. No light-coloured tail patch or spots are seen.
White variants of fallow deer in the Beijing Zoo
  • Leucistic (white, but not albino): Fawns are cream-coloured; adults become pure white, especially in winter. Dark eyes and nose are seen. The coat has no spots.[6]

Most herds consist of the common coat variation, yet animals of the menil coat variation are not rare. The melanistic coat variation is generally rarer, and the white coat variation is very much rarer still, although wild New Zealand herds often have a high melanistic percentage.[7]

A skeleton of a buck (male) exhibited at the Mammal Gallery in the Natural History Museum of Pisa University
A pair of European fallow deer antlers

Only bucks have antlers, which are broad and shovel-shaped (palmate) from three years. In the first two years the antler is a single spike. They are grazing animals; their preferred habitat is mixed woodland and open grassland. During the rut, bucks spread out and females move between them; at that time of year fallow deer are relatively ungrouped compared with the rest of the year, when they try to stay together in groups of up to 150.

Agile and fast in case of danger, fallow deer can run at a maximum speed of 50 km/h (30 mph)[8] over short distances. Being naturally less muscular than other cervids such as the roe deer, they are not as fast. Fallow deer can also jump up to 1.75 m (5 ft 9 in) high and up to 5 m (16 ft) in length.

History[edit]

Skeleton of the extinct subspecies Dama dama geiselana

The European fallow deer was native to most of Europe during the last interglacial. Towards the end of the Pleistocene (during the last Ice Age) the distribution was restricted to the Middle East and refugia in parts of the Mediterranean Basin: Sicily, Anatolia and the Balkans.[9] However, the fossil evidence of the species' prehistoric presence in these apparent refugia is extremely fragmentary, contributing to the ongoing confusion about the species' true range.[1] Pleistocene fallow deer were larger, extant populations have evolved into smaller animals.[10] Humans began to expand the distribution of this deer in the last two millennia by introducing it throughout Europe and further afield.[9] In the Levant, fallow deer were an important source of meat in Palaeolithic cultures (420,000–200,000 BC), as is shown by bones, also used for conserving the marrow to be eaten weeks after the kill, found in the Qesem cave,[11] but the species appears to have disappeared from the southern Levant in the following Epipalaeolithic Natufian culture, 13,000–7,500 BC, although gazelle and especially roe deer proliferated, perhaps because of climate change (increased aridity and the decrease of wooded areas), in combination with changing land use patterns and hunting pressure.[12] At the same time the taxon persisted in the north in the Galilee region and the north of the West Bank.[10][12]

Distribution[edit]

Native[edit]

Turkey[edit]

Turkey is the only country known to have definitively natural populations of European fallow deer since the Last Glacial Maximum, but populations there (alongside those of the Persian fallow deer, which also formerly occurred in Turkey) have since become endangered and almost fully extirpated. European fallow deer in Anatolia underwent a major population decline due to the spread of agriculture (leading to the deforestation of lowland forests) and hunting, and populations in the Marmara and Aegean regions went extinct by the turn of 20th century. Other wild populations of Turkish fallow deer survived for longer on islands at Ayvalık Islands Nature Park, Gökova, and Adaköy near Marmaris, but also appear to have died out in recent years. Currently, the only extant wild population of the species known to be undoubtedly natural lives in Düzlerçami Game Reserve in the Mount Güllük-Termessos National Park in southern Turkey, although the area has been largely fenced since, making the population only semi-wild. This population is very few in number and is genetically distinct from other European fallow deer.[1][13]

A 2024 study suggests that the Turkish populations of fallow deer are ancestral to most fallow deer found throughout Europe as well as introduced populations worldwide. The translocations of fallow deer out of Turkey were facilitated by Roman-era trade networks. The only other refugium found was one in the Balkans, whose surviving descendants are significantly fewer in number. [14][15]

Native but originally extinct[edit]

Southern Balkans[edit]

On mainland Greece and some Greek islands, such as Corfu, Kythira, and Thasos, that were connected to mainland due to lower sea level or proximity to land, fallow deer were present during the last ice age.[16] A belief arose that the species was almost extinct in Greece, returning during the Neolithic.[16] Contrary to that, remains indicate that reduced numbers survived in several parts of the country like in Thessaly, Peloponnese and Central Greece, increasing and becoming common during mid Neolithic, but mostly east of Pindus mountain range and especially in Macedonia and Thrace.[16][17] During the Neolithic period and the Bronze Age, the species survived on the islands of Corfu and Thasos, appeared on Euboea, and began to be introduced by man to other islands, including Crete, some of the Cyclades, Rhodes, Chios, Lesbos, Samos and Sporades.[16][18] Early-historic-period remains have been found in eastern Greece and on the islands of Thasos, Chios, Rhodes and Crete.[16] A few surviving individuals were observed on Samos in 1700, while the species became extinct on Lesbos late in the Ottoman period.[17][19] On the Greek mainland, wild fallow deer survived until the 16th century in northeastern Chalkidiki, until the 19th century in the forests of Mount Olympus, Vermio Mountains, Arakynthos, Evrytania and Boeotia and until the 1910s in Thesprotia. The last individuals were hunted in Acarnania during the 1930s.[17][20][21][22][23][24][25][26][27]

