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A king-sized theropod coprolite
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4899-5034-5_8openalex-snapshot
Phosphates and Fossil Preservation
inferredcites →https://doi.org/10.1016/0031-0182(91)90062-vopenalex-snapshot
Prey bone utilization by predatory dinosaurs
inferredcites →https://doi.org/10.1016/0300-9629(75)90121-8openalex-snapshot
Gastric digestion in some raptors
inferredcites →https://doi.org/10.1016/0300-9629(91)90507-9openalex-snapshot
Comparative physiology of the vertebrate digestive system
inferredcites →https://doi.org/10.1017/s0094837300004048openalex-snapshot
Crocodilian scatology, microvertebrate concentrations, and enamel-less teeth
inferredcites →https://doi.org/10.1038/382706a0openalex-snapshot
Bite-force estimation for Tyrannosaurus rex from tooth-marked bones
inferredcites →https://doi.org/10.1080/02724634.1995.10011257openalex-snapshot
Body mass, bone “strength indicator,” and cursorial potential ofTyrannosaurus rex
inferredcites →https://doi.org/10.1080/02724634.1995.10011575openalex-snapshot
Implications of body-mass estimates for dinosaurs
inferredcites →https://doi.org/10.1080/02724634.1996.10011297openalex-snapshot
Bite marks attributable toTyrannosaurus rex: Preliminary description and implications
inferredcites →https://doi.org/10.1111/j.1469-7998.1985.tb04915.xopenalex-snapshot
Long‐bone circumference and weight in mammals, birds and dinosaurs
inferredcites →https://doi.org/10.2307/1444685openalex-snapshot
The Behavioral Ecology of the Komodo Monitor
inferredcites →https://doi.org/10.2307/1941052openalex-snapshot
A Consideration of the Trophic Dynamics of a Late Cretaceous Large‐Dinosaur Community (Oldman Formation)
inferredcites →https://doi.org/10.2307/3515235openalex-snapshot
Dinosaurs, dung beetles, and conifers; participants in a Cretaceous food web
inferredcites →https://doi.org/10.5860/choice.30-0309openalex-snapshot
Taphonomy: releasing the data locked in the fossil record
inferredcites →https://doi.org/10.5860/choice.32-2751openalex-snapshot
The palaeobiology of trace fossils
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
Of the 200 inferred citing records listed on this page, 31 match the GBIF occurrence-download DOI prefix (10.15468/dl.).
inferred← citeshttps://doi.org/10.1038/s41598-017-02161-wzenodo-depositor-declared
The Biomechanics Behind Extreme Osteophagy in Tyrannosaurus rex
inferred← citeshttps://doi.org/10.4202/app.2009.0133zenodo-depositor-declared
New Information on Scavenging and Selective Feeding Behaviour of Tyrannosaurids
inferred← citeshttps://doi.org/10.1002/1096-8644(200010)113:2<217::aid-ajpa6>3.0.co;2-gopenalex-snapshot
Recognizing hominoid-modified bones: The taphonomy of colobus bones partially digested by free-ranging chimpanzees in the Kibale Forest, Uganda
inferred← citeshttps://doi.org/10.1002/9780470515655.ch12openalex-snapshot
Natural History and Behavioural Homology
inferred← citeshttps://doi.org/10.1002/ar.22491openalex-snapshot
Tooth‐On‐Tooth Interlocking Occlusion Suggests Macrophagy in the Mesozoic Marine Crocodylomorph Dakosaurus
inferred← citeshttps://doi.org/10.1002/ar.24602openalex-snapshot
Biomechanics of juvenile tyrannosaurid mandibles and their implications for bite force: Evolutionary biology
inferred← citeshttps://doi.org/10.1002/ar.25021openalex-snapshot
Rare juvenile material constrains estimation of skeletal allometry in Gryposaurus notabilis (Dinosauria: Hadrosauridae)
inferred← citeshttps://doi.org/10.1002/ar.25299openalex-snapshot
Functional morphology of the Triassic apex predator Saurosuchus galilei (Pseudosuchia: Loricata) and convergence with a post‐Triassic theropod dinosaur
inferred← citeshttps://doi.org/10.1002/ar.25326openalex-snapshot
Comparative cranial biomechanics reveal that Late Cretaceous tyrannosaurids exerted relatively greater bite force than in early‐diverging tyrannosauroids
inferred← citeshttps://doi.org/10.1002/ar.25419openalex-snapshot
Cranial and postcranial anatomy of a juvenile baurusuchid (Notosuchia, Crocodylomorpha) and the taxonomical implications of ontogeny
