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138 results for “Cervidae”
Distribution. Iran and Israel (reintroduced). The map includes both the native relict population and the reintroduced ones. in Cervidae
Distribution. Iran and Israel (reintroduced). The map includes both the native relict population and the reintroduced ones.
Subspecies and Distribution. C.e.elaphusLinnaeus,1758—GreatBritainandcontinentalEurope. C.e.bactrianusLydekker,1900—WTurkestan(Kazakhstan,Uzbekistan,Tajikistan&NAfghanistan). C.e.barbarusBennett,1833—AtlasMts(Algeria,Tunisia). C.e.corsicanusErxleben,1777—Corsica(extinct,reintroducedin1985),Sardinia. C.e.maralGray,1850—Anatolia,Caucasus,andNWIran. C. e. yarkandensis Blanford, 1892 — E Turkestan (S Xinjiang, China). It has been introduced into Chile, Argentina, Australia, and New Zealand. in Cervidae
Subspecies and Distribution. C.e.elaphusLinnaeus,1758—GreatBritainandcontinentalEurope. C.e.bactrianusLydekker,1900—WTurkestan(Kazakhstan,Uzbekistan,Tajikistan&NAfghanistan). C.e.barbarusBennett,1833—AtlasMts(Algeria,Tunisia). C.e.corsicanusErxleben,1777—Corsica(extinct,reintroducedin1985),Sardinia. C.e.maralGray,1850—Anatolia,Caucasus,andNWIran. C. e. yarkandensis Blanford, 1892 — E Turkestan (S Xinjiang, China). It has been introduced into Chile, Argentina, Australia, and New Zealand.
Subspecies and Distribution. C.c.canadensisErxleben,1777—NorthAmerica. C.c.alashanicusBobrinskii&Flerov,1935—NChina(HelanShanMts,Ningxia&NeiMongol). C.c.sibiricusSevertzov,1873—fromTienShantoAltaiandWBaikal(KirgyzstanandNXinjiangtoSSiberiaandNMongolia). C. c. xanthopygus Milne-Edwards, 1867 — SW Siberia, Ussuriland, and Manchuria. in Cervidae
Subspecies and Distribution. C.c.canadensisErxleben,1777—NorthAmerica. C.c.alashanicusBobrinskii&Flerov,1935—NChina(HelanShanMts,Ningxia&NeiMongol). C.c.sibiricusSevertzov,1873—fromTienShantoAltaiandWBaikal(KirgyzstanandNXinjiangtoSSiberiaandNMongolia). C. c. xanthopygus Milne-Edwards, 1867 — SW Siberia, Ussuriland, and Manchuria.
On followmg pages 30 Barasıngha (Huoervus duvıuoelıı) 31 Chınose Water Deer (Hydroporos ınermısl 32 Western Roe Deer (Capreolus aıpmolus), 33 Eastern Roe Deer (Capraolus pyyaryus) in Cervidae
On followmg pages 30 Barasıngha (Huoervus duvıuoelıı) 31 Chınose Water Deer (Hydroporos ınermısl 32 Western Roe Deer (Capreolus aıpmolus), 33 Eastern Roe Deer (Capraolus pyyaryus)
On followıng pages 16 Calamıan Deer (Axıs calamıanensıs) 17 Common Fallow Deer (Dama dama) 18 Persnun Fallow Deer (Dama mesopotamıca) 19 Sambar (Rusa unıoolon 20 Javan Deer (Rusa tlmoœnsls). 21 Phılıppıne Spotted Deer (Rusa alfredh 22 Phılıppıne Brown Deer (Husa manannal in Cervidae
On followıng pages 16 Calamıan Deer (Axıs calamıanensıs) 17 Common Fallow Deer (Dama dama) 18 Persnun Fallow Deer (Dama mesopotamıca) 19 Sambar (Rusa unıoolon 20 Javan Deer (Rusa tlmoœnsls). 21 Phılıppıne Spotted Deer (Rusa alfredh 22 Phılıppıne Brown Deer (Husa manannal
Fig. 4 in Axis axis (Artiodactyla: Cervidae)
Fig. 4.—Feeding association of Axis axis and Semnopithecus in India. Photo by Paul Wild used with permission.
Fig. 3 in Axis axis (Artiodactyla: Cervidae)
Fig. 3.—Dorsal, ventral, and lateral view of skull and lateral view of mandible of adult male Axis axis (DMNS [Denver Museum of Nature & Science] ZM.6800) from San Diego Zoo, San Diego, California. Photograph by René O'Connell, Image Archivist, Denver Museum of Nature & Science used with permission.
Figure 1 in The complete mitochondrial genome of the Chinese Sika deer (Cervus nippon Temminck, 1838), and phylogenetic analysis among Cervidae, Moschidae and Bovidae
Figure 1. Molecular phylogenetic tree derived from complete DNA sequence of 12 mitochondrial protein-coding genes using Bayesian inference and maximum parsimony analysis. The numbers beside the nodes are Bayesian posterior probabilities and bootstrap proportions. Equus asinus and Equus caballus were set as out-groups.
Figure 2 in Global phylogeography of the genus Capreolus (Artiodactyla: Cervidae), a Palaearctic meso-mammal
Figure 2. Phylogeny of Capreolus obtained from the Bayesian analysis of 54 mtDNA haplotypes (925 nt) under the TIM3 model of sequence evolution. Branch length units are expected substitutions per site. Bayesian posterior probability and bootstrap values for NJ, MP and ML, respectively, are shown for the main haplogroups (inner nodes) shared by all trees. Only values over 50% are indicated. A mitochondrial CR sequence of Cervus elaphus was used as an outgroup.
