Showing posts with label Saurischia. Show all posts
Showing posts with label Saurischia. Show all posts

Friday, February 15, 2019

[Paleontology • 2019] Nhandumirim waldsangae • A New Dinosaur with Theropod Affinities from the Late Triassic Santa Maria Formation, South Brazil


Nhandumirim waldsangae 

Marsola, Bittencourt, Butler, Da Rosa, Sayão & Langer, 2019

ABSTRACT
The Late Triassic (Carnian) upper Santa Maria Formation of south Brazil has yielded some of the oldest unequivocal records of dinosaurs. Here, we describe a new saurischian dinosaur from this formation, Nhandumirim waldsangae, gen. et sp. nov., based on a semiarticulated skeleton, including trunk, sacral, and caudal vertebrae, one chevron, right ilium, femur, partial tibia, fibula, and metatarsals II and IV, as well as ungual and non-ungual phalanges. The new taxon differs from all other Carnian dinosauromorphs through a unique combination of characters, some of which are autapomorphic: caudal centra with sharp longitudinal ventral keels; brevis fossa extending for less than three-quarters of the ventral surface of the postacetabular ala of the ilium; dorsolateral trochanter ending well distal to the level of the femoral head; distal part of the tibia with a mediolaterally extending tuberosity on its cranial surface and a tabular caudolateral flange; conspicuous, craniomedially oriented semicircular articular facet on the distal fibula; and a straight metatarsal IV. This clearly distinguishes Nhandumirim waldsangae from both Saturnalia tupiniquim and Staurikosaurus pricei, which were collected nearby and at a similar stratigraphic level. Despite not being fully grown, the differences between Nhandumirim waldsangae and those saurischians cannot be attributed to ontogeny. The phylogenetic position of Nhandumirim waldsangae suggests that it represents one of the earliest members of Theropoda. Nhandumirim waldsangae shows that some typical theropod characters were already present early in dinosaur evolution, and it represents possibly the oldest record of the group known in Brazil.


  Silhouette depicting the preserved bones of Nhandumirim waldsangae, gen. et sp. nov. (LPRP/USP 0651).


SYSTEMATIC PALEONTOLOGY 

DINOSAURIFORMES Novas, 1992, sensu Nesbitt, 2011 
DINOSAURIA Owen, 1842, sensu Padian and May, 1993 

SAURISCHIA Seeley, 1887, sensu Gauthier, 1986 
cf. THEROPODA Marsh, 1881, sensu Gauthier, 1986 

NHANDUMIRIM WALDSANGAE, gen. et sp. nov


Etymology— The generic name combines the Portuguese derivatives of the indigenous Tupi-Guarani words ‘Nhandu’ (running bird, common rhea) and ‘Mirim’ (small), in reference to the size and inferred cursorial habits of the new dinosaur. The specific epithet name refers to the Waldsanga site, the historic outcrop (Langer, 2005a) that yielded this new species.


Júlio C. A. Marsola, Jonathas S. Bittencourt, Richard J. Butler, Átila A. S. Da Rosa, Juliana M. Sayão and Max C. Langer. 2019. A New Dinosaur with Theropod Affinities from the Late Triassic Santa Maria Formation, South Brazil. Journal of Vertebrate Paleontology. e1531878 DOI: 10.1080/02724634.2018.1531878   

Parente do tiranossauro viveu no Brasil há 233 milhões de anos jornal.usp.br/ciencias/ciencias-biologicas/parente-do-tiranossauro-viveu-no-brasil-ha-233-milhoes-de-anos via @usponline 

Thursday, February 14, 2019

[Paleontology • 2019] Mnyamawamtuka moyowamkia • A New African Titanosaurian Sauropod Dinosaur from the middle Cretaceous Galula Formation (Mtuka Member), Rukwa Rift Basin, Southwestern Tanzania


Mnyamawamtuka moyowamkia 
Gorscak & O’Connor. 2019

Abstract
The African terrestrial fossil record has been limited in its contribution to our understanding of both regional and global Cretaceous paleobiogeography, an interval of significant geologic and macroevolutionary change. A common component in Cretaceous African faunas, titanosaurian sauropods diversified into one of the most specious groups of dinosaurs worldwide. Here we describe the new titanosaurian Mnyamawamtuka moyowamkia gen. et sp. nov. from the Mtuka Member of the Galula Formation in southwest Tanzania. The new specimen preserves teeth, elements from all regions of the postcranial axial skeleton, parts of both appendicular girdles, and portions of both limbs including a complete metatarsus. Unique traits of M. moyowamkia include the lack of an interpostzygapophyseal lamina in posterior dorsal vertebrae, pronounced posterolateral expansion of middle caudal centra, and an unusually small sternal plate. Phylogenetic analyses consistently place M. moyowamkia as either a close relative to lithostrotian titanosaurians (e.g., parsimony, uncalibrated Bayesian analyses) or as a lithostrotian and sister taxon to Malawisaurus dixeyi from the nearby Aptian? Dinosaur Beds of Malawi (e.g., tip-dating Bayesian analyses). M. moyowamkia shares a few features with M. dixeyi, including semi-spatulate teeth and a median lamina between the neural canal and interpostzygapophyseal lamina in anterior dorsal vertebrae. Both comparative morphology and phylogenetic analyses support Mnyamawamtuka as a distinct and distant relative to Rukwatitan bisepultus and Shingopana songwensis from the younger Namba Member of the Galula Formation with these results largely congruent with newly constrained ages for the Mtuka Member (Aptian–Cenomanian) and Namba Member (Campanian). Coupled with recent discoveries from the Dahkla Oasis, Egypt (e.g., Mansourasaurus shahinae) and other parts of continental Afro-Arabia, the Tanzania titanosaurians refine perspectives on the development of African terrestrial faunas throughout the Cretaceous—a critical step in understanding non-marine paleobiogeographic patterns of Africa that have remained elusive until the past few years.


