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Scutarx

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oval-shaped parapophyses that are oriented posteriorly, and each one begins a pronounced ridge that reaches the centrum's posterior edge. The dorsoventral and mediolateral sides of the centra are concave, forming distinct but shallow lateral fossae that make contact with the neural arch dorsally. At the base of the neural arch, the diapophyses are positioned centrally. The best-preserved vertebra reveals that they are oval in cross-section, bent ventrolaterally, and somewhat elongate. In the back, the neural canal is rounded. The matching centrum face is shorter than the complete neural arch. The zygapophyses are well formed, long, and inclined at a 45-degree angle.
1923: 126: 422: 814:. In contrast to the equilateral triangles observed in the trunk series, the form of that protuberance is more like a right triangle in the cervical paramedian osteoderms. The osteoderms are slightly arched when seen from the back. As is characteristic for aetosaurians, the median margins are thick dorsoventrally and sigmoidal in medial view. The "tongue-and-groove" lateral articular surfaces found in other aetosaurias are absent in 797: 1941: 382:. The Camp Butte, Lot's Wife, Jasper Forest, Jim Camp Wash, and Martha's Butte beds may be found in the PEFO area of the Sonsela Member. Lot's Wife, Jasper Forest, and Martha's Butte beds form cliffs, whereas the Lot's Wife and Marthas Butte beds are slope-forming units with a larger proportion of mudrocks than sandstones. These locations all show neighboring floodplain facies connected to a braided river system. 108: 780:
ventrolateral hook, a thin bone flange that starts on the dorsal side of the tuberculum continues laterally and confluences with the rib body. The posterodorsal surface of the rib is lined by a deep, elongate groove created by the flange. The rib is flattened dorsally and develops a slender anterior blade. The transverse processes of the dorsal vertebrae are fused with the single-headed, posteriormost ribs.
447:, which played a significant role in a variety of Late Triassic terrestrial faunas with a widespread range and high species diversity. Measuring between one and three meters in length, with strongly armored bodies and tails, it had a crucial ecological function of being the earliest and one of only two clades of big herbivorous archosaurs from the Late Triassic. Aetosauria is divided into two main clades: 679:
anterolateral edges are dorsoventrally thick, rugose, anteromedially sloping regions that are posteriorly bordered by a narrow, curving ridge. For articulation with the nasals, the front borders of the frontals are thick and rugose. Almost transverse is the frontal/nasal suture. The distinct, elevated midline ridge that is found in other aertosaurs is however absent from the frontal of
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arch of the previous vertebra when combined with the flat prezygapophyses. Between the ventromedial borders of the prezygapophyses, a horizontal ventral bar covers the neural canal's entrance. The centroprezygapophyseal fossa (cprf), which is ventrolateral to the prezygapophysis, is a deep depression that is posteriorly bounded by the major strut of the transverse process.
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curvature of the anterior and posterior plate edges is minor. These osteoderms are dorsoventrally thinner and less arched in posterior view than the osteoderms that are located more anterior. Although there might be an individual difference, the dorsal eminence is significantly offset medially and slightly more developed, becoming elevated and more pyramidal in form.
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The related lateral osteoderm has a minor overlap with the sigmoidal lateral border in the anterior region, which is just posterior to the anterior bar. The osteoderm is hardly curved in the posterior view. The osteoderm is more sharply arched in those that are thought to be located more posteriorly.
