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/><title>Chinleana</title><subtitle type="html">Discussion of Late Triassic paleontology and other assorted topics.</subtitle><link rel="http://schemas.google.com/g/2005#feed" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/posts/default" /><link rel="alternate" type="text/html" href="http://chinleana.fieldofscience.com/" /><link rel="next" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default?start-index=26&amp;max-results=25&amp;redirect=false&amp;v=2" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><generator version="7.00" uri="http://www.blogger.com">Blogger</generator><openSearch:totalResults>665</openSearch:totalResults><openSearch:startIndex>1</openSearch:startIndex><openSearch:itemsPerPage>25</openSearch:itemsPerPage><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" type="application/atom+xml" href="http://feeds.feedburner.com/Chinleana" /><feedburner:info uri="chinleana" /><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="hub" href="http://pubsubhubbub.appspot.com/" /><feedburner:emailServiceId>Chinleana</feedburner:emailServiceId><feedburner:feedburnerHostname>http://feedburner.google.com</feedburner:feedburnerHostname><entry gd:etag="W/&quot;CU8FQXw7eip7ImA9WhFSEEw.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-4227940932662272414</id><published>2013-06-11T22:08:00.001-07:00</published><updated>2013-06-11T22:10:10.202-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-06-11T22:10:10.202-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="histology" /><category scheme="http://www.blogger.com/atom/ns#" term="taxonomy" /><category scheme="http://www.blogger.com/atom/ns#" term="aetosaurs" /><title>Two New Aetosaur Papers Including a New Taxon, Stenomyti huangae, from the Chinle Formation of Colorado</title><content type="html">&lt;strong&gt;&lt;span style="font-size: x-small;"&gt;Taborda, J. R. A., Cerda, I. A., and J. B. Desojo. 2013. Growth curve of &lt;em&gt;Aetosauroides scagliai&lt;/em&gt; Casamiquela 1960 (Pseudosuchia: Aetosauria) inferred from osteoderm histology. From Nesbitt, S. J., Desojo, J. B., and R. B. Irmis (eds.), Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin Geological Society Special Publications 379. &lt;/span&gt;&lt;/strong&gt;&lt;a href="http://sp.lyellcollection.org/content/early/2013/06/07/SP379.19.abstract"&gt;&lt;strong&gt;&lt;span style="font-size: x-small;"&gt;doi:10.1144/SP379.19&lt;/span&gt;&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;strong&gt;Abstract -&lt;/strong&gt; Recent palaeohistological studies on paramedian osteoderms of &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;aetosaurs revealed the presence of growth lines (lines of arrested &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;growth or LAGs) and a minimal or nonexistent secondary remodelling in &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;the bone matrix of these elements. This feature allows the age of i&lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;ndividuals to be estimated through growth line count. In the present &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;contribution we study the growth curve of the South American aetosaur &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;em&gt;Aetosauroides scagliai.&lt;/em&gt; We estimated the age (obtained from LAG &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;counting) and body size (body length and body mass were used as&lt;/span&gt;&lt;br /&gt;
&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;proxies) of different aetosaur specimens in order to reconstruct the &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;growth curve of the South American species. The data obtained for &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;em&gt;Aetosauroides scagliai&lt;/em&gt; were compared with that of other aetosaurs, &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;such as &lt;em&gt;Neoaetosauroides engaeus, Aetosaurus ferratus, &lt;/em&gt;&lt;/span&gt;&lt;em&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;em&gt;Aetobarbakinoides brasiliensis, Typothorax coccinarum&lt;/em&gt; and&lt;/span&gt;&lt;/em&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;em&gt;Paratypothorax&lt;/em&gt; sp. Our results indicate that, if body length is &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;considered as proxy, all studied aetosaur specimens have a similar or &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;almost identical growth rate. However, important variations arose &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;among aetosaur taxa if body mass is considered as proxy, which would &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;be related to a body morphology ranging from slender (e.g. &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;em&gt;Aetobarbakinoides brasiliensis&lt;/em&gt;) to very wide (&lt;em&gt;Typothorax coccinarum&lt;/em&gt;) &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;morphotypes. In comparison with extant pseudosuchians (i.e. &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;crocodylians), &lt;em&gt;Aetosauroides scagliai&lt;/em&gt; possesses a relatively lower &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;growth rate.&lt;/span&gt;&lt;br /&gt;
&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;/span&gt;&lt;br /&gt;
&lt;strong&gt;&lt;span style="font-size: x-small;"&gt;Small, B. J., and J. W. Martz. 2013. A new aetosaur from the Upper Triassic Chinle Formation of the Eagle Basin, Colorado, USA.:  From Nesbitt, S. J., Desojo, J. B., and R. B. Irmis (eds.), Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin Geological Society Special Publications 379 &lt;/span&gt;&lt;/strong&gt;&lt;a href="http://sp.lyellcollection.org/content/early/2013/06/07/SP379.18.abstract"&gt;&lt;strong&gt;&lt;span style="font-size: x-small;"&gt;doi:10.1144/SP379.18&lt;/span&gt;&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;
&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;strong&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/span&gt;&lt;br /&gt;
&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;strong&gt;Abstract -&lt;/strong&gt; A small aetosaur skull and skeleton and referred material from the &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;Chinle Formation, Eagle Basin of Colorado, USA, is described as a new &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;taxon, &lt;em&gt;Stenomyti huangae&lt;/em&gt; gen. et sp. nov, distinguished from other &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;aetosaurs by the following autapomorphies: three premaxillary teeth; &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;four palpebrals; pronounced midline ridge on frontals and parietals; &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;paired ridges flanking midline ridge on parietal and frontal; &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;exclusion of quadratojugal from ventral margin of skull by contact &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;between jugal and quadrate; exclusion of postorbital from i&lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;nfratemporal fenestra; infratemporal fenestra a horizontally oriented &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;oval that embays the posterior edge of the jugal; retroarticular &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;process longer than distance between articular glenoid and posterior &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;edge of external mandibular fenestra; oval to irregularly shaped &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;ventral osteoderms that do not contact each other. Paramedian and &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;lateral osteoderms of S. huangae are nearly identical to those of &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;em&gt;Aetosaurus ferratus&lt;/em&gt;, and other shared cranial characters suggest that&lt;/span&gt;&lt;br style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;" /&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;these taxa are closely related and lie outside the clade &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;Typothoracisinae + &lt;/span&gt;&lt;wbr style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;/wbr&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;Desmatosuchinae. This discovery indicates that other &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;reports of Aetosaurus across Laurasia based on osteoderms should be &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;reassessed. Similar confusion with the osteoderms of other &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;non-typothoracisine/&lt;/span&gt;&lt;wbr style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;/wbr&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;desmatosuchine aetosaurs such as &lt;em&gt;Aetosauroides&lt;/em&gt;, &lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;Stagonolepis and &lt;em&gt;Calyptosuchus&lt;/em&gt; suggests that osteoderms are not always r&lt;/span&gt;&lt;span style="-webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;eliable taxonomic indicators.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br /&gt;
&lt;br /&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=aGpXAd_SmqE:0VKjPFABUyg:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=aGpXAd_SmqE:0VKjPFABUyg:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=aGpXAd_SmqE:0VKjPFABUyg:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=aGpXAd_SmqE:0VKjPFABUyg:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=aGpXAd_SmqE:0VKjPFABUyg:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=aGpXAd_SmqE:0VKjPFABUyg:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=aGpXAd_SmqE:0VKjPFABUyg:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=aGpXAd_SmqE:0VKjPFABUyg:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=aGpXAd_SmqE:0VKjPFABUyg:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=aGpXAd_SmqE:0VKjPFABUyg:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/aGpXAd_SmqE" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/4227940932662272414/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/06/two-new-aetosaur-papers-including-new.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4227940932662272414?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4227940932662272414?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/aGpXAd_SmqE/two-new-aetosaur-papers-including-new.html" title="Two New Aetosaur Papers Including a New Taxon, &lt;i&gt;Stenomyti huangae&lt;/i&gt;, from the Chinle Formation of Colorado" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/06/two-new-aetosaur-papers-including-new.html</feedburner:origLink></entry><entry gd:etag="W/&quot;Ck8BRn85cSp7ImA9WhFTFEQ.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-3321936793470835896</id><published>2013-06-05T20:54:00.001-07:00</published><updated>2013-06-05T20:54:17.129-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-06-05T20:54:17.129-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="dinosauriformes" /><category scheme="http://www.blogger.com/atom/ns#" term="dental wear" /><category scheme="http://www.blogger.com/atom/ns#" term="feeding" /><title>Dental Microwear of the Late Triassic Dinosauriform Silesaurus opolensis</title><content type="html">&lt;strong&gt;Kubo, T.,&amp;nbsp;and M. O. Kubo. 2013. Dental microwear of a Late Triassic dinosauriform, &lt;em&gt;Silesaurus opolensis&lt;/em&gt;. Acta Palaeontologica Polonica (in press).&lt;br /&gt;doi: &lt;/strong&gt;&lt;a href="http://dx.doi.org/10.4202/app.2013.0027" target="_blank"&gt;&lt;strong&gt;http://dx.doi.org/10.4202/app.&lt;wbr&gt;&lt;/wbr&gt;2013.0027&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;&lt;br /&gt;&lt;strong&gt;Abstract -&lt;/strong&gt; &lt;em&gt;Silesaurus opolensis&lt;/em&gt; belongs to Silesauridae, the closest sister group&lt;br /&gt;to dinosaurs. The present study analyzed the dental &amp;nbsp;microwear patterns of &lt;em&gt;Silesaurus opolensis&lt;/em&gt;. Low pit-to-scratch ratios imply they did not feed on hard objects. Unimodal distributions of both wear-facet and non-facet scratch orientations indicate simple orthal jaw movement. Scratch orientation and density differ between microscopic regions in &lt;em&gt;Silesaurus&lt;/em&gt;, and unlike hadrosaurid dinosaurs, the microwear patterns of small areas are not identical to those of whole teeth.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=KJkN6lejq50:TEdRKjhO_Uw:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=KJkN6lejq50:TEdRKjhO_Uw:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=KJkN6lejq50:TEdRKjhO_Uw:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=KJkN6lejq50:TEdRKjhO_Uw:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=KJkN6lejq50:TEdRKjhO_Uw:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=KJkN6lejq50:TEdRKjhO_Uw:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=KJkN6lejq50:TEdRKjhO_Uw:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=KJkN6lejq50:TEdRKjhO_Uw:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=KJkN6lejq50:TEdRKjhO_Uw:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=KJkN6lejq50:TEdRKjhO_Uw:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/KJkN6lejq50" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/3321936793470835896/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/06/dental-microwear-of-late-triassic.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/3321936793470835896?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/3321936793470835896?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/KJkN6lejq50/dental-microwear-of-late-triassic.html" title="Dental Microwear of the Late Triassic Dinosauriform &lt;i&gt;Silesaurus opolensis&lt;/i&gt;" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/06/dental-microwear-of-late-triassic.html</feedburner:origLink></entry><entry gd:etag="W/&quot;DUQEQXo_cCp7ImA9WhFTEko.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-2333417573261878143</id><published>2013-06-03T09:35:00.000-07:00</published><updated>2013-06-03T09:35:00.448-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-06-03T09:35:00.448-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="tracks" /><category scheme="http://www.blogger.com/atom/ns#" term="Archosauriformes" /><title>Analysis of Triassic Archosauriform Trackways</title><content type="html">&lt;b&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;Kubo, T. and M. O. Kubo. 2013.&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;Analysis of Triassic archosauriform trackways: difference in&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;stride/foot ratio between dinosauromorphs and other archosauriforms.&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;Palaios 28: 259-265&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;doi:10.2110/palo.2012.p12-099r&lt;/span&gt;&lt;br style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;" /&gt;&lt;/b&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;&lt;b&gt;Abstract &lt;/b&gt;- Fossilized trackways have rarely been analyzed quantitatively to&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;examine major trends and patterns in evolution despite their potential&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;utility, especially in understanding locomotory evolution. In the&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;present study, trackways of Triassic archosauriforms were analyzed.&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;The analyses showed foot and stride lengths of archosauriforms&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;increased from the Early to Middle Triassic, especially those of&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;dinosauromorphs, which tripled. Dinosauromorphs were much smaller in&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;foot length and stride length compared to other archosauriforms during&lt;/span&gt;&lt;br style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;" /&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;the Early Triassic. They reached similar stride length compared with&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;other archosauriforms during the Middle Triassic and similar foot&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;length in the Late Triassic. Stride/foot ratio is significantly higher&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;in dinosauromorphs compared to other archosauriforms throughout the&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;Triassic. This relatively long stride length of dinosauromorphs is&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;attributed to either faster speed or higher relative hip height that&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;was probably caused by their digitigrade foot posture. Analyses of&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;trackway data sets, especially in combination with precise trackmaker&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;assignment and age determination, would bring us more thorough&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;knowledge about locomotory evolution of tetrapods that complements&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;body fossil evidence.&lt;/span&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=YE5-RjOcTtU:9WFb4kccxNw:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=YE5-RjOcTtU:9WFb4kccxNw:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=YE5-RjOcTtU:9WFb4kccxNw:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=YE5-RjOcTtU:9WFb4kccxNw:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=YE5-RjOcTtU:9WFb4kccxNw:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=YE5-RjOcTtU:9WFb4kccxNw:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=YE5-RjOcTtU:9WFb4kccxNw:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=YE5-RjOcTtU:9WFb4kccxNw:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=YE5-RjOcTtU:9WFb4kccxNw:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=YE5-RjOcTtU:9WFb4kccxNw:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/YE5-RjOcTtU" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/2333417573261878143/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/06/analysis-of-triassic-archosauriform.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2333417573261878143?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2333417573261878143?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/YE5-RjOcTtU/analysis-of-triassic-archosauriform.html" title="Analysis of Triassic Archosauriform Trackways" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/06/analysis-of-triassic-archosauriform.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CkIAQXs8eSp7ImA9WhFTEUQ.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-2594079687559751401</id><published>2013-06-02T09:29:00.000-07:00</published><updated>2013-06-02T09:29:00.571-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-06-02T09:29:00.571-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="synapsids" /><category scheme="http://www.blogger.com/atom/ns#" term="Permian" /><title>The Early Evolution of Synapsids</title><content type="html">Brocklehurst, N., Kammerer, C. F., and J.&amp;nbsp;Frobisch. 2013. The early evolution of synapsids, and the influence of sampling on their fossil record. Paleobiology 39:470-490.&amp;nbsp;DOI: 10.1666/12049&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;Abstract -&lt;/b&gt; Synapsids dominated the terrestrial realm between the late Pennsylvanian and the Triassic.&lt;br /&gt;
Their early evolution includes some of the first amniotes to evolve large size, herbivory, and macropredators. However, little research has focused on the changes in diversity occurring during this early phase in their evolutionary history, with more effort concentrating on later events such the Permo-Triassic extinction. Here we assess synapsid diversity, at both the species and genus levels, between the Carboniferous (Moscovian) and the Middle Permian (Capitanian). A raw, taxic diversity (richness) estimate is generated, and we use two separate methods to correct for sampling biases in this curve. To remove the effect of anthropogenic sampling bias, we apply a recently published modification of the residual diversity method, and then generate a supertree, using matrix representation with parsimony to infer ghost lineages and obtain a phylogenetic diversity estimate. The general diversity pattern reflects the initial diversification of synapsids in the late Pennsylvanian and early Cisuralian, which was followed by an extinction event during the Sakmarian. Diversity recovered during the Artinskian and Kungurian, coinciding with the radiation of Caseidae, although other families begin to decline. A second extinction event occurred across the Kungurian/Roadian boundary, in which Edaphosauridae and Ophiacodontidae died out although Caseidae and Therapsida diversified. The sampling-corrected curves reveal further extinction during the Roadian, although therapsids were again unaffected. Pelycosaurian-grade synapsids survived during the Wordian and Capitanian, but were a minor part of an otherwise therapsid-dominated fauna. Evidence of significant anthropogenic sampling bias calls&lt;br /&gt;
into question previous diversity studies that have not employed sampling correction.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=HKCsdBfEr_k:Y8d0Crqcek8:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=HKCsdBfEr_k:Y8d0Crqcek8:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=HKCsdBfEr_k:Y8d0Crqcek8:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=HKCsdBfEr_k:Y8d0Crqcek8:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=HKCsdBfEr_k:Y8d0Crqcek8:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=HKCsdBfEr_k:Y8d0Crqcek8:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=HKCsdBfEr_k:Y8d0Crqcek8:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=HKCsdBfEr_k:Y8d0Crqcek8:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=HKCsdBfEr_k:Y8d0Crqcek8:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=HKCsdBfEr_k:Y8d0Crqcek8:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/HKCsdBfEr_k" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/2594079687559751401/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/06/the-early-evolution-of-synapsids.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2594079687559751401?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2594079687559751401?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/HKCsdBfEr_k/the-early-evolution-of-synapsids.html" title="The Early Evolution of Synapsids" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/06/the-early-evolution-of-synapsids.html</feedburner:origLink></entry><entry gd:etag="W/&quot;AkEEQH07eip7ImA9WhFTEUw.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-1537712500994117693</id><published>2013-06-01T13:30:00.000-07:00</published><updated>2013-06-01T13:30:01.302-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-06-01T13:30:01.302-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="tetrapod evolution" /><category scheme="http://www.blogger.com/atom/ns#" term="turtle shell origin" /><title>New Hypothesis on the Evolutionary Origin of the Turtle Shell (with video)</title><content type="html">&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;This recent early online paper has been getting a lot of attention lately regarding the origin of turtles and their phylogenetic relationships. There is also &lt;a href="http://www.youtube.com/watch?v=qIOPDysP74g"&gt;this associated video on YouTube&lt;/a&gt; depicting this new hypothesis of the evolution of the turtle shell.&lt;/span&gt;&lt;br /&gt;
&lt;b&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;&lt;br /&gt;&lt;/span&gt;&lt;/b&gt;
&lt;b&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;Lyson, T. R., Bever, G. S., Scheyer, T. M., Hsiang, A. Y., &amp;nbsp;and&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;J. A. Gauthier. 2013.&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;Evolutionary Origin of the Turtle Shell.&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;Current Biology.&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;doi:&amp;nbsp;&lt;/span&gt;&lt;a href="http://dx.doi.org/10.1016/j.cub.2013.05.003" style="background-color: white; color: #1155cc; font-family: arial, sans-serif; font-size: 13px;" target="_blank"&gt;http://dx.doi.org/10.1016/j.&lt;wbr&gt;&lt;/wbr&gt;cub.2013.05.003&lt;/a&gt;&lt;/b&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;&lt;b&gt;Abstract - &lt;/b&gt;The origin of the turtle shell has perplexed biologists for more than&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;two centuries. It was not until &lt;i&gt;Odontochelys semitestacea&lt;/i&gt; was&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;discovered, however, that the fossil and developmental data could be&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;synthesized into a model of shell assembly that makes predictions for&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;the as-yet unestablished history of the turtle stem group. We build on&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;this model by integrating novel data for&lt;i&gt; Eunotosaurus africanus&lt;/i&gt;—a Late&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;Guadalupian (~260 mya) Permian reptile inferred to be an early stem&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;turtle. &lt;i&gt;Eunotosaurus&lt;/i&gt; expresses a number of relevant characters,&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;including a reduced number of elongate trunk vertebrae (nine), nine&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;pairs of T-shaped ribs, inferred loss of intercostal muscles,&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;reorganization of respiratory muscles to the ventral side of the ribs,&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;(sub)dermal outgrowth of bone from the developing perichondral collar&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;of the ribs, and paired gastralia that lack both lateral and median&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;elements. These features conform to the predicted sequence of&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;character acquisition and provide further support that &lt;i&gt;E. africanus&lt;/i&gt;,&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;&lt;i&gt;O. semitestacea&lt;/i&gt;, and &lt;i&gt;Proganochelys quenstedti&lt;/i&gt; represent successive&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;divergences from the turtle stem lineage. The initial transformations&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;of the model thus occurred by the Middle Permian, which is congruent&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;with molecular-based divergence estimates for the lineage, and remain&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: white; color: #222222; font-family: arial, sans-serif; font-size: 13px;"&gt;viable whether turtles originated inside or outside crown Diapsida.&lt;/span&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ubBagIiSuQQ:S6hxjBffy3U:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ubBagIiSuQQ:S6hxjBffy3U:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ubBagIiSuQQ:S6hxjBffy3U:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ubBagIiSuQQ:S6hxjBffy3U:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=ubBagIiSuQQ:S6hxjBffy3U:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ubBagIiSuQQ:S6hxjBffy3U:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=ubBagIiSuQQ:S6hxjBffy3U:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ubBagIiSuQQ:S6hxjBffy3U:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ubBagIiSuQQ:S6hxjBffy3U:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=ubBagIiSuQQ:S6hxjBffy3U:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/ubBagIiSuQQ" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/1537712500994117693/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/06/new-hypothesis-on-evolutionary-origin.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/1537712500994117693?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/1537712500994117693?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/ubBagIiSuQQ/new-hypothesis-on-evolutionary-origin.html" title="New Hypothesis on the Evolutionary Origin of the Turtle Shell (with video)" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/06/new-hypothesis-on-evolutionary-origin.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CUAGSH04cSp7ImA9WhFTEU0.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-6921309889753061436</id><published>2013-06-01T09:22:00.000-07:00</published><updated>2013-06-01T09:22:09.339-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-06-01T09:22:09.339-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="North America" /><category scheme="http://www.blogger.com/atom/ns#" term="Late Triassic" /><category scheme="http://www.blogger.com/atom/ns#" term="dicynodont" /><category scheme="http://www.blogger.com/atom/ns#" term="Synapsida" /><title>Revisiting the Dicynodonts of Western North America</title><content type="html">&lt;b&gt;&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;Kammerer, C. F., Fröbisch, J., and Angielczyk, K. D. 2013. On the validity and phylogenetic position of&amp;nbsp;&lt;/span&gt;&lt;em style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;Eubrachiosaurus browni,&lt;/em&gt;&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;&amp;nbsp;a kannemeyeriiform dicynodont (Anomodontia) from Triassic North America. &lt;a href="http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0064203"&gt;PLoS ONE 8(5): e64203. doi:10.1371/journal.pone.0064203&lt;/a&gt;&lt;/span&gt;&lt;/b&gt;&lt;br /&gt;
&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;/span&gt;
&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;&lt;b&gt;Abstract - &lt;/b&gt;The large dicynodont&amp;nbsp;&lt;/span&gt;&lt;em style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;Eubrachiosaurus browni&lt;/em&gt;&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;&amp;nbsp;from the Upper Triassic Popo Agie Formation of Wyoming is redescribed.&amp;nbsp;&lt;/span&gt;&lt;em style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;Eubrachiosaurus&lt;/em&gt;&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;&amp;nbsp;is a valid taxon that differs from&amp;nbsp;&lt;/span&gt;&lt;em style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;Placerias hesternus&lt;/em&gt;&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;, with which it was previously synonymized, by greater anteroposterior expansion of the scapula dorsally and a very large, nearly rectangular humeral ectepicondyle with a broad supinator process. Inclusion of&amp;nbsp;&lt;/span&gt;&lt;em style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;Eubrachiosaurus&lt;/em&gt;&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;&amp;nbsp;in a revised phylogenetic analysis of anomodont therapsids indicates that it is a stahleckeriid closely related to the South American genera&amp;nbsp;&lt;/span&gt;&lt;em style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;Ischigualastia&lt;/em&gt;&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;&amp;nbsp;and&amp;nbsp;&lt;/span&gt;&lt;em style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;Jachaleria&lt;/em&gt;&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;. The recognition of&amp;nbsp;&lt;/span&gt;&lt;em style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;Eubrachiosaurus&lt;/em&gt;&lt;span style="background-color: white; color: #333333; font-family: arial, sans-serif; font-size: 13px; line-height: 18px;"&gt;&amp;nbsp;as a distinct lineage of North American dicynodonts, combined with other recent discoveries in the eastern USA and Europe, alters our perception of Late Triassic dicynodont diversity in the northern hemisphere. Rather than being isolated relicts in previously therapsid-dominated regions, Late Triassic stahleckeriid dicynodonts were continuing to disperse and diversify, even in areas like western North America that were otherwise uninhabited by coeval therapsids (i.e., cynodonts).&lt;/span&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=EbE0kh_UnRA:JKBDbzAToQU:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=EbE0kh_UnRA:JKBDbzAToQU:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=EbE0kh_UnRA:JKBDbzAToQU:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=EbE0kh_UnRA:JKBDbzAToQU:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=EbE0kh_UnRA:JKBDbzAToQU:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=EbE0kh_UnRA:JKBDbzAToQU:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=EbE0kh_UnRA:JKBDbzAToQU:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=EbE0kh_UnRA:JKBDbzAToQU:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=EbE0kh_UnRA:JKBDbzAToQU:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=EbE0kh_UnRA:JKBDbzAToQU:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/EbE0kh_UnRA" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/6921309889753061436/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/06/revisiting-dicynodonts-of-western-north.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/6921309889753061436?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/6921309889753061436?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/EbE0kh_UnRA/revisiting-dicynodonts-of-western-north.html" title="Revisiting the Dicynodonts of Western North America" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/06/revisiting-dicynodonts-of-western-north.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CE8ERnwyeip7ImA9WhBaGUo.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-38492544357868440</id><published>2013-05-30T21:00:00.000-07:00</published><updated>2013-05-30T21:00:07.292-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-05-30T21:00:07.292-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="tracks" /><category scheme="http://www.blogger.com/atom/ns#" term="China" /><category scheme="http://www.blogger.com/atom/ns#" term="Middle Triassic" /><title>Chirotherium Trackways from the Middle Triassic of China</title><content type="html">&lt;strong&gt;Xing, L., Klein, H., Lockley, M. G., Li, J., Zhang, J., Matsukawa, M., and J. Xiao. 2013.&amp;nbsp;Chirotherium trackways from the Middle Triassic of Guizhou, China. Ichnos 20: 99-107. DOI:10.1080/10420940.2013.&lt;wbr&gt;&lt;/wbr&gt;788505&lt;br /&gt;&lt;br /&gt;Abstract -&lt;/strong&gt; Triassic tetrapod footprints from China are less well known than those from the Jurassic and Cretaceous. Archosaurian trackways of the ichnogenus &lt;em&gt;Chirotherium&lt;/em&gt; were found in the Middle Triassic Guanling Formation in Zhenfeng County (Guizhou Province) at the southwestern edge of the Yangtze plate in the early 1960s but were not correctly identified and adequately described until 40 years later. Here we give a detailed re-description and review of the trackways, which are known from two localities near the villages of Niuchang and Longchang. They occur on the bedding surface of a mud-cracked argillaceous dolostone deposited in a near-shore, shallow-water environment. Their morphology and general trackway pattern indicate that they pertain to the ichnospecies &lt;em&gt;Chirotherium barthii&lt;/em&gt;, well known from Middle Triassic&lt;br /&gt; track surfaces of Europe, North and South America, and northern Africa. A peculiarity of the trackways from China are the low pace angulation and stride length, reflecting slow-moving trackmakers, which were basal crown-group archosaurs, possibly early&lt;br /&gt; representatives of the dinosaur-bird line or, alternatively, stem-group crocodylians. These tracks constitute the only chirotheriid record known from Asia thus far and indicate a Pangea-wide distribution for this ichnotaxon. Biostratigraphically, assemblages with &lt;em&gt;C. barthii&lt;/em&gt; are characteristic of the early Anisian, an age assignment already supported for the Guanling Formation based on conodont and bivalve biostratigraphy. In contrast, however, radiometric data from an interlayered ash bed indicate a Ladinian age.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ZzDEizaxEBA:o6eT2i6FK1k:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ZzDEizaxEBA:o6eT2i6FK1k:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ZzDEizaxEBA:o6eT2i6FK1k:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ZzDEizaxEBA:o6eT2i6FK1k:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=ZzDEizaxEBA:o6eT2i6FK1k:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ZzDEizaxEBA:o6eT2i6FK1k:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=ZzDEizaxEBA:o6eT2i6FK1k:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ZzDEizaxEBA:o6eT2i6FK1k:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=ZzDEizaxEBA:o6eT2i6FK1k:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=ZzDEizaxEBA:o6eT2i6FK1k:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/ZzDEizaxEBA" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/38492544357868440/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/05/chirotherium-trackways-from-middle.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/38492544357868440?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/38492544357868440?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/ZzDEizaxEBA/chirotherium-trackways-from-middle.html" title="Chirotherium Trackways from the Middle Triassic of China" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/05/chirotherium-trackways-from-middle.html</feedburner:origLink></entry><entry gd:etag="W/&quot;A0AEQHw5eyp7ImA9WhBaF0Q.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-5081206167720957233</id><published>2013-05-28T20:55:00.000-07:00</published><updated>2013-05-28T20:55:01.223-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-05-28T20:55:01.223-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Temnospondyli" /><category scheme="http://www.blogger.com/atom/ns#" term="tetrapod evolution" /><category scheme="http://www.blogger.com/atom/ns#" term="Late Triassic" /><title>High Environmental and Metabolic Plasticity as a Successful Evolutionary Strategy in a Long-lived Homeostatic Triassic Temnospondyl.</title><content type="html">&lt;strong&gt;Sanchez S., and R. R. Schoch. 2013. Bone histology reveals a high environmental and metabolic plasticity as a successful evolutionary strategy in a long-lived homeostatic Triassic temnospondyl. Evolutionary Biology (early online) &lt;/strong&gt;&lt;a href="http://link.springer.com/article/10.1007/s11692-013-9238-3"&gt;&lt;strong&gt;DOI: 10.1007/s11692-013-9238-3&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;
&lt;br /&gt;&lt;strong&gt;Abstract -&lt;/strong&gt; Evolutionary stasis (long-term stability of morphology in an evolving lineage) is a pattern for which explanations are usually elusive. The Triassic tetrapod &lt;em&gt;Gerrothorax pulcherrimus&lt;/em&gt;, a gill-bearing temnospondyl, survived for 35 million years in the Germanic Basin of Central Europe persisting throughout the dinosaur-dominated Late Triassic Period. This evolutionary stasis coincides with the occurrence of this species in a wide range of habitats and environmental conditions. By the combination of palaeoecological and palaeohistological analyses, we found great ecological flexibility in &lt;em&gt;G. pulcherrimus&lt;/em&gt; and present substantial evidence of developmental and&lt;br /&gt; metabolic plasticity despite the morphological stasis. We conclude that &lt;em&gt;G. pulcherrimus&lt;/em&gt; could show the capacity to settle in water bodies too harsh or unpredictable for most other tetrapods. This would have been made possible by a unique life history strategy that involved a wide reaction norm, permitting adjustment to fluctuating conditions such as salinity and level of nutrients. Growth rate, duration of juvenile period, age at maturity, and life span were all subject to broad variation within specimens of &lt;em&gt;G. pulcherrimus&lt;/em&gt; in one single lake and in between different lakes. In addition to providing a better understanding of fossil ecosystems, this study shows the potential of such a methodology to encourage palaeobiologists and evolutionary biologists to consider the mechanisms of variation in extant and fossil organisms by using a similar time-scope reference.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=Us_7WPXbdsQ:qfLR8-jJcrI:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=Us_7WPXbdsQ:qfLR8-jJcrI:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=Us_7WPXbdsQ:qfLR8-jJcrI:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=Us_7WPXbdsQ:qfLR8-jJcrI:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=Us_7WPXbdsQ:qfLR8-jJcrI:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=Us_7WPXbdsQ:qfLR8-jJcrI:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=Us_7WPXbdsQ:qfLR8-jJcrI:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=Us_7WPXbdsQ:qfLR8-jJcrI:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=Us_7WPXbdsQ:qfLR8-jJcrI:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=Us_7WPXbdsQ:qfLR8-jJcrI:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/Us_7WPXbdsQ" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/5081206167720957233/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/05/high-environmental-and-metabolic.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/5081206167720957233?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/5081206167720957233?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/Us_7WPXbdsQ/high-environmental-and-metabolic.html" title="High Environmental and Metabolic Plasticity as a Successful Evolutionary Strategy in a Long-lived Homeostatic Triassic Temnospondyl." /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/05/high-environmental-and-metabolic.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CE8MQH4zfip7ImA9WhBaF0w.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-2618850541331227223</id><published>2013-05-27T20:48:00.000-07:00</published><updated>2013-05-27T20:48:01.086-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-05-27T20:48:01.086-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="palynology" /><category scheme="http://www.blogger.com/atom/ns#" term="Ischigualasto" /><category scheme="http://www.blogger.com/atom/ns#" term="Late Triassic" /><title>A New Late Triassic Phytogeographical Scenario in Westernmost Gondwana.</title><content type="html">&lt;strong&gt;Césari, S. N.,&amp;nbsp;&amp;nbsp;and Colombi, C. E.&amp;nbsp;2013. A new Late Triassic phytogeographical scenario in westernmost Gondwana. Nature Communications 4, Article number: 1889 &lt;a href="http://www.nature.com/ncomms/journal/v4/n5/full/ncomms2917.html"&gt;doi:10.1038/ncomms2917&lt;/a&gt;&lt;br /&gt;&lt;br /&gt;&amp;nbsp;Abstract -&lt;/strong&gt; Floral provincialism within the Southern Hemisphere during the Late&lt;br /&gt; Triassic (230 Ma) is characterized by the Ipswich and Onslow provinces, recognized originally in eastern Gondwana. However, new palynological assemblages from the Ischigualasto Formation, northwestern Argentina (231–225 Ma), change the phytogeographic interpretation for the Carnian–Norian in the westernmost Gondwana,&lt;br /&gt;which was previously considered part of the southern floral Ipswich province. Here we show the presence of diagnostic Euramerican species within assemblages dominated by Gondwanan taxa that allows us to refer the palynofloras to the Onslow province. Our new data extend the Onslow floral belt, previously recognized from the western edge of Tethys to Timor, to the western margin of South America. This has implications for palaeophytogeography, palaeoclimate reconstructions and the palaeoecology of a Triassic ecosystem, which has yielded significant vertebrate remains and is regarded important in the early evolution of groups such as the Dinosauria.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=8bcnS9syhRY:jgZDwlgMK8U:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=8bcnS9syhRY:jgZDwlgMK8U:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=8bcnS9syhRY:jgZDwlgMK8U:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=8bcnS9syhRY:jgZDwlgMK8U:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=8bcnS9syhRY:jgZDwlgMK8U:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=8bcnS9syhRY:jgZDwlgMK8U:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=8bcnS9syhRY:jgZDwlgMK8U:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=8bcnS9syhRY:jgZDwlgMK8U:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=8bcnS9syhRY:jgZDwlgMK8U:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=8bcnS9syhRY:jgZDwlgMK8U:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/8bcnS9syhRY" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/2618850541331227223/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/05/a-new-late-triassic-phytogeographical.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2618850541331227223?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2618850541331227223?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/8bcnS9syhRY/a-new-late-triassic-phytogeographical.html" title="A New Late Triassic Phytogeographical Scenario in Westernmost Gondwana." /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/05/a-new-late-triassic-phytogeographical.html</feedburner:origLink></entry><entry gd:etag="W/&quot;DEIAQngzfip7ImA9WhBaFk8.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-7664419682951397904</id><published>2013-05-26T20:44:00.001-07:00</published><updated>2013-05-26T20:49:03.686-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-05-26T20:49:03.686-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Asia" /><category scheme="http://www.blogger.com/atom/ns#" term="Late Triassic" /><category scheme="http://www.blogger.com/atom/ns#" term="chronostratigraphy" /><title>New Stratigraphy, Geochronology, and Paleontology from the Late Triassic of Laos</title><content type="html">Note that 225-221 Ma&amp;nbsp;is now considered to be Norian...&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Blanchard, S., Rossignol, C., Bourquin, S., Dabard, M.-P., Hallot, E., Nalpas, T., Poujol, M., Battail, B., Jalil, N.-E., Steyer, J.-S., Vacant, R., Véran, M., Bercovici, A., Diez, J. B., Paquette, J.-L., Khenthavong, B. and Vongphamany, S. 2013. Late Triassic volcanic activity in South-East Asia: new stratigraphical, geochronological and paleontological evidence from the Luang Prabang Basin (Laos). &lt;/strong&gt;&lt;a href="http://www.sciencedirect.com/science/article/pii/S1367912013001442"&gt;&lt;strong&gt;Journal of Asian Earth Sciences 70-71: 8–26&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt;.&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; In South-East Asia, sedimentary basins displaying continental Permian and Triassic deposits have been poorly studied. Among these, the Luang Prabang Basin (North Laos) represents a potential key target to constrain the stratigraphic and structural evolutions of South-East Asia. A combined approach involving sedimentology, palaeontology, geochronology and structural analysis, was thus implemented to study the basin. It resulted in a new geological map, in defining new formations, and in proposing a complete revision of the Late Permian to Triassic stratigraphic succession as well as of the structural organization of the basin. Radiometric ages are used to discuss the synchronism of volcanic activity and sedimentation.&lt;br /&gt;
&lt;br /&gt;
The Luang Prabang Basin consists of an asymmetric NE-SW syncline with NE-SW thrusts, located at the contact between Late Permian and Late Triassic deposits. The potential stratigraphic gap at the Permian–Triassic boundary is therefore masked by deformation in the basin. The Late Triassic volcaniclastic continental deposits are representative of alluvial plain and fluvial environments. The basin was fed by several sources, varying from volcanic, carbonated to silicic (non-volcanic). U–Pb dating of euhedral zircon grains provided maximum sedimentation ages. The stratigraphic vertical succession of these ages, from ca. 225, ca. 220 to ca. 216 Ma, indicates that a long lasting volcanism was active during sedimentation and illustrates significant variations in sediment preservation rates in continental environments (from ∼100 m/Ma to ∼3 m/Ma). Anhedral inherited zircon grains gave older ages. A large number of them, at ca. 1870 Ma, imply the reworking of a Proterozoic basement and/or of sediments containing fragments of such a basement. In addition, the Late Triassic (Carnian to Norian) sediments yielded to a new dicynodont skull, attributed to the Kannemeyeriiform group family, from layers dated in between ∼225 and ∼221 Ma (Carnian).&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=dOGS93xLriQ:QWQtUt6Nvkw:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=dOGS93xLriQ:QWQtUt6Nvkw:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=dOGS93xLriQ:QWQtUt6Nvkw:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=dOGS93xLriQ:QWQtUt6Nvkw:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=dOGS93xLriQ:QWQtUt6Nvkw:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=dOGS93xLriQ:QWQtUt6Nvkw:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=dOGS93xLriQ:QWQtUt6Nvkw:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=dOGS93xLriQ:QWQtUt6Nvkw:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=dOGS93xLriQ:QWQtUt6Nvkw:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=dOGS93xLriQ:QWQtUt6Nvkw:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/dOGS93xLriQ" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/7664419682951397904/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/05/new-stratigraphy-geochronology-and.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/7664419682951397904?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/7664419682951397904?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/dOGS93xLriQ/new-stratigraphy-geochronology-and.html" title="New Stratigraphy, Geochronology, and Paleontology from the Late Triassic of Laos" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/05/new-stratigraphy-geochronology-and.html</feedburner:origLink></entry><entry gd:etag="W/&quot;D04HR30-fip7ImA9WhBaFk8.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-6345435543752585814</id><published>2013-05-14T21:23:00.002-07:00</published><updated>2013-05-26T20:38:56.356-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-05-26T20:38:56.356-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Ischigualasto" /><category scheme="http://www.blogger.com/atom/ns#" term="eucynodontia" /><category scheme="http://www.blogger.com/atom/ns#" term="Late Triassic" /><category scheme="http://www.blogger.com/atom/ns#" term="Argentina" /><title>A New Non-mammaliaform Eucynodont from the Ischigualasto Formation of Argentina</title><content type="html">&lt;strong&gt;Martínez, R. N., Fernandez, E., and O. A. Alcober. 2013.  A new non-mammaliaform eucynodont from the Carnian-Norian Ischigualasto Formation, Northwestern Argentina. Revista Brasileira de Paleontologia 16: 61-76. &lt;a href="http://www.sbpbrasil.org/revista/edicoes/16_1/05_Martinez_et_al.pdf"&gt;doi:10.4072/rbp.2013.1.05&lt;/a&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; The record of non-mammaliaformes eucynodonts from the Carnian-Norian Ischigualasto Formation is diverse and abundant, including a medium to large size herbivore and small carnivores. Here is described a new small eucynodont from the Ischigualasto Formation, on the basis of a partial skull. The new taxon is characterized by palatal process of the premaxilla extending posterior to the level of the first postcanine; deep and large maxillary laterodorsal fossa that opens at the level of the root of the upper canine; and postorbital bar diverging posterolaterally at very low angle (35.6°) from the anteroposterior axis of the skull. Results from a phylogenetic analysis supports the new genus placement as a probainognathian eucynodont, more derived than &lt;em&gt;Probainognathus&lt;/em&gt; Romer, and more closely related to &lt;em&gt;Ecteninion&lt;/em&gt; Martinez, May &amp;amp; Forster and &lt;em&gt;Trucidocynodon&lt;/em&gt; Oliveira, Soares &amp;amp; Schultz than to any other eucynodont. Ecteniniidae is proposed as a new clade including the new genus, &lt;em&gt;Ecteninion&lt;/em&gt; and &lt;em&gt;Trucidocynodon&lt;/em&gt;, and in the phylogenetic hypothesis represents the sister-group of Prozostrodontia (&lt;em&gt;Prozostrodon&lt;/em&gt; Bonaparte &amp;amp; Barberena, Tritylodontidae and Mammaliaformes). Additionally, the new taxon from the Ischigualasto Formation shows that the &lt;em&gt;Scaphonyx-Exaeretodon-Herrerasaurus&lt;/em&gt; biozone has similar cynodont diversity than the supposedly contemporaneous &lt;em&gt;Hyperodapedon&lt;/em&gt; Assemblage Zone of Santa Maria 2 Sequence, in Southern Brazil.&lt;br /&gt;
&lt;br /&gt;
&lt;div class="im" style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #500050; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;
&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;/span&gt;&amp;nbsp;&lt;/div&gt;
&lt;div class="im" style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #500050; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;
&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;/span&gt;&amp;nbsp;&lt;/div&gt;
&lt;div class="im" style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #500050; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;
&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;/span&gt;&amp;nbsp;&lt;/div&gt;
&lt;div class="im" style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #500050; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;
&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;/span&gt;&amp;nbsp;&lt;/div&gt;
&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=-hh4HYaM86w:9-Fl2WvmPrQ:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=-hh4HYaM86w:9-Fl2WvmPrQ:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=-hh4HYaM86w:9-Fl2WvmPrQ:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=-hh4HYaM86w:9-Fl2WvmPrQ:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=-hh4HYaM86w:9-Fl2WvmPrQ:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=-hh4HYaM86w:9-Fl2WvmPrQ:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=-hh4HYaM86w:9-Fl2WvmPrQ:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=-hh4HYaM86w:9-Fl2WvmPrQ:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=-hh4HYaM86w:9-Fl2WvmPrQ:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=-hh4HYaM86w:9-Fl2WvmPrQ:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/-hh4HYaM86w" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/6345435543752585814/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/05/a-new-non-mammaliaform-eucynodont-from.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/6345435543752585814?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/6345435543752585814?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/-hh4HYaM86w/a-new-non-mammaliaform-eucynodont-from.html" title="A New Non-mammaliaform Eucynodont from the Ischigualasto Formation of Argentina" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/05/a-new-non-mammaliaform-eucynodont-from.html</feedburner:origLink></entry><entry gd:etag="W/&quot;D04GQXs_eyp7ImA9WhBUF08.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-7018192046156051294</id><published>2013-05-04T20:52:00.000-07:00</published><updated>2013-05-04T20:52:00.543-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-05-04T20:52:00.543-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="histology" /><category scheme="http://www.blogger.com/atom/ns#" term="Rauisuchids" /><category scheme="http://www.blogger.com/atom/ns#" term="growth rates" /><title>Osteoderm Microstructure of “Rauisuchian” Archosaurs from South America</title><content type="html">&lt;strong&gt;Cerda, I. A., J. B. Desojo, T. M. Scheyer&amp;nbsp;and C. L. Schultz. In Press. Osteoderm microstructure of “rauisuchian” archosaurs from South America. Geobios (accepted manuscript) doi: &lt;/strong&gt;&lt;a href="http://dx.doi.org/10.1016/j.geobios.2013.01.004" target="_blank"&gt;&lt;strong&gt;http://dx.doi.org/10.1016/j.&lt;wbr&gt;&lt;/wbr&gt;geobios.2013.01.004&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;&lt;br /&gt;&lt;strong&gt;Abstract -&lt;/strong&gt; In this contribution we analyze and discuss the microanatomy and histology of postcranial osteoderms of a number of “rauisuchians” from different localities of South America (Argentina and Brazil). The studied sample includes osteoderms of &lt;em&gt;Fasolasuchus tenax&lt;/em&gt;, &lt;em&gt;Prestosuchus chiniquensis&lt;/em&gt;, &lt;em&gt;Saurosuchus galilei&lt;/em&gt; and an undetermined rauisuchian from Brazil. The bone microanatomy of the osteoderms is variable: whereas some specimens have a rather compact structure, others show a diploe architecture with a central cancellous core bordered by two compact cortices. Both external and basal cortices are mainly composed of poorly vascularized, fine and coarse parallel fibred bone and networks of interwoven and mineralized fiber bundles. The internal region of the non-remodeled specimens consists of a well-vascularized core in which the intrinsic fibers exhibit important variations (even in the same specimen), ranging from coarse, parallel-fibred to woven-fibred bone tissues. Lines of arrested growth (LAGs) are well recorded in both basal and external cortices. Differences in the bone microstructure (compact vs. diploe) could be related to the age, sex and reproductive status of the sampled individuals. Hence, age estimation based on the count of LAGs in rauisuchian osteoderms appears to be reliable only in the early stages of ontogeny. The bone microstructure suggests that rauisuchian osteoderms were originated through a mechanism that involves both intramembranous and metaplastic ossifications.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=oqGv01QIIdA:S4bWfuoSJ5A:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=oqGv01QIIdA:S4bWfuoSJ5A:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=oqGv01QIIdA:S4bWfuoSJ5A:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=oqGv01QIIdA:S4bWfuoSJ5A:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=oqGv01QIIdA:S4bWfuoSJ5A:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=oqGv01QIIdA:S4bWfuoSJ5A:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=oqGv01QIIdA:S4bWfuoSJ5A:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=oqGv01QIIdA:S4bWfuoSJ5A:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=oqGv01QIIdA:S4bWfuoSJ5A:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=oqGv01QIIdA:S4bWfuoSJ5A:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/oqGv01QIIdA" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/7018192046156051294/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/05/osteoderm-microstructure-of-rauisuchian.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/7018192046156051294?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/7018192046156051294?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/oqGv01QIIdA/osteoderm-microstructure-of-rauisuchian.html" title="Osteoderm Microstructure of “Rauisuchian” Archosaurs from South America" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/05/osteoderm-microstructure-of-rauisuchian.html</feedburner:origLink></entry><entry gd:etag="W/&quot;A0QERn09eSp7ImA9WhBUFk4.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-2575850738458792564</id><published>2013-05-03T20:48:00.000-07:00</published><updated>2013-05-03T20:48:27.361-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-05-03T20:48:27.361-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="mass extinction" /><category scheme="http://www.blogger.com/atom/ns#" term="biodiversity" /><category scheme="http://www.blogger.com/atom/ns#" term="Permo-Triassic" /><title>Provincialization of Terrestrial Faunas Following the End-Permian Mass Extinction.</title><content type="html">&lt;strong&gt;Sidor, C. A., D. A. Vilhena,&amp;nbsp;K. D. Angielczyk, A. K. Huttenlocker, S. J. Nesbitt, B. R. Peecook, J.&amp;nbsp;S. Steyer, R. M. H. Smith, and L. A. Tsuji. 2013. Provincialization of terrestrial faunas following the end-Permian mass extinction. Proceedings of the National Academy of Sciences (advance online publication)&lt;br /&gt; &lt;/strong&gt;&lt;a href="http://www.pnas.org/content/early/2013/04/24/1302323110.abstract?sid=ca247696-0f82-4a3b-97ae-ff99a2fcd07b"&gt;&lt;strong&gt;doi: 10.1073/pnas.1302323110&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;
&lt;br /&gt;&lt;strong&gt;Abstract -&lt;/strong&gt; &amp;nbsp;In addition to their devastating effects on global biodiversity, mass extinctions have had a long-term influence on the history of life by eliminating dominant lineages that suppressed ecological change. Here, we test whether the end-Permian mass extinction (252.3 Ma) affected the distribution of tetrapod faunas within the southern hemisphere and apply quantitative methods to analyze four components of biogeographic structure: connectedness, clustering, range size, and endemism. For all four components, we detected increased provincialism between our Permian and Triassic datasets. In southern Pangea, a more homogeneous and broadly distributed fauna in the Late Permian (Wuchiapingian, ~257 Ma) was replaced by a provincial and biogeographically fragmented fauna by Middle Triassic times (Anisian, ~242 Ma). Importantly in the Triassic, lower latitude basins in Tanzania and Zambia included dinosaur predecessors and other archosaurs unknown elsewhere. The recognition of heterogeneous tetrapod communities in the Triassic implies that the end-Permian mass extinction afforded ecologically marginalized lineages the ecospace to diversify, and that biotic controls (i.e., evolutionary incumbency) were fundamentally reset. Archosaurs, which began diversifying in the Early Triassic, were likely beneficiaries of this ecological release and remained dominant for much of the later Mesozoic.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=xzP0rY87NIg:UGZkfMQtI48:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=xzP0rY87NIg:UGZkfMQtI48:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=xzP0rY87NIg:UGZkfMQtI48:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=xzP0rY87NIg:UGZkfMQtI48:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=xzP0rY87NIg:UGZkfMQtI48:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=xzP0rY87NIg:UGZkfMQtI48:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=xzP0rY87NIg:UGZkfMQtI48:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=xzP0rY87NIg:UGZkfMQtI48:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=xzP0rY87NIg:UGZkfMQtI48:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=xzP0rY87NIg:UGZkfMQtI48:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/xzP0rY87NIg" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/2575850738458792564/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/05/provincialization-of-terrestrial-faunas.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2575850738458792564?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2575850738458792564?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/xzP0rY87NIg/provincialization-of-terrestrial-faunas.html" title="Provincialization of Terrestrial Faunas Following the End-Permian Mass Extinction." /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/05/provincialization-of-terrestrial-faunas.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CUAHRXs7cSp7ImA9WhBVGUQ.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-6187775801675562061</id><published>2013-04-26T09:28:00.000-07:00</published><updated>2013-04-26T09:28:54.509-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-04-26T09:28:54.509-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="pterosaurs" /><category scheme="http://www.blogger.com/atom/ns#" term="ornithodira" /><category scheme="http://www.blogger.com/atom/ns#" term="Triassic" /><title>Overview of the Triassic Pterosaur Record</title><content type="html">Another paper from the upcoming volume on Triassic archosaurs.&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Dalla Vecchia, F. 2013. Triassic Pterosaurs. &lt;span style="font-family: AdvPS6F0B; font-size: xx-small;"&gt;&lt;span style="font-family: AdvPS6F0B; font-size: xx-small;"&gt;&lt;span style="font-size: small;"&gt;From N&lt;span style="font-family: AdvPS836F;"&gt;&lt;span style="font-family: AdvPS836F;"&gt;esbitt&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;, S. J., D&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS836F;"&gt;&lt;span style="font-family: AdvPS836F;"&gt;esojo&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;, J. B. &amp;amp; I&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS836F;"&gt;&lt;span style="font-family: AdvPS836F;"&gt;rmis&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;, R. B. (eds) 2013. &lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F0B;"&gt;&lt;span style="font-family: AdvPS6F0B;"&gt;Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin. Geological Society, London, Special Publications, &lt;span style="font-family: AdvPS6F01;"&gt;&lt;span style="font-family: AdvPS6F01;"&gt;379&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;, &lt;a href="http://dx.doi.org/10.1144/SP379.14"&gt;http://&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;dx.doi.org&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvP4C4E59;"&gt;&lt;span style="font-family: AdvP4C4E59;"&gt;/&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;10.1144&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvP4C4E59;"&gt;&lt;span style="font-family: AdvP4C4E59;"&gt;/&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;SP379.14&lt;/span&gt;&lt;/span&gt;&lt;/a&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;strong&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/span&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; Pterosaurs are a clade of highly specialized, volant archosauromorphs recorded from the Upper Triassic to the uppermost Cretaceous.                     Problematic remains referred to the Pterosauria are reported from the Triassic of Europe and both North and South America,                     but unequivocal pterosaur specimens are only known from the Alps (Italy, Austria and Switzerland: &lt;em&gt;Preondactylus buffarinii&lt;/em&gt;, &lt;em&gt;Austriadactylus cristatus&lt;/em&gt;, &lt;em&gt;Peteinosaurus zambellii&lt;/em&gt;, &lt;em&gt;Eudimorphodon ranzii&lt;/em&gt;, &lt;em&gt;Carniadactylus rosenfeldi&lt;/em&gt;, &lt;em&gt;Caviramus schesaplanensis&lt;/em&gt; and &lt;em&gt;Raeticodactylus filisurensis&lt;/em&gt;) and Greenland (‘&lt;em&gt;Eudimorphodon’ cromptonellus&lt;/em&gt;). Pterosaurs are diagnosed mostly by features associated with the advent of powered flight. They are generally considered                     to be archosaurians more closely related to dinosaurs than to crocodilians, but non-archosaurian positions have also been                     proposed. There is a lack of general agreement about ingroup relationships, particularly among the basal pterosaurs. Triassic                     pterosaurs differ from other non-pterodactyloid pterosaurs in features of the dentition and caudal vertebral column. A ‘Big                     Bang’ model for their early history fits better with the fossil record: the earliest unequivocal pterosaurs show a sudden                     and geographically limited appearance in the fossil record, as well as a relatively high burst of diversity and considerable                     morphologic disparity. Absence of pterosaur remains from deposits where they are expected to be found suggests that they had                     not yet evolved in pre-Norian times.&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/w02Hx09kTL8" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/6187775801675562061/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/04/overview-of-triassic-pterosaur-record.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/6187775801675562061?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/6187775801675562061?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/w02Hx09kTL8/overview-of-triassic-pterosaur-record.html" title="Overview of the Triassic Pterosaur Record" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/04/overview-of-triassic-pterosaur-record.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CEADQng4fSp7ImA9WhBVGE8.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-1173567138040892137</id><published>2013-04-24T09:59:00.000-07:00</published><updated>2013-04-24T09:59:33.635-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-04-24T09:59:33.635-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Proterosuchus" /><category scheme="http://www.blogger.com/atom/ns#" term="tracks" /><category scheme="http://www.blogger.com/atom/ns#" term="silesaurid" /><category scheme="http://www.blogger.com/atom/ns#" term="Rauisuchids" /><category scheme="http://www.blogger.com/atom/ns#" term="evolution" /><category scheme="http://www.blogger.com/atom/ns#" term="Doswelliidae" /><category scheme="http://www.blogger.com/atom/ns#" term="basal archosaurs" /><title>Six New Papers from the Forthcoming Volume 'Anatomy, Phylogeny, and Palaeobiology of Early Archosaurs and their Kin.</title><content type="html">