         

Systematic paleontology
DINOSAURIA  
SAURISCHIA  

SAUROPODA 
TITANOSAURIFORMES 
TITANOSAURIA 

LITHOSTROTIA  

MNYAMAWAMTUKA MOYOWAMKIA, gen. et sp. nov.

Etymology: Mnyamawamtuka (Mm-nya-ma-wah-mm-too-ka), ‘mnyama’ is the Kiswahili word for ‘animal’ or ‘beast’ and acts as a conceptual proxy to the titans in Titanosauria, and ‘wa Mtuka' is Kiswahili for ‘of the Mtuka’ in reference to the river drainage that yielded the type specimen. Moyowamkia (Mm-oh-yo-wa-mm-key-ah), ‘moyo’ is the Kiswahili word for heart and ‘wa mkia’ is Kiswahili for ‘of the tail’, in reference to the posterolateral expansion of the posterior centrum on the middle caudal vertebrae that gives the posterior centrum surface a heart-shape outline.

Holotype: RRBP 05834, a partial skeleton including an anterior cervical vertebral neural arch and four cervical vertebral centra, seven partial dorsal vertebrae, a sacral neural arch, three partial sacral centra, three sacral ribs, seven caudal vertebral neural arches and seven centra, four chevrons, numerous dorsal rib fragments, a right scapula, a right sternal plate, a partial left humerus and distal right humerus, partial left ulna, right metacarpal I and left metacarpal III, a partial left ischium, a partial right pubis, partial left and right femora, left tibia and partial right tibia, a left fibula, left metatarsal I, left metatarsal II, right metatarsal III, left metatarsal IV, left metatarsal V, two pedal phalanges, a left ungual, and numerous unidentifiable fragments. The majority of the fossils were prepared at the Ohio University Fossil Preparation Facility, with some of the first-discovered elements prepared by J. P. Cavigelli. Preperation used standard manual and technical techniques including hand tools and pneumatic air scribes. Repository information of RRBP 05834 is the Rukwa Rift Basin Project, Tanzanian Antiquities Unit, Dar es Salaam, Tanzania. The fossils are, at time of publication, on temporary loan and deposited at Ohio University in Athens, Ohio. All of the fossils are accessible by request. Research casts will permanently be housed at Ohio University and in the collections at Denver Museum of Science and Nature.

Fig 1. Map of research area. Map of Africa, A, with expanded regional map of the Rukwa Rift Basin of Tanzania, B, with the type localities of Mnyamawamtuka moyowamkia and Rukwatitan bisepultus quarry near the Galula study area, C, and the Shingopana songwensis quarry near the Nsungwe study area, D. Malawi Dinosaur Beds (DB) marked in B to demonstrate the proximity of the deposits to the Galula Formation.


Fig 2. Quarry map of the Mtuka bonebed locality RRBP 2004–06. Recovered elements of Mnyamawamtuka moyowamkia are color-coded and separated by dashed lines according to the year they were collected. The quarry map is represented as a four-by-six-meter grid. Unmarked elements on the map are either fragments or unidentified.

Abbreviations: cac, caudal vertebral centrum; cana, caudal vertebral neural arch; cr, cervical rib; cvc, cervical vertebral centrum; dc, dorsal vertebral centrum; dic, distal caudal vertebra; dr, dorsal rib; dv, dorsal vertebra; fem, femur; fib, fibula; ha, haemal arch; hum, humerus; isc, ischium; mtc I, metacarpal I; sac, sacral centrum; scap, scapula; sp, sternal plate; sr, sacral rib; tib, tibia; ul, ulna; un, ungual.

Type locality and horizon: The specimen was recovered in the Mtuka Member of the Cretaceous Galula Formation. The Mtuka Member is dominated by coarse sandstone fluvial deposits and abundant overbank siltstone and mudstone lenses within an extensive fluvial braidplain system. The holotype of M. moyowamkia was recovered from a quarry developed along the Mtuka River drainage in southwestern Tanzania (Fig 1). The quarry is roughly 20 kilometers south of Lake Rukwa near the coordinates of 32° 34’ E and 8° 34’ S. The initial discovery was made in 2004 at locality RRBP 2004–06, with additional elements recovered sequentially during the 2005–2008 field seasons by the Rukwa Rift Basin Project field teams (Fig 2). Generally, larger and more complete elements, such as appendicular remains, were recovered in the western part of the quarry whereas smaller and more fragmented elements were recovered from the eastern part of the quarry, indicating short-distance transport (Fig 2). Excavation permits were issued by The United Republic of Tanzania, Ministry of Natural Resources and Tourism, Antiquities Unit, P.O. Box 2280, Dar es Salaam, Tanzania to P. M. O’Connor under the specific permit numbers: 14–2004; EA 402/605/01; EA 402/605/01/78; EA 402/605/01/20; and EA 402/604/01/7. In a broader context, the M. moyowamkia discovery and excavation was made in the early years of the Rukwa Rift Basin Project with the aim of addressing the paucity of fossils recovered from the Cretaceous of sub-Saharan Africa.

Age and distribution: The materials were recovered from the Mtuka Member of the Galula Formation of the Red Sandstone Group, Rukwa Rift Basin, southwestern Tanzania. Based on previous lines of evidence, including faunal data within the overlying Namba Member, the age of the Galula Formation was best constrained to the middle Cretaceous (Aptian–Cenomanian) with potential dates of 100–110 Ma. However, new paleomagnetic data place the Mtuka Member (i.e., the specific unit from which M. moyowamkia was recovered) within the Cretaceous long normal with estimates of Aptian–Cenomanian for the unit and a younger date for the overlying Namba Member as either Campanian or Cenomanian–Santonian.

