John B. Scannella’s research while affiliated with Montana State University and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (37)


The left tarsometatarsus of Avisaurus darwini (DDM 1577.730) in A) dorsal, B) plantar, C) right lateral, D) left lateral, E) proximal, and F) distal aspects. Abbreviations: dlp, distal lateral projection; dmp, distal medial projection; dvf, distal vascular foramen; fo, fossa (collateral ligament fossa); is, intermetatarsalian space; lc, lateral cotyle; lf, laterally-projecting flange; mc, medial cotyle; mtII, metatarsal II; mtIII, metatarsal III; mtIV, metatarsal IV; pf, proximoplantar fossae; pl, proximal labrum; pp, plantar projection; tct, m. tibialis cranialis tubercle. Scale bar 10mm. Line illustrations done by Samantha Clark.
The left partial tarsometatarsus of Avisaurus sp
MOR3070 in A) dorsal, B) plantar, and C) proximal aspects. The distal portion of metatarsal II is placed in the approximate place if it was articulated. Abbreviations: dr, dorsal ridge: lc, lateral cotyle; lf, laterally-projecting flange; mc, medial cotyle; mtII, metatarsal II; mtIII, metatarsal III; mtIV, metatarsal IV; pf, proximoplantar fossae; pl, proximal labrum; tct, m. tibialis cranialis tubercle. Scale bar 10mm. Line illustrations done by Samantha Clark.
The partial left tarsometatarsus of Magnusavis ekalakaensis (CCM V2019.5.1) in A) dorsal, B) plantar, and C) distal aspects, D) and the single preserved pedal phalanx in dorsal and right lateral aspects. Abbreviations; mtII, metatarsal II; mtIII, metatarsal III; pp, proximal projection; psf, plantar supratrochanter fossa; tct, m. tibialis cranialis tubercle. Scale bar 10mm. Line illustrations done by Samantha Clark.
Tarsometatarsus size variation among the Avisauridae and close relatives
A) Avisaurus darwini, B) MOR3070, C) Avisaurus archibaldi, D) Gettyia, E) Soroavisaurus, F) Mirarce, G) Intiornis, H) Neuquenornis. All to scale. Scale bar 10 mm.
Phylogenetic placement of new Hell Creek enantiornithines based on cladistic analysis
A) A subset of the strict consensus tree focusing on taxa around the Avisauridae, and B) the full 50% majority tree. In the majority tree, the newly diagnosed Avisauridae family is comprised of six taxa, two of which are described in this publication. C) A 1.8 m tall human to scale with A. darwini (maroon), the largest known Early Cretaceous enantiornithine Pengornis (black), a medium-sized early enantiornithine, Imparavis (white), and finally, a minuscule enantiornithine, Elektorornis (smaller inset black). The extant Buteo jamaicensis (Red-tailed Hawk) is shown in grey.

+7

New enantiornithine diversity in the Hell Creek Formation and the functional morphology of the avisaurid tarsometatarsus
  • Article
  • Full-text available

October 2024

·

170 Reads

Alexander D. Clark

·

Jessie Atterholt

·

John B. Scannella

·

[...]

·

Enantiornithines were the most diverse group of birds during the Cretaceous, comprising over half of all known species from this period. The fossil record and subsequently our knowledge of this clade is heavily skewed by the wealth of material from Lower Cretaceous deposits in China. In contrast, specimens from Upper Cretaceous deposits are rare and typically fragmentary, yet critical for understanding the extinction of this clade across the K-Pg boundary. The most complete North American Late Cretaceous enantiornithine is Mirarce eatoni, a member of the diverse clade Avisauridae. Except for Mirarce, avisaurids are known only from isolated hindlimb elements from North and South America. Here we describe three new enantiornithines from the Maastrichtian Hell Creek Formation, two of which represent new avisaurid taxa. These materials represent a substantial increase in the known diversity of Enantiornithes in the latest Cretaceous. Re-examination of material referred to Avisauridae through phylogenetic analysis provides strong support for a more exclusive Avisauridae consisting of six taxa. Exploration of the functional morphology of the avisaurid tarsometatarsus indicates potential strong constriction and raptorial attributes. The lower aspect ratio of the tarsometatarsus facilitates a more biomechanically efficient lever system which in extant birds of prey equates to lifting proportionally heavier prey items. In addition, the proportional size and distal position of the m. tibialis cranialis tubercle of the tarsometatarsus is similar to the morphology seen in extant birds of prey. Together with the deeply-grooved metatarsal trochlea facilitating robust and likely powerful pedal digits, morphologies of the hindlimb suggest avisaurids as Late Cretaceous birds of prey.