You can access the abstracts electronically &lt;a href="http://sp.lyellcollection.org/online-first/379"&gt;here&lt;/a&gt;.&lt;br /&gt;
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&lt;strong&gt;Mastrantonio, B. M., Schultz, C. L., Desojo, J. B., and J.&amp;nbsp; Bittencourt Garcia. 2013. The braincase of &lt;em&gt;Prestosuchus chiniquensis&lt;/em&gt; (Archosauria: Suchia)From: Nesbitt, S. J., Desojo, J. B. &amp;amp; Irmis, R. B. (eds) 2013. Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin. Geological Society, London, Special Publications, 379, doi:10.1144/SP379.10&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; The osteology of an almost complete braincase of the rauisuchian archosaurs &lt;em&gt;Prestosuchus chiniquensis&lt;/em&gt; from the Middle Triassic of Brazil is described for first time, based on two specimens (UFRGS-PV-0629-T and UFRGS-PV-0156-T). A comparative description with other taxa of rauisuchians is presented that forms the basis of a phylogenetic analysis. To perform the phylogenetic analysis, we describe and discuss each character codification for a modified version of the recent matrices of Gower (2002), Gower &amp;amp; Nesbitt (2006) and Brusatte et al.(2010). The analysis resulted in two most parsimonious trees that differ from the topologies recovered by Gower (2002) in a few aspects within Rauisuchia, and &lt;em&gt;Prestosuchus chiniquensis&lt;/em&gt; was unequivocally depicted as deeply nested within Pseudosuchia, as the sister taxon of &lt;em&gt;Batrachotomus kuperferze&lt;/em&gt;llensis in both topologies, supported by a single synapomorphy: the reduced to small ﬁssure of the post-temporal fenestra between parietal, supraoccipital and exoccipital-opisthotic.&lt;br /&gt;
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&lt;strong&gt;Sues, H.-D., Desojo, J. B., and M. D. Ezcurra. 2013. Doswelliidae: a clade of unusual armoured archosauriforms from the Middle and Late Triassic. From: Nesbitt, S. J., Desojo, J. B. &amp;amp; Irmis, R. B. (eds) 2013. Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin. Geological Society, London, Special Publications, 379, first published on April 23, 2013, doi:10.1144/SP379.13&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; Doswelliidae is a clade of armoured non-archosaurian archosauriform reptiles more closely related to Archosauria than are Proterosuchidae, Erythrosuchidae and possibly Euparkeria capensis. It is currently known from the late Middle Triassic (Ladinian) of Germany, the late Middle to early Late Triassic (Ladinian–Carnian) of Argentina and Brazil, and the Late Triassic (Carnian–Norian) of the USA. To date, two unambiguous synapomorphies diagnose Doswelliidae: (i) osteoderm ornamentation coarse, incised, and composed of central regular pits of subequal size and shape, and (ii) osteoderms with anterior articular lamina. Five taxa are currently recognized: &lt;em&gt;Archeopelta arborensis&lt;/em&gt;, &lt;em&gt;Doswellia kaltenbachi&lt;/em&gt;, &lt;em&gt;Doswellia sixmilensis&lt;/em&gt;, &lt;em&gt;Tarjadia ruthae&lt;/em&gt; and a new taxon from Germany. Based on skeletal features and occurrence, doswelliid archosauriforms may have had a semi-aquatic mode of life.&lt;br /&gt;
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&lt;strong&gt;Langer, M. C., and J. Ferigolo. 2013. The Late Triassic dinosauromorph &lt;em&gt;Sacisaurus agudoensis&lt;/em&gt; (Caturrita Formation; Rio Grande do Sul, Brazil): anatomy and affinities. From: Nesbitt, S. J., Desojo, J. B. &amp;amp; Irmis, R. B. (eds) 2013. Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin.&amp;nbsp; Geological Society, London, Special Publications, 379, first published on April 23, 2013, doi:10.1144/SP379.16&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract - &lt;/strong&gt;Silesauridae is an exclusively Triassic group of dinosauromorphs, knowledge on the diversity of which has increased dramatically in the last few years. Silesaurid relationships are still contentious, as a result in part of different homology statements, particularly regarding the typical edentulous mandible tip of these animals. One of the most complete silesaurids yet discovered is &lt;em&gt;Sacisaurus agudoensis&lt;/em&gt; from the Caturrita Formation (Late Triassic: Norian) of Rio Grande do Sul, Brazil, represented by numerous isolated bones recovered from a single site. The anatomy of&lt;em&gt; S. agudoensis&lt;/em&gt; is fully described for the first time here, and comparisons are provided to other basal dinosauromorphs. &lt;em&gt;S. agudoensis&lt;/em&gt; is a small-bodied animal (less than 1 m in length) that possesses a dentition consisting of leaf-shaped crowns with large denticles in the carinae, a plesiomorphic propubic pelvis with an almost fully closed acetabulum, elongate distal hindlimbs suggesting well-developed cursorial ability, and a laterally projected outer malleolus in the tibia. All previous numerical phylogenies supported a non-dinosaur dinosauromorph affinity for Silesauridae, but the reanalysis of one of those studies suggests that a position within Dinosauria is not unlikely, with silesaurids forming the basal branch of the ornithischian lineage.&lt;br /&gt;
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&lt;strong&gt;Turner, A. H., and S. J. Nesbitt. 2013. Body size evolution during the Triassic archosauriform radiation. From: Nesbitt, S. J., Desojo, J. B. &amp;amp; Irmis, R. B. (eds) 2013. Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin.&amp;nbsp; Geological Society, London, Special Publications, 379, first published on April 23, 2013, doi:10.1144/SP379.15&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; The first large (&amp;gt;1 m) diapsids appeared near the Permian–Triassic extinction and a subset of diapsids, the archosauriforms, expanded their body size range soon after in the Early–Middle Triassic. Here, we examine body size at key evolutionary events within Archosauriformes during the Triassic and through the end-Triassic extinction. Using femoral length as a body size proxy and a temporally calibrated phylogeny of Archosauriformes, we estimate ancestral body sizes using a maximum likelihood approach and test for the presence of an adapative radiation by comparing the fit of competing evolutionary models. Archosauriform body size is characterized by punctuated change with more change occurring early in the Triassic. Archosaurs crossing the Triassic–Jurassic boundary show a wide range in ancestral size, and dinosaurs (sauropodomorphs and theropods) are considerably larger in the Jurassic. Crocodylomorph origins are characterized by a drop in body size; however, both the relative amount of change and the rate of change are matched among other archosaur clades. Archosauriforms increase in absolute body size through the Triassic and evidence suggests that a directional trend in size increase occurred in the early Mesozoic. The morphological signature of adaptive radiation is rare in comparative data from extant animals but is present at the origination of Archosauriformes.&lt;br /&gt;
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&lt;strong&gt;Niedźwiedzki, G., Brusatte, S. L., and R. J. Butler. 2013. &lt;em&gt;Prorotodactylus&lt;/em&gt; and &lt;em&gt;Rotodactylus&lt;/em&gt; tracks: an ichnological record of dinosauromorphs from the Early–Middle Triassic of Poland. From: Nesbitt, S. J., Desojo, J. B. &amp;amp; Irmis, R. B. (eds) 2013. Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin. Geological Society, London, Special Publications, 379, first published on April 23, 2013, doi:10.1144/SP379.12&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; We present the first comprehensive description of &lt;em&gt;Prorotodactylus&lt;/em&gt; and &lt;em&gt;Rotodactylus&lt;/em&gt;&amp;nbsp; dinosauromorph tracks from the Early and Middle Triassic of the Holy Cross Mountains, Poland. We describe and comprehensively figure tracks that have been mentioned briefly in previous accounts as well as new, recently discovered material, and analyse the variation and stratigraphic distribution of these specimens. Tracks have been recorded from four sites – Koszary, Stryczowice, Wióry and Baranów – which span the early Olenekian – early Anisian (c.250–246 Ma). These tracks therefore represent an ichnological record of the evolutionary succession of early dinosauromorphs during the earliest part of their evolutionary history. Recognized track types include cf. &lt;em&gt;Prorotodactylus&lt;/em&gt; isp., &lt;em&gt;Prorotodactylus &lt;/em&gt;isp., &lt;em&gt;Prorotodactylus&lt;/em&gt; &lt;em&gt;mirus&lt;/em&gt;, &lt;em&gt;Rotodactylus cursorius&lt;/em&gt;, &lt;em&gt;Rotodactylus&lt;/em&gt; isp. and cf. &lt;em&gt;Rotodactylus&lt;/em&gt; isp. At least three distinct Early and early Middle Triassic early dinosauromorph ichnofaunas can be recognized. The oldest, which is early Olenekian in age, is characterized by the presence of &lt;em&gt;Prorotodactylus&lt;/em&gt; isp., cf.&lt;em&gt;Prorotodactylus&lt;/em&gt; isp. and non-archosaurian archosauromorph or archosaur tracks (e.g. &lt;em&gt;Synaptichnium &lt;/em&gt;isp., &lt;em&gt;Protochirotherium&lt;/em&gt; isp.), recorded at the Stryczowice and Koszary sites. The following assemblage, recorded at the late Olenekian Wióry site, displays the highest ichnodiversity of dinosauromorphs, with four track types present (&lt;em&gt;Prorotodactylus&lt;/em&gt; isp., &lt;em&gt;Prorotodactylus mirus&lt;/em&gt;, &lt;em&gt;Rotodactylus cursorius&lt;/em&gt; and cf. &lt;em&gt;Rotodactylus&lt;/em&gt; isp.). The youngest site, Baranów, includes &lt;em&gt;Rotodactylus&lt;/em&gt; isp., as well as other larger dinosauromorph tracks. The first body fossil evidence of dinosauromorphs is a few million years younger than the youngest Polish tracks, so &lt;em&gt;Prorotodactylus&lt;/em&gt; and &lt;em&gt;Rotodactylus&lt;/em&gt; tracks currently provide the oldest record of dinosauromorph morphology, biology and evolution.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Ezcurra, M. D., Butler, R. J., and D. J. Gower. 2013. ‘Proterosuchia’: the origin and early history of Archosauriformes.. From: Nesbitt, S. J., Desojo, J. B. &amp;amp; Irmis, R. B. (eds) 2013. Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin. Geological Society, London, Special Publications, 379, first published on April 23, 2013, doi:10.1144/SP379.11&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; The earliest history of Archosauriformes is mainly represented by members of Proterosuchidae and Erythrosuchidae, which are known worldwide from latest Permian to Middle Triassic beds. These two groups were historically combined within ‘Proterosuchia’, with approximately 30 nominal species. Two morphotypes have been recognized among proterosuchians: proterosuchids with a generally more sprawling gait and elongated and low skulls with an overhanging premaxilla, and the more heavily built erythrosuchids, with a probably less sprawling gait and large, presumably hypercarnivorous, skulls. The systematics of ‘Proterosuchia’ was relatively chaotic throughout most of the twentieth century, but currently there exists consensus regarding the non-monophyly of proterosuchians and their phylogenetic position outside all other archosauriforms. In contrast, the delimitation and taxonomic content of Proterosuchidae and Erythrosuchidae remain unstable. Few studies of proterosuchian palaeobiology have been carried out. Current lines of evidence favour a predominantly terrestrial lifestyle for proterosuchians. Limb bone histology indicates rapid continuous growth rates in &lt;em&gt;Proterosuchus&lt;/em&gt; and &lt;em&gt;Erythrosuchus&lt;/em&gt; before reaching sexual maturity. A better knowledge of proterosuchian anatomy, systematics, evolution and ecology is important for advancing understanding of the origin and early radiation of Archosauriformes and the patterns of biotic recovery following the Permo-Triassic mass extinction event. There remains much research to be carried out in proterosuchian palaeobiology.&lt;br /&gt;