Fig 3. Teeth associated with Mnyamawamtuka moyowamkia skeleton.
Teeth recovered from the Mnyamawamtuka moyowamkia quarry. A–D, tooth Morph A; E–F, tooth Morph B; and G–J, tooth Morph C. A, G, distal; B, E, H, labial; C, I, mesial; D, J, lingual; and F, occlusal views. Abbreviations: labwf, labial wear facet; linwf, lingual wear facet. Scale bar equals 1 cm.

Diagnosis: 
 ...
Mnyamawamtuka moyowamkia is diagnosed by the following suite of autapomorphies: (1) middle and posterior dorsal vertebrae with vertical lamina between neural canal and interprezygapophyseal lamina that bifurcates dorsally; (2) posterior dorsal vertebra with no interpostzygapophyseal lamina as the postspinal lamina continues to the dorsal margin of the neural canal; (3) prominent dorsolateral expansion on the posterior centrum of the middle caudal vertebra; (4) curved crest with accompanying fossa within the dorsomedial region of the proximal scapular blade; (5) sternal plate unusually small, estimated to be, at most, 42% of humerus length.
....


Eric Gorscak and Patrick M. O’Connor. 2019. A New African Titanosaurian Sauropod Dinosaur from the middle Cretaceous Galula Formation (Mtuka Member), Rukwa Rift Basin, Southwestern Tanzania.  PLoS ONE. 14(2): e0211412. DOI:  10.1371/journal.pone.0211412
Mnyamawamtuka: New dinosaur with heart-shaped tail provides evolutionary clues for African continent  phys.org/news/2019-02-mnyamawamtuka-dinosaur-heart-shaped-tail-evolutionary.html via @physorg_com

    

Saturday, December 8, 2018

[Paleontology • 2018] Volgatitan simbirskiensis • The Oldest Titanosaurian Sauropod of the Northern Hemisphere


Volgatitan simbirskiensis
Averianov & Efimov, 2018

"Titanosaur" by Olorotitan 

ABSTRACT
Volgatitan simbirskiensis, gen. et sp. nov., is described based on a series of anterior and middle caudal vertebrae from a single individual discovered in the Lower Cretaceous (upper Hauterivian, Speetoniceras versicolor ammonite Zone) marine deposits at Slantsevy Rudnik vertebrate locality near Ulyanovsk City, Russia. The new taxon is characterized by strongly procoelous anterior and middle caudal vertebrae, a long centrum of the first caudal vertebra, a strong ventral ridge in the anterior and middle caudal vertebrae, a neural arch positioned at the anterior half of the centrum, hyposphene-hypantrum articulation in the anterior caudal vertebrae, and somphospondylous bone texture. Phylogenetic analysis places the new taxon as a lithostrotian titanosaur, a basal member of the lineage leading to the Lognkosauria. This lineage previously contained only South American taxa with body mass reaching 60–70 tons. Volgatitan gen. nov. is the first European and the geologically oldest representative of this lineage. Its body mass is estimated as 17.3 tons. Discovery of Volgatitan gen. nov. suggests that the lithostrotian lineage leading to the Lognkosauria had a wider distribution in the Early Cretaceous and became extinct everywhere except South America by the end of the Early Cretaceous.

KEYWORDS: Dinosauria, Sauropoda, Titanosauriformes, Titanosauria, Lithostrotia, Early Cretaceous, Eastern Europe, Russia


Volgatitan simbirskiensis anterior caudal vertebra (holotype),
in right lateral (A), anterior (B), left lateral (C), posterior (D), dorsal (E), and ventral (F) views. 



Alexander Averianov and Vladimir Efimov. 2018. The Oldest Titanosaurian Sauropod of the Northern Hemisphere. Biological Communications. 63(3), 145–162. DOI:  10.21638/spbu03.2018.301

Scientists from St Petersburg and Ulyanovsk have described a new giant dinosaur  english.spbu.ru/news/2482-scientists-from-st-petersburg-and-ulyanovsk-have-described-a-new-giant-dinosaur

    

Sunday, November 4, 2018

[Paleontology • 2018] Lavocatisaurus agrioensis • A New Rebbachisaurid Sauropod from the Aptian–Albian, Lower Cretaceous Rayoso Formation, Neuquén, Argentina


Lavocatisaurus agrioensis 
Canudo, Carballido, Garrido & Salgado, 2018

Illustration: Gabriel Lio. 

Rebbachisaurids are a group of basal diplodocimorph sauropods that diversified in Gondwana at the end of the Early Cretaceous and the beginning of the Late Cretaceous. It is a group of great palaeobiogeographical interest, for it  clearly illustrates various processes of dispersal throughout Gondwana and to Laurasia prior to the breakup of Africa and South America. However, the relationships within the group are still under discussion owing to the scarcity of cranial material that would help clarify them. In the present paper we describe the new rebbachisaurid Lavocatisaurus agrioensis gen. et  sp. nov. from the Aptian–Albian (Lower Cretaceous) of Neuquén (Argentina). Remains have been recovered belonging to an adult specimen (holotype) and two immature specimens (paratypes). Taken together, almost all the bones of the taxon are represented, including most of the cranium. Lavocatisaurus agrioensis gen. et sp. nov. is the first rebbachisaurid from Argentina with an almost complete cranium, making it possible to recognize differences with respect to other rebbachisaurids, such as the highly derived Nigersaurus. Among its most notable characters are the presences of a large preantorbital fenestra and maxillary teeth that are significantly larger than those of the dentary. Our phylogenetic study places Lavocatisaurus amongst basal rebbachisaurids, as the sister lineage to Khebbashia (the clade formed by Limaysaurinae + Rebbachisaurinae). This position, which is somewhat more derived than that previously suggested for Comahuesaurus and Zapalasaurus (the Argentinean rebbachisaurids closest in geographical and geological terms), reaffirms the presence of different basal rebbachisaurid lineages in the Early Cretaceous of Patagonia.