In Bulgaria, the autochthonous population of fallow deer is believed to have declined and disappeared after the 9th or 10th centuries, and the species was reintroduced there much more recently.[28] The species remained in European Turkey into the 19th century.[29] A male fallow deer was captured in Thrace in 1977 and translocated to Düzlerçamı, suggesting that a small population existed there at that time.[30] In Albania (possibly in Butrint), the fallow deer seemed to be plentiful during the first half of 19th century.[31]

A 2024 genetic study suggests that the Balkans served as one of two refugia for fallow deer during the glacial periods, alongside Anatolia. Members of this population were also translocated around Europe during the Iron Age and Roman Empire, but have largely been replaced by Turkish-origin fallow deer (including in their native Balkans) aside from parts of southern Europe. The Balkan fallow deer are thought to represent the ancestors of modern Iberian, Italian, and Rhodes fallow deer, with the Rhodes population dating back to Neolithic translocations.[14][15]

Possible native populations[edit]

Aside from Turkey, other areas of Europe that could have potentially served as refuges for the species during the last ice age include parts of the eastern Mediterranean, including most of the Italian Peninsula, parts of the Balkans, and the Greek island of Rhodes, all of which still host populations of this species. However, palaeontological and archaeozoological evidence of the species' diffusion into these areas during the ice age is very fragmentary, thus whether the present populations in these areas are truly native descendants of relict populations or were introduced by humans is unknown. Presently, the IUCN Red List's range map lists European fallow deer as being native to Italy, Turkey, Rhodes, and most of the Balkans, as having a population of uncertain origin in central Bosnia and Herzegovina, and being introduced to the rest of Europe. In the text, though, all the eastern Mediterranean populations aside from Turkey are listed as having an uncertain origin.[1] A 2024 study suggests that Italian and Iberian populations descend from a now-extinct Balkan population that was translocated early on.[14]

Rhodes, Greece[edit]

The Rhodian population of European fallow deer is smaller on average than those of central and northern Europe, though they are similarly coloured. European fallow deer are said to have been introduced to Rhodes in Neolithic times; although fossils of the species on Rhodes do indeed go back to Neolithic times, no major evidence has been found of domestication, so they could be considered native.[1] In 2005, the Rhodian fallow deer was found to be genetically distinct from all other populations and to be of urgent conservation concern.[32] At the entrance to the harbour of Rhodes city, statues of a fallow deer buck and doe now grace the location where the Colossus of Rhodes once stood.[33] A 2024 study suggests them to be a basal lineage of the Balkan fallow deer, originating from a very early translocation.[14]

Introduced[edit]

Outside of Europe, this species has been introduced to Algeria, Antigua and Barbuda, Argentina, Australia, Canada, Cape Verde, Chile, the Comoros, Cyprus, the Falkland Islands, Fernando Pó, Israel, Lebanon, Madagascar, Mauritius, Mayotte, Morocco, New Zealand, Peru, Réunion, São Tomé, the Seychelles, South Africa, Tunisia, and the United States.[34]

Australia[edit]

European fallow deer were introduced to Tasmania in 1830 and to mainland Australia in the 1880s. The deer can now be found in all Australian jurisdictions, except Western Australia and the Northern Territory. The European fallow deer is the most widespread and numerous of introduced deer species in Australia.[35] Proper control of deer populations in New South Wales (NSW) was precluded for some years by the classification of these deer as "game animals", as well as being a feral pest species.[36] This led to an explosion in numbers, a vast increase in range in that state, impacts on agricultural production, increased environmental damage, and a dramatic increase in vehicle accidents involving deer.[37] This policy has since been reversed on privately held land only, and on such land the deer is once again only classified as a feral pest species; they remain game animals on public land. The NSW government now asks the public to assist by not transporting or releasing feral deer onto any land, implying that intentional release of deer has been a factor in the vast increase in range in NSW in recent years.[38][39]

Argentina[edit]

The European fallow deer was introduced to Victoria Island in Neuquén Province by billionaire Aaron Anchorena, who intended to increase hunting opportunities. He freed wildlife of European and Asian origin, making them common inhabitants of the island.

