|狭脸剑龙“苏菲”（NHMUK PV R36730）的化石，位于伦敦自然历史博物馆|
剑龙（属名：Stegosaurus，发音：//）是植食性装甲类恐龙的一个属，生存于距今1.55亿年至1.5亿年的晚侏罗世启莫里阶至提通阶早期，化石产自美国西部和葡萄牙，目前已有80多件残骸被发现。本属含有3个公认物种，分别为狭脸剑龙（S. stenops）、蹄足剑龙（S. ungulatus）和沟纹剑龙（S. sulcatus），三者皆生存于莫里逊组。剑龙与雷龙、梁龙、腕龙、异特龙和角鼻龙共享栖息地，后两者可能会捕食剑龙。
剑龙遗骸最早由奥塞内尔·查利斯·马什（Othniel Charles Marsh）在骨头大战期间发现于恐龙岭国家地标（Dinosaur Ridge National Landmark）。第一批已知骨骼过于零碎，因此这种动物的真实面貌（包括姿势与骨板的排列方式）在多年以后才得到深入了解。尽管剑龙在书籍和电影中很受欢迎，但其骨骼直到20世纪中期才成为大型自然历史博物馆的主要展品，由于缺乏完整骨骼，许多博物馆不得不将几个不同标本拼接以进行展示。剑龙是一种广为人所知的恐龙，在电影、邮票和其它媒体中都有出现。
剑龙是发现于骨头大战期间的恐龙物种之一，由奥塞内尔·查利斯·马什在1877年根据科罗拉多州莫里逊北部发现的遗骸所命名。这些最早发现的骨骼随后成为剑龙的正模标本。马什将其叙述成类似海龟的水生动物，并将属名取为Stegosaurus（“屋顶蜥蜴”），因为他最初认为这些骨板平铺在动物背上，像屋顶上的瓦片般重叠。在接下来的几年里，人们发现了大量剑龙化石，马什也在1877年至1897年间发表了几篇关于剑龙的论文。1878年，爱德华·德林克·科普（Edward Drinker Cope）根据花园公园乳头山附近科普3号采石场中的化石碎片而命名了另一种剑龙类――Hypsirhophus。许多后期研究人员认为Hypsirhophus是剑龙的异名，尽管彼得·加尔东在2010年指出两者的椎骨存在差异。
马什于1879年命名了第二种剑龙，并对目前收集到的所有化石进行更详细的叙述。1881年，他将一块髋骨命名为第三个物种――近亲剑龙（Stegosaurus "affinis"）。人们普遍认为该物种的叙述不充分，因此将其视为裸名。其正模标本后来遗失。马什继续收集和研究新的剑龙标本，并在1887年命名了三个新种：狭脸剑龙（Stegosarus stenops）、双丛剑龙（S. duplex）和沟纹剑龙（S. sulcatus）。尽管还没有完全准备好，但几乎完整的剑龙标本让马什完成了重建骨架的首次尝试。马什于1891年出版第一本重建书，内容是用狭脸剑龙化石来填补蹄足剑龙（S. ungulatus）化石的缺失部分。然而，理查德·莱德克在1893年误将马什的画重新发布并标名为Hypsirhophus。
下一个被命名的剑龙物种是马氏剑龙（S. marshi），由弗雷德里克·卢卡斯（Frederick Lucas）叙述于1901年。卢卡斯在同年晚些时候将该物种建立为新属装甲龙。卢卡斯还重新研究了剑龙的生前外观问题并得出结论：骨板成对排列，沿背部分成两排且位于肋骨基部上方。卢卡斯委托查尔斯·耐特（Charles R. Knight）根据他的新解释制作蹄足剑龙的复原图。然而，卢卡斯在第二年写道，他现在相信剑龙的骨板可能是交错排列的。1910年，理查德·斯旺·卢尔（Richard Swann Lull）认为狭脸剑龙的骨板交替形式可能是由于死后的骨骼移所位造成。他在皮博迪自然史博物馆（Peabody Museum of Natural History）带领众人建成有史以来第一座剑龙骨架，并将骨板成对摆放。查尔斯·惠特尼·吉尔摩（Charles Wihtney Gilmore）于1914年对卢尔的解释表示反对，并指出一些狭脸剑龙标本（包括现已完全准备好的正模标本）的骨板皆成排交替保存并靠近背部顶端，且没有证据表明骨板位置在石化过程中发生过移动。吉尔摩和卢卡斯的解释成为普遍接受的标准。1924年，皮博迪博物馆的剑龙骨架亦被改动以反映这一点。
- 到1891年，马什发表了一张更广为人知的剑龙复原图，其背部只有一排骨板。这种复原很早就被废弃，因为马什不太了解骨板是如何嵌入皮肤，在这种排列方式中，骨板被认为重叠过多。20世纪80年代，斯蒂芬·泽尔卡斯（Stephen Czerkas）根据鬣蜥背棘的排列方式对其进行修改并重新使用。
