First complete sauropod dinosaur skull from the Cretaceous of the Americas and the evolution of sauropod dentition (original) (raw)
Related papers
2010 Abydosaurus scientific paper
Sauropod dinosaur bones are common in Mesozoic terrestrial sediments, but sauropod skulls are exceedingly rare-cranial materials are known for less than one third of sauropod genera and even fewer are known from complete skulls. Here we describe the first complete sauropod skull from the Cretaceous of the Americas, Abydosaurus mcintoshi, n. gen., n. sp., known from 104.46±0.95 Ma (megannum) sediments from Dinosaur National Monument, USA. Abydosaurus shares close ancestry with Brachiosaurus, which appeared in the fossil record ca. 45 million years earlier and had substantially broader teeth. A survey of tooth shape in sauropodomorphs demonstrates that sauropods evolved broad crowns during the Early Jurassic but did not evolve narrow crowns until the Late Jurassic, when they occupied their greatest range of crown breadths. During the Cretaceous, brachiosaurids and other lineages independently underwent a marked diminution in tooth breadth, and before the latest Cretaceous broad-crowned sauropods were extinct on all continental landmasses. Differential survival and diversification of narrow-crowned sauropods in the Late Cretaceous appears to be a directed trend that was not correlated with changes in plant diversity or abundance, but may signal a shift towards elevated tooth replacement rates and highwear dentition. Sauropods lacked many of the complex herbivorous adaptations present within contemporaneous ornithischian herbivores, such as beaks, cheeks, kinesis, and heterodonty. The spartan design of sauropod skulls may be related to their remarkably small size-sauropod skulls account for only 1/200th of total body volume compared to 1/30th body volume in ornithopod dinosaurs.
Advanced titanosaurian sauropods, such as nemegtosaurids and saltasaurids, were diverse and one of the most important groups of herbivores in the terrestrial biotas of the Late Cretaceous. However, little is known about their rise and diversification prior to the Late Cretaceous. Furthermore, the evolution of their highly-modified skull anatomy has been largely hindered by the scarcity of well-preserved cranial remains. A new sauropod dinosaur from the Early Cretaceous of Brazil represents the earliest advanced titanosaurian known to date, demonstrating that the initial diversification of advanced titanosaurians was well under way at least 30 million years before their known radiation in the latest Cretaceous. The new taxon also preserves the most complete skull among titanosaurians, further revealing that their low and elongated diplodocid-like skull morphology appeared much earlier than previously thought.
A complete skull of an Early Cretaceous sauropod and the evolution of advanced titanosaurians
PLOS One, 2011
Advanced titanosaurian sauropods, such as nemegtosaurids and saltasaurids, were diverse and one of the most important groups of herbivores in the terrestrial biotas of the Late Cretaceous. However, little is known about their rise and diversification prior to the Late Cretaceous. Furthermore, the evolution of their highly-modified skull anatomy has been largely hindered by the scarcity of well-preserved cranial remains. A new sauropod dinosaur from the Early Cretaceous of Brazil represents the earliest advanced titanosaurian known to date, demonstrating that the initial diversification of advanced titanosaurians was well under way at least 30 million years before their known radiation in the latest Cretaceous. The new taxon also preserves the most complete skull among titanosaurians, further revealing that their low and elongated diplodocid-like skull morphology appeared much earlier than previously thought.
Journal of Vertebrate …, 2010
More than any other sauropod dinosaur group, the long-necked herbivores belonging to Diplodocoidea have been defined by their skulls. Their unique skull shape, which is extremely elongate antorbitally, with a transversely broad, square snout packed at its anterior extreme with narrow-crowned, pencil-like teeth, has served as a touchstone for describing the biology of these animals ever since the discovery of the first skull in the late 19th century. In particular, the unusual diplodocoid skull has been discussed frequently in the context of examining feeding behavior, spawning hypotheses ranging from branch stripping, propalinal shearing, and aquatic plant 'grazing.' Here, we describe a juvenile skull of Diplodocus (Carnegie Museum 11255) that does not share the unusually blunted snout and anteriorly sequestered teeth seen in adult specimens, suggesting that adults and juveniles may have differed greatly in their feeding behavior, an ontogenetic distinction that may be unique among sauropodomorphs.
Biology of the sauropod dinosaurs: the evolution of gigantism
The herbivorous sauropod dinosaurs of the Jurassic and Cretaceous periods were the largest terrestrial animals ever, surpassing the largest herbivorous mammals by an order of magnitude in body mass. Several evolutionary lineages among Sauropoda produced giants with body masses in excess of 50 metric tonnes by conservative estimates. With body mass increase driven by the selective advantages of large body size, animal lineages will increase in body size until they reach the limit determined by the interplay of bauplan, biology, and resource availability. There is no evidence, however, that resource availability and global physicochemical parameters were different enough in the Mesozoic to have led to sauropod gigantism.We review the biology of sauropod dinosaurs in detail and posit that sauropod gigantism was made possible by a specific combination of plesiomorphic characters (phylogenetic heritage) and evolutionary innovations at different levels which triggered a remarkable evolutionary cascade. Of these key innovations, the most important probably was the very long neck, the most conspicuous feature of the sauropod bauplan. Compared to other herbivores, the long neck allowed more efficient food uptake than in other large herbivores by covering a much larger feeding envelope and making food accessible that was out of the reach of other herbivores. Sauropods thus must have been able to take up more energy from their environment than other herbivores.The long neck, in turn, could only evolve because of the small head and the extensive pneumatization of the sauropod axial skeleton, lightening the neck. The small head was possible because food was ingested without mastication. Both mastication and a gastric mill would have limited food uptake rate. Scaling relationships between gastrointestinal tract size and basal metabolic rate (BMR) suggest that sauropods compensated for the lack of particle reduction with long retention times, even at high uptake rates.The extensive pneumatization of the axial skeleton resulted from the evolution of an avian-style respiratory system, presumably at the base of Saurischia. An avian-style respiratory system would also have lowered the cost of breathing, reduced specific gravity, and may have been important in removing excess body heat. Another crucial innovation inherited from basal dinosaurs was a high BMR. This is required for fueling the high growth rate necessary for a multi-tonne animal to survive to reproductive maturity.The retention of the plesiomorphic oviparous mode of reproduction appears to have been critical as well, allowing much faster population recovery than in megaherbivore mammals. Sauropods produced numerous but small offspring each season while land mammals show a negative correlation of reproductive output to body size. This permitted lower population densities in sauropods than in megaherbivore mammals but larger individuals.Our work on sauropod dinosaurs thus informs us about evolutionary limits to body size in other groups of herbivorous terrestrial tetrapods. Ectothermic reptiles are strongly limited by their low BMR, remaining small. Mammals are limited by their extensive mastication and their vivipary, while ornithsichian dinosaurs were only limited by their extensive mastication, having greater average body sizes than mammals.
