Пахицефалозавры: Исчезнувший отряд динозавров.

Extinct clade of dinosaurs

Pachycephalosauria (,/p//æ//k//ɪ//s//ɛ//f//əl//ə/'/s//ɔː//r//i//ə//, // /,/k//ɛ//f// /; from Greek παχυκεφαλόσαυρος for 'thick headed lizards') is a clade of ornithischian dinosaurs. Along with Ceratopsia, it makes up the clade Marginocephalia. With the exception of two species, most pachycephalosaurs lived during the Late Cretaceous Period, dating between about 85.8 and 66 million years ago. The oldest known pachycephalosaur is currently Sinocephale bexelli from the Late Cretaceous of China. In 2017, a phylogenetic analysis conducted by Han and colleagues identified Stenopelix as a member of the Ceratopsia.

Pachycephalosaurs were bipedal ornithischians characterized by their thickened skulls. They had a bulky torso with an expanded gut cavity and broad hips, short forelimbs, long legs, a short, thick neck, and a heavy tail. Large orbits and a large optic nerve point to pachycephalosaurs having good vision, and uncharacteristically large olfactory lobes indicate that they had a good sense of smell relative to other dinosaurs. They were fairly small dinosaurs, with most falling in the range of in length and the largest, Pachycephalosaurus wyomingensis, estimated to measure long and weigh The characteristic skull of pachycephalosaurs is a result of the fusion and thickening of the frontals and parietals, accompanied by the closing of the supratemporal fenestra. In some species this takes the form of a raised dome; in others, the skull is flat or wedge shaped. While the flat headed pachycephalosaurs are traditionally regarded as distinct species or even families, they may represent juveniles of dome headed adults.

Most pachycephalosaurid remains are not complete, usually consisting of portions of the frontoparietal bone that forms the distinctive dome. This can make taxonomic identification a difficult task, as the classification of genera and species within Pachycephalosauria relies almost entirely on cranial characteristics. Consequently, improper species have historically been appointed to the clade. For instance, Majungatholus, once thought to be a pachycephalosaur, is now recognized as a specimen of the abelisaurid theropod Majungasaurus, and Yaverlandia, another dinosaur initially described as a pachycephalosaurid, has also since been reclassified as a coelurosaur (Naish in ). Further complicating matters are the diverse interpretations of ontogenetic and sexual features in pachycephalosaurs. A 2009 paper proposed that Dracorex and Stygimoloch were just early growth stages of Pachycephalosaurus, rather than distinct genera. The same conclusion had previously been reached by George Olshevsky in 1991, who classified heterodontosaurids as basal pachycephalosaurs on the basis of perceived cranial kinesis, the presence of fanglike premaxillary teeth, and the prominent diastema present in many genera.

The Pachycephalosauria was first named as a suborder of the order Ornithischia by They included within it only one family, the Pachycephalosauridae. Later researchers, such as Michael Benton, have ranked it as an infraorder of a suborder Cerapoda, which unites the ceratopsians and ornithopods. In 2006, Robert Sullivan published a re evaluation of pachycephalosaur taxonomy. Sullivan considered attempts by Maryańska and Osmólska to restrict the definition of Pachycephalosauria redundant with their Pachycephalosauridae, since they were diagnosed by the same anatomical characters. Sullivan also rejected attempts by , in his phylogenetic studies, to re define Pachycephalosauridae to include only "dome skulled" species (including Stegoceras and Pachycephalosaurus), while leaving more "basal" species outside that family in Pachycephalosauria. Therefore, Sullivan's use of Pachycephalosauridae is equivalent to Sereno and Benton's use of Pachycephalosauria. Sullivan diagnosed the Pachycephalosauridae based only on characters of the skull, with the defining character being a dome shaped frontoparietal skull bone. According to Sullivan, the absence of this feature in some species assumed to be primitive led to the split in classification between domed and non domed pachycephalosaurs; however, discovery of more advanced and possibly juvenile pachycephalosaurs with flat skulls (such as Dracorex hogwartsia) show this distinction to be incorrect. Sullivan also pointed out that the original diagnosis of Pachycephalosauridae centered around "flat to dome like" skulls, so the flat headed forms should be included in the family. In a paper published in 2003, Thomas E. Williamson and Thomas D. Carr discovered a clade of the Pachycephalosauridae that was a sister taxa to the genus Stegoceras, made up of "all other dome headed pachycephalosaurians; this was referred to as Pachycephalosaurinae

