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Three-dimensional preservation of foot movements in Triassic theropod dinosaurs
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0031-0182(82)90005-0openalex-snapshot
Speeds and gaits of dinosaurs
inferredcites →https://doi.org/10.1016/0160-9327(92)90032-kopenalex-snapshot
Tracking dinosaurs. A new look at an ancient world
inferredcites →https://doi.org/10.1016/s0031-0182(98)00043-1openalex-snapshot
A Late Triassic lake system in East Greenland: facies, depositional cycles and palaeoclimate
inferredcites →https://doi.org/10.1017/s0094837300009866openalex-snapshot
Caudofemoral musculature and the evolution of theropod locomotion
inferredcites →https://doi.org/10.1038/294747a0openalex-snapshot
Estimates of dinosaur speeds from a new trackway site in Texas
inferredcites →https://doi.org/10.1038/361064a0openalex-snapshot
Primitive dinosaur skeleton from Argentina and the early evolution of Dinosauria
inferredcites →https://doi.org/10.1080/02724634.1992.10011473openalex-snapshot
Procompsognathus: theropod, “thecodont” or both?
inferredcites →https://doi.org/10.1080/02724634.1994.10011523openalex-snapshot
New information on the systematics and postcranial skeleton ofHerrerasaurus ischigualastensis(Theropoda: Herrerasauridae) from the Ischigualasto Formation (Upper Triassic) of Argentina
inferredcites →https://doi.org/10.1080/02724634.1998.10011086openalex-snapshot
Type material of the type species of the classic theropod footprint genera Eubrontes, Anchisauripus , and Grallator (Early Jurassic, Hartford and Deerfield basins, Connecticut and Massachusetts, U.S.A.)
inferredcites →https://doi.org/10.1111/j.1096-3642.1923.tb02192.xopenalex-snapshot
On the Origin of Flight in Birds
inferredcites →https://doi.org/10.1111/j.1096-3642.1984.tb00539.xopenalex-snapshot
The avian relationships of Archaeopteryx, and the origin of birds
inferredcites →https://doi.org/10.1111/j.1469-7998.1991.tb03786.xopenalex-snapshot
Hind limb movements of the American alligator (Alligator mississippiensis) and postural grades
inferredcites →https://doi.org/10.1126/science.207.4436.1198openalex-snapshot
Swimming Ability of Carnivorous Dinosaurs
inferredcites →https://doi.org/10.15468/11srqkopenalex-snapshot
Stance and gait in theropod dinosaurs
inferredcites →https://doi.org/10.5281/zenodo.13525207openalex-snapshot
Triassic reptile footprint faunules from Milford, New Jersey
inferredcites →https://doi.org/10.5281/zenodo.16171435openalex-snapshot
Saurischian monophyly and the origin of birds
inferredcites →https://doi.org/10.5962/bhl.title.70405openalex-snapshot
Triassic life of the Connecticut valley,
inferredcites →https://doi.org/10.7146/moggeosci.v32i.140904openalex-snapshot
Late Triassic continental vertebrates and depositional environments of the Fleming Fjord Formation, Jameson Land, East Greenland
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.26879/1389zenodo-depositor-declared
Glossary of fossil tetrapod tracks
inferred← citeshttps://doi.org/10.26879/529zenodo-depositor-declared
Dinosaur tracks from the Langenberg Quarry (Late Jurassic, Germany) reconstructed with historical photogrammetry: Evidence for large theropods soon after insular dwarfism
inferred← citeshttps://doi.org/10.1002/ajpa.22276openalex-snapshot
Holocene footprints in Namibia: The influence of substrate on footprint variability
inferred← citeshttps://doi.org/10.1002/ar.22863openalex-snapshot
Pedal Proportions of Poposaurus gracilis: Convergence and Divergence in the Feet of Archosaurs
inferred← citeshttps://doi.org/10.1002/evan.21963openalex-snapshot
Fossil footprints and what they mean for hominin paleobiology
inferred← citeshttps://doi.org/10.1002/gj.4357openalex-snapshot
First occurrence of sauropod and theropod footprints in the pre‐Campanian deposits of the Nubian Sandstone, south Eastern Desert, Egypt
inferred← citeshttps://doi.org/10.1002/jez.588openalex-snapshot
Scientific rotoscoping: a morphology‐based method of 3‐D motion analysis and visualization
inferred← citeshttps://doi.org/10.1002/jez.b.22697openalex-snapshot
Greater Growth of Proximal Metatarsals in Bird Embryos and the Evolution of Hallux Position in the Grasping Foot
inferred← citeshttps://doi.org/10.1002/jmor.10240openalex-snapshot
Biomechanical modeling and sensitivity analysis of bipedal running ability. II. Extinct taxa
inferred← citeshttps://doi.org/10.1002/jmor.10241openalex-snapshot
Biomechanical modeling and sensitivity analysis of bipedal running ability. I. Extant taxa
inferred← citeshttps://doi.org/10.1002/jmor.1058openalex-snapshot
The morphological basis of hallucal orientation in extant birds
inferred← citeshttps://doi.org/10.1007/978-3-030-95959-3_14openalex-snapshot
Sauropod Ichnology: Overview and New Research Lines from a South American Perspective
