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Temporal range: Late Jurassic, 155–150Ma
|Reconstructed S. stenops skeleton, Senckenberg Museum|
Temporal range: Late Jurassic, 155–150Ma
|Reconstructed S. stenops skeleton, Senckenberg Museum|
Stegosaurus (//, meaning "roof lizard" or "covered lizard" in reference to its bony plates) is a genus of armored stegosaurid dinosaur. They lived during the Late Jurassic period (Kimmeridgian to early Tithonian), some 155 to 150 million years ago in what is now western North America. In 2006, a specimen of Stegosaurus was announced from Portugal, showing that they were present in Europe as well. Due to its distinctive tail spikes and plates, Stegosaurus is one of the most recognizable dinosaurs. At least three species have been identified in the upper Morrison Formation and are known from the remains of about 80 individuals.
A large, heavily built, herbivorous quadruped, Stegosaurus had a distinctive and unusual posture, with a heavily rounded back, short forelimbs, head held low to the ground and a stiffened tail held high in the air. Its array of plates and spikes has been the subject of much speculation. The spikes were most likely used for defense, while the plates have also been proposed as a defensive mechanism, as well as having display and thermoregulatory functions. Stegosaurus had a relatively low brain-to-body mass ratio. It had a short neck and small head, meaning it most likely ate low-lying bushes and shrubs. It was the largest of all the stegosaurians (bigger than genera such as Kentrosaurus and Huayangosaurus) and, although roughly bus-sized, it nonetheless shared many anatomical features (including the tail spines and plates) with the other stegosaurian genera.
The quadrupedal Stegosaurus is one of the most easily identifiable dinosaur genera, due to the distinctive double row of kite-shaped plates rising vertically along the rounded back and the two pairs of long spikes extending horizontally near the end of the tail. Although large animals at up to 9 metres (30 ft) in length, the various species of Stegosaurus were dwarfed by their contemporaries, the giant sauropods. Some form of armor appears to have been necessary, as Stegosaurus species coexisted with large predatory theropod dinosaurs, such as Allosaurus and Ceratosaurus.
The hind feet each had three short toes, while each forefoot had five toes; only the inner two toes had a blunt hoof. The phalangeal formula is 2-2-2-2-1, meaning that the innermost finger of the forelimb has two bones, the next has two, etc. All four limbs were supported by pads behind the toes. The forelimbs were much shorter than the stocky hindlimbs, which resulted in an unusual posture. The tail appears to have been held well clear of the ground, while the head of Stegosaurus was positioned relatively low down, probably no higher than 1 meter (3.3 ft) above the ground.
The long and narrow skull was small in proportion to the body. It had a small antorbital fenestra, the hole between the nose and eye common to most archosaurs, including modern birds, though lost in extant crocodylians. The skull's low position suggests that Stegosaurus may have been a browser of low-growing vegetation. This interpretation is supported by the absence of front teeth and their replacement by a horny beak or rhamphotheca. Stegosaurian teeth were small, triangular and flat; wear facets show that they did grind their food. The inset placement in the jaws suggests that Stegosaurus had cheeks to keep food in their mouths while they chewed.
Despite the animal's overall size, the braincase of Stegosaurus was small, being no larger than that of a dog. A well-preserved Stegosaurus braincase allowed Othniel Charles Marsh to obtain in the 1880s a cast of the brain cavity or endocast of the animal, which gave an indication of the brain size. The endocast showed that the brain was indeed very small, maybe the smallest among the dinosaurs. The fact that an animal weighing over 4.5 metric tons (5 short tons) could have a brain of no more than 80 grams (2.8 oz) contributed to the popular old idea that all dinosaurs were unintelligent, an idea now largely rejected. Actual brain anatomy in Stegosaurus is poorly known, but the brain itself was however small even for a dinosaur, fitting well with a slow herbivorous lifestyle and limited behavioural complexity.