inferred← citeshttps://doi.org/10.1002/ar.70126openalex-snapshot
Comparative cranial biomechanics reveal macroevolutionary trends in theropod dinosaurs, with emphasis on Tyrannosauroidea
inferred← citeshttps://doi.org/10.1002/ar.70170openalex-snapshot
Inter‐ and intraspecific variation in theropod dinosaur dental microwear and its palaeoecological implications
inferred← citeshttps://doi.org/10.1002/gj.70253openalex-snapshot
How Do Vertebrate Droppings Fossilise? Biogenic Versus Diagenetic Signals in Coprolites Evidenced by Elemental Mappings
inferred← citeshttps://doi.org/10.1002/spp2.1474openalex-snapshot
Tough to digest: first record of Teleosauroidea (Thalattosuchia) in a regurgitalite from the Upper Jurassic of north‐eastern Italy
inferred← citeshttps://doi.org/10.1002/spp2.70100openalex-snapshot
Digestion corrosion marks on a hatchling Allosaurus (Dinosauria, Theropoda) maxilla from the Upper Jurassic of Guimarota (Leiria, Portugal)
inferred← citeshttps://doi.org/10.1007/978-3-031-28624-7_5openalex-snapshot
Critical Thinking Identifies Misconceptions and False Trails
inferred← citeshttps://doi.org/10.1007/978-3-540-68211-0_2openalex-snapshot
Entfaltung der Organismen in der Erdgeschichte
inferred← citeshttps://doi.org/10.1007/978-3-642-32836-7_2openalex-snapshot
Entfaltung der Organismen in der Erdgeschichte
inferred← citeshttps://doi.org/10.1007/978-3-662-07144-1_2openalex-snapshot
Entfaltung der Organismen in der Erdgeschichte
inferred← citeshttps://doi.org/10.1007/s00114-010-0659-xopenalex-snapshot
Shark-bitten vertebrate coprolites from the Miocene of Maryland
inferred← citeshttps://doi.org/10.1007/s11692-022-09561-5openalex-snapshot
The Tyrant Lizard King, Queen and Emperor: Multiple Lines of Morphological and Stratigraphic Evidence Support Subtle Evolution and Probable Speciation Within the North American Genus Tyrannosaurus
inferred← citeshttps://doi.org/10.1007/s13358-013-0057-zopenalex-snapshot
A new method to determine volume of bromalites: morphometrics of Lower Permian (Archer City Formation) heteropolar bromalites
inferred← citeshttps://doi.org/10.1007/s13358-018-0171-zopenalex-snapshot
Regurgitated ammonoid remains from the latest Devonian of Morocco
inferred← citeshttps://doi.org/10.1007/s44288-026-00454-0openalex-snapshot
The dentition of tyrannosauroid theropods: a review
inferred← citeshttps://doi.org/10.1016/b978-0-12-819770-7.00009-8openalex-snapshot
Evolution of birds
inferred← citeshttps://doi.org/10.1016/b978-0-443-38351-9.00008-6openalex-snapshot
Vertebrate coprolites
inferred← citeshttps://doi.org/10.1016/b978-044452949-7/50138-8openalex-snapshot
The Trace-Fossil Record of Vertebrates
inferred← citeshttps://doi.org/10.1016/bs.apar.2015.06.002openalex-snapshot
Constraining the Deep Origin of Parasitic Flatworms and Host-Interactions with Fossil Evidence
inferred← citeshttps://doi.org/10.1016/j.cretres.2005.03.001openalex-snapshot
Trace fossils and pseudofossils from the Wealden strata (non-marine Lower Cretaceous) of southern England
inferred← citeshttps://doi.org/10.1016/j.cretres.2012.03.018openalex-snapshot
Tyrannosaur feeding traces on Deinocheirus (Theropoda:?Ornithomimosauria) remains from the Nemegt Formation (Late Cretaceous), Mongolia
inferred← citeshttps://doi.org/10.1016/j.cretres.2017.02.010openalex-snapshot
First report on vertebrate coprolites from the Upper Cretaceous (Santonian) Csehbánya Formation of Iharkút, Hungary
inferred← citeshttps://doi.org/10.1016/j.cretres.2019.104343openalex-snapshot
Food web reconstruction through isotopic compositions of fossil faeces: Insights into the ecology of a late Barremian freshwater ecosystem (Las Hoyas, Cuenca, Spain)
inferred← citeshttps://doi.org/10.1016/j.cretres.2020.104409openalex-snapshot
The late Barremian ecosystem of Las Hoyas sustained by fishes and shrimps as inferred from coprofabrics
inferred← citeshttps://doi.org/10.1016/j.cretres.2024.105939openalex-snapshot
A rich coprolite assemblage from Angeac-Charente (France): A glimpse into trophic interactions within an Early Cretaceous freshwater swamp