Key words: Dinosauria, Rebbachisauridae, phylogeny, Cretaceous, Rayoso Formation, Argentina.


Fig. 2. Rebbachisaurid sauropod Lavocatisaurus agrioensis gen. et sp. nov. from Agrio del Medio (Argentina), Aptian–lower Albian. A. MOZ-Pv1232, axis in lateral view (A1, photograph; A2, drawing); eight cervical vertebrae in lateral view view (A3, photograph; A4, drawing, ); anterior caudal vertebra in lateral view (A5); middle caudal vertebra in lateral view (A6); posterior caudal vertebra in lateral view (A7); posteriormost caudal vertebra in lateral view (A8); left tibia in lateral view (A9). B. MOZ-Pv 1255, left scapula from a juvenile specimen, in lateral view. C. Skeletal reconstruction based on the holotype and paratype specimens. Scale bars 10 cm. 

Saurischia Seeley, 1887
Sauropoda Marsh, 1878
Diplodocoidea Marsh, 1878 sensu Upchurch, 1995
Diplodocimorpha Calvo and Salgado, 1995
Rebbachisauridae Bonaparte, 1997

Genus Lavocatisaurus nov.

Etymology: In honour of the French researcher René Lavocat (1909–2007), who described Rebbachisaurus, the first known representative of Rebbachisauridae.

Lavocatisaurus agrioensis sp. nov.

Etymology: In reference to the locality of Agrio del Medio, from which the new species was found


Illustration: Gabriel Lio.  

Conclusions: 
Lavocatisaurus agrioensis is the first of the South American rebbachisaurids that preserves the rostral region of the cranium, which has allowed us to undertake a reliable enough reconstruction of the skull. The skull has a combination of morphological characters that justifies its definition as a new taxon within Rebbachisauridae along with the less derived rebbachisaurids from the Early Cretaceous of Argentina such as Zapalasaurus and Comahuesaurus. Our phylogenetic study situates Lavocatisaurus as the sister lineage of Khebbashia (Fig. 5). Lavocatisaurus is the most derived basal rebbachisaurid known to date, providing reliable information on the evolutionary steps that occurred just prior to the diversification of Rebbachisaurinae.


José I. Canudo, José L. Carballido, Alberto Garrido and Leonardo Salgado. 2018. A New Rebbachisaurid Sauropod from the Aptian–Albian, Lower Cretaceous Rayoso Formation, Neuquén, Argentina. Acta Palaeontologica Polonica. in press. DOI: 10.4202/app.00524.2018 

Scientists discover a new species of dinosaur 110 million years old in Argentina


Friday, October 12, 2018

[Paleontology • 2018] The Smallest Diplodocid Skull Reveals Cranial Ontogeny and Growth-Related Dietary Changes in the Largest Dinosaurs


Life reconstruction of CMC VP14128. Note the cranial morphologies interpreted to denote differing feeding strategies: in CMC VP14128 the narrow snout with posteriorly elongated and morphologically varied tooth row for bulk feeding vs. the widened snout with anteriorly restricted peg-shaped teeth for ground-level browsing in adults. Also note the camouflaged ontogenetic color change suggesting young diplodocids may have sought forested refuge.

in Woodruff, Carr, Storrs, et al., 2018. 
Reconstruction by A. Atuchin.

Abstract
Sauropod dinosaurs were the largest terrestrial vertebrates; yet despite a robust global fossil record, the paucity of cranial remains complicates attempts to understand their paleobiology. An assemblage of small diplodocid sauropods from the Upper Jurassic Morrison Formation of Montana, USA, has produced the smallest diplodocid skull yet discovered. The ~24 cm long skull is referred to cf. Diplodocus based on the presence of several cranial and vertebral characters. This specimen enhances known features of early diplodocid ontogeny including a short snout with narrow-crowned teeth limited to the anterior portion of the jaws and more spatulate teeth posteriorly. The combination of size plus basal and derived character expression seen here further emphasizes caution when naming new taxa displaying the same, as these may be indicative of immaturity. This young diplodocid reveals that cranial modifications occurred throughout growth, providing evidence for ontogenetic dietary partitioning and recapitulation of ancestral morphologies.




Figure 1: Skeletal reconstruction of CMC VP14128 to scale with a mature Diplodocus carnegii (dark grey). Grey bones are missing, while those in ivory are those present in CMC VP14128. Skeletal reconstruction based on the Diplodocus by S. Hartman. Silhouettes by S. Hartman and PhyloPic (Creative Commons Attribution-ShareAlike 3.0 Unported; phylopic.orgcreativecommons.org), modifications made. Skeletal reconstruction of CMC VP14128 redrawn from D. carnegii skeletal by S. Hartman (skeletaldrawing.com). Human scale is Andrew Carnegie at his natural height of 1.6 m. Skeletal and silhouettes to scale. (B) CMC VP14128 in right lateral view with accompanying schematic. (C) CMC VP14128 in left lateral view with accompanying schematic. Schematics by DCW. The four portions of the skull numbered on accompanying schematics.

 Lateral views and schematics to scale. a: angular, al: alisphenoid, aof: antorbital fenestra, d: dentary, f: frontal, h: hyoid, l: lacrimal, m: maxilla, n: nasal, oc: occipital condyle, os: orbitosphenoid, p: parietal, paof: preantorbital fenestra, pf: prefrontal, pm: premaxilla, po: postorbital, pro: prootic, q: quadrate, sa: surangular, sq: squamosal. L and r before bone denotes if it is left or right.

