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term="reconstructions" /><category term="isotopes" /><category term="great books" /><category term="feeding" /><category term="Temnospondyli" /><category term="Pseudosuchia" /><category term="evolution" /><category term="sauropodomorphs" /><category term="PDFs" /><category term="Carbon isotopes" /><category term="Diapsids" /><category term="Connecticut Volunteers" /><category term="Scenery" /><category term="Rhychosauria" /><category term="procolophonids" /><category term="tracks" /><category term="SVP" /><category term="South Africa" /><category term="museum exhibits" /><category term="dinosaurs" /><category term="fossil eggs" /><category term="insect predation" /><category term="readers" /><category term="blogroll updates" /><category term="vacation" /><category term="Protorosauria" /><category term="field notes" /><category term="vertebrates" /><category term="communication" /><category term="Science" /><category term="Triassic Sites" /><category term="Desmatosuchus" /><category term="expansion" /><category term="Germany" /><category term="truly wierd" /><category term="Jeff Martz" /><category term="cynodont" /><category term="Chinle" /><category term="ornithodira" /><category term="non-Triassic" /><category term="plate tectonics" /><category term="Chinlechelys" /><category term="CAMP" /><category term="data" /><category term="outreach" /><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>598</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;CU8CRnw8cCp7ImA9WhVVF0w.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-4763974759988274485</id><published>2012-05-10T22:24:00.001-07:00</published><updated>2012-05-10T22:24:27.278-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-05-10T22:24:27.278-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Temnospondyli" /><category scheme="http://www.blogger.com/atom/ns#" term="capitosauria" /><category scheme="http://www.blogger.com/atom/ns#" term="functional morphology" /><title>Skull Mechanics of Capitosaurs (Amphibia: Temnospondyli)</title><content type="html">&lt;strong&gt;Fortuny, J., Marcé-Nogué, J., Gil, L. and Galobart, À. 2012. Skull Mechanics and the Evolutionary Patterns of the Otic Notch Closure in Capitosaurs (Amphibia: Temnospondyli). The Anatomical Record (advance online publication) doi: 10.1002/ar.22486 &lt;/strong&gt;&lt;a href="http://onlinelibrary.wiley.com/doi/10.1002/ar.22486/abstract"&gt;&lt;strong&gt;http://onlinelibrary.wiley.com/doi/10.1002/ar.22486/abstract&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; Capitosaurs were among the largest amphibians that have ever lived. Their members displayed an amphibious lifestyle. We provide new information on functional morphology data, using finite element analysis (FEA) which has palaeoecological implications for the group. Our analyses included 17 taxa using (2D) plate models to test four loading cases (bilateral, unilateral and lateral bitings and skull raising system simulation). Our results demonstrates that, when feeding, capitosaurs concentrated the stress at the circumorbital region of the capitosaur skull and cranial sutures probably played a key role in dissipating and absorbing the stress generated during biting. Basal members (as &lt;em&gt;Wetlugasaurus&lt;/em&gt;) were probably less specialized forms, while during Middle- and Late Triassic the group radiated into different ecomorphotypes with closed otic notch forms (as &lt;em&gt;Cyclotosaurus&lt;/em&gt;) resulting in the strongest skulls during biting. Previous interpretations discussed a trend from an open to closed otic notch associated with lateral repositioning of the tabular horns, but the analysis of the skull-raising system reveals that taxa exhibiting posteriorly directed tabular horns display similar results during skull raising to those of closed otic notch taxa. Our results suggest that various constraints besides otic notch morphology, such as the elongation of the tabular horns, snout length, skull width and position, and size of the orbits affect the function of the skull. On the light of our results, capitosaur skull showed a trend to reduce the stresses and deformation during biting. Capitosaurs could be considered crocodilian analogues as they were top-level predators in fluvial and brackish Triassic ecosystems.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-4763974759988274485?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/Gf2wlmashTI" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/4763974759988274485/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/05/skull-mechanics-of-capitosaurs-amphibia.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4763974759988274485?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4763974759988274485?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/Gf2wlmashTI/skull-mechanics-of-capitosaurs-amphibia.html" title="Skull Mechanics of Capitosaurs (Amphibia: Temnospondyli)" /><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/2012/05/skull-mechanics-of-capitosaurs-amphibia.html</feedburner:origLink></entry><entry gd:etag="W/&quot;DkYNQnc6cSp7ImA9WhVVFEg.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-523447075813312165</id><published>2012-05-07T22:16:00.001-07:00</published><updated>2012-05-07T22:16:33.919-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-05-07T22:16:33.919-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="China" /><category scheme="http://www.blogger.com/atom/ns#" term="Paleobotany" /><category scheme="http://www.blogger.com/atom/ns#" term="Late Triassic" /><title>A New Neocalamites from the Upper Triassic of China</title><content type="html">&lt;strong&gt;Zan, S.-Q., Axsmith, B. J, Escapa, I., Fraser, N. C., Liu, F.-X., and D.-E. Xing. 2012. A new &lt;em&gt;Neocalamites&lt;/em&gt; (Sphenophyta) with prickles and attached cones from the Upper Triassic of China. Palaeoworld (accepted manuscript). &lt;/strong&gt;&lt;a href="http://dx.doi.org/10.1016/j.palwor.2012.04.001" id="ddDoi" target="doilink"&gt;&lt;span style="color: #316c9d;"&gt;&lt;strong&gt;http://dx.doi.org/10.1016/j.palwor.2012.04.001&lt;/strong&gt;&lt;/span&gt;&lt;/a&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; Remains of the extinct sphenophyte (horsetail) &lt;em&gt;Neocalamites&lt;/em&gt; are most widespread in the Middle–Upper Triassic and are typically represented by stem and leaf fragments. Here we report on spectacular new finds of &lt;em&gt;Neocalamites&lt;/em&gt; from the Late Triassic Yangcaogou Formation in Liaoning Province, China that include bedding surfaces dominated by nearly complete aerial stems with attached leaf whorls and rare bractless cones. They reveal a monopodial growth habit for the stems, which are covered with downward projecting prickles that probably provided protection against herbivores. These features provide the basis for a new proposed species, &lt;em&gt;Neocalamites horridus&lt;/em&gt;. The nodes bear whorls of very long leaves mainly free to their bases, and one specimen bears an attached cone on a long peduncle. Identical dispersed cones have also been recovered. The leaves of adjacent monopodial stems most likely interlocked to support growth in large stands akin to the role now played by branches in large modern &lt;em&gt;Equisetum&lt;/em&gt; species. The new Chinese &lt;em&gt;Neocalamites&lt;/em&gt; is among the most confidently reconstructed species, and indicates a greater diversity of sphenophyte morphology during the Mesozoic than previously realized.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-523447075813312165?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=LEZgOpAh_NQ:P5uI2vNlg98: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=LEZgOpAh_NQ:P5uI2vNlg98: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=LEZgOpAh_NQ:P5uI2vNlg98: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=LEZgOpAh_NQ:P5uI2vNlg98:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=LEZgOpAh_NQ:P5uI2vNlg98:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=LEZgOpAh_NQ:P5uI2vNlg98:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=LEZgOpAh_NQ:P5uI2vNlg98:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=LEZgOpAh_NQ:P5uI2vNlg98: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=LEZgOpAh_NQ:P5uI2vNlg98:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=LEZgOpAh_NQ:P5uI2vNlg98:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/LEZgOpAh_NQ" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/523447075813312165/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/05/new-neocalamites-from-upper-triassic-of.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/523447075813312165?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/523447075813312165?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/LEZgOpAh_NQ/new-neocalamites-from-upper-triassic-of.html" title="A New &lt;i&gt;Neocalamites&lt;/i&gt; from the Upper 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/2012/05/new-neocalamites-from-upper-triassic-of.html</feedburner:origLink></entry><entry gd:etag="W/&quot;A0YESXg_eSp7ImA9WhVVEUU.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-5429952395180889761</id><published>2012-05-03T22:23:00.002-07:00</published><updated>2012-05-04T20:38:28.641-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-05-04T20:38:28.641-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Petrified Forest" /><category scheme="http://www.blogger.com/atom/ns#" term="apomorphy-based identifications" /><category scheme="http://www.blogger.com/atom/ns#" term="phytosaur" /><title>Introducing Protome batalaria, a New Phytosaur from the Chinle Formation of Petrified Forest National Park, Arizona</title><content type="html">In the Fall of 2004 Michelle Stocker and I were out at the Battleship NW fossil locality in Petrified Forest National Park&amp;nbsp;with several researchers from Northern Arizona University. They were working on completing the geological map of the area and had noted that they could not get the current stratigraphic scheme we were using (introduced in 2002) to work out on the map.&amp;nbsp; The stratigraphic position of this quarry was an important issue behind this work as I had just collected a good skeleton of the aetosaur &lt;em&gt;Calyptosuchus wellesi&lt;/em&gt; here just above a prominent sandstone that previous workers had correlated to the "Sonsela Sandstone Bed". If this bed correlation was correct then the specimen would be from the Revueltian biozone. This was problematic because &lt;em&gt;Calyptosuchus&lt;/em&gt; is considered an index taxon of the Adamanian.&amp;nbsp; As we hemmed and hawed back and forth and discussed various possible correlations to work out these problems, Michelle noted some scraps of bone in unconsolidated sand&amp;nbsp;at top of this bed and very near to where we were standing. She was very surprised, as was I, when she reached down and pulled up part of the skull roof of a phytosaur. &lt;br /&gt;
&lt;br /&gt;
After the NAU researchers moved on to complete their work, we examined Michelle's new "quarry" much closer.&amp;nbsp; By literally sifting our fingers through the loose sand we easily collected numerous parts of the skull including large portions of the rostrum and skull roof. We also uncovered a ramus of the mandible, but this was actually in-situ in the bedrock just underneath the loose sand. We were able to jacket this element, but it was wintertime and I distinctly remember how frozen our hands were after each application of a plaster bandage.&amp;nbsp; Luckily the truck was very nearby, so after each application we would run to the running truck to stick our hands under the heater. &lt;br /&gt;
&lt;br /&gt;
Back in the lab we were able to piece back together much of the skull and it later became part of the focus of Michelle's Masters Thesis. Prior to this Randall Irmis and I mentioned (and figured) this specimen in a 2005 paper where we referred it to "&lt;em&gt;Leptosuchus&lt;/em&gt;" &lt;em&gt;adamanensis&lt;/em&gt; based on the overall morphology of the squamosals following work by Long and Murry. However, Michelle's detailed phylogenetic analysis in her thesis suggested something different, specifically the specimen did not form a clade with &lt;em&gt;Smilosuchus adamanensis&lt;/em&gt; and instead was something else.&lt;br /&gt;
&lt;br /&gt;
In her new paper in the Journal of Vertebrate Paleontology Michelle has&amp;nbsp;described this specimen&amp;nbsp;as&amp;nbsp;a new taxon, which she names &lt;em&gt;Protome batalaria&lt;/em&gt;. The name reflects the condition of the specimen, "face of an animal" and where it was found "warship" (for the Battleship Quarry).&amp;nbsp;It can be diagnosed by a unique combination of characters as well as three autapomorphies of the braincase and lower jaw. Her phylogenetic analysis recovers it as a non-pseudopalatine leptosuchomorph.&lt;br /&gt;
&lt;br /&gt;
Important discussion in her paper revolves around the importance of the use of apomorphies to describe and classify specimens. In this particular case past workers (myself) had focused on the generally morphology of the squamosal and robustness of the specimen to make a taxonomic assignment and ignored other discrete apomorphies of the material, which a phylogenetic analysis later determined to be&amp;nbsp;of significance. &amp;nbsp;Thus the longtime practice of assigning isolated phytosaur squamosals to taxa based on general similarity and utilizing these for Late Triassic biochronology is called into question. This general squamosal morphology used to assign (fragmentary and complete) specimens to &lt;em&gt;Rutiodon&lt;/em&gt; or &lt;em&gt;Leptosuchus&lt;/em&gt; instead just appears to&amp;nbsp;be a shared character of non-pseudopalatine leptosuchomorphs, a paraphyletic assemblage.&lt;br /&gt;