inferred← citeshttps://doi.org/10.1016/j.cub.2016.02.055openalex-snapshot
A Fish-Eating Enantiornithine Bird from the Early Cretaceous of China Provides Evidence of Modern Avian Digestive Features
inferred← citeshttps://doi.org/10.1016/j.cub.2019.06.020openalex-snapshot
Microraptor with Ingested Lizard Suggests Non-specialized Digestive Function
inferred← citeshttps://doi.org/10.1016/j.cub.2026.08.054openalex-snapshot
Bird feathers from a Late Cretaceous coprolite
inferred← citeshttps://doi.org/10.1016/j.earscirev.2016.08.014openalex-snapshot
Vertebrate coprolites (fossil faeces): An underexplored Konservat-Lagerstätte
inferred← citeshttps://doi.org/10.1016/j.gca.2011.03.032openalex-snapshot
Calcium isotopes in fossil bones and teeth — Diagenetic versus biogenic origin
inferred← citeshttps://doi.org/10.1016/j.gca.2025.05.006openalex-snapshot
Combined Ca, Sr isotope and trace element analyses of Late Cretaceous dinosaur teeth: assessing diet versus diagenesis
inferred← citeshttps://doi.org/10.1016/j.geobios.2006.02.002openalex-snapshot
The appendicular skeleton of Suuwassea emilieae (Sauropoda: Flagellicaudata) from the Upper Jurassic Morrison Formation of Montana (USA)
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110679openalex-snapshot
Morphological evolution and functional consequences of giantism in tyrannosauroid dinosaurs
inferred← citeshttps://doi.org/10.1016/j.jas.2009.11.029openalex-snapshot
Identification of fragmentary bone from the Pacific
inferred← citeshttps://doi.org/10.1016/j.jhevol.2014.10.016openalex-snapshot
Ancient human microbiomes
inferred← citeshttps://doi.org/10.1016/j.marpetgeo.2025.107531openalex-snapshot
Phosphatized embryo-like fossils from the Chang 73 sub-member, middle-upper Triassic Yanchang Formation, Ordos Basin, northwest China: Affinity, preservation and paleoecological implications
inferred← citeshttps://doi.org/10.1016/j.micron.2008.02.004openalex-snapshot
Principles of demineralization: Modern strategies for the isolation of organic frameworks
inferred← citeshttps://doi.org/10.1016/j.palaeo.2008.03.030openalex-snapshot
Preservation of primary stable isotope signals in dinosaur remains, and environmental gradients of the Late Cretaceous of Montana and Alberta
inferred← citeshttps://doi.org/10.1016/j.palaeo.2011.07.013openalex-snapshot
An exceptionally rich hyaena coprolites concentration in the Late Miocene mammal fossil site of La Roma 2 (Teruel, Spain): Taphonomical and palaeoenvironmental inferences
inferred← citeshttps://doi.org/10.1016/j.palaeo.2011.09.006openalex-snapshot
Morphology and composition of bone-bearing coprolites from the Late Permian Beaufort Group, Karoo Basin, South Africa
inferred← citeshttps://doi.org/10.1016/j.palaeo.2013.11.019openalex-snapshot
Coprolite evidence for carnivorous predation in a Late Devonian pelagic environment of southern Laurussia
inferred← citeshttps://doi.org/10.1016/j.palaeo.2014.05.035openalex-snapshot
Phosphatized coprolites from the middle Cambrian (Stage 5) Duyun fauna of China
inferred← citeshttps://doi.org/10.1016/j.palaeo.2014.06.013openalex-snapshot
Putative dicynodont coprolites from the Upper Triassic of Poland
inferred← citeshttps://doi.org/10.1016/j.palaeo.2014.09.032openalex-snapshot
Taphonomic and paleoecologic investigations of the Late Cretaceous (Santonian) Iharkút vertebrate assemblage (Bakony Mts, Northwestern Hungary)
inferred← citeshttps://doi.org/10.1016/j.palaeo.2015.04.009openalex-snapshot
Coprolites of Late Triassic carnivorous vertebrates from Poland: An integrative approach
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.02.036openalex-snapshot
Dietary and environmental implications of Early Cretaceous predatory dinosaur coprolites from Teruel, Spain
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.02.057openalex-snapshot
Reduction of vertebrate coprolite diversity associated with the end-Permian extinction event in Vyazniki region, European Russia
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.04.003openalex-snapshot
An Early Triassic polar predator ecosystem revealed by vertebrate coprolites from the Bulgo Sandstone (Sydney Basin) of southeastern Australia