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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/MxCxmvAz19A" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/1173567138040892137/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/04/six-new-papers-from-forthcoming-volume.html#comment-form" title="2 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/1173567138040892137?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/1173567138040892137?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/MxCxmvAz19A/six-new-papers-from-forthcoming-volume.html" title="Six New Papers from the Forthcoming Volume 'Anatomy, Phylogeny, and Palaeobiology of Early Archosaurs and their Kin." /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>2</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/04/six-new-papers-from-forthcoming-volume.html</feedburner:origLink></entry><entry gd:etag="W/&quot;C0EARHk9eyp7ImA9WhBVE08.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-8024651500242492498</id><published>2013-04-16T09:49:00.001-07:00</published><updated>2013-04-18T14:47:25.763-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-04-18T14:47:25.763-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Germany" /><category scheme="http://www.blogger.com/atom/ns#" term="Middle Triassic" /><category scheme="http://www.blogger.com/atom/ns#" term="Doswelliidae" /><category scheme="http://www.blogger.com/atom/ns#" term="Archosauriformes" /><title /><content type="html">A new interpretation of material of an armored archosauriform from the Middle Triassic of Germany that solves the mystery of the purported Middle Triassic aetosaur.&amp;nbsp; Instead this specimen is from a taxon more closely to &lt;em&gt;Doswellia kaltenbachi&lt;/em&gt;. This new taxon supports the growing realization that doswelliids had a broader range geographically and temporally.&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Schoch, R. R., and H.-D. Sues. 2013. A new archosauriform reptile from the Middle Triassic (Ladinian) of Germany. Journal of Systematic Palaeontology (advance online publication) &lt;/strong&gt;&lt;strong&gt;&lt;a href="http://www.tandfonline.com/doi/abs/10.1080/14772019.2013.781066"&gt;DOI:10.1080/14772019.2013.781066&lt;/a&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;strong&gt;Abstract-&lt;/strong&gt; Numerous well-preserved skeletal remains of a distinctive armoured &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;archosauriform reptile from the Lower Keuper (Erfurt Formation; Middle &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;Triassic: Ladinian: Longobardian) of Baden-Württemberg (Germany) &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;represent a new taxon,&lt;em&gt; Jaxtasuchus salomoni&lt;/em&gt; gen. et sp. nov. The &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;dermal armour of &lt;em&gt;Jaxtasuchus&lt;/em&gt; comprises transverse rows of four &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;rectangular osteoderms each in the cervical, dorsal and caudal &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;regions, with the individual plates closely resembling those of &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;em&gt;Doswellia kaltenbachi&lt;/em&gt; from Carnian strata in North America. The long &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;and low maxilla of Jaxtasuchus held at least 15 teeth. The labial and &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;lingual surfaces of the tall, only slightly recurved crowns of the &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;maxillary teeth bear distinct vertical ridges and smooth mesial and &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;distal carinae. The cervical region of the vertebral column is long. &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;Phylogenetic analysis places Jaxtasuchus as the sister taxon to&lt;/span&gt;&lt;br /&gt;
&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;&lt;em&gt;Doswellia&lt;/em&gt; in Doswelliidae sensu Desojo et al. (2011). Doswelliidae is &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;diagnosed by the coarsely reticulate, incised ornamentation of &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;osteoderms composed of central regular pits of subequal size and &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;contour, and a mostly smooth anterior articular lamina on each &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;osteoderm. The discovery of &lt;em&gt;Jaxtasuchus&lt;/em&gt; confirms that Doswelliidae had &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;a wide palaeogeographical distribution during the latter half of the &lt;/span&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #222222; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/normal arial, sans-serif; letter-spacing: normal; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0px;"&gt;Triassic.&lt;/span&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/JcXxVisdhwI" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/8024651500242492498/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/04/a-new-interpretation-of-material-of.html#comment-form" title="2 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/8024651500242492498?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/8024651500242492498?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/JcXxVisdhwI/a-new-interpretation-of-material-of.html" title="" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>2</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/04/a-new-interpretation-of-material-of.html</feedburner:origLink></entry><entry gd:etag="W/&quot;C0UERHw6eCp7ImA9WhBWEE0.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-5937026982313189020</id><published>2013-04-03T08:00:00.000-07:00</published><updated>2013-04-03T08:00:05.210-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-04-03T08:00:05.210-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="diet" /><category scheme="http://www.blogger.com/atom/ns#" term="Archosauromorphs" /><category scheme="http://www.blogger.com/atom/ns#" term="functional morphology" /><title>Morphology and Diversity of the Mandibular Symphysis of Archosauriforms</title><content type="html">