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differ noticeably from each other, and this coincides with the loss of distinct parapophyses and diapophyses along the series. The centra also become dorsoventrally taller than they are anteroposteriorly. Regarding the existence of the different vertebral laminae and related fossae, the properties of
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In comparison to the centrum height, the neural spine is short (32.3 mm). The spine is mediolaterally enlarged at the distal end and is anteroposteriorly elongate, measuring the same length as the neural arch's proximal section. Spinoprezygapophyseal and spinopostzygapophyseal laminae are paired
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The frontal's exceptional dorsoventral thickness is obvious, with dorsoventral thickness 0.35 times the element's midline length. The posterior frontal edge is inclined posterolaterally in the dorsal view so that the lateral frontal margin is longer than the medial frontal margin, creating a separate
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An extended, thin "tube" that bends anteroventrally and widens medially into two broad sheets of bone that meet in a median symphysis makes up the pubis' body. The front and posterior contours of the pubic are convex, rarely extending over the puboischiadic plate's ventral edge dorsoventrally due to
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The anterior bar is consistently wide over the osteoderm's lateral section, but it dramatically narrows medially before swelling once again at the anteromedial projection, making it profoundly concave. This is known as scalloping. This "scalloping" of the anterior bar is a synapomorphy found in all
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The dorsal eminence is reduced to a raised, anteroposteriorly elongate keel with a posterior projection that reaches beyond the posterior boundary of the osteoderm, and the posterior dorsal caudal paramedians become longer than broad. They presumably continue until they develop into long strips of
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The anterior bars of the cervical osteoderms, which are well-developed and have pronounced anteromedial projections, are thick dorsoventrally. The lateral edges are extremely sigmoidal and devoid of anterolateral projections. The ornamentation on the dorsal surface is minimally developed, with few
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The prezygapophyses are inclined at around 45 degrees from the horizontal. There is a large, sub-triangular spinoprezygapophyseal fossa between the prezygapophyses and ventral to the base of the neural spine that is well-developed. This produces a wide shelf for the posterior section of the neural
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In both the anterior and posterior views, the centrum faces are subcircular, somewhat concave, and have slightly flared rims. Each centrum has two concave, ventromedially inclined, rectangular surfaces that are separated by a sharp, deep mid-line keel. The anteroventral corners of the centrum have
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One of the most often discovered vertebrate fossils in the Petrified Forest National Park (PEFO), Arizona's Upper Triassic Chinle Formation are aetosaurians. Four fragmentary skeletons that were believed to be a new taxon were discovered during paleontological research in the park between 2001 and
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While it can be challenging to distinguish the osteoderm transition between the cervical and trunk series, anterior dorsal trunk osteoderms are considered to have greater width/length ratios and be dorsoventrally thinner than the cervical paramedian osteoderms. The triangular protuberance is also
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While comparable and have a wider width/length ratio of 2.05 than their more anterior counterparts, the cervical paramedian osteoderms lack a pronounced sigmoidal lateral border. Even though the margin has a considerable anterolateral projection, it remains sigmoidal. Moreover, the anterolateral
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The anterior and mid-trunk ribs are double-headed. They extend laterally and then sharply turn ventrolaterally and then gradually turn more ventrally. The rib body is oval in cross-section, flattening more distally; it is broadest at the point of the sharp ventrolateral turn. Just lateral to the
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The centra's articular faces are rounded, somewhat concave, and have wide rims that flare outward. The centrum has a ventral surface that is thin and smooth, profoundly concave lateral sides, and is longer (45.78 mm) than it is tall (41.81 mm). The neural canal is broad, and the neural
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The element's main body is thick in the dorsoventral region, and the dorsomedial portion of the element is slightly twisted such that the dorsal surface is visibly concave. A thin layer of hematite covers any surface ornamentation. The sutural surface for the ascending process of the maxilla is
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For Scutarx deltatylus, the trunk-caudal transition exhibits a noticeable height increase from the mid-trunk area to the anterior dorsal caudal region. The dorsal prominence is a large pyramid with a vertical keel at the back. The anterior caudal osteoderms are identical to those in the trunk.
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The postzygapophyses are likewise situated around 45 degrees above the horizontal in posterior view. On the posterior aspect, they have a triangular shape and a lateral postzygadiapophyseal lamina that is well developed. In dorsal view, that lamina creates a wide dorsal ledge of the transverse
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process and continues laterally to the diapophysis. Along the transverse process, the shelf is larger proximally and narrower distally. There are two shallow postzygapophyseal spinodiapophyseal fossae located along the shelf's dorsal surface, between the postzygapophyses and the neural spine.
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The frontals' dorsal surfaces are rugose and decorated with deep indentations, some of which are connected to longer grooves. There are broader, anteroposteriorly directed grooves anteriorly and laterally over the rounded orbits that indicate the higher center of the frontals. The frontals'
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The frontal/parietal suture is clearly apparent at the posterior boundary of the frontals, making it clear that these parts were not fused. The posterolateral section defines the dorsal boundary of the supratemporal fenestra. The top part of the skull's back is made up of posterior flanges
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the neural spine are the same as those of the mid-trunk vertebrae. Fossil records show that the prezygodiapophyseal laminae of the mid and posterior trunk vertebrae have significantly more pronounced development and lateral extension when compared to neural spines.
