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Lazarussuchus

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618:, while the Menat specimen does not. However, this difference can only be properly evaluated in 3 dimensional specimens. Matsumoto and colleagues (2013) declined to create a new species for the Menat specimen despite it being "most certainly specifically distinct" because "species diagnoses must be based on clear morphological differences and this is problematic for the Menat specimen" going on to state that "Size and preservation could .... explain many or all of the observed differences between the specimens". 1750: 136: 2116: 2099: 115: 451: 415:
in France. The specimen, which is an almost complete articulated skeleton (BDL 1819) is largely preserved as an impression, with remnants of disintegrating bone and some preserved soft tissue. The remains were not assigned to a species however, because it could not be robustly diagnosed separately
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but the crest on the ribs of the 9th vertebra is limited. In the Menat specimen, the crest is present on all cervical ribs, including a particularly strong crest on the rib of the ninth vertebra. However, this contrast may be due to missalignment of vertebral counts as mentioned previously. The
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preserves some remnants of soft tissue, but no scales, which shows that the hindfoot (pes) was not webbed, and a dark stained region with a crenellated edge is present above the caudal vertebrae of the tail, suggestive of a crest similar to those found in some living reptiles, like the
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equal or nearly equal in length to the parietal plate, directed posteriorly with less than 30 degrees of angulation and only weakly concave, resulting in the upper temporal fenestra being elongated and almost rectangular in shape, with an anterior-posterior long axis, nine
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is distinguished by having postparietal processes only 1/3 of the length of the parietal plate, which are angulated greater than 45 degrees laterally and a concave lateral margin, resulting in the upper temporal fenestrae being smaller and more ovoid in comparison to
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Matsumoto, Ryoko; Dong, Liping; Wang, Yuan; Evans, Susan E. (2019). "The first record of a nearly complete choristodere (Reptilia: Diapsida) from the Upper Jurassic of Hebei Province, People's Republic of China". Journal of Systematic Palaeontology. 0 (0): 1–18.
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are present, the posterior portion of the trunk vertebrae have spinous processes below the postzygapophyses that act as additional articular surfaces, four functional sacral vertebrae are present, of which the first is a sacrodorsal, and a slender T-shaped
387:, was described from isolated skull bones and vertebrae from the Early-Middle Miocene sediments of the Merkur-North locality in the north-west Czech Republic. The species was named after Zdeněk Dvořák who had collected the specimens. In 2008, remains of 1591:
Evans, Susan E.; Hecht, Max K. (1993). "A History of an Extinct Reptilian Clade, the Choristodera: Longevity, Lazarus-Taxa, and the Fossil Record". In Max K. Hecht; Ross J. MacIntyre; Michael T. Clegg (eds.).
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was initially interpreted as the basalmost member of Choristodera, meaning that its lineage must have been the earliest to branch off from the group. Since the first definitive choristoderes appear in the
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was described as T-shaped in its initial description, however the main part of the bone is not visible, and only a strong lateral process is visible. In contrast, the Menat specimen interclavicle is
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Böhme, M. Ectothermic vertebrates (Teleostei, Allocaudata, Urodela, Anura, Testudines, Choristodera, Crocodylia, Squamata) from the Upper Oligocene of Oberleichtersbach (Northern Bavaria, Germany).
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Matsumoto, R.; Buffetaut, E.; Escuillie, F.; Hervet, S.; Evans, S. E. (2013). "New material of the choristodere Lazarussuchus (Diapsida, Choristodera) from the Paleocene of France".
728:, although there is still a gap between the disappearance of small-bodied, lizard-like choristoderes at the end of the Early Cretaceous and their reappearance in the form of 577:
The Menat specimen is distinguished by having 40 maxillary teeth and a total of 52 teeth in the upper jaw as opposed to 11 premaxillary and 24 maxillary tooth positions in
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Böhme, Madelaine; Spassov, Nikolai; Fuss, Jochen; Tröscher, Adrian; Deane, Andrew S.; Prieto, Jérôme; Kirscher, Uwe; Lechner, Thomas; Begun, David R. (2019-11-21).
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in the Paleocene. Possible lizard-like choristoderes have been found in Late Cretaceous North American deposits, although their remains are very fragmentary.
