Fact-checked by Grok 2 weeks ago

Denversaurus

Denversaurus is a genus of herbivorous nodosaurid ankylosaurian dinosaur that lived during the late Maastrichtian stage of the Late Cretaceous period, approximately 66 million years ago, in what is now western North America.^[1] The type and only recognized species is D. schlessmani, known from a partial skeleton including skull fragments, vertebrae, limb bones, and over 100 osteoderms recovered from the Hell Creek Formation in the Badlands of South Dakota.^[1] This armored dinosaur measured about 6 meters (20 feet) in length and weighed around 3 tonnes, ranking among the largest members of the Nodosauridae family.^[1] Named in 1988 by paleontologist Robert T. Bakker, Denversaurus schlessmani honors the Schlessman family, supporters of the Denver Museum of Natural History where the specimen is housed, and reflects the genus's distinctive "Denver lizard" etymology.^[1] The fossils, originally collected in 1922 and initially misidentified as belonging to the related genus Edmontonia, reveal unique features such as a broad, smooth skull with eye sockets positioned at the extreme rear corners, prominent laterally oriented shoulder spines, and extensive bony armor plating covering the body.^[1]^[2] These adaptations likely served defensive purposes against predators, with the downward-facing snout suggesting a low-browsing feeding strategy on vegetation near the ground.^[1] Within Ankylosauria, Denversaurus belongs to the subfamily Nodosauridae, characterized by lacking a tail club and instead relying on widespread osteoderms for protection; it is often grouped with genera like Edmontonia and Panoplosaurus in the potential clade Panoplosauridae due to shared cranial traits such as broader, smoother skulls compared to other nodosaurs.^[2] As one of the last surviving nodosaurs before the Cretaceous–Paleogene extinction event, Denversaurus provides insights into the final diversity of armored ornithischians in Laramidia, the western landmass of North America during the Late Cretaceous.^[1]

Discovery and naming

Known specimens

The holotype specimen of Denversaurus, cataloged as DMNH 468, consists of a partial skull lacking the lower jaws and more than 100 associated osteoderms. It was collected in 1922 by Philip Reinheimer from the lower portion of the Hell Creek Formation in Corson County, South Dakota, and represents material discovered prior to its initial description as Edmontonia sp. by Carpenter and Breithaupt in 1986.^[3] The specimen was found in a crushed state and is housed in the collections of the Denver Museum of Nature and Science. In 1988, Bakker formally named this material as the holotype of the new species Denversaurus schlessmani. Referred specimens of Denversaurus are limited to isolated osteoderms and fragmentary postcranial elements from the Hell Creek and Lance Formations. Notable among these are osteoderms originally described by Marsh in 1891 as dermal armor associated with the ceratopsid Agathaumas sylvestris, which were later recognized as belonging to a nodosaurid and reassigned to Denversaurus. Additional isolated osteoderms have been reported from the Hell Creek Formation in Montana and the Lance Formation in Wyoming, providing evidence of the genus's distribution across the northern Western Interior of North America during the late Maastrichtian stage, approximately 68–66 million years ago.^[4] No complete or near-complete skeletons of Denversaurus are known, and the holotype lacks postcranial skeletal elements beyond the osteoderms. All specimens derive from Maastrichtian-aged deposits of the uppermost Cretaceous Period.^[4]

