View source for Mymoorapelta

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{{Short description|Extinct genus of ornithischian dinosaur}}
{{Automatic taxobox
| fossil_range = [[Late Jurassic]], {{Fossil range|155|150}}
| image = Mymoorapelta maysi.jpg
| image_caption = Reconstructed skeleton in [[Wyoming Dinosaur Center]]
| display_parents = 2
| taxon = Mymoorapelta
| authority = Kirkland et Carpenter, 1994
| type_species = {{extinct}}'''''Mymoorapelta maysi'''''
| type_species_authority = [[James Kirkland (paleontologist)|Kirkland]] and [[Kenneth Carpenter|Carpenter]], [[1994 in paleontology|1994]]
}}

'''''Mymoorapelta''''' (Meaning "Shield from the Mygatt-Moore Quarry" after a combination of the names of the discoverers of the Mygatt-Moore Quarry that fossils were originally collected from, and the Greek word πέλτα, meaning "shield") is a [[Nodosauridae|nodosaurid]] [[ankylosaur]] from the Late [[Jurassic]] ([[Kimmeridgian]]-[[Tithonian]], around 155 to 150 million years ago) [[Morrison Formation]] (Brushy Basin Member) of western [[Colorado]] and central [[Utah]], [[United States|USA]]. The animal is known from a single species, '''''Mymoorapelta maysi''''', and few specimens are known. The most complete specimen is the [[holotype]] individual from the Mygatt-Moore Quarry, which includes {{Dinogloss|osteoderms}}, a partial {{Dinogloss|skull}}, {{Dinogloss|vertebrae}}, and other bones. It was initially described by [[James Kirkland (paleontologist)|James Kirkland]] and [[Kenneth Carpenter]] in 1994. Along with ''[[Gargoyleosaurus]]'', it is one of the earliest known nodosaurids.

''Mymoorapelta'' is one of the smaller known nodosaurids, with the estimated length of the largest specimen only reaching {{Convert|3|m|ft}}. It had a narrow snout and almost triangular skull in dorsal view, with two large horns pointing backwards from the brow and two horns below these that pointed backwards and down on the {{Dinogloss|jugal}}. Five different armor types have been observed in ''Mymoorapelta'', ranging from elongated, sharp spines on the side of the body to a giant {{Dinogloss|sacral}} shield composed of tiny osteoderms, called ''ossicles'', that covered the top of the pelvis. In contrast to the club-tailed ankylosaurids, the tail bore spikes that ''Mymoorapelta'' likely used for defense. 

''Mymoorapelta'' was a low browser in the Morrison ecosystem, feeding on [[cycad]]s and [[conifer]]s, in contrast to the high-browsing ''[[Apatosaurus]]'' known from the same quarries. Other dinosaur groups were also present, including the large [[Theropoda|theropods]] ''[[Allosaurus]]'' and ''[[Ceratosaurus]]'' and possibly the [[ornithischia]]n ''[[Nanosaurus]]''. Both of the theropods have also been found in association with the animal, and we have evidence that the former preyed on ''Mymoorapelta.''  

== Discovery and naming ==
[[File:Mygatt-Moore Quarry.png|left|thumb|Map of the location of Mygatt-Moore Quarry, where ''Mymoorapelta'' fossils were first discovered.]]
The Mygatt-Moore Quarry was first discovered in March of 1981 by hikers Vanetta Moore and Pete and Marilyn Mygatt in [[Mesa County, Colorado|Mesa County]], west-central [[Colorado]]. The quarry's strata come from the Brushy Basin Member of the [[Morrison Formation]], which dates to the [[Late Jurassic|Upper Jurassic]].<ref name=":0">Kirkland, J. I., & Carpenter, K. (1994). [https://www.researchgate.net/profile/James-Kirkland-5/publication/286694749_North_America's_first_pre-Cretaceous_ankylosaur_Dinosauria_from_the_Upper_Jurassic_Morrison_Formation_of_western_Colorado/links/569549ca08ae820ff074b132/North-Americas-first-pre-Cretaceous-ankylosaur-Dinosauria-from-the-Upper-Jurassic-Morrison-Formation-of-western-Colorado.pdf North America's first pre-cretaceous ankylosaur (Dinosauria) from the Upper Jurassic Morrison Formation of western Colorado.] ''Brigham Young University Geology Studies'', ''40'', 25-42.</ref><ref>{{Cite web |last=Sullivan |first=Sharon |title=Huge dinosaur bone unearthed at quarry |url=https://www.aspentimes.com/news/huge-dinosaur-bone-unearthed-at-quarry/ |access-date=2022-08-18 |website=www.aspentimes.com |date=24 September 2007 |language=en-US}}</ref> Fossils of ''Mymoorapelta'' were first discovered in the quarry in 1990, and since then over 160 elements have been found scattered over {{Convert|25|m|yd}} of the {{Convert|150|m2|sqft|adj=on}} quarry.<ref name=":1">Foster, J., Hunt-Foster, R., Gorman, M., Trujillo, K., Suarez, C., McHugh, J., ... & Schoenstein, H. (2018). Paleontology, taphonomy, and sedimentology of the Mygatt-Moore Quarry, a large dinosaur bonebed in the Morrison formation, western Colorado—implications for Upper Jurassic dinosaur preservation modes. ''Geology of the Intermountain West'', ''5'', 23-93.</ref><ref name=":0" /> A few of these elements are part of a single adult individual and were described by American paleontologists [[James Kirkland (paleontologist)|James Kirkland]] and [[Kenneth Carpenter]] in 1994. This specimen (MWC 1815) would be designated the holotype of the species and includes a left {{Dinogloss|ilium}} (hip bone) with preserved bitemarks.<ref name=":0" /> Kirkland and Carpenter named the species ''Mymoorapelta maysi'', the generic name deriving from the names of Marilyn Mygatt and the Moores, who had discovered the quarry, and the Greek root ''pelta'', meaning "shield", due to the preserved armor.<ref name=":0" /> The specific name is after Chris Mays, the president of the [[Dinamation|Dinamation International Corporation]] and Society, who funded the initial excavation of the Mygatt-Moore Quarry.<ref name=":0" /><ref name=":1" /> ''Mymoorapelta'' was the first Jurassic [[Ankylosauria|ankylosaur]] named from North America, with the closely related ''[[Gargoyleosaurus]]'' being named four years later in 1998.<ref name=":5">Carpenter, K., Miles, C. and Cloward, K. (1998). "Skull of a Jurassic ankylosaur (Dinosauria)." ''Nature'' 393: 782–783.</ref><ref name=":0" /> Other parts of the type specimen that were excavated from the quarry include several {{Dinogloss|dorsal}} (back) and {{Dinogloss|caudal}} (tail) vertebrae, {{Dinogloss|ribs}}, isolated limb bones, and many osteoderms, including the signature triangular cervical spine of basal ankylosaurs.<ref name=":2">Hunt, A. P., & Scheetz, R. D. (1998). [https://www.researchgate.net/profile/James-Kirkland-5/publication/286681879_Ankylosaur_Dinosauria_specimens_from_the_Upper_Jurassic_Morrison_Formation/links/5894979892851c54574b9f38/Ankylosaur-Dinosauria-specimens-from-the-Upper-Jurassic-Morrison-Formation.pdf Ankylosaur (Dinosauria) specimens from the Upper Jurassic Morrison Formation] ''The Upper Jurassic Morrison Formation: An Interdisciplinary Study: Denver Museum of Natural History, Denver, USA: May 26-28, 1994'', ''22'', 145-177.</ref><ref name=":1" /><ref name=":0" /> Some osteoderms which have been found in the quarry and referred to ''Mymoorapelta'' come from a higher stratigraphic layer, suggesting that a second individual is preserved.<ref name=":1" />[[File:Holotype left ilium of Mymoorapelta maysii (MWC 1815).png|thumb|Left [[ilium (bone)|ilium]] of the [[holotype]] (MWC 1815)]]