Excellent study that demonstrates changes in mandibular symphyses through individual clades; &amp;nbsp;changes&amp;nbsp;that appear to&amp;nbsp;be influenced by changes in dental morphology, which presumably reflect differences in diet. This paper is part of the upcoming volume on early archosaurs.&lt;br /&gt;
&lt;div class="MsoNormal" style="line-height: normal; margin: 0in 0in 0pt; mso-layout-grid-align: none; mso-pagination: widow-orphan;"&gt;
&lt;b style="mso-bidi-font-weight: normal;"&gt;&lt;span style="font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt;&lt;/span&gt;&lt;/b&gt;&amp;nbsp;&lt;/div&gt;
&lt;div class="MsoNormal" style="line-height: normal; margin: 0in 0in 0pt; mso-layout-grid-align: none; mso-pagination: widow-orphan;"&gt;
&lt;b style="mso-bidi-font-weight: normal;"&gt;&lt;span style="font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt;Holliday, C. M., and S. J. Nesbitt.
2013. Morphology and diversity of the mandibular symphysis of archosauriforms &lt;i style="mso-bidi-font-style: normal;"&gt;In&lt;/i&gt; Nesbitt, S. J., Desojo, J. B. and R.
B. Irmis (eds) Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and
their Kin. Geological Society, London, Special Publications, 379, &lt;a href="http://dx.doi.org/10.1144/SP379.2"&gt;&lt;span style="color: blue;"&gt;http://dx.doi.org/10.1144/SP379.2&lt;/span&gt;&lt;/a&gt;&lt;/span&gt;&lt;/b&gt;&lt;/div&gt;
&lt;div class="MsoNormal" style="line-height: normal; margin: 0in 0in 0pt; mso-layout-grid-align: none; mso-pagination: widow-orphan;"&gt;
&lt;span style="font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt;&lt;o:p&gt;&amp;nbsp;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;b style="mso-bidi-font-weight: normal;"&gt;&lt;span style="font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt;Abstract:&lt;/span&gt;&lt;/b&gt;&lt;span style="font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt; Archosauromorphs
radiated into numerous trophic niches during the Mesozoic, many of which were
accommodated by particular suites of cranial adaptations and feeding
behaviours. The mandibular symphysis, the joint linking the mandibles, is a
poorly understood craniomandibular joint that may offer significant insight
into skull function and feeding ecology. Using comparative data from extant
amniotes, we investigated the skeletal anatomy and osteological correlates of relevant
soft tissues in a survey of archosauromorph mandibular symphyses. Characters
were identified and their evolution mapped using a current phylogeny of archosauriforms
with the addition of non-archosauriform archosauromorphs. Extinct taxa with the
simple Class I condition (e.g. proterochampsids, ‘rauisuchians’), rugose Class
II (aetosaurs, protosuchians, silesaurids) and interdigitating Class III
symphyses (e.g. phytosaurs, crocodyliforms) and finally fused Class IV (avians)
build the joints in expected ways, although they differ in the contributions of
bony elements and Meckel’s cartilage. Optimization of the different classes of
symphyses across archosauromorph clades indicates that major iterative
transitions from plesiomorphic Class I to derived, rigid Class II–IV symphyses
occurred along the lines to phytosaurs, aetosaurs, a subset of poposauroids, crocodyliformes,
pterosaurs and birds. These transitions in symphyseal morphology also appear to
track changes in dentition and potentially diet.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;br /&gt;