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features. The posterior plate edge is touched by the low, wide, and mounded dorsal eminence. Also medially offset and closer to the midline margin is the eminence. The osteoderm's posteromedial corner contains the distinctive triangle protuberance used to identify
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posteroventrally sloping contours that make connection with the opisthotics' paroccipital processes ventrally.  The posterior process of the squamosal is in touch with the parietal flanges laterally and the supraoccipital in medial position.
436:. The Late Triassic (Carnian/Norian) aetosaurs were armored archosaurian reptiles. They are commonly found in India, North Africa, North America, and South America. These rare, highly derived archosaurs are easily distinguished from other 789:
its short length. As opposed to the robust, knob-like projections, the distal extremities of the pubes are shaped like elongate commata, which are thin and curve towards the symphysis. A unique character of the pubis of
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The breadth and length of dorsal mid-caudal paramedians are almost comparable. The prominent dorsal eminence and the anteromedial and anterolateral projections of the anterior bar are still present in those osteoderms.
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posterolateral process. Its anterior part connects posteriorly to the parietal and laterally to the postfrontal. The frontal creates the dorsal edge of the orbit just in front of the posterolateral process.
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of Texas. Four partial skeletons including much of the carapace, vertebral column as well as the shoulder and pelvic girdles have been collected from PEFO between 2002 and 2009. The locations where the
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The presence of a large, triangular boss in the posteromedial corner of the dorsal surface of the dorsal paramedian osteoderms is the primary morphological characteristic that distinguishes
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A robust, wide sacral rib that laterally extends anterodorsally to touch the posterodorsal border of the left ilium is a recognizable feature of this element.
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There is a little embayment on the underside of the dorsal eminence and a smooth ventral surface to the dorsal trunk paramedian osteoderms.
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markedly posteroventrally concave. The dorsal edge of the external naris is formed by the anterior nasal narrowing mediolaterally.
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from the early Revueltian of Arizona, this significantly increases the record of non-desmatosuchin aetosaurs in the Revueltian.
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Greek for “triangular protuberance” -delta meaning triangle and -tylos meaning “knob, knot, swelling, callous, protuberance”).
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is notable because it is from the lowermost Revueltian teilzone. With the sole other record being a reported specimen of
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In Texas, the Cooper Canyon Formation's uppermost and the majority of its middle part are Revueltian in age. While the
1184:"New insights into Late Triassic dinosauromorph-bearing assemblages from Texas using apomorphy-based identifications" 1218:
Nesbitt, Sterling; Stocker, Michelle; Parker, William; Wood, Thomas; Sidor, Christian; Angielczyk, Kenneth (2017).
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more equally sized. These osteoderms are difficult to distinguish from those in the anterior caudal area.
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archosaurs by the presence of an elongated, occasionally spiky, premaxilla and substantial dermal armor.
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is prevalent in the fossil record because it may be an indicator taxon for the late Adamanian biozone.
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is the presence of two large pubic foremen, a characteristic seen in only one other aetosaur.
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arch's canal-lateral borders are medium-thin and have strong anterior edges in anterior view.
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The neural spines and transverse processes of the mid- and posterior trunk vertebrae of
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also possess deep, round parabasisphenoid recess, a trait apomorphic to this taxon.
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Latin for “shield fortress” -scutum meaning “shield” and -arx meaning “fortress”;
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fossils were found at around the same level as the lowest recorded occurrence of
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has been identified through phylogenetic analysis as the sister taxon of
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2009. This genoholotype was later named in 2016 by William G. Parker as
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vertically along the anterior and posterior edges of the neural spine.
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fossils were gathered are all found in the lower Sonsela Member of the
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Fossils of Scutarx have been found in the Triassic Chinle Formation of
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from other aetosaurs. Both morphologically and stratigraphically,
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are “medium sized” paramedian osteoderms belonging to the clade
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It was originally believed that aetosaurs were primarily
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belong to the family of Stagonolepididae of the clade
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Reyes, William; Parker, William; Marsh, Adam (2021).