Download

Figure 7. Reconstruction of the diagenetic history of Brachylophosaurus canadensis MOR 2598, summarizing macroscale and microscale events effecting its skeletal elements after death. Events are classified into approximate taphonomic stages, with a visual portrayal of the diagenetic processes affecting the bones during each stage shown at left.
Summary of the REE composition of the left tibia of Brachylophosaurus canadensis MOR 2598. Qualitative ∑REE content is based on the value shown in Table 1 (256 ppm) in comparison to values from other Mesozoic bones (as listed in the main text). Abbreviations: DMD, double medium diffusion sensu [80]; LREEs, light rare earth elements.
Taphonomic and Diagenetic Pathways to Protein Preservation, Part II: The Case of Brachylophosaurus canadensis Specimen MOR 2598

August 2022

·

201 Reads

·

6 Citations

Biology

Recent recoveries of peptide sequences from two Cretaceous dinosaur bones require paleontologists to rethink traditional notions about how fossilization occurs. As part of this shifting paradigm, several research groups have recently begun attempting to characterize biomolecular decay and stabilization pathways in diverse paleoenvironmental and diagenetic settings. To advance these efforts, we assessed the taphonomic and geochemical history of Brachylophosaurus canadensis specimen MOR 2598, the left femur of which was previously found to retain endogenous cells, tissues, and structural proteins. Combined stratigraphic and trace element data show that after brief fluvial transport, this articulated hind limb was buried in a sandy, likely-brackish, estuarine channel. During early diagenesis, percolating groundwaters stagnated within the bones, forming reducing internal microenvironments. Recent exposure and weathering also caused the surficial leaching of trace elements from the specimen. Despite these shifting redox regimes, proteins within the bones were able to survive through diagenesis, attesting to their remarkable resiliency over geologic time. Synthesizing our findings with other recent studies reveals that oxidizing conditions in the initial ~48 h postmortem likely promote molecular stabilization reactions and that the retention of early-diagenetic trace element signatures may be a useful proxy for molecular recovery potential.


Comparative cranial osteology of subadult eucentrosauran ceratopsid dinosaurs from the Two Medicine Formation, Montana, indicates sequence of ornamentation development and complex supraorbital ontogenetic change