- 蹄足剑龙（Stegosaurus ungulatus）意为“有蹄的屋顶蜥蜴”，由马什在1879年根据怀俄明州科摩崖（12号采石场，靠近Robber's Roost）发现的遗骸所命名，可能是狭脸剑龙的异名。该物种长达9米（29.5英尺），为本属最长的物种。在葡萄牙发现的一件零碎标本已初步确认为该物种，其年代可追溯至启莫里阶晚期至提通阶早期。蹄足剑龙可根据更长的后肢、成比例缩小且末端更尖、基部更宽、尖部更窄的骨板和尾刺前方几个小而平的刺状骨板而区别于狭脸剑龙，这些刺状骨板似乎是成对分布的，因为至少有一对骨板形状相同且对称；蹄足剑龙的股骨和髋骨似乎也长于其它物种。正模标本中发现了八根尖刺，尽管它们分散在原来的位置，但通常被解释为表明这只动物具有四对尾刺，因为目前并未发现保存有完整尾刺的标本，也没有发现同时保存八根尾刺的其他标本。这对额外的尖刺可能来自另一个体，虽然没有发现其它额外骨骸，但如果在原址进行更多挖掘，这些骨头可能会被发现。其它采石场的标本（例如13号采石场发现的尾巴，现为美国自然历史博物馆合成骨架AMNH 650的一部分）根据尾椎形状而归类于蹄足剑龙，然而，这些标本也只有四根尾刺保存下来。1910年，理查德·斯旺·卢尔（Richard Swann Lull）将正模标本（YPM 1853）并入皮博迪自然史博物馆（Peabody Museum of Natural History）中的世界上第一具剑龙骨架。最初，骨板被成对安装在肋骨底部上方，但在1924年被重新安装并沿背部中线交错排列。美国国家自然历史博物馆从同一采石场发现的其他标本包括尾椎和一个额外的大型骨板（USNM 7414），与YPM 1853属于同一个体。
- Stegosaurus stenops, meaning "narrow-faced roof lizard", was named by Marsh in 1887, with the holotype having been collected by Marshall Felch at Garden Park, north of Cañon City, Colorado, in 1886. This is the best-known species of Stegosaurus, mainly because its remains include at least one complete articulated skeleton. It had proportionately large, broad plates and rounded tail plates. Articulated specimens show that the plates were arranged alternating in a staggered double row. S. stenops is known from at least 50 partial skeletons of adults and juveniles, one complete skull, and four partial skulls. It was shorter than other species, at 7米（23英尺）. Found in the Morrison Formation, Colorado, Wyoming, and Utah.
- Stegosaurus sulcatus, meaning "furrowed roof lizard", was described by Marsh in 1887 based on a partial skeleton. It has traditionally been considered a synonym of S. armatus, though more recent studies suggest it is not. S. sulcatus is distinguished mainly by its unusually large, furrowed spikes with very large bases. A spike associated with the type specimen, originally thought to be a tail spike, may in fact come from the shoulder or hip, since its base is much larger than the corresponding tail vertebrae. A review published by Maidment and colleagues in 2008 regarded it as an indeterminate species possibly not even belonging to Stegosaurus at all, but to a different genus. Peter Galton suggested it should be considered a valid species due to its unique spikes.