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can be distinguished from the closely related taxas
268: 1968: 1848: 1779: 1751: 1742: 1678: 1616: 1576: 1565: 1539: 1492: 1465: 1321:Desmet, Hilde; Antczak, Mateusz; Bodzioch, Adam. 888:, like more aetosaurs however, are herbivores. 1182:Lessner, Emily; Parker, William; Marsh, Adam. 310:lived around 230 million years ago during the 1387: 868:. Recent aetosaur skull finds, such those of 294:, most commonly regarded by its species name 8: 716:have a broad contact and are not elongate. 1956: 1789: 1748: 1623: 1582: 1573: 1547: 1536: 1471: 1462: 1410: 1394: 1380: 1372: 443:Aetosauria is an early-diverging clade of 106: 20: 1289: 1279: 1153: 1143: 1053: 1043: 795: 700:Unlike those of other aetosaurians like 897: 1121: 1119: 1021: 1019: 1017: 1015: 1013: 1011: 1009: 1007: 1005: 1003: 1001: 999: 997: 995: 993: 991: 989: 953: 951: 949: 947: 945: 943: 941: 939: 937: 935: 933: 931: 929: 927: 925: 923: 921: 7: 1257: 1255: 1253: 1213: 1211: 1177: 1175: 1173: 1117: 1115: 1113: 1111: 1109: 1107: 1105: 1103: 1101: 1099: 1083: 1081: 987: 985: 983: 981: 979: 977: 975: 973: 971: 969: 919: 917: 915: 913: 911: 909: 907: 905: 903: 901: 563: 541: 516: 491: 481: 1342:Journal of Vertebrate Paleontology 1224:Journal of Vertebrate Paleontology 115:Life restoration and size diagram 14: 1940: 1939: 1921: 124: 367:Petrified Forest National Park 1: 2070:Fossil taxa described in 2016 1354:10.1080/02724634.2020.1876080 1236:10.1080/02724634.2017.1393431 474:, all forming a clade within 2035:Late Triassic pseudosuchians 425:Desmatosuchia skeletal mount 2045:Late Triassic North America 2086: 2050:Aetosaurs of North America 571:Adamanasuchus eisenhardtae 465:Adamanasuchus eisenhardtae 350:Adamanasuchus eisenhardtae 1935: 1918: 1792: 1626: 1585: 1550: 1535: 1516: 1474: 1461: 1409: 598: 583: 568: 561: 546: 539: 521: 514: 496: 489: 267: 260: 121:Scientific classification 119: 114: 105: 23: 16:Extinct genus of reptiles 1262:Parker, William (2018). 1197:Benton, Micheal (1988). 1126:Parker, William (2016). 1026:Parker, William (2016). 958:Parker, William (2014). 871:Neoaetosauroides engaeus 754:Posterior trunk vertebra 2040:Paleontology in Arizona 703:Stagonolepis robertsoni 371:Cooper Canyon Formation 290:is an extinct genus of 877:Aetosauroides scagliai 801: 709:Aetosauroides scagliai 426: 2007:Paleobiology Database 1088:Small, Bryan (2001). 799: 724:Post cranial skeleton 586:Calyptosuchus wellesi 424: 344:Calyptosuchus wellesi 2065:Triassic extinctions 471:Calytosuchus wellesi 402:Desmatosuchus smalli 361:History of discovery 800:Aetosaur osteoderms 369:of Arizona and the 353:. Because of this, 1281:10.7717/peerj.5455 1145:10.7717/peerj.1583 1045:10.7717/peerj.1583 886:Scutarx deltatylus 816:Scutarx deltatylus 812:Scutarx deltatylus 802: 791:Scutarx deltatylus 760:Scutarx deltatylus 733:Mid trunk vertebra 718:Scutarx deltatylus 714:Scutarx deltatylus 601:Scutarx deltatylus 427: 397:Scutarx deltatylus 296:Scutarx deltatylus 273:Scutarx