Most of the information known about Stegosaurus comes from the remains of mature animals; however more recently juvenile remains of Stegosaurus have been found. One sub-adult specimen, discovered in 1994 in Wyoming, is 4.6 meters (15 ft) long and 2 meters (7 ft) high, and is estimated to have weighed 2.3 metric tons (2.6 short tons) while alive. It is on display in the University of Wyoming Geological Museum. Even smaller skeletons, 210 centimeters (6.9 ft) long and 80 centimeters (2.6 ft) tall at the back, are on display at the Denver Museum of Nature & Science.
Stegosaurus was the first-named genus of the family Stegosauridae. It is the type genus that gives its name to the family. Stegosauridae is one of two families within the infraorder Stegosauria, with the other being Huayangosauridae. Stegosauria lies within the Thyreophora, or armored dinosaurs, a suborder which also includes the more diverse ankylosaurs. The stegosaurs were a clade of animals similar in appearance, posture and shape that mainly differed in their array of spikes and plates. Among the closest relatives to Stegosaurus are Wuerhosaurus from China and Kentrosaurus from east Africa.
The origin of Stegosaurus is uncertain, as few remains of basal stegosaurs and their ancestors are known. Recently, stegosaurids have been shown to be present in the lower Morrison Formation, existing several million years before the occurrence of Stegosaurus itself, with the discovery of the related Hesperosaurus from the early Kimmeridgian. The earliest stegosaurid (the genus Lexovisaurus) is known from the Oxford Clay Formation of England and France, giving it an age of early to middle Callovian.
The earlier and more basal genus Huayangosaurus from the Middle Jurassic of China (some 165 million years ago) predates Stegosaurus by 20 million years and is the only genus in the family Huayangosauridae. Earlier still is Scelidosaurus, from Early Jurassic England, which lived approximately 190 million years ago. Interestingly, it possessed features of both stegosaurs and ankylosaurs. Emausaurus from Germany was another small quadruped, while Scutellosaurus from Arizona in the USA was an even earlier genus and was facultatively bipedal. These small, lightly armored dinosaurs were closely related to the direct ancestor of both stegosaurs and ankylosaurs. A trackway of a possible early armored dinosaur, from around 195 million years ago, has been found in France.
Stegosaurus, one of the many dinosaurs first collected and described in the Bone Wars, was originally named by Othniel Charles Marsh in 1877, from remains recovered north of Morrison, Colorado. These first bones became the holotype of Stegosaurus armatus. Marsh initially believed the remains were from an aquatic turtle-like animal, and the basis for its scientific name, 'roof(ed) lizard' was due to his early belief that the plates lay flat over the animal's back, overlapping like the shingles (tiles) on a roof. A wealth of Stegosaurus material was recovered over the next few years and Marsh published several papers on the genus. Initially, several species were described. However, many of these have since been considered to be invalid or synonymous with existing species, leaving two well-known and one poorly known species. Confirmed Stegosaurus remains have been found in the Morrison Formation's stratigraphic zones 2–6, with additional remains possibly referrable to Stegosaurus recovered from stratigraphic zone 1.
Susannah Maidment and colleagues in 2008 proposed extensive alterations to the taxonomy of Stegosaurus. They advocated synonymizing S. stenops and S. ungulatus (sometimes considered valid; see below) with S. armatus, and sinking Hesperosaurus and Wuerhosaurus into Stegosaurus, with their type species becoming Stegosaurus mjosi and Stegosaurus homheni, respectively. They regarded S. longispinus as dubious. Thus, their conception of Stegosaurus would include three valid species (S. armatus, S. homheni, and S. mjosi) and would range from the Late Jurassic of North America and Europe to the Early Cretaceous of Asia. However, this classification scheme has not generally been followed by other researchers. Galton, for example, has stated that Wuerhosaurus differs enough from Stegosaurus to be retained as a distinct genus.