&lt;br /&gt;
As recommended by Michelle it is now necessary to go back to collections such as those from the Petrified Forest and look carefully at all of the specimens assigned to "&lt;em&gt;Leptosuchus&lt;/em&gt;" and sort them out using apomorphies. Hopefully this will provide a clear distribution pattern and biochronological signal for these specimens,&amp;nbsp;testing their importance in phytosaur biochronology and biogeography.&amp;nbsp; Overall this&amp;nbsp;new paper provides a great description and&amp;nbsp;discussion that Michelle should be proud of and&amp;nbsp;will be landmark (along with her 2010 paper) for sorting out the labyrinth that is phytosaur taxonomy.&lt;br /&gt;
&lt;br /&gt;
By the way, the stratigraphic problem mentioned at the beginning of this post was finally figured out by Jeff Martz and I in 2009 when we discovered that the bed in question was definitely not the "Sonsela Sandstone Bed", but rather an isolated sandstone lens in the older Lot's Wife Beds and &amp;nbsp;Adamanian in age. &lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Stocker, M. R.&amp;nbsp;2012. A new phytosaur (Archosauriformes, Phytosauria) from the Lot’s Wife beds (Sonsela Member) within the Chinle Formation (Upper Triassic) of Petrified Forest National Park, Arizona. Journal of Vertebrate Paleontology 32(3): 573-586 &lt;/strong&gt;&lt;a href="http://www.tandfonline.com/doi/abs/10.1080/02724634.2012.649815"&gt;&lt;strong&gt;DOI:10.1080/02724634.2012.649815&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; A new phytosaur taxon from Petrified Forest National Park, Arizona, is here described based on cranial material from a single individual. This specimen previously was included in an extensive phylogenetic analysis, and it was found to possess a combination of character states that differs from all known phytosaur taxa in addition to two autapomorphies within the braincase and an autapomorphy of the mandible. The new taxon adds to the taxonomic diversity recognized from the Sonsela Member of the Chinle Formation. The continued increase in phytosaur diversity emphasizes the need to more accurately characterize and identify taxa within a phylogenetic systematic context in order to produce a more refined signal for biostratigraphic correlations, biochronologic inferences, and faunal dynamics during the Late Triassic.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-5429952395180889761?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=9R7mWALZPw8:9w01qxNn7fs: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=9R7mWALZPw8:9w01qxNn7fs: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=9R7mWALZPw8:9w01qxNn7fs: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=9R7mWALZPw8:9w01qxNn7fs:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=9R7mWALZPw8:9w01qxNn7fs:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=9R7mWALZPw8:9w01qxNn7fs:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=9R7mWALZPw8:9w01qxNn7fs:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=9R7mWALZPw8:9w01qxNn7fs: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=9R7mWALZPw8:9w01qxNn7fs:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=9R7mWALZPw8:9w01qxNn7fs:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/9R7mWALZPw8" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/5429952395180889761/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/05/introducing-protome-batalaria-new.html#comment-form" title="1 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/5429952395180889761?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/5429952395180889761?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/9R7mWALZPw8/introducing-protome-batalaria-new.html" title="Introducing &lt;i&gt;Protome batalaria&lt;/i&gt;, a New Phytosaur from the Chinle Formation of Petrified Forest National Park, Arizona" /><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/2012/05/introducing-protome-batalaria-new.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CEMERnk8eyp7ImA9WhVWGEw.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-880330847651183727</id><published>2012-04-30T12:00:00.000-07:00</published><updated>2012-04-30T12:00:07.773-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-04-30T12:00:07.773-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="tracks" /><category scheme="http://www.blogger.com/atom/ns#" term="Trace Fossils" /><category scheme="http://www.blogger.com/atom/ns#" term="Europe" /><title>New Triassic Trackway from Switzerland</title><content type="html">&lt;br /&gt;
&lt;div class="Abstract" lang="en"&gt;
&lt;a href="" name="Abs1"&gt;&lt;/a&gt;
&lt;div class="normal"&gt;
&lt;div class="text"&gt;
&lt;div class="authors"&gt;
&lt;b&gt;Cavin, L., Avanzini, M., Bernardi, M., Piuz, A., Proz, P.-A., Meister, C., Boissonnas, J., and C. A. Meyer. 2012. New vertebrate trackway from the autochthonous cover of the Aiguilles Rouges Massif and reevaluation of the dinosaur record in the Valais, SW Switzerland. Swiss Journal of Palaeontology [online first]&amp;nbsp;&lt;span class="doi"&gt;&lt;a href="http://www.springerlink.com/content/m05vv41332844252/"&gt;&lt;span class="label"&gt;DOI:&lt;/span&gt; &lt;span class="value"&gt;10.1007/s13358-012-0040-0&lt;/span&gt;&lt;/a&gt;&lt;/span&gt;&lt;/b&gt;&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;div class="normal"&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;/div&gt;
&lt;div class="normal"&gt;
&lt;b&gt;Abstract - &lt;/b&gt;A new tracksite located in the Mesozoic autochthonous series 
covering the Aiguilles Rouges Massif, circa 7&amp;nbsp;km to the NNE of the tracksite of 
the Vieux Emosson, is briefly described. The trampled bed is most likely coeval 
with the outcrop in the Vieux Emosson area. Two poorly preserved quadrupedal 
trackways, almost parallel, measure 9.8 and 8&amp;nbsp;m in length, respectively. They 
are referred to the Chirotheriidae ABEL, 1835 form-family. A short and 
well-preserved quadrupedal trackway, composed of two manus-pes couples, is 
assigned to &lt;i&gt;Chirotherium&lt;/i&gt; cf&lt;i&gt;. barthii&lt;/i&gt; KAUP, 1835. A 
reinterpretation of the Vieux Emosson ichnotaxa reveals that most tracks, if not 
all, belong to indeterminate chirotheriid and that no clear evidence of dinosaur 
footprints is observed. The trampled bed of the cover of the Aiguilles Rouges 
Massif probably forms a megatracksite, which is Early or Middle Triassic in age. &amp;nbsp;&lt;/div&gt;
&lt;/div&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-880330847651183727?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=tg9oV3E31aE:ArTApf4IUm8: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=tg9oV3E31aE:ArTApf4IUm8: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=tg9oV3E31aE:ArTApf4IUm8: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=tg9oV3E31aE:ArTApf4IUm8:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=tg9oV3E31aE:ArTApf4IUm8:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=tg9oV3E31aE:ArTApf4IUm8:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=tg9oV3E31aE:ArTApf4IUm8:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=tg9oV3E31aE:ArTApf4IUm8: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=tg9oV3E31aE:ArTApf4IUm8:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=tg9oV3E31aE:ArTApf4IUm8:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/tg9oV3E31aE" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/880330847651183727/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/04/new-triassic-trackway-from-switzerland.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/880330847651183727?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/880330847651183727?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/tg9oV3E31aE/new-triassic-trackway-from-switzerland.html" title="New Triassic Trackway from Switzerland" /><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/2012/04/new-triassic-trackway-from-switzerland.html</feedburner:origLink></entry><entry gd:etag="W/&quot;Ak8DQHg_fip7ImA9WhVWEk4.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-6987622116360346433</id><published>2012-04-23T20:40:00.001-07:00</published><updated>2012-04-23T20:41:11.646-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-04-23T20:41:11.646-07:00</app:edited><title>Could it Be? An Non-Archosaurian Archosauriform that is Actually a Dinosaur?</title><content type="html">The past eight years have seen quite a few cases where purported Triassic dinosaurs actually turned out to be non-dinosaurian archosauriforms...&lt;em&gt;Revueltosaurus, Shuvosaurus, Azendohsaurus&lt;/em&gt;... finally the dinosaurs get one back. Moreover there are no Jurassic or Chinese phytosaur specimens.&amp;nbsp; &lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Barrett, P. M., and X. Xu. 2012. The enigmatic reptile &lt;em&gt;Pachysuchus imperfectus&lt;/em&gt; Young, 1951 from the lower Lufeng Formation (Lower Jurassic) of Yunnan, China.&amp;nbsp;Vertebrata PalAsiatica 50:151-159. [&lt;a href="http://english.ivpp.cas.cn/sp/PalAsiatica/vp_list/201202/t20120209_81207.html"&gt;Free download here&lt;/a&gt;]&lt;/strong&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;span style="font-family: FzBookMaker1DlFont1; font-size: xx-small;"&gt;&lt;span style="font-family: FzBookMaker1DlFont1; font-size: xx-small;"&gt;&lt;span style="font-size: small;"&gt;&lt;strong&gt;Abstract -&lt;/strong&gt; Phytosaurs are generally considered to have become extinct at the end of the Triassic Period, but several records have suggested that they survived into the basal Jurassic in Europe and Asia. The Asian record consists of Pachysuchus imperfectus from the lower Lufeng Formation (?Hettangian-Sinemurian) of Yunnan, China. However, this specimen differs from phytosaurs in numerous aspects and is more likely a poorly preserved, indeterminate sauropodomorph dinosaur skull. The referred specimens of this species are also regarded as indeterminate, thereby removing the post-Triassic record of phytosaurs from Asia. The European records of Jurassic phytosaurs are also shown to be doubtful, suggesting that this clade was restricted to the Late Triassic.&lt;/span&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-6987622116360346433?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/GWi74k4bb70" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/6987622116360346433/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/04/could-it-be-archosauriform-that-is.html#comment-form" title="9 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/6987622116360346433?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/6987622116360346433?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/GWi74k4bb70/could-it-be-archosauriform-that-is.html" title="Could it Be? An Non-Archosaurian Archosauriform that is Actually a Dinosaur?" /><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>9</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2012/04/could-it-be-archosauriform-that-is.html</feedburner:origLink></entry><entry gd:etag="W/&quot;C0UDQ3g9fyp7ImA9WhVQFEo.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-7512576464028588689</id><published>2012-04-03T09:41:00.000-07:00</published><updated>2012-04-03T09:41:12.667-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-04-03T09:41:12.667-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Early Jurassic" /><category scheme="http://www.blogger.com/atom/ns#" term="ICZN" /><category scheme="http://www.blogger.com/atom/ns#" term="sauropodomorphs" /><title>Neotype Proposal for Anchisaurus polyzelus</title><content type="html">&lt;br /&gt;