&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=kKz_myX7p8o:KAiYk5M4Hf4:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=kKz_myX7p8o:KAiYk5M4Hf4:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=kKz_myX7p8o:KAiYk5M4Hf4:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=kKz_myX7p8o:KAiYk5M4Hf4:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=kKz_myX7p8o:KAiYk5M4Hf4:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=kKz_myX7p8o:KAiYk5M4Hf4:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=kKz_myX7p8o:KAiYk5M4Hf4:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=kKz_myX7p8o:KAiYk5M4Hf4:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=kKz_myX7p8o:KAiYk5M4Hf4:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=kKz_myX7p8o:KAiYk5M4Hf4:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/kKz_myX7p8o" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/5937026982313189020/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/04/morphology-and-diversity-of-mandibular.html#comment-form" title="1 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/5937026982313189020?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/5937026982313189020?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/kKz_myX7p8o/morphology-and-diversity-of-mandibular.html" title="Morphology and Diversity of the Mandibular Symphysis of Archosauriforms" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>1</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/04/morphology-and-diversity-of-mandibular.html</feedburner:origLink></entry><entry gd:etag="W/&quot;Dk8EQXwyfyp7ImA9WhBXGUw.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-4580403816071364134</id><published>2013-04-02T08:00:00.000-07:00</published><updated>2013-04-02T08:00:00.297-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-04-02T08:00:00.297-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Paleobotany" /><category scheme="http://www.blogger.com/atom/ns#" term="Petrified Forest" /><category scheme="http://www.blogger.com/atom/ns#" term="Chinle Formation" /><title>New Occurrences of the Controversial Late Triassic Plant Fossil Sanmiguelia</title><content type="html">&lt;span style="font-family: Times-Roman; font-size: x-small;"&gt;&lt;span style="font-family: Times-Roman; font-size: x-small;"&gt;&lt;span style="font-size: small;"&gt;