Susannah Maidment and colleagues in 2008 proposed extensive alterations to the taxonomy of Stegosaurus. They advocated synonymizing S. stenops and S. ungulatus 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 was not followed by other researchers, and a 2017 cladistic analysis co-authored by Maidment with Thomas Raven rejects the synonymy of Hesperosaurus with Stegosaurus. In 2015, Maidment et al. revised their suggestion due to the recognition by Galton of S. armatus as a nomen dubium and its replacement by S. stenops as type species.
Doubtful species and junior synonyms[编辑]
- Stegosaurus armatus, meaning "armored roof lizard", was the first species to be found and the original type species named by O.C. Marsh in 1877. It is known from a partial skeleton, and more than 30 fragmentary specimens have been referred to it. However, the type specimen was very fragmentary, consisting only of a partial tail, hips, and leg, parts of some back vertebrae, and a single fragmentary plate (the presence of which was used to give the animal its name). No other plates or spikes were found, and the entire front half of the animal appears not to have been preserved. Because the type specimen is very fragmentary, it is extremely difficult to compare it with other species based on better specimens, and it is now generally considered to be a nomen dubium. Because of this, it was replaced by S. stenops as the type species of Stegosaurus in a ruling of the ICZN in 2013.
- Stegosaurus "affinis", named by Marsh in 1881, is only known from a pubis which has since been lost. Because Marsh did not provide an adequate description of the bone with which to distinguish a new species, this name is considered a nomen nudum.
- Diracodon laticeps was described by Marsh in 1881, from some jawbone fragments. Bakker resurrected D. laticeps in 1986 as a senior synonym of S. stenops, although others note that the material is not diagnostic and is only referable to Stegosaurus sp., making it a nomen dubium.
- Stegosaurus duplex, meaning "two plexus roof lizard" (in allusion to the greatly enlarged neural canal of the sacrum which Marsh characterized as a "posterior brain case"), was named by Marsh in 1887 (including the holotype specimen). The disarticulated bones were actually collected in 1879 by Edward Ashley at Como Bluff. Marsh initially distinguished it from S. ungulatus based on the fact that each sacral (hip) vertebra bore its own rib, which he claimed was unlike the anatomy of S. ungulatus; however, the sacrum of S. ungulatus had not actually been discovered. Marsh also suggested that S. duplex may have lacked armor, since no plates or spikes were found with the specimen, though a single spike may actually have been present nearby, and re-examination of the site maps has shown that the entire specimen was found highly disarticulated and scattered. It is generally considered a synonym of S. ungulatus today, and parts of the specimen were actually incorporated into the Peabody Museum S. ungulatus skeletal mount in 1910.
- Stegosaurus marshi, which was described by Lucas in 1901, was renamed Hoplitosaurus in 1902.
- Stegosaurus priscus, described by Nopcsa in 1911, was reassigned to Lexovisaurus, and is now the type species of Loricatosaurus.
- Stegosaurus longispinus was named by Charles W. Gilmore. It is now the type species of the genus Alcovasaurus.
- Stegosaurus madagascariensis from Madagascar is known solely from teeth and was described by Piveteau in 1926. The teeth were variously attributed to a stegosaur, the theropod Majungasaurus, a hadrosaur or even a crocodylian, but is now considered a possible ankylosaur.
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 individuals could grow up to 9米（29.5英尺） in length and 5.3～7公噸（5.8～7.7短噸） in weight, the various species of Stegosaurus were dwarfed by 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.
Most of the information known about Stegosaurus comes from the remains of mature animals; more recently, though, juvenile remains of Stegosaurus have been found. One subadult specimen, discovered in 1994 in Wyoming, is 4.6米（15.1英尺） long and 2米（6.6英尺） high, and is estimated to have weighed 2.4 metric tons (2.6 short tons) while alive. It is on display in the University of Wyoming Geological Museum.
