In 1834, physician Johann Friedrich Engelhardt discovered some vertebrae and leg bones at Heroldsberg near Nuremberg, Germany. Three years later German palaeontologist Hermann von Meyer designated them as the type specimen of a new genus, Plateosaurus. Since then, remains of well over 100 individuals of Plateosaurus have been discovered at various locations throughout Europe.
Von Meyer's original short description from 1837 did not provide an etymology for Plateosaurus, but noted (as translated into English by British biologist Thomas Henry Huxley in 1870): "The bones belong to a gigantic Saurian, which, in virtue of the mass and hollowness of its limb-bones, is allied to Iguanodon and to Megalosaurus, and will belong to the second division of my Saurian system." Von Meyer later gave the formal name Pachypodes or Pachypoda ("thick feet") to his second division of "Saurians with Limbs Similar to Heavy Land Mammalia", but the group was a synonym of Richard Owen's Dinosauria from 1842.
The ribs were connected to the dorsal (trunk) vertebrae with two joints, acting together as a simple hinge joint, which has allowed researchers to reconstruct the inhaled and exhaled positions of the ribcage. The difference in volume between these two positions defines the air exchange volume (the amount of air moved with each breath), determined to be approximately 20 L for a P. engelhardti individual estimated to have weighed 690 kg, or 29 mL/kg bodyweight. This is a typical value for birds, but not for mammals, and indicates that Plateosaurus probably had an avian-style flow-through lung, although indicators for postcranial pneumaticity (air sacs of the lung invading the bones to reduce weight) can be found on the bones of only a few individuals, and were only recognised in 2010. Combined with evidence from bone histology this indicates that Plateosaurus was endothermic.
From 1980 on, a better understanding of dinosaur biomechanics, and studies by palaeontologists Andreas Christian and Holger Preuschoft on the resistance to bending of the back of Plateosaurus, led to widespread acceptance of an erect, digitigrade limb posture and a roughly horizontal position of the back. Many researchers were of the opinion that Plateosaurus could use both quadrupedal gaits (for slow speeds) and bipedal gaits (for rapid locomotion), and Wellnhofer insisted that the tail curved strongly downward, making a bipedal posture impossible. However, Moser showed that the tail was in fact straight.
The bipedal-quadrupedal consensus was changed by a detailed study of the forelimbs of Plateosaurus by Bonnan and Senter (2007), which clearly showed that Plateosaurus was incapable of pronating its hands. The pronated position in some museum mounts had been achieved by exchanging the position of radius and ulna in the elbow. The lack of forelimb pronation meant that Plateosaurus was an obligate (i.e. unable to walk in any other way) biped. Further indicators for a purely bipedal mode of locomotion are the great difference in limb length (the hind limb is roughly twice as long as the forelimb), the very limited motion range of the forelimb, and the fact that the centre of mass rests squarely over the hind limbs. A recent study based on the cross-sectional geometry of long limb bones, comparisons with extant taxa and inference models also confirmed a bipedal posture and erect stance for Plateosaurus.
Important cranial characteristics (such as jaw articulation) of most "prosauropods" are closer to those of herbivorous reptiles than those of carnivorous ones, and the shape of the tooth crown is similar to that of modern herbivorous or omnivorous iguanas. The maximum width of the crown was greater than that of the root for the teeth of most "prosauropods", including Plateosaurus; this results in a cutting edge similar to those of extant herbivorous or omnivorous reptiles. Paul Barrett proposed that prosauropods supplemented their mostly herbivorous diets with small prey or carrion, thus making them omnivores.
Long-bone histology also allows estimating the age a specific individual reached. Sander and Klein found that some individuals were fully grown at 12 years of age, others were still slowly growing at 20 years, and one individual was still growing rapidly at 18 years. The oldest individual found was 27 years and still growing; most individuals were between 12 and 20 years old. However, some may well have lived much longer, because the fossils from Frick and Trossingen are all animals that died in accidents, and not from old age. Due to the absence of individuals smaller than 4.8 metres (16 ft) long, it is not possible to deduce a complete ontogenetic series for Plateosaurus or determine the growth rate of animals less than 10 years of age.
A different school of thought developed almost half a century later, with palaeontologist David Weishampel suggesting that the skeletons from the lower layers stemmed from a herd that died catastrophically in a mudflow, while those in the upper layers accumulated over time. Weishampel explained the curious monospecific assemblage by theorising that Plateosaurus were common during this period. This theory was erroneously attributed to Seemann in a popular account of the plateosaurs in the collection of the Institute and Museum for Geology and Palaeontology, University of Tübingen, and has since become the standard explanation on most internet sites and in popular books on dinosaurs. Rieber proposed a more elaborate scenario, which included the animals dying of thirst or starvation, and being concentrated by mudflows.
A detailed re-assessment of the taphonomy by palaeontologist Martin Sander of the University of Bonn, Germany, found that the mud-miring hypothesis first suggested by Fraas is true: animals above a certain body weight sank into the mud, which was further liquefied by their attempts to free themselves. Sander's scenario, similar to that proposed for the famous Rancho La Brea Tar Pits, is the only one explaining all taphonomic data. The degree of completeness of the carcasses was not influenced by transport, which is obvious from the lack of indications for transport before burial, but rather by how much the dead animals were scavenged. Juveniles of Plateosaurus and other taxa of herbivores were too light to sink into the mud or managed to extract themselves, and were thus not preserved. Similarly, scavenging theropods were not trapped due to their lower body weights, combined with proportionally larger feet. There is no indication of herding, or of catastrophic burial of such a herd, or catastrophic accumulation of animals that previously died isolated elsewhere.
Meyer, H. von (1837). "Mitteilung an Prof. Bronn (Plateosaurus engelhardti)" [message to Prof. Bronn (Plateosaurus engelhardti)]. Neues Jahrbuch für Geologie und Paläontologie (in German). 1837: 316. https://archive.org/details/cbarchive_108435_1837mitteilunganprofbronnplate1833
Meyer, H. von (1837). "Mitteilung an Prof. Bronn (Plateosaurus engelhardti)" [message to Prof. Bronn (Plateosaurus engelhardti)]. Neues Jahrbuch für Geologie und Paläontologie (in German). 1837: 316. https://archive.org/details/cbarchive_108435_1837mitteilunganprofbronnplate1833
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Jaekel, O. (1913–1914). "Über die Wirbeltierfunde in der oberen Trias von Halberstadt" [About the vertebrate finds in the Upper Triassic of Halberstadt]. Paläontologische Zeitschrift (in German). 1: 155–215. doi:10.1007/BF03160336. S2CID 128404687. Archived (PDF) from the original on 2013-12-28. https://publikationsserver.tu-braunschweig.de/receive/dbbs_mods_00059197
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