In 1998, a partial skeleton referred to ''Mymoorapelta'' was described by Kirkland ''et al'' from Cactus Park, Colorado, though at the time the fossil was still undergoing [[fossil preparation]].<ref name=":2" /> The skeleton preserved [[Fossil#Casts and molds|natural molds]] and body fossils of the sacrum, caudal vertebrae, {{Dinogloss|chevrons}} (bones attached to the underside of the tail vertebrae in [[dinosaur]]s), {{Dinogloss|pes}} (foot), and many pieces of the dermal armor, including parts of the sacral shield, which was a type of armor that would cover the top of the pelvis. Though skull material was mentioned to be preserved it is still in preparation and undescribed.<ref name=":7">Foster, J. (2007). Jurassic West: The Dinosaurs of the Morrison Formation and Their World. Indiana University Press. pp. 327–329. {{ISBN|978-0-253-34870-8}}</ref><ref name=":0" /> Some of the material, namely from the pes and sacral shield, was preserved in articulation making it the only known articulated specimen of the taxon.<ref name=":2" /> In a 2010 abstract, Kirkland and colleagues mentioned the discovery of many more elements of ''Mymoorapelta'' at Mygatt-Moore Quarry including a nearly complete skull and every postcranial element except the pubis and femur.<ref name=":2" /><ref name=":3">Kirkland, J. I., Hunt-Foster, R. K., Foster, J. R., & Loewen, M. (2010). Newly recovered skeletal elements of the Late Jurassic dinosaur Mymoorapelta from its type locality in the Morrison Formation permits re-evaluation of ankylosaur phylogeny. ''Journal of Vertebrate Paleontology'', ''30'', 116A.</ref><ref name=":1" /> All of the fossils found at Mygatt-Moore Quarry and Cactus Park are currently deposited in the [[Dinosaur Journey Museum|Dinosaur Journey Museum of Western Colorado]] in [[Fruita, Colorado|Fruita]].<ref name=":1" /><ref name=":0" /> 2015 saw the presentation of an abstract by Katie Tremaine ''et al'' that mentions a new ''Mymoorapelta'' specimen unearthed at [[Hanksville-Burpee Quarry]] near [[Hanksville, Utah]].<ref name=":8">Tremaine, K., D’Emic, M., Williams, S., Hunt-Foster, R.K., Foster, J., and Mathews, J., (2015), Paleoecological implications of a new specimen of the ankylosaur Mymoorapelta maysi from the Hanksville-Burpee Quarry, latest Jurassic (Tithonian) Morrison Formation (Brushy Basin Member) [abs.]: Journal of Vertebrate Paleontology Program and Abstracts, p. 226.</ref> The specimen includes one individual preserving: 24 osteoderms, three ribs, one vertebra, and a femur, though more material has yet to be excavated. The discovery of a single, dorsal osteoderm that had been collected from the Peterson Quarry outside of [[Albuquerque, New Mexico|Albuquerque]], [[New Mexico]] was described in 2016.<ref name=":9">Burns, M. E., & Lucas, S. G. (2016). [https://books.google.com/books?id=au2oDQAAQBAJ&dq=mymoorapelta&pg=PA9 Biostratigraphy of Ankylosaur (Dinosauria: Ornithischia) Osteoderms from New Mexico.] ''Fossil Record 4: Bulletin 67'', ''67'', 9.</ref> The osteoderm is [[Morphology (biology)|morphologically]] (based on external anatomy) similar to ''Mymoorapelta'', however it is [[Stratigraphy|stratigraphically]] (based on rock layers) closer to ''Gargoyleosaurus.''<ref name=":9" />

== Description ==
[[File:Mymoorapelta size.png|thumb|Diagram illustrating the size of  ''Mymoorapelta''.]]
''Mymoorapelta'' is one of the smallest ankylosaurs known and the smallest known [[Quadrupedalism|quadrupedal]] dinosaur from the Morrison Formation. However, few individuals have been found and only a portion of the known material has been described in detail. The Cactus Park specimen is the largest described individual, with its length being estimated at around {{Convert|3|m|ft}} long in 1998.<ref name=":2" /> Body mass estimates based on the type specimen give a weight of around {{Convert|300|-|562|kg|lb}}.<ref>{{Cite journal |last1=Farlow |first1=James O. |last2=Coroian |first2=Dan |last3=Currie |first3=Philip J. |last4=Foster |first4=John R. |last5=Mallon |first5=Jordan C. |last6=Therrien |first6=François |date=2022-07-11 |title="Dragons" on the landscape: Modeling the abundance of large carnivorous dinosaurs of the Upper Jurassic Morrison Formation (USA) and the Upper Cretaceous Dinosaur Park Formation (Canada) |journal=The Anatomical Record |volume=306 |issue=7 |language=en |pages=1669–1696 |doi=10.1002/ar.25024 |pmid=35815600 |s2cid=250422526 |issn=1932-8486|doi-access=free }}</ref><ref name=":7" /><ref>{{Cite book|last=Paul|first=Gregory S.|url=http://worldcat.org/oclc/985402380|title=The Princeton Field Guide to Dinosaurs|year=2016|publisher=Princeton University Press|isbn=978-1-78684-190-2|oclc=985402380|pages=252}}</ref>

=== Skull and dentition ===
[[File:Gargoyleosaurus skull.jpg|left|thumb|Skull of the similar ''[[Gargoyleosaurus]],'' also from the [[Morrison Formation]].]]
The {{Dinogloss|skull}} specifically has not been described in detail, but the preserved [[Morphology (biology)|morphology]] (external anatomy) is very similar to that of ''Gargoyleosaurus'', which also hails from the Morrison Formation.<ref name=":3" /> It had a narrow snout and almost triangular shaped skull in [[Anatomical terms of location|dorsal (top) view]], with two large horns pointing backward from the back of the brow, and two horns below these that pointed backward and down from the {{Dinogloss|jugal}} (cheek bone). A preserved jugal described in 1998 has a wedge-shaped, armored morphology and projects ventrolaterally (down and outwards) like in ankylosaurids.<ref name=":2" /> The {{Dinogloss|premaxillae}} (bones at the tip of the snout) probably possessed a narrow, toothed, and trapezoidal muzzle like in ''Gargoyleosaurus''.<ref name=":15">{{Cite journal |last1=Ősi |first1=Attila |last2=Prondvai |first2=Edina |last3=Mallon |first3=Jordan |last4=Bodor |first4=Emese Réka |date=2016-07-20 |title=Diversity and convergences in the evolution of feeding adaptations in ankylosaurs (Dinosauria: Ornithischia) |url=http://www.tandfonline.com/action/showCitFormats?doi=10.1080/08912963.2016.1208194 |journal=Historical Biology |language=en |volume=29 |issue=4 |pages=539–570 |doi=10.1080/08912963.2016.1208194 |s2cid=55372674 |issn=0891-2963}}</ref> In the back of the skull, the {{Dinogloss|quadrate}}-articular area (place of contact between the skull and lower jaw) faces slightly medially (towards the midline of the body), and is subtly lengthened anteroposteriorly (front to back). The distal surface of the quadrate, especially on the medial condyle, is robust and elongated anteroposteriorly. In all ankylosaurs, the jaw joint (joint connecting the skull to the jaw bone) is placed ventrally to the [[Occlusion (dentistry)|occlusal plane]] (contact surface between teeth). The {{Dinogloss|coronoid process}} (bony projection on the lower jaw) is very well developed in nodosaurids, and the jaw joint is well depressed in turn, which corresponds to a higher relative [[Bite force quotient|bite force]]. 

