- Related Topics:
- saurischian
- ornithischian
- theropod
- Sauropodomorpha
- cerapod
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During the decades that followed Owen’s announcement, many other kinds of dinosaurs were discovered and named in England and Europe: Massospondylus in 1854, Scelidosaurus in 1859, Bothriospondylus in 1875, and Omosaurus in 1877. Popular fascination with the giant reptiles grew, reaching a peak in the 1850s with the first attempts to reconstruct the three animals on which Owen based Dinosauria—Iguanodon, Megalosaurus, and Hylaeosaurus—for the first world exposition, the Great Exhibition of 1851 in London’s Crystal Palace. A sculptor under Owen’s direction (Waterhouse Hawkins) created life-size models of these two genera, and in 1854 they were displayed together with models of other extinct and living reptiles, such as plesiosaurs, ichthyosaurs, and crocodiles.
By the 1850s it had become evident that the reptile fauna of the Mesozoic Era was far more diverse and complex than it is today. The first important attempt to establish an informative classification of the dinosaurs was made by the English biologist T.H. Huxley as early as 1868. Because he observed that these animals had legs similar to birds as well as other birdlike features, he established a new order called Ornithoscelida. He divided the order into two suborders. Dinosauria was the first and included the iguanodonts, the large carnivores (or megalosaurids), and the armoured forms (including Scelidosaurus). Compsognatha was the second order, named for the very small birdlike carnivore Compsognathus.
Huxley’s classification was replaced by a radically new scheme proposed in 1887 by his fellow Englishman H.G. Seeley, who noticed that all dinosaurs possessed one of two distinctive pelvic designs, one like that of birds and the other like that of reptiles. Accordingly, he divided the dinosaurs into the orders Ornithischia (having a birdlike pelvis) and Saurischia (having a reptilian pelvis). Ornithischia included four suborders: Ornithopoda (Iguanodon and similar herbivores), Stegosauria (plated forms), Ankylosauria (Hylaeosaurus and other armoured forms), and Ceratopsia (horned dinosaurs, just then being discovered in North America). Seeley’s second order, the Saurischia, included all the carnivorous dinosaurs, such as Megalosaurus and Compsognathus, as well as the giant herbivorous sauropods, including Cetiosaurus and several immense “brontosaur” types that were turning up in North America. In erecting Saurischia and Ornithischia, Seeley cast doubt on the idea that Dinosauria was a natural grouping of these animals. This uncertainty persisted for a century thereafter, but it is now understood that the two groups share unique features that indeed make the Dinosauria a natural group.
In 1878 a spectacular discovery was made in the town of Bernissart, Belgium, where several dozen complete articulated skeletons of Iguanodon were accidentally uncovered in a coal mine during the course of mining operations. Under the direction of the Royal Institute of Natural Science of Belgium, thousands of bones were retrieved and carefully restored over a period of many years. The first skeleton was placed on exhibit in 1883, and today the public can view an impressive herd of Iguanodon. The discovery of these multiple remains gave the first hint that at least some dinosaurs may have traveled in groups and showed clearly that some dinosaurs were bipedal (walking on two legs). The supervisor of this extraordinary project was Louis Dollo, a zoologist who was to spend most of his life studying Iguanodon, working out its structure, and speculating on its living habits.f
American hunting expeditions
England and Europe produced most of the early discoveries and students of dinosaurs, but North America soon began to contribute a large share of both. One leading student of fossils was Joseph Leidy of the Academy of Natural Sciences in Philadelphia, who named some of the earliest dinosaurs found in America, including Palaeoscincus, Trachodon, Troodon, and Deinodon. Unfortunately, some names given by Leidy are no longer used, because they were based on such fragmentary and undiagnostic material. Leidy is perhaps best known for his study and description of the first dinosaur skeleton to be recognized in North America, that of a duckbill, or hadrosaur, found at Haddonfield, New Jersey, in 1858, which he named Hadrosaurus foulkii. Leidy’s inference that this animal was probably amphibious influenced views of dinosaur life for the next century.