&lt;b&gt;Galton, P.M. 2012.&amp;nbsp;Case 3561 &lt;i&gt;Anchisaurus&lt;/i&gt; Marsh, 1885 (Dinosauria, Sauropodomorpha):&amp;nbsp;proposed conservation of usage by designation of a neotype for its&amp;nbsp;type species &lt;i&gt;Megadactylus polyzelus&lt;/i&gt; Hitchcock, 1865.&amp;nbsp;Bulletin of Zoological Nomenclature 69 (1): &lt;a href="http://iczn.org/content/case-3561-anchisaurus-marsh-1885-dinosauria-sauropodomorpha-proposed-conservation-usage-desi"&gt;44-50&lt;/a&gt;.&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;Abstract - &lt;/b&gt;The purpose of this application, under Article 75.5 of the Code, is to&amp;nbsp;conserve the usage of the name &lt;i&gt;Anchisaurus&lt;/i&gt; Marsh, 1885 (Lower&amp;nbsp;Jurassic, Connecticut Valley, northeastern U.S.A.) that is based on&amp;nbsp;&lt;i&gt;Megadactylus polyzelus&lt;/i&gt; Hitchcock, 1865. It is proposed to replace the&amp;nbsp;fragmentary and non-diagnostic holotype of &lt;i&gt;M. polyzelus&lt;/i&gt; with a&amp;nbsp;diagnostic neotype, an almost complete skull and skeleton (YPM 1883,&amp;nbsp;holotype of A. colurus Marsh, 1891). This specimen has formed the&amp;nbsp;basis for the concept of &lt;i&gt;Anchisaurus&lt;/i&gt;, the first basal sauropodomorph&amp;nbsp;genus from the U.S.A. and still the best represented from there since&amp;nbsp;it was illustrated by Marsh (1892, 1893), and of &lt;i&gt;A. polyzelus&lt;/i&gt; since it&amp;nbsp;was illustrated by Galton (1976). &lt;i&gt;Anchisaurus&lt;/i&gt; is the basis for&amp;nbsp;ANCHISAURIDAE Marsh, 1885, the first basal sauropodomorph family to be&amp;nbsp;named, and for the Anchisauria Galton &amp;amp; Upchurch, 2004.&lt;br /&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/J8PJjdif0uk" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/7512576464028588689/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/04/neotype-proposal-for-anchisaurus.html#comment-form" title="3 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/7512576464028588689?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/7512576464028588689?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/J8PJjdif0uk/neotype-proposal-for-anchisaurus.html" title="Neotype Proposal for &lt;i&gt;Anchisaurus polyzelus&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>3</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2012/04/neotype-proposal-for-anchisaurus.html</feedburner:origLink></entry><entry gd:etag="W/&quot;D0QERns5cCp7ImA9WhVQEkQ.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-5999868622783346612</id><published>2012-04-01T07:46:00.001-07:00</published><updated>2012-04-01T08:48:27.528-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-04-01T08:48:27.528-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="April 1" /><title>First Multi-taxic Multi-component Ornithischian and Sauropodomorph Dinosaur Bonebed from the Upper Triassic of North America</title><content type="html">&lt;br /&gt;
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&lt;div class="MsoNormal" style="background: white; line-height: 140%;"&gt;
&lt;b&gt;&lt;span style="font-family: &amp;quot;Times New Roman&amp;quot;,&amp;quot;serif&amp;quot;; mso-fareast-font-family: &amp;quot;Times New Roman&amp;quot;;"&gt;Cubo, J., LeRoy, N., Martinez-Maza, C., and L. Montes. 2012. Paleohistological estimation of bone growth rate in extinct archosaurs. Paleobiology 38:335-339.&amp;nbsp;&lt;/span&gt;&lt;span style="background-color: transparent;"&gt;doi: &lt;/span&gt;&lt;a href="http://dx.doi.org/10.1666/08093.1" style="background-color: transparent;"&gt;http://dx.doi.org/10.1666/08093.1&lt;/a&gt;&lt;/b&gt;&lt;/div&gt;
&lt;div class="MsoNormal" style="background: white; line-height: 140%;"&gt;
&lt;b style="background-color: white; font-family: 'Times New Roman', serif; line-height: 140%;"&gt;&lt;br /&gt;&lt;/b&gt;&lt;/div&gt;
&lt;div class="MsoNormal" style="background: white; line-height: 140%;"&gt;
&lt;b style="background-color: white; font-family: 'Times New Roman', serif; line-height: 140%;"&gt;Abstract -&lt;/b&gt;&lt;span style="background-color: white; font-family: 'Times New Roman', serif; line-height: 140%;"&gt; The
clade Archosauria contains two very different sister groups in terms of
diversity (number of species) and disparity (phenotypic variation): Crurotarsi
(taxa more closely related to crocodiles than to birds) and Ornithodira
(pterosaurs and dinosaurs including birds). The extant species of Crurotarsi
may constitute a biased sample of past biodiversity regarding growth patterns
and metabolic rates. Bone histological characters can be conserved over
hundreds of millions of years in the fossil record and potentially contain
information about individual age at death, age at sexual maturity, bone growth
rates, and basal metabolic rates of extinct vertebrates. Using a sample of
extant amniotes, we have constructed a paleobiological model to estimate bone
growth rate from bone histological traits. Cross-validation tests show that
this model is reliable. We then used it to estimate bone growth rates in a
sample of extinct archosaurs including Crurotarsi and Ornithodira. After
testing for phylogenetic signal, optimization of femoral growth rates through
squared change parsimony onto a time-calibrated tree of amniotes shows two
divergent evolutionary trends: whereas bone growth rates increase from the last
common ancestor of Ornithodira to extant birds, they decrease from the last
common ancestor of Crurotarsi to extant crocodiles. However, we conclude, on
the basis of recent evidence for unidirectional airflow in the lungs of
alligators, that crocodiles may have retained the capacity of growing at high
rates.&lt;/span&gt;&lt;/div&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-804845746036418565?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/A8E4ZReowVQ" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/804845746036418565/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/paleohistological-estimation-of-bone.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/804845746036418565?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/804845746036418565?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/A8E4ZReowVQ/paleohistological-estimation-of-bone.html" title="Paleohistological Estimation of Bone Growth Rate in Extinct Archosaurs" /><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/2012/03/paleohistological-estimation-of-bone.html</feedburner:origLink></entry><entry gd:etag="W/&quot;A0UFRn8_fCp7ImA9WhVQEUk.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-3083290693149822354</id><published>2012-03-30T16:13:00.001-07:00</published><updated>2012-03-30T16:13:37.144-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-30T16:13:37.144-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="climate" /><category scheme="http://www.blogger.com/atom/ns#" term="palynology" /><category scheme="http://www.blogger.com/atom/ns#" term="Triassic-Jurassic" /><title>Vegetation History and Climate Change Across the Tr/J Boundary</title><content type="html">&lt;br /&gt;
&lt;div class="last" style="background: white;"&gt;
&lt;b&gt;Bonis, N. R., and W. M.&amp;nbsp;Kürschner. 2012. Vegetation history, diversity patterns, and climate change across the Triassic/Jurassic boundary. Paleobiology 38:240-264.&amp;nbsp;&lt;span style="background-color: transparent;"&gt;doi: &lt;/span&gt;&lt;a href="http://dx.doi.org/10.1666/09071.1" style="background-color: transparent;"&gt;http://dx.doi.org/10.1666/09071.1&lt;/a&gt;&lt;/b&gt;&lt;/div&gt;
&lt;div class="last" style="background: white;"&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;/div&gt;
&lt;div class="last" style="background: white;"&gt;
&lt;b&gt;Abstract - &lt;/b&gt;High-resolution palynological data sets
from shallow marine Triassic-Jurassic (Tr/J) boundary beds of two principal
sections in Europe (Hochalplgraben in Austria and St. Audrie's Bay in the
United Kingdom) were analyzed to reconstruct changes in vegetation,
biodiversity, and climate. In Hochalplgraben, a hardwood gymnosperm forest with
conifers and seed ferns is replaced by vegetation with dominant ferns, club
mosses and liverworts, which concurs with an increased diversification of spore
types during the latest Rhaetian. Multivariate statistical analysis reveals a
trend to warmer and wetter conditions across the Tr/J boundary in
Hochalplgraben. The vegetation changes in St. Audrie's Bay are markedly
different. Here, a mixed gymnosperm forest is replaced by monotonous vegetation
consisting mainly of Cheirolepidiaceae (80–100%). This change is caused by a
transition to a warmer and more arid climate. The observed diversity decrease
in St. Audrie's Bay affirms this interpretation. Although both sections show major
vegetation changes, neither of them demonstrates a distinctive floral mass
extinction. A compilation of Tr/J boundary sections across the world
demonstrates the presence of Cheirolepidiaceae-dominated forests in the
Pangaean interior and increases in abundance of spore-producing plants adjacent
to the Tethys Ocean. We propose that the non-uniform vegetation changes
reflected in the Tr/J palynological records are the result of environmental
changes caused by Central Atlantic Magmatic Province volcanism. The increase in
greenhouse gases caused a warmer climate and an enhanced thermal contrast
between the continent and the seas. Consequently, the monsoon system got
stronger and induced a drier continental interior and more intensive rainfall
near the margins of the Tethys Ocean.&lt;/div&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-3083290693149822354?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/iNgom5kkLtQ" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/3083290693149822354/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/vegetation-history-and-climate-change.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/3083290693149822354?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/3083290693149822354?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/iNgom5kkLtQ/vegetation-history-and-climate-change.html" title="Vegetation History and Climate Change Across the Tr/J Boundary" /><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/2012/03/vegetation-history-and-climate-change.html</feedburner:origLink></entry><entry gd:etag="W/&quot;DE4DSH06fSp7ImA9WhVRGUo.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-317118612262871630</id><published>2012-03-28T16:22:00.001-07:00</published><updated>2012-03-28T16:22:59.315-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-28T16:22:59.315-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="pneumaticity" /><category scheme="http://www.blogger.com/atom/ns#" term="evolution" /><category scheme="http://www.blogger.com/atom/ns#" term="functional morphology" /><category scheme="http://www.blogger.com/atom/ns#" term="archosauria" /><title>Postcranial Skeletal Pneumaticity in Triassic Archosaurs</title><content type="html">&lt;br /&gt;
&lt;b&gt;Butler, R. J.,&amp;nbsp;Barrett, P. M., and D. J. Gower. 2012. Reassessment of the evidence for postcranial skeletal pneumaticity in Triassic archosaurs, and the early evolution&amp;nbsp;&lt;/b&gt;&lt;b&gt;of the avian respiratory system. PLoS ONE 7(3): e34094. &lt;a href="http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0034094"&gt;doi:10.1371/journal.pone.0034094&lt;/a&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;Abstract -&lt;/b&gt; Uniquely among extant vertebrates, birds possess complex respiratory systems characterised by the combination of small,&amp;nbsp;rigid lungs, extensive pulmonary air sacs that possess diverticula that invade (pneumatise) the postcranial skeleton,&amp;nbsp;unidirectional ventilation of the lungs, and efficient crosscurrent gas exchange. Crocodilians, the only other living&amp;nbsp;archosaurs, also possess unidirectional lung ventilation, but lack true air sacs and postcranial skeletal pneumaticity (PSP).&amp;nbsp;PSP can be used to infer the presence of avian-like pulmonary air sacs in several extinct archosaur clades (non-avian&amp;nbsp;theropod dinosaurs, sauropod dinosaurs and pterosaurs). However, the evolution of respiratory systems in other archosaurs,&amp;nbsp;especially in the lineage leading to crocodilians, is poorly documented. Here, we use mCT-scanning to investigate the&amp;nbsp;vertebral anatomy of Triassic archosaur taxa, from both the avian and crocodilian lineages as well as non-archosaurian&amp;nbsp;diapsid outgroups. Our results confirm previous suggestions that unambiguous evidence of PSP (presence of internal&amp;nbsp;pneumatic cavities linked to the exterior by foramina) is found only in bird-line (ornithodiran) archosaurs. We propose that&amp;nbsp;pulmonary air sacs were present in the common ancestor of Ornithodira and may have been subsequently lost or reduced&amp;nbsp;in some members of the clade (notably in ornithischian dinosaurs). The development of these avian-like respiratory features&amp;nbsp;might have been linked to inferred increases in activity levels among ornithodirans. By contrast, no crocodile-line archosaur&amp;nbsp;(pseudosuchian) exhibits evidence for unambiguous PSP, but many of these taxa possess the complex array of vertebral&amp;nbsp;laminae and fossae that always accompany the presence of air sacs in ornithodirans. These laminae and fossae are likely&amp;nbsp;homologous with those in ornithodirans, which suggests the need for further investigation of the hypothesis that a&amp;nbsp;reduced, or non-invasive, system of pulmonary air sacs may be have been present in these taxa (and secondarily lost in&amp;nbsp;extant crocodilians) and was potentially primitive for Archosauria as a whole.&lt;br /&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-317118612262871630?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/ysjgFhPWrzA" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/317118612262871630/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/postcranial-skeletal-pneumaticity-in.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/317118612262871630?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/317118612262871630?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/ysjgFhPWrzA/postcranial-skeletal-pneumaticity-in.html" title="Postcranial Skeletal Pneumaticity in Triassic Archosaurs" /><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/2012/03/postcranial-skeletal-pneumaticity-in.html</feedburner:origLink></entry><entry gd:etag="W/&quot;C0UERn49eyp7ImA9WhVRFE8.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-8874341389020378302</id><published>2012-03-22T06:00:00.000-07:00</published><updated>2012-03-22T06:00:07.063-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-22T06:00:07.063-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Taphonomy" /><category scheme="http://www.blogger.com/atom/ns#" term="rhynchosaurs" /><category scheme="http://www.blogger.com/atom/ns#" term="India" /><category scheme="http://www.blogger.com/atom/ns#" term="Upper Triassic" /><title>Taphonomy of an Upper Triassic Rhynchosaur Bonebed From India</title><content type="html">&lt;br /&gt;
