| Rileyleff/sandbox Temporal range: Jurassic - Late Cretaceous,
| |
|---|---|
Scientific classification 
| |
| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Clade: | Dinosauria |
| Clade: | †Ornithischia |
| Clade: | †Neornithischia |
| Clade: | †Ornithopoda |
| Clade: | †Hadrosauriformes |
| Family: | †Iguanodontidae Huxley, 1870 |
| Subgroups | |
Iguanodontidae is a family of iguanodontians belonging to Styracosterna, a derived clade within Ankylopollexia. Some evidence dates the origination of Iguanodontidae to approximately 200 million years ago during the Jurassic Period in North America.[1] The most recent iguanodontid fossils have been dated to approximately 65 million years ago, which temporally corresponds with the Cretaceous-Paleogene extinction event.[2][3] Iguanodontids were most prevalent during the Early Cretaceous Period, and became widely distributed during this time.Cite error: The <ref> tag name cannot be a simple integer (see the help page).
Iguanodontids, characterized by their elongated maxillae, were herbivorous and typically large in size.Cite error: The <ref> tag name cannot be a simple integer (see the help page). This family exhibited locomotive dynamism; there exists evidence for both bipedalism and quadrupedalism within iguanodontid species, supporting the idea that individual organisms were capable of both locomoting exclusively with their hind limbs and locomoting quadrupedally.[4] Iguanodontids possess hoof-like second, third, and fourth digits, and in some cases, a specialized thumb spike and an opposable fifth digit.[5] Their skull construction allows for a strong chewing mechanism called a transverse power stroke.[6] This, paired with their bilateral dental occlusion, made them extremely effective as herbivores.[7] Members of Iguanodontidae are thought to have had a diet that consisted of both gymnosperms and angiosperms, the latter of which co-evolved with the iguanodontids in the Cretaceous period.[8]
There is no consensus on the phylogeny of Iguanodontidae. Iguanodontidae is most frequently characterized as paraphyletic with respect to Hadrosauridae, although some researchers advocate for a monophyletic view of the family.[9]Cite error: The <ref> tag name cannot be a simple integer (see the help page). Additionally, some analyses have supported a reduction of the number of constituent genera within Iguanodontidae.[10]
Anatomy
editSkull and Mandible
editThe upper surface of a typical iguanodontid skull has a convex curve that extends from the snout to just past the orbit, where the skull flattens out to form a roughly level plane directly above the braincase.[6] The antorbital fenestra, an opening in the skull anterior to the eye sockets, is reduced in size in iguanodontids. Their maxillae are roughly triangular, fairly flat, and sport thickened bony walls. An elongated maxilla is characteristic of the family. [11] Iguanodontid dentaries are very long as well, and become increasingly thick towards the back of the skull. A pair of bony processes extending from the maxilla insert into the jugal and lacrimal, respectively. The iguanodontid jugal has particularly deep crevices that serve to mediate this contact. The lacrimal process constitutes the rostral margin of the reduced antorbital fenestra.[6]
Teeth
editIguanodontids are generally limited to the possession of single replacement tooth at each position, although exceptions exist. The most primitive example bears positions for 13 maxillary and 14 dentary teeth. More derived forms have a larger number of positions per row. For example, I. bernissartensis is able to accommodate up to 29 maxillary and 25 dentary teeth. Iguanodontids exhibit contact between maxillary and dentary teeth upon closure of the jaw. [7]They have a thick layer of enamel over the lip-facing (labial) surface of the crown, a robust primary ridge beginning at the base of the crown, and a denticulate margin. Most members of the family have maxillary tooth crowns lanceolate in shape. The labial surface of the teeth has some grooves, while the tongue-facing (lingual) surface is smooth. Iguanodontids have lost their premaxillary teeth.[6]
Manus and Pes
edit