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being just over 30 centimetres (0.98 ft), and a skull length of around 4.5 centimetres (1.8 in) According to Matsumoto and colleagues (2013)
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Evans, Susan E.; Klembara, Jozef (2005). "A choristoderan reptile (Reptilia: Diapsida) from the Lower Miocene of northwest Bohemia (Czech Republic)".
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are broad and sickle shaped, and are large relative to the size of the vertebrae, the ectepicondylar groove of the humerus is bridged to form a
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came from the Late Oligocene, meaning that it extended the fossil range of Choristodera by several million years. At the time of its discovery
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was considered an example of the Lazarus effect because its "unexpected" presence followed a long gap in the choristodere fossil record.
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Hecht, M.K. (1992). "A new choristodere (Reptilia, Diapsida) from the Oligocene of France: an example of the Lazarus effect".
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from the two named species. In 2019, in the supplementary information for the paper describing the remains of the extinct ape
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from the early Miocene of the Czech Republic. It was not a large animal; with the total preserved body and tail length of
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specimen suggesting a vertebra could be missing or obscured. The ribs tuberculum and capitulum are joined by a crest in
135: 399:, Germany. Remains included 25 bones, and was suggested to probably represent a new species. In 2013, a specimen of 1776: 1699: 1420: 337:
with preserved soft tissue was found from the Late Paleocene of France, but has not been assigned to a species.
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went extinct at the start of the Eocene, possibly due to climatic changes happening at this time, known as the
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with a antero-medial to posterolateral long axis, and the trunk vertebrae lack articular spinal processes.
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Dong, Liping; Matsumoto, Ryoko; Kusuhashi, Nao; Wang, Yuanqing; Wang, Yuan; Evans, Susan E. (2020-08-02).
510: 2235: 2207: 2119: 1769: 615: 585:. The Menat specimen is interpreted to have 10 cervical vertebrae, as opposed to the nine reported for 412: 610:
in shape, but the lateral processes are incomplete, making comparison difficult. The type specimen of
1708: 1651: 1639: 1538: 1524:"Supplementary Information:A new Miocene ape and locomotion in the ancestor of great apes and humans" 1472: 1374: 1865: 1755: 657:
is the youngest member of the group Choristodera and the only choristodere to have lived after the
435: 417: 1675: 1570: 1488: 1432: 557: 518: 271: 130: 2212: 700:, it was placed as the sister group of neochoristoderes. Matsumoto and colleagues (2013) placed 2194: 2186: 2010: 1667: 1605: 1562: 1554: 1424: 1169: 721: 548: 392: 2199: 1973: 1716: 1659: 1597: 1546: 1480: 1416: 1382: 717: 502: 2065: 2028: 820: 685: 662: 498: 408: 291: 1640:"A new choristodere (Reptilia: Choristodera) from an Aptian–Albian coal deposit in China" 696:
of choristoderes spanning at least 100 million years. However in the 2005 description of
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fossils, and resembled the most primitive choristodere known, the Middle-Late Jurassic
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and possibly Late Miocene deposits (~56-20 or possibly 11.6 million years ago) in
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is assumed to have fed on invertebrates. At Oberleichtersbach and Merkur-North,
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is distinguished from all other known choristoderes by the presence of paired
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like in appearance, with the total preserved body and tail length of
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were described in 1992 from a mostly complete articulated skeleton (
325:("unexpected") (Hecht, 1992) from the late Oligocene of France. and 713: 449: 442:
stage of the Late Miocene, approximately 11.62 million years ago.
