A large iguanodont from the Upper Barremian of the Paris Basin

The remains of an ornithopod dinosaur from the Upper Barremian (Lower Cretaceous) of Auxerre (Burgundy, France) are described. They consist of several vertebrae and a fragmentary scapula. Despite obvious morphological and dimensional affinities with the species Iguanodon bernissartensis, the state of the specimen does not allow any identification more precise than Iguanodontia indet. Reappraisal of the French Upper Barremian record of medium and large-sized ornithopods reveals that no specimen can be definitely determined to the specific level.     

A new herrerasaurid (Dinosauria, Saurischia) from the Upper Triassic Ischigualasto Formation of northwestern Argentina

Herrerasauridae comprises a basal clade of dinosaurs best known from the Upper Triassic of Argentina and Brazil, which have yielded remains of Herrerasaurus ischigualastensis and Staurikosaurus pricei, respectively. Systematic opinion regarding the position of Herrerasauridae at the base of Dinosauria has varied. Here we describe a new herrerasaurid, Sanjuansaurus gordilloi gen. n., sp. n., based on a partial skeleton from Carnian-age strata of the the Upper Triassic Ischigualasto Formation of northwestern Argentina. The new taxon is diagnosed by numerous features, including long, band-shaped and posterolaterally oriented transverse process on the posterior cervical vertebrae; neural spines of the sixth to eighth dorsal vertebrae, at least, bearing acute anterior and posterior processes; scapula and coracoid with everted lateral margins of the glenoid; and short pubis (63% of the femoral length). Phylogenetic analysis placed Sanjuansaurus within a monophyletic Herrerasauridae, at the base of Theropoda and including Herrerasaurus and Staurikosaurus. The presence of Sanjuansaurus at the base of the Ischigualasto Formation, along with other dinosaurs such as Herrerasaurus, Eoraptor, Panphagia, and Chromogisaurus suggests that saurischian dinosaurs in southwestern Pangea were already widely diversified by the late Carnian rather than increasing in diversity across the Carnian-Norian boundary.     

The hand structure of Carnotaurus sastrei (Theropoda,Abelisauridae): implications for hand diversity and evolution in abelisaurids

Abstract: Carnotaurus sastrei is an abelisaurid dinosaur from the Late Cretaceous of Argentina that has very reduced, but robust, forelimbs and derived hands with four digits, including a large, conical‐shaped metacarpal IV lacking an articulation for a phalanx. The analysis presented in this work highlights a series of additional autapomorphies of C. sastrei. For example, the proximal phalanges are longer than the metacarpals in digits II and III, and digit III includes only one phalanx besides the ungual. The hand of Carnotaurus shares several features with those of Aucasaurus and Majungasaurus, but the hands of the latter genera also display autapomorphies, indicating that the diversity in abelisaurid hand structure is similar to the diversity of cranial protuberances of these dinosaurs.     

Evolution of dinosaur epidermal structures

Spectacularly preserved non-avian dinosaurs with integumentary filaments/feathers have revolutionized dinosaur studies and fostered the suggestion that the dinosaur common ancestor possessed complex integumentary structures homologous to feathers. This hypothesis has major implications for interpreting dinosaur biology, but has not been tested rigorously. Using a comprehensive database of dinosaur skin traces, we apply maximum-likelihood methods to reconstruct the phylogenetic distribution of epidermal structures and interpret their evolutionary history. Most of these analyses find no compelling evidence for the appearance of protofeathers in the dinosaur common ancestor and scales are usually recovered as the plesiomorphic state, but results are sensitive to the outgroup condition in pterosaurs. Rare occurrences of ornithischian filamentous integument might represent independent acquisitions of novel epidermal structures that are not homologous with theropod feathers.     

Sauropod dinosaurs evolved moderately sized genomes unrelated to body size

Sauropodomorph dinosaurs include the largest land animals to have ever lived, some reaching up to 10 times the mass of an African elephant. Despite their status defining the upper range for body size in land animals, it remains unknown whether sauropodomorphs evolved larger-sized genomes than non-avian theropods, their sister taxon, or whether a relationship exists between genome size and body size in dinosaurs, two questions critical for understanding broad patterns of genome evolution in dinosaurs. Here we report inferences of genome size for 10 sauropodomorph taxa. The estimates are derived from a Bayesian phylogenetic generalized least squares approach that generates posterior distributions of regression models relating genome size to osteocyte lacunae volume in extant tetrapods. We estimate that the average genome size of sauropodomorphs was 2.02 pg (range of species means: 1.77–2.21 pg), a value in the upper range of extant birds (mean = 1.42 pg, range: 0.97–2.16 pg) and near the average for extant non-avian reptiles (mean = 2.24 pg, range: 1.05–5.44 pg). The results suggest that the variation in size and architecture of genomes in extinct dinosaurs was lower than the variation found in mammals. A substantial difference in genome size separates the two major clades within dinosaurs, Ornithischia (large genomes) and Saurischia (moderate to small genomes). We find no relationship between body size and estimated genome size in extinct dinosaurs, which suggests that neutral forces did not dominate the evolution of genome size in this group.     