December 2021

·

176 Reads

·

3 Citations

Acta Palaeontologica Polonica

The eucentrosauran centrosaurines Einiosaurus procurvicornis and Achelousaurus horneri are the two most commonly recovered ceratopsids from the Campanian Two Medicine Formation of northwestern Montana, USA. Einiosaurus procurvicornis is known from at least 15 individuals recovered from two monospecific bonebeds, while Achelousaurus horneri is primarily known from one articulated adult cranium as well as two isolated subadult individuals previously referred to the taxon. Previous assessments of ontogeny in these taxa, alongside closely related centrosaurines, focused primarily on crania of mature individuals and disarticulated elements of immature individuals. Here we describe an articulated subadult Einiosaurus procurvicornis skull (MOR 456 8-8-87-1) from the Einiosaurus procurvicornis type locality bonebed and compare its cranial ornamental development with the only identically sized articulated subadult eucentrosauran skull from the Two Medicine Formation, MOR 591. These individuals represent the only known articulated subadult skulls from the hypothesized eucentrosauran lineage in the Two Medicine Formation, thereby enabling comparison of early ontogenetic developmental sequence and timing of all three primary cranial ornaments (nasal, supraorbital, and parietosquamosal frill). Comparison indicates that parietosquamosal frill and supraorbital ornamentation development may have preceded nasal horncore development in these taxa. MOR 456 8-8-87-1 fills a gap between the plesiomorphic morphology of juvenile Einiosaurus procurvicornis supraorbital horncores and the rounded, spheroid mass of bone which characterizes adults. The complete left squamosal of MOR 456 8-8-87-1 is of adult size, in contrast to its shorter face and immature facial ornamentation, which suggests that in Einiosaurus procurvicornis, the face and facial ornamentation development occurred after the parietosquamosal frill had reached adult size.


Figure 2. Quarry map from the 2002 field season at the MOR 1125 quarry. Only bones discovered during that field season are shown. Select identifiable bones are identified as labeled. Although the large tree trunk was found above all the bones in the central region of the quarry, it is shown behind them to allow the bones to be better seen. Scale bar as indicated.
Figure 5. REE composition of the femur of MOR 1125. (A) Three-point moving average profile of La concentrations in the outermost 7 mm of the bone. (B) Average NASC-normalized REE composition of the fossil specimen as a whole. (C,D) Ternary diagrams of NASC-normalized REE. (C) Average composition of the bone. (D) REE compositions divided into data from each individual laser transect (~5 mm of data each). Compositional data from the transect that included the outer bone edge is denoted by a dark diamond; all other internal transect data are indicated by gray circles. The 2σ circle represents two standard deviations based on ±5% relative standard deviation.
Figure 8. (Ce/Ce*)N vs. (Pr/Pr*)N plot (after [66]) of five-point averages along the transect across the cortex of MOR 1125 recorded by LA-ICPMS. Separate fields (labeled by blue text) are as follows: 1, neither Ce nor La anomaly; 2a, no Ce and positive La anomaly; 2b, no Ce and negative La anomaly; 3a, positive Ce and negative La anomaly; 3b, negative Ce and positive La anomaly; 4a, negative Ce and negative La anomaly; 4b, positive Ce and positive La anomaly. Measurements from the outer 1 Figure 8. (Ce/Ce*) N vs. (Pr/Pr*) N plot (after [66]) of five-point averages along the transect across the cortex of MOR 1125 recorded by LA-ICPMS. Separate fields (labeled by blue text) are as follows: 1, neither Ce nor La anomaly; 2a, no Ce and positive La anomaly; 2b, no Ce and negative La anomaly; 3a, positive Ce and negative La anomaly; 3b, negative Ce and positive La anomaly; 4a, negative Ce and negative La anomaly; 4b, positive Ce and positive La anomaly. Measurements from the outer 1 mm of the external cortex are plotted as black triangles, and all measurements from deeper within the bone are plotted as grey diamonds. (Ce/Ce*) N and (Pr/Pr*) N anomalies, comparing observed (Ce, Pr) versus expected (Ce*, Pr*) concentrations of each element, are calculated as in the Materials and Methods section of the text. Yttrium/holmium (Y/Ho) ratios are slightly above chondritic (26) [67] near the cortical margin and through most of the external cortex (range ~30-70). Deeper in the bone, Y/Ho anomalies become increasingly positive through the middle cortex, forming a broad peak near 24 mm of ~90-250, then gently decline through the innermost cortex to values of ~60-100 at the end of the transect (Figure S2). When averaged for the entire transect, the Y/Ho anomaly is positive (59; Table 1).
Figure 9. Reconstruction of the taphonomic and diagenetic history of Tyrannosaurus rex MOR 1125. (A) Generalized postmortem history of the carcass, sans disarticulation. Reprinted in modified form with permission from ref. [108]. Copyright 2016 Porto Editora. (B) Synopsis of macroscale, microscale, and nanoscale (molecular level) processes inferred to have taken place during each taphonomic stage in the decay of this specimen, as portrayed in (A). Nanoscale processes of biomolecular decay and stabilization based on propositions by [29,30,109,110]. Black Tyrannosaurus silhouette by Scott Hartman, www.phylopic.org (accessed on 8 August 2021), CC BY-NC-SA-3.0. Autolysis, REE uptake, biomolecular lysis, and glycation images each respectively modified, with permission, from [38,111-114]. Hydrolysis image modified from [115], and oxidation and crosslinking images modified from [109], each under CC BY-4.0 licenses.
Summary of the REE composition of the right femur of Tyrannosaurs rex MOR 1125. Qualitative ∑REE content is based on the value shown in Table 1 (596 ppm) in comparison to values from other Mesozoic bones (as listed in the main text). Abbreviations: DMD-double medium diffusion sensu [44]; LREE-light rare earth elements.
Taphonomic and Diagenetic Pathways to Protein Preservation, Part I: The Case of Tyrannosaurus rex Specimen MOR 1125