&lt;b&gt;Mukherje, D. and &amp;nbsp;&amp;amp; S. Ray. 2012.&amp;nbsp;Taphonomy of an Upper Triassic vertebrate bonebed: A new rhynchosaur&amp;nbsp;&lt;/b&gt;&lt;b&gt;(Reptilia; Archosauromorpha) accumulation from India.&amp;nbsp;Palaeogeography, Palaeoclimatology, Palaeoecology (advance online publication)&amp;nbsp;&lt;a href="http://dx.doi.org/10.1016/j.palaeo.2012.03.010"&gt;http://dx.doi.org/10.1016/j.palaeo.2012.03.010&lt;/a&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;Abstract -&lt;/b&gt; The Upper Triassic Tiki Formation of India is a rich storehouse of&amp;nbsp;varied vertebrate fossil assemblages. So far, there is no information&amp;nbsp;on taphonomic signatures of the Tiki vertebrate assemblages in&amp;nbsp;comparison to that of other fossiliferous horizons of India. We report&amp;nbsp;a new, low diversity, mono-dominant, multitaxic vertebrate&amp;nbsp;accumulation where rhynchosaurs constitute the dominant component. The&amp;nbsp;formation of the rhynchosaur bonebed is attributed to biological&amp;nbsp;aggregation with a hydraulic overprint resulting in a mixed-origin&amp;nbsp;concentration. Other taxa include rauisuchid, phytosaur, small&amp;nbsp;indeterminate archosaur and cynodonts. Taphonomic study based on 617&amp;nbsp;skeletal specimens of rhynchosaurs collected from nine sites within an&amp;nbsp;area of about 250x217 sq m shows that most of the specimens are&amp;nbsp;disarticulated and disassociated but in close spatial proximity to one&amp;nbsp;another; some are associated specimens and few are articulated. About&amp;nbsp;13 to 20 individuals of rhynchosaur at different ontogenetic stages&amp;nbsp;are estimated from the specimens collected, suggesting gregarious&amp;nbsp;behaviour, possibly herding. These specimens show varying degree of&amp;nbsp;weathering, breakage, encrustation, abrasion and deformation. The&amp;nbsp;bonebed is preserved within the Tiki red mudstone unit and is found in&amp;nbsp;association with paleosol profiles, suggesting prolonged subaerial&amp;nbsp;exposure. Spatial distribution and relative bone frequencies show&amp;nbsp;differential susceptibility of the skeletal specimens to fluvial&amp;nbsp;transport. 55.4% of the collected skeletal specimens belonged to&amp;nbsp;Voorhies Group I, whereas 12.4% and 24% constituted Voorhies Group II&amp;nbsp;and III respectively, and 8.2% of the collected specimens belonged to&amp;nbsp;the intermediate group I and II. It appears that the animals&amp;nbsp;concentrated in the vicinity of the water sources during prolonged&amp;nbsp;period of aridity and died possibly during high seasonal rainfall that&amp;nbsp;resulted in a major flood event. Subsequently, the soft tissues&amp;nbsp;decomposed, and the skeletons suffered prolonged subaerial exposure&amp;nbsp;when the water receded leading to disarticulation and fragmentation&amp;nbsp;followed by minor dispersion by low velocity water currents. This&amp;nbsp;resulted in segregation of skeletal specimens, which were gradually&amp;nbsp;covered by mud deposited during later flooding events. Based on the&amp;nbsp;known flora and fauna, the Tiki Upper Triassic ecosystem is&amp;nbsp;reconstructed for the first time. In the aquatic ecosystem, the&amp;nbsp;metoposaurid labyrinthodonts occupied the top of the food pyramid&amp;nbsp;together with the semi-aquatic parasuchids, which occupied an&amp;nbsp;ecological niche similar to that of the present day crocodilians. The&amp;nbsp;abundance of herbivorous rhynchosaurs at the base with few large and&amp;nbsp;carnivorous rauisuchids and parasuchids at the top suggest a trophic&amp;nbsp;structure similar to that of a modern day terrestrial ecosystem.&lt;br /&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-8874341389020378302?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=bJmGUkRImZo:qWWpIFTMKN0: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=bJmGUkRImZo:qWWpIFTMKN0: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=bJmGUkRImZo:qWWpIFTMKN0: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=bJmGUkRImZo:qWWpIFTMKN0:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=bJmGUkRImZo:qWWpIFTMKN0:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=bJmGUkRImZo:qWWpIFTMKN0:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=bJmGUkRImZo:qWWpIFTMKN0:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=bJmGUkRImZo:qWWpIFTMKN0: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=bJmGUkRImZo:qWWpIFTMKN0:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=bJmGUkRImZo:qWWpIFTMKN0:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/bJmGUkRImZo" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/8874341389020378302/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/taphonomy-of-upper-triassic-rhynchosaur.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/8874341389020378302?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/8874341389020378302?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/bJmGUkRImZo/taphonomy-of-upper-triassic-rhynchosaur.html" title="Taphonomy of an Upper Triassic Rhynchosaur Bonebed From India" /><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/2012/03/taphonomy-of-upper-triassic-rhynchosaur.html</feedburner:origLink></entry><entry gd:etag="W/&quot;DEMER3Y7cSp7ImA9WhVRE0g.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-4091784698286326344</id><published>2012-03-21T12:00:00.000-07:00</published><updated>2012-03-21T12:00:06.809-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-21T12:00:06.809-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="phylogenetic analysis" /><category scheme="http://www.blogger.com/atom/ns#" term="turtles" /><title>Revised Phylogeny of Basal Turtles</title><content type="html">&lt;br /&gt;
&lt;b&gt;Anquetin, J. 2012. Reassessment of the phylogenetic interrelationships of basal turtles (Testudinata). Journal of Systematic Palaeontology 10:3-45. doi: http://dx.doi.org/10.1080/14772019.2011.558928&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;Abstract -&lt;/b&gt; Recent discoveries from the Late Triassic and Middle Jurassic have significantly improved the fossil record of early turtles.&amp;nbsp;These new forms offer a unique opportunity to test the interrelationships of basal turtles. Nineteen fossil species are added&amp;nbsp;to the taxon sample of the most comprehensive morphological phylogenetic analysis of the turtle clade. Among these&amp;nbsp;additional species are recently discovered forms (e.g. &lt;i&gt;Odontochelys semitestacea, Eileanchelys waldmani, Condorchelys&amp;nbsp;antiqua&lt;/i&gt;), taxa generally omitted from previous analyses (e.g. chengyuchelyids, &lt;i&gt;Sichuanchelys chowi&lt;/i&gt;) and species included&amp;nbsp;in a phylogenetic analysis for the first time (&lt;i&gt;Naomichelys speciosa&lt;/i&gt; and &lt;i&gt;Siamochelys peninsularis&lt;/i&gt;). The coding of several&amp;nbsp;characters is reassessed in the light of recent observations, but also in order to reduce unwarranted assumptions on character&amp;nbsp;and character state homologies. Additional characters from previous analyses, as well as five new ones, are also included,&amp;nbsp;resulting in a data matrix of 178 characters scored for 86 turtle species and seven fossil outgroups. The dataset resolves&amp;nbsp;the relationships of most newly included taxa, with the exception of &lt;i&gt;S. chowi&lt;/i&gt; and ‘&lt;i&gt;Chengyuchelys&lt;/i&gt;’ &lt;i&gt;dashanpuensis&lt;/i&gt;. The&amp;nbsp;phylogenetic placement of &lt;i&gt;Heckerochelys romani&lt;/i&gt;, &lt;i&gt;Condorchelys antiqua&lt;/i&gt; and &lt;i&gt;Eileanchelys waldmani&lt;/i&gt; as stem turtles more&amp;nbsp;derived than &lt;i&gt;Kayentachelys aprix &lt;/i&gt;but more basal than &lt;i&gt;Meiolania platyceps&lt;/i&gt; and &lt;i&gt;Mongolochelys efremovi&lt;/i&gt; is corroborated. The&amp;nbsp;relationships of chengyuchelyids remain unclear and they are unstable with respect to stem turtles. In contrast to previous&amp;nbsp;analyses, &lt;i&gt;Arundelemys dardeni&lt;/i&gt; is placed within pleurosternids and &lt;i&gt;Siamochelys peninsularis&lt;/i&gt; falls within xinjiangchelyids.&amp;nbsp;Perhaps the most salient conclusion of the present study is the placement of &lt;i&gt;Naomichelys speciosa&lt;/i&gt; as a basal member of a&amp;nbsp;clade uniting meiolaniids, &lt;i&gt;Mongolochelys efremovi &lt;/i&gt;and &lt;i&gt;Otwayemys cunicularius&lt;/i&gt;. This clade of rather large stem turtles had&amp;nbsp;a worldwide spread during the Mesozoic at least, and persisted until the Pleistocene with meiolaniids.&lt;br /&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-4091784698286326344?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/ZXCKXvCyCOQ" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/4091784698286326344/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/revised-phylogeny-of-basal-turtles.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4091784698286326344?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4091784698286326344?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/ZXCKXvCyCOQ/revised-phylogeny-of-basal-turtles.html" title="Revised Phylogeny of Basal Turtles" /><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/2012/03/revised-phylogeny-of-basal-turtles.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CUYAQX07fip7ImA9WhVRE0w.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-3072539241751762704</id><published>2012-03-20T23:59:00.000-07:00</published><updated>2012-03-20T23:59:00.306-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-20T23:59:00.306-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Early Triassic" /><category scheme="http://www.blogger.com/atom/ns#" term="functional morphology" /><category scheme="http://www.blogger.com/atom/ns#" term="procolophonids" /><title>Further Evidence of Burrowing in Procolophonid Parareptiles</title><content type="html">&lt;br /&gt;
&lt;div class="caption"&gt;
&lt;b&gt;MacDougall, M. J., Modesto, S. P., and J. Botha-Brink. 2012.&amp;nbsp;The postcranial skeleton of the Early Triassic parareptile &lt;i&gt;Sauropareion anoplus&lt;/i&gt;, with a discussion of possible life history.&amp;nbsp;&lt;em&gt;Acta Palaeontologica Polonica&lt;/em&gt; in press. Available 
online 27 Feb 2012 &lt;a href="http://www.app.pan.pl/article/item/app20110099.html"&gt;doi: http://dx.doi.org/10.4202/app.2011.0099.&lt;/a&gt;&lt;/b&gt;&lt;/div&gt;
&lt;div class="caption"&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;/div&gt;
&lt;br /&gt;

&lt;div class="ce_text"&gt;

&lt;div id="abstract"&gt;

&lt;/div&gt;
&lt;b&gt;Abstract - &lt;/b&gt;The skeletal anatomy of the Early Triassic (Induan) procolophonid reptile 
&lt;i&gt;Sauropareion anoplus&lt;/i&gt; is described on the basis of three partial skeletons from 
Vangfontein, Middelburg District, South Africa. Together these three specimens 
preserve the large majority of the pectoral and pelvic girdles, articulated 
forelimbs and hindlimbs, and all but the caudal portion of the vertebral column, 
elements hitherto undescribed. Our phylogenetic analysis of the Procolophonoidea 
is consonant with previous work, positing &lt;i&gt;S. anoplus&lt;/i&gt; as the sister taxon to a 
clade composed of all other procolophonids exclusive of &lt;i&gt;Coletta seca&lt;/i&gt;. Previous 
studies have suggested that procolophonids were burrowers, and this seems to 
have been the case for &lt;i&gt;S. anoplus&lt;/i&gt;, based on comparisons with characteristic 
skeletal anatomy of living digging animals, such as the presence of a 
spade-shaped skull, robust phalanges, and large unguals.&lt;/div&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-3072539241751762704?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=Ayx43B1z-04:abUV2ppUg4M: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=Ayx43B1z-04:abUV2ppUg4M: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=Ayx43B1z-04:abUV2ppUg4M: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=Ayx43B1z-04:abUV2ppUg4M:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=Ayx43B1z-04:abUV2ppUg4M:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=Ayx43B1z-04:abUV2ppUg4M:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=Ayx43B1z-04:abUV2ppUg4M:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=Ayx43B1z-04:abUV2ppUg4M: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=Ayx43B1z-04:abUV2ppUg4M:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=Ayx43B1z-04:abUV2ppUg4M:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/Ayx43B1z-04" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/3072539241751762704/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/further-evidence-of-burrowing-in.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/3072539241751762704?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/3072539241751762704?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/Ayx43B1z-04/further-evidence-of-burrowing-in.html" title="Further Evidence of Burrowing in Procolophonid Parareptiles" /><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/2012/03/further-evidence-of-burrowing-in.html</feedburner:origLink></entry><entry gd:etag="W/&quot;Ck8EQXo6cCp7ImA9WhVREkU.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-4955655442052137341</id><published>2012-03-20T15:00:00.000-07:00</published><updated>2012-03-20T15:00:00.418-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-20T15:00:00.418-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="China" /><category scheme="http://www.blogger.com/atom/ns#" term="Early Triassic" /><category scheme="http://www.blogger.com/atom/ns#" term="Coelocanths" /><title>Earliest Evidence of Ovoviviparity in Coelocanths</title><content type="html">&lt;b&gt;Wen, W., Zhang, Q.-Y., Hu, S.-X., Benton, M. J., Zhou, C.-Y., Tao, X., Yuan, H.-J., and Z.-Q., Chen. 2012. Coelacanths from the Middle Triassic Luoping Biota, Yunnan, South China, with the earliest evidence of ovoviviparity. Acta Palaeontologica Polonica in press. Available online 08 Mar 2012 &lt;a href="http://www.app.pan.pl/article/item/app20110066.html"&gt;doi: http://dx.doi.org/10.4202/app.2011.0066&lt;/a&gt;&lt;/b&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;div class="ce_text"&gt;