Canada[edit]

The European fallow deer is listed as an invasive species in the province of British Columbia.[40] In 2021, the Canadian federal government, local First Nations, and local residents put forward a plan to eradicate the fallow deer population on Sidney Island, a small island located off the southwest coast of British Columbia.[41]

Great Britain and Ireland[edit]

The European fallow deer was spread across Central Europe by the Romans. Recent finds at Fishbourne Roman Palace show that European fallow deer were introduced into southern England in the first century AD.[42] Fallow deer were established in Britain by the fourth century AD. Genetic studies have shown that this population became extinct and the fallow deer was re-introduced from Anatolia prior to the Norman conquest, not introduced from Scilly by the Normans as had previously been believed. Deer from England are a likely source of their re-introduction elsewhere in northern Europe.[43]

European fallow deer are now widespread on the UK mainland and are present in most of England and Wales south of a line drawn from the Wash to the Mersey. Populations in the New Forest and the Forest of Dean are long-standing, and many of the other populations originated from park escapees. They are not quite so widespread in the northern parts of England, but are present in most lowland areas and also in parts of Scotland, principally in Strathtay and around Loch Lomond. According to the British Deer Society distribution survey 2007, they have increased in range since the previous survey in 2000, although the increase in range is not as spectacular as for some of the other deer species.

A significant number of the European fallow deer in the Forest of Dean and in Epping Forest are of the black variety. One particularly interesting population, known as "long-haired fallow deer", inhabit Mortimer Forest on the England/Wales border; a significant part of the population has long body hair with distinct ear tufts.[44]

A historical herd is at Phoenix Park in Ireland, where a herd of 400–450 European fallow deer descends from the original herd introduced in the 1660s.[45] In a 2023 study, this herd was shown to comprise the first wild deer outside of North America to have contracted SARS-CoV-2, raising concerns about a potential natural reservoir arising within European deer herds.[46]

Three of the fallow deer colour variants found at the Fossil Rim Wildlife Center in Texas

New Zealand[edit]

From 1860, European fallow deer were introduced into New Zealand. Significant herds exist in a number of low-altitude forests.[47]

South Africa[edit]

European fallow deer are popular in the rural areas of KwaZulu-Natal for hunting purposes, in parts of the Gauteng Province to beautify ranches, and in the Eastern Cape where they were introduced on game farms for the hunting industry because of their exotic qualities. European fallow deer adapted extremely well to the South African environment with access to savanna grasslands and particularly in the cooler climate ranges such as the highveld.

Sweden[edit]

One noted historical herd of European fallow deer is located in the Ottenby nature reserve in Öland, where Charles X Gustav of Sweden erected a dry stone wall some 4 km long to enclose a royal fallow deer herd in the mid-17th century; the herd still exists as of 2006.[48]

United States[edit]

In recent times, European fallow deer have been introduced in parts of the United States. A small feral population exists on one barrier island in Georgia.[49] Fallow deer have also been introduced in Texas, along with many other exotic deer species, where they are often hunted on large game ranches.

In Pennsylvania, European fallow deer are considered livestock, since no feral animals are breeding in the wild. Occasional reports of wild European fallow deer in Pennsylvania and Indiana are generally attributed to escapes from preserves or farms.

A herd of white European fallow deer is located near Argonne National Laboratories in northeastern Illinois.[50]

White European fallow deer near Argonne National Labs in Westmont, Illinois, U.S.

A small herd of 15 mostly white European fallow deer resides at the Belle Isle Nature Zoo on Belle Isle in Detroit, Michigan. Until the turn of the 21st century, this herd had the run of the island; the herd was thereafter confined, with extirpation being the initial goal.[citation needed]

A small herd, believed to be the oldest in the United States, exists in the Land Between the Lakes National Recreation Area (LBL) in far western Kentucky and Tennessee. The European fallow deer herd in the LBL "was brought to LBL by the Hillman Land Company in 1918. LBL's herd is believed to be the oldest population of fallow deer in the country, and at one time was the largest. Today, the herd numbers fewer than 150 and hunting of fallow deer is not permitted. Although LBL's wildlife management activities focus on native species, the fallow herd is maintained for wildlife viewing and because of its historical significance."[51]

European fallow deer are present in the Point Reyes National Seashore, California, and Mendocino County near Ridgewood Ranch, west of Redwood Valley, California; some of them are leucistic.[citation needed]

Mating system[edit]

European fallow deer are highly dimorphic, polygynous breeders;[52][53] the breeding season or rut lasts about 135 days.[52] In the Northern Hemisphere, the breeding season tends to occur in the second half of October, while it occurs in April in the Southern Hemisphere, some matings can still occur before and after.[52][54] This mating behaviour within the rut most often occurs in leks, where males congregate in small groups on mating territories in which the females’ only purpose for visiting these territories is for copulation.[52][54] Variation within European fallow deer mating systems occurs; other than the traditional behaviour of lekking, different types of mating behaviours can include harems, dominance groups, stands, temporary stands, and multiple stands.[55] Different populations, environmental variation, size, and even age can determine the type of variation within a European fallow deer mating system,[55] but lekking behaviour is the most commonly found and studied in nature; variation can be explained by three characteristics (1) the optimal strategy under specific environmental or social conditions, (2) the strategy of an individual may be dependent on the strategies of other individual males within the same population, and (3) individual males may be less capable at gaining access to females, since they can be outcompeted by other males that are more capable.[54]