Systematic Paleontology

Saurischia Seeley 1887
Sauropodomorpha von Huene 1932

Sauropoda Marsh 1878
Diplodocoidea Marsh 1884
Flagellicaudata Harris and Dodson 2004

Diplodocidae Marsh 1884

cf. Diplodocus Marsh 1878.

....



Figure 5: Life reconstruction of CMC VP14128. Note the cranial morphologies interpreted to denote differing feeding strategies: in CMC VP14128 the narrow snout with posteriorly elongated and morphologically varied tooth row for bulk feeding vs. the widened snout with anteriorly restricted peg-shaped teeth for ground-level browsing in adults. Also note the camouflaged ontogenetic color change suggesting young diplodocids may have sought forested refuge. Reconstruction by A. Atuchin.

Conclusions: 
Within Dinosauria, there are small bodied taxa that display basal and derived characters and occupy unusual basal phylogenetic positions. The validity and position of such taxa has been disputed, and regarding sauropodomorph phylogeny, we would advocate that the combination of basal and derived characters and basal phylogenetic recovery should be recognized as an indicator of an immature ontogimorph – instead of a distinct taxon. In light of the current wealth of information pertaining to dinosaur ontogeny, we can no longer assume that all morphological differences correspond with phylogenetic distinctiveness. Accounting for ontogeny could prove as test for our phylogenies. Recognizing the ontogenetic age of immature specimens provides important insights into the life history of these animals. The immature Diplodocus specimen CMC VP14128 extends our understanding of the ontogeny of the genus and the evolution of diplodocids into new areas, where:

(1) The combination of basal and derived characters in the juvenile is broadly congruent with the phylogenetic transition from eusauropods to diplodocoids.
(2) The plesiomorphic tooth morphology is retained in immature Diplodocus and lost with maturity, and we predict this growth pattern will be seen in all other diplodocoids.
(3) As first proposed by Whitlock et al. (2010), tooth and skull morphology indicate that during growth Diplodocus inhabited different trophic levels/niches, where juveniles were generalists (i.e., browsers; Fig. 5) and more mature individuals were specialists (i.e., ground-level browsing), a pattern that we predict is ancestral for Diplodocoidea.


D. Cary Woodruff, Thomas D. Carr, Glenn W. Storrs, Katja Waskow, John B. Scannella, Klara K. Nordén and John P. Wilson. 2018. The Smallest Diplodocid Skull Reveals Cranial Ontogeny and Growth-Related Dietary Changes in the Largest Dinosaurs. Scientific Reports. 8, Article number: 14341. DOI:  10.1038/s41598-018-32620-x 

Tiny Skull Illuminates the Lives of Giant Dinosaur  po.st/WYNAw9 via @SmithsonianMag

     

Friday, September 14, 2018

[Paleontology • 2018] Yizhousaurus sunae • A New Sauropodiform Dinosaur with A ‘Sauropodan’ Skull from the Lower Jurassic Lufeng Formation of Yunnan Province, China


Yizhousaurus sunae 
Zhang, You, Wang & Chatterjee, 2018


Abstract
The Early Jurassic Lufeng Formation of Yunnan Province in southwestern China is one of the best fossil localities in the world for understanding the early radiation of sauropodomorph dinosaurs. It has yielded a rich assemblage of complete and three-dimensionally preserved skeletons of herbivorous dinosaurs that provide crucial morphological information for systematic and evolutionary studies. Here we describe a new taxonYizhousaurus sunae gen. et sp. nov., represented by a nearly complete skeleton with an exquisitely preserved skull and mandible. Yizhousaurus is distinguished from other non-sauropodan sauropodomorphs by a unique combination of plesiomorphic and apomorphic features, which increases our understanding of the anatomical variation on the relatively conservative ‘prosauropod’ cranial plan. Phylogenetic analysis resolves Yizhousaurus as a sauropodiform, showcasing a mosaic character suite combining plesiomorphic states in the postcranial skeleton with some more ‘sauropodan’-like features in the skull. Furthermore, Yizhousaurus is placed closer to the base of Sauropoda than other non-sauropodan sauropodomorphs currently known from the Lufeng Formation, adding another taxon to enrich the Lower Jurassic Lufeng dinosaur fauna.

Figure 2 Status of preservation of Yizhousaurus sunae gen. et sp. nov.
 (A) The reconstruction in sketch of Yizhousaurus in left lateral view (drawn by Xiao-Cong Guo), regions in red rim represent absent elements; (B), the original burial map of Yizhousaurus 
(drawn by Qian-Nan Zhang).

Systematic Paleontology

Dinosauria Owen, 1842
Saurischia Seeley, 1887
Sauropodomorpha von Huene, 1932
Massopoda Yates, 2007

Sauropodiformes Sereno, 2007 

Yizhousaurus sunae gen. et sp. nov.

Holotype: LFGT (Bureau of Land and Resources of Lufeng County, Yunnan, China) -ZLJ0033. An undistorted skeleton about 7 meters long, including a well-preserved skull and mandible, a mostly complete vertebral series (9 cervicals, 14 dorsals, 3 sacrals and 5 anterior caudals), pectoral and pelvic girdles, forelimbs (lacking both carpi) and both femora (Fig. 2A).

Type locality and horizon: The specimen was collected near Duwafang Village, Chuanjie Town, Lufeng County, Chuxiong Yi Autonomous Prefecture, Yunnan Province, China (Fig. 1); the skeleton was excavated in the uppermost layer of the Zhangjiaao Member of the Lower Jurassic Lufeng Formation.

Etymology: The generic name Yizhou refers to the Chuxiong Yi Autonomous Prefecture of Yunnan Province. The specific name is in honor of Professor Ai-Ling Sun, for her great contribution to Chinese vertebrate fossils, including those from Lufeng.