Etymology and taxonomic history

The genus name Denversaurus combines "Denver," honoring the city and the Denver Museum of Nature and Science that houses the holotype specimen, with the Greek sauros ("lizard"). The species epithet schlessmani commemorates philanthropist Lee E. Schlessman, whose family donated the fossil to the museum.^[1]^[5] In 1988, paleontologist Robert T. Bakker formally described and named Denversaurus schlessmani as a distinct genus of nodosaurid ankylosaur based on the holotype specimen DMNH 468 from the Hell Creek Formation of South Dakota; Bakker distinguished it from the related genus Edmontonia primarily by features of the skull and armor arrangement.^[1] Prior to this, elements of Denversaurus had a complex history of misidentification: in 1891, Othniel Charles Marsh described isolated osteoderms from the Lance Formation of Wyoming (including USNM 5793, a cervical half-ring) as dermal armor belonging to the ceratopsid Agathaumas sylvestris (then considered a junior synonym of Triceratops), though these were later recognized as nodosaurid in origin.^[6] From the 1920s through the 1980s, additional Denversaurus material from formations such as the Hell Creek and Lance was routinely referred to Edmontonia longiceps, Ankylosaurus, or simply as indeterminate nodosaurids; for instance, in 1986, Kenneth Carpenter and Brent Breithaupt described DMNH 468 (then undesignated as holotype) as Edmontonia sp., noting its crushed preservation but affirming its Maastrichtian age and nodosaurid affinities.^[7] Subsequent taxonomic revisions have affirmed Denversaurus as a valid, distinct nodosaurid. In 2015, Michael E. Burns's doctoral thesis analyzed intraspecific variation among Late Cretaceous North American nodosaurids and concluded that Denversaurus warrants separation from Edmontonia, supported by unique cranial sculpturing and osteoderm morphology resembling that of Panoplosaurus.^[8] A 2023 phylogenetic analysis by Thomas J. Raven and colleagues further validated this distinction, recovering Denversaurus as a separate taxon from Edmontonia longiceps within Nodosauridae and emphasizing its basal position relative to other panoplosaurins.^[9] Amid ongoing debates over synonymy—particularly whether Denversaurus represents a junior synonym of Edmontonia or Panoplosaurus—a 2024 reappraisal of global ankylosaur diversity by Sergio Soto-Acuña and coauthors reinforced its validity by incorporating it into broader phylogenetic matrices, highlighting diagnostic armor patterns that exclude conspecificity with other genera.^[10]

Description

Overall morphology

Denversaurus was a quadrupedal herbivorous dinosaur characterized by a low-slung, tank-like body plan, with an estimated length of 5.5–6 meters and a body mass of approximately 3 tonnes, based on scaling methods applied to the partial holotype skeleton including cranial material. This robust build featured a broad dorsal surface extensively armored with osteoderms, providing substantial protection, while lacking a tail club—a key distinction from ankylosaurine ankylosaurs. The overall form emphasized stability and defense, with the animal's posture adapted for grazing near ground level in its Late Cretaceous environment. The limbs of Denversaurus were pillar-like and heavily built to support its substantial weight, with robust forelimbs and hindlimbs contributing to a stable quadrupedal stance. Estimated shoulder height reached about 1.5 meters, underscoring the low-slung nature of its body and facilitating a posture suited to foraging in dense vegetation. This limb configuration, combined with the armored torso, formed a defensive profile that prioritized weight-bearing efficiency over speed. In overall morphology, Denversaurus exhibited a form similar to that of Panoplosaurus but appeared more robust, with enhanced body proportions for greater mass and stability. It shared the presence of prominent shoulder spines with Edmontonia but differed in their more horizontal orientation, reflecting variations in armor distribution among closely related nodosaurids.

Skull and osteoderms

The skull of Denversaurus exhibits distinctive proportions, with the holotype (DMNS 4680) measuring 496 mm in length and 346 mm in width across the posterior skull table. This structure features a notably wide posterior table, rearward-positioned orbits, and a broad snout that exceeds the width seen in Panoplosaurus. Cranial sculpturing is inflated, displaying visible sulci and doming over the orbits, contributing to its derived morphology among nodosaurids.^[11] Dentition in Denversaurus comprises leaf-shaped teeth with thick enamel adapted for grinding tough vegetation, typical of nodosaurids; these teeth feature labiolingually compressed crowns with a distally offset apex and prominent cingulum, facilitating a shearing and grinding mechanism. Osteoderms form the primary armor, with over 100 keeled, polygonal plates recovered from the holotype, ranging 10–20 cm in diameter and arranged in a non-segmented mosaic pattern along the dorsal and lateral surfaces of the back and flanks. These osteoderms lack fusion into a tail club, distinguishing Denversaurus from ankylosaurines, and include rounded cervical and pectoral forms similar to those in Panoplosaurus. The combination of a broad skull with rearward orbits and the absence of tail club fusion represents key autapomorphies for Denversaurus, supporting its validity as a distinct nodosaurid taxon separate from Edmontonia.