Vestigial skeletal structures in dinosaurs

The existence of vestigial structures is one of the main lines of evidence for macroevolution. Here I introduce a phylogenetic bracketing approach to the identification of vestigial structures and apply it to Dinosauria. According to this approach, a structure is considered vestigial if, in comparison with its homolog in at least three successive outgroups, it is reduced to one-third or less its size relative to adjacent structures and if at least distally it has lost the specialized morphology present in the three outgroups. This approach identifies fingers IV and V as vestigial in dinosaurs in general, II–V in sauropods, III in Tyrannosauridae and Caudipteryx , II and III in Shuvuuia and I and III in modern birds. The entire forelimb distal to the elbow is vestigial in Abelisauridae. Vestigial parts of the pelvic girdle and hindlimb include the pubic shaft in Iguanodontia and Ceratopsia, the entire pubis in Ankylosauria, the first metatarsal in derived Iguanodontia, the first metatarsal shaft in Theropoda and the fifth toe in dinosaurs in general. Derived Centrosaurinae and some Chasmosaurus exhibit vestigial supraorbital horns. Some centrosaurines have a vestigial nasal horn. The antorbital cavity is vestigial in Thyreophora, Iguanodontia and Ceratopsidae. I recommend that this information be exploited to increase public awareness of the evidence for macroevolution.     

A revision of the sauropod dinosaur genus ‘Bothriospondylus’ with a redescription of the type material of the Middle Jurassic form ‘B. madagascariensis’

Abstract: The sauropod dinosaur ‘Bothriospondylus’, originally named on the basis of Late Jurassic remains from England, is demonstrated to be invalid, and the characters used to diagnose it are shown to be obsolescent features which are widespread throughout Sauropoda. Material referred to this genus spans a temporal range from the Middle Jurassic until the early Late Cretaceous and has been described from five different countries, across three continents. These remains represent a wide array of sauropod groups, comprising non‐neosauropod eusauropods, a macronarian, titanosauriforms (including at least one definite brachiosaurid) and a rebbachisaurid. The type material of the Middle Jurassic ‘B. madagascariensis’ represents a derived non‐neosauropod eusauropod and possesses two potential autapomorphies. However, as a result of the fragmentary nature of the material and the uncertainty surrounding its association, a new taxon is not erected. Of the numerous specimens referred to ‘Bothriospondylus’, however, several remains are considered diagnostic: Ornithopsis hulkei (Early Cretaceous, UK), Lapparentosaurus madagascariensis (Middle Jurassic, Madagascar) and Nopcsaspondylus alarconensis (early Late Cretaceous, Argentina). At least three types of sauropod were present in the Bathonian (Middle Jurassic) of north‐west Madagascar, with a basal eusauropod (Archaeodontosaurus), a more derived eusauropod (‘B. madagascariensis’) and a titanosauriform (Lapparentosaurus) all approximately contemporaneous. Palaeocontinental reconstructions suggest that Middle Jurassic Madagascan sauropods would still have been capable of global biotic interchange, and this is perhaps reflected in their diverse assemblage. Re‐evaluation of these Malagasy forms has shed new light on this important time period in sauropod evolution.     

A longirostrine tyrannosauroid from the Early Cretaceous of China

The fossil record of tyrannosauroid theropods is marked by a substantial temporal and morphological gap between small-bodied, Barremian taxa, and extremely large-bodied taxa from the latest Cretaceous. Here we describe a new tyrannosauroid, Xiongguanlong baimoensis n. gen. et sp., from the Aptian–Albian Xinminpu Group of western China that represents a phylogenetic, morphological, and temporal link between these disjunct portions of tyrannosauroid evolutionary history. Xiongguanlong is recovered in our phylogenetic analysis as the sister taxon to Tyrannosauridae plus Appalachiosaurus, and marks the appearance of several tyrannosaurid hallmark features, including a sharp parietal sagittal crest, a boxy basicranium, a quadratojugal with a flaring dorsal process and a flexed caudal edge, premaxillary teeth bearing a median lingual ridge, and an expanded axial neural spine surmounted by distinct processes at its corners. Xiongguanlong is characterized by a narrow and elongate muzzle resembling that of Alioramus. The slender, unornamented nasals of Xiongguanlong are inconsistent with recent hypotheses of correlated progression in tyrannosauroid feeding mechanics, and suggest more complex patterns of character evolution in the integration of feeding adaptations in tyrannosaurids. Body mass estimates for the full-grown holotype specimen of Xiongguanlong fall between those of Late Cretaceous tyrannosaurids and Barremian tyrannosauroids, suggesting that the trend of increasing body size observed in North American Late Cretaceous Tyrannosauridae may extend through the Cretaceous history of Tyrannosauroidea though further phylogenetic work is required to corroborate this.     

Necks for sex: sexual selection as an explanation for sauropod dinosaur neck elongation

The immensely long neck of a sauropod is one of the most familiar and striking of anatomical specializations among dinosaurs. Here, I use recently collected neontological and paleontological information to test the predictions of two competing hypotheses proposed to explain the significance of the long neck. According to the traditional hypothesis, neck elongation in sauropods increased feeding height, thereby reducing competition with contemporaries for food. According to the other hypothesis, which is advanced for the first time here, neck elongation in sauropods was driven by sexual selection. Available data match the predictions of the sexual selection hypothesis and contradict the predictions of the feeding competition hypothesis. It is therefore more plausible that increases in sauropod neck lengths were driven by sexual selection than by competition for foliage.