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.12.003openalex-snapshot
Taphonomical and palaeoecological investigation of the Late Cretaceous (Maastrichtian) Tuştea vertebrate assemblage (Romania; Haţeg Basin) - insights into a unique dinosaur nesting locality
inferred← citeshttps://doi.org/10.1016/j.palaeo.2017.05.033openalex-snapshot
Residues from the Upper Permian carnivore coprolites from Vyazniki in Russia - key questions in reconstruction of feeding habits
inferred← citeshttps://doi.org/10.1016/j.palaeo.2017.07.032openalex-snapshot
Carnivore coprolites from the lower Carnian (Upper Triassic) Chañares Formation, northwestern Argentina
inferred← citeshttps://doi.org/10.1016/j.palaeo.2018.04.003openalex-snapshot
Palaeobotany and palynology of coprolites from the Late Triassic Chañares Formation of Argentina: implications for vegetation provinces and the diet of dicynodonts
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.02.002openalex-snapshot
Bromalites from a turtle-dominated fossil assemblage from the Triassic of Poland
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.109318openalex-snapshot
Bioerosion on vertebrate remains from the Upper Cretaceous of the Haţeg Basin, Romania and its taphonomic implications
inferred← citeshttps://doi.org/10.1016/j.palaeo.2020.109999openalex-snapshot
A theropod dinosaur feeding site from the Upper Jurassic of the Junggar Basin, NW China
inferred← citeshttps://doi.org/10.1016/j.palaeo.2022.111084openalex-snapshot
Vertebrate coprolites from Middle Triassic Chang 7 Member in Ordos Basin, China: Palaeobiological and palaeoecological implications
inferred← citeshttps://doi.org/10.1016/j.pgeola.2011.03.007openalex-snapshot
A new hypothesis for the origin of the supposed giant snail Dinocochlea from the Wealden of Sussex, England
inferred← citeshttps://doi.org/10.1016/j.quaint.2010.06.022openalex-snapshot
The larger Carnivora of the West Runton Freshwater Bed
inferred← citeshttps://doi.org/10.1016/j.tree.2006.01.002openalex-snapshot
Ecological and evolutionary implications of dinosaur feeding behaviour
inferred← citeshttps://doi.org/10.1016/j.yqres.2009.06.006openalex-snapshot
Lipid analysis of a ground sloth coprolite
inferred← citeshttps://doi.org/10.1017/jpa.2022.16openalex-snapshot
Carnivorous reptile feeding strategies and postmortem food-processing behaviors: tooth traces on bones from the Upper Triassic Grabowa Formation (southern Poland)
inferred← citeshttps://doi.org/10.1017/s0022336000018199openalex-snapshot
Gut contents from a Cretaceous Tyrannosaurid: Implications for theropod dinosaur digestive tracts
inferred← citeshttps://doi.org/10.1017/s0031182006000138openalex-snapshot
Evidence of intestinal parasites of dinosaurs
inferred← citeshttps://doi.org/10.1017/s1089332600001030openalex-snapshot
The Fossil Record of Predation: An Overview of Analytical Methods
inferred← citeshttps://doi.org/10.1017/s1089332600001042openalex-snapshot
Analyses of Coprolites Produced by Carnivorous Vertebrates
inferred← citeshttps://doi.org/10.1017/s108933260000111xopenalex-snapshot
The Fossil Record of Predation in Dinosaurs
inferred← citeshttps://doi.org/10.1038/35059070openalex-snapshot
Cranial design and function in a large theropod dinosaur
inferred← citeshttps://doi.org/10.1038/nature01532openalex-snapshot
Cannibalism in the Madagascan dinosaur Majungatholus atopus
inferred← citeshttps://doi.org/10.1038/nature02699openalex-snapshot
Gigantism and comparative life-history parameters of tyrannosaurid dinosaurs
inferred← citeshttps://doi.org/10.1038/s41598-018-32202-xopenalex-snapshot
Exceptional dinosaur fossils reveal early origin of avian-style digestion
inferred← citeshttps://doi.org/10.1038/s41598-018-37540-4openalex-snapshot
Tyrannosaurid-like osteophagy by a Triassic archosaur
inferred← citeshttps://doi.org/10.1038/s41598-022-24602-xopenalex-snapshot
Intestinal preservation in a birdlike dinosaur supports conservatism in digestive canal evolution among theropods
inferred← citeshttps://doi.org/10.1038/s41598-025-33381-0openalex-snapshot