The second, third, and fourth digits of the iguanodontid forelimb are close together. In some cases, it is possible that digits three and four were bound into a single structure by layers of skin, a specialized adaptation for quadruped locomotion.[5] In addition, the wrist bones are fused into a block, and the thumb bones are fused into a spike-like point. In species of genus Iguanodon, the fifth digit is long, flexible, and opposable. On the hind limb, digits two, three, and four are wide and short, with blunt claws that resemble hooves.[6]
Body
editAll of the cervical vertebrae have ribs attached. The initial set are linear; the rest are two-headed. Tendons along the neural arches were ossified, limiting mobility in the backbone in exchange for reinforcement. A similar ossification is seen in the tail. [11]Iguanodontids have a rod-shaped pubis that extends parallel to the ischium. The paired sternal bones are often hatchet-shaped. The humerus has a shallow curve, in contrast to the straight ulna and radius. The ilium is thinner at the anterior end than it is at the posterior. Evidence suggests that these dinosaurs do not have plated, armored skin.[6]
Locomotion
edit
Fossilized footprints provide evidence for both quadrupedality and bipedialty within representative iguanodontid gerena like Iguanodon. It is thought that iguanodontids are primarily quadruped but can optionally walk on two limbs. The ossification of tendons along the neural arches may have played a role in facilitating the dynamic pedality of iguanodontids, as the ossified tendons could help withstand the additional stress incurred on the backbone by standing upright.[11] Some research suggests that organism size plays a role in the determination of pedality, where larger organisms are more likely to choose to walk on all fours than their smaller counterparts.[4]
Diet
editIguanodontids are low-browsing herbivores that fed extensively on gymnosperms like ferns and horsetails, especially during the early Cretaceous period. These dinosaurs were very effective as herbivores due in part to their combination of bilateral dental occlusion with the transverse power stroke of their chewing mechanism. Additionally, iguanodontids lack a rigid secondary palate, which helps to mitigate torsional stresses during occlusion, a feature that enhanced their ability to break down plant matter.[6] Additionally, the iguanodontids co-evolved with the radiation of angiosperms in the Cretaceous period. Angiosperms typically develop more rapidly and lower to the ground than gymnosperms; their proliferation provided a wealth of easily accessible food for the members of Iguanodontidae.[8]
Phylogeny
editIn the past, Iguanodontidae became a repository for any ornithopod that did not belong in either Camptosauridae, Hadrosauridae, or Hypsilophodontidae. A number of studies suggest that Iguanodontidae as traditionally defined is paraphyletic with respect to Hadrosauridae.[9] That is, iguanodontids represent successive steps in the acquisition of advanced hadrosaurean characteristics between hypsilophodontids and hadrosaurs, and in this view cannot be defined as a single distinct clade.[12] Nevertheless, some researchers have found support for a monophyletic Iguanodontidae consisting of a handful of genera including Barilium, Bolong, Iguanodon, Jinzhousaurus, Mantellisaurus, and Proa.[13][14] After some recent cladistic analyses, Iguanodontidae is becoming more restricted in its number of constituent genera. For example, Ouranosaurus, once thought to be an Iguanodontid, is now considered to be a basal Hadrosaurid.[15][16] Some researchers dispute the status of iguanodontidae as a family given its increasingly limited quantity of constituent genera.[10]
Biogeography
editThe earliest traditional iguanodontids were found in the Jurassic in North America.[17] In the early cretaceous, the family dispersed across the northern hemisphere, later expanding into the southern hemisphere. [18]The group became very successful; fossilized remains are widespread across the globe. Several fossils dated to the Cretaceous period were found across Europe, South America, Africa, and North America. A small number of fossils have been discovered in Australia and Antarctica as well, dating back to the mid-Cretaceous and the late Cretaceous, respectively.[19][20]
References
edit- ^ Young, C (1948). "Fossil crocodiles in China, with notes on dinosaurian remains associated with the Kansu crocodiles". Bulletin of the Geological Society of China: 255-288.
- ^ Casanovas-Cladellas, M.L. (1985). "Orthomerus (Hadrosauridae, Ornithopoda) del Cretácico Superior del yacimento de "Els Nerets" (Tremp, España)": 155–162.