Classification

Taxonomic revisions

In 1988, Robert T. Bakker erected Denversaurus schlessmani as a new genus and species within the Nodosauridae, distinguishing it from Edmontonia primarily based on a wider skull and differences in osteoderm morphology. During the 1990s and 2000s, several researchers, including Walter P. Coombs Jr. and Kenneth Carpenter, proposed that Denversaurus represented a junior synonym of Edmontonia longiceps, arguing that the diagnostic features overlapped significantly with known Edmontonia material. This view was later challenged by Carpenter in 2001, who rejected the synonymy on the grounds of distinct geographic distributions (Lance and Hell Creek formations in Wyoming and South Dakota for Denversaurus versus Edmonton Formation in Alberta for Edmontonia) and stratigraphic separation in the Late Maastrichtian. The modern consensus affirms the validity of Denversaurus as a distinct nodosaurid genus, as detailed in Michael E. Burns's 2015 doctoral thesis, which placed it within the subtribe Panoplosaurini alongside Panoplosaurus and Edmontonia, emphasizing intraspecific variation in armor and cranial features that support separation from Edmontonia. Recent studies from 2023 to 2024 have further resolved Denversaurus's taxonomic status amid broader revisions to Edmontonia. Raven and colleagues (2023) upheld Denversaurus as valid and distinct from Edmontonia longiceps in their comprehensive ankylosaur phylogeny, based on reanalysis of cranial and postcranial traits.^[12] Similarly, Soto-Acuña et al. (2024), in reappraising southern high-latitude ankylosaurs, supported Denversaurus's independence while dismissing Chassternbergia (another taxon proposed by Bakker in 1988 for Edmontonia rugosidens material) as a nomen dubium due to insufficient distinguishing features.^[10]

Phylogenetic position

Denversaurus is classified within the family Nodosauridae, a clade of armored ornithischian dinosaurs belonging to the suborder Ankylosauria and the larger group Thyreophora, and is specifically assigned to the subtribe Panoplosaurini based on shared derived traits with other Late Cretaceous nodosaurids.^[13] This placement reflects its position among non-ankylosaurine ankylosaurs characterized by extensive body armor but lacking the tail club typical of ankylosaurids. Key synapomorphies supporting its nodosaurid affinities include a broad, low skull with a wide posterior region and keeled osteoderms distributed across the body, without the development of a tail club, features particularly shared with the closely related Panoplosaurus.^[13] These traits distinguish Denversaurus from more basal thyreophorans and align it with derived nodosaurids that emphasized passive defense through dermal armor rather than active weaponry. Cladistic analyses have consistently supported its nodosaurid position, though relationships within the family vary by dataset. In a comprehensive matrix incorporating intraspecific variation among Late Cretaceous nodosaurids, Burns (2015) recovered Denversaurus as the sister taxon to Panoplosaurus, forming a tight panoplosaurin clade defined by enhanced cranial robustness and armor patterning.^[13] Conversely, the broader phylogenetic analysis by Raven et al. (2023), which incorporated global thyreophoran taxa and refined character scorings, positioned Denversaurus as basal to the Edmontonia + Struthiosaurus clade, highlighting its role as a transitional form within Nodosauridae. As a taxon from the late Maastrichtian Hell Creek Formation, Denversaurus exemplifies the persistence and final diversification of nodosaurids in western North America toward the end of the Cretaceous, surviving as one of the last representatives of Thyreophora before the K-Pg mass extinction abruptly terminated the group.^[13]

Paleobiology

Locomotion and sensory adaptations

Denversaurus exhibited a quadrupedal gait characterized by a stable, low center of gravity, inferred from its broad pelvic structure and robust limb bones that supported a heavily armored body.^[14] The forelimbs featured high elbow extension moment arms due to elongated olecranon processes, enabling effective weight-bearing and a wide-gauge stance typical of nodosaurids.^[14] This configuration, combined with columnar limb posture, indicates deliberate, energy-efficient movement suited to foraging in forested environments, with no skeletal evidence for bipedal capabilities.^[15] Robust hindlimbs and overall body proportions suggest slow locomotion, with maximum speeds estimated at 5–10 km/h based on comparative analyses of ankylosaur trackways and limb scaling.^[16] Such velocities align with the limited agility imposed by extensive armor, prioritizing stability over rapid evasion; trackway evidence from related nodosaurids confirms a walking gait without transitions to faster gaits.^[17] Sensory adaptations in Denversaurus are inferred from cranial features shared with other nodosaurids, including moderately enlarged olfactory bulbs relative to brain size in taxa like Pawpawsaurus (olfactory ratio ≈46), comparable to that in Panoplosaurus, indicating a well-developed sense of smell for detecting vegetation or foraging opportunities.^[18] This supports chemical sensing as a primary foraging mechanism in low-light or dense habitats.^[18] Eye orbits positioned laterally on the skull provided a broad field of view, exceeding 180 degrees monocularly, to monitor for predators approaching from the rear or sides.^[19] The skull's compact, heavily ossified structure, with a short lagena in the inner ear, suggests limited auditory acuity tuned to low frequencies (around 2–4 kHz), potentially for detecting distant vibrations rather than high-pitched sounds.^[20] This aligns with observations in related nodosaurids like Struthiosaurus, where reduced hearing capacity complemented reliance on visual and olfactory cues for predator detection.^[21] Osteoderms in Denversaurus formed a continuous dermal armor that provided passive protection against predation, distributing impact forces across the body and enhancing overall stability during movement.^[21] The weight of these bony plates, concentrated along the back and flanks, lowered the center of gravity further but likely reduced lateral mobility, as evidenced by restricted neck flexibility in nodosaurids bearing similar integumentary structures.^[21] This trade-off underscores armor's role in defensive posture over agile evasion.^[18]