Female European fallow deer are polyestrous; they are receptive to males during multiple periods of estrus throughout the mating season while not gestating.[52][56] Male rut behaviour includes licking and sniffing around the anus and vulva to determine whether a female is fertile.[52] Males produce high-pitched whines repeatedly to initiate mating; following this display, a female may allow the male to mount; copulation can last as long as 5 minutes.[52]

Ecology and mating system characteristics[edit]

Fallow deer herd

Many deer species—including European fallow deer—have a social organization that can be tremendously plastic depending on their environment, meaning that group size and habitat type are closely linked to herd size.[57] Most of the detailed research on the ecological characteristics and behaviour of European fallow deer occurs in large blocks of woodland, which means some bias may be present.[57] European fallow deer can be found in a variety of habitats, which can range from cool and wet to hot and dry.[52] European fallow deer seem to have a preference for older forests with dispersed areas of grass, trees, and a variety of other vegetation.[52] The largest herd occurs right before the rutting season, while the smallest groups are females with fawns.[52] Throughout a large portion of the year, the sexes remain separated and only congregate during the mating months, but other patterns may be described, such as bachelor groups and even mixed groups.[57]

Male European fallow deer produce low-frequency vocalizations called groans; the sound of these groans results from the consistent and complex shape of the vocal tract involving the oral and nasal cavities.[58]

Ruts are characterized by males gaining the best territory possible to increase their odds for mating, and are often characterized by the presence of females on stands.[52] During this time, males stop feeding to defend their ruts from subordinate males. Males defending this territory often lose an average of 17% of their body weight, and the liver exhibits steatosis, which is reversible.[52] Throughout breeding seasons, the males may obtain the same rut; in some cases, ruts can be held by more than one individual; some possibilities for this include high population density and less rut space, or more suitable habitats, which can be shared.[57]

Parental care[edit]

Mother European fallow deer and fawn

After a female is impregnated, gestation lasts up to 245 days. Usually one fawn is born; twins are rare.[52] The females can conceive when they are 16 months old, whereas the males can successfully breed at 16 months, but most do not breed until they are 48 months old.[52] The females can become very cagey just before they give birth to their fawn and find secluded areas such as a bush or cave; sometimes females give birth near the herd.[52] As soon as the female gives birth, the she then licks the fawn to clean it; this helps initiate the maternal bond between the two, and only females provide parental investment; males do not participate in rearing the fawn.[52][54]

After the birth of the fawn occurs, the females do not return to the herd for at least 10 days and for most of the days the mother is separated from the fawn, returning only to feed the fawn.[52] The nursing period lasts about 4 months and happens every 4 hours each day.[52] Rumination is a critical part of development in the fawn's life, and this develops about 2 to 3 weeks into the fawn's life.[52] Females initiate the weaning periods for the fawn, which lasts about 20 days; 3 to 4 weeks; later, the fawn will start to follow its mother, and they will finally rejoin the herd together.[52] The mother frequently licks the fawn's anal area to stimulate suckling, urination, and defecation, which is a critical part of the development of the fawn.[52] Weaning is completed at around 7 months, and at around 12 months, the fawn is independent; after the 135 days of reproduction, the rut comes to an end, which can be characterized by the changes in group size and behaviour.[52]

Contests and weaponry[edit]

European fallow deer bucks fighting at Charlecote Park

Since European fallow deer are polygynous species that congregate once every year, males must fight to obtain access to estrous females.[59][54] The relationship between antler size and body condition can be treated as indicators to reflect body condition within a given year.[60] These secondary sexual characteristics can have dual functions, which include the attractiveness of males, which females can ultimately choose, and fighting ability of the male.[61][62][63][59] It was found that males with larger antlers had higher mating success, where males with asymmetrical antlers did not.[60] When males develop their antlers, trade-offs are made between reproduction and survival.[59] Genetic variations exist within fallow deer populations with variable antler growth, males that exhibited faster-growing antlers early in life are able to grow longer antlers without any significant cost; this shows that there is phenotypic variation among fallow deer populations.[59]

Aggressive behaviour is often observed when individuals are seeking out mates, scarce resources, and even territories.[64] Species that compete using their weapons usually engage with mutual agreement, but if any noticeable asymmetries are seen, such as a broken or lost weapon, this may alter the behaviour of an individual to engage in a fight.[64] Likelihood and severity of antler damage were looked at in fallow deer, to test whether antler damage was associated with contest tactics and duration, and if an association existed with the tendency for individuals to engage in fighting.[64] Individuals with undamaged antlers were more likely to attack, using high-risk tactics that included jumping, clashing, or backward-pushing behaviour, this was exhibited by both contestants; dominant males were more likely to have damaged antlers.[64] Dominance ranks exist within fallow deer populations, which can be linked to aggression level and body size; when competing for a male, however, how ranks are obtained is not studied extensively.[65]