&lt;div id="abstract"&gt;
&lt;/div&gt;
&lt;b&gt;Abstract - &lt;/b&gt;The fossil record of coelacanths is patchy, with very few taxa known from the 
Triassic of Asia. We report here two new genera and species of coelacanths from 
the Luoping Biota, a recently found site of exceptional fossil preservation from 
Yunnan, South China. The first new taxon, &lt;i&gt;Luopingcoelacanthus eurylacrimalis&lt;/i&gt;, is 
based on four specimens, which together show most aspects of the anatomy. One 
specimen shows two small coelacanths inside the ventral portion of the abdominal 
cavity, and these are interpreted as intrauterine embryos, close to birth size, 
based on comparisons with previously reported embryos of the fossil coelacanths 
&lt;i&gt;Rhabdoderma&lt;/i&gt; and &lt;i&gt;Undina&lt;/i&gt;, and the extant genus &lt;i&gt;Latimeria&lt;/i&gt;. Our new find extends the 
evidence for ovoviviparity in coelacanths back from the Late Jurassic to the 
Middle Triassic. The second new taxon, &lt;i&gt;Yunnancoelacanthus acrotuberculatus&lt;/i&gt;, is 
based on one specimen, and differs from&lt;i&gt; Luopingcoelacanthus&lt;/i&gt; in the dentary, 
lachrymojugal, number of rays of the first dorsal fin, and especially in the 
ornament on dermal bones and scales. A cladistic analysis shows that the new 
taxa are closest relatives to the derived clade Latimerioidei. The relatively 
high diversity of coelacanths in the Early Triassic, and adaptations of living 
&lt;i&gt;Latimeria&lt;/i&gt; to low-oxygen conditions, suggests that the group may have included 
‘disaster taxa’ that benefited from anoxic and dysoxic ocean conditions in the 
aftermath of the end-Permian mass extinction.&lt;/div&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-4955655442052137341?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=24rI5MKYnms:qX6G2F7deJo: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=24rI5MKYnms:qX6G2F7deJo: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=24rI5MKYnms:qX6G2F7deJo: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=24rI5MKYnms:qX6G2F7deJo:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=24rI5MKYnms:qX6G2F7deJo:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=24rI5MKYnms:qX6G2F7deJo:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=24rI5MKYnms:qX6G2F7deJo:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=24rI5MKYnms:qX6G2F7deJo: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=24rI5MKYnms:qX6G2F7deJo:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=24rI5MKYnms:qX6G2F7deJo:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/24rI5MKYnms" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/4955655442052137341/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/earliest-evidence-of-ovoviviparity-in.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4955655442052137341?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4955655442052137341?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/24rI5MKYnms/earliest-evidence-of-ovoviviparity-in.html" title="Earliest Evidence of Ovoviviparity in Coelocanths" /><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/2012/03/earliest-evidence-of-ovoviviparity-in.html</feedburner:origLink></entry><entry gd:etag="W/&quot;C0ECQXgzeyp7ImA9WhVREks.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-3382352209180667576</id><published>2012-03-20T09:41:00.000-07:00</published><updated>2012-03-20T09:41:00.683-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-20T09:41:00.683-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="vertebrae" /><category scheme="http://www.blogger.com/atom/ns#" term="evolution" /><category scheme="http://www.blogger.com/atom/ns#" term="sauropodomorphs" /><title>Early Evolution of Postcranial Skeletal Pneumaticity in Sauropodomorph Dinosaurs</title><content type="html">&lt;br /&gt;
&lt;div class="abstractSection"&gt;

&lt;h3 class="abstractTitle"&gt;
&lt;/h3&gt;
&lt;div class="last"&gt;
I don't think I've posted this paper previously, but it has been in press for a year...&lt;/div&gt;
&lt;div class="last"&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;/div&gt;
&lt;div class="last"&gt;
&lt;b&gt;Yates, A. M., Wedel, M. J., and M. F. Bonnan. 2012.&amp;nbsp;The early evolution of postcranial skeletal pneumaticity in sauropodomorph 
dinosaurs.&amp;nbsp;Acta Palaeontologica Polonica 57:85-100. &amp;nbsp;&lt;/b&gt;&lt;/div&gt;
&lt;b&gt;doi: &lt;a href="http://dx.doi.org/10.4202/app.2010.0075"&gt;http://dx.doi.org/10.4202/app.2010.0075&lt;/a&gt;&lt;/b&gt;&lt;div class="last"&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;/div&gt;
&lt;div class="last"&gt;
&lt;b&gt;Abstract - &lt;/b&gt;Postcranial skeletal pneumaticity (PSP) is present in a range of 
basal sauropodomorphs spanning the basal sauropodomorph—sauropod transition. We 
describe the PSP of five taxa, &lt;i&gt;Plateosaurus engelhardti, Eucnemesaurus 
fortis, Aardonyx celestae, Antetonitrus ingenipes&lt;/i&gt;, and an unnamed basal 
sauropod from Spion Kop, South Africa (hereafter referred to as the Spion Kop 
sauropod). The PSP of &lt;i&gt;Plateosaurus&lt;/i&gt; is apparently sporadic in its 
occurrence and has only been observed in very few specimens, in which it is of 
very limited extent, affecting only the posterior cervical vertebrae and 
possibly the mid dorsals in one specimen. The PSP of &lt;i&gt;Eucnemesaurus, Aardonyx, 
Antetonitrus&lt;/i&gt;, and the Spion Kop sauropod consists of subfossae 
(fossa within-fossa structures) that excavate the vertices of the posterior 
infradiapophyseal fossae of the posterior dorsal vertebrae. These subfossae 
range from simple shallow depressions (&lt;i&gt;Eucnemesaurus&lt;/i&gt;) to deep, 
steepsided, internally subdivided and asymmetrically developed chambers 
(&lt;i&gt;Antetonitrus&lt;/i&gt;). The middle and anterior dorsal vertebrae of these taxa 
lack PSP, demonstrating that abdominal air sacs were the source of the invasive 
diverticula. The presence of pneumatic features within the infradiapophyseal 
fossae suggest that the homologous fossae of more basal saurischians and 
dinosauriforms were receptacles that housed pneumatic diverticula. We suggest 
that it is probable that rigid non-compliant lungs ventilated by compliant 
posterior air sacs evolved prior to the origination of Dinosauria.&lt;/div&gt;
&lt;/div&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-3382352209180667576?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/b_7HAgJFJDw" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/3382352209180667576/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/early-evolution-of-postcranial-skeletal.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/3382352209180667576?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/3382352209180667576?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/b_7HAgJFJDw/early-evolution-of-postcranial-skeletal.html" title="Early Evolution of Postcranial Skeletal Pneumaticity in Sauropodomorph Dinosaurs" /><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/2012/03/early-evolution-of-postcranial-skeletal.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CUYFR3s_eCp7ImA9WhVREUo.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-8833672070290532397</id><published>2012-03-19T09:05:00.000-07:00</published><updated>2012-03-19T09:05:16.540-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-19T09:05:16.540-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="India" /><category scheme="http://www.blogger.com/atom/ns#" term="cynodont" /><category scheme="http://www.blogger.com/atom/ns#" term="Early Triassic" /><title>Panchetocynodon damodarensis, a New Cynodont from the Lower Triassic of India</title><content type="html">&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;Das, D. P., and A. Gupta. 2012.&amp;nbsp;New cynodont record from the lower Triassic Panchet Formation, Damodar valley.&amp;nbsp;Earth and Environmental Science Journal of the Geological Society of India&amp;nbsp;Volume 79, Number 2, 175-180&amp;nbsp;&lt;a href="http://www.springerlink.com/content/u85484576365lp51/"&gt;DOI: 10.1007/s12594-012-0022-2&lt;/a&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;Abstract -&lt;/b&gt; This paper reports the find of a new non-mammalian cynodont from the&amp;nbsp;Lower Triassic Panchet Formation of the Damodar valley, West Bengal,&amp;nbsp;India. The fossil, recovered from a clay pellet rich calcareous&amp;nbsp;sandstone bed, is a part of left lower jaw having five post canines&amp;nbsp;that are damaged to various extents. A combination of mammal-like&amp;nbsp;advanced characters such as much enlarged dentary, reduced post&amp;nbsp;dentary bones, high coronoid process, large masseteric fossa, each&amp;nbsp;post canine with a large central cusp flanked by a distal and a mesial&amp;nbsp;accessory cusps with two additional lingually positioned cingular&amp;nbsp;cusps, incipient root division and clearly demarcated crown-root&amp;nbsp;juncture prompted to erect a new taxon &lt;i&gt;Panchetocynodon damodarensis&amp;nbsp;&lt;/i&gt;gen. et sp. nov.&lt;br /&gt;
&lt;br /&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-8833672070290532397?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=vKlBPQSIvb4:rv4w87323r4: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=vKlBPQSIvb4:rv4w87323r4: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=vKlBPQSIvb4:rv4w87323r4: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=vKlBPQSIvb4:rv4w87323r4:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=vKlBPQSIvb4:rv4w87323r4:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=vKlBPQSIvb4:rv4w87323r4:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=vKlBPQSIvb4:rv4w87323r4:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=vKlBPQSIvb4:rv4w87323r4: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=vKlBPQSIvb4:rv4w87323r4:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=vKlBPQSIvb4:rv4w87323r4:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/vKlBPQSIvb4" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/8833672070290532397/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/panchetocynodon-damodarensis-new.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/8833672070290532397?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/8833672070290532397?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/vKlBPQSIvb4/panchetocynodon-damodarensis-new.html" title="&lt;i&gt;Panchetocynodon damodarensis&lt;/i&gt;, a New Cynodont from the Lower Triassic of India" /><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/2012/03/panchetocynodon-damodarensis-new.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CE8BRXozfyp7ImA9WhVSGUw.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-8381151716613497802</id><published>2012-03-16T08:47:00.003-07:00</published><updated>2012-03-16T08:47:34.487-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-16T08:47:34.487-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Pseudosuchia" /><category scheme="http://www.blogger.com/atom/ns#" term="Gracilisuchus" /><category scheme="http://www.blogger.com/atom/ns#" term="Argentina" /><title>Hind limb osteology of Gracilisuchus stipanicicorum</title><content type="html">&lt;br /&gt;
