Showing posts with label Sauropod. Show all posts
Showing posts with label Sauropod. Show all posts

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

    

Tuesday, February 5, 2019

[Paleontology • 2019] Bajadasaurus pronuspinax • A New Long-spined Dinosaur from Patagonia sheds light on Sauropod Defense System


Bajadasaurus pronuspinax
Gallina, Apesteguía, Canale & Haluza, 2019

DOI: 10.1038/s41598-018-37943-3
Illustration: Jorge A. González

Abstract
Dicraeosaurids are a group of sauropod dinosaurs characterized by a distinctive vertebral column with paired, long, neural spines, present in an extreme fashion in the South American form Amargasaurus cazaui. This distinctive morphology has been interpreted as a support structure for a thermoregulatory sail, a padded crest for display, a dorsal hump acting as fat reservoir, and even as inner cores for dorsal horns. Other inferred functions (if any) of this structure were related to sexual display and/or defense strategies. Here we describe a new dicraeosaurid sauropod, Bajadasaurus pronuspinax gen. et sp. nov., from Patagonia which preserves the most complete skull of the group and has extremely elongate bifid cervical neural spines that point permanently forward, irrespective of the neck position. Although much shorter versions of this neural spine configuration were already recorded for other dicraeosaurid taxa, the long, anteriorly bent spines of this new dinosaur support the hypothesis that these elongate spines of dicraeosaurid sauropods served as passive defense structures.




Figure 1 Skeletal reconstruction of Bajadasaurus pronuspinax gen. et sp. nov. (MMCh-PV 75), location and quarry map. 
(A) The neck and skull reconstruction in left lateral view, showing preserved bones in white. The complete anterior cervical vertebra is located tentatively in the fifth position (see Description). The total count of cervical elements, as well as the relative extension of the neural spines, is based in the complete series of the related taxon Amargasaurus, the other dicraeosaurid with extremely elongated bifid neural spines along the neck.
 (B) A map of the surrounding area of the Ezequiel Ramos Mexía lake (Neuquén Province, Argentina) showing the type locality of Bajadasaurus (Bajada Colorada) indicated by a white star. 

(C) A quarry map showing the association and location of the remains in the field. at, atlas; ax, axis; cv, cervical vertebra; d, dentary; f, frontal; m, maxilla; po, postorbital; pt, pterygoid; qj, quadratojugal.


Illustration: Jorge A. González

Systematic palaeontology
SAUROPODA Marsh 1878
DIPLODOCOIDEA Marsh 1884
FLAGELLICAUDATA Harris & Dodson 2004

DICRAEOSAURIDAE Huene 1927

Bajadasaurus pronuspinax gen. et sp. nov.

Etymology: Generic name from Bajada (Spanish for downhill, in reference to the locality Bajada Colorada) and saurus (Greek, lizard). Specific epithet from pronus (Latin, bent over forward) and spinax (Greek, spine), referring to the anteriorly pointed, curved, neural spines of the cervical vertebrae.


    



Pablo A. Gallina, Sebastián Apesteguía, Juan I. Canale and Alejandro Haluza. 2019. A New Long-spined Dinosaur from Patagonia sheds light on Sauropod Defense System. Scientific Reports. 9: 1392. DOI: 10.1038/s41598-018-37943-3

  

    

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

Wednesday, July 25, 2018

[Paleontology • 2018] Lingwulong shenqi • A New Middle Jurassic Diplodocoid Suggests An Earlier Dispersal and Diversification of Sauropod Dinosaurs


Lingwulong shenqi
Xu, Upchurch, Mannion, Barrett, Regalado-Fernandez, Mo, Ma & Liu, 2018


Abstract
The fragmentation of the supercontinent Pangaea has been suggested to have had a profound impact on Mesozoic terrestrial vertebrate distributions. One current paradigm is that geographic isolation produced an endemic biota in East Asia during the Jurassic, while simultaneously preventing diplodocoid sauropod dinosaurs and several other tetrapod groups from reaching this region. Here we report the discovery of the earliest diplodocoid, and the first from East Asia, to our knowledge, based on fossil material comprising multiple individuals and most parts of the skeleton of an early Middle Jurassic dicraeosaurid. The new discovery challenges conventional biogeographical ideas, and suggests that dispersal into East Asia occurred much earlier than expected. Moreover, the age of this new taxon indicates that many advanced sauropod lineages originated at least 15 million years earlier than previously realised, achieving a global distribution while Pangaea was still a coherent landmass.


