Bovidae, Gray, 1821
publication ID |
https://doi.org/10.5252/g2011n4a7 |
DOI |
https://doi.org/10.5281/zenodo.4608725 |
persistent identifier |
https://treatment.plazi.org/id/03F88A03-B63B-3C07-0E5D-FA09FE0C5BD3 |
treatment provided by |
Felipe (2021-03-11 13:57:40, last updated 2024-11-27 10:15:08) |
scientific name |
Bovidae |
status |
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Bovidae View in CoL indet.
LOCALITY. — Quarry 1, Ivand district, northwest of Tabriz, Iran.
MATERIAL EXAMINED. — Fragmentary right mandible with m2-m3 ( HMNH-IV 59; Table 3 View TABLE ), right m1 ( HM-
NH-IV 65; Table 3 View TABLE ), broken right m2 ( HMNH-IV 68; Table 3 View TABLE ), left maxilla with DP2-M1 ( HMNH-IV 70; Table 3 View TABLE ), fragmentary right maxilla with M1-M2 (HMNH- IV 64; Table 3 View TABLE ), fragmentary right maxilla with P4-M1 ( HMNH-IV 58; Table 3 View TABLE ), fragmentary left maxilla with M1-M2 ( HMNH-IV 57; Table 3 View TABLE ).
DESCRIPTION
The mandibles and maxillae are too fragmentary to provide any detailed character. DP2 is heavily worn and is long and narrow. The parastyle is prominent but low. There is no mesostyle, and the metastyle is weak. The paracone is the highest cusp, and the metacone is slightly lower. The protocone is large and located anteriorly to the paracone. The hypocone is larger than the protocone. There is no central fossette visible on the occlusal surface. DP3 is longer than DP2 and is submolarized. The parastyle is strong and well separated from the paracone by a wide groove. The mesostyle, however, is less developed, and the metastyle is the least developed. The anterior rib is very strong, and the posterior rib is weak. The central cavities bear a simple enamel outline. DP4 is highly molarized and, except for its smaller size, closely resembles molars. The central fossettes are open in the medium wear.
P4 is subtriangular. The hypocone is relatively well developed, though smaller than protocone, thus rendering the inner wall a less angled shape. The parastyle and metastyle are well developed, while the mesostyle is weak.
On M1, the parastyle is robust, the mesostyle is well developed as a vertical ridge, and the metastyle projects much less. The anterior rib is large, and the posterior rib is weak. There is no basal pillar. M2 closely resembles M 1 in tooth morphology. The hypocone triangle is relatively short and is rounder than the protocone triangle. The metastyle is slightly more developed.
m1 shows a rectangular occlusal outline. The parastylid, metastylid, and the entostylid are much reduced. The lingual wall is flat with slightly convex metaconid and entoconid. The protoconid and hypoconid on m2 are triangle shaped. The parastylid is slightly more developed than the metastylid and entostylid. There is no goat fold but there is a low basal pillar. m3 resembles m2, except for its strongly labially offset hypoconulid with a central cavity.
COMPARISON
With no cranial or horn-cores found, discussing the systematic position of these isolated fragmentary materials in detail is difficult. Based on size and morphology, these teeth are tentatively assigned to one form herein, pending the discovery of better specimens.
This form, like Urmiatherium polaki Rodler, 1889 , features a developed parastyle, very strong mesostyles, a prominent anterior rib, and a concave labial metacone wall on the upper molars. It differs by having a lower tooth crown, no additional cavities near the central lingual edge of the occlusal surface on the upper molars, a convex shape of the lingual wall, and the well developed basal pillars on the lower molars.
De Mecquenem (1924, 1925) reported some material of Palaeoryx pallasi (Wagner, 1857) from Maragheh. The size of the present form from Ivand locality is comparable to this Maragheh
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taxon. They share similar tooth morphology, such as strong parastyles and mesostyles, weak metastyles, developed anterior ribs, no basal pillars on the upper molars, a slightly convex lingual wall of the lower molars, low but distinct basal pillars, triangular labial lobes on the lower molars, and strongly labially offset hypoconulids on m3. The skull figured by de Mecquenem (1924, 1925: pl. 4, fig. 1), however, was believed to be that of a Miotragocerus Stromer, 1928 (= Tragoportax Pilgrim, 1937 ) by Bohlin (1936) and Gentry (1971, 2000). Gentry (1971) further stated that there was no other convincing evidence of Palaeoryx pallasi from Maragheh. Given these poor materials and pending the discovery of more complete fossils, we avoid naming them.
ANTOINE P. O. & SARAC G. 2005. - Rhinocerotidae (Mammalia, Perissodactyla) from the Late Miocene of Akkasdagi, Turkey, in SEN S. (ed.), Geology, mammals and environments at Akkasdagi, Late Miocene of Central Anatolia. Geodiversitas 27 (4): 601 - 632.
BOHLIN B. 1936. - Bemerkungen uber einige pontischen Antilopen-Gattungen. Arkiv for Zoologi 28 A (18): 1 - 22.
DE MECQUENEM R. 1924. - Contribution a l'etude des fossiles de Maragha. Annales de Paleontologie 13: 135 - 160.
DE MECQUENEM R. 1925. - Contribution a l'etude des fossiles de Maragha. Annales de Paleontologie 14: 1 - 64.
DENG T. 2002. - Limb bones of Chilotherium wimani (Perissodactyla, Rhinocerotidae) from the Late Miocene of the Linxia Basin in Gansu, China. Vertebrata PalAsiatica 40 (4): 305 - 316.
GENTRY A. W. 1971. - The earliest goats and other antelopes from the Samos Hipparion fauna. Bulletin of the British Museum (Natural History), Geology 20: 231 - 296.
GENTRY A. W. 2000. - Caprinae and Hippotragini (Bovidae, Mammalia) in the Upper Miocene, in VRBA E. S. & SCHALLER G. B. (eds), Antelopes, Deer and Relatives: Fossil Record, Behavioral Ecology, Systematics and Conservation. Yale University Press, New Haven: 65 - 83.
HUTTUNEN K. & GOHLICH U. B. 2002. - A partial skeleton of Prodeinotherium bavaricum (Proboscidea, Mammalia) from the middle Miocene of Unterzolling (Upper Freshwater Molasse, Germany). Geobios 35 (4): 489 - 514.
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