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climate. Occurring alongside fish, frogs, turtles, squamates and
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by the premaxillae and wedged between the anterior tips of the
434:, Bavaria, Germany. The Hammerschmiede locality has been dated 593:, and there is a gap between the 8th and 9th vertebrae of the 530: 614:
has plantar tubercles present on the proximal portion of the
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bones are fused into a combined postorbitofrontal, the lower
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10.1671/0272-4634(2005)025[0171:ACRRDF]2.0.CO;2
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Phylogeny from the analysis of Dong and colleagues (2020):
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of Asia, united by the shared condition of closed lower
629:, alongside other unspecified cranial bone differences. 581:, however, it cannot be ruled out that these are due to 489:
in the anterior part of the rostrum, the slender paired
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being just over 30 centimetres. A complete specimen of
1742:- brief article on the fossil record of choristoderes 361:
aged sediments of the Armissan limestone quarry near
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were reported from the Upper Oligocene sediments of
246: 223: 2143: 2027: 1972: 1927: 1876: 1849: 454:Restoration of the skull of the Menat specimen of 1322:was found in continental lake deposits, with a 357:no Re 437, coll. Gennevaux 92813) found in the 286:of Europe. It is the youngest known member of 1777: 716:of small-bodied choristoderes known from the 8: 547:is distinguished by having the postparietal 2131: 1933: 1924: 1920: 1855: 1846: 1800: 1784: 1770: 1762: 1314:Although no gut contents have been found, 373:", as the remains were the youngest known 113: 20: 1720: 1458: 1456: 1454: 1452: 1450: 1448: 1446: 369:, France. The genus was named after the " 621:The premaxilla of the Oberleichtersbach 1360: 1358: 1356: 1354: 1352: 1348: 1586: 1584: 1510:Courier Forschungsinstitut Senckenberg 1402: 1400: 1398: 1396: 1633: 1631: 7: 1504: 1502: 1644:Journal of Systematic Palaeontology 1204: 1161: 1099: 1087: 1041: 1011: 955: 904: 826: 816: 773: 748: 738: 529:are broad and flattened, the trunk 318:. Two species have been named: the 1625:doi:10.1080/14772019.2018.1494220. 1465:Journal of Vertebrate Paleontology 1409:Journal of Vertebrate Paleontology 669:. The first discovered fossils of 14: 525:and postorbitofrontal bones, the 513:are closed by the joining of the 2115: 2114: 2097: 1748: 667:Paleocene-Eocene Thermal Maximum 349:, belonging to the type species 134: 1722:10.5209/rev_jige.2010.v36.n2.11 541:is slender and parallel sided. 481:high on the rostrum, elongated 1693:Matsumoto R, Evans SE (2010). 1596:. Springer. pp. 323–338. 107:(Possible Late Miocene record) 1: 2271:Fossil taxa described in 1992 1664:10.1080/14772019.2020.1749147 1594:Evolutionary Biology, vol. 27 1387:10.1016/S0016-6995(09)90041-9 688:, the lineage represented by 294:. Fossils have been found in 274:'s crocodile") is an extinct 2256:Oligocene reptiles of Europe 2246:Paleocene reptiles of Europe 1485:10.1080/02724634.2012.716274 465:was small and superficially 403:was described from the late 2241:Paleocene first appearances 1602:10.1007/978-1-4615-2878-4_8 458:in dorsal and lateral views 422:, indeterminate remains of 383:. In 2005 another species, 2292: 2276:Prehistoric reptile genera 2261:Miocene reptiles of Europe 1700:Journal of Iberian Geology 646:, lizards and crocodiles. 