New paper extending the biostratigraphic range of the enigmatic Late Triassic plant &lt;em&gt;Sanmiguelia&lt;/em&gt;. These new finds also alter the plant-based biostratigraphic scheme proposed by Ash in 1980.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br /&gt;
&lt;span style="font-family: Times-Roman; font-size: x-small;"&gt;&lt;span style="font-family: Times-Roman; font-size: x-small;"&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;br /&gt;
&lt;span style="font-family: Times-Roman; font-size: x-small;"&gt;&lt;span style="font-family: Times-Roman; font-size: x-small;"&gt;&lt;div class="MsoNormal" style="line-height: normal; margin: 0in 0in 0pt; mso-layout-grid-align: none; mso-pagination: widow-orphan;"&gt;
&lt;span&gt;&lt;span style="font-size: small;"&gt;

&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class="MsoNormal" style="line-height: normal; margin: 0in 0in 0pt; mso-layout-grid-align: none; mso-pagination: widow-orphan;"&gt;
&lt;span style="font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt;&lt;strong&gt;Ash,
S.R. and S. T. Hasiotis, S.T. 2013. New occurrences of the controversial Late
Triassic plant fossil &lt;i&gt;Sanmiguelia &lt;/i&gt;Brown and associated ichnofossils in
the Chinle Formation of Arizona and Utah, USA. Neues Jahrbuch für Geologie und
Paläontologie Abhandlungen 268: 65–82.&lt;/strong&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class="MsoNormal" style="line-height: normal; margin: 0in 0in 0pt; mso-layout-grid-align: none; mso-pagination: widow-orphan;"&gt;
&amp;nbsp;&lt;/div&gt;
&lt;div class="MsoNormal" style="line-height: normal; margin: 0in 0in 0pt; mso-layout-grid-align: none; mso-pagination: widow-orphan;"&gt;
&lt;span style="font-size: small;"&gt;

&lt;/span&gt;&lt;b&gt;&lt;span style="font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt;Abstract:
&lt;/span&gt;&lt;/b&gt;&lt;span style="font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt;Fragments
of the rare and distinctive palm-like leaves of the controversial Late Triassic
plant &lt;i&gt;Sanmiguelia &lt;/i&gt;have been discovered recently in both Petrified Forest
National Park, Arizona and Arches National Park, Utah. Although, the new
specimens do not clarify the classification of this intriguing fossil, they do
confirm that it occurs in all members of the Chinle Formation except for the
very lowest units, the Shinarump, Mesa Redondo, and Temple Mountain members.
Furthermore, their discovery in Petrified Forest National Park extends the
known geographical distribution of the fossil into east-central Arizona and
demonstrates that it is a characteristic member of the Late Triassic flora of
the American southwest and requires a revision of the Chinle floral zone scheme
proposed and revised earlier by Ash (1980). In Petrified Forest National Park
the leaves are associated with several types of ichnofossils including &lt;i&gt;Scoyenia&lt;/i&gt;,
&lt;i&gt;Arenicolites&lt;/i&gt;, &lt;i&gt;Cylindrichum&lt;/i&gt;, cf. &lt;i&gt;Scolicia&lt;/i&gt;, cf. &lt;i&gt;Beaconites&lt;/i&gt;,
&lt;i&gt;Selenchnites&lt;/i&gt;, and other trace fossils in open nomenclature. These trace
fossils suggest that &lt;i&gt;Sanmiguelia &lt;/i&gt;was preserved in high moisture,
imperfectly drained, water-margin setting inhabited by phytosaurs, snails,
horseshoe crabs, and a variety of arthropods such as beetles and dipteran
larvae and record high water table conditions punctuated by flooding and overbank
deposition. The findings reported here generally support and improve on
previous interpretations of the paleoenvironment inhabited by the &lt;i&gt;Sanmiguelia
&lt;/i&gt;plant.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class="MsoNormal" style="line-height: normal; margin: 0in 0in 0pt; mso-layout-grid-align: none; mso-pagination: widow-orphan;"&gt;
&lt;span style="font-size: small;"&gt;

&lt;/span&gt;&lt;/div&gt;
&lt;/span&gt;&lt;div class="MsoNormal" style="line-height: normal; margin: 0in 0in 0pt; mso-layout-grid-align: none; mso-pagination: widow-orphan;"&gt;
&lt;br /&gt;&lt;/div&gt;
&lt;/span&gt;&lt;div class="MsoNormal" style="line-height: normal; margin: 0in 0in 0pt; mso-layout-grid-align: none; mso-pagination: widow-orphan;"&gt;
&lt;br /&gt;&lt;/div&gt;
&lt;span style="font-family: Times-Roman; font-size: x-small;"&gt;&lt;span style="font-family: Times-Roman; font-size: x-small;"&gt;&lt;/span&gt;&lt;/span&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=T0MyQanpSAg:hxlaz9nsYZE:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=T0MyQanpSAg:hxlaz9nsYZE:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=T0MyQanpSAg:hxlaz9nsYZE:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=T0MyQanpSAg:hxlaz9nsYZE:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=T0MyQanpSAg:hxlaz9nsYZE:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=T0MyQanpSAg:hxlaz9nsYZE:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=T0MyQanpSAg:hxlaz9nsYZE:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=T0MyQanpSAg:hxlaz9nsYZE:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=T0MyQanpSAg:hxlaz9nsYZE:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=T0MyQanpSAg:hxlaz9nsYZE:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/T0MyQanpSAg" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/4580403816071364134/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/04/new-occurrences-of-controversial-late.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4580403816071364134?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4580403816071364134?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/T0MyQanpSAg/new-occurrences-of-controversial-late.html" title="New Occurrences of the Controversial Late Triassic Plant Fossil &lt;i&gt;Sanmiguelia&lt;/i&gt;" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/04/new-occurrences-of-controversial-late.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CUAMQnwyeip7ImA9WhBXGEk.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-7076127031590773896</id><published>2013-04-01T12:16:00.001-07:00</published><updated>2013-04-01T12:16:23.292-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-04-01T12:16:23.292-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="crocodylomorphs" /><category scheme="http://www.blogger.com/atom/ns#" term="Triassic-Jurassic" /><category scheme="http://www.blogger.com/atom/ns#" term="Pseudosuchia" /><category scheme="http://www.blogger.com/atom/ns#" term="disparity" /><title>Triassic–Jurassic Mass Extinction as Trigger for the Mesozoic Radiation of Crocodylomorphs</title><content type="html">