Endurance rivalry[edit]

Male fallow deer are highly competitive during the rutting season; successful mating depends mainly on body size and dominance rank.[66] Many factors can determine the seasonal reproductive success of an individual male fallow deer; these factors include body size, which can affect reproduction and survival.[66] The amount of time spent in a lek can be an important factor in determining male reproductive success; energy can play an important role for the duration of competitive leks.[67] Among ungulates, European fallow deer exhibit one of the most outstanding examples of sexual dimorphism, as males are much larger than females.[66] For sexual selection to lead to the evolution of sexual dimorphism, where males are bigger than females, advantages must be present: (1) Advantages during combat, (2) Endurance rivalry advantage, (3) Female preference for larger males, and (4) Advantages during sperm competition.[63][66] Sexual selection has chosen bigger males over an evolutionary time scale and conferred advantages during competition of mates by a variety of mechanisms, which are intrasexual competition, access to females, and resource accessibility, which affects attractiveness to females.[66]

Body size is important during male-male agonistic interactions and endurance rivalry, while females tend to have a preference for larger males.[68] Dominance rank is a good indicator of body size and body mass, but age was not an important factor.[66] In a study done by McElligott et al. (2001), it was found that mating success was related to body size, pre-rut and rut rank.[66] Similarly, in another study, researchers found that age, weight, and display effort were all significant factors in determining mating success; in both studies, mating success was measured by the frequency of copulations,[68][66] which means that a variety of factors in different fallow deer populations can affect the overall energy allocation which will ultimately affect mating success. Maternal investment early in life can be critical to the development of body size, since it can be quite variable at that stage depending on resources and habitat type.[66] Mature male body size can be a better indicator of overall male quality rather than body mass, since body mass depends on a variety of resources each year and is not a static trait; body mass can be a complex trait to measure.[66]

Threats[edit]

Since the 20th century, a serious decline in the populations of European fallow deer has been seen in Turkey, the only region where it is definitely thought to be native, and it has disappeared from almost all regions where it was formerly found aside from Düzlerçami Game Reserve in the Mount Güllük-Termessos National Park, where a semiwild, genetically distinct population exists. The Turkish government undertook a breeding program at Düzlerçami starting in 1966, with the population growing from 7 to 500 animals, but it underwent a massive collapse until 2000 due to reasons not fully understood, but thought to be linked to urbanization, recreational activities, and poaching, and numbered less than 30 (with only 10 individuals roaming outside the fenced areas) individuals by 2007 and less than 130 individuals by 2010. This population remains at risk from inbreeding and poaching. Reintroduction to other areas of Turkey has not been successful but should still be considered to increase the species' population.[1][13]

The population on Rhodes, which is of uncertain origin, but is known to be very genetically distinct from others, is also of major conservation concern.[32] It numbers around 400-500 animals and is at risk from poaching and wildfires. The population is also at risk of outbreeding depression, as in some parts of Rhodes, mainland European fallow deer are kept in fenced areas; these deer could escape and breed with the Rhodian fallow deer. Rhodian fallow deer also damage summer crops and due to a lack of a compensation system, persecution against the population could happen. A reduction of water resources on the island due to climate change could also affect the animals. Despite this, there are signs of population recovery on Rhodes as of 2008 due to conservation measures.[1]

Despite these threats, the European fallow deer is common across the other areas where it could potentially be native, as well as the areas throughout Europe that it was introduced to early on, thus it is considered to be of least concern by the IUCN Red List.[1]

See also[edit]

References[edit]