Stegosaurus was the largest stegosaur, possibly weighing up to 5,000 kilograms (5.5 short tons). Soon after its discovery, Marsh considered Stegosaurus to have been bipedal, due to its short forelimbs. He had changed his mind however, by 1891, after considering the heavy build of the animal. Although Stegosaurus is undoubtedly now considered to have been quadrupedal, there has been some discussion over whether it could have reared up on its hind legs, using its tail to form a tripod with its hind limbs and browsing for higher foliage. This has been proposed by Bakker and opposed by Carpenter.
Stegosaurus did have very short forelimbs, in relation to its hind legs. Furthermore, within the hindlimbs, the lower section (comprising the tibia and fibula) was short compared with the femur. This suggests that it couldn't walk very fast, as the stride of the back legs at speed would have overtaken the front legs, giving a maximum speed of 6–7 kilometers per hour (4–5 mi/hr).
Tracks discovered by Matthew Mossbrucker (Morrison Natural History Museum, Colorado) suggest that Stegosaurus lived in multi-age herds. One group of tracks is interpreted as showing four or five baby stegosaurs moving in the same direction, while another has a juvenile stegosaur track with an adult track overprinting it. Stegosaurus may have preferred drier settings than other common Morrison Formation dinosaurs, such as Allosaurus, Apatosaurus, Camarasaurus, and Diplodocus.
Juveniles of Stegosaurus have been preserved, probably showing the growth of the genus. Kentrosaurus is also known from juvenile specimens, and they can be identified as different genders. The two juveniles are both relatively small, with the smaller individual being 1.5 m (4.9 ft) long, and the larger having a length of 2.6 m (8.5 ft). The specimens can be identified as not mature because they lack the fusion of the scapula and coracoid, and the lower hind limbs. Also, the pelvic region of the specimens are similar to Kentrosaurus juveniles.
The most recognizable features of Stegosaurus are its dermal plates, which consisted of 17 separate flat plates. These were highly modified osteoderms (bony-cored scales), similar to those seen in crocodiles and many lizards today. They were not directly attached to the animal's skeleton, instead arising from the skin. The largest plates were found over the animal's hips and measured 60 centimeters (2 ft) wide and 60 centimeters tall.
One of the major subjects of books and articles about Stegosaurus is the plate arrangement. The argument has been a major one in the history of dinosaur reconstruction. Four possible plate arrangements have been mooted over the years:
In the past, some palaeontologists, notably Robert Bakker, have speculated that the plates may have been mobile to some degree, although others disagree. Bakker suggested that the plates were the bony cores of pointed horn-covered plates that a Stegosaurus could flip from one side to another in order to present a predator with an array of spikes and blades that would impede it from closing sufficiently to attack the Stegosaurus effectively. The plates would naturally sag to the sides of the Stegosaurus, the length of the plates reflecting the width of the animal at that point along its spine. His reasoning for these plates to be covered in horn is that the surface fossilized plates have a resemblance to the bony cores of horns in other animals known or thought to bear horns, and his reasoning for the plates to be defensive in nature is that the plates had insufficient width for them to stand erect easily in such a manner as to be useful in display without continuous muscular effort. Stegosaurus stenops also had disk-shaped plates, on its hips.
The function of the plates has been much debated. Initially thought of as some form of armor, they appear to have been too fragile and ill-placed for defensive purposes, leaving the animal's sides unprotected. The plates' large size suggests that they may have served to increase the apparent height of the animal, in order either to intimidate enemies or to impress other members of the same species, in some form of sexual display, although both male and female specimens seemed to have had the same plates. More recently, researchers have proposed that they may have helped to control the body temperature of the animal, in a similar way to the sails of the pelycosaurs Dimetrodon and Edaphosaurus (and modern elephant and rabbit ears). The plates had blood vessels running through grooves and air flowing around the plates would have cooled the blood. 2010 structural comparisons of Stegosaurus plates to Alligator osteoderms seems to support the conclusion that the potential for a thermoregulatory role in the plates of Stegosaurus definitely exists. This hypothesis has been seriously questioned, since its closest relatives, such as Kentrosaurus, had more low surface area spikes than plates, implying that cooling was not important enough to require specialized structural formations such as plates. Another possible function is that the plates may have helped the animal increase heat absorption from the sun. Since there was a cooling trend towards the end of the Jurassic, a large ectothermic reptile might have used the increased surface area afforded by the plates to absorb radiation from the sun.