inferred← citeshttps://doi.org/10.1007/978-3-031-56355-3_5openalex-snapshot
The Dinosaur Footprints in the Cretaceous Aeolian Deposits of Sanfranciscana Basin
inferred← citeshttps://doi.org/10.1007/978-3-319-08572-2_5openalex-snapshot
The Role of Substrate in Track Formation and Topology
inferred← citeshttps://doi.org/10.1007/978-3-319-68009-5_12openalex-snapshot
Late Triassic Nonmarine Vertebrate and Invertebrate Trace Fossils and the Pattern of the Phanerozoic Record of Vertebrate Trace Fossils
inferred← citeshttps://doi.org/10.1007/978-3-662-08865-4_10openalex-snapshot
Sauropod Tracks — a geometric morphometric study
inferred← citeshttps://doi.org/10.1007/978-94-017-9597-5_3openalex-snapshot
The Mesozoic Vertebrate Radiation in Terrestrial Settings
inferred← citeshttps://doi.org/10.1007/bf03043770openalex-snapshot
DinoMorph: Parametric modeling of skeletal structures
inferred← citeshttps://doi.org/10.1007/s00114-007-0310-7openalex-snapshot
Behavioral and faunal implications of Early Cretaceous deinonychosaur trackways from China
inferred← citeshttps://doi.org/10.1007/s00114-008-0488-3openalex-snapshot
The evolutionary continuum of limb function from early theropods to birds
inferred← citeshttps://doi.org/10.1007/s001140050715openalex-snapshot
The oldest known tracks of web-footed birds from the Lower Cretaceous of South Korea
inferred← citeshttps://doi.org/10.1007/s00265-011-1226-yopenalex-snapshot
From dummies to animations: a review of computer-animated stimuli used in animal behavior studies
inferred← citeshttps://doi.org/10.1007/s10211-014-0209-1openalex-snapshot
The importance of syntax in a dynamic visual signal: recognition of jacky dragon displays depends upon sequence
inferred← citeshttps://doi.org/10.1007/s41513-017-0036-0openalex-snapshot
The evolution of ornithischian quadrupedality
inferred← citeshttps://doi.org/10.1007/s41513-018-0080-4openalex-snapshot
Can undertracks show higher morphologic quality than surface tracks? Remarks on large amphibian tracks from the Early Permian of France
inferred← citeshttps://doi.org/10.1007/s41513-022-00192-5openalex-snapshot
Vertebrate ichnofauna from Sierra de las Cabras tracksite (Late Miocene, Jumilla, SE Spain). Mammalian ichnofauna
inferred← citeshttps://doi.org/10.1007/s41513-023-00226-6openalex-snapshot
What do their footprints tell us? Many questions and some answers about the life of non-avian dinosaurs
inferred← citeshttps://doi.org/10.1016/j.beproc.2008.03.003openalex-snapshot
Considerations in video playback design: Using optic flow analysis to examine motion characteristics of live and computer-generated animation sequences
inferred← citeshttps://doi.org/10.1016/j.cretres.2010.11.003openalex-snapshot
A reassessment of large theropod dinosaur tracks from the mid-Cretaceous (late Albian–Cenomanian) Winton Formation of Lark Quarry, central-western Queensland, Australia: A case for mistaken identity
inferred← citeshttps://doi.org/10.1016/j.cretres.2011.07.001openalex-snapshot
A protoceratopsid skeleton with an associated track from the Upper Cretaceous of Mongolia
inferred← citeshttps://doi.org/10.1016/j.cretres.2012.07.001openalex-snapshot
Dinosaur footprints from the Lower Cretaceous of the Algarve Basin (Portugal): New data on the ornithopod palaeoecology and palaeobiogeography of the Iberian Peninsula
inferred← citeshttps://doi.org/10.1016/j.cretres.2014.10.001openalex-snapshot
Dinosaur natural track casts from the Lower Cretaceous Hekou Group in the Lanzhou-Minhe Basin, Gansu, Northwest China: Ichnology, track formation, and distribution
inferred← citeshttps://doi.org/10.1016/j.cretres.2015.05.008openalex-snapshot
The longest theropod trackway from East Asia, and a diverse sauropod-, theropod-, and ornithopod-track assemblage from the Lower Cretaceous Jiaguan Formation, southwest China
inferred← citeshttps://doi.org/10.1016/j.cretres.2017.07.008openalex-snapshot
Vertebrate tracks from the Paso Córdoba fossiliferous site (Anacleto and Allen formations, Upper Cretaceous), Northern Patagonia, Argentina: Preservational, environmental and palaeobiological implications
inferred← citeshttps://doi.org/10.1016/j.cretres.2018.04.005openalex-snapshot
Multiple parallel deinonychosaurian trackways from a diverse dinosaur track assemblage of the Lower Cretaceous Dasheng Group of Shandong Province, China
inferred← citeshttps://doi.org/10.1016/j.cretres.2019.06.009openalex-snapshot
Dinosaur tracks from the Lower Cretaceous Xiguayuan Formation in the Luanping Basin, Hebei Province, China
inferred← citeshttps://doi.org/10.1016/j.cretres.2020.104626openalex-snapshot
Dinosaur trampling from the Aptian of Araripe Basin, NE Brazil, as tools for paleoenvironmental interpretation
inferred← citeshttps://doi.org/10.1016/j.cretres.2020.104733openalex-snapshot
