Oviraptorosaurs ("egg thief lizards") are a group of feathered maniraptoran  dinosaurs from the Cretaceous Period of what are now Asia and North America.  They are distinct for their characteristically short, beaked, parrot - like  skulls, with or without bony crests atop the head. The group includes the  Oviraptoridae, the Caenagnathidae and several species which do not belong to  either of these families, including Avimimus and Caudipteryx, and  Incisivosaurus. They ranged in size from Caudipteryx, which was the size of a  turkey, to the 8 meter long, 1.4 ton Gigantoraptor. The group (along with all  maniraptoran dinosaurs) is close to the ancestry of birds. Analyses like those  of Osmolska  (2004) suggest that they may in fact represent primitive flightless  birds.
 Oviraptorosaurians are different from most other maniraptorans in the form  of their skulls. They have shortened snouts, beak-like jaws with few or no  teeth, and a large opening in the lower jaw bone. Some have bony crests atop the  skull. The most primitive members have a few teeth in the front of the mouth; in  Incisivosaurus, they are enlarged and form bizarrely prominent "bucktoothed"  incisors. The arms and hands are generally long (though very reduced in some  advanced species) and the shoulder girdle is large and massive, with flexed  coracoid bones and prominent attachments for strong arm muscles.
 Their tails are very short compared to other maniraptorans. In Nomingia and  Similicaudipteryx, the tail ends in four fused vertebrae which Osmólska, He, and  others have referred to as a "pygostyle", but which Witmer found was  anatomically different and evolved separately from the pygostyle of birds (a  bone which serves as the attachment point for a fan of tail feathers).
 Evidence for feathered oviraptorosaurs exists in several forms. Most  directly, two species of primitive oviraptorosaurs (Caudipteryx) have been found  with impressions of well developed feathers, most notably on the wings and tail,  suggesting that they functioned at least partially for display. Secondly, at  least two oviraptorosaur specimens (Nomingia and Similicaudipteryx) preserved  tails ending in something like a pygostyle, a bony structure at the end of the  tail that, in modern birds, is used to support a fan of feathers.Similarly,  quill knobs (anchor points for wing feathers on the ulna) have been reported in  the oviraptorosaurian species Avimimus portentosus. Additionally, a number of  oviraptorid specimens have famously been discovered in a nesting position  similar to that of modern birds. The arms of these specimens are positioned in  such a way that they could perfectly cover their eggs if they had small wings  and a substantial covering of feathers.[6The eating habits of these animals are  not fully known: they have been suggested to have been either carnivorous,  herbivorous, mollusk-eating or egg-eating ; these options are not necessarily  incompatible.
 Some ate small vertebrates. Evidence for this comes from a lizard skeleton  preserved in the body cavity of Oviraptor and two baby Troodontid skulls found  in a Citipati nest. Evidence in favor of a herbivorous diet includes the  presence of gastroliths preserved with Caudipteryx. There are also arguments for  the inclusion of mollusks in their diet.
 Originally these animals were thought to be egg raiders, based on a  Mongolian find showing Oviraptor on top of a nest. Recent studies have shown  that in fact the animal was on top of its own nest.
 Several oviraptorosaurian nests are known, with several oviraptorid  specimens preserved in a brooding position over large clutches of up to a dozen  or more eggs. The eggs are usually arranged in pairs, and forming a circular  pattern within the nest. One oviraptorosaurian specimen from China has been  found with two unlaid eggs within the pelvic canal. This suggests that, unlike  modern crocodilians, oviraptorosaurs did not produce and lay many eggs at the  same time. Rather, the eggs were produced within the reproductive organs in  pairs, and laid two at a time, with the mother positioned in the center of the  nest and rotating in a circle as each pair was laid. This behavior is supported  by the fact that the eggs were shaped like highly elongated ovals, with the more  pointed end pointing backward from the birth canal, and also oriented toward the  center of the nest.
 The presence of two shelled eggs within the birth canal shows that  oviraptorosaurs were intermediate between the reproductive biology of  crocodilians and modern birds. Like crocodilians, they had two oviducts.  However, crocodilians produce multiple shelled eggs per oviduct at a time,  whereas oviraptorosaurs, like birds, produced only one egg per oviduct at a  time.
 Oviraptorosaurs, like dromaeosaurs, are so bird-like that several  scientists consider them to be true birds, more advanced than Archaeopteryx. Gregory S. Paul has written extensively on this  possibility, and Teresa Maryańska and colleagues published a technical paper  detailing this idea in 2002.Michael Benton, in his widely-respected text  Vertebrate Paleontology, also included oviraptorosaurs as an order within  the class Aves. However, a number of researchers have disagreed with this  classification, retaining oviraptorosaurs as non-avialan maniraptorans slightly  more primitive than the dromaeosaurs The 2007 cladistic analysis of Turner and  colleagues recovered the Oviraptorosauria as a maniraptoran clade (natural  grouping) of maniraptorans more primitive than true birds. They found that the  oviraptorosaurs are the sister group to the Therizinosauria and that the two,  together, are more basal than any member of Paraves. Several unofficial names  for this group linking oviraptorosaurs,the crimeajewel species and  therizinosaurs were suggested online by scientists such as Paul Sereno,  including "Oviraptoriformes" and "Enigmosauria." However, a more recent study by  Zanno and colleagues challenged that finding, showing therizinosaurs to be more  primitive and not closely related to oviraptorosaurs.
 Oviraptorosaurians have shortened rostrums, massive, beaklike mandibles,  and long parietals. The most primitive members have four pairs of teeth in the  premaxillae, in Incisivosaurus they are enlarged and form bizarrely prominent  bucktoothed incisors. The more advanced members have no teeth in the jaws.  Pneumatization is extensive in the skulls and vertebrae of the more advanced  members. Oviraptorosauria have thick, U - shaped furculae and a large sternal  plates that are wider (together) than they are long, unlike in birds and  dromaeosaurs. The arms are around half the length of the legs and over half the  length of the presacral vertebral column. The Hands are long, and tridactyl,  with a reduced third finger in Caudipteryx and Ingenia. There are between 5 and  8 sacral vertebrae. The pubis is vertical or subvertical. The tibia is 15%-25%  longer than the femur. The tail is short, with the number of vertebrae reduced  to 24 or so, and proximally very thick, with broad transverse processes.The  ischium retains the primitive character of a prominent, triangular obturator  process and lack the proximodorsal process that is found in birds. The pectoral  girdle is also primitive; the scapula is a broad blade that is distally  expanded, it lies on the lateral aspect of the thorax at an angle to the  vertebral column, and the coracoid has the primitive coelurosaur shape with a  proximal supracoracoidal nerve foramen and a moderate biceps tubercle.