deltatylus 2022: 2021: 1962:Taxon identifiers 1953: 1952: 1931: 1930: 1916: 1915: 1912: 1911: 1908: 1907: 1904: 1903: 1853:(Desmatosuchinae 1806:Aetobarbakinoides 1738: 1737: 1734: 1733: 1680:Paratypothoracini 1531: 1530: 1527: 1526: 1512: 1511: 647: 646: 638: 637: 629: 628: 620: 619: 611: 610: 511:Stagonolepidoidea 283: 282: 256: 2077: 2015: 2014: 2002: 2001: 1989: 1988: 1987: 1957: 1943: 1942: 1926: 1925: 1830:Neoaetosauroides 1790: 1753:Stagonolepidinae 1749: 1624: 1583: 1574: 1568:Stagonolepididae 1548: 1537: 1472: 1463: 1456: 1455: 1411: 1396: 1389: 1382: 1373: 1366: 1365: 1333: 1327: 1326: 1318: 1312: 1311: 1293: 1283: 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1594: 1586: 1580: 1571: 1566: 1563: 1562: 1560: 1559: 1551: 1545: 1540: 1533: 1532: 1529: 1528: 1525: 1524: 1517: 1514: 1513: 1510: 1509: 1507: 1506: 1505: 1504: 1498: 1496: 1490: 1489: 1487: 1486: 1485: 1484: 1475: 1469: 1459: 1458: 1454: 1453: 1444: 1435: 1429: 1423: 1414: 1407: 1406: 1401: 1399: 1398: 1391: 1384: 1376: 1368: 1367: 1328: 1313: 1249: 1207: 1189: 1169: 1095: 1077: 965: 896: 895: 893: 890: 861: 858: 844: 841: 827: 824: 806: 803: 785: 782: 776: 773: 768: 765: 755: 752: 734: 731: 725: 722: 697: 694: 688: 685: 671: 668: 662: 659: 657: 654: 652: 649: 645: 644: 641: 640: 636: 635: 632: 631: 627: 626: 623: 622: 618: 617: 614: 613: 609: 608: 605: 604: 597: 594: 593: 590: 589: 582: 579: 578: 575: 574: 567: 562: 560: 557: 556: 553: 552: 549:Desmatosuchini 545: 540: 538: 532: 531: 528: 527: 520: 515: 513: 507: 506: 503: 502: 495: 490: 488: 480: 445:Pseudosuchians 418: 417:Classification 415: 362: 359: 281: 280: 277: 265: 264: 258: 257: 243: 239: 238: 230: 226: 225: 217: 213: 212: 204: 197: 196: 191: 184: 183: 178: 171: 170: 165: 161: 160: 155: 151: 150: 145: 141: 140: 135: 131: 130: 117: 116: 112: 111: 103: 102: 94: 89: 84: 79: 74: 69: 64: 59: 54: 49: 44: 39: 38: 36:Carnian–Norian 28: 15: 13: 10: 9: 6: 4: 3: 2: 2082: 2071: 2068: 2066: 2063: 2061: 2060:Norian genera 2058: 2056: 2053: 2051: 2048: 2046: 2043: 2041: 2038: 2036: 2033: 2032: 2030: 2013: 2008: 2004: 2000: 1995: 1991: 1986: 1980: 1976: 1975: 1973: 1971: 1967: 1963: 1958: 1946: 1938: 1937: 1934: 1924: 1897: 1896: 1892: 1890: 1889: 1885: 1883: 1882: 1878: 1875: 1874: 1873:Gorgetosuchus 1870: 1868: 1867: 1866:Desmatosuchus 1863: 1862: 1860: 1857: 1856:sensu stricto 1851: 1847: 1840: 1839: 1835: 1832: 1831: 1827: 1824: 1823: 1822:Chilenosuchus 1819: 1816: 1815: 1814:Calyptosuchus 1811: 1808: 1807: 1803: 1800: 1799: 1798:Adamanasuchus 1795: 1794: 1791: 1788: 1786: 1782: 1778: 1772: 1771: 1767: 1765: 1764: 1760: 1759: 1757: 1754: 1750: 1747: 1745: 1744:Desmatosuchia 1741: 1727: 1726: 1725:Venkatasuchus 1722: 1720: 1719: 1715: 1713: 1712: 1708: 1706: 1705: 1701: 1699: 1698: 1694: 1691: 1690: 1686: 1685: 1683: 1681: 1677: 1671: 1670: 1666: 1664: 1663: 1662:Redondasuchus 1659: 1657: 1656: 1652: 1649: 1648: 1647:Gorgetosuchus 1644: 1641: 1640: 1639:Chilenosuchus 1636: 1634: 1633: 1629: 1628: 1625: 1622: 1619: 1615: 1608: 1607: 