The publication of "Growth and Function of Stegosaurus Plates" by Buffrénil, et al. in 1986 marked a major step out of the realm of speculation and into the realm of science, with its microscopic analyses of multiple Stegosaurus plate specimens, proving unequivocally "extreme vascularization of the outer layer of bone," which was seen by Buffrénil as further evidence the plates "acted as thermoregulatory devices." Later, more comprehensive histological surveys of plate microstructure attributed the vascularization to the need to transport nutrients for rapid plate growth, asserting the plates' physiology, if beneficial, was a side-benefit secondary to their primary function, identification and display.
The latest explanation for Stegosaurus plates' heavily vascular design is that, when under threat, blood could rush into the plates, causing them to "blush" which would add a colorful, red warning, "embellishing" the visual threat display. This "blushing capacity," instead of thermoregulatory functions, may be the plates' purpose, though the two functions certainly could have co-existed. That Stegosaurus plates could "blush" has become the predominant interpretation of plate function since the late 20th century, and is even depicted in the popular BBC documentary Walking with Dinosaurs, with the sudden reddening of the plates used in conjunction with threatening swings of the spiked tail to intimidate and confuse an attacking Allosaurus. It is also possible that this blushing could have been used to attract mates. A study published in 2005 supports the idea of their use in species identification. Researchers believe this may be the function of other unique anatomical features, found in various dinosaur species.
There has been debate about whether the tail spikes were used for display only, as posited by Gilmore in 1914 or used as a weapon. Robert Bakker noted the tail was likely to have been much more flexible than that of other dinosaurs, as it lacked ossified tendons, thus lending credence to the idea of the tail as a weapon. However, as Carpenter has noted, the plates overlap so many tail vertebrae that movement would be limited. Bakker also observed that Stegosaurus could have maneuvered its rear easily, by keeping its large hindlimbs stationary and pushing off with its very powerfully muscled but short forelimbs, allowing it to swivel deftly to deal with attack. More recently, a study of tail spikes by McWhinney et al., which showed a high incidence of trauma-related damage, lends more weight to the position that the spikes were indeed used in combat. This study showed that 9.8% of Stegosaurus specimens examined had injuries to their tail spikes. Additional support for this idea was a punctured tail vertebra of an Allosaurus into which a tail spike fit perfectly.
Stegosaurus stenops had four dermal spikes, each about 60–90 centimeters (2–3 ft) long. Discoveries of articulated stegosaur armor show that, at least in some species, these spikes protruded horizontally from the tail, not vertically as is often depicted. Initially, Marsh described S. armatus as having eight spikes in its tail, unlike S. stenops. However, recent research re-examined this and concluded this species also had four.
Soon after describing Stegosaurus, Marsh noted a large canal in the hip region of the spinal cord, which could have accommodated a structure up to 20 times larger than the famously small brain. This has led to the influential idea that dinosaurs like Stegosaurus had a "second brain" in the tail, which may have been responsible for controlling reflexes in the rear portion of the body. It has also been suggested that this "brain" might have given a Stegosaurus a temporary boost when it was under threat from predators. More recently, it has been argued that this space (also found in sauropods) may have been the location of a glycogen body, a structure in living birds whose function is not definitely known but which is postulated to facilitate the supply of glycogen to the animal's nervous system.