November 2021

·

536 Reads

·

14 Citations

Biology

Many recent reports have demonstrated remarkable preservation of proteins in fossil bones dating back to the Permian. However, preservation mechanisms that foster the long-term stability of biomolecules and the taphonomic circumstances facilitating them remain largely unexplored. To address this, we examined the taphonomic and geochemical history of Tyrannosaurus rex specimen Museum of the Rockies (MOR) 1125, whose right femur and tibiae were previously shown to retain still-soft tissues and endogenous proteins. By combining taphonomic insights with trace element compositional data, we reconstruct the postmortem history of this famous specimen. Our data show that following prolonged, subaqueous decay in an estuarine channel, MOR 1125 was buried in a coarse sandstone wherein its bones fossilized while interacting with oxic and potentially brackish early-diagenetic groundwaters. Once its bones became stable fossils, they experienced minimal further chemical alteration. Comparisons with other recent studies reveal that oxidizing early-diagenetic microenvironments and diagenetic circumstances which restrict exposure to percolating pore fluids elevate biomolecular preservation potential by promoting molecular condensation reactions and hindering chemical alteration, respectively. Avoiding protracted interactions with late-diagenetic pore fluids is also likely crucial. Similar studies must be conducted on fossil bones preserved under diverse paleoenvironmental and diagenetic contexts to fully elucidate molecular preservation pathways.


Figure Captions: 1360 1361
Comparisons of tyrannosaurid embryo dimensions to previous hypothetical hatchlings. 1356
Baby tyrannosaurid bones and teeth from the Late Cretaceous of western North America

January 2021

·

1,490 Reads

·

18 Citations

Abstract: Tyrannosaurids were the apex predators of Late Cretaceous Laurasia and their status as dominant carnivores has garnered considerable interest since their discovery, both in the popular and scientific realms. As a result, they are well studied and much is known of their anatomy, diversity, growth, and evolution. In contrast, little is known of the earliest stages of tyrannosaurid development. Tyrannosaurid eggs and embryos remain elusive, and juvenile specimens — although known — are rare. Perinatal tyrannosaurid bones and teeth from the Campanian–Maastrichtian of western North America provide the first window into this critical period of the life of a tyrannosaurid. An embryonic dentary (cf. Daspletosaurus) from the Two Medicine Formation of Montana, measuring just 3 cm long, already exhibits distinctive tyrannosaurine char- acters like a “chin” and a deep Meckelian groove, and reveals the earliest stages of tooth development. When considered to- gether with a remarkably large embryonic ungual from the Horseshoe Canyon Formation of Alberta, minimum hatchling size of tyrannosaurids can be roughly estimated. A perinatal premaxillary tooth from the Horseshoe Canyon Formation likely pertains to Albertosaurus sarcophagus and it shows small denticles on the carinae. This tooth shows that the hallmark characters that distinguish tyrannosaurids from other theropods were present early in life and raises questions about the ontogenetic variability of serrations in premaxillary teeth. Sedimentary and taphonomic similarities in the sites that pro- duced the embryonic bones provide clues to the nesting habits of tyrannosaurids and may help to refine the prospecting search image in the continued quest to discover baby tyrannosaurids.