Diverse preserved dinosaur footprint assemblage from Jurassic–Cretaceous transition eolian dune deposits of western Shandong Province, China
inferred← citeshttps://doi.org/10.1016/j.cretres.2022.105292openalex-snapshot
New evidence for avian and small non-avian theropod ichnotaxa from the Lower Cretaceous of Canada: Implications for theropod ichnodiversity
inferred← citeshttps://doi.org/10.1016/j.cretres.2022.105446openalex-snapshot
Dinosaur tracks from the Sítio Pereiros ichnosite, Triunfo Basin (Lower Cretaceous) and the dinosaur diversity in the Rio do Peixe basins, Northeastern Brazil
inferred← citeshttps://doi.org/10.1016/j.cretres.2023.105516openalex-snapshot
Dinosaur swim tracks from the Lower Cretaceous of La Rioja, Spain: An ichnological approach to non-common behaviours
inferred← citeshttps://doi.org/10.1016/j.cretres.2024.105981openalex-snapshot
The impact of microbial mats in promoting record of Maastrichtian crocodylomorph tracks from Yacoraite Formation, Argentina
inferred← citeshttps://doi.org/10.1016/j.crpv.2005.09.002openalex-snapshot
The evolution of locomotion in archosaurs
inferred← citeshttps://doi.org/10.1016/j.crpv.2008.02.005openalex-snapshot
Microscopic, chemical and molecular methods for examining fossil preservation
inferred← citeshttps://doi.org/10.1016/j.earscirev.2019.04.008openalex-snapshot
Defining the morphological quality of fossil footprints. Problems and principles of preservation in tetrapod ichnology with examples from the Palaeozoic to the present
inferred← citeshttps://doi.org/10.1016/j.earscirev.2020.103319openalex-snapshot
Reply to discussion of “Defining the morphological quality of fossil footprints. Problems and principles of preservation in tetrapod ichnology with examples from the Palaeozoic to the present” by Marchetti et al. (2019)
inferred← citeshttps://doi.org/10.1016/j.earscirev.2020.103320openalex-snapshot
Discussion: Defining the morphological quality of fossil footprints. Problems and principles of preservation in tetrapod ichnology with examples from the Palaeozoic to the present by Lorenzo Marchetti et al.
inferred← citeshttps://doi.org/10.1016/j.eve.2026.100129openalex-snapshot
The ichnotaphonomic window in lacustrine subaqueous littoral deposits: an example of bird and mammal footprints from the Miocene of northwest Argentina
inferred← citeshttps://doi.org/10.1016/j.geobios.2024.12.002openalex-snapshot
Diversity of the pterodactyloid ichnites of Crayssac (Lower Tithonian, Late Jurassic, southwestern France)
inferred← citeshttps://doi.org/10.1016/j.gsf.2017.12.012openalex-snapshot
Theropod assemblages and a new ichnotaxon Gigandipus chiappei ichnosp. nov. from the Jiaguan Formation, Lower Cretaceous of Guizhou Province, China
inferred← citeshttps://doi.org/10.1016/j.gsf.2021.101181openalex-snapshot
Largest dinosaur tracksite in China (Cretaceous, Zhaojue area, Sichuan Province): On the verge of destruction
inferred← citeshttps://doi.org/10.1016/j.jafrearsci.2024.105306openalex-snapshot
Evidence of theropod dinosaurs in the upper hauterivian–lower barremian of Jebel Kebar (central Tunisia): Paleobiogeographic implications
inferred← citeshttps://doi.org/10.1016/j.jafrearsci.2025.105676openalex-snapshot
The uncertain representativeness of theropod footprint morphometric data
inferred← citeshttps://doi.org/10.1016/j.jhevol.2013.03.009openalex-snapshot
The relationship between plantar pressure and footprint shape
inferred← citeshttps://doi.org/10.1016/j.jhevol.2017.08.013openalex-snapshot
Hominin track assemblages from Okote Member deposits near Ileret, Kenya, and their implications for understanding fossil hominin paleobiology at 1.5 Ma
inferred← citeshttps://doi.org/10.1016/j.jhevol.2018.03.006openalex-snapshot
A biplanar X-ray approach for studying the 3D dynamics of human track formation
inferred← citeshttps://doi.org/10.1016/j.jop.2024.01.001openalex-snapshot
Substrate control in track registration and preservation: insights across the Triassic–Jurassic boundary in southern Africa
inferred← citeshttps://doi.org/10.1016/j.jsames.2020.102936openalex-snapshot
Fossil footprints as biosedimentary structures for paleoenvironmental interpretation: Examples from Gondwana
inferred← citeshttps://doi.org/10.1016/j.jsames.2024.104962openalex-snapshot
Tetradactyl footprints and plant material from the Jurassic-Cretaceous boundary, Tarapaca Region, Northern Chile
inferred← citeshttps://doi.org/10.1016/j.palaeo.2004.12.022openalex-snapshot
True tracks, undertracks and eroded tracks, experimental work with tetrapod tracks in laboratory and field
inferred← citeshttps://doi.org/10.1016/j.palaeo.2006.10.013openalex-snapshot
Sequence stratigraphic controls on synsedimentary cementation and preservation of dinosaur tracks: Example from the lower Cretaceous, (Upper Albian) Dakota Formation, Southeastern Nebraska, U.S.A.