Stegosaurus and related genera were herbivores. However, their teeth and jaws are very different from those of other herbivorous ornithischian dinosaurs, suggesting a different feeding strategy that is not yet well understood. The other ornithischians possessed teeth capable of grinding plant material and a jaw structure capable of movements in planes other than simply orthal (i.e. not only the fused up-down motion stegosaur jaws were likely limited to). Unlike the sturdy jaws and grinding teeth common to its fellow ornithischians, Stegosaurus (and all stegosaurians) had small, peg-shaped teeth that have been observed with horizontal wear facets associated with tooth-food contact and their unusual jaws were probably capable of only orthal (up-down) movements. Their teeth were "not tightly pressed together in a block for efficient grinding," and there is no evidence in the fossil record of stegosaurians using gastroliths—the stone(s) some dinosaurs (and some present-day bird species) ingested—to aid the grinding process, so how exactly Stegosaurus obtained and processed the amount of plant material required to sustain its size remains "poorly understood."
The stegosaurians were geographically widely distributed in the late Jurassic. Palaeontologists believe it would have eaten plants such as mosses, ferns, horsetails, cycads and conifers or fruits. Grazing on grasses, seen in many modern mammalian herbivores, would not have been possible for Stegosaurus, as grasses did not evolve until late into the Cretaceous Period, long after Stegosaurus had become extinct.
One hypothesized feeding behavior strategy considers them to be low-level browsers, eating low-growing fruit of various non-flowering plants, as well as foliage. This scenario has Stegosaurus foraging at most one meter above the ground. On the other hand, if Stegosaurus could have raised itself on two legs, as suggested by Bakker, then it could have browsed on vegetation and fruits quite high up, with adults being able to forage up to 6 meters (20 ft) above the ground.
A detailed computer analysis of the biomechanics of Stegosaurus's feeding behavior was performed in 2010, using two different three-dimensional models of Stegosaurus teeth given realistic physics and properties. Bite force was also calculated using these models and the known skull proportions of the animal as well as simulated tree branches of different size and hardness. The resultant bite forces calculated for Stegosaurus were 140.1 N (Newton), 183.7 N, and 275 N (for anterior, middle and posterior teeth, respectively), which means that its bite force was less than half that of a Labrador retriever. This indicates that Stegosaurus could have easily bitten through smaller green branches, but would have had difficulty with anything over 12 mm in diameter. Stegosaurus, therefore, probably browsed primarily among smaller twigs and foliage, and would have been unable to handle larger plant parts unless the animal was capable of biting much more efficiently than predicted in this study.
The Morrison Formation is interpreted as a semiarid environment with distinct wet and dry seasons, and flat floodplains. Vegetation varied from river-lining forests of conifers, tree ferns, and ferns (gallery forests), to fern savannas with occasional trees such as the Araucaria-like conifer Brachyphyllum.The flora of the period has been revealed by fossils of green algae, fungi, mosses, horsetails, ferns, cycads, ginkgoes, and several families of conifers. Animal fossils discovered include bivalves, snails, ray-finned fishes, frogs, salamanders, turtles, sphenodonts, lizards, terrestrial and aquatic crocodylomorphans, several species of pterosaur, numerous dinosaur species, and early mammals such as docodonts, multituberculates, symmetrodonts, and triconodonts.
Dinosaurs that lived alongside Stegosaurus included theropods Allosaurus, Saurophaganax, Torvosaurus, Ceratosaurus, Marshosaurus, Stokesosaurus and Ornitholestes. Sauropods dominated the region, and included Brachiosaurus, Apatosaurus, Diplodocus, Camarasaurus, and Barosaurus. Other ornithischians included Camptosaurus, Gargoyleosaurus,Dryosaurus, and Othnielosaurus. Stegosaurus is commonly found at the same sites as Allosaurus, Apatosaurus, Camarasaurus, and Diplodocus.
Proportions and anatomy of endocasts of Stegosaurus vary little from those of ancestral archosaurs, with an elongated shape, large olfractory lobes, and extremely narrow cerebral hemispheres. Lack of surface detail suggest that the brain did not fill the braincase. EQ estimates are below 0,6 (Hoppson, 1977), agreeing well with predictions of a slow herbivorous lifestyle.
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