  1. ^ a b c d e f g h i Masseti, M.; Mertzanidou, D. (2008). "Dama dama". IUCN Red List of Threatened Species. 2008: e.T42188A10656554. doi:10.2305/IUCN.UK.2008.RLTS.T42188A10656554.en. Retrieved 19 November 2021.
  2. ^ Lemoine, Rhys T.; Svenning, Jens‐Christian (2022-03-03). "Nativeness is not binary—a graduated terminology for native and non‐native species in the Anthropocene". Restoration Ecology. 30 (8). doi:10.1111/rec.13636. ISSN 1061-2971. S2CID 246251260.
  3. ^ Wilson, D. E.; Reeder, D. M., eds. (2005). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. ISBN 978-0-8018-8221-0. OCLC 62265494.
  4. ^ Burnie D and Wilson DE (Eds.), Animal: The Definitive Visual Guide to the World's Wildlife. DK Adult (2005), ISBN 0789477645
  5. ^ "The British Deer Society". Archived from the original on 2014-05-23. Retrieved 2009-04-16.
  6. ^ Prior, John. Dear Watch. David & Charles Inc., 1987. p. 80.
  7. ^ "New Zealand Hunting Info". Archived from the original on 2018-06-20. Retrieved 2012-09-01.
  8. ^ "The Deer of the Ranch of America". Archived from the original on 2020-07-31. Retrieved 2012-06-08.
  9. ^ a b Fernández-García, J. L. (2012) The endangered Dama dama mesopotamica: genetic variability, allelic loss and hybridization signals. Contributions to Zoology, 81.4, 223-233.
  10. ^ a b Kolska Horwitz, Liora (September 1986). "Faunal Remains from the Early Iron Age Site on Mount Ebal". Tel Aviv: Journal of the Institute of Archaeology of Tel Aviv University. 13/14: 173–189. Retrieved 12 September 2020.
  11. ^ "Israel cave bones: Early humans 'conserved food to eat later'". BBC News. London. 2019-10-10. Retrieved 2019-12-14.
  12. ^ a b Davies, S. J. M. (1982). "Climatic change and the advent of domestication: the succession of ruminant Artiodactyla in the late Pleistocene-Holocene in the Israel region". Paléorient. 8 (2): 5–15. doi:10.3406/paleo.1982.4317. Retrieved 12 September 2020.
  13. ^ a b Arslangündoğdu, Zeynel; Kasparek, Max; Sarbaçak, Halil; Kaçar, M. Süleyman; Yöntem, Osman; Şahin, M. Tuğrul (2010-01-01). "Development of the population of the European Fallow Deer, Dama dama dama (Linnaeus, 1758), in Turkey". Zoology in the Middle East. 49 (1): 3–12. doi:10.1080/09397140.2010.10638383. ISSN 0939-7140. S2CID 88172579.
  14. ^ a b c d Baker, K. H.; Gray, H. W. I.; Lister, A. M.; Spassov, N.; Welch, A. J.; Trantalidou, K.; De Cupere, B.; Bonillas, E.; De Jong, M.; Çakırlar, C.; Sykes, N.; Hoelzel, A. R. (2024-02-12). "Ancient and modern DNA track temporal and spatial population dynamics in the European fallow deer since the Eemian interglacial". Scientific Reports. 14 (1): 3015. doi:10.1038/s41598-023-48112-6. ISSN 2045-2322. PMC 10861457.
  15. ^ a b University, Durham. "Genetic analysis and archaeological insight combine to reveal the ancient origins of the fallow deer". phys.org. Retrieved 2024-02-12.
  16. ^ a b c d e Yiannouli E. & Trantalidou K. 1999: The fallow deer (Dama dama Linnaeus, 1758): Archaeological presence and representation in Greece. The Holocene History of the European Vertebrate Fauna. Modern Aspects of Research. Workshop, 6th to 9nth April 1998, Berlin: 247-281.
  17. ^ a b c Trantalidou K. 2002: The Rhodian fallow deer. Game and trophy since prehistoric times, M. Μasseti (ed.), Island of deer. Natural history of the fallow deer of Rhodes and the vertebrates of the Dodecanese (Greece), Rhodes, Prefecture of Rhodes, 159-164.
  18. ^ Dermitzakis M.D. & P.Y. Sondaar 1985: The Quaternary Fossil Mammals from North-eastern of Kerkyra (Corfu) Island (Ionian Sea, Greece). Rapports et Proces-Verbaux des Reunions Commission Internationale pour l'Exploration Scientifique de la Mer Mediterranee Monaco 292: 155-156.
  19. ^ Tournefort, J.P. 1717: Relation d’un Voyage du Levant, fait par ordre du Roy. Contenant l’histoire ancienne & moderne de plusieurs Isles de l’Archipel, de Constantinople, des côtes de la Mer Noire, de l’Armenie, de la Georgie, des frontières de Perse & de l’Asie Mineure. Avec les plans des villes & des lieux considérables; Les Plans des Villes & des Lieux conſiderables; le Genie, les Mæurs , le Commerce & la Religion des differens Peuples qui les habitent; Et l'Explication des Médailles & des Monumens Antiques. Enrichie de Descriptions & de Figures d'un grand nombre de Plantes rares, de divers Animaux; Et de plusieurs Observations touchant l'Histoire Naturelle. Amsterdam 604p.