Most ankylosaurs have [[heterodont]] dentition (variation in tooth morphology), but not in ''Gargoyleosaurus,'' which shows only subtle morphological differences in the premaxillary, maxillary, and dentary teeth. Ankylosaur teeth are compressed labiolingually and are phylliform (leaf-shaped), with an apical cusp and secondary cusps along the mesial and distal edges. Nodosaurid teeth are blade-like, larger, and usually more complex than the basic cusps of ankylosaurids, having a larger crown, a rough enamel surface, confluent fluting with grooves of the marginal cusps, and a crenelated {{Dinogloss|cingulum}} (shelf-like bulge surrounding the base of a [[Glossary of dinosaur anatomy#tooth crown|tooth crown]]). The wear facets on Ankylosaur teeth vary greatly, but in nodosaurids they are usually more extensive and steeply inclined than in ankylosaurids, demonstrating underlying patterns of shape-constrained function. In early nodosaurids like ''Gargoyleosaurus'' and ''[[Gastonia (dinosaur)|Gastonia]]'', the {{Dinogloss|pterygoid}} (a [[Glossary of dinosaur anatomy#dermal|dermal]], [[Glossary of dinosaur anatomy#paired|paired]] bone of the [[Glossary of dinosaur anatomy#palate|palate]]) is not yet well developed anteroposteriorly and mediolaterally, but in later species they are much wider, with more robust lateral wings, and they are more expanded anteroposteriorly than in basal forms, reaching the level of the distal quadrate condyles. This suggests more developed pterygoid muscles in later nodosaurids than in ankylosaurids, reflecting a more efficient jaw adductor system in nodosaurids. The mandibular adductor chamber and the coronoid process are generally taller in nodosaurids than in ankylosaurs, suggesting differences in the size and attachment of muscles.<ref name=":15" />

=== Postcranial skeleton ===
[[File:Mymoorapelta dorsal vertebra fruita.jpg|thumb|right|A {{Dinogloss|dorsal vertebra}} in anterior view at the [[Dinosaur Journey Museum|Dinosaur Journey Museum, Fruita]].]]A large part of the postcranial (behind the skull) skeleton of ''Mymoorapelta'' is known. For instance, many {{Dinogloss|cervical vertebrae}} (vertebrae of the neck) are known, though many of them have not been fully researched or excavated. In the cervicals, the faces (ends) of the {{Dinogloss|centra}} are wider than they are tall and display a heart-shaped morphology. The centra overall are anteroposteriorly short with lengths that are around equal to their width. The {{Dinogloss|neural spines}} are short and thick,and possess round, circular neural canals. A deep, tear-shaped fossa (small opening in bone) is present between the {{Dinogloss|postzygapophyses}} (backwards projections of the vertebral arch).<ref name=":2" /> Several dorsal (back, sometimes referred to as thoracic) vertebrae are known from ''Mymoorapelta,'' and they are unique when compared to those of Cretaceous nodosaurids. The centra are cylindrical, longer posteriorly, and less laterally compressed than those of other, later nodosaurids like ''[[Sauropelta]]'' and ''[[Dracopelta]]''. The anterior dorsals are unique in that they bear a triangular pit between the {{Dinogloss|prezygapophyses}} (forwards projections of the vertebral arch), which are also much more elongate at the anterior end of the vertebra. Meanwhile, the postzygapophyses are truncated at the posterior end, with the left and right postzygapophyses divided by a large groove. The mid dorsal vertebrae differ in that they are rounded ventrally and have a weak keel at the bottom. The transverse processes of the dorsal vertebrae do not ascend steeply and are instead gradually heightened, similar to the condition in basal ankylosaurs, and differing from that of nodosaurids. ''Mymoorapelta'' has 13 ribs, all of which have triangular cross-sections and a weak T-shape, in contrast to other ankylosaurs. ''Mymoorapelta'' is also one of the few ankylosaurs with 4 sacral ribs, a trait it shares with only 3 other taxa.<ref name=":2" /><ref name=":10">Raven, T. J. (2021). ''The Taxonomic, Phylogenetic, Biogeographic and Macroevolutionary History of the Armoured Dinosaurs (Ornithischia: Thyreophora)''(Doctoral dissertation, University of Brighton).</ref> 

[[File:Mymoorapelta maysi.png|right|thumb|[[Life restoration]]]]
The caudal (tail) vertebrae of ''Mymoorapelta'' and other nodosaurids are longer than they are wide, and dorsoventrally (top-bottom) flattened with a reduction of the neural spines when compared to the anterior caudals. The haemal spine takes on a rounded, hatchet-shaped appearance. The prezygapophyses are short and extend past the anterior edge of the centra by only 25% or less. This trait is only present in nodosaurids and basal anklosaurs, but in taxa like ''Liaoningosaurus'' and more derived ankylosaurids they overlap by at least 50% of its length, making them more fused together. ''Mymoorapelta'' lacks tail club handles or tail club knobs, as in other nodosaurids, giving them less ankylosis. The transition from anterior to posterior caudal vertebrae is less abrupt compared to ankylosaurids, which have an abrupt transition at the midcaudals, the lack of this abrupt transition would give the tail more flexibility, which is unique to nodosaurids when compared to the strongly fused tails of ankylosaurids.<ref name=":4">Arbour, V. M., & Currie, P. J. (2015). [https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/joa.12363 Ankylosaurid dinosaur tail clubs evolved through stepwise acquisition of key features.] ''Journal of anatomy'', ''227''(4), 514-523.</ref> The vertebral centra and neural spines are much shorter when compared to ''Gargoyleosaurus.''<ref name=":2" /> ''Mymoorapelta,'' like other dinosaurs, preserves chevrons along the undersides of the caudal vertebrae, and just like in many other ankylosaurs, the chevrons are strongly fused to the lower posterior part of the centra, and the haemal arches extend parallel to the elongate vertebral centra. The extension of these arches is greater anteriorly than posteriorly, forming a continuous bony structure underneath the haemal canal. One of the preserved chevrons measures {{Convert|9.1|cm|in}} and is strongly recurved posteriorly.<ref name=":0" /><ref name=":2" />

The scapular spine forms a vertical ridge opposite the glenoid in ''Mymoorapelta,'' as in other ankylosaurids and in an indeterminate ankylosaur scapula found in the nearby [[Dry Mesa Quarry]]. In the pelvic region, ''Mymoorapelta'' displays an intermediate between some features of basal and more derived ankylosaurs. The ischium is bent as in other nodosaurids and polacanthines, indicating that a straight ischium is a derived feature in ankylosaurids. In the forelimbs, the ulna has a broad, massive olecranon process that preserves rugosities. The coronoid process develops about 1/3rd of the way down the ulna's shaft, compared to 1/4th of the way down in taxa like ''[[Stegopelta]]'' and ''[[Polacanthus]].'' In the pes (foot), the genus preserves short, wide metapodials with long phalanges, with the distal phalanges looking triangular and pointed in side view, contrary to other nodosaurids like ''[[Edmontonia]]''.<ref name=":0" /><ref name=":2" />