Early Permian terrestrial apex predator regurgitalite indicates opportunistic feeding behaviour
inferred← citeshttps://doi.org/10.1038/s41598-025-90032-0openalex-snapshot
Determining whether a phosphatic concretion containing a Cretaceous juvenile crocodylian is a coprolite or a non-fecal concretion
inferred← citeshttps://doi.org/10.1038/s44358-026-00191-9openalex-snapshot
Progress and future directions in dinosaur palaeontology
inferred← citeshttps://doi.org/10.1038/srep03348openalex-snapshot
The oldest known communal latrines provide evidence of gregarism in Triassic megaherbivores
inferred← citeshttps://doi.org/10.1038/srep12338openalex-snapshot
Developmental and evolutionary novelty in the serrated teeth of theropod dinosaurs
inferred← citeshttps://doi.org/10.1046/j.1095-8312.2002.00098.xopenalex-snapshot
Feeding ecology of North American gopher snakes (Pituophis catenifer, Colubridae)
inferred← citeshttps://doi.org/10.1073/pnas.1011924108openalex-snapshot
Herbivorous ecomorphology and specialization patterns in theropod dinosaur evolution
inferred← citeshttps://doi.org/10.1073/pnas.1117727108openalex-snapshot
Additional specimen of Microraptor provides unique evidence of dinosaurs preying on birds
inferred← citeshttps://doi.org/10.1080/02724631003762906openalex-snapshot
Coprolites from the Pipe Creek Sinkhole (Late Neogene, Grant County, Indiana, U.S.A.)
inferred← citeshttps://doi.org/10.1080/02724634.2010.483535openalex-snapshot
A description of Deinonychus antirrhopus bite marks and estimates of bite force using tooth indentation simulations
inferred← citeshttps://doi.org/10.1080/02724634.2019.1667814openalex-snapshot
Bones of pycnodontiform fishes (Actinopterygii: Pycnodontiformes) in coprolites from the Barremian fossil site of Las Hoyas (Cuenca, Spain)
inferred← citeshttps://doi.org/10.1080/02724634.2021.1999251openalex-snapshot
The cranial anatomy of the long-snouted tyrannosaurid dinosaur Qianzhousaurus sinensis from the Upper Cretaceous of China
inferred← citeshttps://doi.org/10.1080/02724634.2022.2144337openalex-snapshot
Generalist diet of Microraptor zhaoianus included mammals
inferred← citeshttps://doi.org/10.1080/03949370.2014.928655openalex-snapshot
Unexpected behavior in the Cretaceous: tooth-marked bones attributable to tyrannosaur play
inferred← citeshttps://doi.org/10.1080/0891296021000050755openalex-snapshot
Maximum Bite Force and Prey Size of Tyrannosaurus rex and Their Relationships to the Inference of Feeding Behavior
inferred← citeshttps://doi.org/10.1080/08912963.2011.631703openalex-snapshot
A call to search for fossilised gastric pellets
inferred← citeshttps://doi.org/10.1080/08912963.2015.1111886openalex-snapshot
Sublethal injuries in non-marine microconchid tubeworms from the Lower Carboniferous of West Virginia, USA
inferred← citeshttps://doi.org/10.1080/10420940.2015.1030073openalex-snapshot
Gar-Bitten Coprolite From South Carolina, USA
inferred← citeshttps://doi.org/10.1080/10420940.2017.1386662openalex-snapshot
Turtle Shell Impression in a Coprolite from South Carolina, USA
inferred← citeshttps://doi.org/10.1080/10420940.2026.2659169openalex-snapshot
Exploring the paleoecology and taphonomy of upper cretaceous bromalites from the cerro del pueblo formation, Northern Mexico
inferred← citeshttps://doi.org/10.1080/10420940.2026.2666124openalex-snapshot
Microcoprolite morphotypes from the Revueltian (Upper Triassic: Norian) age Homestead Site, Garita Creek Formation, east-central New Mexico, USA
inferred← citeshttps://doi.org/10.1081/fst-120002927openalex-snapshot
COMPUTATIONAL STUDY OF N@C60, P@C60, AND As@C60
inferred← citeshttps://doi.org/10.1086/686094openalex-snapshot
Body Size as a Driver of Scavenging in Theropod Dinosaurs
inferred← citeshttps://doi.org/10.1098/rsbl.2003.0097openalex-snapshot
Tyrannosaurus en pointe: allometry minimized rotational inertia of large carnivorous dinosaurs
inferred← citeshttps://doi.org/10.1098/rsos.181042openalex-snapshot
Beetle-bearing coprolites possibly reveal the diet of a Late Triassic dinosauriform