&lt;b&gt;Lecuona, A., and J. B. Desojo 2011.&amp;nbsp;Hind limb osteology of &lt;i&gt;Gracilisuchus&lt;/i&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;&lt;i&gt;stipanicicorum&lt;/i&gt; (Archosauria: Pseudosuchia).&amp;nbsp;Earth and Environmental Science Transactions of the Royal Society of Edinburgh, 102, 105–128.&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;Abstract -&lt;/b&gt; &lt;i&gt;Gracilisuchus stipanicicorum&lt;/i&gt; Romer, 1972, from the Middle-Late Triassic of the&amp;nbsp;Ischigualasto–Villa Unio´n Basin of Argentina, is an extinct pseudosuchian archosaur on the stem to&amp;nbsp;Crocodylomorpha. The pelvic girdle and hind limb anatomy of a referred specimen of &lt;i&gt;Gracilisuchus&amp;nbsp;&lt;/i&gt;&lt;i&gt;stipanicicorum&lt;/i&gt; is described and compared with that from a broad range of archosauriform taxa,&amp;nbsp;including basal members such as crurotarsans and basal ornithodirans. The description of this&amp;nbsp;specimen reveals new information on the anatomy of the pelvic girdle and hind limb of &lt;i&gt;Gracilisuchus&lt;/i&gt;,&amp;nbsp;through a detailed examination of some anatomical regions barely or not previously described, as&amp;nbsp;well as reinterpretations of previous features. The phylogenetic affinities of &lt;i&gt;Gracilisuchus&lt;/i&gt; within the&amp;nbsp;Archosauria remain to be tested, but &lt;i&gt;Gracilisuchus&lt;/i&gt; shares two putative synapomorphies with some&amp;nbsp;non-crocodyliform crocodylomorphs, providing tentative support for the monophyly of Sphenosuchia&amp;nbsp;(e.g., Sereno &amp;amp; Wild 1992; Wu &amp;amp; Chatterjee 1993) and the close relationship of &lt;i&gt;Gracilisuchus&amp;nbsp;&lt;/i&gt;to that clade. These characteristics are: (i) the morphology and poor development of the femoral&amp;nbsp;fourth trochanter, closely resembling the condition of &lt;i&gt;Pseudhesperosuchus&lt;/i&gt; and &lt;i&gt;Trialestes&lt;/i&gt;; and (ii) a&amp;nbsp;poor anterior development of the femoral head, shared with &lt;i&gt;Pseudhesperosuchus&lt;/i&gt;. On the other hand&amp;nbsp;there are characters that reject the inclusion of &lt;i&gt;Gracilisuchus&lt;/i&gt; within Crocodylomorpha (Nesbitt&amp;nbsp;2011), such as the absence of an imperforated acetabulum, and that rather suggests a sister-taxon&amp;nbsp;position to Crocodylomorpha.&lt;br /&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-8381151716613497802?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=qbpvqZAE3Oc:lxOfrtBNQn4: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=qbpvqZAE3Oc:lxOfrtBNQn4: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=qbpvqZAE3Oc:lxOfrtBNQn4: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=qbpvqZAE3Oc:lxOfrtBNQn4:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=qbpvqZAE3Oc:lxOfrtBNQn4:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=qbpvqZAE3Oc:lxOfrtBNQn4:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=qbpvqZAE3Oc:lxOfrtBNQn4:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=qbpvqZAE3Oc:lxOfrtBNQn4: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=qbpvqZAE3Oc:lxOfrtBNQn4:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=qbpvqZAE3Oc:lxOfrtBNQn4:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/qbpvqZAE3Oc" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/8381151716613497802/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/hind-limb-osteology-of-gracilisuchus.html#comment-form" title="3 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/8381151716613497802?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/8381151716613497802?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/qbpvqZAE3Oc/hind-limb-osteology-of-gracilisuchus.html" title="Hind limb osteology of &lt;i&gt;Gracilisuchus stipanicicorum&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>3</thr:total><feedburner:origLink>http://chinleana.fieldofscience.com/2012/03/hind-limb-osteology-of-gracilisuchus.html</feedburner:origLink></entry><entry gd:etag="W/&quot;DEQEQHs5eyp7ImA9WhVSEk8.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-6548232467417564876</id><published>2012-03-08T06:00:00.000-07:00</published><updated>2012-03-08T10:05:01.523-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-08T10:05:01.523-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Antarctica" /><category scheme="http://www.blogger.com/atom/ns#" term="apomorphy-based identifications" /><category scheme="http://www.blogger.com/atom/ns#" term="Therapsida" /><title>Reevaluation of Therapsid Fossils from Antarctica</title><content type="html">&lt;strong&gt;Huttenlocker, A. K.,&amp;nbsp;and C. A. Sidor. 2012. Taxonomic Revision of Therocephalians (Therapsida: Theriodontia) from the Lower Triassic of Antarctica. &lt;a href="http://digitallibrary.amnh.org/dspace/handle/2246/6163"&gt;American Museum Novitates Number 3738 :1-19. &lt;/a&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; We reevaluate the taxonomic status of therocephalian fossils recovered from the lower Fremouw Formation (Lower Triassic) of the central Transantarctic Mountains, Antarctica. The material, which includes mostly fragmentary juvenile specimens, is reidentified using an apomorphy-based approach. We recognize the presence of three higher-level taxa: Eutherocephalia, Akidnognathidae, and Baurioidea. The only genus-level identification is for a partial lower jaw and pterygoid tentatively attributed to the baurioid, &lt;em&gt;Ericiolacerta parva&lt;/em&gt;. An indeterminate theriodont partial skull is reassigned to the therocephalian family Akidnognathidae. The holotypes of &lt;em&gt;Pedaeosaurus parvus&lt;/em&gt; and &lt;em&gt;Rhigosaurus glacialis&lt;/em&gt; are represented by indeterminate juvenile baurioids and, in the absence of clear autapomorphies, are considered nomina dubia. The results of the taxonomic revision indicate that the therocephalian fauna of Antarctica lacks endemic genera and thus corresponds to that of the Triassic Lystrosaurus Assemblage Zone fauna of South Africa's Karoo Basin. More generally, we consider the southern Gondwanan basins of South Africa and Antarctica to sample a broadly distributed Lower Triassic tetrapod fauna, although the latter basin documents the first occurrence of several taxa (e.g., &lt;em&gt;Kombuisia&lt;/em&gt;, &lt;em&gt;Palacrodon&lt;/em&gt;). More precise (i.e., species-level) identifications are needed to better constrain the biogeographic signal for therocephalians, but the presence of juveniles strongly suggests that this group of therapsids, like dicynodonts, were year-round high-latitude inhabitants during Early Triassic times.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-6548232467417564876?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/vxunXumS9XY" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/6548232467417564876/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/reevaluation-of-therapsis-fossils-from.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/6548232467417564876?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/6548232467417564876?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/vxunXumS9XY/reevaluation-of-therapsis-fossils-from.html" title="Reevaluation of Therapsid Fossils from Antarctica" /><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/2012/03/reevaluation-of-therapsis-fossils-from.html</feedburner:origLink></entry><entry gd:etag="W/&quot;DEAMSHkzfip7ImA9WhVSEUo.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-9185604262292193160</id><published>2012-03-07T20:19:00.003-07:00</published><updated>2012-03-07T20:19:49.786-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-07T20:19:49.786-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="basal dinosaurs" /><category scheme="http://www.blogger.com/atom/ns#" term="Brazil" /><category scheme="http://www.blogger.com/atom/ns#" term="sauropodomorphs" /><title>Possible New Plateosaurid Sauropodomorph From Brazil</title><content type="html">&lt;strong&gt;B&lt;span class="smallcaps"&gt;ittencourt&lt;/span&gt;, J.S., L&lt;span class="smallcaps"&gt;eal&lt;/span&gt;, L.A., L&lt;span class="smallcaps"&gt;anger&lt;/span&gt;, M.C. &amp;amp; A&lt;span class="smallcaps"&gt;zevedo&lt;/span&gt;, S.A.K., &lt;i&gt;iFirst&lt;/i&gt; article. An additional basal sauropodomorph specimen from the Upper Triassic Caturrita Formation, southern Brazil, with comments on the biogeography of plateosaurids. &lt;a href="http://www.tandfonline.com/doi/abs/10.1080/03115518.2012.634111"&gt;&lt;i&gt;Alcheringa&lt;/i&gt;, 1–10&lt;/a&gt;. &lt;/strong&gt;&lt;div class="first"&gt;
&lt;br /&gt;&lt;/div&gt;
&lt;strong&gt;Abstract - &lt;/strong&gt;We describe an additional saurischian specimen from the Caturrita Formation (Norian) of the Parana Basin, southern Brazil. This material was collected in the 1950s and remained unstudied due to its fragmentary condition. Detailed comparisons with other saurischians worldwide reveal that some characters of the ilium, including the low ventral projection of the medial wall of the acetabulum and its concave ventral margin, together with the short triangular shape of the pre-acetabular process and its mound-like dorsocaudal edge, resemble those of sauropodomorphs such as &lt;i&gt;Plateosaurus&lt;/i&gt; and &lt;i&gt;Riojasaurus&lt;/i&gt;. This set of traits suggests that MN 1326-V has affinities with basal Sauropodomorpha, probably closer to plateosaurians than to &lt;i&gt;Saturnalia&lt;/i&gt;-like taxa. Previous records of this clade in the Caturrita Formation include &lt;i&gt;Unaysaurus&lt;/i&gt;, which has been related to &lt;i&gt;Plateosaurus&lt;/i&gt; within Plateosauridae. Alternative schemes suggest that plateosaurids include &lt;i&gt;Plateosaurus&lt;/i&gt; plus the Argentinean ‘prosauropods’ &lt;i&gt;Coloradisaurus&lt;/i&gt; and &lt;i&gt;Riojasaurus&lt;/i&gt;. Both hypotheses raise biogeographic questions, as a close relationship between faunas from South America and Europe excluding Africa and North America is not supported by geological and biostratigraphical evidence. Additionally, the absence of plateosaurids in other continents suggests that the geographical distribution of this taxon is inconsistent with the geological history of western Pangaea, and this demands further investigations of the phylogeny of sauropodomorphs or improved sampling.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-9185604262292193160?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/N1u1XCHYxp4" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/9185604262292193160/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/possible-new-plateosaurid.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/9185604262292193160?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/9185604262292193160?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/N1u1XCHYxp4/possible-new-plateosaurid.html" title="Possible New Plateosaurid Sauropodomorph From Brazil" /><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/2012/03/possible-new-plateosaurid.html</feedburner:origLink></entry><entry gd:etag="W/&quot;DkIESX89fCp7ImA9WhVSEEg.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-4949615742685423544</id><published>2012-03-06T10:21:00.003-07:00</published><updated>2012-03-06T10:21:48.164-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-06T10:21:48.164-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Temnospondyli" /><category scheme="http://www.blogger.com/atom/ns#" term="South America" /><title>Arachana nigra, a New Temnospondyl from the Permo-Triassic of Uruguay</title><content type="html">&lt;br /&gt;
&lt;div class="abstract svAbstract"&gt;
&lt;div id="spar0005"&gt;
&lt;/div&gt;
&lt;div&gt;
&lt;b&gt;Piñeiro, G., Ramos, A., and C. Marsicano. 2012.&amp;nbsp;A rhinesuchid-like temnospondyl from the Permo-Triassic of 
Uruguay. Compte Rendus Palevol 11:65-78.&amp;nbsp;&lt;/b&gt;&lt;a href="http://dx.doi.org/10.1016/j.crpv.2011.07.007"&gt;&lt;b&gt;http://dx.doi.org/10.1016/j.crpv.2011.07.007&lt;/b&gt;&lt;/a&gt;&lt;/div&gt;
&lt;div&gt;
&lt;b&gt;&amp;nbsp;&lt;/b&gt;&lt;/div&gt;
&lt;div&gt;
&lt;b&gt;Abstract - &lt;/b&gt;A new temnospondyl species, &lt;em&gt;Arachana nigra,&lt;/em&gt; from the 
Permo-Triassic Buena Vista Formation of Uruguay is described. The holotypic and 
only known specimen consists of an almost complete skull lacking most of the 
snout, the tabular horns and the posterolateral corners of the skull table. As 
with other specimens from the same unit, &lt;em&gt;Arachana&lt;/em&gt; shows a transitional 
morphology. It shares several characters with rhinesuchids, such as the large 
size and the general shape of the skull, orbits positioned slightly posterior to 
the skull roof mid-length, a coarsely pitted dermal ornamentation lacking 
pustules, and a smoothly convex cheek contour. The palatal ramus of the 
pterygoid suturing with the vomer, and excluding the palatine and ectopterygoid 
from the margin of the interpterygoid vacuity, and the presence of a small 
basioccipital, visible in both occipital and ventral view, also resemble the 
conditions found in rhinesuchids and other basal temnospondyls. Other characters 
present in &lt;em&gt;Arachana,&lt;/em&gt; however, are commonly found in lydekkerinids, but 
are absent in almost all rhinesuchids: supratemporal excluded from otic notch; 
supraorbital and infraorbital sensory sulci encroaching the lacrimal, although 
lacking a step-like lacrimal flexure; otic notch not deeply incised; 
post-temporal fenestra large and rounded; occipital condyles well-separated from 
each other; palatine tooth row behind the palatine tusk reduced; pterygoid 
corpus slightly ornamented; and presence of an interorbital depression. This 
combination of primitive and derived characters is consistently present in most 
components of the Buena Vista fauna, which could thus be transitional between 
typical Permian and Triassic tetrapod communities found elsewhere. The location 
of the PTB in the Uruguayan sequence is controversial, mainly due to the lack of 
clear faunal correlations with other well-known sequences, such as those of 
southern Africa and Russia. Moreover, the mosaic-like character combinations in 
most of the recorded tetrapods ally them to both Triassic and Paleozoic groups, 
and this has complicated even more the possibility of age assignment. 