A chasmosaurine ceratopsid premaxilla from the basal sandstone of the Hell Creek Formation, Montana

November 2020

·

57 Reads

Vertebrate Anatomy Morphology Palaeontology

A well-preserved large chasmosaurine ceratopsid premaxilla (MOR 1122 7-22-00-1) collected from the basal sandstone of the Cretaceous Hell Creek Formation (HCF) represents one of the stratigraphically lowest ceratopsid occurrences in the formation. The specimen was discovered in 2000, during the excavation of a large Torosaurus latus skull (MOR 1122) which was later hypothesized to represent an advanced growth stage of the more commonly recovered HCF ceratopsid Triceratops. MOR 1122 7-22-00-1 compares favorably with the incomplete premaxillae of the MOR 1122 skull and reveals details of premaxilla morphology from this stratigraphic zone. It preserves large, closely spaced ventromedial foramina, a narrow triangular process, and a thin septal flange at the base of the narial strut. The nasal process is narrow, caudally inclined and has a forked dorsal surface which appears to represent an intermediate between the morphology expressed in the slightly stratigraphically lower ceratopsid Eotriceratops xerinsularis from the Horseshoe Canyon Formation of Alberta and specimens recovered higher in the HCF. MOR 1122 7-22-00-1 expresses a deep recess extending medial to the strut of the triangular process, a feature shared with other HCF ceratopsid specimens but not Eotriceratops or other earlier occurring triceratopsin taxa. The morphology of MOR 1122 7-22-00-1 is consistent with noted stratigraphic trends in HCF ceratopsids and highlights the increased complexity of the narial region in uppermost Cretaceous triceratopsins.