  20. ^ Μπάου Ν. 1872 Παληά κυνήγια στην Αθήνα, Αναδρομή στα περασμένα.
  21. ^ Sforza, C. 1948: Jugoslavia: storia e ricordi.
  22. ^ Sidiropoulos, Polymeni, & Legakis (2016). The evolution of Greek fauna since classical times. The Historical Review/La Revue Historique, 13, 127-146.
  23. ^ Μιγκλή Δ. 2006 Οικολογία και ηθολογία ενός απομονωμένου πληθυσμού Πλατωνιών (Dama dana L.) στη νήσο Λήμνο. Μεταπτυχιακή ∆ιπλωματική Εργασία, ΑΠΘ. Θεσσαλονίκη. Σελ. 50.
  24. ^ Belon, P. 1555: Les observations de plusieurs singularitez et choses memorables, trouvées en Grece, Asie, Iudée, Egypte, Arabie, et autres pays estranges.
  25. ^ Bowen, G.F. 1852: Mount Athos, Thessaly, and Epirus: A Diary of a Journey from Constantinople to Corfu. London.
  26. ^ Leak, W.M. 1835: Travels in Northern Greece. Vol. III. London 620p.
  27. ^ Μπάου, Ν. 1952: Ο λήσταρχος. Κυνηγετικά Νέα 247(9): 333-334.
  28. ^ Boev Z. 2016: Subfossil Vertebrate Fauna from Forum Serdica (Sofia, Bulgaria), 16-18th Century A.D. Acta zool. bulg., 68(3): 415-424.
  29. ^ Ünal Y. & Çulhacı H. 2018: Investigation of fallow deer (Cervus dama L.) population densities by camera trap method in Antalya Düzlerçamı Eşenadası Breeding Station. Turkish Journal of Forestry 19(1): 57-62.
  30. ^ Arslangündoğdu Z., Kasparek M., Sarıbaşak H., Kaçar M.S., Yöntem O. & Şahin M.T. 2010: Development of the population of the European Fallow Deer, Dama dama dama (Linnaeus, 1758), in Turkey. Zoology in the Middle East 49(1): 3-12.
  31. ^ Best, J.J. 1842: Excursions in Albania; Compromising a Description of the Wild Boar, Deer and Woodcock shooting in that country.
  32. ^ a b Masseti, M; Cavallaro, A.; Pecchioli, E.; Vernesi, C. (2006-11-11), "Artificial Occurrence of the Fallow Deer, Dama dama dama (L., 1758), on the Island of Rhodes (Greece): Insight from mtDNA Analysis", Human Evolution, 21 (2): 167–175, doi:10.1007/s11598-006-9014-9, S2CID 84328010
  33. ^ "Rhodian Deer Statues in Rhodes, Greece". GPSmyCity. Retrieved 2022-07-06.
  34. ^ Long, J. L. (2003). Introduced Mammals of the World: Their History, Distribution and Influence (Cabi Publishing) ISBN 9780643067141.
  35. ^ "DeerScan > Fallow deer in Australia". www.feralscan.org.au. Retrieved 2021-01-30.
  36. ^ "Game and pests". www.dpi.nsw.gov.au. 2017. Retrieved 2021-01-30.
  37. ^ "Wild deer problem on the rise in NSW as calls grow to declare the animal a pest". www.abc.net.au. 2017-08-01. Retrieved 2021-01-30.
  38. ^ NSW Department of Primary Industry, Primefact (September 2019). "Feral deer in New South Wales" (PDF).
  39. ^ Langford, Ben (2019-08-25). "Game over! Govt's change on deer kill rules welcomed". St George & Sutherland Shire Leader. Retrieved 2021-01-30.
  40. ^ Ministry of Forests, Lands. "Invasive Mammals - Province of British Columbia". www2.gov.bc.ca. Retrieved 2021-05-18.
  41. ^ "Plan moves ahead to wipe out non-native deer population on B.C. island". CBC News. 2021-05-18. Retrieved 2021-05-18.
  42. ^ Sykes, N. J.; White, J.; Hayes, T. J.; Palmer, M. R. (2006), "Tracking animals using strontium isotopes in teeth: the role of fallow deer (Dama dama) in Roman Britain", Antiquity, 80 (310): 948–959, doi:10.1017/S0003598X00094539, PMID 19395750, S2CID 160712869
  43. ^ Karis H. Baker; Holly Miller; Sean Doherty; et al. (12 February 2024). Melinda Zeder (ed.). "The 10,000-year biocultural history of fallow deer and its implications for conservation policy". PNAS. 121 (8): e2310051121. doi:10.1073/pnas.2310051121.
  44. ^ "Unique deer living in Shropshire forest". BBC. 5 January 2011.
  45. ^ "Phoenix Park – Fauna". Archived from the original on 2010-06-04. Retrieved 2009-07-15.
  46. ^ Rains, Molly (19 July 2023). "Dublin deer herd first in Europe to be infected with COVID-19 virus, raising concerns about further spread". Science. Archived from the original on 19 July 2023. Retrieved 8 August 2023.
  47. ^ Hunting: Things to do