Differential Diagnosis: A medium-sized sauropodiform distinguished from other non-sauropodan sauropodomorphs with respect to the following unique combination of character states (autapomorphies marked with *): lateral plates appressed to the labial sides of the premaxillary and maxillary teeth but not the dentary teeth*; anteroposterior expansion at the dorsal end of the maxillary ascending ramus; antorbital fenestra anteroposteriorly narrow and pipe-shaped in outline*; lacrimal shaft vertical with respect to the maxillary ramus*; transverse width of the ventral process of the postorbital greater than its anteroposterior width at midshaft; anterior tip of the dentary anterodosally curved over the alveolar margin*; tiny external mandibular fenestra (about 5% of the mandibular length)*; broad axial intercentrum wider than its centrum; deep depressions on the lateral surfaces of centra of dorsal vertebrae 3–6; hyposphenes of the anterior dorsals equal to their neural canals in height; and subelliptical cross-section of the midshaft of the femur.
.....

Comment: Yizhousaurus sunae was briefly reported as a basal sauropod at the Geological Society of America Conference in 2010, but has never received formal study. In addition, its fourth and fifth caudal vertebrae are fused together, which is considered pathological in nature.




Qian-Nan Zhang, Hai-Lu You, Tao Wang and Sankar Chatterjee. 2018. A New Sauropodiform Dinosaur with A ‘Sauropodan’ Skull from the Lower Jurassic Lufeng Formation of Yunnan Province, China. Scientific Reports.  8,  13464.  DOI:  10.1038/s41598-018-31874-9

 Chatterjee, Sankar; Wang, T.; Pan, S.G.; Dong, Z.; Wu, X.C.; Upchurch, P. 2010. A Complete Skeleton of A Basal Sauropod Dinosaur from the early Jurassic of China and the Origin of Sauropoda. Geological Society of America Abstracts with Programs. 42 (5): 26.

Found: First complete remains of early sauropod dinosaur  phys.org/news/2010-10-early-sauropod-dinosaur.html via @physorg_com

Thursday, September 13, 2018

[Paleontology • 2018] Qiupanykus zhangi • A New Alvarezsaurid Dinosaur from the Late Cretaceous Qiupa Formation of Luanchuan, Henan Province, central China


Qiupanykus zhangi  
Lü, Xu, Chang, Jia, Zhang, Gao, Zhang, Zhang & Ding, 2018

 DOI:  10.31035/cg2018005 
Illustration: Zhao Chuang. 

An alvarezsaurid dinosaur skeleton was discovered from the Late Cretaceous Qiupa Formation of Luanchuan, Henan Province of centtral China. It represents a new alvarezsaurid dinosaur Qiupanykus zhangi gen. et sp. nov. A phylogenetic analysis recovers Qiupanykus nested within the unresolved clade, which includes Asian and north American taxa. The skeleton of the new specimen is preserved in association with eggshells. The eggshell morphologies show that these eggs belong to oviraptorid eggs, skeletal remains of which were discovered from the same area. The alvarezsaurid skeleton associated with eggshell fragments may indicate that these eggs were broken by the strong thumb-claws of the former and that alvarezsaurid dinosaurs may be egg-eaters.

Keywords: Vertebrate paleontology, alvarezsaurid dinosaur, Qiupanykus, Late Cretaceous, central China


Figure 2. The photograph (a) and outline drawings (b) of Qiupanykus zhangi.
 Abbreviations: cd: caudal vertebrae; f: femur; hc: haemal arch; il: ilium; mt(II-IV): metatarsls II-IV; ti: tibia; p: pubis; pp: pedal phalanx; sv: sacral vertebrae.

Systematic paleontology

Maniraptora (Gauthier, 1986)
Alvarezsauridae (Bonaparte JF, 1991)

Qiupanykus zhangi gen. et sp. nov.

Etymology: The generic name refers to the Qiupa town, Luanchuan County, where the specimen was discovered. The specific name is in honor of Shuancheng Zhang for his logistic support with fossil searching and excavations in the field.

Holotype: Incomplete skeleton comprising most posterior axial elements and most of hindlimb elements. The specimen 41HIII-0101 is housed in the collections of the Henan Geological Museum, Zhengzhou, China.

Holotype locality and horizon: The specimen (41HIII-0101) was found in Guanping, Qiupa Town, Luanchuan County of Henan Province; Qiupa Formation (Bureau of Geology and Mineral Resources of Henan Province, 1989; Lü JC et al., 2007)

Diagnosis: A small-sized alvarezsaurid dinosaur with the following combination of characters: posterior sacral vertebrae bearing a strong ventral keel; proximal caudals with transverse processes centrally positioned on centrum; pubic articular surface of the pubic peduncle of ilium is reduced and knob-like; fibular crest of tibia large and quadrangular; functional sacrum made up of eight vertebral elements (two anterior caudal plus six sacral vertebrae); a small pneumatic foramen is present in caudal vertebrae.
....

Figure 4. Life scene of Qiupanykus zhangi. 
(drawn by Zhao Chuang)

Behaviour of alvarezsaurid dinosaurs
The skeleton of Qiupanykus is associated with an eggshell fragment near its tail. The thickness of the eggshell fragment is 1.8 mm. Some features, such as linearituberculate ornamentation type, including nodes and short ridges, two structural layers (non-prismatic), and relatively thick shell, are all identical to the Luanchuan oviraptorosaur eggshells (Tanaka K et al., 2011). Using the formula (Elongatoolithidae) by Tanaka K et al. (2016), the estimated egg mass of the eggshell is: Log10 egg mass = 1.569×log10 (1.8)+2.655, the thickness of the egg shell is 1.8 mm, then the Egg mass is 1136.377 g (95% CI: 715 g to 1809 g). The femur circumference of Qiupanykus is 17.09 mm. Based on the formula (log10 BM = 2.754×log10(femur circumference-0.683) by Campione NE et al. (2014), the estimated body mass for Qiupanykus: is 515 g (log10 BM = 2.754×log10 17.09-0.683). The estimated egg mass is much heavier than the estimated body mass of Qiupanykus. Thus, the egg could not be laid by Qiupanykus.