Systematic paleontology
Sauropoda Marsh, 1878
Neosauropoda Bonaparte, 1986
Diplodocoidea (Marsh, 1884)

Dicraeosauridae Janensch, 1929

Lingwulong shenqi gen. et sp. nov.

Etymology: Lingwu, after the region where the specimens were found; long, the Mandarin Chinese for ‘dragon’; and shenqi, the Mandarin Chinese for ‘amazing’, reflecting the unexpected discovery of a dicraeosaurid in the Middle Jurassic of China.

Horizon and locality: Yanan Formation, late Early to early Middle Jurassic (late Toarcian–Bajocian), Lingwu Geopark, near Ciyaopu, Ningxia Hui Autonomous Region, China.

Diagnosis: Autapomorphies: prefrontal anterior process directed laterally; orbital dorsal margin strongly ornamented by deep, longitudinal grooves and tubercles; long-axes of the free tips of the basal tubera directed anteromedially; capitate process mediolaterally long (length:height ratio c. 5.0); occipital condyle articular surface wide transversely (width:height ratio c. 1.54); lateral surface of cervical prezygapophyseal process bears a ridge formed by a linear array of tubercles; subcircular facet-like region at the summit of metapophyses in middle cervical-anterior dorsal vertebrae; small process projects anterodorsally from the anterior margin of the transverse process, near its distal end, in anterior dorsal vertebrae; anterior dorsal metapophyses twisted along their length; anterior caudal neural spines bear subtriangular facet-like areas, extending from summit to spine mid-height.




Fig. 1 Cranial material of Lingwulong shenqi. Braincase in:
 left lateral (a), dorsal (b), occipital (c), and ventral (d) views. Dentary teeth in occlusal view (e). The 5th and 6th left dentary tooth crowns in labial view (f).

 Abbreviations: bpp, basipterygoid process; bt, basal tubera; f, frontal; fps, frontoparietal suture; gt, grooves and tubercles; pf, prefrontal; llp, ‘leaf’-like process; oc, occipital condyle; p, parietal; pcp, capitate process; paf, proatlantal facet; pag, proatlantal groove; pfap, prefrontal anterior process; po, postorbital; povp, postorbital ventral process; pp, paroccipital process; sc, sagittal crest; so, supraoccipital; sq, squamosal; sqhp, squamosal hook-like process; sqvp, squamosal ventral process; stf, supratemporal fenestra; wf, wear facet. Scale bars = 20 mm for a–e and 10 mm for f

Fig. 2 Skeletal reconstruction and exemplar skeletal remains of Lingwulong shenqi.
 Silhouette showing preserved elements (a); middle cervical vertebra in left lateral (b) and anterior (c) views; anterior dorsal vertebra in left lateral (d) and anterior (e) views; posterior dorsal vertebra in lateral view (f); sacrum and ilium in left lateral view (g); anterior caudal vertebra in left lateral (h) and anterior (i) views; right scapulocoracoid in lateral view (j); right humerus in anterior view (k); left pubis in lateral view (l); right ischium in lateral (m) views; right femur in posterior view (n); and right tibia in lateral view (o).

Abbreviations: ap, ambiens process; ar, acromial ridge; ip, iliac peduncle; naf, notch anterior to glenoid; np, neural spine; podl, postzygodiapophyseal lamina; ppr, prezygapophyseal process ridge; prp, prezygapophysis; pvf, posteroventral fossa; slf, shallow lateral fossa; spol, spinopostzygapophyseal lamina; sprl, spinoprezygapophyseal lamina; wls, wing-like structure. Scale bars = 100 cm for a and 5 cm for b–o

Fig. 3 Time-calibrated evolutionary tree for Eusauropoda. Agreement subtree produced in TNT, with additional diplodocid taxa incorporated (see Supplementary Note 4). All macronarian taxa have been combined into a single lineage, and non-sauropod sauropodomorphs have been removed, in order to enhance clarity (see Supplementary Fig. 13 for the full version of this tree). Silhouettes of dinosaurs drawn by Scott Hartman, Mike Taylor, and Mathew Wedel, and available at Phylopic (phylopic.org) under a Creative Commons Attribution 3.0 Unported license. Global paleogeographic reconstructions from the Paleobiology Database (paleobiodb.org)
  


Xing Xu, Paul Upchurch, Philip D. Mannion, Paul M. Barrett, Omar R. Regalado-Fernandez, Jinyou Mo, Jinfu Ma and Hongan Liu. 2018. A New Middle Jurassic Diplodocoid Suggests An Earlier Dispersal and Diversification of Sauropod Dinosaurs. Nature Communications. 9, 2700.  DOI:  10.1038/s41467-018-05128-1

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