=== Armor ===
[[File:Mymoorapelta plates fruita.jpg|thumb|right|Three of the thin, triangular plates on display at the Dinosaur Journey Museum, Fruita.]] 
A prominent feature of ''Mymoorapelta'' was its armor, which mostly consisted of large spiked osteoderms (bony armor) protruding from the lateral and dorsal sides of the body. These have not been found in articulation, so their exact placement on the body is unknown, though their position can be surmised based on the well preserved skeletons of other nodosaurids and ankylosaurs. In ''Mymoorapelta'', there are five different preserved armor types: elongated spines with a large, hollow base; thin triangular plates with a narrow, asymmetrical base; small bladelike spines with a rounded, solid base; isolated, flat, keeled scutes; and scutes fused into a single plate of armor. The large spine is assumed to have extended from the base of the neck outward laterally, with the point curving posteriorly.<ref name=":2" /><ref name=":0" /> Evidence from ''[[Borealopelta]]'' also supports the extension of the spike by a large keratin sheath.<ref name=":6">{{Cite journal |last1=Brown |first1=Caleb M. |last2=Henderson |first2=Donald M. |last3=Vinther |first3=Jakob |last4=Fletcher |first4=Ian |last5=Sistiaga |first5=Ainara |last6=Herrera |first6=Jorsua |last7=Summons |first7=Roger E. |date=2017-08-21 |title=An Exceptionally Preserved Three-Dimensional Armored Dinosaur Reveals Insights into Coloration and Cretaceous Predator-Prey Dynamics |url=https://www.cell.com/current-biology/abstract/S0960-9822(17)30808-4 |journal=Current Biology |language=English |volume=27 |issue=16 |pages=2514–2521.e3 |doi=10.1016/j.cub.2017.06.071 |issn=0960-9822 |pmid=28781051|bibcode=2017CBio...27E2514B |s2cid=5182644 |hdl=1721.1/118950 |hdl-access=free }}</ref> The aforementioned thin triangular plates, of which eight are known, are preserved similarly to those in ''Polacanthus'' further down the body.<ref>Hulke, J. W. (1887). VII. [https://royalsocietypublishing.org/doi/pdf/10.1098/rstb.1887.0007 Supplemental note on ''Polacanthus foxii'', describing the dorsal shield and some parts of the endoskeleton, imperfectly known in 1881.] ''Philosophical Transactions of the Royal Society of London.(B.)'', (178), 169-172.</ref><ref name=":0" /> It was theorized by Kirkland and Carpenter that the largest of these plates were attached to the proximal part of the tail, and protruded laterally along the sides of the body. A specimen of ''Mymoorapelta'' preserves one of these at {{Convert|11|cm|in}} in length.<ref name=":2" /><ref name=":0" /> A single, small triangular plate was reported in 1994 and it preserves a thin, bladelike morphology, though its position is unknown.<ref name=":0" /> Twelve of the previously mentioned keeled, flat scutes were recovered from a specimen of ''Mymoorapelta'' in 1994, they preserve a keeled oval shape and an external surface that bears uniform, weak pitting, and a privation of [[Neurovascular unit|neurovascular grooves]] (the system that controls blood flow and [[homeostasis]]) and {{Dinogloss|foramina}} (small openings within bones).<ref name=":0" /> In the internal structure of the scutes, half of the space is made up of [[Trabecula|trabecular bone]], while the rest is made up of thick external and basal [[Cortex (anatomy)|cortices]].<ref>{{Cite journal |last1=Burns |first1=Michael E. |last2=Currie |first2=Philip J. |date=2014-06-07 |title=External and internal structure of ankylosaur (Dinosauria, Ornithischia) osteoderms and their systematic relevance |url=https://doi.org/10.1080/02724634.2014.840309 |journal=Journal of Vertebrate Paleontology |volume=34 |issue=4 |pages=835–851 |doi=10.1080/02724634.2014.840309 |bibcode=2014JVPal..34..835B |s2cid=85943454 |issn=0272-4634}}</ref>

Lastly, a small fragment of dermal armor preserves a rosette (a large osteoderm surrounded by smaller osteoderms, forming a flower-like arrangement) formed by a large central scute surrounded on all sides by smaller ossicles.<ref name=":2" /><ref name=":0" /> This piece of armor comes from the sacral shield, which is a large plate of small, connected armor across the sacrum and pelvis for protection. A more complete sacral shield was preserved in the Cactus Park specimen, with estimates placing the complete sacral shield at {{Convert|70|cm|in}} in width for a pelvis that is {{Convert|50|cm|in}} wide.<ref name=":2" /><ref name=":0" /> The sacral shield also preserves two middle rows of larger scutes, with each row preserving seven.<ref name=":2" /> ''Mymoorapelta'' preserves a category 2 sacral shield, which is characterized by bosses (keeled osteoderms) that border tubercles (elevated knobs) as well as rosettes of co-ossified osteoderms. This category of sacral shield is mostly found in the "polacanthids",<ref>BLOws, W. T. (2001). 17. Dermal Armor of the Polacanthine Dinosaurs. ''The armored dinosaurs'', 363.</ref><ref name=":11">{{Cite journal |last1=Arbour |first1=Victoria M. |last2=Burns |first2=Michael E. |last3=Currie |first3=Philip J. |date=2011 |title=A review of pelvic shield morphology in ankylosaurs (Dinosauria: Ornithischia) |url=https://www.cambridge.org/core/journals/journal-of-paleontology/article/abs/review-of-pelvic-shield-morphology-in-ankylosaurs-dinosauria-ornithischia/984D0154571F625C142E0D51180D86B9 |journal=Journal of Paleontology |language=en |volume=85 |issue=2 |pages=298–302 |doi=10.1666/10-071.1 |bibcode=2011JPal...85..298A |s2cid=129637814 |issn=0022-3360}}</ref> but the status of this group is generally unstable, and the trait is also known in some ankylosaurids like ''[[Shamosaurus]]''.<ref name=":12">{{Cite journal |last1=Thompson |first1=Richard S. |last2=Parish |first2=Jolyon C. |last3=Maidment |first3=Susannah C. R. |last4=Barrett |first4=Paul M. |date=2012-06-01 |title=Phylogeny of the ankylosaurian dinosaurs (Ornithischia: Thyreophora) |url=https://doi.org/10.1080/14772019.2011.569091 |journal=Journal of Systematic Palaeontology |volume=10 |issue=2 |pages=301–312 |doi=10.1080/14772019.2011.569091 |bibcode=2012JSPal..10..301T |s2cid=86002282 |issn=1477-2019}}</ref><ref>Tumanova, T. A. (1987). The armored dinosaurs of Mongolia. Academy of Sciences of the USSR.</ref><ref name=":11" /> The category 2 shield is most similar to that of category 3, though the latter preserves polygonal osteoderms that lack rosettes.<ref name=":11" /> However, [[Victoria Arbour]] ''et al.'' (2011) suggested that category 1 shields could simply be an ontogenetic (growth) stage of category 2, as they have very similar morphology but are not co-ossified, which is an ontogenetic trait present in extant armored animals like armadillos and alligators.<ref name=":11" /><ref>{{Cite journal |last1=Vickaryous |first1=Matthew K. |last2=Hall |first2=Brian K. |date=2006 |title=Osteoderm morphology and development in the nine-banded armadillo,Dasypus novemcinctus (Mammalia, Xenarthra, Cingulata) |url=https://onlinelibrary.wiley.com/doi/10.1002/jmor.10475 |journal=Journal of Morphology |language=en |volume=267 |issue=11 |pages=1273–1283 |doi=10.1002/jmor.10475|pmid=17051548 |s2cid=23338307 }}</ref><ref>{{Cite journal |last1=Vickaryous |first1=Matthew K. |last2=Hall |first2=Brian K. |date=2008 |title=Development of the dermal skeleton in Alligator mississippiensis (Archosauria, Crocodylia) with comments on the homology of osteoderms |journal=Journal of Morphology |language=en |volume=269 |issue=4 |pages=398–422 |doi=10.1002/jmor.10575|pmid=17960802 |s2cid=5927674 |doi-access=free }}</ref> The current categorisation of sacral shields into distinct categories finds its origins in a 2011 paper by Arbour, Michael E. Burns and [[Philip J. Currie]], and gives three distinct characteristics, one for each of the three categories. Category 1 shields are characterized by non-coosified osteoderms, category 2 shields by coossified rosettes, and category 3 by uniformly sized coossified polygons.<ref>{{Cite journal |last1=Arbour |first1=Victoria M. |last2=Burns |first2=Michael E. |last3=Currie |first3=Philip J. |date=2011 |title=A review of pelvic shield morphology in ankylosaurs (Dinosauria: Ornithischia) |url=http://dx.doi.org/10.1666/10-071.1 |journal=Journal of Paleontology |volume=85 |issue=2 |pages=298–302 |doi=10.1666/10-071.1 |bibcode=2011JPal...85..298A |s2cid=129637814 |issn=0022-3360}}</ref> 