{{cite journal}}: Cite journal requires|journal=(help) - ^ Renne, Paul R.; Deino, Alan L.; Hilgen, Frederik J.; Kuiper, Klaudia F.; Mark, Darren F.; Mitchell, William S.; Morgan, Leah E.; Mundil, Roland; Smit, Jan (7 February 2013). "Time Scales of Critical Events Around the Cretaceous-Paleogene Boundary". Science. 339 (6120): 684–687. Bibcode:2013Sci...339..684R. doi:10.1126/science.1230492. PMID 23393261.
- ^ a b Galton, Peter (1976). "The Dinosaur Vectisaurus valdensis (Ornithischia: Iguanodontidae) from the Lower Cretaceous of England". Journal of Paleontology. 50 (5): 976–984.
- ^ a b Moratalla, J.J. (1992). "A Quadrupedal Ornithopod Trackway from the Lower Cretaceous of La Rioja (Spain): Inferences on Gait and Hand Structure". Journal of Vertebrate Paleontology. 12 (2): 150–157.
- ^ a b c d e f g Godefroit, Pascal (2012). Bernissart Dinosaurs and Early Cretaceous Terrestrial Ecosystems.
- ^ a b Weishampel, David (2012). Evolution of Jaw Mechanisms in Ornithopod Dinosaurs.
- ^ a b Barrett, P.M. (2001). "Did Dinosaurs invent flowers? Dinosaur-angiosperm coevolution revisited". Biol. Revs. 76: 411–447.
- ^ a b Sereno, Paul. "Phylogeny of the bird-hipped dinosaurs". national geographic research. 2: 234–256.
- ^ a b Weishampel, David (1990). The Dinosauria.
- ^ a b c Lucas, Spencer (1998). Lower and Middle Cretaceous Terrestrial Ecosystems: Bulletin 14.
- ^ Wang, Xaolin (2001). "A new iguanodontid (Jin- zhousaurus yangi gen. et sp. nov.) from the Yixian For- mation of western Liaoning, China". Chinese Science Bulletin. 46 (19).
- ^ Godefroit P, Escuillié F, Bolotsky YL, Lauters P. 2012. A new basal hadrosauroid dinosaur from the Upper Cretaceous of Kazakhstan. In: Godefroit P, ed. Bernissart dinosaurs and Early Cretaceous terrestrial ecosystems. Bloomington & Indianapolis: Indiana University Press, 335–358.
- ^ Norman, D. B. (2015), On the history, osteology, and systematic position of the Wealden (Hastings group) dinosaur Hypselospinus fittoni (Iguanodontia: Styracosterna). Zoological Journal of the Linnean Society, 173: 92–189. doi: 10.1111/zoj.12193
- ^ McDonald, A.T.; Kirkland, J.I.; DeBlieux, D.D.; Madsen, S.K.; Cavin, J.; Milner, A.R.C.; Panzarin, L. (2010). Farke, Andrew Allen (ed.). "New Basal Iguanodontians from the Cedar Mountain Formation of Utah and the Evolution of Thumb-Spiked Dinosaurs". PLoS ONE. 5 (11): e14075. doi:10.1371/journal.pone.0014075. PMC 2989904. PMID 21124919.
{{cite journal}}: CS1 maint: unflagged free DOI (link) - ^ Andrew T. McDonald (2011). "The taxonomy of species assigned to Camptosaurus (Dinosauria: Ornithopoda)" (PDF). Zootaxa. 2783: 52–68.
- ^ Lucas, Spencer (1994). Dinosaurs: The Textbook.
- ^ Benton, Michael (2003). The Age of Dinosaurs in Russia and Mongolia.
- ^ Case, J.A. (2007). "dromaeosaur from the Maastrichtian of James Ross Island and the Late Cretaceous Antarctic dinosaur fauna". United States Geological Survey and the National Academies.
- ^ King, G.M. (1996). Reptiles and Herbivory. p. 72.