Figure 1. Skeletal reconstruction of CMC VP14128 to scale with a mature D. carnegii (dark grey). Grey bones are missing, while those in ivory are those present in CMC VP14128. Skeletal reconstruction based on the Diplodocus by S. Hartman. Silhouettes by S. Hartman and PhyloPic (Creative Commons Attribution-ShareAlike 3.0 Unported; http://phylopic.org/image/3cb1d5bf-7db5-4db2-82a6-4c39f6a4441b/; https://creativecommons. org/licenses/by-sa/3.0/), modifications made. Skeletal reconstruction of CMC VP14128 redrawn from D. carnegii skeletal by S. Hartman (http://www.skeletaldrawing.com/sauropods-and-kin/diplodocus). Human scale is Andrew Carnegie at his natural height of 1.6 m. Skeletal and silhouettes to scale. (B) CMC VP14128 in right lateral view with accompanying schematic. (C) CMC VP14128 in left lateral view with accompanying schematic. Schematics by DCW. The four portions of the skull numbered on accompanying schematics. Lateral views and schematics to scale. a: angular, al: alisphenoid, aof: antorbital fenestra, d: dentary, f: frontal, h: hyoid, l: lacrimal, m: maxilla, n: nasal, oc: occipital condyle, os: orbitosphenoid, p: parietal, paof: preantorbital fenestra, pf: prefrontal, pm: premaxilla, po: postorbital, pro: prootic, q: quadrate, sa: surangular, sq: squamosal. L and r before bone denotes if it is left or right.
Figure 2. Cranial ontogeny in Diplodocus sp. (A) CMC VP14128; (B) CM 11255 (redrawn from Whitlock et al. 3 ); (C) CM 11161 (redrawn from Wilson and Sereno 69 ). Skull drawings by K. Scannella. Skulls to scale. (D) Silhouettes of CMC VP14128 and a mature D. carnegii to illustrate body length differences between skulls of A and C size. Diplodocus silhouette by S. Hartman and PhyloPic (Creative Commons Attribution-ShareAlike 3.0 Unported; http://phylopic.org/image/3cb1d5bf-7db5-4db2-82a6-4c39f6a4441b/; https://creativecommons.org/licenses/ by-sa/3.0/), modifications made. Skeletal reconstruction of CMC VP14128 redrawn from D. carnegii skeletal by S. Hartman (http://www.skeletaldrawing.com/sauropods-and-kin/diplodocus). (E) Transformation grid highlighting the ontogenetic cranial changes. Adult skull is the same in part C (Wilson and Sereno 69 ).
Figure 3. The dental morphotypes in CMC VP14128. Pre-and maxillary teeth of CMC VP14128 in right and left lateral. Drawing by K. Scannella. Red outlines highlight the zoomed in views on the right. Note the combination of diplodocid peg and camarasaurid spatulate tooth forms. Camarasaurus sp. with the spatulate tooth form (SMA 0002). Diplodocus longus with the peg tooth form (USNM 2672). Camarasaurus and Diplodocus skull modified from McIntosh 70. Skulls not to scale.
Figure 4. Dendrograms of parsimony (left column) and Bayesian (right column) phylogenetic analyses. (A-C) Consist of cranial and postcranial characters, while (D,E) consist of only cranial characters. (A and D) CMC VP14128 coded into the matrix of Whitlock 11. (B and E) CMC VP14128 coded into the matrix of Tschopp et al. 12. (C and F) CMC VP14128 coded into a combined matrix.
Life reconstruction of CMC VP14128. Note the cranial morphologies interpreted to denote differing feeding strategies: in CMC VP14128 the narrow snout with posteriorly elongated and morphologically varied tooth row for bulk feeding vs. the widened snout with anteriorly restricted peg-shaped teeth for ground-level browsing in adults. Also note the camouflaged ontogenetic color change suggesting young diplodocids may have sought forested refuge. Reconstruction by A. Atuchin.
The Smallest Diplodocid Skull Reveals Cranial Ontogeny and Growth-Related Dietary Changes in the Largest Dinosaurs

October 2018

·

1,727 Reads

·

33 Citations

Sauropod dinosaurs were the largest terrestrial vertebrates; yet despite a robust global fossil record, the paucity of cranial remains complicates attempts to understand their paleobiology. An assemblage of small diplodocid sauropods from the Upper Jurassic Morrison Formation of Montana, USA, has produced the smallest diplodocid skull yet discovered. The ~24 cm long skull is referred to cf. Diplodocus based on the presence of several cranial and vertebral characters. This specimen enhances known features of early diplodocid ontogeny including a short snout with narrow-crowned teeth limited to the anterior portion of the jaws and more spatulate teeth posteriorly. The combination of size plus basal and derived character expression seen here further emphasizes caution when naming new taxa displaying the same, as these may be indicative of immaturity. This young diplodocid reveals that cranial modifications occurred throughout growth, providing evidence for ontogenetic dietary partitioning and recapitulation of ancestral morphologies.




Citations (16)


... Phylogenetically and physiologically informative tissues were probed by synchrotron [34] to support the previous identification of reproductive tissues in dinosaurs [35,36]. Technologies continue to broaden not only the type of questions to be asked, but the type of fossils we can analyze, from coprolites [33], teeth [37], and invertebrates [22,38,39] to dinosaurs [25,34,[40][41][42][43][44], mammals [45], and our own lineage [29,32,46]. ...