inferred← citeshttps://doi.org/10.1098/rspb.2004.2755openalex-snapshot
Cranial mechanics and feeding inTyrannosaurus rex
inferred← citeshttps://doi.org/10.1098/rspb.2009.1029openalex-snapshot
A new North American therizinosaurid and the role of herbivory in ‘predatory’ dinosaur evolution
inferred← citeshttps://doi.org/10.1101/2024.12.06.627300openalex-snapshot
Convincing Evidence of Carnivorous Diet in Alvarezsaurian Dinosaur
inferred← citeshttps://doi.org/10.1111/brv.12666openalex-snapshot
Assessing ontogenetic maturity in extinct saurian reptiles
inferred← citeshttps://doi.org/10.1111/brv.12743openalex-snapshot
The diet of early birds based on modern and fossil evidence and a new framework for its reconstruction
inferred← citeshttps://doi.org/10.1111/ecog.02817openalex-snapshot
A recipe for scavenging in vertebrates – the natural history of a behaviour
inferred← citeshttps://doi.org/10.1111/evo.12119openalex-snapshot
PISCIVORY IN THE FEATHERED DINOSAURMICRORAPTOR
inferred← citeshttps://doi.org/10.1111/gbi.70030openalex-snapshot
Mineralization Controls Informative Biomarker Preservation Associated With Soft Part Fossilization in Deep Time
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2004.00432.xopenalex-snapshot
Early Triassic coprolites from Australia and their palaeobiological significance
inferred← citeshttps://doi.org/10.1111/j.1502-3931.2009.00187.xopenalex-snapshot
Feeding behaviour and bone utilization by theropod dinosaurs
inferred← citeshttps://doi.org/10.1111/j.1502-3931.2010.00257.xopenalex-snapshot
Coprolite morphotypes from the Upper Cretaceous of Sweden: novel views on an ancient ecosystem and implications for coprolite taphonomy
inferred← citeshttps://doi.org/10.1111/j.1949-8594.2011.00087.xopenalex-snapshot
A “Coprolitic Vision” for Earth Science Education
inferred← citeshttps://doi.org/10.1111/jzo.12109openalex-snapshot
The role of the neck in the feeding behaviour of the T yrannosauridae: inference based on kinematics and muscle function of extant avians
inferred← citeshttps://doi.org/10.1111/let.12330openalex-snapshot
Multi-proxy analyses of Late Cretaceous coprolites from Germany
inferred← citeshttps://doi.org/10.1111/let.12431openalex-snapshot
Morphological and compositional analyses of coprolites from the Upper Cretaceous Bauru Group reveal dietary habits of notosuchian fauna
inferred← citeshttps://doi.org/10.1111/let.12438openalex-snapshot
Coprolites in natural traps: direct evidence of bone‐eating carnivorans from the Late Miocene Batallones‐3 site, Madrid, Spain
inferred← citeshttps://doi.org/10.1111/pala.12409openalex-snapshot
First record of Mesozoic scroll coprolites: classification, characteristics, elemental composition and probable producers
inferred← citeshttps://doi.org/10.1111/pala.12453openalex-snapshot
The evolution of the modern avian digestive system: insights from paravian fossils from the Yanliao and Jehol biotas
inferred← citeshttps://doi.org/10.1111/pala.12546openalex-snapshot
Mammal‐bearing gastric pellets potentially attributable to Troodon formosus at the Cretaceous Egg Mountain locality, Two Medicine Formation, Montana, USA
inferred← citeshttps://doi.org/10.1111/pala.12632openalex-snapshot
First application of dental microwear texture analysis to infer theropod feeding ecology
inferred← citeshttps://doi.org/10.1126/sciadv.adi0505openalex-snapshot
Exceptionally preserved stomach contents of a young tyrannosaurid reveal an ontogenetic dietary shift in an iconic extinct predator
inferred← citeshttps://doi.org/10.1126/science.1193304openalex-snapshot
Tyrannosaur Paleobiology: New Research on Ancient Exemplar Organisms
inferred← citeshttps://doi.org/10.1139/cjes-2020-0177openalex-snapshot
Mandibular force profiles and tooth morphology in growth series of Albertosaurus sarcophagus and Gorgosaurus libratus (Tyrannosauridae: Albertosaurinae) provide evidence for an ontogenetic dietary shift in tyrannosaurids 1
inferred← citeshttps://doi.org/10.1139/e10-072openalex-snapshot
On gregarious behavior inAlbertosaurusThis article is one of a series of papers published in this Special Issue on the themeAlbertosaurus.