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 likely replacement by a horny beak or rhamphotheca. The lower jaw had flat downward and upward extensions that would have completely hidden the teeth when viewed from the side, and these probably supported a turtle-like beak in life. The presence of a beak extended along much of the jaws may have precluded the presence of cheeks in these species. Such an extensive beak was probably unique to Stegosaurus and some other advanced stegosaurids among ornithischians, which usually had beaks restricted to the jaw tips. Other researchers have interpreted these ridges as modified versions of similar structures in other ornithischians which might have supported fleshy cheeks, rather than beaks. Stegosaurian teeth were small, triangular, and flat; wear facets show that they did grind their food.
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 the brain was indeed very small, the smallest proportionally of all dinosaur endocasts then known. The fact that an animal weighing over 4.5 metric tons (5 short tons) could have a brain of no more than 80 g（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 small even for a dinosaur, fitting well with a slow, herbivorous lifestyle and limited behavioral complexity.
In Stegosaurus stenops there are 27 bones in the vertebral column anterior to the sacrum, a varying number of vertebrae in the sacrum, with four in most subadults, and around 46 caudal (tail) vertebrae. The presacrals are divided into cervical (neck) and dorsal (back) vertebrae, with around 10 cervicals and 17 dorsals, the total number being one greater than in Hesperosaurus, two greater than Huayangosaurus, although Miragaia preserves 17 cervicals and an unknown number of dorsals. The first cervical vertebra is the axis bone, which is connected and often fused to the atlas bone. Farther posteriorly, the proportionately larger the cervicals become, although they do not change greatly in anything other than size. Past the first few dorsals, the centrum of the bones become more elongate front-to-back, and the transverse processes become more elevated dorsal. The sacrum of S. stenops includes four sacral vertebrae, but one of the dorsals is also incorporated into the structure. In some specimens of S. stenops, a caudal is also incorporated, as a caudosacral. In Hesperosaurus there are two dorsosacrals, and only four fused sacrals, but in Kentrosaurus there may be as many as seven vertebrae in the sacrum, with both dorsosacrals and caudosacrals. S. stenops preserves 46 caudal vertebrae, and up to 49, and along the series both the centrums and the neural spines become smaller, until the neural spines disappear at caudal 35. Around the middle of the tail, the neural spines become bifurcated, meaning they are divided near the top.
With multiple well-preserved skeletons, S. stenops preserves all regions of the body, including the limbs. The scapula (shoulder blade) is sub-rectangular, with a robust blade. Though it is not always perfectly preserved, the acromion ridge is slightly larger than in Kentrosaurus. The blade is relatively straight, although it curves towards the back. There is a small bump on the back of the blade, that would have served as the base of the triceps muscle. Articulated with the scapula, the coracoid is sub-circular. The hind feet each had three short toes, while each fore foot had five toes; only the inner two toes had a blunt hoof. The phalangeal formula is 2-2-2-2-1, meaning the innermost finger of the fore limb has two bones, the next has two, etc. All four limbs were supported by pads behind the toes. The fore limbs were much shorter than the stocky hind limbs, 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米（3.3英尺） above the ground.
The most recognizable features of Stegosaurus are its dermal plates, which consisted of between 17 and 22 separate plates and flat spines. 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 hips and could measure over 60 cm（24英寸） wide and 60 cm（24英寸） tall.
In a 2010 review of Stegosaurus species, Peter Galton suggested that the arrangement of the plates on the back may have varied between species, and that the pattern of plates as viewed in profile may have been important for species recognition. Galton noted that the plates in S. stenops have been found articulated in two staggered rows, rather than paired. Fewer S. ungulatus plates have been found, and none articulated, making the arrangement in this species more difficult to determine. However, the type specimen of S. ungulatus preserves two flattened spine-like plates from the tail that are nearly identical in shape and size, but are mirror images of each other, suggesting that at least these were arranged in pairs. Many of the plates are manifestly chiral and no two plates of the same size and shape have been found for an individual; however plates have been correlated between individuals. Well preserved integumentary impressions of the plates of Hesperosaurus show a smooth surface with long and parallel, shallow grooves. This indicates that the plates were covered in keratinous sheaths.
