Matthew T. Carrano

The osteology of Masiakasaurus knopfleri, a small abelisauroid (Dinosauria: Theropoda) from the Late Cretaceous of Madagascar

Abstract We describe the osteology of the new small theropod dinosaur Masiakasaurus knopfleri, from the Late Cretaceous Maevarano Formation of northwestern Madagascar. Approximately 40% of the skeleton is known, including parts of the jaws, axial column, forelimb, pelvic girdle, and hind limb. The jaws of Masiakasaurus are remarkably derived, bearing a heterodont, procumbent dentition that is unknown elsewhere among dinosaurs. The vertebrae are similar to those of abelisauroids in the reduction of the neural spine, lack of pleurocoelous fossae on the centrum, and extensively pneumatized neural arch. The limb skeleton is relatively gracile and bears numerous abelisauroid synapomorphies, including a rounded humeral head, peg-and-socket iliac-pubic articulation, prominent femoral medial epicondyle, expanded tibial cnemial crest, and double-grooved pedal unguals. The femora and tibiae show evidence of dimorphism. More specific features shared between Masiakasaurus, the Argentine Noasaurus, and the Indian Laevisuchus suggest that these taxa form a clade (Noasauridae) within Abelisauroidea. This is supported by a cladistic phylogenetic analysis of 158 characters and 23 theropod taxa. Additionally, Ceratosauria is rendered paraphyletic in favor of a sister-taxon relationship between Neoceratosauria and Tetanurae that is exclusive of Coelophysoidea. The unique dental and jaw specializations of Masiakasaurus suggest deviation from the typical theropod diet. Finally, the distribution of noasaurids further supports a shared biogeographic history between South America, Madagascar, and India into the Late Cretaceous.

The Phylogeny of Ceratosauria (Dinosauria: Theropoda)

Synopsis Recent discoveries and analyses have drawn increased attention to Ceratosauria, a taxonomically and morphologically diverse group of basal theropods. By the time of its first appearance in the Late Jurassic, the group was probably globally distributed. This pattern eventually gave way to a primarily Gondwanan distribution by the Late Cretaceous. Ceratosaurs are one of several focal groups for studies of Cretaceous palaeobiogeography and their often bizarre morphological developments highlight their distinctiveness. Unfortunately, lack of phylogenetic resolution, shifting views of which taxa fall within Ceratosauria and minimal overlap in coverage between systematic studies, have made it difficult to explicate any of these important evolutionary patterns. Although many taxa are fragmentary, an increase in new, more complete forms has clarified much of ceratosaur anatomy, allowed the identification of additional materials and increased our ability to compare specimens and taxa. We studied nearly 40 ceratosaurs from the Late Jurassic‐Late Cretaceous of North and South America, Europe, Africa, India and Madagascar, ultimately selecting 18 for a new cladistic analysis. The results suggest that Elaphrosaurus and its relatives are the most basal ceratosaurs, followed by Ceratosaurus and Noasauridae + Abelisauridae (= Abelisauroidea). Several additional forms were identified as noasaurids, including Genusaurus. Within Abelisauridae, our analysis reveals a clade including Majungasaurus and the Indian forms, as well as a more weakly supported clade comprising Carnotaurus and Ilokelesia. These results greatly clarify the sequence of character acquisition leading to, and within, Abelisauroidea. Thanks to new noasaurid materials (particularly Masiakasaurus), numerous formerly ambiguous characters can now be resolved as either abelisaurid, noasaurid or abelisauroid synapomorphies. Skull and forelimb shortening, for example, now appear to be features confined to Abelisauridae. Nevertheless, a great deal of phylogenetic resolution is lacking, particularly among noasaurids, which hampers attempts to glean meaningful biogeographical information from the phylogeny. As a result, tem poral and geographical sampling biases are probably contributing to the apparent patterns in the data and we suggest that definitive answers must await new discoveries. None of the recent ceratosaurian discoveries bear directly on the controversy surrounding latest Cretaceous ceratosaur biogeography.