inferred← citeshttps://doi.org/10.1371/journal.pbio.1000321openalex-snapshot
Studying Function and Behavior in the Fossil Record
inferred← citeshttps://doi.org/10.1371/journal.pone.0011998openalex-snapshot
Convergent Evolution in Aquatic Tetrapods: Insights from an Exceptional Fossil Mosasaur
inferred← citeshttps://doi.org/10.1371/journal.pone.0013419openalex-snapshot
Cannibalism in Tyrannosaurus rex
inferred← citeshttps://doi.org/10.1371/journal.pone.0044012openalex-snapshot
Abdominal Contents from Two Large Early Cretaceous Compsognathids (Dinosauria: Theropoda) Demonstrate Feeding on Confuciusornithids and Dromaeosaurids
inferred← citeshttps://doi.org/10.1371/journal.pone.0196982openalex-snapshot
Exceptional coprolite association from the Early Cretaceous continental Lagerstätte of Las Hoyas, Cuenca, Spain
inferred← citeshttps://doi.org/10.1371/journal.pone.0233115openalex-snapshot
High frequencies of theropod bite marks provide evidence for feeding, scavenging, and possible cannibalism in a stressed Late Jurassic ecosystem
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inferred← citeshttps://doi.org/10.1649/0010-065x(2006)60[120:fraeos]2.0.co;2openalex-snapshot
Fossil Record and Evolution of Scarabaeoidea (Coleoptera: Polyphaga)
inferred← citeshttps://doi.org/10.1666/0022-3360(2001)075<0401:gcfact>2.0.co;2openalex-snapshot
GUT CONTENTS FROM A CRETACEOUS TYRANNOSAURID: IMPLICATIONS FOR THEROPOD DINOSAUR DIGESTIVE TRACTS
inferred← citeshttps://doi.org/10.1666/0094-8373(2002)028<0527:dampc>2.0.co;2openalex-snapshot
Dinosaurian and mammalian predators compared
inferred← citeshttps://doi.org/10.1666/08020.1openalex-snapshot
Stable isotope evidence for changes in dietary niche partitioning among hadrosaurian and ceratopsian dinosaurs of the Hell Creek Formation, North Dakota
inferred← citeshttps://doi.org/10.1669/0883-1351(2003)018<0286:rpoumt>2.0.co;2openalex-snapshot
Remarkable Preservation of Undigested Muscle Tissue Within a Late Cretaceous Tyrannosaurid Coprolite from Alberta, Canada
inferred← citeshttps://doi.org/10.1671/0272-4634(2000)020[0619:tcbot]2.0.co;2openalex-snapshot
The crushing bite of tyrannosaurids
inferred← citeshttps://doi.org/10.1671/0272-4634(2007)27[32:caomct]2.0.co;2openalex-snapshot
CRANIOFACIAL ANATOMY OF MAJUNGASAURUS CRENATISSIMUS (THEROPODA: ABELISAURIDAE) FROM THE LATE CRETACEOUS OF MADAGASCAR
inferred← citeshttps://doi.org/10.2110/palo.2003.p03-98openalex-snapshot
Carnivore Coprolites from the Upper Triassic Ischigualasto Formation, Argentina: Chemistry, Mineralogy, and Evidence for Rapid Initial Mineralization
inferred← citeshttps://doi.org/10.2110/palo.2008.p08-132ropenalex-snapshot
A PHOSPHATIC COPROLITE LACKING DIAGENETIC PERMINERALIZATION FROM THE UPPER CRETACEOUS HELL CREEK FORMATION, NORTHEASTERN MONTANA: IMPORTANCE OF DIETARY CALCIUM PHOSPHATE IN PRESERVATION
