| A standard protocol for documenting modern and fossil ichnological data |
32 |
| Cope's rule and the adaptive landscape of dinosaur body size evolution |
18 |
| Probabilistic methods surpass parsimony when assessing clade support in phylogenetic analyses of discrete morphological data |
13 |
| Probabilistic methods outperform parsimony in the phylogenetic analysis of data simulated without a probabilistic model |
12 |
| A new phylogenetic hypothesis of turtles with implications for the timing and number of evolutionary transitions to marine lifestyles in the group |
11 |
| Ontogeny of the Massospondylus labyrinth: implications for locomotory shifts in a basal sauropodomorph dinosaur |
10 |
| Sediment-encased maturation: a novel method for simulating diagenesis in organic fossil preservation |
10 |
| Spatiotemporal sampling patterns in the 230 million year fossil record of terrestrial crocodylomorphs and their impact on diversity |
10 |
| Increased pliosaurid dental disparity across the Jurassic-Cretaceous transition |
10 |
| JOURNEYS THROUGH DISCRETE-CHARACTER MORPHOSPACE: SYNTHESIZING PHYLOGENY, TEMPO, AND DISPARITY |
9 |
| Experimental analysis of soft-tissue fossilization: opening the black box |
9 |
| Integrating 2D and 3D shell morphology to disentangle the palaeobiology of ammonoids: a virtual approach |
9 |
| Three new naraoiid species from the Burgess Shale, with a morphometric and phylogenetic reinvestigation of Naraoiidae |
8 |
| Use and misuse of discrete character data for morphospace and disparity analyses |
8 |
| Small carbonaceous fossils (SCFs) from the Terreneuvian (lower Cambrian) of Baltica |
7 |
| Time for a rethink: time sub-sampling methods indisparity-through-time analyses |
7 |
| Impact of the Late Triassic mass extinction on functional diversity and composition of marine ecosystems |
7 |
| Ontogenetic trajectories of septal spacing in Early Jurassic belemnites from Germany and France, and their palaeobiological implications |
6 |
| Homologous shell microstructures in Cambrian hyoliths and molluscs |
6 |
| Body size changes in bivalves of the family Limidae in the aftermath of the end-Triassic mass extinction: the Brobdingnag effect |
6 |
| The hatching mechanism of 130-million-year-old insects: an association of neonates, egg shells and egg bursters in Lebanese amber |
6 |
| Cambrian petalonamid Stromatoveris phylogenetically links Ediacaran biota to later animals |
6 |
| Evolution of jaw disparity in fishes |
6 |
| Virtual endocasts of fossil Sciuroidea: brain size reduction in the evolution of fossoriality |
6 |
| Baltoscandian conodont biofacies fluctuations and their link to Middle Ordovician (Darriwilian) global cooling |
6 |
| Flight reconstruction of two European enantiornithines (Aves, Pygostylia) and the achievement of bounding flight in Early Cretaceous birds |
6 |
| Plywood-like shell microstructures in hyoliths from the middle Cambrian (Drumian) Gowers Formation, Georgina Basin, Australia |
6 |
| Show me your yttrium, and I will tell you who you are: implications for fossil imaging |
5 |
| Computed tomography scanning as a tool for linking the skeletal and otolith-based fossil records of teleost fishes |
5 |
| Evidence for heterochrony in the cranial evolution of fossil crocodyliforms |
5 |
| Total-evidence approach reveals an extinct lineage of Paederinae rove beetles from Cretaceous Burmese amber |
5 |
| THE DIVERSE DIETARY PROFILES OF MIS 3 CAVE BEARS FROM THE ROMANIAN CARPATHIANS: INSIGHTS FROM STABLE ISOTOPE (delta C-13 AND delta N-15) ANALYSIS |
5 |
| Phylogeny and evolutionary history of diplobathrid crinoids (Echinodermata) |
5 |
| Ecological stasis in Spinicaudata (Crustacea, Branchiopoda)? Early Cretaceous clam shrimp of the Yixian Formation of north-east China occupied a broader realized ecological niche than extant members of the group |
5 |
| A fish and tetrapod fauna from Romer's Gap preserved in Scottish Tournaisian floodplain deposits |
5 |
| Convergence and functional evolution of longirostry in crocodylomorphs |
4 |
| Tooth microwear and occlusal modes of euharamiyidans from the Jurassic Yanliao Biota reveal mosaic tooth evolution in Mesozoic allotherian mammals |
4 |
| POST-METAMORPHIC ALLOMETRY IN THE EARLIEST ACROTRETOID BRACHIOPODS FROM THE LOWER CAMBRIAN (SERIES 2) OF SOUTH CHINA, AND ITS IMPLICATIONS |
4 |
| First record of Mesozoic scroll coprolites: classification, characteristics, elemental composition and probable producers |
4 |
| THE LATE NEOGENE RODENT SUCCESSION OF THE GUADIX-BAZA BASIN (SOUTH-EASTERN SPAIN) AND ITS MAGNETOSTRATIGRAPHIC CORRELATION |
4 |
| Increases in sampling support the southern Gondwanan hypothesis for the origin of dinosaurs |
4 |
| Anatomical and ontogenetic reassessment of the Ediacaran frond Arborea arborea and its placement within total group Eumetazoa |
4 |
| Biases with the Generalized Euclidean Distance measure in disparity analyses with high levels of missing data |
4 |
| Quantifying the completeness of the bat fossil record |
4 |
| Electron backscatter diffraction (EBSD) analysis of maniraptoran eggshells with important implications for microstructural and taphonomic interpretations |
4 |
| NOVEL DATA ON AETOSAUR (ARCHOSAURIA, PSEUDOSUCHIA) OSTEODERM MICROANATOMY AND HISTOLOGY: PALAEOBIOLOGICAL IMPLICATIONS |
4 |
| The oldest shipworms (Bivalvia, Pholadoidea, Teredinidae) preserved with soft parts (western France): insights into the fossil record and evolution of Pholadoidea |
3 |
| GUT EVOLUTION IN EARLY CAMBRIAN TRILOBITES AND THE ORIGIN OF PREDATION ON INFAUNAL MACROINVERTEBRATES: EVIDENCE FROM MUSCLE SCARS IN MESOLENELLUS |
3 |
| ADDITIONAL INFORMATION ON THE PRIMITIVE CONTOUR AND WING FEATHERING OF PARAVIAN DINOSAURS |
3 |
| The early composition and evolution of the turtle shell (Reptilia, Testudinata) |
3 |