The phylogeny of Tetanurae (Dinosauria: Theropoda)

Tetanuran theropods represent the majority of Mesozoic predatory dinosaur diversity and the lineage leading to extant Aves. Thus their history is relevant to understanding the evolution of dinosaur diversity, Mesozoic terrestrial ecosystems, and modern birds. Previously, the fragmentary and poorly sampled fossil record of basal (non-coelurosaur) tetanurans led to uncertainties regarding their basic interrelationships. This in turn prevented determining the relationships of many incompletely known taxa that nonetheless document a global radiation spanning more than 120 million years. We undertook an exhaustive examination of all basal tetanurans and all existing character data, taking advantage of recent discoveries and adding new morphological, temporal and geographic data. Our cladistic analysis of 61 taxa achieved significantly improved phylogenetic resolution. These results position several ‘stem’ taxa basal to a succession of monophyletic clades (Megalosauroidea, Allosauroidea and Coelurosauria). Megalosauroids include nearly 20 taxa arrayed amongst a basalmost clade (Piatnitzkysauridae, fam. nov.) and the sister taxa Spinosauridae and Megalosauridae; the latter includes two subfamilies, Megalosaurinae and Afrovenatorinae subfam. nov. Allosauroidea contains a diverse Metriacanthosauridae (= Sinraptoridae), Neovenatoridae, Carcharodontosauridae and a reduced Allosauridae. Finally, we assessed more than 40 fragmentary forms and hundreds of additional reported tetanuran occurrences. Tetanuran evolution was characterized by repeated acquisitions of giant body size and at least two general skull forms, but few variations in locomotor morphology. Despite parallel diversification of multiple lineages, there is evidence for a succession of ‘dominant’ clades. Tetanurae first appeared by the Early Jurassic and was globally distributed by the Middle Jurassic. Several major clades appeared prior to the breakup of Pangaea; as such their absence in specific regions, and at later times, must be due to poor sampling, dispersal failure and/or regional extinction. Finally, we outline a general perspective on Mesozoic terrestrial biogeography that should apply to most clades that appeared before the Late Jurassic.

Testing the effect of the rock record on diversity: a multidisciplinary approach to elucidating the generic richness of sauropodomorph dinosaurs through time

The accurate reconstruction of palaeobiodiversity patterns is central to a detailed understanding of the macroevolutionary history of a group of organisms. However, there is increasing evidence that diversity patterns observed directly from the fossil record are strongly influenced by fluctuations in the quality of our sampling of the rock record; thus, any patterns we see may reflect sampling biases, rather than genuine biological signals. Previous dinosaur diversity studies have suggested that fluctuations in sauropodomorph palaeobiodiversity reflect genuine biological signals, in comparison to theropods and ornithischians whose diversity seems to be largely controlled by the rock record. Most previous diversity analyses that have attempted to take into account the effects of sampling biases have used only a single method or proxy: here we use a number of techniques in order to elucidate diversity. A global database of all known sauropodomorph body fossil occurrences (2024) was constructed. A taxic diversity curve for all valid sauropodomorph genera was extracted from this database and compared statistically with several sampling proxies (rock outcrop area and dinosaur‐bearing formations and collections), each of which captures a different aspect of fossil record sampling. Phylogenetic diversity estimates, residuals and sample‐based rarefaction (including the first attempt to capture ‘cryptic’ diversity in dinosaurs) were implemented to investigate further the effects of sampling. After ‘removal’ of biases, sauropodomorph diversity appears to be genuinely high in the Norian, Pliensbachian–Toarcian, Bathonian–Callovian and Kimmeridgian–Tithonian (with a small peak in the Aptian), whereas low diversity levels are recorded for the Oxfordian and Berriasian–Barremian, with the Jurassic/Cretaceous boundary seemingly representing a real diversity trough. Observed diversity in the remaining Triassic–Jurassic stages appears to be largely driven by sampling effort. Late Cretaceous diversity is difficult to elucidate and it is possible that this interval remains relatively under‐sampled. Despite its distortion by sampling biases, much of sauropodomorph palaeobiodiversity can be interpreted as a reflection of genuine biological signals, and fluctuations in sea level may account for some of these diversity patterns.