228:Lazarussuchus inexpectatus 2251:Eocene reptiles of Europe 2110: 2095: 1936: 1923: 1919: 1900: 1858: 1845: 1799: 1551:10.1038/s41586-019-1731-0 1227: 1209: 1202: 1184: 1166: 1159: 1135: 1119: 1104: 1097: 1085: 1061: 1046: 1039: 1016: 1009: 975: 960: 953: 924: 909: 902: 882: 864: 849: 831: 824: 814: 796: 778: 771: 753: 746: 355:Claude Bernard University 243: 238: 222: 215: 131:Scientific classification 129: 121: 112: 23: 16:Extinct genus of reptiles 625:is shorter than that of 436:magnetostratigraphically 282:reptile, known from the 256:Evans and Klembara, 2005 2266:Burdigalian extinctions 1333:belonging to the genus 852:Ikechosaurus sunailinae 537:, and the blade of the 428:Hammerschmiede clay pit 426:were reported from the 637:The Menat specimen of 459: 2208:Paleobiology Database 661:. The crocodile-like 650:Age and relationships 453: 345:The first remains of 29:Temporal range: Late 1512:260, 161–183 (2008). 692:implied a very long 1756:Paleontology portal 1713:2010JIbG...36..253M 1656:2020JSPal..18.1223D 1543:2019Natur.575..489B 1477:2013JVPal..33..319M 1379:1992Geobi..25..115H 1007:"Allochoristodera" 438:to the base of the 722:temporal fenestrae 712:position within a 558:cervical vertebrae 511:temporal fenestrae 485:which replace the 483:premaxillary bones 460: 413:Menat, Puy-de-Dôme 122:Reconstruction of 2223: 2222: 2195:Open Tree of Life 2137:Taxon identifiers 2128: 2127: 2106: 2105: 2093: 2092: 2089: 2088: 2011:Khurendukhosaurus 1915: 1914: 1911: 1910: 1896: 1895: 1650:(15): 1223–1242. 1611:978-1-4613-6248-7 1537:(7783): 489–493. 1306: 1305: 1297: 1296: 1288: 1287: 1279: 1278: 1270: 1269: 1261: 1260: 1252: 1251: 1243: 1242: 1170:Khurendukhosaurus 1148: 1147: 1074: 1073: 997: 996: 988: 987: 937: 936: 885:Tchoiria klauseni 602:interclavicle of 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1906: 1905: 1899: 1886: 1885: 1884: 1883: 1881: 1879: 1875: 1867: 1863: 1862: 1861: 1860: 1857: 1854: 1852: 1848: 1844: 1836: 1832: 1830: 1826: 1824: 1820: 1818: 1814: 1812: 1808: 1807: 1802: 1798: 1794: 1787: 1782: 1780: 1775: 1773: 1768: 1767: 1764: 1757: 1746: 1741: 1738: 1737: 1733: 1723: 1718: 1714: 1710: 1706: 1702: 1701: 1696: 1689: 1686: 1681: 1677: 1673: 1669: 1665: 1661: 1657: 1653: 1649: 1645: 1641: 1634: 1632: 1628: 1621: 1618: 1613: 1607: 1603: 1599: 1595: 1587: 1585: 1581: 1576: 1572: 1568: 1564: 1560: 1556: 1552: 1548: 1544: 1540: 1536: 1532: 1525: 1518: 1515: 1511: 1505: 1503: 1499: 1494: 1490: 1486: 1482: 1478: 1474: 1470: 1466: 1459: 1457: 1455: 1453: 1451: 1449: 1447: 1443: 1438: 1434: 1430: 1426: 1422: 1418: 1414: 1410: 1403: 1401: 1399: 1397: 1393: 1388: 1384: 1380: 1376: 1372: 1368: 1361: 1359: 1357: 1355: 1353: 1349: 1342: 1340: 1339: 1337: 1332: 1331:crocodillians 1329: 1325: 1321: 1317: 1316:Lazarussuchus 1309: 1302: 1301: 1293: 1292: 1284: 1283: 1275: 1274: 1266: 1265: 1257: 1256: 1248: 1247: 1239: 1238: 1235: 1234: 1232: 