A new study that contrasts that of Brusatte et al. (2008), who had found a significant dropoff in pseudosuchian disparity through the end Triassic extinction.&lt;br /&gt;
&lt;b style="mso-bidi-font-weight: normal;"&gt;&lt;span style="color: #231f20; font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt;&lt;/span&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b style="mso-bidi-font-weight: normal;"&gt;&lt;span style="color: #231f20; font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt;Toljagić, O., and R. J. Butler.
2013 Triassic–Jurassic mass extinction as trigger for the Mesozoic radiation of
crocodylomorphs. Biology Letters 9: 20130095. http://dx.doi.org/10.1098/rsbl.2013.0095&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;br /&gt;


&lt;br /&gt;
&lt;b style="mso-bidi-font-weight: normal;"&gt;&lt;span style="color: #231f20; font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt;Abstract -&lt;/span&gt;&lt;/b&gt;&lt;span style="color: #231f20; font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; font-size: 12pt;"&gt; Pseudosuchia,
one of the two main clades of Archosauria (Reptilia: Diapsida), suffered a
major decline in lineage diversity during the Triassic–Jurassic (TJ) mass
extinction (approx. 201 Ma). Crocodylomorpha, including living crocodilians and
their extinct relatives, is the only group of pseudosuchians that survived into
the Jurassic.We reassess changes in pseudosuchian morphological diversity
(disparity) across this time interval, using considerably larger sample sizes
than in previous analyses. Our results show that metrics of pseudosuchian disparity
did not change significantly across the TJ boundary, contrasting with previous
work suggesting low pseudosuchian disparity in the Early Jurassic following the
TJ mass extinction. However, a significant shift in morphospace occupation
between Late Triassic and Early Jurassic taxa is recognized, suggesting that
the TJ extinction of many pseudosuchian lineages was followed by a major and
geologically rapid adaptive radiation of crocodylomorphs. This marks the onset
of the spectacularly successful evolutionary history of crocodylomorphs in
Jurassic and Cretaceous ecosystems.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;br /&gt;


&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=0F711CcMKhc:aTIRqaIfzBw:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=0F711CcMKhc:aTIRqaIfzBw:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=0F711CcMKhc:aTIRqaIfzBw:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=0F711CcMKhc:aTIRqaIfzBw:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=0F711CcMKhc:aTIRqaIfzBw:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=0F711CcMKhc:aTIRqaIfzBw:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=0F711CcMKhc:aTIRqaIfzBw:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=0F711CcMKhc:aTIRqaIfzBw:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=0F711CcMKhc:aTIRqaIfzBw:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=0F711CcMKhc:aTIRqaIfzBw:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/0F711CcMKhc" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/7076127031590773896/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/04/triassicjurassic-mass-extinction-as.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/7076127031590773896?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/7076127031590773896?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/0F711CcMKhc/triassicjurassic-mass-extinction-as.html" title="Triassic–Jurassic Mass Extinction as Trigger for the Mesozoic Radiation of Crocodylomorphs" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/04/triassicjurassic-mass-extinction-as.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CUYMR3g4fCp7ImA9WhBQGEQ.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-274839336860219722</id><published>2013-03-21T12:12:00.002-07:00</published><updated>2013-03-21T12:13:06.634-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-03-21T12:13:06.634-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="CAMP" /><category scheme="http://www.blogger.com/atom/ns#" term="Newark Supergroup" /><category scheme="http://www.blogger.com/atom/ns#" term="end Triassic extinction" /><title>New Data Linking the End-Triassic Extinction with the Central Atlantic Magmatic Province.</title><content type="html">Out today in Science Express. This study also provides support for the accuracy of the astrochronologically tuned time scale proposed for the Late Triassic Newark Supergroup&amp;nbsp;sequence.&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Blackburn, T. J., Olsen, P. E., Bowring, S. A., McLean, N. M., Kent, D. V., Puffer, J., McHone, G., Rasbury, E. T., and M. Et-Touhami. 2013. Zircon U-Pb Geochronology Links the End-Triassic Extinction with the&amp;nbsp;Central Atlantic Magmatic Province. Science Express. &lt;/strong&gt;&lt;a href="http://www.sciencemag.org/content/early/recent"&gt;&lt;strong&gt;http://www.sciencemag.org/content/early/recent&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; / 21 March 2013 / Page 1/ 10.1126/science.1234204&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; The end-Triassic extinction is characterized by major losses in both terrestrial and&amp;nbsp; marine diversity, setting the stage for dinosaurs to dominate Earth for the next 136&amp;nbsp;million years. Despite the approximate coincidence between this extinction and&amp;nbsp; flood basalt volcanism, existing geochronologic dates have insufficient resolution&amp;nbsp; to confirm eruptive rates required to induce major climate perturbations. Here we&amp;nbsp;present new zircon U-Pb geochronologic constraints on the age and duration of flood basalt volcanism within the Central Atlantic Magmatic Province. This&amp;nbsp;chronology demonstrates synchroneity between the earliest volcanism and&amp;nbsp;extinction, tests and corroborates the existing astrochronologic time scale, and shows that the release of magma and associated atmospheric flux occurred in four pulses over ~600,000 years, indicating expansive volcanism even as the biologic recovery was under way.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=w62tW_7Wpa8:6DjJ9o9kCSM:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=w62tW_7Wpa8:6DjJ9o9kCSM:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=w62tW_7Wpa8:6DjJ9o9kCSM:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=w62tW_7Wpa8:6DjJ9o9kCSM:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=w62tW_7Wpa8:6DjJ9o9kCSM:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=w62tW_7Wpa8:6DjJ9o9kCSM:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=w62tW_7Wpa8:6DjJ9o9kCSM:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=w62tW_7Wpa8:6DjJ9o9kCSM:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=w62tW_7Wpa8:6DjJ9o9kCSM:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=w62tW_7Wpa8:6DjJ9o9kCSM:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/w62tW_7Wpa8" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/274839336860219722/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/03/new-data-linking-end-triassic.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/274839336860219722?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/274839336860219722?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/w62tW_7Wpa8/new-data-linking-end-triassic.html" title="New Data Linking the End-Triassic Extinction with the Central Atlantic Magmatic Province." /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/03/new-data-linking-end-triassic.html</feedburner:origLink></entry><entry gd:etag="W/&quot;AkIBSH0zcSp7ImA9WhBSGEk.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-2679837884018570393</id><published>2013-02-25T20:15:00.002-07:00</published><updated>2013-02-25T20:15:59.389-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-02-25T20:15:59.389-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Late Triassic" /><category scheme="http://www.blogger.com/atom/ns#" term="Germany" /><category scheme="http://www.blogger.com/atom/ns#" term="archosauria" /><title>Reevaluation of the Enigmatic Archosaur Dyoplax arenaceus from the Upper Triassic of Germany</title><content type="html">&lt;strong&gt;Maisch, M. W., Matzke, A. T.,&amp;nbsp;and T. Rathgeber. 2013. Re-evaluation of the enigmatic archosaur &lt;em&gt;Dyoplax arenaceus&lt;/em&gt; O. Fraas, 1867 from the Schilfsandstein (Stuttgart Formation, lower Carnian, Upper Triassic) of Stuttgart, Germany. Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen 267(3): 353-362&lt;br /&gt; DOI: &lt;/strong&gt;&lt;a href="http://dx.doi.org/10.1127/0077-7749/2013/0317" target="_blank"&gt;&lt;strong&gt;http://dx.doi.org/10.1127/&lt;wbr&gt;&lt;/wbr&gt;0077-7749/2013/0317&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;
&lt;br /&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; The holotype and only specimen of the small suchian archosaur &lt;em&gt;Dyoplax arenaceus&lt;/em&gt; O. Fraas, 1867 from the Stuttgart-Formation (Schilfsandstein) of southwestern Germany is partially redescribed and re-evaluated. The type locality can be identified as Stuttgart, not Stuttgart-Feuerbach as erroneously suggested by previous authors. A re-description of the skull and the dorsal armour provides several new characters and a restoration of the skull is attempted for the first time. The phylogenetic placement of &lt;em&gt;Dyoplax&lt;/em&gt; is discussed. Although it is agreed with previous authors that the taxon is not an aetosaur, its placement in Crocodylomorpha is questioned. Instead we demonstrate that &lt;em&gt;Dyoplax&lt;/em&gt; has several important cranial and postcranial features in common with &lt;em&gt;Erpetosuchus&lt;/em&gt; from the Late Triassic of Scotland and North America, and it is tentatively re-assigned to ?Erpetosuchidae.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=MK8LRjSBGvU:IHvKIuRUfdg:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=MK8LRjSBGvU:IHvKIuRUfdg:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=MK8LRjSBGvU:IHvKIuRUfdg:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=MK8LRjSBGvU:IHvKIuRUfdg:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=MK8LRjSBGvU:IHvKIuRUfdg:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=MK8LRjSBGvU:IHvKIuRUfdg:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=MK8LRjSBGvU:IHvKIuRUfdg:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=MK8LRjSBGvU:IHvKIuRUfdg:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=MK8LRjSBGvU:IHvKIuRUfdg:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=MK8LRjSBGvU:IHvKIuRUfdg:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/MK8LRjSBGvU" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/2679837884018570393/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/02/reevaluation-of-enigmatic-archosaur.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2679837884018570393?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2679837884018570393?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/MK8LRjSBGvU/reevaluation-of-enigmatic-archosaur.html" title="Reevaluation of the Enigmatic Archosaur &lt;i&gt;Dyoplax arenaceus&lt;/i&gt; from the Upper Triassic of Germany" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/02/reevaluation-of-enigmatic-archosaur.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CE8ERXs-eip7ImA9WhBSEkk.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-2012608406239301484</id><published>2013-02-18T20:00:00.000-07:00</published><updated>2013-02-18T20:00:04.552-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-02-18T20:00:04.552-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="United States" /><category scheme="http://www.blogger.com/atom/ns#" term="chemostratigraphy" /><category scheme="http://www.blogger.com/atom/ns#" term="Permo-Triassic" /><title>Latest Permian Strata Preserved in the Western U.S.?</title><content type="html">&lt;strong&gt;Saltzman, M. R., and A. R. C. Sedlacek. 2013.&amp;nbsp;Chemostratigraphy indicates a relatively complete Late Permian to Early Triassic sequence in the western United&amp;nbsp;States. Geology (early online) &lt;a href="http://geology.gsapubs.org/content/early/2013/02/07/G33906.1.abstract"&gt;doi:10.1130/G33906.1&lt;/a&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;br /&gt;&lt;strong&gt;Abstract -&lt;/strong&gt; Although the latest Permian mass extinction and associated δ13C excursion are well documented from the Tethys Ocean, carbonate rocks preserving these events in the eastern Panthalassic Ocean (western Pangea) are unknown. We present δ13Ccarb from the Gerster and Thaynes (Permian and Triassic) Formations in the western United States and document a negative excursion with no evidence for major breaks in continuity. To further constrain the age of the δ13Ccarb excursion in the absence of index fossils, we analyzed the same samples for 87Sr/86Sr. When examining our new carbon and Sr data in the context of biostratigraphy and sequence stratigraphy, we conclude that parts of the western United States may preserve carbonate successions that span the latest Permian extinction.&lt;br /&gt;
&lt;b&gt;&lt;br /&gt;
&lt;span style="font-family: Times-Bold; font-size: xx-small;"&gt;&lt;br /&gt;
&lt;span style="font-family: Times-Bold; font-size: xx-small;"&gt;&lt;br /&gt;
&lt;div align="LEFT"&gt;
&amp;nbsp;&lt;/div&gt;
&lt;/span&gt;&lt;br /&gt;
&amp;nbsp;&lt;/span&gt;&lt;br /&gt;&lt;/b&gt;&lt;br /&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=uvj4JG3VMSc:pJaTY6B3mBQ:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=uvj4JG3VMSc:pJaTY6B3mBQ:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=uvj4JG3VMSc:pJaTY6B3mBQ:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=uvj4JG3VMSc:pJaTY6B3mBQ:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=uvj4JG3VMSc:pJaTY6B3mBQ:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=uvj4JG3VMSc:pJaTY6B3mBQ:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=uvj4JG3VMSc:pJaTY6B3mBQ:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=uvj4JG3VMSc:pJaTY6B3mBQ:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=uvj4JG3VMSc:pJaTY6B3mBQ:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=uvj4JG3VMSc:pJaTY6B3mBQ:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/uvj4JG3VMSc" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/2012608406239301484/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/02/latest-permian-strata-preserved-in.html#comment-form" title="2 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2012608406239301484?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2012608406239301484?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/uvj4JG3VMSc/latest-permian-strata-preserved-in.html" title="Latest Permian Strata Preserved in the Western U.S.?" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>2</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/02/latest-permian-strata-preserved-in.html</feedburner:origLink></entry><entry gd:etag="W/&quot;D0UASH85cSp7ImA9WhBSEUs.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-836142251834456175</id><published>2013-02-17T22:27:00.000-07:00</published><updated>2013-02-17T22:27:29.129-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-02-17T22:27:29.129-07:00</app:edited><title>Triassic Marine Flooding Event Identified by a Vertebrate Bonebed </title><content type="html">&lt;strong&gt;Reolid, M., Pérez-Valera, F., Benton, M. J., and J. Reolid. 2013. Marine flooding event in continental Triassic facies identified by a nothosaur and placodont bonebed (South Iberian Paleomargin). Facies (early online)&amp;nbsp;&lt;/strong&gt;&lt;a href="http://doi10.1007/s10347-013-0360-6"&gt;&lt;strong&gt;DOI 10.1007/s10347-013-0360-6&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; Sudden marine flooding within otherwise continental successions of the Triassic is unusual. The Tabular Cover of the SE paleomargin of the Iberian Massif is characterized by continental Triassic redbed facies composed of sandstones and siltstones, with gypsum-rich levels in the transition to Jurassic limestones. These Triassic deposits were developed in a fluvial-coastal system and they are 300&amp;nbsp;m thick in the Puente Génave-Villarrodrigo area, eastern Jaén Province, Spain. An unexpected sandstone-limestone unit in the lower part of this formation, recognized over more than 30&amp;nbsp;km, contains marine reptile bones in a storm bed or tsunami deposit. The lower part of this unit is characterized by a sandstone with sedimentary structures indicative of high-energy conditions as well as by fossil remains of marine reptiles. This bed ranges from 0 to 90&amp;nbsp;cm in thickness, and in some outcrops pinches out rapidly within a few meters. The upper part of the studied unit is a limestone with common trace fossils and abundant remains of marine reptiles, comprising isolated and fragmented pieces of sauropterygians (nothosaurs, pachypleurosaurs, and placodonts). Most abundant are vertebrae and ribs. In some outcrops, the top of this bed presents a dense accumulation of well-preserved small gastropods. The limestone is overlain by red siltstones and sandstones. The studied unit is interpreted as a marine deposit representing a high-energy event and records exceptional marine flooding in a distal fluvial environment, in fact the only open-marine deposit in the Villarrodrigo section. The sedimentary structures in the lower part of the unit are typical of high-energy deposits and indicate deposition in a single episode, probably related to a storm surge or a tsunami. The fragmentation, disarticulation, and dispersion of the vertebrate bones and the imbrication of bioclasts are consistent with a high-energy event that favored the concentration of bones according to size and density.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=7FInF8taPeU:sKjCW823cuI:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=7FInF8taPeU:sKjCW823cuI:I9og5sOYxJI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=I9og5sOYxJI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=7FInF8taPeU:sKjCW823cuI:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=7FInF8taPeU:sKjCW823cuI:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=7FInF8taPeU:sKjCW823cuI:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=7FInF8taPeU:sKjCW823cuI:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=7FInF8taPeU:sKjCW823cuI:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=7FInF8taPeU:sKjCW823cuI:cGdyc7Q-1BI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?d=cGdyc7Q-1BI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=7FInF8taPeU:sKjCW823cuI:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=7FInF8taPeU:sKjCW823cuI:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/7FInF8taPeU" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/836142251834456175/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/02/triassic-marine-flooding-event.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/836142251834456175?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/836142251834456175?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/7FInF8taPeU/triassic-marine-flooding-event.html" title="Triassic Marine Flooding Event Identified by a Vertebrate Bonebed " /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/02/triassic-marine-flooding-event.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CEAMQXkyfip7ImA9WhBTGUQ.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-3050821119249434329</id><published>2013-02-15T22:33:00.000-07:00</published><updated>2013-02-15T22:33:00.796-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-02-15T22:33:00.796-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="rauisuchia" /><category scheme="http://www.blogger.com/atom/ns#" term="Pseudosuchia" /><title>Two New 'Rauisuchid' Papers</title><content type="html">&lt;strong&gt;Weinbaum, J. C. 2013. Postcranial skeleton of &lt;em&gt;Postosuchus kirkpatricki&lt;/em&gt; (Archosauria: Paracrocodylomorpha), from the upper Triassic of the United States. In Nesbitt, S. J., Desojo, J. B.&amp;nbsp;and R. B.&amp;nbsp;Irmis, (eds) Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin. Geological Society, London, Special Publications, 379, &lt;/strong&gt;&lt;a href="http://dx.doi.org/10.1144/SP379.7"&gt;&lt;strong&gt;http://dx.doi.org/10.1144/SP379.7&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; &lt;em&gt;Postosuchus kirkpatricki&lt;/em&gt; is a Late Triassic (Norian) ‘rauisuchid’ archosaur from North America. The initial description of the &lt;em&gt;Postosuchus&lt;/em&gt; type material included elements from two poposaurids. This confusion has prevented adequate description of the material. Recent examination of the type material and other specimens of &lt;em&gt;Postosuchus&lt;/em&gt;, and of related taxa, has helped clarify the osteology of &lt;em&gt;Postosuchus&lt;/em&gt;. The type specimens represent c. 75% of the skeleton. Together with other referred material, &lt;em&gt;Postosuchus&lt;/em&gt; remains one of the most completely known rauisuchids. The paratype skeleton, which is relatively complete, would have been c. 3.5–4 m in length, and the holotype would have been closer to 5–6 m.&lt;br /&gt;&lt;br /&gt;Analysis of the postcranial skeleton of &lt;em&gt;Postosuchus&lt;/em&gt; suggests that it may have been an obligate biped (based in part on limb proportions, which are similar to some theropod dinosaurs, the size of the manus (30% of the size of the pes) and the highly reduced nature of the digits and vertebral measurements). Possible postcranial autapomorphies of &lt;em&gt;Postosuchus&lt;/em&gt; include a large, rugose triangular supra-acetabular buttress confluent with the dorsal margin of the iliac blade, and a symmetrical pes with digits two and three being roughly equal in length.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;