inferred← citeshttps://doi.org/10.1016/j.palaeo.2008.08.014openalex-snapshot
Application of neoichnological studies to behavioural and taphonomic interpretation of fossil bird-like tracks from lacustrine settings: The Late Triassic–Early Jurassic? Santo Domingo Formation, Argentina
inferred← citeshttps://doi.org/10.1016/j.palaeo.2010.03.009openalex-snapshot
Tetrapod tracks in a marginal lacustrine setting (Middle Triassic, Argentina): Taphonomy and significance
inferred← citeshttps://doi.org/10.1016/j.palaeo.2015.03.028openalex-snapshot
Application of vertebrate trace fossils to palaeoenvironmental analysis
inferred← citeshttps://doi.org/10.1016/j.palaeo.2018.01.009openalex-snapshot
Palaeoichnology of an MIS 3 cave bear settlement – Urşilor Cave (Western Carpathians, Romania)
inferred← citeshttps://doi.org/10.1016/j.palaeo.2018.05.016openalex-snapshot
Tetrapod track assemblages from Lower Cretaceous desert facies in the Ordos Basin, Shaanxi Province, China, and their implications for Mesozoic paleoecology
inferred← citeshttps://doi.org/10.1016/j.palwor.2014.10.010openalex-snapshot
Large theropod trackway from the Lower Jurassic Zhenzhuchong Formation of Weiyuan County, Sichuan Province, China: Review, new observations and special preservation
inferred← citeshttps://doi.org/10.1016/j.palwor.2021.09.001openalex-snapshot
Dinoturbation in Upper Jurassic siliciclastic levels at Cabo Mondego (Lusitanian Basin, Portugal): evidences in a fluvial-dominated deltaic succession
inferred← citeshttps://doi.org/10.1016/j.palwor.2024.03.005openalex-snapshot
Diversity and discrimination of large ornithopods revealed through their tracks (Lower Cretaceous, Spain): A phenetic correlation approach
inferred← citeshttps://doi.org/10.1016/j.palwor.2026.201147openalex-snapshot
Middle Jurassic isolated dinosaur tracks from Msemrir (Central High Atlas, Morocco): Evidence for theropod occurrence and paleogeographic distribution
inferred← citeshttps://doi.org/10.1016/j.palwor.2026.201155openalex-snapshot
A running ornithopod trackway from the Hasandong Formation (Lower Cretaceous, Korea): Evidence of a ‘Goldilocks’ substrate window and rapid avulsion burial
inferred← citeshttps://doi.org/10.1016/j.pgeola.2026.101189openalex-snapshot
New theropod tracks from the Callovian of Tunisia: implications for Middle Jurassic theropod diversity along the northern margin of Gondwana
inferred← citeshttps://doi.org/10.1016/j.quascirev.2019.01.013openalex-snapshot
Following the last Neanderthals: Mammal tracks in Late Pleistocene coastal dunes of Gibraltar (S Iberian Peninsula)
inferred← citeshttps://doi.org/10.1016/s1095-6433(02)00158-7openalex-snapshot
The evolution of hindlimb tendons and muscles on the line to crown-group birds
inferred← citeshttps://doi.org/10.1017/pab.2020.46openalex-snapshot
How to build a dinosaur: Musculoskeletal modeling and simulation of locomotor biomechanics in extinct animals
inferred← citeshttps://doi.org/10.1017/s0016756816000546openalex-snapshot
Crouching theropod at the seaside. Matching footprints with metatarsal impressions and theropod authopods: a morphometric approach
inferred← citeshttps://doi.org/10.1017/s0094837300026981openalex-snapshot
Invention by evolution: Functional analysis in paleobiology
inferred← citeshttps://doi.org/10.1017/s1755691011020032openalex-snapshot
Implications of the Newark Supergroup-based astrochronology and geomagnetic polarity time scale (Newark-APTS) for the tempo and mode of the early diversification of the Dinosauria
inferred← citeshttps://doi.org/10.1038/nature00818openalex-snapshot
Bird-like fossil footprints from the Late Triassic
inferred← citeshttps://doi.org/10.1038/s41467-024-44832-zopenalex-snapshot
Articular surface interactions distinguish dinosaurian locomotor joint poses
inferred← citeshttps://doi.org/10.1038/s41598-024-55805-zopenalex-snapshot
Rethinking the four-wing problem in plesiosaur swimming using bio-inspired decentralized control
inferred← citeshttps://doi.org/10.1038/s41598-025-31361-yopenalex-snapshot
Footprint morphology sheds light on running strategies in non-avian theropods
inferred← citeshttps://doi.org/10.1038/srep28766openalex-snapshot
Footprints reveal direct evidence of group behavior and locomotion in Homo erectus
inferred← citeshttps://doi.org/10.1073/pnas.1416252111openalex-snapshot
The birth of a dinosaur footprint: Subsurface 3D motion reconstruction and discrete element simulation reveal track ontogeny
inferred← citeshttps://doi.org/10.1073/pnas.2527222122openalex-snapshot
Identifying variation in dinosaur footprints and classifying problematic specimens via unbiased unsupervised machine learning
inferred← citeshttps://doi.org/10.1080/00241160410002036openalex-snapshot
Vertical sections through dinosaur tracks (Late Triassic lake deposits, East Greenland) – undertracks and other subsurface deformation structures revealed
inferred← citeshttps://doi.org/10.1080/00288306.2009.9518464openalex-snapshot
First New Zealand record of probable dinosaur footprints from the Late Cretaceous North Cape Formation, northwest Nelson
inferred← citeshttps://doi.org/10.1080/0035919x.2021.1964104openalex-snapshot
Bipedal leaping Jurassic vertebrates in Southern Africa: proposed new ichnotaxon and inferred palaeoenvironment
inferred← citeshttps://doi.org/10.1080/02724634.2012.694591openalex-snapshot
Reevaluation of the Lark Quarry dinosaur Tracksite (late Albian–Cenomanian Winton Formation, central-western Queensland, Australia): no longer a stampede?