1603: 1600: 1599: 1598:Coahomasuchus 1595: 1593: 1592: 1588: 1587: 1584: 1581: 1579: 1575: 1572: 1569: 1564: 1558: 1557: 1556:Aetosauroides 1553: 1552: 1549: 1546: 1543: 1538: 1534: 1522: 1521: 1515: 1502: 1501: 1500: 1499: 1497: 1495: 1491: 1483: 1479: 1478: 1477: 1476: 1473: 1470: 1468: 1464: 1460: 1452: 1448: 1445: 1443: 1439: 1436: 1434: 1430: 1428: 1424: 1422: 1418: 1417: 1412: 1408: 1404: 1397: 1392: 1390: 1385: 1383: 1378: 1377: 1374: 1363: 1359: 1355: 1351: 1347: 1343: 1339: 1332: 1329: 1324: 1317: 1314: 1309: 1305: 1301: 1297: 1292: 1287: 1282: 1277: 1273: 1269: 1265: 1258: 1256: 1254: 1250: 1245: 1241: 1237: 1233: 1229: 1225: 1221: 1214: 1212: 1208: 1200: 1193: 1190: 1185: 1178: 1176: 1174: 1170: 1165: 1161: 1156: 1151: 1146: 1141: 1137: 1133: 1129: 1122: 1120: 1118: 1116: 1114: 1112: 1110: 1108: 1106: 1104: 1102: 1100: 1096: 1091: 1084: 1082: 1078: 1073: 1069: 1065: 1061: 1056: 1051: 1046: 1041: 1037: 1033: 1029: 1022: 1020: 1018: 1016: 1014: 1012: 1010: 1008: 1006: 1004: 1002: 1000: 998: 996: 994: 992: 990: 988: 986: 984: 982: 980: 978: 976: 974: 972: 970: 966: 961: 954: 952: 950: 948: 946: 944: 942: 940: 938: 936: 934: 932: 930: 928: 926: 924: 922: 920: 918: 916: 914: 912: 910: 908: 906: 904: 902: 898: 891: 889: 887: 883: 879: 878: 873: 872: 867: 859: 857: 853: 849: 842: 840: 836: 832: 825: 823: 819: 817: 813: 804: 798: 794: 792: 783: 781: 774: 772: 766: 764: 761: 753: 751: 747: 743: 739: 732: 730: 723: 721: 719: 715: 711: 710: 705: 704: 695: 693: 686: 684: 682: 676: 669: 667: 660: 655: 650: 643: 642: 634: 633: 625: 624: 616: 615: 607: 606: 603: 602: 596: 595: 592: 591: 588: 587: 581: 580: 577: 576: 573: 572: 566: 565: 559: 558: 555: 554: 551: 550: 544: 543: 537: 534: 533: 530: 529: 526: 525: 519: 518: 512: 509: 508: 505: 504: 501: 500: 494: 493: 487: 484: 483: 479: 477: 473: 472: 467: 466: 461: 458: 454: 450: 449:Desmatosuchia 446: 441: 439: 435: 431: 423: 416: 414: 412: 406: 404: 403: 398: 394: 393: 388: 383: 381: 377: 372: 368: 360: 358: 356: 352: 351: 346: 345: 340: 336: 331: 329: 325: 321: 320:Late Triassic 318:stage of the 317: 313: 309: 305: 301: 297: 293: 289: 288: 275: 274: 266: 263: 259: 252: 251: 244: 241: 240: 237: 231: 228: 227: 224: 218: 215: 214: 211: 205: 202: 199: 198: 195: 192: 189: 186: 185: 182: 179: 176: 173: 172: 169: 166: 163: 162: 159: 156: 153: 152: 149: 146: 143: 142: 139: 136: 133: 132: 127: 122: 118: 113: 109: 104: 97: 92: 87: 82: 77: 72: 67: 62: 57: 52: 47: 42: 32: 31:Late Triassic 26: 22: 19: 1969: 1893: 1886: 1879: 1871: 1864: 1855: 1837: 1836: 1828: 1820: 1812: 1804: 1796: 1784: 1770:Stagonolepis 1768: 1761: 1723: 1718:Tecovasuchus 1716: 1709: 1702: 1695: 1687: 1667: 1660: 1655:Kryphioparma 1653: 1645: 1637: 1632:Apachesuchus 1630: 1604: 1596: 1589: 1578:Aetosaurinae 1554: 1518: 1482:Pseudosuchia 1467:Pseudosuchia 1446: 1442:Pseudosuchia 1437: 1345: 1341: 1331: 1316: 1271: 1267: 1227: 1223: 1192: 1135: 1131: 1035: 1031: 885: 876: 869: 863: 854: 850: 846: 837: 833: 829: 820: 815: 811: 808: 790: 787: 778: 