Transitional faunas associated with the PTB, such as the Russian Uppermost 
Permian faunas, could be equivalent to the unique Colonia Orozco fauna. If true, 
this scenario will substantially change estimates about survivorship rates, 
suggesting a speciation rate increase in temnospondyls after the 
Permian-Triassic event. Based on taxonomic, phylogenetic, and geochronologic 
data, the Buena Vista fauna allows us to quantify faunal turnover across the PTB 
and in the aftermath of the end Permian extinction event.&lt;/div&gt;
&lt;/div&gt;
&lt;hr id="Résumé" /&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-4949615742685423544?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=rjcuD23To84:8kcCIEO61yk: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=rjcuD23To84:8kcCIEO61yk: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=rjcuD23To84:8kcCIEO61yk: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=rjcuD23To84:8kcCIEO61yk:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=rjcuD23To84:8kcCIEO61yk:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=rjcuD23To84:8kcCIEO61yk:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=rjcuD23To84:8kcCIEO61yk:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=rjcuD23To84:8kcCIEO61yk: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=rjcuD23To84:8kcCIEO61yk:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=rjcuD23To84:8kcCIEO61yk:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/rjcuD23To84" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/4949615742685423544/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/arachana-nigra-new-temnospondyl-from.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4949615742685423544?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4949615742685423544?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/rjcuD23To84/arachana-nigra-new-temnospondyl-from.html" title="&lt;i&gt;Arachana nigra&lt;/i&gt;, a New Temnospondyl from the Permo-Triassic of Uruguay" /><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/2012/03/arachana-nigra-new-temnospondyl-from.html</feedburner:origLink></entry><entry gd:etag="W/&quot;DEMERXc_eyp7ImA9WhVSEE0.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-2728851972521338493</id><published>2012-03-05T21:00:00.000-07:00</published><updated>2012-03-05T21:00:04.943-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-05T21:00:04.943-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="non-Triassic" /><category scheme="http://www.blogger.com/atom/ns#" term="tetrapod evolution" /><title>"Romer's Gap" Is Filled</title><content type="html">Taking a quick break from all of the current Triassic papers because this is pretty significant for the field of vertebrate paleontology.&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Smithson, T. R.,Wood, S. P., Marshall, J. E. A., and J. A. Clack. 2012. Earliest Carboniferous tetrapod and arthropod faunas from Scotland populate Romer's Gap. PNAS [advance online] &lt;a href="http://www.pnas.org/content/early/2012/02/27/1117332109.abstract?sid=77288ea0-6da6-4f1e-b892-abece2f20bab"&gt;doi: 10.1073/pnas.1117332109&lt;/a&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; Devonian tetrapods (limbed vertebrates), known from an increasingly large number of localities, have been shown to be mainly aquatic with many primitive features. In contrast, the post-Devonian record is marked by an Early Mississippian temporal gap ranging from the earliest Carboniferous (Tournaisian and early Viséan) to the mid-Viséan. By the mid-Viséan, tetrapods had become effectively terrestrial as attested by the presence of stem amniotes, developed an essentially modern aspect, and given rise to the crown group. Up to now, only two localities have yielded tetrapod specimens from the Tournaisian stage: one in Scotland with a single articulated skeleton&lt;br /&gt;and one in Nova Scotia with isolated bones, many of uncertain identity. We announce a series of discoveries of Tournaisian-age localities in Scotland that have yielded a wealth of new tetrapod and arthropod fossils. These include both terrestrial and aquatic forms and new taxa. We conclude that the gap in the fossil record has been an artifact of collection failure.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-2728851972521338493?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=IHQgB3LFcy4:WD-5o53Es5U: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=IHQgB3LFcy4:WD-5o53Es5U: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=IHQgB3LFcy4:WD-5o53Es5U: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=IHQgB3LFcy4:WD-5o53Es5U:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=IHQgB3LFcy4:WD-5o53Es5U:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=IHQgB3LFcy4:WD-5o53Es5U:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=IHQgB3LFcy4:WD-5o53Es5U:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=IHQgB3LFcy4:WD-5o53Es5U: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=IHQgB3LFcy4:WD-5o53Es5U:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=IHQgB3LFcy4:WD-5o53Es5U:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/IHQgB3LFcy4" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/2728851972521338493/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/romers-gap-is-filled.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2728851972521338493?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2728851972521338493?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/IHQgB3LFcy4/romers-gap-is-filled.html" title="&quot;Romer's Gap&quot; Is Filled" /><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/2012/03/romers-gap-is-filled.html</feedburner:origLink></entry><entry gd:etag="W/&quot;D0EEQXkyfSp7ImA9WhVTGUQ.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-4246394823046961599</id><published>2012-03-05T18:00:00.000-07:00</published><updated>2012-03-05T18:00:00.795-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-05T18:00:00.795-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="Taphonomy" /><category scheme="http://www.blogger.com/atom/ns#" term="basal dinosaurs" /><title>Evidence of Avian-like Behavior in a Basal Saurischian Dinosaur</title><content type="html">There has been a rash of Triassic vertebrate papers in the last two weeks.&amp;nbsp; Here is one that looks at the taphonomy of a specimen of the basal saurischian &lt;em&gt;Guaibasaurus&lt;/em&gt; and suggests that it had a avian style of resting.&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Agnolin, F.,&amp;nbsp;and Martinelli, A.G. 2012. &lt;em&gt;Guaibasaurus candelariensis&lt;/em&gt; (Dinosauria, Saurischia) and the early origin of avian-like resting posture. Alcheringa (1–5) [advance online] &lt;a href="http://www.tandfonline.com/doi/abs/10.1080/03115518.2012.634203"&gt;DOI:10.1080/03115518.2012.634203&lt;/a&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Abstract -&lt;/strong&gt; A specimen of the basal saurischian &lt;em&gt;Guaibasaurus candelariensis&lt;/em&gt; Bonaparte, Ferigolo and Ribeiro (UFRGS-PV-0725-T) from the Faxinal do Soturno locality, Rio Grande do Sul State, Brazil (Caturrita Formation; Late Triassic) lacks any sign of post-mortem transport and burial deformation, and exhibits features (flexed forelimbs, folded hindlimbs under the body and curved neck) that indicate a typical avian-like resting position. The presence in &lt;em&gt;Guaibasaurus&lt;/em&gt; of an avian-like resting posture and related physiological implications would extend this unique trait, previously considered restricted to derived maniraptoran theropods, to the base of the Theropoda (or even&lt;br /&gt;Saurischia) clade.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-4246394823046961599?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=qJj_uZVp3jc:azJj0HBE29E: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=qJj_uZVp3jc:azJj0HBE29E: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=qJj_uZVp3jc:azJj0HBE29E: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=qJj_uZVp3jc:azJj0HBE29E:4cEx4HpKnUU"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=qJj_uZVp3jc:azJj0HBE29E:4cEx4HpKnUU" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=qJj_uZVp3jc:azJj0HBE29E:-BTjWOF_DHI"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=qJj_uZVp3jc:azJj0HBE29E:-BTjWOF_DHI" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/Chinleana?a=qJj_uZVp3jc:azJj0HBE29E: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=qJj_uZVp3jc:azJj0HBE29E:gIN9vFwOqvQ"&gt;&lt;img src="http://feeds.feedburner.com/~ff/Chinleana?i=qJj_uZVp3jc:azJj0HBE29E:gIN9vFwOqvQ" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/qJj_uZVp3jc" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/4246394823046961599/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/evidence-of-avian-like-behavior-in.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4246394823046961599?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4246394823046961599?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/qJj_uZVp3jc/evidence-of-avian-like-behavior-in.html" title="Evidence of Avian-like Behavior in a Basal Saurischian Dinosaur" /><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/2012/03/evidence-of-avian-like-behavior-in.html</feedburner:origLink></entry><entry gd:etag="W/&quot;Ck4ERngzcSp7ImA9WhVTGUo.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-4031203841961126325</id><published>2012-03-05T11:08:00.001-07:00</published><updated>2012-03-05T11:08:27.689-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-05T11:08:27.689-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="phylogenetic analysis" /><category scheme="http://www.blogger.com/atom/ns#" term="Longisquama" /><category scheme="http://www.blogger.com/atom/ns#" term="Chroniosuchia" /><category scheme="http://www.blogger.com/atom/ns#" term="osteoderms" /><title>Another Example of the Phylogenetic Utility of Osteoderms in Triassic Vertebrates</title><content type="html">&lt;strong&gt;Buchwitz, M., C. Foth, I. Kogan, and S. Voigt. 2012.&lt;/strong&gt; &lt;strong&gt;On the use 
of osteoderm features in a phylogenetic approach on the internal relationships 
of the Chroniosuchia (Tetrapoda: Reptiliomorpha). Palaeontology [Early View]. &lt;/strong&gt;&lt;a href="http://onlinelibrary.wiley.com/doi/10.1111/j.1475-4983.2012.01137.x/abstract"&gt;&lt;strong&gt;DOI: 10.1111/j.1475-4983.2012.01137.x&lt;/strong&gt;&lt;/a&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;Abstract: &lt;/b&gt; Chroniosuchians are an enigmatic Permian to Triassic group 
of crocodile-like basal tetrapods. Their conspicuous dorsal osteoderm systems 
include most of the group’s yet documented postcranial morphological variability 
but have hardly been considered in cladistic approaches. Aiming at the 
clarification of the internal relationships of the Chroniosuchia, we have 
carried out a parsimony analysis including, among others, 23 morphological and 
osteohistological osteoderm characters and 12 chroniosuchian taxa. According to 
the most parsimonious trees, taxa usually referred to Chroniosuchidae form a 
paraphyletic succession with &lt;em&gt;Madygenerpeton pustulatus&lt;/em&gt; and 
&lt;em&gt;Chroniosaurus dongusensis&lt;/em&gt; as the basalmost chroniosuchians and 
&lt;em&gt;Uralerpeton tverdochlebovae&lt;/em&gt; as the sister group of Bystrowianidae 
(hypothesis A). However, the concurrent hypothesis of a basal split into 
monophyletic subtaxa Chroniosuchidae and Bystrowianidae (hypothesis B) is only 
slightly less parsimonious and supported by an alternative analysis which 
includes embolomeres as the only reptiliomorph outgroup. Searching for the 
better hypothesis, we compare the respective order of branching to the order of 