inferred← citeshttps://doi.org/10.1080/02724634.2016.1116995openalex-snapshot
Evolution of the hallux in non-avian theropod dinosaurs
inferred← citeshttps://doi.org/10.1080/02724634.2017.1314298openalex-snapshot
Neither bones nor feet: track morphological variation and ‘preservation quality’
inferred← citeshttps://doi.org/10.1080/02724634.2020.1781142openalex-snapshot
Hitchcock’s Leptodactyli, Penetrative Tracks, and Dinosaur Footprint Diversity
inferred← citeshttps://doi.org/10.1080/02724634.2026.2706201openalex-snapshot
A large tridactyl trackway from the Upper Cretaceous Hell Creek Formation of North Dakota, likely attributable to an adult Tyrannosaurus rex
inferred← citeshttps://doi.org/10.1080/03115518.2011.597564openalex-snapshot
A polar dinosaur-track assemblage from the Eumeralla Formation (Albian), Victoria, Australia
inferred← citeshttps://doi.org/10.1080/03115518.2026.2697810openalex-snapshot
Investigation of finger motion in two quadrupedal dinosaurs: the sauropod Camarasaurus and stegosaur Stegosaurus
inferred← citeshttps://doi.org/10.1080/03949370.2012.711370openalex-snapshot
Efficiency of aggressive and submissive visual displays against environmental motion noise in Jacky dragon ( Amphibolurus muricatus )
inferred← citeshttps://doi.org/10.1080/08912961003789867openalex-snapshot
Didactyl, tridactyl and tetradactyl theropod trackways from the Lower Jurassic of Morocco: evidence of limping, labouring and other irregular gaits
inferred← citeshttps://doi.org/10.1080/08912963.2017.1370588openalex-snapshot
A diversified vertebrate ichnite fauna from the Dasheng Group (Lower Cretaceous) of southeast Shandong Province, China
inferred← citeshttps://doi.org/10.1080/08912963.2018.1516766openalex-snapshot
A review of the concepts of ‘axony’ and their bearing on tetrapod ichnology
inferred← citeshttps://doi.org/10.1080/08912963.2020.1810681openalex-snapshot
Hidden for one hundred years: a diverse theropod ichnoassemblage and cross-sectional tracks from the historic Early Jurassic Tsikoane ichnosite (Clarens Formation, northern Lesotho, southern Africa)
inferred← citeshttps://doi.org/10.1080/08912963.2022.2069020openalex-snapshot
How to verify fossil tracks: the first record of dinosaurs from Palestine
inferred← citeshttps://doi.org/10.1080/08912963.2023.2196683openalex-snapshot
Autopod and track morphology elucidate on the putative producer in hadrosauriform ornithopods: a case study of manus tracks from the Frontier Formation (Coniacian), Montana
inferred← citeshttps://doi.org/10.1080/08912963.2023.2220121openalex-snapshot
Early Jurassic theropod elongate tracks with metatarsal marks from Yunnan, China
inferred← citeshttps://doi.org/10.1080/08912963.2025.2610322openalex-snapshot
The abundance and diversity of penetrative tracks: a critical re-evaluation of theropod ichnotaxa
inferred← citeshttps://doi.org/10.1080/08912963.2026.2676032openalex-snapshot
New theropod remains from the Lower Jurassic Fengjiahe Formation of Yunnan, China
inferred← citeshttps://doi.org/10.1080/10420940.2010.510026openalex-snapshot
Range of Experimental Dinosaur (Hypsilophodon foxii) Footprints Due to Variation in Sand Consistency: How Wet Was the Track?
inferred← citeshttps://doi.org/10.1080/10420940.2013.817405openalex-snapshot
Review of Dinosaur Tail Traces
inferred← citeshttps://doi.org/10.1080/10420940.2013.877006openalex-snapshot
Ichnology of an Extant Belly-Dragging Lizard—Analogies to Early Reptile Locomotion?