Rates of Dinosaur Body Mass Evolution Indicate 170 Million Years of Sustained Ecological Innovation on the Avian Stem Lineage

Early dinosaurs showed rapid evolutionary rates, which were sustained on the line leading to birds. Maintenance of evolvability in key lineages might explain the uneven distribution of trait diversity among groups of animal species.

Taxon distributions and the tetrapod track record

Abstract Vertebrate tracks are a unique, abundant source of fossil data that supplements the skeletal record in many ways. However, the utility of ichnofossil data depends on how specifically the authors of tracks can be identified. Despite this fact, there is little consensus about how to identify potential trackmakers, and existing methods differ in their bases, assumptions, and corresponding implications. In this paper we support the proposal that trackmakers should be identified primarily by skeletal structures that are both preserved in the ichnofossils and synapomorphies of some body-fossil clade. This synapomorphy-based technique enables certain taxa to be positively identified as candidate trackmakers and others to be excluded from consideration. In addition, the diagnostic level of the synapomorphy (i.e., to a higher or lower level) corresponds to that of the trackmaker. Additional features, such as body size and provenance, can be used in association with synapomorphies as additional differentiae of trackmaker identity. Trackway analyses are dependent on the level of trackmaker diagnosis, but not all analyses require the same diagnostic specificity. Palichnostratigraphic correlations to the stage level are shown to require at least a genus-level identification of a trackmaker, whereas studies of vertebrate distributions (i.e., origins, extinctions, ranges) accommodate much coarser designations. Anachronistic occurrences of trace and body fossils result in range extensions for either the skeletal taxon or the feature in question. For example, the temporal distribution of theropods can be extended on the basis of the footprint record, resulting in an earlier estimated divergence time for Dinosauria.

Sea level, dinosaur diversity and sampling biases: investigating the 'common cause' hypothesis in the terrestrial realm

The fossil record is our primary window onto the diversification of ancient life, but there are widespread concerns that sampling biases may distort observed palaeodiversity counts. Such concerns have been reinforced by numerous studies that found correlations between measures of sampling intensity and observed diversity. However, correlation does not necessarily mean that sampling controls observed diversity: an alternative view is that both sampling and diversity may be driven by some common factor (e.g. variation in continental flooding driven by sea level). The latter is known as the ‘common cause’ hypothesis. Here, we present quantitative analyses of the relationships between dinosaur diversity, sampling of the dinosaur fossil record, and changes in continental flooding and sea level, providing new insights into terrestrial common cause. Although raw data show significant correlations between continental flooding/sea level and both observed diversity and sampling, these correlations do not survive detrending or removal of short-term autocorrelation. By contrast, the strong correlation between diversity and sampling is robust to various data transformations. Correlations between continental flooding/sea level and taxic diversity/sampling result from a shared upward trend in all data series, and short-term changes in continental flooding/sea level and diversity/sampling do not correlate. The hypothesis that global dinosaur diversity is tied to sea-level fluctuations is poorly supported, and terrestrial common cause is unsubstantiated as currently conceived. Instead, we consider variation in sampling to be the preferred null hypothesis for short-term diversity variation in the Mesozoic terrestrial realm.

Geological and anthropogenic controls on the sampling of the terrestrial fossil record: a case study from the Dinosauria

Abstract Dinosaurs provide excellent opportunities to examine the impact of sampling biases on the palaeodiversity of terrestrial organisms. The stratigraphical and geographical ranges of 847 dinosaurian species are analysed for palaeodiversity patterns and compared to several sampling metrics. The observed diversity of dinosaurs, Theropoda, Sauropodomorpha and Ornithischia, are positively correlated with sampling at global and regional scales. Sampling metrics for the same region correlate with each other, suggesting that different metrics often capture the same signal. Regional sampling metrics perform well as explanations for regional diversity patterns, but correlations with global diversity are weaker. Residual diversity estimates indicate that sauropodomorphs diversified during the Late Triassic, but major increases in the diversity of theropods and ornithischians did not occur until the Early Jurassic. Diversity increased during the Jurassic, but many groups underwent extinction during the Late Jurassic or at the Jurassic/Cretaceous boundary. Although a recovery occurred during the Cretaceous, only sauropodomorphs display a long-term upward trend. The Campanian–Maastrichtian diversity ‘peak’ is largely a sampling artefact. There is little evidence for a gradualistic decrease in diversity prior to the end-Cretaceous mass extinction (except for ornithischians), and when such decreases do occur they are small relative to those experienced earlier in dinosaur evolution. Supplementary material: The full data set and details of analyses are available at www.geolsoc.org.uk/SUP18487 The same materials (in the form of an Excel workbook) are also available from the first author on request.