The cladogram presented here follows an analysis by
Cladogram after
Below is a cladogram published by Dieudonné and colleagues (2020) which controversially found heterodontosauridae to be paraphyletic with respect to pachycephalosauria. This analysis was proposed as a hypothesis for the complete lack of Jurassic and Early Cretaceous pachycephalosaur fossils, even though they should have existed if the modern understanding of ornithischian phylogeny is correct. However, this hypothesis has not been widely accepted.

The small size of most pachycephalosaur species and lack of skeletal adaptation indicates that they were not climbers and primarily ate food close to the ground. Mallon et al. (2013) examined herbivore coexistence on the island continent of Laramidia, during the Late Cretaceous and concluded that pachycephalosaurids were generally restricted to feeding on vegetation at, or below, the height of 1 meter. They exhibit heterodonty, having different tooth morphology between the premaxillary teeth and maxillary teeth. Front teeth are small and peg like with an ovular cross section and were most likely used for grabbing food. In some species, the last premaxillary tooth was enlarged and canine like. Back teeth are small and triangular with denticles on the front and back of the crown, used for mouth processing. In species in which the dentary has been found, mandibular teeth are similar in size and shape to those in the upper jaw. Wear patterns on the teeth vary by species, indicating a range of food preferences which could include seeds, stems, leaves, fruits, and possibly insects. A very wide rib cage and large gut cavity extending all the way to the base of the tail suggests the use of fermentation to digest food. It has been suggested that a pachycephalosaur could make its head, neck, and body horizontally straight, in order to transmit stress during ramming. However, in no known dinosaur could the head, neck, and body be oriented in such a position. Instead, the cervical and anterior dorsal vertebrae of pachycephalosaurs show that the neck was carried in an "S" or U shaped curve. Also, the rounded shape of the skull would lessen the contacted surface area during head butting, resulting in glancing blows. Other possibilities include flank butting, defense against predators, or both. The relatively wide build of pachycephalosaurs (which would protect vital internal organs from harm during flank butting) and the squamosal horns of the Stygimoloch (which would have been used to great effect during flank butting) add credence to the flank butting hypothesis. A histological study conducted by argued against the battering ram hypothesis. They argued that the dome was "an ephemeral ontogenetic stage", the spongy bone structure could not sustain the blows of combat, and the radial pattern was simply an effect of rapid growth. Later biomechanical analyses by and concluded, however, that the domes could withstand combat stresses. instead argued that the dome functioned for species recognition. There is evidence that the dome had some form of external covering, and it is reasonable to consider the dome may have been brightly covered, or subject to change color seasonally. The frequency of trauma was comparable across the different genera in this family, despite the fact that these genera vary with respect to the size and architecture of their domes, and fact that they existed during varying geologic periods. where intra specific combat behavior is not expected. Histological examination reveals that pachycephalosaurid domes are composed of a unique form of fibrolamellar bone which contains fibroblasts that play a critical role in wound healing, and are capable of rapidly depositing bone during remodeling. Peterson et al. (2013) concluded that, taken together, the frequency of lesion distribution and the bone structure of frontoparietal domes lend strong support to the hypothesis that pachycephalosaurids used their unique cranial structures for agonistic behavior.

Pachycephalosaurs lived exclusively in Laurasia, being found in western North America and central Asia. Pachycephalosaurs originated in Asia and had two major dispersal events, resulting in the two separate waves of pachycephalosaur evolution observed in Asia. The first, occurring before the late Santonian or early Campanian, involved a migration from Asia to North America, most likely by way of the Bering Land Bridge. This migration was by a common ancestor of Stygimoloch, Stegoceras, Tylocephale, Prenocephale, and Pachycephalosaurus. The second event occurred before the middle Campanian, and involved a migration back into Asia from North America by a common ancestor of Prenocephale and Tylocephale. Two species originally reported to be pachycephalosaurs discovered outside this range, Yaverlandia bitholus of England and Majungatholus atopus of Madagascar, have recently been shown to actually be theropods.