  48. ^ Environmental Baseline Study, Lumina Technologies, Öland, Sweden, July, 2004
  49. ^ Morse, Brian W.; Miller, Debra L.; Miller, Karl V.; Baldwin, Charles A. (April 2009). "Population Health of Fallow Deer (Dama Dama) on Little St. Simons Island, Georgia, USA". Journal of Wildlife Diseases. 45 (2): 411–421. doi:10.7589/0090-3558-45.2.411. PMID 19395750. S2CID 24723221. Retrieved 16 September 2020.
  50. ^ And another in Willits CA. on the famous Sea Biscuit Ranch. They number about 50 and have resided there for the last 50 years Herd of white deer roams Argonne campus. Archived 2011-06-15 at the Wayback Machine
  51. ^ "Western Kentucky Wildlife Viewing". Archived from the original on 27 December 2010.
  52. ^ a b c d e f g h i j k l m n o p q r s t u v Feldhamer, G. A., Farris-Renner, K. C., & Barker, C. M. (1988). Dama dama. Mammalian Species, 97(317), 1–8. doi:10.2307/3504141.
  53. ^ McElligot, A. G., Mattiangeli, V., Mattiello, S., Verga, M., Reynolds, C. A., & Hayden, T. (1998). Fighting tactics of fallows bucks (Dama dama, Cervidae): Reducing the Risks of Serious Conflict. Ethology, 104(9), 789–803. doi:10.1111/j.1439-0310.1998.tb00112.x.
  54. ^ a b c d e Thirgood, S. J. (1991). Alternative Mating Strategies and Reproductive Success in Fallow Deer. Behaviour, 116(1/2), 1–10. doi:10.1163/156853990X00338. JSTOR 4534906.
  55. ^ a b Langbein, J. & Thirgood, S. J. (1989). Variation in Mating Systems of Fallow Deer (Dama dama) in Relation to Ecology. Ethology, 83(3), 195–214. doi:10.1111/j.1439-0310.1989.tb00529.x.
  56. ^ "Estrus | reproductive cycle".
  57. ^ a b c d Putman, R. J. (1986). Grazing in temperate ecosystems: Large herbivores and the ecology of the New Forest. Croom Helm: Beckenham.
  58. ^ Reby, D; Wyman, M; Frey, R; Charlton, B; Dalmont, J; Gilbert, J (2018). "Vocal tract modelling in fallow deer: are male groans nasalized?". The Journal of Experimental Biology. 221 (17): jeb179416. doi:10.1242/jeb.179416. PMID 29941611.
  59. ^ a b c d Bergeron, P., Festa-Bianchet, M., von Hardenberg, A., & Bassano, B. (2008). Heterogeneity in Male Horn Growth and Longevity in a Highly Sexually Dimorphic Ungulate. Oikos, 117(1), 77–82. doi:10.1111/j.2007.0030-1299.16158.x. JSTOR 40235456.
  60. ^ a b Ciuti, S., & Apollonio, M. (2011). Do Antlers Honestly Advertise the Phenotypic Quality of Fallow Buck (Dama dama) in a Lekking Population? Ethology, 117(2), 133–144. doi:10.1111/j.1439-0310.2010.01862.x.
  61. ^ Darwin, C. (1859). On the Origin of Species by Means of Natural Selection. (Murray, London).
  62. ^ Darwin, C. (1871) The Descent of Man, and Selection in Relation to Sex.
  63. ^ a b Andersson M. (1994). Sexual selection. Princeton University Press, Princeton, New Jersey
  64. ^ a b c d Jennings, D. J., Boys, R. J., & Gammell, M. P. (2017). Weapon damage is associated with contest dynamics but not mating success in fallow deer (Dama dama). Biology Letters, 13(11), 20170565. doi:10.1098/rsbl.2017.0565.
  65. ^ Jennings, D. J., Carlin, C. M., Hayden, T. J., & Gammell, M. P. (2010). Investment in fighting in relation to body condition, age and dominance rank in the male fallow deer, Dama dama. Animal Behaviour, 79(6), 1293–1300. doi:10.1016/j.anbehav.2010.02.031.
  66. ^ a b c d e f g h i j McElligott, A. G., Gammell, M. P., Harty, H. C., Paini, D. R., Murphy, D. T., Walsh, J. T., & Hayden, T. J. (2001). Sexual size dimorphism in fallow deer (Dama dama): Do larger, heavier males gain greater mating success? Behavioral Ecology and Sociobiology, 49(4), 266–272. doi:10.1007/s002650000293. JSTOR 4601886.
  67. ^ Craig, A. S., Herman, L. M., Gabriele, C. M., & Pack, A. A. (2003). Migratory timing of humpback whales (Megaptera novaengliae) in the central North Pacific varies with age, sex and reproductive status. Behaviour, 140(8), 981–1001. doi:10.1163/156853903322589605. JSTOR 4536074.
  68. ^ a b Alonso, J. C., Magaña, M., Palacín, C., & Carlos, M. A. (2010). Correlates of male mating success in great bustard leks: the effects of age, weight, and display effort. Behavioral Ecology and Sociobiology, 64(10), 1589–1600. doi:10.1007/s00265-010-0972-6. JSTOR 40863226.

Further reading[edit]

External links[edit]