On the upper surface of the back and tail, the skin was covered in small osteoderms, which are sometimes referred to as ossicles, in-between larger plates of armor as inferred by ''Sauropelta'',<ref>{{Cite journal |last=Carpenter |first=Kenneth |date=1984-12-01 |title=Skeletal reconstruction and life restoration of Sauropelta (Ankylosauria: Nodosauridae) from the Cretaceous of North America |url=http://www.nrcresearchpress.com/doi/10.1139/e84-154 |journal=Canadian Journal of Earth Sciences |language=en |volume=21 |issue=12 |pages=1491–1498 |doi=10.1139/e84-154 |bibcode=1984CaJES..21.1491C |issn=0008-4077}}</ref> though ossicles themselves are not known confidently outside of the sacral shield in ''Mymoorapelta''.<ref name=":2" /><ref name=":0" /> The armor of ''Mymoorapelta'' differs from that of ''Gargoyleosaurus'' in that the former has solid conical armor compared to the thin-walled armor of the latter.<ref name=":5" />

== Paleobiology ==
=== Diet and feeding ===
[[File:Mymoorapelta in side view.jpg|thumb|right|Reconstructed skeleton shown from the side, WDC]] 
''Mymoorapelta'' was a low-browsing herbivore like its relatives, likely feeding on the [[fern]]s, [[cycad]]s, and [[conifer]]s that dominated the [[flora]] of its time due to the lack of complex [[Poaceae|grasses]] in the Jurassic.<ref name=":13">{{Cite journal |last1=Prasad |first1=Vandana |last2=Strömberg |first2=Caroline A. E. |last3=Alimohammadian |first3=Habib |last4=Sahni |first4=Ashok |date=2005-11-18 |title=Dinosaur Coprolites and the Early Evolution of Grasses and Grazers |url=https://www.science.org/doi/10.1126/science.1118806 |journal=Science |language=en |volume=310 |issue=5751 |pages=1177–1180 |bibcode=2005Sci...310.1177P |doi=10.1126/science.1118806 |issn=0036-8075 |pmid=16293759 |s2cid=1816461}}</ref> Nodosaurids like ''Mymoorapelta'' had narrow snouts, an adaptation seen today in animals that are selective browsers as opposed to the wide muzzles of [[Grazing|grazers]].<ref>Carpenter, Kenneth. (1997). "Ankylosauria". In Currie, Philip J.; Padian, Kevin (eds.). The Encyclopedia of Dinosaurs. Berkeley: University of California Press. pp. 16–17.</ref><ref name=":15" /> In ankylosaurs, the Jurassic and mid-Cretaceous forms with narrow and pointed muzzles were apparently the most selective feeders, akin to extant mammalian browsers. This is in stark contrast to the later ankylosaurs that were adapted to bulk feeding on food with lower nutritional value. The preservation of complete a {{Dinogloss|hyoid}} in taxa like the ankylosaurid ''[[Pinacosaurus]]'' and the nodosaurid ''Edmontonia'' demonstrate that ankylosaurs had fleshy, muscular tongues that could have assisted with feeding on plants that grew low to the ground.<ref name=":16">{{Cite journal |last1=Hill |first1=Robert V. |last2=D'Emic |first2=Michael D. |last3=Bever |first3=G. S. |last4=Norell |first4=Mark A. |date=2015 |title=A complex hyobranchial apparatus in a Cretaceous dinosaur and the antiquity of avian paraglossalia: Dinosaur Hyobranchial Apparatus |journal=Zoological Journal of the Linnean Society |language=en |volume=175 |issue=4 |pages=892–909 |doi=10.1111/zoj.12293|doi-access=free }}</ref><ref name=":15" /> Tongue protrusion and prehension is not confidently known, but lingual food manipulation could have been used in later ankylosaurids to crop food, like in giraffes. The preservation of cheek plates in ''Edmontonia'' and ''Panoplosaurus'' provide evidence for fleshy cheeks and chewing, with the cheek covering the tooth rows both for defense and to prevent food loss when eating.<ref>{{Cite journal |last=Vickaryous |first=Matthew K. |date=2006-12-11 |title=New information on the cranial anatomy of Edmontonia rugosidens Gilmore, a Late Cretaceous nodosaurid dinosaur from Dinosaur Provincial Park, Alberta |url=http://www.tandfonline.com/doi/abs/10.1671/0272-4634%282006%2926%5B1011%3ANIOTCA%5D2.0.CO%3B2 |journal=Journal of Vertebrate Paleontology |language=en |volume=26 |issue=4 |pages=1011–1013 |doi=10.1671/0272-4634(2006)26[1011:NIOTCA]2.0.CO;2 |s2cid=130696265 |issn=0272-4634}}</ref> 

Tooth occlusion is not directly preserved in ''Mymoorapelta'' or its close relative ''Gargoyleosaurus'', but it has been found in other nodosaurids from the Cretaceous. The earliest evidence of nodosaurid dental occlusion is in ''Sauropelta,'' which demonstrated a basic motion, in that the power strokes moved vertically. In contrast to later nodosaurids, tooth-to-tooth contact was incidental or local when present and a biphasial jaw mechanism was lacking in both ''Mymoorapelta'' and ''Gargoyleosaurus''.<ref name=":15" />  Ankylosaurs generally demonstrate more variable wear patterns than the contemporary [[Ceratopsidae|ceratopsids]] and [[Hadrosauridae|hadrosaurids]] of the Cretaceous. Even though ankylosaurs may not have fed on [[Fiber|fibrous]] and [[woody plant]]s, they may have had a varied diet which included tough leaves and pulpy fruits.<ref name=":16" />

=== Habitat preference ===
Due to competition with [[Diplodocidae|Diplodocid]] sauropods, ''Mymoorapelta'' seems more adapted for open environments.<ref>Whitlock, J., Trujillo, K., & Hanik, G. (2018). Assemblage-level structure in Morrison Formation dinosaurs, western interior, USA. ''Geology of the Intermountain West'', ''5'', 9-22.</ref> ''Mymoorapelta'' has a very limited known distribution, having only been found at two sites in Western Colorado, in addition to the Hanksville-Burpee and potential Albuquerque specimens.<ref name=":0" /><ref name=":2" /><ref name=":8" /><ref name=":9" /> This could be due to ''Mymoorapelta'' preferring to feed on a specific variety of plant, constricting its possible distribution. The Hanksville-Burpee specimen's [[taphonomy]] (how and where it decomposed to end up as a fossil) suggests that the individual had died inland, contrary to the coastal distribution previously inferred for nodosaurids.<ref name=":8" /><ref>Butler, R. J., & Barrett, P. M. (2008). Palaeoenvironmental controls on the distribution of Cretaceous herbivorous dinosaurs. ''Naturwissenschaften'', ''95''(11), 1027-1032.</ref><ref>Coombs Jr, W. P. (1995). A nodosaurid ankylosaur (Dinosauria: Ornithischia) from the Lower Cretaceous of Texas. ''Journal of vertebrate Paleontology'', ''15''(2), 298-312.</ref>