1225: 1224: 1221: 1220: 1217: 1216: 1215:lingyuanensis 1214: 1213:Hyphalosaurus 1207: 1206: 1200: 1199: 1196: 1195: 1192: 1190: 1189: 1188:Hyphalosaurus 1182: 1181: 1178: 1177: 1174: 1173: 1171: 1164: 1163: 1157: 1156: 1153: 1152: 1144: 1143: 1140: 1139: 1133: 1132: 1129: 1128: 1125: 1123: 1122:Lazarussuchus 1117: 1116: 1113: 1112: 1109: 1108: 1102: 1101: 1095: 1094: 1093:Lazarussuchus 1090: 1089: 1083: 1082: 1079: 1078: 1070: 1069: 1066: 1065: 1059: 1058: 1055: 1054: 1051: 1050: 1044: 1043: 1037: 1036: 1032: 1031: 1028: 1027: 1024: 1023: 1021: 1020:Monjurosuchus 1014: 1013: 1006: 1005: 1002: 1001: 993: 992: 984: 983: 980: 979: 978:S. dakotensis 973: 972: 969: 968: 965: 964: 958: 957: 951: 950: 949:Simoedosaurus 946: 945: 942: 941: 933: 932: 929: 928: 922: 921: 918: 917: 914: 913: 907: 906: 900: 899: 898:Champsosaurus 895: 894: 891: 890: 887: 886: 880: 879: 876: 875: 872: 871: 869: 862: 861: 858: 857: 854: 853: 847: 846: 843: 842: 839: 838: 837:pijiagouensis 836: 829: 828: 822: 819: 818: 812: 811: 808: 807: 804: 803: 801: 800:Coeruleodraco 794: 793: 790: 789: 786: 785: 783: 776: 775: 769: 768: 765: 764: 761: 759: 758: 751: 750: 744: 741: 740: 736: 733: 731: 730:Lazarussuchus 727: 726:Lazarussuchus 723: 719: 715: 711: 707: 706:Lazarussuchus 703: 699: 695: 694:ghost lineage 691: 690:Lazarussuchus 687: 682: 681:Lazarussuchus 678: 676: 675:Lazarussuchus 672: 671:Lazarussuchus 668: 664: 660: 656: 655:Lazarussuchus 649: 647: 645: 640: 639:Lazarussuchus 632: 630: 628: 624: 623:Lazarussuchus 619: 617: 613: 609: 605: 600: 596: 592: 588: 584: 580: 575: 573: 568: 564: 563:interclavicle 559: 554: 553:parietal bone 550: 546: 542: 540: 536: 532: 528: 527:cervical ribs 524: 520: 519:quadratojugal 516: 512: 508: 504: 500: 496: 492: 488: 484: 480: 476: 475:Lazarussuchus 472: 468: 464: 463:Lazarussuchus 457: 456:Lazarussuchus 452: 445: 443: 441: 437: 433: 429: 425: 424:Lazarussuchus 421: 420: 414: 410: 406: 402: 401:Lazurussuchus 398: 394: 390: 389:Lazarussuchus 386: 382: 381: 376: 372: 368: 364: 360: 356: 352: 348: 347:Lazarussuchus 340: 338: 336: 335:Lazarussuchus 332: 328: 324: 321: 317: 313: 309: 305: 304:Early Miocene 301: 297: 293: 289: 285: 281: 277: 273: 269: 268: 267:Lazarussuchus 253: 252: 245: 244: 242: 237: 230: 229: 221: 218: 214: 207: 206: 205:Lazarussuchus 199: 196: 195: 192: 186: 183: 182: 179: 176: 173: 172: 169: 166: 163: 162: 159: 156: 153: 152: 149: 146: 143: 142: 137: 132: 128: 125: 124:Lazarussuchus 120: 116: 111: 103: 98: 93: 88: 83: 78: 73: 68: 63: 58: 53: 48: 42: 36: 32: 26: 25:Lazarussuchus 22: 19: 2236:Choristodera 2144: 2078: 2071: 2064: 2059:Liaoxisaurus 2057: 2050: 2045:Ikechosaurus 2043: 2036: 2017: 2016: 2009: 2002: 1995: 1988: 1981: 1961: 1954: 1947: 1940: 1929:Choristodera 1904:Choristodera 1902: 1878:Choristodera 1821:Superclass: 1793:Choristodera 1704: 1698: 1688: 1647: 1643: 1620: 1593: 1534: 1530: 1517: 1509: 1468: 1464: 1412: 1408: 1370: 1366: 1336:Diplocynodon 1334: 1328:alligatoroid 1319: 1315: 1313: 1310:Paleoecology 1229: 1228: 1211: 1210: 1186: 1185: 1168: 1167: 1137: 1136: 1121: 1120: 1106: 1105: 1092: 1091: 1064:P. proseilus 1063: 1062: 1049:P. proseilus 1048: 1047: 1033: 1018: 1017: 977: 976: 962: 961: 947: 926: 925: 911: 910: 896: 884: 883: 866: 865: 851: 850: 835:Ikechosaurus 