Temporal range: Late Triassic, 228–210 Ma
|Desmatosuchus from Petrified Forest National Park, Arizona|
The living animals were large quadrupeds that were upwards of 4.5 meters in length. Their spines had amphicoelus centra and 3 sacral vertebrae. Their scapulae had large acromion processes. Their forelimbs were much shorter than their hindlimbs, with humeri less than two-thirds the length of their femurs. Their pelvic girdles consisted of a long pubis with a strong symphysis in the middle, a plate-like ischium, a highly recurved ilium, and a deep, imperforate acetabulum. They had relatively long, straight femurs, crurotarsal ankles, and calcaneal tubers that gave them large heels.
Their skulls were relatively small relative to their bodies, on average about 37 centimeters long, 18 centimeters wide, and 15 centimeters high. Their braincases were very firmly fused with the skull roof and palate. They had slender,forked premaxillae that turned up and expanded in the front, creating a shovel-like structure. Desmatosuchus is unique among aetosaurs in that its species are the only known aetosaurs that lacked teeth on their premaxillae. Their premaxillae fit loosely together with their maxillae, indicating flexibility at that joint. Their maxilla contained 10 to 12 teeth. Desmatosuchus also had very thin vomers, which bounded the medial side of the internal nares. These internal nares were relatively large, roughly half the length of the entire palate. Their lower jaw typically carried 5 or 6 teeth, and had a toothless beak on the end. The dentary was about half the length of the lower jaw, with the front portion being toothless and covered by a horny sheath. Behind the dentary was a moderately large mandibular fenestra.
Individuals of Desmatosuchus were heavily armored. The carapace was made up of two rows of median scutes surrounded by two more rows of lateral scutes. The lateral scutes have well-developed spines that point out laterally and dorso-posteriorly. There are typically five rows of spines, and they increase in size anteriorly. The front spine is much larger, around 28 centimeters long, and is recurved. The fourth spine varies in length in each specimen, but remains shorter than the fifth in all of them. Desmatosuchus are the only aetosaurs known to have possessed spines like these.
Discovery and classification
The first Desmatosuchus discovery occurred in the late 19th century when E.D. Cope classified armor from the Dockum Group in Texas, USA, as the new species Episcoposaurus haplocerus. Case later classified a partial skeleton found in the Tecovas Formation as Desmatosuchus spurensis. Since the localities of Cope and Case were only a few kilometers apart, the two taxa were synonymized into Desmatosuchus haplocerus, the initial type species of the genus.
A revision of Desmatosuchus by Parker (2008) found the lectotype of Episcoposaurus haplocerus to be referable to Desmatosuchus but indeterminate at the species level. Therefore, E. haplocerus was considered to be a nomen dubium and D. spurensis was named the type species of the genus. Two species were accepted as valid: D. spurensis and D. smalli, named after Brian J. Small for his contribution to the study of this genus. Desmatosuchus chamaensis is recognized as a distinct genus, but there is some dispute about whether the name Heliocanthus or Rioarribasuchus applies.
Bones and armor pieces of Desmatosuchus are abundant in the Dockum formation, Chinle formation, and Post quarry, indicating that they were widespread and abundant during the Late Triassic. It is possible that Desmatosuchus traveled in packs or family units. This is evidenced by several findings of multiple Desmatosuchus skeletons in relatively small areas.
Desmatosuchus had blunt, bulbous, slightly recurved teeth. Furthermore, they are believed to have had homodont dentition. This, combined with its shovel like snout, indicate that Desmatosuchus fed by digging up soft vegetation. This method of feeding is further evidenced by its toothless premaxilla and dentary tip, which were covered in horny sheaths. These sheaths protected the bones and could be used for cutting or holding objects. It is believed that Desmatosuchus dug for food in the soft mud near bodies of water due to the abundance of lakes and rivers in the Dockum area and the fact that Desmatosuchus scutes are often found among parts of other reptiles that are known to have fed along waterways. It is unknown whether or not Desmatosuchus replaced their teeth and, if so, how. The low number of Desmatosuchus teeth that have been discovered indicates that they were only held in place by soft tissue connections. The jaw articulation point is below the tooth line, holding its upper and lower tooth rows parallel while biting in a way that is reminiscent of ornithischian dinosaurs.
The armor and spikes of Desmatosuchus were its only ways to defend itself from predators. The lateral spike rows showed variation in size among individuals, especially the second most anterior spike. This spike was always shorter than the one in front of it, but to what extent varied drastically. This variation may indicate sexual dimorphism. It has also been hypothesized as a form of sexual display. Aside from this armor, Desmatosuchus was defenseless from attacks from carnivores. Several Desmatosuchus bones have been found amongst skeletons of Postosuchus, indicating predation by Postosuchus. The herd nature of Desmatosuchus apparently did little to discourage predators, as Postosuchus along with several other Late Triassic carnivores also traveled in groups.
Most thecodonts of the Late Triassic lacked certain pelvic features that aided locomotion, such as a deep acetabulum or a crest over the acetabulum. This, in spite of their upright posture, rendered them only slightly more mobile than sprawling reptiles. Desmatosuchus possessed both of these features, along with its long femur and elongate pubis, making it more mobile than most thecodonts of its time. This mobility, along with the Desmatosuchus' size, abundance, and specialized beak made it the chief herbivore in the Dockum area.
It has also been suggested that Desmatosuchus could have been omnivorous or even an insectivore. This is because of several similarities between Desmatosuchus and armadillos. For instance, both groups are armored. They possess long snouts that lack teeth on the end. Also, there is evidence of bees, wasps, and termites in the Late Triassic, meaning that Desmatosuchus had access to insects that armadillos prey on. Their teeth are somewhat similar in shape, although armadillos have more peg like teeth. Both Desmatosuchus and armadillos typically carry around 6 teeth on their dentaries. Both armadillos and Desmatosuchus have hypertrophied processes present on their limbs, which indicates large limb muscles. This connection is more tenuous, however, since Desmatosuchus have a crest over their hind limbs but lack one on their forelimbs, meaning that they likely didn't have the musculature for digging with their arms the way armadillos do. In spite of these parallels, the general consensus is still that Desmatosuchus was most likely herbivorous. 
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