inferred← citeshttps://doi.org/10.1080/10420940.2016.1223655openalex-snapshot
Hoof-Like Unguals, Skin, and Foot Movements Deduced from Deltapodus Casts of the Galve Basin (Upper Jurassic-Lower Cretaceous, Teruel, Spain)
inferred← citeshttps://doi.org/10.1080/10420940.2016.1265524openalex-snapshot
Traces of Floating Archosaurs: An Interpretation of the Enigmatic Trace Fossils from the Triassic of the Tabular Cover of Southern Spain
inferred← citeshttps://doi.org/10.1080/10420940.2017.1337634openalex-snapshot
Crossing Slopes: Unusual Trackways of Recent Birds and Implications for Tetrapod Footprint Preservation
inferred← citeshttps://doi.org/10.1080/10420940.2018.1532902openalex-snapshot
Evidence for Bipedal Prosauropods as the LikelyEubrontesTrack-Makers
inferred← citeshttps://doi.org/10.1080/10420940009380161openalex-snapshot
An amended description of the theropod footprintBueckeburgichnus maximusKuhn 1958, and its bearing on the megalosaur tracks debate
inferred← citeshttps://doi.org/10.1080/10420940390255501openalex-snapshot
Pterosaur Stance and Gait and the Interpretation of Trackways
inferred← citeshttps://doi.org/10.1080/10420940490428625openalex-snapshot
A Diverse Dinosaur-Bird Footprint Assemblage from the Lance Formation, Upper Cretaceous, Eastern Wyoming: Implications for Ichnotaxonomy
inferred← citeshttps://doi.org/10.1080/10420940591008999openalex-snapshot
Excavated andIn SituDinosaur Footprints from the Murray Quarry (Early Jurassic East Berlin Formation), Holyoke, Massachusetts, USA
inferred← citeshttps://doi.org/10.1080/10420940600739781openalex-snapshot
The Syngenetic Structure Suite of Dinosaur Footprints in Finely Laminated Sandstones: Site n°1 of Bin el Ouidane (1BO; Central Atlas, Morocco)
inferred← citeshttps://doi.org/10.1080/10420940600864712openalex-snapshot
The Impact of Sediment Consistency on Track and Undertrack Morphology: Experiments with Emu Tracks in Layered Cement
inferred← citeshttps://doi.org/10.1080/10420940601006859openalex-snapshot
Dinosaur Tracks as Paleogeographic Constraints: New Scenarios for the Cretaceous Geography of the Periadriatic Region
inferred← citeshttps://doi.org/10.1080/10420940802471027openalex-snapshot
Formation and Taphonomy of Human Footprints in Microbial Mats of Present-Day Tidal-flat Environments: Implications for the Study of Fossil Footprints
inferred← citeshttps://doi.org/10.1080/14772019.2010.509356openalex-snapshot
Bird tracks from the Upper Cretaceous Cantwell Formation of Denali National Park, Alaska, USA: a new perspective on ancient northern polar vertebrate biodiversity
inferred← citeshttps://doi.org/10.1086/512758openalex-snapshot
Preservation and Erosion of Theropod Tracks in Eolian Deposits: Examples from the Middle Jurassic Entrada Sandstone, Utah, U.S.A.
inferred← citeshttps://doi.org/10.1086/521608openalex-snapshot
Dinosaur Tectonics: A Structural Analysis of Theropod Undertracks with a Reconstruction of Theropod Walking Dynamics
inferred← citeshttps://doi.org/10.1093/icb/icac009openalex-snapshot
What is Stance Phase on Deformable Substrates?
inferred← citeshttps://doi.org/10.1093/icb/icac049openalex-snapshot
Walking—and Running and Jumping—with Dinosaurs and their Cousins, Viewed Through the Lens of Evolutionary Biomechanics
inferred← citeshttps://doi.org/10.1093/icb/icy092openalex-snapshot
Anatomy, Animation, and Visual Effects: The Reciprocal Tools of Biology and Film-Making
inferred← citeshttps://doi.org/10.1098/rsbl.2020.0309openalex-snapshot
It's in the loop: shared sub-surface foot kinematics in birds and other dinosaurs shed light on a new dimension of fossil track diversity
inferred← citeshttps://doi.org/10.1098/rsbl.2024.0441openalex-snapshot
Reconstructing dinosaur locomotion
inferred← citeshttps://doi.org/10.1098/rsbl.2025.0191openalex-snapshot
Speed from fossil trackways: calculations not validated by extant birds on compliant substrates
inferred← citeshttps://doi.org/10.1098/rsfs.2020.0075openalex-snapshot
Integration of biplanar X-ray, three-dimensional animation and particle simulation reveals details of human ‘track ontogeny’
inferred← citeshttps://doi.org/10.1098/rsif.2010.0634openalex-snapshot
The ‘Goldilocks’ effect: preservation bias in vertebrate track assemblages
inferred← citeshttps://doi.org/10.1098/rsif.2013.0009openalex-snapshot
Does footprint depth correlate with foot motion and pressure?