=== Limb movements ===

Reconstructions of ankylosaur forelimb musculature made by Coombs in 1978 suggest that the forelimbs bore the majority of the animal's weight and that they were adapted for high force delivery on the front feet, possibly for food gathering. In addition, Coombs suggested that ankylosaurs may have been capable diggers, though the hoof-like structure of the {{Dinogloss|manus}} would have limited fossorial capibilities. Ankylosaurs were likely to have been slow-moving and sluggish animals,<ref>Coombs, W. (1979). "Osteology and myology of the hindlimb in the Ankylosauria (Reptillia, Ornithischia)". ''Journal of Paleontology''. '''53''' (3): 666–84. [[JSTOR (identifier)|JSTOR]] 1304004.</ref><ref>Coombs, W. (1978). "Forelimb muscles of the Ankylosauria (Reptilia, Ornithischia)". ''Journal of Paleontology''. '''52''' (3): 642–57. [[JSTOR (identifier)|JSTOR]] 1303969.</ref> though they may have been capable of quick movements when necessary.<ref>{{Cite journal |last=Coombs |first=Walter P. |date=1978-12-01 |title=Theoretical Aspects of Cursorial Adaptations in Dinosaurs |url=https://www.journals.uchicago.edu/doi/10.1086/410790 |journal=The Quarterly Review of Biology |volume=53 |issue=4 |pages=393–418 |doi=10.1086/410790 |s2cid=84505681 |issn=0033-5770}}</ref> ''Mymoorapelta'' preserves very short limbs with even shorter distal limb elements, which is in contrast to the longer distal limb elements known in other nodosaurids but similar to the condition found in ankylosaurids and ''Polacanthus''.<ref name=":3" />

=== Armor and tail ===
[[File:Mymoorapelta tail and hip armor.jpg|thumb|right|Reconstructed tail and hip armor, WDC]] 
The scientific literature mostly considers the armor of ankylosauroids to have been used for defensive purposes, mainly to fend off any attacking carnivores.<ref>{{Cite journal |last1=Scheyer |first1=Torsten M. |last2=Sander |first2=P. Martin |date=2004-12-10 |title=Histology of ankylosaur osteoderms: implications for systematics and function |url=http://dx.doi.org/10.1671/0272-4634(2004)024[0874:hoaoif]2.0.co;2 |journal=Journal of Vertebrate Paleontology |volume=24 |issue=4 |pages=874–893 |doi=10.1671/0272-4634(2004)024[0874:hoaoif]2.0.co;2 |s2cid=86333501 |issn=0272-4634}}</ref> The tails of these animals have a complex evolutionary history, with basal taxa like ''Mymoorapelta'' possessing a flexible tail with pointed osteoderms on either side and on top. The aforementioned flexibility of the tail would allow for a greater range of motion than the stiff tails of later ankylosaurids and nodosaurids.<ref>{{Cite journal |last1=Arbour |first1=Victoria M. |last2=Currie |first2=Philip J. |date=2015-08-31 |title=Ankylosaurid dinosaur tail clubs evolved through stepwise acquisition of key features |url=http://dx.doi.org/10.1111/joa.12363 |journal=Journal of Anatomy |volume=227 |issue=4 |pages=514–523 |doi=10.1111/joa.12363 |pmid=26332595 |issn=0021-8782|pmc=4580109 }}</ref> It is thought that the tail could also have been used in defense against predators, though more recent findings by Arbour ''et al''. in 2022 also consider the possibility that the tails of ankylosaurids were used for intraspecific combat and might have primarily evolved to fill a function here, which might indicate a similar use in more basal taxa like ''Mymoorapelta'' and ''Gargoyleosaurus''.<ref>{{Cite journal |last1=Arbour |first1=Victoria M. |last2=Zanno |first2=Lindsay E. |last3=Evans |first3=David C. |date=2022 |title=Palaeopathological evidence for intraspecific combat in ankylosaurid dinosaurs |journal=Biology Letters |language=en |volume=18 |issue=12 |pages=20220404 |doi=10.1098/rsbl.2022.0404 |issn=1744-957X |pmc=9727678 |pmid=36475422 }}</ref>

== Classification ==

''Mymoorapelta'' is one of the [[Basal (phylogenetics)|basalmost]] known genera of [[Nodosauridae]], an extinct family of medium to large, heavily built, quadrupedal, [[herbivorous]] dinosaurs which possess small, leaf-shaped teeth. The clade was named in 1890 by Othniel Charles Marsh, who designated the Cretaceous genus ''[[Nodosaurus]]'' as the type genus based on the heavy dermal armor, solid bones, large forelimbs, and ungulate feet it preserves.<ref>Marsh, O. C. (1890). Description of new dinosaurian reptiles. ''American Journal of Science'', ''3''(229), 81-86. Chicago</ref><ref>{{Cite journal |last=Marsh |first=Othniel Charles |date=1889-08-01 |title=Notice of gigantic horned Dinosauria from the Cretaceous |url=https://www.ajsonline.org/content/s3-38/224/173 |journal=American Journal of Science |language=en |volume=s3-38 |issue=224 |pages=173–176 |bibcode=1889AmJS...38..173M |doi=10.2475/ajs.s3-38.224.173 |issn=0002-9599 |s2cid=131187857 |access-date=2022-08-10 |archive-date=2021-10-19 |archive-url=https://web.archive.org/web/20211019182409/https://www.ajsonline.org/content/s3-38/224/173 |url-status=dead }}</ref> Nodosaurids first evolved in the [[Late Jurassic]] (ca. 155 mya), with ''Mymoorapelta'' and the similarly sized ''Gargoyleosaurus'' being early members of the evolutionary radiation which would continue into the Cretaceous in accordance with [[Cope's rule|Cope's Rule]].<ref>{{Cite journal |last1=Hone |first1=D. W. E. |last2=Keesey |first2=T. M. |last3=Pisani |first3=D. |last4=Purvis |first4=A. |date=2005-02-22 |title=Macroevolutionary trends in the Dinosauria: Cope's rule: Dinosaurs obey Cope's rule |journal=Journal of Evolutionary Biology |language=en |volume=18 |issue=3 |pages=587–595 |doi=10.1111/j.1420-9101.2004.00870.x |pmid=15842488 |s2cid=14122343|doi-access=free }}</ref><ref name=":52">Carpenter, K., Miles, C. and Cloward, K. (1998). "Skull of a Jurassic ankylosaur (Dinosauria)." ''Nature'' 393: 782–783.</ref> The nodosaurids went extinct in the [[Late Cretaceous]] (ca. 66 mya) during the [[Cretaceous–Paleogene extinction event]] along with the other non-avian dinosaurs. 