833: 832: 798: 797: 780: 779: 755: 754: 743:Choristodera 742: 734: 729: 725: 705: 701: 697: 689: 680: 679: 674: 670: 654: 653: 638: 636: 626: 622: 620: 611: 603: 598: 594: 590: 586: 578: 576: 571: 566: 544: 543: 474: 470: 462: 461: 455: 423: 418: 400: 395:in northern 388: 384: 378: 375:choristodere 350: 346: 344: 334: 330: 326: 322: 320:type species 288:Choristodera 266: 265: 264: 250: 249: 227: 226: 217:Type species 204: 203: 191:Choristodera 123: 24: 18: 1963:Irenosaurus 1949:Cteniogenys 1324:subtropical 963:S. lemoinei 757:Cteniogenys 702:Cteniogenys 633:Soft tissue 507:postfrontal 503:postorbital 491:nasal bones 446:Description 380:Cteniogenys 233:Hecht, 1992 210:Hecht, 1992 39:61–20  2230:Categories 2052:Kosmodraco 1887:see below↓ 1866:Sauropsida 1851:Sauropsida 1833:Subclass: 1829:Sauropsida 1471:(2): 319. 1343:References 1138:L. dvoraki 802:jurassicus 708:in a more 698:L. dvoraki 567:L. dvoraki 495:anteriorly 385:L. dvoraki 327:L. dvoraki 314:, and the 280:amphibious 270:(meaning " 251:L. dvoraki 1823:Tetrapoda 1809:Kingdom: 1680:219047160 1672:1477-2019 1575:207888156 1559:0028-0836 1493:129438118 1429:0272-4634 1022:splendens 583:allometry 549:processes 515:squamosal 440:Tortonian 405:Paleocene 341:Discovery 154:Kingdom: 148:Eukaryota 31:Paleocene 2154:Wikidata 2120:Category 2080:Tchoiria 1835:Diapsida 1817:Chordata 1815:Phylum: 1811:Animalia 1567:31695194 1437:84097919 912:C. gigas 868:Tchoiria 784:pygmaeus 608:rhomboid 487:maxillae 419:Danuvius 363:Narbonne 284:Cenozoic 178:Reptilia 168:Chordata 164:Phylum: 158:Animalia 144:Domain: 33:- Early 2200:4127340 2187:1188761 2174:4822407 2160:Q222698 1990:Shokawa 1827:Class: 1709:Bibcode 1652:Bibcode 1539:Bibcode 1473:Bibcode 1375:Bibcode 1367:Geobios 1231:Shokawa 870:namsari 710:derived 644:tuatara 551:of the 539:scapula 535:foramen 432:Pforzen 397:Bavaria 312:Germany 272:Lazarus 197:Genus: 184:Order: 174:Class: 35:Miocene 2213:202121 1678:  1670:  1608:  1573:  1565:  1557:  1531:Nature 1491:  1435:  1427:  1172:orlovi 659:Eocene 467:lizard 308:France 2182:IRMNG 1676:S2CID 1571:S2CID 1527:(PDF) 1489:S2CID 1433:S2CID 714:clade 523:jugal 479:nares 430:near 411:near 407:aged 276:genus 2169:GBIF 1864:see 1668:ISSN 1606:ISBN 1563:PMID 1555:ISSN 1425:ISSN 1233:ikoi 1191:sp. 1124:sp. 760:sp. 531:ribs 505:and 367:Aude 47:PreꞒ 1717:doi 1660:doi 1598:doi 1547:doi 1535:575 1481:doi 1417:doi 1383:doi 365:in 278:of 2232:: 2210:: 2197:: 2184:: 2171:: 2156:: 1715:. 1705:36 1703:. 1697:. 1674:. 1666:. 1658:. 1648:18 1646:. 1642:. 1630:^ 1604:. 1583:^ 1569:. 1561:. 1553:. 1545:. 1533:. 1529:. 1501:^ 1487:. 1479:. 1469:33 1467:. 1445:^ 1431:. 1423:. 1413:25 1411:. 1395:^ 1381:. 1371:25 1369:. 1351:^ 565:. 521:, 517:, 310:, 302:, 298:, 97:Pg 41:Ma 1785:e 1778:t 1771:v 1725:. 1719:: 1711:: 1682:. 1662:: 1654:: 1614:. 1600:: 1577:. 1549:: 1541:: 1495:. 1483:: 1475:: 1439:. 1419:: 1389:. 1385:: 1377:: 1338:. 247:† 224:† 201:† 188:† 102:N 92:K 87:J 82:T 77:P 72:C 67:D 62:S 57:O 52:Ꞓ

Index

Paleocene
Miocene
Ma
PreꞒ

O
S
D
C
P
T
J
K
Pg
N

Scientific classification
Edit this classification
Eukaryota
Animalia
Chordata
Reptilia
Choristodera
Lazarussuchus
Type species
Lazarus
genus
amphibious
Cenozoic
Choristodera

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