&lt;strong&gt;De Franca, M. A. G., Langer, M. C., and J. Ferigolo. 2013. The skull anatomy of &lt;em&gt;Decuriasuchus quartacolonia&lt;/em&gt; (Pseudosuchia: Suchia: Loricata) from the middle Triassic of Brazil. In Nesbitt, S. J., Desojo, J. B.&amp;nbsp;and R. B.&amp;nbsp;Irmis, (eds) Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin. Geological Society, London, Special Publications, 379, &lt;a href="http://sp.lyellcollection.org/content/early/2013/02/12/SP379.8.abstract"&gt;doi:10.1144/SP379.8&lt;/a&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract - &lt;/strong&gt;Unlike most rauisuchians, which are known based on partially preserved specimens, fossils attributed to &lt;em&gt;Decuriasuchus quartacolonia&lt;/em&gt; include a monotaxonomic assemblage composed of nine associated individuals (MCN-PV10.105a–i), three with almost complete skulls (MCN-PV10.105a,c,d), and a partial disarticulated skull (MCN-PV10.004) collected in the Middle Triassic (Ladinian, &lt;em&gt;Dinodontosaurus&lt;/em&gt; Biozone) beds of the Santa Maria Formation, in south Brazil. Because of its completeness and possible phylogenetic position, as one of the most basal loricatans, &lt;em&gt;D. quartacolonia&lt;/em&gt; is a key taxon for anatomic, evolutionary and biomechanical studies of rauisuchians. The comparative description of its osteology reveals that the skull and mandible of &lt;em&gt;D.quartacolonia&lt;/em&gt; are very similar to those of cf. &lt;em&gt;Prestosuchus chiniquensis&lt;/em&gt; and &lt;em&gt;Saurosuchus galilei&lt;/em&gt;, sharing a drop-shaped subnarial fenestra, a subtriangular antorbital fenestra with an elongated and narrow anterior point, a ‘roman nosed’ nasal, and a posteroventrally oriented ridge on the lateral surface of the ventral ramus of the squamosal. Among the differences are the autapomorphies of &lt;em&gt;D.quartacolonia&lt;/em&gt;: numerous maxillary teeth (17), lateral expansion of the nasal/lacrimal covering the antorbital fenestra dorsally, and squamosal and quadratojugal forming a subtriangular projection that invades the lower temporal fenestra.&lt;strong&gt;&lt;span style="-webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px; background-color: white; color: #403838; display: inline !important; float: none; font-size-adjust: none; font-stretch: normal; font: 13px/19px &amp;quot;Lucida Sans Unicode&amp;quot;, Arial, &amp;quot;Lucida Grande&amp;quot;, Tahoma, Verdana, Helvetica, sans-serif; letter-spacing: normal; orphans: 2; text-align: justify; text-indent: 0px; text-transform: none; white-space: normal; widows: 2; word-spacing: 0px;"&gt;&lt;/span&gt;&lt;/strong&gt;&lt;br /&gt;


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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/g08hbeKEGmk" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/3050821119249434329/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/02/two-new-rauisuchid-papers.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/3050821119249434329?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/3050821119249434329?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/g08hbeKEGmk/two-new-rauisuchid-papers.html" title="Two New 'Rauisuchid' Papers" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/02/two-new-rauisuchid-papers.html</feedburner:origLink></entry><entry gd:etag="W/&quot;D0cDSHgyfCp7ImA9WhBTGU0.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-4941401402876653760</id><published>2013-02-14T22:11:00.000-07:00</published><updated>2013-02-14T22:11:19.694-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2013-02-14T22:11:19.694-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="dinosauriformes" /><category scheme="http://www.blogger.com/atom/ns#" term="dinosauromorpha" /><title>New Basal Dinosauromorph Synthesis Paper</title><content type="html">A solid review of our current knowledge of non-dinosaurian dinosauromorphs such as lagerpetids and silesaurids.&lt;br /&gt;
&lt;strong&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Langer, M. C., Nesbitt, S. J., Bittencourt, J. S., and R. B. Irmis. 2013. Non-Dinosaurian Dinosauromorpha. &lt;em&gt;In&lt;/em&gt; &lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;N&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS836F;"&gt;&lt;span style="font-family: AdvPS836F;"&gt;esbitt&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;, S. J., D&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS836F;"&gt;&lt;span style="font-family: AdvPS836F;"&gt;esojo&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;, J. B.&amp;nbsp;and R. B.&amp;nbsp;I&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS836F;"&gt;&lt;span style="font-family: AdvPS836F;"&gt;rmis&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;, (eds) &lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F0B;"&gt;&lt;span style="font-family: AdvPS6F0B;"&gt;Anatomy, Phylogeny and Palaeobiology of &lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F0B;"&gt;&lt;span style="font-family: AdvPS6F0B;"&gt;Early Archosaurs and their Kin&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;. Geological Society, London, Special Publications, &lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F01;"&gt;&lt;span style="font-family: AdvPS6F01;"&gt;379&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;, &lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;a href="http://dx.doi.org/10.1144/SP379.9"&gt;&lt;strong&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;http:&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvP4C4E59;"&gt;&lt;span style="font-family: AdvP4C4E59;"&gt;//&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;dx.doi.org&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvP4C4E59;"&gt;&lt;span style="font-family: AdvP4C4E59;"&gt;/&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;10.1144&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvP4C4E59;"&gt;&lt;span style="font-family: AdvP4C4E59;"&gt;/&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: AdvPS6F00;"&gt;&lt;span style="font-family: AdvPS6F00;"&gt;SP379.9&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;
&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; 

Ichnological evidence suggests that dinosauromorphs originated by the Early Triassic, and skeletal remains of non-dinosaur representatives of the clade occur from the Anisian to the end of the Triassic. These taxa are small- to medium-sized, vary in feeding and locomotor features, and occurred over most of western Pangaea. They include the small lagerpetids from the Mid–Late Triassic of Argentina and the United States, and the larger, quadrupedal Silesauridae, with records in the Middle Triassic of Africa and Argentina, and in the Late Triassic of Europe, the Americas and northern Africa. The former group represents the earliest diverging dinosauromorphs, whereas silesaurids are more closely related to Dinosauria. Other dinosauromorphs include the archetypal early dinosauriform &lt;em&gt;Marasuchus lilloensis&lt;/em&gt; (Middle Triassic of Argentina) and poorly known/controversial taxa such as &lt;em&gt;Lewisuchus admixtus&lt;/em&gt; and &lt;em&gt;Saltopus elginensis&lt;/em&gt;. The earliest diverging dinosauromorphs may have preyed on small animals (including insects), but cranio-dental remains are rare; by contrast, most silesaurids probably included plant material in their diet, as indicated by their modified jaw apparatus and teeth. Our knowledge of the anatomy and thus relationships of non-dinosaurian Dinosauromorpha is still deficient, and we suspect that future discoveries will continue to reveal novel patterns and hypotheses of palaeobiology and biogeography.&lt;br /&gt;


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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/2Kke0DIvACQ" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/4941401402876653760/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2013/02/new-basal-dinosauromorph-synthesis-paper.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4941401402876653760?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4941401402876653760?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/2Kke0DIvACQ/new-basal-dinosauromorph-synthesis-paper.html" title="New Basal Dinosauromorph Synthesis Paper" /><author><name>Bill Parker</name><uri>http://www.blogger.com/profile/05941940882532354219</uri><email>noreply@blogger.com</email><gd:image rel="http://schemas.google.com/g/2005#thumbnail" width="32" height="24" src="http://3.bp.blogspot.com/_MCznsojQGoc/SnsKlyDSD_I/AAAAAAAAAfY/h0q2V6xt0LI/S220/Rincon+Basin.jpg" /></author><thr:total>0</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2013/02/new-basal-dinosauromorph-synthesis-paper.html</feedburner:origLink></entry></feed>