Diet and feeding mechanics

Denversaurus was an herbivorous low-browser, consuming low-lying vegetation in floodplain environments, such as ferns, horsetails, and possibly cycads or Bennettitales, that were present in the Hell Creek Formation.^[22] No gastroliths have been discovered in association with known Denversaurus specimens, distinguishing it from some other nodosaurids like Borealopelta markmitchelli that possessed stomach stones for grinding plant material.^[23] The feeding apparatus of Denversaurus featured a battery of leaf-shaped, blade-like teeth suited for shearing fibrous vegetation, as evidenced by the morphology of nodosaurid dentition with prominent basal cingula and denticles.^[24] Its relatively wide skull likely accommodated enlarged jaw adductor muscles, enabling a powerful bite to process tough plant matter, though weaker overall than in ceratopsids or hadrosaurids.^[25] A rhamphotheca, or keratinous beak, may have facilitated cropping low-lying foliage prior to mastication, consistent with the predentary structure in nodosaurids.^[23] As a megaherbivore, Denversaurus likely relied on hindgut fermentation for digestion, with symbiotic gut bacteria breaking down cellulose in ingested vegetation, a strategy inferred from its skull ecomorphology and the prevalence of resistant plant tissues in its diet.^[25] Its extensive armor of osteoderms would have provided protection against predators during vulnerable feeding periods in open floodplains.^[24]

Paleoecology

Geological context

Fossils of Denversaurus are primarily recovered from the Hell Creek Formation in South Dakota and Montana, and the Lance Formation in Wyoming, both of which date to the late Maastrichtian stage of the Late Cretaceous, spanning approximately 68 to 66 million years ago. These formations consist of nonmarine sediments deposited during the final retreat of the Western Interior Seaway, marking the transition from marine to fully terrestrial conditions in the region. The Hell Creek Formation is characterized by interbedded sandstones, mudstones, and carbonaceous shales, while the Lance Formation features more fine-grained sandstones and siltstones, reflecting similar depositional regimes but with local variations in sediment supply.^[26]^[27] The taphonomy of Denversaurus specimens indicates burial in fluvial settings, with many preserved in channel-fill sandstones or overbank mudstones that suggest rapid entombment by riverine processes following death on nearby floodplains. This preservation style is common in both formations, where disarticulated skeletons and isolated osteoderms reflect post-mortem transport and exposure in dynamic, low-energy environments prone to seasonal inundation. The warm, humid subtropical paleoclimate, punctuated by periodic flooding, likely contributed to such taphonomic patterns by limiting widespread decay while facilitating localized burial events.^[28]^[27] The paleoenvironment encompassed coastal plains with seasonal wetlands, supporting a diverse flora dominated by angiosperms alongside ferns, conifers, and ginkgos, which formed lowland forests and swampy habitats. This ecosystem was situated near the emerging Laramide Orogeny, where tectonic uplift of the ancestral Rocky Mountains to the west supplied coarse clastics to the basins and influenced regional drainage patterns. Denversaurus distribution is confined to western North America, extending from Montana southward to potentially Texas via debated referrals to the Aguja Formation, with no records from Asia or Europe.^[29]^[27]