Reference:

Paleontology in the 21st Century
Taphonomic and Diagenetic Pathways to Protein Preservation, Part II: The Case of Brachylophosaurus canadensis Specimen MOR 2598

Biology

... This latter process results in more effective adsorption of the LREE and MREE at the edge of the fossils during permineralization, while HREE is less likely scavenged, and it can be relatively more enriched in the interior part of the bones (e.g. Herwartz et al., 2013;Ullmann et al., 2021). Such trends have been reported from many environmental settings (e.g. ...

Taphonomic and Diagenetic Pathways to Protein Preservation, Part I: The Case of Tyrannosaurus rex Specimen MOR 1125

Biology

... The Tyrannosauridae, including Tyrannosaurus rex and its close relatives, is a group of carnivorous theropods with a large body size and a highly specialized body-plan, and stands as one of the most extensively studied theropod groups (Osborn, 1905;Osborn and Brown, 1906;Lambe, 1917;Brochu, 2003;Currie, 2003;Hurum and Sabath, 2003;Horner and Padian, 2004;Brusatte et al., 2010;Tsuihiji et al., 2011;Brusatte and Carr, 2016;Carr, 2020;Woodward et al., 2020;Marshall et al., 2021;Paul et al., 2022;Dalman et al., 2023;Scherer and Voiculescu-Holvad, 2024). As the apex predators of the Late Cretaceous, tyrannosaurids harbor highly specialized feeding apparatuses that have attracted lots of attention (Currie et al., 1990;Abler, 1992;Farlow and Brinkman, 1994;Erickson, 1995;Smith, 2005;Buckley et al., 2010;Reichel, 2012;Owocki et al., 2020;Funston et al., 2021;Holtz, 2021;Therrien et al., 2021). These giant carnivorous dinosaurs, which were hypothesized to employ a unique bone-cracking strategy, exhibit some derived dental features, including extremely thickened teeth and heterodonty (refer to pseudo-heterodonty, sensu Hendrickx et al., 2015) in both morphology and function (Erickson and Olson,1996;Hurum and Currie, 2000;Meers, 2002;Brochu, 2003;Rayfield, 2004;Smith, 2005;Hone and Watabe, 2010;Reichel, 2010;DePalma II et al., 2013;Gignac and Erickson, 2017;Peterson et al., 2021;Rowe and Snively, 2022;Winkler et al., 2022;Therrien et al., 2023). ...

Baby tyrannosaurid bones and teeth from the Late Cretaceous of western North America

... Diplodocoidea. Diplodocoid dentition differed from earlier sauropodomorphs in having both narrow-crowned teeth (SI > 4) and teeth that are restricted to the anterior portion of the jaw in adults Woodruff et al. 2018). Although the shapes of diplodocoid teeth are similar along the tooth row, they vary in size, which is the primitive condition in Sauropodomorpha. ...

The Smallest Diplodocid Skull Reveals Cranial Ontogeny and Growth-Related Dietary Changes in the Largest Dinosaurs

... Cranial sutures are boundary areas between bones, comprising a soft tissue component and the contacting bone edges (Curtis et al. 2013). Sutures are, however, not only sites of bone deposition during growth, but also determine the biomechanics of the skull (Bailleul et al. 2016). Essentially, they serve as critical elements in the dissipation and reduction of stress (Curtis et al. 2013). ...

Fusion Patterns in the Skulls of Modern Archosaurs Reveal That Sutures Are Ambiguous Maturity Indicators for the Dinosauria

... Bader et al. (2009) described root etching from the Upper Jurassic fluvial deposits of the Morrison Formation, USA, as small, 'thin, curvilinear, branching grooves' forming irregular dendritic or looping patterns. In that case, root etchings typically occur on burried bones or where bone surfaces have prolonged contact with soil (Paes Neto et al., 2018), usually forming a shallow and dendritic shape with damage to the bone's integrity (e.g., Fisher, 1995;Pokines and Baker, 2013;Keenan and Scannella, 2014). However, recent etching patterns on fossil bones display haloes of chemical activity that appear as grey, white, or yellow discolorations on the bone surface (e.g., Stewart, 1979) and, if the phenomena continue, shallow grooves are produced on the bone surface (Binford, 1981;Ehrenreich, 1995;Bader et al., 2009). ...

