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Jump to: ,
Parent taxa:
(check the following menu and phylogeny - the taxon in bold refers to the topic on this page)


Taxonomy Phylogeny

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  • Families: See phylogeny section
`--
   |-Walangania africanus
   |-Orygotherium escheri
   `--+--
      `--+--
         `--+--
            |-Dromomerycidae (jnr syn. Palaeomerycidae?)
            `--+--
               `--viagra dosage


Cervidae


The large cervids (back), and (front) (viagra dosage,,,) (c) Stanton F. Fink



Cervidae are ruminant artiodactyls, commonly known as Deer

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this section from

Deer differ from other ruminants in that they have antlers instead of horns. Antlers are bony growths that develop each year (usually in summer) and, in general, it is only male deer that develop them (although there are exceptions). A young buck's first pair of antlers grow from two tiny bumps on their head that they have had from birth. The antlers grow wrapped in a thick layer of velvet and remain that way for several months, until the bone inside is hard; later the velvet is torn away (not shed contrary to popular belief). The one way that many hunters are able to track main paths that the deer travel on is because of their "rubs". A rub is used to deposit scent from glands near the eye and forehead and physically mark territory. During the mating season, bucks use their antlers to fight one another for the opportunity to attract mates in a given herd. The two bucks circle each other, bend back their legs, lower their heads, and charge.

A doe generally has one or two fawns at a time (triplets, while not unknown, are uncommon). The gestation period is anywhere between 160 days (just over 5 months) in the musk deer to ten months for the roe deer. Most fawns are born with their fur covered with white spots, though they lose their spots once they get older (excluding the Fallow Deer who keeps its spots for life). In the first twenty minutes of a fawn's life, the fawn begins to take its first steps. Its mother licks it clean until it is almost free of scent, so predators will not find it. Its mother leaves often, and the fawn does not like to be left behind. Sometimes its mother must gently push it down with her foot. The fawn stays hidden in the grass for one week until it is strong enough to walk with its mother. The fawn and its mother stay together for about one year. A male usually never sees his mother again, but females sometimes come back with their own fawns and form small herds.

Deer generally have lithe, compact bodies and long, powerful legs suited for rugged woodland terrain. Deer are also excellent swimmers. Their lower cheek teeth have crescent ridges of enamel, which enable them to grind a wide variety of vegetation. Snow on a Deer's back can stay for hours. Deer are ruminants or cud-chewers and have a four-chambered stomach. Nearly all deer have a facial gland in front of each eye. The gland contains a strongly scented pheromone, used to mark its home range. Bucks of a wide range of species open these glands wide when angry or excited. All deer have a liver without a gallbladder. The Chinese water deer is the only species that differs from others in that they have no antlers and bear upper canines developed into tusks.

Deer are selective feeders. They feed on leaves. They have small, unspecialised stomachs by herbivore standards, and high nutrition requirements. Rather than attempt to digest vast quantities of low-grade, fibrous food as, for example, sheep and cattle do, deer select easily digestible shoots, young leaves, fresh grasses, soft twigs, fruit, fungi, and lichens.

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There are about 34 of deer worldwide, divided into two broad groups: the mostly Old World that includes the subfamilies and , and the mostly New World including the subfamilies and (often referred to as Odocoileinae).

It is thought that the Telemetacarpalia evolved about 5 million years ago in the forests of North America and Siberia, while the Plesiometacarpalia originated in Asia.

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Cervidae
   |  i. s.:  Tuoc, Dung et al. 1994
   |         
   |          Lartet 1839 [incl. Cosoryx]
   |           |--D. dichotomus
   |           |--D. furcatus (Leidy 1869) [=Cosoryx furcatus; incl. C. ramosus Cope 1874]
   |           |--D. gemmifer (Cope 1873) [=Cosoryx gemmifer]
   |           |--D. necatus (Leidy 1854) [=Merycodus necatus; incl. Cervus warrenii Leidy 1858]
   |           |--D. tehuanus Cope 1876
   |           |--D. teres (Cope 1874) [=Cosoryx teres]
   |           `--D. trilateralis Cope 1876
   |-- [Plesiometacarpalia]
   |    |--
   |    `-- [Muntiacinae]
   |         |--
   |         `-- Milne-Edwards 1871
   |              `--
   `-- [Odocoileinae, Telemetacarpalia]
        |--
        `--+--Alceini [Alcinae, Alcini]
           |    |--
           |    |--
           |    `-- Gray 1821
           |         |--* (Linnaeus 1758)
           |         `--
           `--Capreolini
                |--
                |-- Swinhoe 1870 [Hydropotinae, Hydropotini]
                |    `--
                `-- Gray 1821
                     |--*
                     |--C. matheronis (Gervais 1850)
                     `--C. pygargus
Inorganic: Alces alces minilorientalus  1987
           Capreolus capreolus minilorientalus  1987

* Type species of generic name indicated

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Cope, E. D. 1876. Report upon the extinct Vertebrata obtained in New Mexico by parties of the expedition of 1874. Geographical Surveys West of the One Hundredth Meridian 4(2): i-iv, 1-370.

Deng T., Wang X., Ni X. & Liu L. 2004. Sequence of the Cenozoic mammalian faunas of the Linxia Basin in Gansu, China. Acta Geologica Sinica (English Edition) 78 (1): 8-14.

Forsten, A. 1999. Snout proportions in some Eurasian hipparions (Mammalia, Equidae): taxonomic and functional implications. Geodiversitas 21 (2): 255-278.

Gilbert, C., A. Ropiquet & A. Hassanin. 2006. Mitochondrial and nuclear phylogenies of Cervidae (Mammalia, Ruminantia): Systematics, morphology, and biogeography. Molecular Phylogenetics and Evolution 40 (1): 101-117.

Hamilton, W. R. 1978. Cervidae and Palaeomerycidae. In Evolution of African Mammals (V. J. Maglio & H. B. S. Cooke, eds.) pp. 496-508. Harvard University Press: Cambridge (Massachusetts).

Hughes, S., T. J. Hayden, C. J. Douady, C. Tougard, M. Germonpré, A. Stuart, L. Lbova, R. F. Carden, C. Hänni & L. Say. 2006. Molecular phylogeny of the extinct giant deer, Megaloceros giganteus. Molecular Phylogenetics and Evolution 40 (1): 285-291.

Lister, A. M., C. J. Edwards, D. A. W. Nock, M. Bunce, I. A. van Pijlen, D. G. Bradley, M. G. Thomas & I. Barnes. 2005. The phylogenetic position of the ‘giant deer’ Megaloceros giganteus. Nature 438: 850-853.

Miller, S. A., & J. P. Harley. 1996. Zoology (3rd ed.) Wm. C. Brown Publishers: Dubuque (Iowa).

1987. New facts: Homo and all Vertebrata were born simultaneously in the former Paleozoic in Japan. Original Report of the Okamura Fossil Laboratory 15: 347-573.

Randi, E., N. Mucci, M. Pierpaoli & E. Douzery. 1998. New phylogenetic perspectives on the Cervidae (Artiodactyla) are provided by the mitochondrial cytochrome b gene. Proceedings of the Royal Society of London Series B – Biological Sciences 265: 793-801.

Timm, R. M., & J. H. Brandt. 2001. Pseudonovibos spiralis (Artiodactyla: Bovidae): New information on this enigmatic south-east Asian ox. Journal of Zoology 253: 157-166.

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