first occurrences in the fossil record, demonstrating that hypothesis A provides 
a better stratigraphic fit than hypothesis B. Accordingly, the last common 
ancestor of the yet known chroniosuchians had a series of broad complexly 
interlocking ‘chroniosuchid’ osteoderms that served as a protection carapace 
apart from supporting the trunk during terrestrial locomotion. The later 
evolution of chroniosuchian carapaces was marked by a stepwise increase in 
flexibility and size reduction, which resulted in a loss of protective function 
and in a reduction in trunk support function. The flexibility increase is 
paralleled by the evolution of the Crocodylomorpha whose extant members do not 
possess as extensively interlocking osteoderm systems as some of their Mesozoic 
relatives.&lt;br /&gt;
&lt;br /&gt;
In addition you can read about more new articles on &lt;em&gt;Kyrgyzsaurus &lt;/em&gt;and &lt;i&gt;Longisquama&lt;/i&gt; &lt;a href="http://triassiccritters.blogspot.com/2012/02/new-papers-on-kyrgyzsaurus.html"&gt;here&lt;/a&gt;.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-4031203841961126325?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/51Y-CrQ4InQ" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/4031203841961126325/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/another-example-of-phylogenetic-utility.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4031203841961126325?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/4031203841961126325?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/51Y-CrQ4InQ/another-example-of-phylogenetic-utility.html" title="Another Example of the Phylogenetic Utility of Osteoderms in Triassic Vertebrates" /><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/2012/03/another-example-of-phylogenetic-utility.html</feedburner:origLink></entry><entry gd:etag="W/&quot;CUMHSXo-cSp7ImA9WhVTGEk.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-2247770963901759503</id><published>2012-03-03T23:40:00.001-07:00</published><updated>2012-03-03T23:43:58.459-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-03-03T23:43:58.459-07:00</app:edited><title>Chanaresuchus ischigualastensis, a New Proterochampsid from the Late Triassic of Argentina and a Temporal Range Extension for the Genus Chanaresuchus</title><content type="html">This is a short communication in the new issue of the Journal of Vertebrate Paleontology. As such there is no abstract available.&lt;br /&gt;
&lt;br /&gt;
&lt;strong&gt;Trotteyn, M. J., Martinez, R. N., and O. A. Alcober. 2012. A new proterochampsid &lt;i&gt;Chanaresuchus ischigualastensis&lt;/i&gt; (Diapsida, Archosauriformes) in the early Late Triassic Ischigualasto Formation, Argentina. Journal of Vertebrate Paleontology 32:485-489. &lt;/strong&gt;&lt;strong&gt;&lt;a href="http://www.tandfonline.com/doi/abs/10.1080/02724634.2012.645975"&gt;DOI:10.1080/02724634.2012.645975&lt;/a&gt;&lt;/strong&gt;&lt;br /&gt;
&lt;br /&gt;
The specimen includes much of an articulated skeleton including a well preserved skull. This is the first occurrence of &lt;em&gt;Chanaresuchus&lt;/em&gt; outside of the Chanares Formation and marks an extension of the taxon into the Late Triassic. As the authors state, this is interesting because it demonstrates only a species level turnover for&amp;nbsp;the clade between the late Middle and early Late Triassic faunas in the Ischiguasto Basin. Several therapsids also show the same pattern. This also marks the presence of two different proterochampsids in the Ischigualasto Formation.&lt;br /&gt;
&lt;br /&gt;
From the discussion: "&lt;span style="font-family: TimesTen-Roman; font-size: xx-small;"&gt;&lt;span style="font-family: TimesTen-Roman; font-size: xx-small;"&gt;&lt;span style="font-size: small;"&gt;PVSJ 567 is assignable to &lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;i&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;Chanaresuchus &lt;/span&gt;&lt;/span&gt;&lt;/i&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;on the basis of diagnostic &lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;characters shared with &lt;/span&gt;&lt;/span&gt;&lt;i&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;Chanaresuchus bonapartei &lt;/span&gt;&lt;/span&gt;&lt;/i&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;&lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;(e.g., &lt;/span&gt;&lt;/span&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;skull ornamented by longitudinal crests and depressions on the dorsal surfaces of the premaxillae, maxillae, and nasals; lateral fossa in the centra of presacral vertebrae; low deltopectoral crest on the humerus; absence of phalanges on pedal digit V). PVSJ 567 exhibits several differences from &lt;/span&gt;&lt;/span&gt;&lt;i&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;Chanaresuchus bonapartei &lt;/span&gt;&lt;/span&gt;&lt;/i&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;and can be assigned to a new species, &lt;/span&gt;&lt;/span&gt;&lt;i&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;&lt;span style="font-family: TimesTen-Italic;"&gt;C. ischigualastensis &lt;/span&gt;&lt;/span&gt;&lt;/i&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;(e.g., basal tubera wide with rostrolateral contour transversely&amp;nbsp;&lt;span style="font-family: TimesTen-Roman; font-size: xx-small;"&gt;&lt;span style="font-family: TimesTen-Roman; font-size: xx-small;"&gt;&lt;span style="font-size: small;"&gt;oriented; paroccipital processes distally expanded; articular &lt;/span&gt;&lt;span style="font-size: small;"&gt;surface of caudal prezygapophyses elliptical and notably anteriorly &lt;/span&gt;&lt;span style="font-size: small;"&gt;developed; astragalus lacking perforations in the posterior &lt;/span&gt;&lt;span style="font-size: small;"&gt;sulcus; osteoderms with longitudinal dorsal sulcus).&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br /&gt;
&lt;span style="font-family: TimesTen-Roman;"&gt;&lt;span style="font-family: TimesTen-Roman;"&gt;&lt;span style="font-family: TimesTen-Roman; font-size: xx-small;"&gt;&lt;span style="font-family: TimesTen-Roman; font-size: xx-small;"&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br /&gt;
&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-2247770963901759503?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/RA7764maq1k" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/2247770963901759503/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/03/chanaresuchus-ischigualastensis-new.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2247770963901759503?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/2247770963901759503?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/RA7764maq1k/chanaresuchus-ischigualastensis-new.html" title="&lt;i&gt;Chanaresuchus ischigualastensis&lt;/i&gt;, a New Proterochampsid from the Late Triassic of Argentina and a Temporal Range Extension for the Genus &lt;i&gt;Chanaresuchus&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/2012/03/chanaresuchus-ischigualastensis-new.html</feedburner:origLink></entry><entry gd:etag="W/&quot;DEEDQ3g6eSp7ImA9WhVTFEs.&quot;"><id>tag:blogger.com,1999:blog-5519292617097628087.post-691838487886535425</id><published>2012-02-28T15:04:00.001-07:00</published><updated>2012-02-28T15:04:32.611-07:00</updated><app:edited xmlns:app="http://www.w3.org/2007/app">2012-02-28T15:04:32.611-07:00</app:edited><category scheme="http://www.blogger.com/atom/ns#" term="microvertebrates" /><category scheme="http://www.blogger.com/atom/ns#" term="faunal assemblages" /><title>Diverse New Microvertebrate Assemblage from the Late Triassic of North Carolina</title><content type="html">&lt;br /&gt;
&lt;b&gt;Heckert, A. B., Mitchell, J. S., Schneider, V. P., and P. E. Olsen. 2012.&amp;nbsp;Diverse New Microvertebrate Assemblage from the Upper Triassic Cumnock&amp;nbsp;Formation, Sanford Subbasin, North Carolina, USA.&amp;nbsp;Journal of Paleontology 86(2): 368-390&amp;nbsp;&lt;a href="http://www.bioone.org/doi/abs/10.1666/11-098.1"&gt;doi: http://dx.doi.org/10.1666/11-098.1&lt;/a&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;Abstract -&lt;/b&gt; The Moncure microvertebrate locality in the Cumnock Formation, Sanford&amp;nbsp;sub-basin, North Carolina, dramatically increases the known Late&amp;nbsp;Triassic age vertebrate assemblage from the Deep River Basin. The&amp;nbsp;50,000 recovered microvertebrate fossils include osteichthyans,&amp;nbsp;amphibians, and numerous lepidosauromorph, archosauriform, and&amp;nbsp;synapsid amniotes. Actinopterygian fossils consist of thousands of&amp;nbsp;scales, teeth, skull, and lower jaw fragments, principally of&amp;nbsp;redfieldiids and semionotids. Non-tetrapod sarcopterygians include the&amp;nbsp;dipnoan &lt;i&gt;Arganodus&lt;/i&gt; sp., the first record of lungfish in the Newark&amp;nbsp;Supergroup. Temnospondyls are comparatively rare but the preserved&amp;nbsp;centra, teeth, and skull fragments probably represent small (juvenile)&amp;nbsp;metoposaurids. Two fragmentary teeth are assigned to the unusual&amp;nbsp;reptile &lt;i&gt;Colognathus obscurus &lt;/i&gt;(Case). Poorly preserved but intriguing&amp;nbsp;records include acrodont and pleurodont jaw fragments tentatively&amp;nbsp;assigned to lepidosaurs. Among the archosauriform teeth is a taxon&amp;nbsp;distinct from &lt;i&gt;R. callenderi &lt;/i&gt;that we assign to &lt;i&gt;Revueltosaurus olseni&lt;/i&gt;&amp;nbsp;new combination, a morphotype best assigned to cf. &lt;i&gt;Galtonia&lt;/i&gt;, the first&amp;nbsp;Newark Supergroup record of &lt;i&gt;Crosbysaurus&lt;/i&gt; sp., and several other&amp;nbsp;archosauriform tooth morphotypes, as well as grooved teeth assigned to&amp;nbsp;the recently named species &lt;i&gt;Uatchitodon schneideri&lt;/i&gt;. Synapsids&amp;nbsp;represented by molariform teeth include both “traversodontids”&amp;nbsp;assigned to aff. Boreogomphodon and the “dromatheriid” &lt;i&gt;Microconodon&lt;/i&gt;.&amp;nbsp;These records are biogeographically important, with many new records&amp;nbsp;for the Cumnock Formation and/or the Newark Supergroup. In particular,&amp;nbsp;&lt;i&gt;Colognathus&lt;/i&gt;, &lt;i&gt;Crosbysaurus&lt;/i&gt;, and &lt;i&gt;Uatchitodon&lt;/i&gt; are known from basins of&amp;nbsp;Adamanian age in the southwestern U.S.A. These new records include&amp;nbsp;microvertebrate taxa more typical of non-Newark basins (abundant&amp;nbsp;archosauriforms, temnospondyls, lungfish) as well as more typical&amp;nbsp;Newark osteichthyans and synapsid-rich faunal elements.&lt;br /&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5519292617097628087-691838487886535425?l=chinleana.fieldofscience.com' alt='' /&gt;&lt;/div&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/Chinleana/~4/E4EgMU6nQfs" height="1" width="1"/&gt;</content><link rel="replies" type="application/atom+xml" href="http://chinleana.fieldofscience.com/feeds/691838487886535425/comments/default" title="Post Comments" /><link rel="replies" type="text/html" href="http://chinleana.fieldofscience.com/2012/02/diverse-new-microvertebrate-assemblage.html#comment-form" title="0 Comments" /><link rel="edit" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/691838487886535425?v=2" /><link rel="self" type="application/atom+xml" href="http://www.blogger.com/feeds/5519292617097628087/posts/default/691838487886535425?v=2" /><link rel="alternate" type="text/html" href="http://feedproxy.google.com/~r/Chinleana/~3/E4EgMU6nQfs/diverse-new-microvertebrate-assemblage.html" title="Diverse New Microvertebrate Assemblage from the Late Triassic of North Carolina" /><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/2012/02/diverse-new-microvertebrate-assemblage.html</feedburner:origLink></entry></feed>