Contemporaneous fauna and interactions

Denversaurus inhabited the Maastrichtian Hell Creek and Lance Formations alongside a rich vertebrate assemblage that included the dominant theropod predator Tyrannosaurus rex, large ceratopsians such as Triceratops horridus, hadrosaurs like Edmontosaurus annectens, basal ornithopods including Thescelosaurus neglectus, and the ankylosaurid Ankylosaurus magniventris.^[30] Other co-occurring taxa encompassed crocodylomorphs, turtles, and a variety of smaller vertebrates, reflecting a complex floodplain and riverine ecosystem.^[30] Fossils of Denversaurus itself are rare, often represented by isolated teeth and osteoderms that show signs of transport, comprising less than 2% of dinosaurian material in multitaxic bonebeds like the Tooth Draw locality.^[30] In this community, Denversaurus served as an armored low-level grazer among a diverse array of herbivores, potentially engaging in niche partitioning to minimize competition—for instance, by targeting vegetation inaccessible to taller browsers such as hadrosaurs and ceratopsians. Direct evidence of interactions remains limited; while Tyrannosaurus and other theropods preyed on large herbivores like Edmontosaurus and Triceratops—as evidenced by bite marks on bones—no such predation scars have been documented on Denversaurus specimens, likely due to its extensive armor providing effective defense.^[30] Denversaurus contributed to the waning nodosaurid diversity in the latest Cretaceous, with ankylosaurids like Ankylosaurus more prevalent and no indications of competitive overlap between these armored clades.^[7] This entire fauna, including Denversaurus, succumbed to the K-Pg mass extinction event.^[7]