Stegosaurus was the first-named genus of the family Stegosauridae. It is the type genus that gives its name to the family. The Stegosauridae are one of two families within the infraorder Stegosauria, with the other being the Huayangosauridae. The infraorder 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 – Mya) antedates Stegosaurus by 20 million years and is the only genus in the family Huayangosauridae. Earlier still is Scelidosaurus, from Early Jurassic England, which lived about 190 Mya. It possessed features of both stegosaurs and ankylosaurs. Emausaurus from Germany was another small quadruped, while Scutellosaurus from Arizona 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 Mya, has been found in France.
Posture and movement[编辑]
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, some discussion has occurred over whether it could have reared up on its hind legs, using its tail to form a tripod with its hind limbs, to browse for higher foliage. This has been proposed by Bakker and opposed by Carpenter. A study by Mallison (2010) found support for a rearing up posture in Kentrosaurus, though not for ability for the tail to act as a tripod.
Stegosaurus had short fore limbs in relation to its hind limb. Furthermore, within the hind limbs, the lower section (comprising the tibia and fibula) was short compared with the femur. This suggests it could not 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 km/h（3.7～4.3 mph）. Tracks discovered by Matthew Mossbrucker (Morrison Natural History Museum, Colorado) suggest that Stegosaurus lived and traveled in multiple-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.
As the plates would have been obstacles during copulation, it is possible the female stegosaur laid on her side as the male mounted her from behind. Another suggestion is that the female would stand on all fours but squat the fore limbs and raise the tail slightly to the side as the male rested its fore limbs on her broad pelvis. However, this would not explain how their reproductive organs can touch as there is no evidence of muscle attachments for a mobile penis nor a baculum in dinosaurs.
The function of Stegosaurus' plates has been much debated. Marsh suggested that they functioned as some form of armor, though Davitashvili (1961) disputed this, claiming that they were too fragile and ill-placed for defensive purposes, leaving the animal's sides unprotected. Nevertheless, others have continued to support a defensive function. Bakker suggested in 1986 that the plates were covered in horn comparing the surface of the fossilized plates to the bony cores of horns in other animals known or thought to bear horns. Christiansen and Tschopp (2010), having studied a well-preserved specimen of Hesperosaurus with skin impressions, concluded that the plates were covered in a keratin sheath which would have strengthened the plate as a whole and provided it with sharp cutting edges. Bakker stated that Stegosaurus could flip its osteoderms from one side to another to present a predator with an array of spikes and blades that would impede it from closing sufficiently to attack the Stegosaurus effectively. He contends that they had insufficient width for them to stand erect easily in such a manner as to be useful in display without continuous muscular effort. Mobility of the plates, however, has been disputed by other paleontologists.
Another possible function of the plates is 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. Buffrénil, et al. (1986) found "extreme vascularization of the outer layer of bone", which was seen as evidence that the plates "acted as thermoregulatory devices". Likewise, 2010 structural comparisons of Stegosaurus plates to Alligator osteoderms seem to support the conclusion that the potential for a thermoregulatory role in the plates of Stegosaurus definitely exists.
The thermoregulation hypothesis has been seriously questioned, since other stegosaurs 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. However, it has also been suggested that the plates could have helped the animal increase heat absorption from the sun. Since a cooling trend occurred 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. Christiansen and Tschopp (2010) state that the presence of a smooth, insulating keratin covering would have hampered thermoregulation, but such a function cannot be entirely ruled out as extant cattle and ducks use horns and beaks to dump excess heat despite the keratin covering. Histological surveys of plate microstructure attributed the vascularization to the need to transport nutrients for rapid plate growth.
The vascular system of the plates have been theorized to have played a role in threat displaying as Stegosaurus could have pumped blood into them, causing them to "blush" and give a colorful, red warning. However, Christiansen and Tschopp (2010) consider this unlikely, as stegosaur plates were covered in horn rather than skin. The plates' large size suggests that they may have served to increase the apparent height of the animal, either to intimidate enemies or to impress other members of the same species in some form of sexual display. A 2015 study of the shapes and sizes of Hesperosaurus plates suggested that they were sexually dimorphic, with wide plates belonging to males and taller plates belonging to females. Christiansen and Tschopp (2010) proposed that the display function would have been reinforced by the horny sheath which would have increased the visible surface and such horn structures are often brightly colored. Some have suggested that plates in stegosaurs were used to allow individuals to identify members of their species. The use of exaggerated structures in dinosaurs as species identification has been questioned, as no such function exists in modern species.