Scientific reports, 2018
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 partition...
How to get big in the Mesozoic: The Evolution of the sauropodomorph body plan
Sauropod (or, more correctly, eusauropod) dinosaurs are highly distinctive, not only in their overall body form, but also in respect to many details of their anatomy. In comparison with basal dinosaurs, typical sauropods are characterized by small skulls, elongate necks, massive bodies, and an obligatory quadrupedal stance with elongate forelimbs and straight limbs in general. Tracing the anatomical changes that led to this distinctive body plan through sauropodomorph evolution is problematic as a result of the incompleteness of many basal taxa and phylogenetic uncertainty at the base of the clade. The decrease in skull size in sauropodomorphs seems to be abrupt at the base of the clade, but it is even more pronounced toward sauropods. Major changes in the sauropod skull are a relative shortening and broadening of the snout and an enlargement and retraction of the nares. Although the ultimate causes for these evolutionary changes are certainly manifold, most if not all of them seem to be related to the ecological and biomechanical requirements of the transition from a carnivorous to an herbivorous lifestyle, in which the skull is mainly used as a cropping device. A relatively elongate neck seems to be ancestral for sauropodomorphs, but the neck is further elongated on the lineage toward sauropods, especially by incorporation of two additional vertebrae at the base of Sauropoda. The relatively simple structure of the cervical vertebrae in basal sauropodomorphs might be a secondary reduction relative to basal saurischians as a result of changes in neck biomechanics in connection with the reduction of the size of the skull. Thus, the more complicated structure of sauropod cervicals probably reflects changing biomechanical requirements in connection with an elongation of the neck and an increase in body size, as does the opisthocoelous structure of the cervical vertebral centra. Limb evolution in sauropodomorphs is dominated by adaptations toward increasing body size and thus graviportality, with the limbs getting straighter and the distal limb segments relatively shorter. Body size increase in sauropodomorphs seems to have been rapid but even-paced, with the ancestral body size of the clade being in the 0–10 kg category, and the ancestral body size for sauropods probably being in the 1,000–10,000 kg category.
Amygdalodon patagonicus is the oldest record of Sauropoda from South America and is known from several teeth and fragmentary postcranial remains. Here we describe in detail its dental morphology, characterized by the presence of broad spatulated teeth (with low SI values) and the absence of denticles in their crowns. The enamel bears a particular wrinkling pattern composed only of apicobasally-aligned pits, which are frequently joined to each other by a continuous sulcus. Some worn teeth have large wear-facets that extend over only one of the crown’s edges. This unique combination of characters provides a proper diagnosis for Amygdalodon. Despite the fragmentary available material, Amygdalodon is here interpreted as a non-eusauropod sauropod based on the results of a phylogenetic analysis. The presence of derived dental characters in Amygdalodon, such as the presence of tooth-tooth occlusion, shows several features previously thought to diagnose Eusauropoda or Gravisauria appeared earlier during the early evolution of sauropods.
Sauroposeidon Proteles,A New Sauropod from the Early Cretaceous
2000
Sauroposeidon proteles, a new brachiosaurid sauropod, is represented by an articulated series of four mid-cervical vertebrae recovered from the Antlers Formation (Aptian-Albian) of southeastern Oklahoma. Most Early Cretaceous North American sauropod material has been referred to Pleurocoelus, a genus which is largely represented by juvenile material and is not well understood. Regardless of the status and affinities of Pleurocoelus, the new taxon is morphologically and proportionally distinct. Among well-known sauropod taxa, Sauroposeidon is most similar to Brachiosaurus; particularly noteworthy are the neural spines, which are set forward on the centra and are not bifurcate, and the extremely elongate cervical ribs. Sauroposeidon and Brachiosaurus also share a derived pattern of pneumatic vertebral ultrastructure and a mid-cervical transition point, at which neural spine morphology changes from very low (anteriorly) to very high (posteriorly). Autapomorphies of Sauroposeidon include posterior placement of the diapophyses, hypertrophied pneumatic fossae in the lateral faces of the neural spines and centra, and an extraordinary degree of vertebral elongation (e.g., C8 ϭ 1.25 m; 25% longer than Brachiosaurus). Additional sauropod material from the Early Cretaceous Cloverly Formation may be referrable to the new Oklahoma sauropod, which appears to be the last of the giant North American sauropods and represents the culmination of brachiosaurid trends towards lengthening and lightening of the neck.