References

[1]
Discovery of New Dinosaur Species Reported - The New York Times
Sep 20, 1988 · They carry their heads with the snouts facing directly downward. The full scientific name for the species is Denversaurus schlessmanni, honoring ...
[2]
GEOL 104 Thyreophora
Aug 29, 2025 · Edmontonia, Denversaurus, and Panoplosaurus are the best known examples. These have broader, smoother skulls than most "nodosaurs", and ...
[3]
latest cretaceous occurrence of nodosaurid ankylosaurs - jstor
EDMONTONIA sp. Referred Material-DMNH 468, complete skull. (lacking lower jaws) and associated plates; lower Hell.
[4]
[PDF] VERTEBRATE PALEONTOLOGY OF MONTANA - MBMG
Mary. River Formation has also yielded a few mammal taxa. (see Hunter and others, 2010). l. Late Cretaceous (Maastrichtian: 66.8–66 Ma). Hell Creek Formation.
[5]
Denversaurus - Paleofile.com
Holotype: DMNH 468 Locality: Near southwest corner of sec. 25, T20N, R21E, Carson County, South Dakota. Horizon: Lower Hell Creek Formation.
[6]
(PDF) Armor for Agathaumas: The fossils behind Charles Knight's ...
May 1, 2023 · The fossils described by O.C. Marsh as Triceratops dermal armor and his skeletal reconstruction of Triceratops, from Marsh (1891a) and (1891b) ...
[7]
[PDF] Latest Cretaceous Occurrence of Nodosaurid Ankylosaurs ...
Author(s): Kenneth Carpenter and Brent Breithaupt. Source: Journal of Vertebrate Paleontology, Vol. 6, No. 3 (Sep. 2, 1986), pp. 251-257. Published by: The ...
[8]
Intraspecific Variation in the Armoured Dinosaurs (Dinosauria - ERA
In addition to Edmontonia spp. and Panoplosaurus mirus, Denversaurus schlessmani Bakker, 1988, is likely valid. It also allows for most currently-known ...
[9]
Raven et al. 2023 on ankylosaur phylogeny missed the shortest ...
May 21, 2023 · Raven et al. accept Denversaurus as a distinct genus from Edmontonia longiceps (Carpenter [1990] listed Denversaurus schlessmani as Edmontonia ...
[10]
(PDF) A new look at the first dinosaur discovered in Antarctica
Apr 29, 2024 · The first dinosaur discovered in the Antarctic continent was the ankylosaur Antarctopelta oliveroi in the 1980s.
[11]
[PDF] Meeting Program & Abstracts - Society of Vertebrate Paleontology
Together, we welcome all of you to Dallas for what is sure to be an enlightening assemblage of the world's most engaged vertebrate paleontologists at the 75th.Missing: thesis | Show results with:thesis
[12]
Dinosaur Tooth Morphology & Wear: Megaherbivores, Alberta
Ankylosaur teeth (Figure 1) bear straight roots and labiolingually compressed, phylliform (leaf-shaped) crowns with a distally-offset apex and apical ...
[13]
Phylogeny of the ankylosaurian dinosaurs (Ornithischia: Thyreophora)
Aug 6, 2025 · It is worth emphasising that a new phylogeny of the Ankylosauria was proposed recently by Raven et al. (2023), who found Nodosauridae to be ...
[14]
[PDF] The phylogenetic relationships and evolutionary history of the ...
This is an Accepted Manuscript of an article published by Taylor & Francis in Journal of Systematic. Palaeontology on the 18 May 2023, the final published ...
[15]
https://bioone.org/journals/acta-palaeontologica-polonica/volume-59/issue-1/app.2012.0065/Osteological-Correlates-for-Quadrupedality-in-Ornithischian-Dinosaurs/10.4202/app.2012.0065.full
[16]
Convergent evolution of quadrupedality in ornithischian dinosaurs ...
Feb 1, 2023 · The ankylosaur Peloroplites is strongly separated from other quadrupedal taxa on PC1 owing to higher elbow medial rotation moment arms. The ...
[17]
Osteological Correlates for Quadrupedality in Ornithischian Dinosaurs
Sep 21, 2012 · ... ankylosaur track occurrences. In : K. Carpenter (ed.), The Armored Dinosaurs , 413–454. Indiana University Press, Bloomington. Google ...
[18]
Speeds and gaits of dinosaurs - ScienceDirect.com
Most quadrupedal dinosaurs seem to have been restricted to a walking gait. Stegosaurs and ankylosaurs may have had maximum speeds as low as 6–8 km/h. Sauropods ...Missing: nodosaurid | Show results with:nodosaurid
[19]
A new purported ankylosaur trackway in the Lower Cretaceous ...
This paper focuses on a new quadrupedal trackway produced by an ankylosaur, discovered at a site near Bisceglie (Bari, southern Italy) (Fig. 1). Footprints ...
[20]
Endocranial Morphology of the Primitive Nodosaurid Dinosaur ... - NIH
Mar 23, 2016 · Olfaction and vomeronasal chemoreception constitute the chemical senses associated with the nasal region, which play an important role in ...Missing: eyes | Show results with:eyes
[21]
Defensive Adaptations and Paleoecology of Ankylosaurus: Insights ...
Jul 30, 2024 · Short but robust limbs supported its massive frame, and its eyes, positioned on the sides of its head, offered a broad field of view to detect ...
[22]
Ankylosaur was sluggish and deaf - Phys.org
Jan 11, 2022 · For example, the inner ears can hint to auditory capacities and skull orientation.Missing: adaptations | Show results with:adaptations
[23]
Neuroanatomy of the nodosaurid Struthiosaurus austriacus ... - Nature
Jan 7, 2022 · Nodosaurids bear long spikes around their neck and shoulder (which likely rather limited their neck mobility) in addition to osteoderms ...
[24]
[PDF] THE LARAMIE FLORA OF THE DENVER ·BASIN
... Laramie is not now known tp extend beyond Colorado. Springs on the south. This paper deals with the plants known from the Laramie of the Denver Basin, which ...
[25]
Dietary palaeoecology of an Early Cretaceous armoured dinosaur ...
Jun 3, 2020 · Highly fragmented woody material and tracheids (4%) are probably derived from twigs processed by the nodosaurid's gastric mill or by its teeth ...
[26]
Skull Ecomorphology of Megaherbivorous Dinosaurs from the ...
Because jaw adductor muscle mass–and by extension, bite force–generally scales positively with skull size (e.g., [87]–[91]), it is likely that ankylosaurs ...
[27]
The Hell Creek Formation and its contribution to the Cretaceous ...
The Hell Creek Formation is the global standard for understanding K–Pg extinction. We present a summary of the current paleontological and sedimentological ...
[28]
[PDF] The Lance Formation Petrography and Stratigraphy, Powder River ...
Deposition of the Upper. Cretaceous Lance Formation ended at the time of the K-T boundary event. The climate very briefly became cooler, but soon it was warmer ...
[29]
Size-driven preservational and macroecological biases in the latest ...
Nov 2, 2021 · ... Denversaurus was based on Edmontonia) or scaled relative to comparable elements (e.g., Sphaerotholus buccholtzae was based on dome length ...
[30]
the late cretaceous (maastrichtian) flora of the hell creek
The megaflora of the Hell Creek Formation is dominated by flowering plants ... The remaining 10 percent of the flora is composed of conifers, cycadophytes, ferns, ...Missing: paleoflora conifers
[31]
[PDF] Hell Creek Formation (Maastrictian), Butte County, South Dakota.
Bakker, R.T. (1988). "Review of the Late Cretaceous Nodosauroid Dinosauria: Denversaurus schlessmani, a new armor-plated dinosaur from the Latest Cretaceous of ...