Thagomizer (tail spikes)[编辑]
Debate has been going on 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, movement would be limited. Bakker also observed that Stegosaurus could have maneuvered its rear easily, by keeping its large hind limbs 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 the 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 fits perfectly.
S. stenops had four dermal spikes, each about 60～90 cm（2.0～3.0英尺） long. Discoveries of articulated stegosaur armor show, at least in some species, these spikes protruded horizontally from the tail, not vertically as is often depicted. Initially, Marsh described S. ungulatus as having eight spikes in its tail, unlike S. stenops. However, recent research re-examined this and concluded this species also had four.
At one time, stegosaurs were described as having a "second brain" in their hips. 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. This "brain" was proposed to have given a Stegosaurus a temporary boost when it was under threat from predators.
This space, however, is more likely to have served other purposes. The sacro-lumbar expansion is not unique to stegosaurs, nor even sauropods. It is also present in birds. In their case, it contains what is called the glycogen body, a structure whose function is not definitely known, but which is postulated to facilitate the supply of glycogen to the animal's nervous system. It also may function as a balance organ, or reservoir of compounds to support the nervous system.
Juveniles of Stegosaurus have been preserved, probably showing the growth of the genus. The two juveniles are both relatively small, with the smaller individual being 1.5米（4.9英尺） long, and the larger having a length of 2.6米（8.5英尺）. 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. One 2009 study of Stegosaurus specimens of various sizes found that the plates and spikes had delayed histological growth in comparison to the skeleton and when the dinosaur reached maturity, growth in the osteoderms may have increased. A 2013 study concluded, based on the rapid deposition of highly vascularised fibrolamellar bone, that Kentrosaurus had a quicker growth rate than Stegosaurus, contradicting the general rule that larger dinosaurs grew faster than smaller ones.
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 to which stegosaur jaws were likely limited). 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 no evidence in the fossil record of stegosaurians indicates use of 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 widely distributed geographically 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 nonflowering plants, as well as foliage. This scenario has Stegosaurus foraging at most 1 m above the ground. Conversely, 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米（20英尺） 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 newtons (N), 183.7 N, and 275 N (for anterior, middle and posterior teeth, respectively), which means its bite force was less than half that of a Labrador retriever. 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. However, a 2016 study indicates that Stegosaurus's bite strength was stronger than previously believed. Comparisons were made between it (represented by a specimen known as "Sophie" from the United Kingdom's Natural History Museum) and two other herbivorous dinosaurs; Erlikosaurus and Plateosaurus to determine if all three had similar bite forces and similar niches. Based on the results of the study, it was revealed that Stegosaurus had a bite similar in strength to that of modern herbivorous mammals, in particular, cattle and sheep. Based on this data, it is likely Stegosaurus also ate woodier, tougher plants such as cycads, perhaps even acting as a means of spreading cycad seeds.
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, ginkoes, and several families of conifers. Animal fossils discovered include bivalves, snails, ray-finned fishes, frogs, salamanders, turtles like Dorsetochelys, sphenodonts, lizards, terrestrial and aquatic crocodylomorphans like Hoplosuchus, several species of pterosaurs such as Harpactognathus and Mesadactylus, numerous dinosaur species, and early mammals such as docodonts (like Docodon), multituberculates, symmetrodonts, and triconodonts.
Dinosaurs that lived alongside Stegosaurus included theropods Allosaurus, Saurophaganax, Torvosaurus, Ceratosaurus, Marshosaurus, Stokesosaurus, Ornitholestes, Coelurus and Tanycolagreus. Sauropods dominated the region, and included Brachiosaurus, Apatosaurus, Diplodocus, Camarasaurus, and Barosaurus. Other ornithischians included Camptosaurus, Gargoyleosaurus, Dryosaurus, Othnielosaurus and Drinker. Stegosaurus is commonly found at the same sites as Allosaurus, Apatosaurus, Camarasaurus, and Diplodocus. Stegosaurus may have preferred drier settings than these other dinosaurs.