Nodosaurids are situated within the group [[Euankylosauria]], together with the closely related family [[Ankylosauridae]]. Nodosaurids differ from ankylosaurids in the fact that ankylosaurids evolved more recently, during the [[Early Cretaceous]], and in several distinct anatomical characteristics; most notably the lack of mace-like tail clubs, with nodosaurs having osteoderm-lined, flexible tails instead, and the possession of sacral shields. Many nodosaurids also had spikes projecting outwards from their shoulders, and two armored half-rings on their neck, among other traits. A third proposed family, [[Polacanthinae|Polacanthidae]], was erected for several genera that were similar to nodosaurids but had more fragile armor and a different distribution. However, it has seen little support from phylogenetic analyses in recent years and is in a state of flux.<ref name=":12" /><ref>{{Cite journal |last1=Zheng |first1=Wenjie |last2=Jin |first2=Xingsheng |last3=Azuma |first3=Yoichi |last4=Wang |first4=Qiongying |last5=Miyata |first5=Kazunori |last6=Xu |first6=Xing |date=2018-02-27 |title=The most basal ankylosaurine dinosaur from the Albian–Cenomanian of China, with implications for the evolution of the tail club |journal=Scientific Reports |language=en |volume=8 |issue=1 |pages=3711 |bibcode=2018NatSR...8.3711Z |doi=10.1038/s41598-018-21924-7 |issn=2045-2322 |pmc=5829254 |pmid=29487376}}</ref><ref name="Riveraetal">{{Cite journal |last1=Rivera-Sylva |first1=Héctor E. |last2=Frey |first2=Eberhard |last3=Stinnesbeck |first3=Wolfgang |last4=Carbot-Chanona |first4=Gerardo |last5=Sanchez-Uribe |first5=Iván E. |last6=Guzmán-Gutiérrez |first6=José Rubén |date=2018 |title=Paleodiversity of Late Cretaceous Ankylosauria from Mexico and their phylogenetic significance |journal=[[Swiss Journal of Palaeontology]] |language=en |volume=137 |issue=1 |pages=83–93 |doi=10.1007/s13358-018-0153-1 |bibcode=2018SwJP..137...83R |issn=1664-2384 |s2cid=134924657|doi-access=free }}</ref> Euankylosauria encompasses all members of Ankylosauria except for the clade [[Parankylosauria]], which is a smaller group known exclusively from a few taxa that lived in the Cretaceous of [[Gondwana]], rather than the euankylosaurs, who were endemic to [[Laurasia]].<ref>{{Cite journal |last1=Soto-Acuña |first1=Sergio |last2=Vargas |first2=Alexander O. |last3=Kaluza |first3=Jonatan |last4=Leppe |first4=Marcelo A. |last5=Botelho |first5=Joao F. |last6=Palma-Liberona |first6=José |last7=Simon-Gutstein |first7=Carolina |last8=Fernández |first8=Roy A. |last9=Ortiz |first9=Héctor |last10=Milla |first10=Verónica |last11=Aravena |first11=Bárbara |last12=Manríquez |first12=Leslie M. E. |last13=Alarcón-Muñoz |first13=Jhonatan |last14=Pino |first14=Juan Pablo |last15=Trevisan |first15=Cristine |date=2021-12-09 |title=Bizarre tail weaponry in a transitional ankylosaur from subantarctic Chile |url=https://www.nature.com/articles/s41586-021-04147-1 |journal=Nature |language=en |volume=600 |issue=7888 |pages=259–263 |doi=10.1038/s41586-021-04147-1 |pmid=34853468 |bibcode=2021Natur.600..259S |s2cid=243794180 |issn=0028-0836}}</ref>[[File:Caudal anatomy of ankylosaurs.jpg|thumb|right|Tail anatomy of [[Ankylosauria|ankylosaurs]], F is ''Mymoorapelta'']]When ''Mymoorapelta'' was originally named, Kirkland and Carpenter placed the taxon as a potential nodosaurid, though at that time there were only a few taxa to compare the material to. The phylogenetic placement was changed in 1998 when it was considered closer to the European polacanthids,<ref name=":2" /> though this affiliation has been doubted.<ref name=":3" /><ref name=":10" /><ref name=":8" /> Matthew Vickaryous et al. (2004) considered the genus Ankylosauria ''[[incertae sedis]],''<ref>Vickaryous, M. K., Maryanska, T. ´ & Weishampel, D. B. (2004). Ankylosauria. Pp. 363–392 in D. B. Weishampel, P. Dodson & H. Osmolska (eds) ´The Dinosauria, 2nd edition. University of California Press, Berkeley</ref> while a [[cladistic analysis]] performed by Thompson ''et al.'' (2011) suggests that ''Mymoorapelta'' is a basal nodosaurid as originally theorized by Kirkland and Carpenter.<ref name=":12" /> A 2010 phylogenetic analysis utilizing undescribed material resulted with ''Mymoorapelta'' as the sister taxon to ''Gargoyleosaurus'' in their own group outside of Polacanthidae, Nodosauridae, and Ankylosauridae.<ref name=":3" /> In a [[2018 in paleontology|2018]] phylogenetic analysis by Rivera-Sylva and colleagues which has been reproduced below, ''Mymoorapelta'' is recovered as a basal nodosaurid in a clade with ''[[Sauroplites]]'' and ''[[Dongyangopelta]]'' that represents the most basal group within Nodosauridae, while ''Gargoyleosaurus'' is recovered as more derived, further proving their distinction.<ref name="Riveraetal" /> Alternatively, ''Mymoorapelta'' may also be an ankylosaur outside both Nodosauridae and Ankylosauridae.<ref name="madzia2021">{{cite journal |last1=Madzia |first1=D. |last2=Arbour |first2=V.M. |last3=Boyd |first3=C.A. |last4=Farke |first4=A.A. |last5=Cruzado-Caballero |first5=P. |last6=Evans |first6=D.C. |year=2021 |title=The phylogenetic nomenclature of ornithischian dinosaurs |journal=PeerJ |volume=9 |pages=e12362 |doi=10.7717/peerj.12362 |pmc=8667728 |pmid=34966571 |doi-access=free }}</ref>

The phylogenetic analyses of Rivera-Sylva and colleagues (left) and Thomas Raven and colleagues (right) found ''Mymoorapelta'' as a basal member of either Nodosauridae or Ankylosauridae.<ref name="Riveraetal"/><ref name="raven2023">{{cite journal |last1=Raven |first1=T. J. |last2=Barrett |first2=P. M. |last3=Joyce |first3=C. B. |last4=Maidment |first4=S. C. R. |year=2023 |title=The phylogenetic relationships and evolutionary history of the armoured dinosaurs (Ornithischia: Thyreophora) |journal=Journal of Systematic Palaeontology |volume=21 |issue=1 |at=2205433 |doi=10.1080/14772019.2023.2205433 |bibcode=2023JSPal..2105433R |s2cid=258802937 }}</ref>
{{col-begin|width=75%}}
{{col-break}}
{{clade| style=font-size:85%; line-height:85%
|label1=[[Nodosauridae]]
|1={{clade
 |1={{clade
  |1=''[[Sauroplites]]''
  |2='''''Mymoorapelta'''''
  |3=''[[Dongyangopelta]]'' }}
 |2={{clade
  |1=''[[Gastonia burgei|Gastonia]]''
  |2={{clade
   |1=''[[Gargoyleosaurus]]''
   |2={{clade
    |1=[[Polacanthinae]]
    |2=[[Nodosaurinae]] }} }} }} }} }}
{{col-break}}
{{clade | style=font-size:85%; line-height:85%;
|label1=[[Ankylosauridae]]
|1={{clade
 |1={{clade
  |1=''[[Borealopelta]]''
  |2={{clade
   |1=''[[Mymoorapelta]]''
   |2=''[[Stegopelta]]'' }} }}
 |2={{clade
  |1={{clade
   |1=''[[Vectipelta]]''
   |2={{clade
    |1=''[[Dongyangopelta]]''
    |2=''[[Zhejiangosaurus]]'' }} }}
  |2={{clade
   |1=''[[Ahshislepelta]]''
   |2={{clade
    |1={{clade
     |1=''[[Aletopelta]]''
     |2=''[[Talarurus]]'' }}
    |2={{clade
     |1=[[Shamosaurinae]]
     |2=[[Ankylosaurinae]] }} }} }} }} }} }}
{{col-end}}