Alvarezsaurid dinosaurs bear highly specialized arms, whose purpose is still a mystery. They are regarded that the special arms were used to burrow (Perle A et al., 1993) or break open termite mounds (like modern anteaters), and possible to feed on insects (Senter P, 2005). However, the skeleton is associated with eggshell fragments from Luanchuan area, and the eggshell fragment morphologies indicate that those eggs belong to oviraptorid eggs (Tanaka K, personal communication, 2017). There is another case found from north-western Patagonia of Argentina, where an alvarezsaurid skeleton is preserved with eggs (Agnolin FL et al., 2012). Although Agnolin et al. thought the eggs associated with the alvarezsaurid Bonapartenykus ultimus were laid by an alvarezsaurid dinosaur, they pointed out that the external ornamentation patterns of Arriagadoolithus expressed on the outer shell surface is similar to elongathoolithid eggs. Arriagadoolithus was possibly laid by oviraptorosaurid dinosaurs. Thus, there are three possibilities about the relationship between the alvarezsaurid skeletons and eggs (egg fragments) associated with them: (1) Eggshell fragments were buried with alvarezsaurid skeleton by coincidence, and the eggshell is nothing to do with the skeleton. (2) The eggs were laid by alvarezsaurid dinosaurs and (3) The eggshell fragments were from eggs broken by alvarezsaurid dinosaurs and the eggs were not laid by them. However, considering the strong thumb claw of alvarezsaurid dinosaurs, we prefer to the third interpretation. Alvarezsaurid dinosaurs perhaps use their special claw to break eggs, and they are perhaps egg-eaters (Fig. 4).


Conclusion: 
The skeleton of Qiupanykus is associated with oviraptorid egg shell fragments suggesting that at least the derived alvarezsaurid dinosaurs may be an egg-eaters, which use their special arms (the strong thumb claws) to pierce the hard eggshell. Qiupanykus is a relatively small sized alvarezsaurid and it represents the youngest alvarezsaurid dinosaur from China so far.




Jun-Chang Lü, Li Xu, Hua-Li Chang, Song-Hai Jia, Ji-Ming Zhang, Dian-Song Gao, Yi-Yang Zhang, Cheng-Jun Zhang and Fang Ding. 2018. A New Alvarezsaurid Dinosaur from the Late Cretaceous Qiupa Formation of Luanchuan, Henan Province, central China. China Geology. 1(1): 28–35. DOI:  10.31035/cg2018005

   

Thursday, June 28, 2018

[Paleontology • 2018] Ceratosaur Palaeobiology: New Insights on Evolution and Ecology of the Southern Rulers


 The hypothetical phylogenetic relationships of ceratosaurs based on current topologies. 
The main source is from Wang et al. (2016).

Hypothetical reconstruction of two abelisaurids showing the soft tissues on the head inferred from osteological morphology of the skull. On the top, Carnotaurus; on the bottom, PycnonemosaurusArt by Maurilio Oliveira. 

in Delcourt, 2018. 

Abstract
Ceratosaur theropods ruled the Southern Hemisphere until the end of the Late Cretaceous. However, their origin was earlier, during the Early Jurassic, a fact which allowed the group to reach great morphological diversity. The body plans of the two main branches (Noasauridae and new name Etrigansauria: Ceratosauridae + Abelisauridae) are quite different; nevertheless, they are sister taxa. Abelisaurids have lost the ability to grasp in the most derived taxa, but the reduced forelimb might have had some display function. The ontogenetic changes are well known in Limusaurus which lost all their teeth and probably changed the dietary preference at maturity. The results presented here suggest that abelisaurids had different soft tissues on the skull. These tissues might have been associated with evolution of a strong cervicocephalic complex and should have allowed derived taxa (e.g. Majungasaurus and Carnotaurus) to have low-displacement headbutting matches. The ability to live in different semi-arid environment plus high morphological disparity allowed the ceratosaurs to become an evolutionary success.


Figure 1 The hypothetical phylogenetic relationships of ceratosaurs based on current topologies. The main source is from Wang et al. (2016). The phylogenetic position of Chenanisaurus is from Longrich et al.(2016) and the Ligabueino, Austrocheirus, Majungasaurinae and Brachyrostra are from Filippi et al.(2011).

 Figure 4 Skin structures inferred for abelisaurids. Dorsal surface of the skull of (A) Rugops (MNN IGU1), (C) Carnotaurus (MACN-CH 894) and dorsal surface of the fused nasal of (B) Abelisaurus (MPCA 11908). Scales bar: 5 cm. 


Figure 6 Hypothetical reconstruction of two abelisaurids showing the soft tissues on the head inferred from osteological morphology of the skull. On the top, Carnotaurus; on the bottom, Pycnonemosaurus.
Art by Maurilio Oliveira.

