Incisivosaurus ("incisor lizard") is a genus of small, probably herbivorous theropod from the early Cretaceous Period of what is now the People's Republic of China. The first specimen to be described (by Xu et al. in 2002), IVPP V13326, is a skull that was collected from the lowermost levels (the fluvial Lujiatun beds) of the Yixian Formation (dating to the Barremian stage about 126 million years ago) in the Sihetun area, near Beipiao, in western Liaoning Province. The most significant, and highly unusual, characteristic of this dinosaur is its apparent adaptation to an herbivorous or omnivorous lifestyle. It was named for its prominent, rodent-like front teeth, which show wear patterns commonly found in plant-eating dinosaurs. The specific name gauthieri honors Jacques Gauthier, a pioneer of the phylogenetic method of classification.
In 2009 the holotype skull was scanned and analyzed in three dimensions. The results indicated that Incisivosaurus had less birdlike air spaces in the skull bones than later oviraptorosaurs did. It also found that Incisivosaurus had reduced olfactory lobes and expanded optic lobes similar to . It suggested that the most birdlike features of may have been convergent with birds.
Incisivosaurus is assumed to have been like most other theropods. Its total body length has been estimated at and its weight at 2–4.6 kg (4.4–10 lbs).
The nature of the feathers preserved in the two Yixian specimens appeared to Xu and colleagues, who described the two feathered specimens, to change with age. The youngest specimen had relatively short primary feathers (those anchored to the hand) compared to its tail feathers. In the older specimen, the primary feathers were the same length as the tail feathers, and secondary feathers (those anchored to the lower arm) were also present. The primary feathers may have grown more slowly than the tail feathers, not reaching equal size until the animal was close to maturity, and the secondary feathers would not appear at all until this more mature stage. This suggests that the wing feathers had little use at a young age, only becoming fully developed with maturity.
Additionally, the youngest specimen's vaned feathers appeared to lack barbs except at the tip, instead consisting of a solid sheet. Xu and colleagues interpreted the stark differences in the feathers of the two specimens as primarily age-related. They speculated that hatchlings would have been covered in natal down like modern birds. As the animal aged, the down would be replaced by vaned pennaceous feathers on the hands and tail, but ribbon-like and primitive in form, similar to the tail feathers of Confuciusornis, Epidexipteryx, and some Enantiornithes. These feathers would be lost through moulting as the animal aged, and replaced with more modern-style barbed feathers. The primary feathers grew more slowly than the tail feathers, not reaching equal size until the animal was close to maturity, and the secondary feathers would not appear at all until this more mature stage. This suggests that the wing feathers had little use at a young age, only becoming fully developed with maturity.
However, feather development specialist Richard Prum disputed the above interpretation of the feathers in a November 2010 letter to the journal Nature. Prum noted that the apparently ribbon-like structure of the juvenile's feathers were consistent with pennaceous feathers in the midst of moulting. In modern birds, new vaned feathers emerge from the feather follicle enclosed in a "pin feather", a solid tube covered in keratin. Usually, the tip of this tube will fall away first, leaving a structure identical to that seen in the fossil. Later, the rest of the sheath falls away when the entire feather has fully developed. Prum also noted, as did Xu and his team, that the structure of the oviraptorosaur feathers is fundamentally different from other prehistoric birds with ribbon-like tail feathers. In those other species, the ribbon portion is formed from a flattened and expanded rachis, or central quill, of the feather, with the feather barbs expanding out at the tip. In the fossil specimen, however, the "ribbon" like portion is the same width as the vaned tip. This is consistent with what is seen in feathers in the process of moulting. Prum concluded that rather than representing an instance of feathers changing in form as the animal aged, this specimen represents the first known fossil evidence of feather moulting.Prum, R.O. (2010). "Moulting tail feathers in a juvenile oviraptorisaur." Nature, 468. Published online 3 November 2010.
Prum also noted that in modern birds, tail feathers moult sequentially, not simultaneously as in the oviraptorosaur specimen. However, the sequential moulting of modern birds is because the birds need to retain their ability to fly during the moult (except in penguins). For lineages more primitive than the advent of flight, like oviraptorosaurs, this would not have been an issue, and all the wing and tail feathers of primitive feathered theropods may have moulted simultaneously, more like penguins than flying birds.
However, Xu et al. (2010) rebutted that the purported moulting evidence is problematic due to the complete absence of previous-generation feathers, and suggested that the feather is too large to be considered as a "pin feather". Other authors agreed with the reply by Xu et al. (2010) that the structures do not represent the "pin feather", though they considered that the specimen might represent a mid to late immature stage.
Classification
Paleobiology
See also
External links
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