770: 759: 757: 748: 744: 740: 736: 727: 717: 713: 707: 701: 699: 690: 680: 677: 673: 664: 600: 599: 584: 569: 547: 522: 499:Aetosaurinae 497: 469: 463: 459: 456: 453:Aetosaurinae 442: 429: 428: 410: 407: 401: 396: 390: 386: 384: 375: 364: 354: 348: 342: 338: 334: 332: 323: 307: 303: 299: 295: 286: 285: 284: 278:Parker, 2016 272: 271: 262:Type species 255:Parker, 2016 249: 248: 200: 194:Pseudosuchia 187: 174: 24: 18: 1881:Longosuchus 1697:Kocurypelta 1230:: 122–141. 835:aetosaurs. 651:Description 181:Archosauria 2029:Categories 1888:Lucasuchus 1785:sensu lato 1689:Garzapelta 1669:Typothorax 1591:Aetosaurus 1542:Aetosauria 1520:Aetosauria 1503:see below↓ 1494:Aetosauria 1433:Sauropsida 1403:Aetosauria 892:References 882:omnivorous 866:herbivores 486:Aetosauria 460:deltatylus 328:Aetosauria 304:deltatylus 223:Aetosauria 1985:Q22911737 1606:Stenomyti 1419:Kingdom: 1362:233616969 1274:: e5455. 1138:: e1583. 1038:: e1583. 805:Osteoderm 144:Kingdom: 138:Eukaryota 1979:Wikidata 1945:Category 1427:Chordata 1425:Phylum: 1421:Animalia 1308:52158424 1300:30186682 1244:89657063 1164:26819845 1064:26819845 687:Parietal 438:Triassic 229:Family: 168:Reptilia 158:Chordata 154:Phylum: 148:Animalia 134:Domain: 1999:8824841 1970:Scutarx 1838:Scutarx 1431:Class: 1291:6118205 1155:4727975 1072:5317139 1055:4727975 681:Scutarx 670:Frontal 457:Scutarx 430:Scutarx 411:Scutarx 387:Scutarx 376:Scutarx 355:Scutarx 339:Scutarx 335:Scutarx 324:Scutarx 312:Carnian 308:Scutarx 300:Scutarx 287:Scutarx 250:Scutarx 242:Genus: 216:Order: 164:Class: 25:Scutarx 2012:347478 1360:  1306:  1298:  1288:  1242:  1162:  1152:  1070:  1062:  1052:  856:bone. 843:Caudal 316:Norian 1447:Clade 1438:Clade 1358:S2CID 1304:S2CID 1268:PeerJ 1240:S2CID 1202:(PDF) 1132:PeerJ 1068:S2CID 1032:PeerJ 826:Trunk 784:Pubis 661:Nasal 656:Skull 201:Clade 188:Clade 175:Clade 1994:GBIF 1480:see 1296:PMID 1160:PMID 1060:PMID 874:and 860:Diet 706:and 468:and 451:and 347:and 314:and 41:Preęž’ 1350:doi 1286:PMC 1276:doi 1232:doi 1150:PMC 1140:doi 1050:PMC 1040:doi 775:Rib 2031:: 2009:: 1996:: 1981:: 1449:: 1440:: 1356:. 1346:40 1344:. 1340:. 1302:. 1294:. 1284:. 1270:. 1266:. 1252:^ 1238:. 1228:37 1226:. 1222:. 1210:^ 1172:^ 1158:. 1148:. 1134:. 1130:. 1098:^ 1080:^ 1066:. 1058:. 1048:. 1034:. 1030:. 968:^ 900:^ 884:. 818:. 478:. 455:. 413:. 322:. 203:: 190:: 177:: 91:Pg 33:, 1876:? 1858:) 1841:? 1833:? 1825:? 1817:? 1809:? 1801:? 1755:? 1692:? 1650:? 1642:? 1620:? 1609:? 1601:? 1395:e 1388:t 1381:v 1364:. 1352:: 1325:. 1310:. 1278:: 1272:6 1246:. 1234:: 1204:. 1186:. 1166:. 1142:: 1136:4 1092:. 1074:. 1042:: 1036:4 962:. 298:( 269:† 246:† 233:† 220:† 207:† 96:N 86:K 81:J 76:T 71:P 66:C 61:D 56:S 51:O 46:ęž’

Index

Late Triassic
Preęž’
ęž’
O
S
D
C
P
T
J
K
Pg
N

Scientific classification
Edit this classification
Eukaryota
Animalia
Chordata
Reptilia
Archosauria
Pseudosuchia
Aetosauriformes
Aetosauria
Stagonolepididae
Scutarx
Type species
Aetosauriformes
Carnian
Norian

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