Figure 1. Distribution ranges for C. capreolus and C in Global phylogeography of the genus Capreolus (Artiodactyla: Cervidae), a Palaearctic meso-mammal
Figure 1. Distribution ranges for C. capreolus and C. pygargus, and the area of putative current sympatry between the rivers Volga and Don (Hewison & Danilkin, 2001). The question mark indicates the area of further putative presence of C. pygargus. Collection sites are as follows: (FRA) France, (SWE) Sweden, (DEN) Denmark, (AUS) Austria, (ITA) Central-southern Italy, (E-AL) Eastern Italian Alps, (N-SP) Northern Spain, (CS-SP) Central-southern Spain, (GRE) Greece, (ROM) Romania, (POL) Poland, (LIT) Lithuania, (CRI) Crimea, (W-RUS) Western Russia, (KYR) Kyrgyzstan, (NE-CH) North-eastern China, (CE-CH) Central-eastern China, (E-RUS) Eastern Russia. Multiple sampling sites for one population are indicated by the same acronym. See Table 1 for details on precise sampling locations and sample sizes.
Figure 3 in Global phylogeography of the genus Capreolus (Artiodactyla: Cervidae), a Palaearctic meso-mammal
Figure 3. Median-joining network based on the data set of C. capreolus and C. pygargus haplotypes. Branch lengths are approximately scaled to the number of nucleotide substitutions occurring along the branches. White circles represent missing haplotypes. The main haplogroups are indicated by curved lines. The number of mutations are reported only for the main haplogroups.
FIGURE 5 in A new species of Euprox (Cervidae, Artiodactyla) from the upper Miocene of the Linxia Basin, Gansu Province, China, with interpretation of its paleoenvironment
FIGURE 5. Antlers of Euprox grandis sp. nov. (V 20081.1-2) a, V 20081.1, left antler, anterior view; b, V 20081.2, right antler, posterior view; scale bar equals 5 cm.
FIGURE 8 in A new species of Euprox (Cervidae, Artiodactyla) from the upper Miocene of the Linxia Basin, Gansu Province, China, with interpretation of its paleoenvironment
FIGURE 8. Phylogenetic relationships of Euprox within Muntiacinae and relevant taxa (Lucentia excluded). Most parsimony tree (L = 47; CI = 0.787; RI = 0.767) with nodes numbers. Bootstrap value figure in brackets under the clade.
FIGURE 2 in A new species of Euprox (Cervidae, Artiodactyla) from the upper Miocene of the Linxia Basin, Gansu Province, China, with interpretation of its paleoenvironment
FIGURE 2. Skull of Euprox grandis sp. nov. (V 20080.1, holotype). a, dorsal view; b, lateral view; c, ventral view; scale bar equals 5 cm; the dash line shows the orientation of the pedicle ridge.
FIGURE 7 in A new species of Euprox (Cervidae, Artiodactyla) from the upper Miocene of the Linxia Basin, Gansu Province, China, with interpretation of its paleoenvironment
FIGURE 7. Phylogenetic relationships of Euprox within Muntiacinae and relevant taxa. a, b, synapomorphies for most parsimony tree 0 and tree 1; c, strict consensus tree (L = 54; CI = 0.722; RI = 0.700) with nodes numbered. Bootstrap value figure in brackets under the clade.
FIGURE 3 in A new species of Euprox (Cervidae, Artiodactyla) from the upper Miocene of the Linxia Basin, Gansu Province, China, with interpretation of its paleoenvironment
FIGURE 3. Occipital view of the skull of Euprox grandis sp. nov. (V 20080.1, holotype). Scale bar equals 5 cm.
FIGURE 4 in A new species of Euprox (Cervidae, Artiodactyla) from the upper Miocene of the Linxia Basin, Gansu Province, China, with interpretation of its paleoenvironment
FIGURE 4. Antlers of Euprox grandis sp. nov. (V 20080.2-3, holotype) a, V 20080.2, left antler, anterior view; b, V 20080.2, left antler, medial view; c, V 20080.3, right antler, posterior view; scale bar equals 5 cm.
Figure 3 in First record of a giant muntjac Muntiacus vuquangensis (Cervidae) from Cambodia
Figure 3: The location of our record of a giant muntjac in Virachey National Park, Cambodia, and locations of other recent (2010–2020) camera-trap photographs of this species from Laos and Vietnam. The range of the giant muntjac was taken from the IUCN distribution map (Timmins et al. 2016) and represents its potential distribution based on habitat and the extent of the Annamite mountain range (figure by Andrew Tilker).
Supplementary material 4 from: Morales-Donoso JA, Vacari GQ, Bernegossi AM, Sandoval EDP, Peres PHF, Galindo DJ, de Thoisy B, Vozdova M, Kubickova S, Barbanti Duarte JM (2023) Revalidation of Passalites Gloger, 1841 for the Amazon brown brocket deer P. nemorivagus (Cuvier, 1817) (Mammalia, Artiodactyla, Cervidae). ZooKeys 1167: 241-264. https://doi.org/10.3897/zookeys.1167.100577
Genetic pairwise Kimura 2 parameter distance of Passalites nemorivagus compared to other Neotropical deer
Supplementary material 3 from: Cifuentes-Rincón A, Morales-Donoso JA, Sandoval EDP, Tomazella IM, Mantellatto AMB, de Thoisy B, Duarte JMB (2020) Designation of a neotype for Mazama americana (Artiodactyla, Cervidae) reveals a cryptic new complex of brocket deer species. ZooKeys 958: 143-164. https://doi.org/10.3897/zookeys.958.50300
Table S3. Cranial measurements of M. americana neotype represented in millimeters
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Allen Brain Atlas
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