Homoplasy and the evolution of dinosaur locomotion

Abstract In this paper, I survey hindlimb and pelvic anatomy across non-avian dinosaurs and analyze these within a cladistic framework to quantify patterns of change within the locomotor apparatus. Specifically, I attempt to identify where homoplasy constitutes parallelism and may thereby be used to infer similar selective pressures on hindlimb function. Traditional methods of discrete character optimization are used along with two methods for evaluating changes in continuous characters in a phylogenetic context (squared-change parsimony and clade rank correlation). Resultant patterns are evaluated in light of the biomechanics of locomotion and the relationship between form and function in extant terrestrial vertebrates. Although non-avian dinosaurian locomotor morphology is strikingly uniform, these analyses reveal the repeated derivations of several morphological features that have potential relevance for hindlimb locomotor function. Anterior and posterior iliac expansion, a medially oriented femoral head, and an elevated femoral lesser trochanter each evolved independently multiple times within Dinosauria. These changes probably reflect enlargement of several hindlimb muscles as well as a general switch in their predominant function from abduction-adduction (characteristic of “sprawling” limb postures) to protraction-retraction (characteristic of parasagittal, or “erect,” limb postures). Several “avian” characteristics are shared with more basal theropods, and many were acquired convergently in other dinosaurian lineages. The evolution of the avian hindlimb therefore represents a cumulative acquisition of characters, many of which were quite far removed in time and function from the origin of flight.

Air-filled postcranial bones in theropod dinosaurs: physiological implications and the 'reptile'-bird transition.

Pneumatic (air‐filled) postcranial bones are unique to birds among extant tetrapods. Unambiguous skeletal correlates of postcranial pneumaticity first appeared in the Late Triassic (approximately 210 million years ago), when they evolved independently in several groups of bird‐line archosaurs (ornithodirans). These include the theropod dinosaurs (of which birds are extant representatives), the pterosaurs, and sauropodomorph dinosaurs. Postulated functions of skeletal pneumatisation include weight reduction in large‐bodied or flying taxa, and density reduction resulting in energetic savings during foraging and locomotion. However, the influence of these hypotheses on the early evolution of pneumaticity has not been studied in detail previously. We review recent work on the significance of pneumaticity for understanding the biology of extinct ornithodirans, and present detailed new data on the proportion of the skeleton that was pneumatised in 131 non‐avian theropods and Archaeopteryx. This includes all taxa known from significant postcranial remains. Pneumaticity of the cervical and anterior dorsal vertebrae occurred early in theropod evolution. This ‘common pattern’ was conserved on the line leading to birds, and is likely present in Archaeopteryx. Increases in skeletal pneumaticity occurred independently in as many as 12 lineages, highlighting a remarkably high number of parallel acquisitions of a bird‐like feature among non‐avian theropods. Using a quantitative comparative framework, we show that evolutionary increases in skeletal pneumaticity are significantly concentrated in lineages with large body size, suggesting that mass reduction in response to gravitational constraints at large body sizes influenced the early evolution of pneumaticity. However, the body size threshold for extensive pneumatisation is lower in theropod lineages more closely related to birds (maniraptorans). Thus, relaxation of the relationship between body size and pneumatisation preceded the origin of birds and cannot be explained as an adaptation for flight. We hypothesise that skeletal density modulation in small, non‐volant, maniraptorans resulted in energetic savings as part of a multi‐system response to increased metabolic demands. Acquisition of extensive postcranial pneumaticity in small‐bodied maniraptorans may indicate avian‐like high‐performance endothermy.