Two Americans whose work during the second half of the 19th century had worldwide impact on the science of paleontology in general, and the growing knowledge of dinosaurs in particular, were O.C. Marsh of Yale College and E.D. Cope of Haverford College, the University of Pennsylvania, and the Academy of Natural Sciences in Philadelphia. All previous dinosaur remains had been discovered by accident in well-populated regions with temperate, moist climates, but Cope and Marsh astutely focused their attention on the wide arid expanses of bare exposed rock in western North America. In their intense quest to find and name new dinosaurs, these scientific pioneers became fierce and unfriendly rivals.
Marsh’s field parties explored widely, exploiting dozens of now famous areas, among them Yale’s sites at Morrison and Canon City, Colorado, and, most important, Como Bluff in southeastern Wyoming. The discovery of Como Bluff in 1877 was a momentous event in the history of paleontology that generated a burst of exploration and study as well as widespread public enthusiasm for dinosaurs. Como Bluff brought to light one of the greatest assemblages of dinosaurs, both small and gigantic, ever found. For decades the site went on producing the first known specimens of Late Jurassic Epoch (163.5 million to 145 million years ago) dinosaurs such as Stegosaurus, Camptosaurus, Camarasaurus, Laosaurus, Coelurus, and others. From the Morrison site came the original specimens of Allosaurus, Diplodocus, Atlantosaurus, and Brontosaurus (later renamed Apatosaurus). Canon City provided bones of a host of dinosaurs, including Stegosaurus, Brachiosaurus, Allosaurus, and Camptosaurus.
Another major historic site was the Lance Creek area of northeastern Wyoming, where J.B. Hatcher discovered and collected dozens of Late Cretaceous horned dinosaur remains for Marsh and for Yale College, among them the first specimens of Triceratops and Torosaurus. Marsh was aided in his work at these and other localities by the skills and efforts of many other collaborators like Hatcher—William Reed, Benjamin Mudge, Arthur Lakes, William Phelps, and Samuel Wendell Williston, to name a few. Marsh’s specimens now form the core of the Mesozoic collections at the National Museum of Natural History of the Smithsonian Institution and the Peabody Museum of Natural History at Yale University.
Cope’s dinosaur explorations ranged as far as, or farther than, Marsh’s, and his interests encompassed a wider variety of fossils. Owing to a number of circumstances, however, Cope’s dinosaur discoveries were fewer and his collections far less complete than those of Marsh. Perhaps his most notable achievement was finding and proposing the names for Coelophysis and Monoclonius. Cope’s dinosaur explorations began in the eastern badlands of Montana, where he discovered Monoclonius in the Judith River Formation of the Late Cretaceous Epoch (100.5 million to 66 million years ago). Accompanying him there was a talented young assistant, Charles H. Sternberg. Later Sternberg and his three sons went on to recover countless dinosaur skeletons from the Oldman and Edmonton formations of the Late Cretaceous along the Red Deer River of Alberta, Canada.
Dinosaur ancestors
During the early decades of dinosaur discoveries, little thought was given to their evolutionary ancestry. Not only were the few specimens known unlike any living animal, but they were so different from any other reptiles that it was difficult to discern much about their relationships. Early on it was recognized that, as a group, dinosaurs appear to be most closely allied to crocodilians, though T.H. Huxley had proposed in the 1860s that dinosaurs and birds must have had a very close common ancestor in the distant past. Three anatomic features—socketed teeth, a skull with two large holes (diapsid), and another hole in the lower jaw—are present in both crocodiles and dinosaurs. The earliest crocodilians occurred nearly simultaneously with the first known dinosaurs, so neither could have given rise to the other. It was long thought that the most likely ancestry of dinosaurs could be found within a poorly understood group of Triassic reptiles termed thecodontians (“socket-toothed reptiles”). Today it is recognized that “thecodontian” is simply a name for the basal, or most primitive, members of the archosaurs (“ruling reptiles”), a group that is distinguished by the three anatomic features mentioned above and that includes dinosaurs, pterosaurs (flying reptiles), crocodiles, and their extinct relatives.