Rafael Delcourt. 2018. Ceratosaur Palaeobiology: New Insights on Evolution and Ecology of the Southern Rulers. Scientific Reports. 8, 9730.  DOI:   10.1038/s41598-018-28154-x 

Tuesday, June 12, 2018

[Paleontology • 2018] Anomalipes zhaoi • A New Caenagnathid Dinosaur from the Upper Cretaceous Wangshi Group of Shandong, China, with Comments on Size Variation Among Oviraptorosaurs


Anomalipes zhaoi 
 Yu, Wang, Chen, Sullivan, Wang, Wang & Xu, 2018


Abstract
The bone-beds of the Upper Cretaceous Wangshi Group in Zhucheng, Shandong, China are rich in fossil remains of the gigantic hadrosaurid Shantungosaurus. Here we report a new oviraptorosaur, Anomalipes zhaoi gen. et sp. nov., based on a recently collected specimen comprising a partial left hindlimb from the Kugou Locality in Zhucheng. This specimen’s systematic position was assessed by three numerical cladistic analyses based on recently published theropod phylogenetic datasets, with the inclusion of several new characters. Anomalipes zhaoi differs from other known caenagnathids in having a unique combination of features: femoral head anteroposteriorly narrow and with significant posterior orientation; accessory trochanter low and confluent with lesser trochanter; lateral ridge present on femoral lateral surface; weak fourth trochanter present; metatarsal III with triangular proximal articular surface, prominent anterior flange near proximal end, highly asymmetrical hemicondyles, and longitudinal groove on distal articular surface; and ungual of pedal digit II with lateral collateral groove deeper and more dorsally located than medial groove. The holotype of Anomalipes zhaoi is smaller than is typical for Caenagnathidae but larger than is typical for the other major oviraptorosaurian subclade, Oviraptoridae. Size comparisons among oviraptorisaurians show that the Caenagnathidae vary much more widely in size than the Oviraptoridae.


Figure 2 Preserved left femur, tibia, and fibula of Anomalipes zhaoi ZCDM V0020.
 Left femur in anterior (a), posterior (b), lateral (c), medial (d) and proximal (e) views.
Left tibia in anterior (f), posterior (g) and distal (j) views. Shading indicates the articular facet for the ascending process of the astragalus.
Left fibula in lateral (h) and medial (i) views.

Abbreviations: act, accessory trochanter; dg, distinct groove; fc, fibular crest; fh, femoral head; ft, fourth trochanter; gt, greater trochanter; if, iliofibularis tubercle; ig, intercondylar groove; lm, lateral malleolus; lr, lateral ridge; lt, lesser trochanter; mm, medial malleolus; pt, posterior trochanter; taf, triangular articular facet. Scale bar 1 cm.

Figure 3 Preserved pedal elements of Anomalipes zhaoi ZCDM V0020.
Left metatarsal III in lateral (a), medial (b), posterior (c), anterior (d), proximal (e) and distal (f) views. Dark lines indicate ridges on the posterior surface of the shaft.
Phalanx IV-1 in lateral (g), medial (h), proximal (i), and distal (j) views. Phalanx II-3 in lateral (k) and medial (l) views.

Abbreviations: fl, flexor tubercle; lc, lateral condyle; lgf, ligament fossa; pdc, proximal dorsal crest; pdl, proximal dorsal lip; vr, ventral ridge; ptaf, proximal triangular articular facet; rlmh, ridge-like medial hemicondyle; vr, ventral ridge (extending to medial hemicondyle). Scale bar 1 cm.


Systematic palaeontology

Theropoda Marsh 1881
Oviraptorosauria Barsbold 1976

Caenagnathidae Sternberg 1940

Anomalipes zhaoi gen.et sp. nov

Etymology: Generic name is a combination of the Latin “Anomalus” and “pes”, referring to the unusual shape of the foot. Specific name is in honour of Xijin Zhao, a Chinese palaeontologist who has made great contributions to research on Zhucheng dinosaur fossils.

Holotype: ZCDM V0020 (Zhucheng Dinosaur Museum, Zhucheng, Shandong, China), an incomplete left hindlimb, including the left femur missing the distal end, the left tibia missing the proximal end, the left fibula missing the distal and proximal ends, a complete metatarsal III and two pedal phalanges. Although these bones are disarticulated, they are inferred to be derived from a single theropod individual given that 1) they were preserved in a small area of less than 0.3 square metres within a Shantungosaurus bonebed; and 2) no other theropod skeletal elements are preserved nearby.

Locality and horizon: Kugou, Zhucheng City, Shandong Province, China. Upper Cretaceous Wangshi Group.

Diagnosis: A new caenagnathid with the following unique combination of features: femoral head anteroposteriorly narrow and somewhat deflected posteriorly; accessory trochanter low; lateral ridge present on femoral lateral surface; weak fourth trochanter present; metatarsal III with triangular proximal articular surface, prominent anterior flange near proximal end, medial hemicondyle much narrower than lateral hemicondyle, and longitudinal groove on distal articular surface; and pedal phalanx II-3 with lateral collateral groove deeper and more dorsally located than medial groove.

Figure 5 Simplified oviraptorosaurian phylogenetic tree, showing size ranges for basal oviraptorosaurs, the Caenagnathidae, and the Oviraptoridae. Grey boxes represent body mass ranges for three oviraptorosaurian groups: basal oviraptorosaurs, oviraptorids, and caenagnathids. See the electronic supplementary material for estimated body masses of various oviraptorosaurian species.

 Abbreviations: Caud: Caudipteryx zoui; Avim: Avimimus portentosus; Conc: Conchoraptor gracilis; Micr: Microvenator celer; Wula: Wulatelong gobiensis; Citi: Citipati osmolskae; Nank: Nankangia jiangxiensisAnom: Anomalipes zhaoi; Neme: Nemegtia barsboldi; Anzu: Anzu wyliei; Giga: Gigantoraptor erlianensis.

Yilun Yu, Kebai Wang, Shuqing Chen, Corwin Sullivan, Shuo Wang, Peiye Wang and Xing Xu. 2018. A New Caenagnathid Dinosaur from the Upper Cretaceous Wangshi Group of Shandong, China, with Comments on Size Variation Among Oviraptorosaurs. Scientific Reports. volume 8, Article number: 5030. DOI: 10.1038/s41598-018-23252-2