inferred← citeshttps://doi.org/10.1098/rsif.2025.0796openalex-snapshot
Penetrative track morphology and sediment parameters: subsurface layers are robust to changes in substrate properties
inferred← citeshttps://doi.org/10.1098/rsos.140225openalex-snapshot
Mitigating the Goldilocks effect: the effects of different substrate models on track formation potential
inferred← citeshttps://doi.org/10.1098/rsos.231091openalex-snapshot
New Middle to ?Late Jurassic dinosaur tracksites in the Central High Atlas Mountains, Morocco
inferred← citeshttps://doi.org/10.1098/rsos.251016openalex-snapshot
Small theropod-dominated dinosaur footprint assemblages in the Middle Jurassic Valtos Sandstone and Kilmaluag Formations on the Isle of Skye, Scotland
inferred← citeshttps://doi.org/10.1098/rspb.2009.1161openalex-snapshot
First record of a pterosaur landing trackway
inferred← citeshttps://doi.org/10.1098/rspb.2010.1746openalex-snapshot
Footprints pull origin and diversification of dinosaur stem lineage deep into Early Triassic
inferred← citeshttps://doi.org/10.1109/mc.2002.1033024openalex-snapshot
Merging fossil specimens with computer-generated information
inferred← citeshttps://doi.org/10.1109/mcg.2016.65openalex-snapshot
Immersive Visualization to Support Scientific Insight
inferred← citeshttps://doi.org/10.1109/tvcg.2019.2898796openalex-snapshot
Developing Virtual Reality Visualizations for Unsteady Flow Analysis of Dinosaur Track Formation using Scientific Sketching
inferred← citeshttps://doi.org/10.1111/brv.12071openalex-snapshot
Locomotion in ornithischian dinosaurs: an assessment using three‐dimensional computational modelling
inferred← citeshttps://doi.org/10.1111/j.0031-0239.2004.00366.xopenalex-snapshot
A Middle Jurassic dinosaur trackway site from Oxfordshire, UK
inferred← citeshttps://doi.org/10.1111/j.1365-3121.2011.01047.xopenalex-snapshot
Exceptional preservation processes of 3D dinosaur footprint casts in Costalomo (Lower Cretaceous, Cameros Basin, Spain)
inferred← citeshttps://doi.org/10.1111/j.1439-0310.2011.01993.xopenalex-snapshot
Aggressive Signal Design in the Jacky Dragon (Amphibolurus muricatus): Display Duration Affects Efficiency
inferred← citeshttps://doi.org/10.1111/j.1469-185x.2009.00094.xopenalex-snapshot
The origin and early evolution of dinosaurs
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2008.00789.xopenalex-snapshot
THREE‐DIMENSIONAL MODELLING AND ANALYSIS OF DINOSAUR TRACKWAYS
inferred← citeshttps://doi.org/10.1111/j.1502-3931.2011.00276.xopenalex-snapshot
Late Jurassic footprints reveal walking kinematics of theropod dinosaurs
inferred← citeshttps://doi.org/10.1111/j.1755-6724.2012.00660.xopenalex-snapshot
An Unusual, Three‐Dimensionally Preserved, Large Hadrosauriform Pes Track from “Mid”‐Cretaceous Jiaguan Formation of Chongqing, China
inferred← citeshttps://doi.org/10.1111/joa.13090openalex-snapshot
Can skeletal surface area predictin vivofoot surface area?
inferred← citeshttps://doi.org/10.1111/jzo.12110openalex-snapshot
Interpreting ecology and behaviour from the vertebrate fossil track record
inferred← citeshttps://doi.org/10.1111/let.12136openalex-snapshot
Corroborating trackmaker identification through footprint functional analysis: the case study of Ichniotherium and Dimetropus
inferred← citeshttps://doi.org/10.1111/pala.12082openalex-snapshot
Oldest known avian footprints from A ustralia: E umeralla F ormation ( A lbian), D inosaur C ove, V ictoria
inferred← citeshttps://doi.org/10.1111/pala.12373openalex-snapshot
A standard protocol for documenting modern and fossil ichnological data
inferred← citeshttps://doi.org/10.1111/pala.12449openalex-snapshot
Shape variability in tridactyl dinosaur footprints: the significance of size and function
inferred← citeshttps://doi.org/10.1111/pala.12502openalex-snapshot
Constructing and testing hypotheses of dinosaur foot motions from fossil tracks using digitization and simulation
inferred← citeshttps://doi.org/10.1111/pala.12584openalex-snapshot
A new solution to an old riddle: elongate dinosaur tracks explained as deep penetration of the foot, not plantigrade locomotion
inferred← citeshttps://doi.org/10.1111/pala.70040openalex-snapshot
Formation, preservation, and interpretation of dinosaur tracks
inferred← citeshttps://doi.org/10.1111/sed.13224openalex-snapshot
Formation and preservation of vertebrate tracks in semi‐liquid sediments: Insights from tidal flats and laboratory experiments
inferred← citeshttps://doi.org/10.1126/sciadv.abe2778openalex-snapshot
The evolution of pelvic limb muscle moment arms in bird-line archosaurs
inferred← citeshttps://doi.org/10.1126/science.284.5423.2137openalex-snapshot
The Evolution of Dinosaurs
inferred← citeshttps://doi.org/10.1130/g23452a.1openalex-snapshot
Were non-avian theropod dinosaurs able to swim? Supportive evidence from an Early Cretaceous trackway, Cameros Basin (La Rioja, Spain)
inferred← citeshttps://doi.org/10.1139/e06-024openalex-snapshot
Simulated weathering of dinosaur tracks and the implications for their characterization