In popular culture[编辑]
One of the most recognizable of all dinosaurs, Stegosaurus has been depicted on film, in cartoons and comics and as children's toys. Due to the fragmentary nature of most early Stegosaurus fossil finds, it took many years before reasonably accurate restorations of this dinosaur could be produced. The earliest popular image of Stegosaurus was an engraving produced by A. Tobin for the November 1884 issue of Scientific American, which included the dinosaur amid a speculative Morrison age landscape. Tobin restored the Stegosaurus as bipedal and long-necked, with the plates arranged along the tail and the back covered in spikes. This covering of spikes might have been based on a misinterpretation of the teeth, which Marsh had noted were oddly shaped, cylindrical, and found scattered, such that he thought they might turn out to be small dermal spines.
Marsh published his more accurate skeletal reconstruction of Stegosaurus in 1891, and within a decade Stegosaurus had become among the most-illustrated types of dinosaur. Artist Charles R. Knight published his first illustration of Stegosaurus ungulatus based on Marsh's skeletal reconstruction in a November 1897 issue of The Century Magazine. This illustration would later go on to form the basis of the stop-motion puppet used in the 1933 film King Kong. Like Marsh's reconstruction, Knight's first restoration had a single row of large plates, though he next used a double row for his more well-known 1901 painting, produced under the direction of Frederic Lucas. Again under Lucas, Knight revised his version of Stegosaurus again two years later, producing a model with a staggered double row of plates. Knight would go on to paint a stegosaur with a staggered double plate row in 1927 for the Field Museum of Natural History, and was followed by Rudolph F. Zallinger, who painted Stegosaurus this way in his "Age of Reptiles" mural at the Peabody Museum in 1947.
Stegosaurus made its major public debut as a paper mache model commissioned by the U.S. National Museum of Natural History for the 1904 Louisiana Purchase Exposition. The model was based on Knight's latest miniature with the double row of staggered plates, and was exhibited in the United States Government Building at the exposition in St. Louis before being relocated to Portland, Oregon for the Lewis and Clark Centennial Exposition in 1905. The model was moved to the Smithsonian National Museum of Natural History (now the Arts and Industries Building) in Washington, D.C. along with other prehistory displays, and to the current National Museum of Natural History building in 1911. Following renovations to the museum in the 2010s, the model was moved once again for display at the Museum of the Earth in Ithaca, New York.
The popularity of Stegosaurus is owed partly to its prominent display in natural history museums. Though considered one of the most distinctive types of dinosaur, Stegosaurus displays were missing from a majority of museums during the first half of the 20th century, due largely to the disarticulated nature of most fossil specimens. Until 1918, the only mounted skeleton of Stegosaurus in the world was O. C. Marsh's type specimen of S. ungulatus at the Peabody Museum of Natural History, which was put on display in 1910. However, this mount was dismantled in 1917 when the old Peabody Museum building was demolished. This historically significant specimen was re-mounted ahead of the opening of the new Peabody Museum building in 1925. 1918 saw the completion of the second Stegosaurus mount, and the first depicting S. stenops. This mount was created under the direction of Charles Gilmore at the U.S. National Museum of Natural History. It was a composite of several skeletons, primarily USNM 6531, with proportions designed to closely follow the S. stenops type specimen, which had been on display in relief nearby since 1918. The aging mount was dismantled in 2003 and replaced with a cast in an updated pose in 2004. A third mounted skeleton of Stegosaurus, referred to S. stenops, was put on display at the American Museum of Natural History in 1932. Mounted under the direction of Charles J. Long, the American Museum mount was a composite consisting of partial remains filled in with replicas based on other specimens. In his article about the new mount for the museum's journal, Barnum Brown described (and disputed) the popular misconception that the Stegosaurus had a "second brain" in its hips. Another composite mount, using specimens referred to S. ungulatus collected from Dinosaur National Monument between 1920 and 1922, was put on display at the Carnegie Museum of Natural History in 1940.
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