An early candidate for the ancestor of dinosaurs was a small basal archosaur from the Early Triassic Epoch (252.2 million to 247.2 million years ago) of South Africa called Euparkeria. New discoveries suggest creatures that are even more dinosaur-like from the Middle Triassic (247.2 million to 237 million years ago) and from an early portion of the Late Triassic (237 million to 201.3 million years ago) of South America; these include Lagerpeton, Lagosuchus, Pseudolagosuchus, and Lewisuchus. Other forms, such as Nyasasaurus and Asilisaurus, date from the Middle Triassic of East Africa; Nyasasaurus is considered by some to be the oldest known member of Dinosauria. Other South American forms such as Eoraptor and Herrerasaurus are particularly dinosaurian in appearance and are sometimes considered dinosaurs.
The earliest appearance of “true dinosaurs” is almost impossible to pinpoint, since it can never be known with certainty whether the very first (or last) specimen of any kind of organism has been found. The succession of deposits containing fossils is discontinuous and contains many gaps; even within these deposits, the fossil record of dinosaurs and other creatures contained within is far from complete. Further complicating matters is that evolution from ancestral to descendant form is usually a stepwise process. Consequently, as more and more gaps are filled between the first dinosaurs and other archosaurs, the number of features distinguishing them becomes smaller and smaller. Currently, paleontologists define dinosaurs as Triceratops (representing Ornithischia), birds (the most recent representatives of the Saurischia), and all the descendants of their most recent common ancestor. That common ancestor apparently had a suite of features not present in other dinosaur relatives, including the loss of the prefrontal bone above the eye, a long deltopectoral crest on the humerus, three or fewer joints on the fourth finger of the hand, three or more hip vertebrae, a fully open hip socket, and a cnemial crest on the shin bone (tibia). These features were passed on and modified in the descendants of the first dinosaurs. Compared with most of their contemporaries, dinosaurs had an improved stance and posture with a resulting improved gait and, in several independent lineages, an overall increase in size. They also were more efficient at gathering food and processing it and apparently had higher metabolic rates and cardiovascular nourishment. All these trends, individually or in concert, probably contributed to the collective success of dinosaurs, which resulted in their dominance among the terrestrial animals of the Mesozoic.
Modern studies
During the first century or more of dinosaur awareness, workers in the field more or less concentrated on the search for new specimens and new types. Their discoveries then required detailed description and analysis, followed by comparisons with other known dinosaurs in order to classify the new finds and develop hypotheses about evolutionary relationships. These pursuits continue, but newer methods of exploration and analysis have been adopted. Emphasis has shifted from purely descriptive procedures to analyses of relationships by using the methods of cladistics, which dispenses with the traditional taxonomic hierarchy in favour of “phylogenetic trees” that are more explicit about evolutionary relationships. Phylogenetic analyses also help us to understand how certain features evolved in groups of dinosaurs and give us insight into their possible functions. For example, in the evolution of horned dinosaurs (ceratopsians), it can be seen that the beak evolved first, followed by the frill, and finally the nose and eye horns, which were differently developed in different groups. The hypothesis that the frill was widely used in defense by ceratopsians such as Protoceratops can thus be tested phylogenetically. On this basis, the idea is now generally rejected because the frill was basically just an open rim of bone in nearly all ceratopsians except Triceratops, which is often pictured charging like a rhinoceros.
Functional anatomic studies extensively use analogous traits of present-day animals that, along with both mechanical and theoretical models, make it possible to visualize certain aspects of extinct animals. For example, estimates of normal walking and maximum running speeds can be calculated on the basis of the analysis of trackways, which can then be combined with biomechanical examination of the legs and joints and reconstruction of limb musculature. Similar methods have been applied to jaw mechanisms and tooth wear patterns to obtain a better understanding of feeding habits and capabilities.

The soft parts of dinosaurs are only imperfectly known. Original colours and patterns cannot be known, but skin textures have occasionally been preserved. Most show a knobby or pebbly surface rather than a scaly texture as in most living reptiles. Impressions of internal organs are rarely preserved, but, increasingly, records of filaments and feathers have been found on some dinosaurs. The discovery of Kulindadromeus zabaikalicus, an early ornithischian dinosaur whose remains show evidence of featherlike structures on its limbs, suggests that feathers may even have been widespread among the dinosaurs. Gastroliths (“stomach stones”) used for processing food in the gizzard have been recovered from a variety of dinosaurs.