Paleobiological implications of a Triceratops bonebed from the Hell Creek Formation, Garfield County, northeastern Montana
  • Citing Article
  • January 2014

Geological Society of America Special Papers

... Bedding consists of trough cross-bedded, planar-bedded, and massive sandstones. It commonly yields macrovertebrate and microvertebrate fossils, often disarticulated and abraded, although partly articulated unabraded material is known [24]. In its uppermost~1-2 m the Apex Sand fines into a siltstone and is overlain by fine grained sediments and isolated channels of the upper Hell Creek Formation fines part 1. ...

A stratigraphic survey of Triceratops localities in the Hell Creek Formation, northeastern Montana (2006--2010)
  • Citing Article
  • January 2014

Geological Society of America Special Papers

... One important caveat for our sample is that stratigraphy in our sample is not well-constrained beyond the level of " formation " . Analysis of morphology in conjunction with precise stratigraphy within the Hell Creek Formation suggests that Triceratops horridus and Triceratops prorsus represent successive species, and potentially an anagenetic lineage [41,42]. Unfortunately we cannot argue anything about this issue without a good resolution of the stratigraphic data. ...

Transitional Triceratops: details of an ontogenetic sequence from the upper middle unit of the Hell Creek Formation, Montana
  • Citing Conference Paper
  • January 2012

... Some of the bones of ceratopsians and hadrosaurs, commonly recovered from the Upper Cretaceous deposits in the Western Interior Basin of North America, contain numerous elongate and puncture marks, which have been identified as bite marks made by tyrannosaurids (e.g., Fiorillo, 1991;Carpenter, 1998;Farlow and Holtz, 2002;Fowler and Sullivan, 2006;Happ, 2008;Hone and Rauhut, 2010;Fowler et al., 2012;Rivera-Sylva et al., 2012;DePalma et al., 2013;Dalman andLucas, 2018c, 2018d). In addition to the tooth-marked bones of herbivorous dinosaurs, are tooth-marked bones of tyrannosaurids, in particular of Albertosaurus, Daspletosaurus, Gorgosaurus, Nanotyrannus, and Tyrannosaurus (e.g., Tanke and Currie, 1998;Peterson et al., 2009;Bell, 2010;Bell and Currie, 2010;Hone and Tanke, 2015). ...

How to eat a Triceratops: large sample of toothmarks provides new insight into the feeding behavior of Tyrannosaurus
  • Citing Conference Paper
  • January 2012

Journal of Verterbrate Paleontology

... Intermediate Campanian chasmosaurine ceratopsids were predicted by Lehman (1998; Fig. S1), who showed successive morphospecies of the Canadian genus Chasmosaurus (Dinosaur Park Formation, Alberta; middle to upper Campanian) with a progressively shallowing embayment of the posterior margin of the parietosquamosal frill. This was contrasted with an opposite trend seen in Pentaceratops sternbergii (Fruitland Formation, New Mexico; upper Campanian) to Anchiceratops ornatus (Horseshoe Canyon Formation, Alberta; lower Maastrichtian), whereupon the midline embayment deepens and eventually closes (Lehman, 1993;Lehman, 1998;Fowler, 2010;Fowler, Scannella & Horner, 2011;Wick & Lehman, 2013). This hypothesis matched the stratigraphic occurrence of taxa known at the time, and is supported by new taxa described since 1998 (Vagaceratops (Chasmosaurus) irvinensis; Kosmoceratops richardsoni; Utahceratops gettyi; and Bravoceratops polyphemus; Holmes et al., 2001;Fowler, 2010;Fowler, Scannella & Horner, 2011;Wick & Lehman, 2013; although see Supporting Information 1). ...

Reassessing ceratopsid diversity using unified frames of reference