inferred← citeshttps://doi.org/10.1144/gsl.sp.2004.228.01.06openalex-snapshot
A new approach to the analysis and interpretation of tracks: examples from the dinosauria
inferred← citeshttps://doi.org/10.1144/pygs.54.3.185openalex-snapshot
Jurassic dinosaur tracks and trackways of the Cleveland Basin, Yorkshire: preservation, diversity and distribution
inferred← citeshttps://doi.org/10.1144/sjg2017-016openalex-snapshot
A sauropod-dominated tracksite from Rubha nam Brathairean (Brothers’ Point), Isle of Skye, Scotland
inferred← citeshttps://doi.org/10.1144/sp334.14openalex-snapshot
Tetrapod footprints - their use in biostratigraphy and biochronology of the Triassic
inferred← citeshttps://doi.org/10.1144/sp434.1openalex-snapshot
Archosaur footprints (cf. Brachychirotherium ) with unusual morphology from the Upper Triassic Fleming Fjord Formation (Norian–Rhaetian) of East Greenland
inferred← citeshttps://doi.org/10.1144/sp434.3openalex-snapshot
The vertebrate-bearing Late Triassic Fleming Fjord Formation of central East Greenland revisited: stratigraphy, palaeoclimate and new palaeontological data
inferred← citeshttps://doi.org/10.1145/1281500.1281628openalex-snapshot
Modern approaches to augmented reality Video files associated with this course are available from the citation page
inferred← citeshttps://doi.org/10.1146/annurev-earth-040610-133502openalex-snapshot
Soft Tissue Preservation in Terrestrial Mesozoic Vertebrates
inferred← citeshttps://doi.org/10.1146/annurev.physiol.70.113006.100438openalex-snapshot
Advances in Comparative Physiology from High-Speed Imaging of Animal and Fluid Motion
inferred← citeshttps://doi.org/10.1186/s12983-020-00363-zopenalex-snapshot
Examining the accuracy of trackways for predicting gait selection and speed of locomotion
inferred← citeshttps://doi.org/10.1242/jeb.00664openalex-snapshot
Introductory tail-flick of the Jacky dragon visual display: signal efficacy depends upon duration
inferred← citeshttps://doi.org/10.1242/jeb.242795openalex-snapshot
Terrestrial force production by the limbs of a semi-aquatic salamander provides insight into the evolution of terrestrial locomotor mechanics
inferred← citeshttps://doi.org/10.1242/jeb.245132openalex-snapshot
Modern three-dimensional digital methods for studying locomotor biomechanics in tetrapods
inferred← citeshttps://doi.org/10.1371/journal.pone.0007331openalex-snapshot
Dynamic Locomotor Capabilities Revealed by Early Dinosaur Trackmakers from Southern Africa
inferred← citeshttps://doi.org/10.1371/journal.pone.0026882openalex-snapshot
Tetradactyl Footprints of an Unknown Affinity Theropod Dinosaur from the Upper Jurassic of Morocco
inferred← citeshttps://doi.org/10.1371/journal.pone.0028964openalex-snapshot
The Predatory Ecology of Deinonychus and the Origin of Flapping in Birds
inferred← citeshttps://doi.org/10.1371/journal.pone.0078733openalex-snapshot
March of the Titans: The Locomotor Capabilities of Sauropod Dinosaurs
inferred← citeshttps://doi.org/10.1371/journal.pone.0090751openalex-snapshot
Dinosaur Footprints and Other Ichnofauna from the Cretaceous Kem Kem Beds of Morocco
inferred← citeshttps://doi.org/10.1371/journal.pone.0093708openalex-snapshot
Intra-Trackway Morphological Variations Due to Substrate Consistency: The El Frontal Dinosaur Tracksite (Lower Cretaceous, Spain)
inferred← citeshttps://doi.org/10.1371/journal.pone.0103613openalex-snapshot
A ‘Terror of Tyrannosaurs’: The First Trackways of Tyrannosaurids and Evidence of Gregariousness and Pathology in Tyrannosauridae
inferred← citeshttps://doi.org/10.1371/journal.pone.0213572openalex-snapshot
A late Pleistocene human footprint from the Pilauco archaeological site, northern Patagonia, Chile
inferred← citeshttps://doi.org/10.1371/journal.pone.0293308openalex-snapshot
Earliest known Gondwanan bird tracks: Wonthaggi Formation (Early Cretaceous), Victoria, Australia
inferred← citeshttps://doi.org/10.1371/journal.pone.0335973openalex-snapshot
Morphotypes, preservation, and taphonomy of dinosaur footprints, tail traces, and swim tracks in the largest tracksite in the world: Carreras Pampa (Upper Cretaceous), Torotoro National Park, Bolivia
inferred← citeshttps://doi.org/10.14241/asgp.2018.010openalex-snapshot
Dinosaur behaviour in an Early Jurassic palaeoecosystem – uppermost Elliot Formation, Ha Nohana, Lesotho
inferred← citeshttps://doi.org/10.1590/s0001-37652011000100005openalex-snapshot
Pelvic and hind limb musculature of Staurikosaurus pricei (Dinosauria: Saurischia)
inferred← citeshttps://doi.org/10.1666/0094-8373(2001)027<0564:tdattt>2.0.co;2openalex-snapshot
Taxon distributions and the tetrapod track record
inferred← citeshttps://doi.org/10.1668/0003-1569(2000)040[0640:tl]2.0.co;2openalex-snapshot
Theropod Locomotion1
inferred← citeshttps://doi.org/10.1671/0272-4634(2008)28[145:iobfae]2.0.co;2openalex-snapshot
Ichnotaxonomy of bird-like footprints: an example from the Late Triassic-Early Jurassic of northwest Argentina
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