inferred← citeshttps://doi.org/10.2110/palo.2009.p09-136ropenalex-snapshot
BITE MARKS ON AN UPPER TRIASSIC DICYNODONTID TIBIA FROM ZAWIERCIE, KRAKOW-CZESTOCHOWA UPLAND, SOUTHERN POLAND
inferred← citeshttps://doi.org/10.2110/palo.2010.p10-088ropenalex-snapshot
MAMMALIAN BITE MARKS ON JUVENILE FUR SEAL BONES FROM THE LATE NEOGENE PURISIMA FORMATION OF CENTRAL CALIFORNIA
inferred← citeshttps://doi.org/10.2110/palo.2012.p12-017ropenalex-snapshot
UPPER PERMIAN VERTEBRATE COPROLITES FROM VYAZNIKI AND GOROKHOVETS, VYATKIAN REGIONAL STAGE, RUSSIAN PLATFORM
inferred← citeshttps://doi.org/10.2110/palo.2015.019openalex-snapshot
A LATE CRETACEOUS SHARK COPROLITE WITH BABY FRESHWATER TURTLE VERTEBRAE INCLUSIONS
inferred← citeshttps://doi.org/10.2110/palo.2017.038openalex-snapshot
COPROLITES IN THE RAVENS THROAT RIVER LAGERSTÄTTE OF NORTHWESTERN CANADA: IMPLICATIONS FOR THE MIDDLE CAMBRIAN FOOD WEB
inferred← citeshttps://doi.org/10.2110/palo.2017.076openalex-snapshot
TYRANNOSAUR CANNIBALISM: A CASE OF A TOOTH-TRACED TYRANNOSAURID BONE IN THE LANCE FORMATION (MAASTRICHTIAN), WYOMING
inferred← citeshttps://doi.org/10.2110/palo.2019.080openalex-snapshot
SPARASSODONTA (METATHERIA) COPROLITES FROM THE EARLY-MID MIOCENE (SANTACRUCIAN AGE) OF PATAGONIA (ARGENTINA) WITH EVIDENCE OF EXPLOITATION BY COPROPHAGOUS INSECTS
inferred← citeshttps://doi.org/10.2110/palo.2019.099openalex-snapshot
DISTINGUISHING REGURGITALITES AND COPROLITES: A CASE STUDY USING A TRIASSIC BROMALITE WITH SOFT TISSUE OF THE PSEUDOSUCHIAN ARCHOSAUR REVUELTOSAURUS
inferred← citeshttps://doi.org/10.2110/palo.2020.043openalex-snapshot
BITE MARKS ON AN AETOSAUR (ARCHOSAURIA, SUCHIA) OSTEODERM: ASSESSING LATE TRIASSIC PREDATOR-PREY ECOLOGY THROUGH ICHNOLOGY AND TOOTH MORPHOLOGY
inferred← citeshttps://doi.org/10.26879/337openalex-snapshot
A revised listing of fossil mammals from the Haasgat cave system ex situ deposits (HGD), South Africa
inferred← citeshttps://doi.org/10.26879/464openalex-snapshot
Ambergris cololites of Pleistocene sperm whales from central Italy and description of the new ichnogenus and ichnospecies Ambergrisichnus alleronae
inferred← citeshttps://doi.org/10.26879/99012openalex-snapshot
Themophysiology and Biology of Giganotosaurs: Comparison with Tyrannosaurus
inferred← citeshttps://doi.org/10.31233/osf.io/nc6tkopenalex-snapshot
Taxonomic status of Nanotyrannus lancensis (Dinosauria: Tyrannosauroidea) — a distinct taxon of small-bodied tyrannosaur
inferred← citeshttps://doi.org/10.3374/0079-032x(2007)48[103:arocph]2.0.co;2openalex-snapshot
A Reevaluation of Cooperative Pack Hunting and Gregariousness in Deinonychus antirrhopus and Other Nonavian Theropod Dinosaurs
inferred← citeshttps://doi.org/10.3374/014.066.0106openalex-snapshot
Documenting Footprints for Tracksites at Dinosaur State Park, Rocky Hill, Connecticut
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