== Paleoecology ==
The Morrison Formation is a sequence of shallow marine and alluvial sediments which, according to [[radiometric dating]], ranges between 156.3 million years old ([[Mega-annum|Ma]]) at its base, to ~150 ma at the top, placing it in the late [[Oxfordian stage|Oxfordian]], [[Kimmeridgian]], and early [[Tithonian]] [[Faunal stages|stages]] of the Upper Jurassic period.<ref>{{Cite journal |last1=Christiansen |first1=E. H. |last2=Kowallis |first2=B. J. |last3=Dorais |first3=M. J. |last4=Hart |first4=G. L. |last5=Mills |first5=C. N. |last6=Pickard |first6=M. |last7=Parks |first7=E. |date=2015 |title=The record of volcanism in the Brushy Basin Member of the Morrison Formation: Implications for the Late Jurassic of western North America |url=https://www.researchgate.net/publication/281118079 |journal=Special Paper of the Geological Society of America |volume=513 |pages=1–XXX |via=ResearchGate}}</ref><ref>{{Cite journal |last1=Trujillo |first1=Kelli |last2=Kowallis |first2=Bart |date=2015-01-20 |title=Recalibrated legacy 40Ar/39Ar ages for the Upper Jurassic Morrison Formation, Western Interior, U.S.A. |journal=Geology of the Intermountain West |volume=2 |pages=1–8 |doi=10.31711/giw.v2.pp1-8 |doi-broken-date=1 November 2024 |issn=2380-7601|doi-access=free }}</ref> The paleoenvironment of the Morrison Formation is interpreted as a [[semiarid]] environment with distinct [[Wet season|wet]] and [[dry season]]s, and flat [[floodplain]]s.<ref name=":7" /> Vegetation varied from river-lining forests of conifers, [[tree fern]]s, and ferns (gallery forests), to fern savannas with occasional trees such as the [[Araucaria]]-like conifer ''[[Brachyphyllum]]''.<ref name=":7" /> The Morrison Basin where dinosaurs lived stretched from New Mexico to Alberta and Saskatchewan, and was formed when the precursors to the [[Front Range]] of the Rocky Mountains started pushing up to the west. The deposits from their east-facing [[drainage basin]]s were carried by streams and [[river]]s and deposited in [[swamp]]y lowlands, lakes, river channels and floodplains.
[[File:Dry season at the Mygatt-Moore Quarry.PNG|thumb|Illustration of the theropods ''[[Ceratosaurus]]'' and ''[[Allosaurus]]'' fighting over food in the Mygatt-Moore Quarry.]]
The Mygatt-Moore Quarry where ''Mymoorapelta'' was first found has been dated between 151.89 and 152.47 million years old, firmly placing it within the Brushy Basin Member of the Morrison Formation. The broader paleoenvironment of the area has been interpreted as a riparian (riverine) ecosystem with abundant flora and a high water table, with the quarry itself having been interpreted as an attritional accumulation of dinosaur fossils at a seasonal waterhole. This has allowed it to become one of the most fossil abundant sites in the United States, with the site notably preserving plants, pollen, coprolites, and even skin impressions preserved alongside dinosaur fossils.<ref name=":14" /> The quarry's abundant plant fossils include [[Equisetum|horsetails]], cycads, [[Ginkgoales|Gingkoales]], [[Czekanowskiales]], and many different Coniferales represented by leaf, wood, and pollen fossils.<ref name=":1" /> Invertebrates represented in the quarry include [[Gastropoda|gastropods]] and, most notably, fossils of fossil [[crayfish]].<ref name=":1" /> 

As for vertebrates, three different kinds of fish have been described from the quarry based on fossils of astonishing quality, including ''[[Hulettia|Hulettia hawesi]]'' and ''[[Morrolepis|Morrolepis schaefferi]]''. The most common fossils from the quarry are dinosaurian in nature. ''[[Allosaurus]],'' a large carnivorous theropod, and ''[[Apatosaurus]]'', a large [[Diplodocidae|diplodocid]] sauropod, are the two most common dinosaurs in the quarry, with ''Mymoorapelta'' being the third most common at the site.<ref name=":1" /> Fossils of several other dinosaurs are known from the quarry, including the theropod ''[[Ceratosaurus]]'', the sauropods ''[[Camarasaurus]]'' and ''[[Diplodocus]]'', and potentially the small ornithischian ''[[Nanosaurus]]''. Remains of other vertebrate groups like [[Crocodyliformes|crocodyliforms]] and [[turtle]]s are rare in the quarry, indicating the lack of continuous standing water in the form of [[lake]]s or [[pond]]s.<ref name=":14" />

Fossils of ''Mymoorapelta'' and the theropod ''Allosaurus'' that preserve bite marks have been described from the Mygatt-Moore Quarry by Stephanie Drumheller ''et al.'' (2020), alongside other bones found with feeding traces.<ref name=":14">{{Cite journal |last1=Drumheller |first1=Stephanie K. |last2=McHugh |first2=Julia B. |last3=Kane |first3=Miriam |last4=Riedel |first4=Anja |last5=D’Amore |first5=Domenic C. |date=2020-05-27 |title=High frequencies of theropod bite marks provide evidence for feeding, scavenging, and possible cannibalism in a stressed Late Jurassic ecosystem |journal=PLOS ONE |language=en |volume=15 |issue=5 |pages=e0233115 |doi=10.1371/journal.pone.0233115 |issn=1932-6203 |pmc=7252595 |pmid=32459808|bibcode=2020PLoSO..1533115D |doi-access=free }}</ref> Unlike the others, the fossils of ''Mymoorapelta'' and ''Allosaurus'' preserve striations that, when measured to determine [[Denticle (tooth feature)|denticle]] (serration) width, produced tooth and body size extrapolations greater than any known specimen of ''Allosaurus'' or ''Ceratosaurus,'' the two large predators of the quarry that are known from osteological remains. The extrapolations are instead coherent either with an unusually large specimen of ''Allosaurus'', or a separate large taxon like ''[[Torvosaurus]]'' or ''[[Saurophaganax]],'' neither of which preserves fossil material within the quarry''.'' The result either increases the known diversity of the site based on [[Trace fossil|ichnological]] evidence alone, or represents powerful evidence of cannibalism in ''Allosaurus''. Based on the position and nutrient value associated with the various skeletal elements with bite marks, it is predicted that ''Mymoorapelta'' was either predated upon or scavenged shortly after death.<ref name=":14" />

==See also==
{{Portal|Dinosaurs}}
* ''[[Gargoyleosaurus]]''
* ''[[Gastonia (dinosaur)|Gastonia]]''
* ''[[Polacanthus]]''
* [[Timeline of ankylosaur research]]

==References==
{{Reflist}}

{{Thyreophora|N.}}
{{Taxonbar|from=Q134139}}

[[Category:Nodosaurids]]
[[Category:Fossil taxa described in 1994]]
[[Category:Dinosaurs of the Morrison Formation]]
[[Category:Taxa named by James I. Kirkland]]
[[Category:Taxa named by Kenneth Carpenter]]
[[Category:Paleontology in Colorado]]
[[Category:Ornithischian genera]]