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{{Short description|Extinct clade of dinosaurs}}
{{Automatic taxobox
{{Automatic taxobox
| fossil_range = [[Late Jurassic]]–[[Late Cretaceous]], {{Fossil range|156|66}}
| fossil_range = [[Late Jurassic]]–[[Late Cretaceous]], {{Fossil range|156.3|66}}
| image = Isle of Wight Mantellisaurus.jpg
| image = Isle of Wight Mantellisaurus.jpg
| image_caption = ''[[Mantellisaurus]]'' skeleton, [[Natural History Museum, London|Natural History Museum]], London
| image_caption = ''[[Mantellisaurus]]'' skeleton, [[Natural History Museum, London|Natural History Museum]], London
| taxon = Ankylopollexia
| taxon = Styracosterna
| authority = [[Paul Sereno|Sereno]], [[1986 in paleontology|1986]]
| authority = [[Paul Sereno|Sereno]], [[1986 in paleontology|1986]]
| subdivision_ranks = Subgroups
| subdivision_ranks = Subgroups
| subdivision =
| subdivision =
*{{extinct}}''[[Camptosaurus]]''
*{{extinct}}''[[Batyrosaurus]]''?
*{{extinct}}''[[Cumnoria]]''
*{{extinct}}''[[Bayannurosaurus]]''
*{{extinct}}''[[Draconyx]]''
*{{extinct}}''[[Calvarius]]''
*{{extinct}}''[[Owenodon]]''
*{{extinct}}''[[Cedrorestes]]''
*{{extinct}}''[[Uteodon]]''
*{{extinct}}''[[Dakotadon]]''
*{{extinct}}'''Styracosterna'''
*{{extinct}}''[[Fukuisaurus]]''
**{{extinct}}''[[Bayannurosaurus]]''
*{{extinct}}''[[Hippodraco]]''
**{{extinct}}''[[Cedrorestes]]''
*{{extinct}}''[[Iguanacolossus]]''
**{{extinct}}''[[Dakotadon]]''
*{{extinct}}''[[Lanzhousaurus]]''
**{{extinct}}''[[Fukuisaurus]]''
*{{extinct}}''[[Lurdusaurus]]''
**{{extinct}}''[[Hippodraco]]''
*{{extinct}}''[[Magnamanus]]''
**{{extinct}}''[[Hypselospinus]]''
*{{extinct}}''[[Osmakasaurus]]''
**{{extinct}}''[[Iguanacolossus]]''
*{{extinct}}''[[Planicoxa]]''
**{{extinct}}''[[Lanzhousaurus]]''
*{{extinct}}''[[Riabininohadros]]''
**{{extinct}}''[[Lurdusaurus]]''
*{{extinct}}''[[Theiophytalia]]''
**{{extinct}}''[[Magnamanus]]''
*{{extinct}}''[[Barilium]]''
**{{extinct}}''[[Osmakasaurus]]''
*{{extinct}}''[[Hypselospinus]]''
**{{extinct}}''[[Planicoxa]]''
*{{extinct}}''[[Proa valdearinnoensis|Proa]]''
**{{extinct}}''[[Proa valdearinnoensis|Proa]]''
*{{extinct}}'''[[Hadrosauriformes]]'''

**{{extinct}}''[[Theiophytalia]]''
**{{extinct}}'''Hadrosauriformes'''
***{{extinct}}''[[Bolong]]''
***{{extinct}}''[[Jinzhousaurus]]''
***{{extinct}}''[[Ouranosaurus]]''
***{{extinct}}''[[Morelladon]]''
***{{extinct}}[[Iguanodontidae]]
***{{extinct}}[[Hadrosauroidea]]
}}
}}
'''Ankylopollexia''' is an extinct [[clade]] of [[ornithischian]] [[dinosaurs]] that lived from the [[Late Jurassic]] to the [[Late Cretaceous]]. It is a derived clade of [[iguanodontian]] [[ornithopod]]s and contains the subgroup Styracosterna.<ref name=McDonaldUpdate /> The name stems from the Greek word, “ankylos”, mistakenly taken to mean stiff, fused (in fact the adjective means bent or curved; used of fingers, it can mean hooked), and the Latin word, “pollex”, meaning thumb. Originally described in 1986 by Sereno, this most likely [[synapomorphic]] feature of a conical thumb spine defines the clade.<ref name=sereno1986>Sereno, P.C. (1986). "Phylogeny of the bird-hipped dinosaurs (order Ornithischia)". National Geographic Research 2 (2): 234–56</ref>


'''Styracosterna''' is an [[extinct]] [[clade]] of [[ornithischian]] [[dinosaurs]] that lived from the [[Late Jurassic]] to the [[Late Cretaceous]]. It is a derived clade of [[ornithopod]]s and contains thumb spiked animals such as ''[[Iguanodon]]'', the crested [[hadrosaurs]], and their many relatives.<ref name=McDonaldUpdate>{{Cite journal | last1 = McDonald | first1 = A. T. | editor1-last = Farke| editor1-first =Andrew A| title = Phylogeny of Basal Iguanodonts (Dinosauria: Ornithischia): An Update | doi = 10.1371/journal.pone.0036745 | journal = PLOS ONE | volume = 7 | issue = 5 | pages = e36745 | year = 2012 | pmid = 22629328| pmc =3358318 | bibcode = 2012PLoSO...736745M | doi-access = free }}</ref>
First appearing around 156 million years ago, in the [[Jurassic]], Ankylopollexia became an extremely successful and widespread clade during the [[Cretaceous]], and were found around the world. The group died out at the end of the [[Maastrichtian]].<ref name=McDonaldUpdate /> Even though they grew to be quite large, comparable to some carnivorous dinosaurs, they were universally [[herbivorous]]. Most ankylopollexians were bipedal.<ref>Foster, J. (2007). ''Camptosaurus dispar''. Jurassic West: The Dinosaurs of the Morrison Formation and Their World. Indiana University Press. p. 219-221</ref>


Likely first appearing during the [[Jurassic]], Styracosterna became an extremely successful and widespread clade during the [[Cretaceous]], and were found around the world. The group died out at the end of the [[Maastrichtian]].<ref name=McDonaldUpdate /> They grew to be quite large, comparable to some carnivorous dinosaurs and they were universally [[herbivorous]].<ref>Foster, J. (2007). ''Camptosaurus dispar''. Jurassic West: The Dinosaurs of the Morrison Formation and Their World. Indiana University Press. p. 219-221</ref>
==History of study==
===First discoveries===


==Size==
===Discovery of hadrosaurs===
[[File:Iguanodontian Sizes.svg|thumb|left|Size of three ankylopollexians (''[[Edmontosaurus]]'', ''[[Iguanodon]]'', and ''[[Camptosaurus]]'') compared to other ornithopods]]

Ankylopollexians varied greatly in size over the course of their evolution.{{citation needed|date=July 2018}}. The largest known ankylopollexian, dating to the late [[Campanian]] age (around 70 million years ago), belonged to the hadrosaurid family, and is named ''[[Shantungosaurus]]''. It was around {{convert|14.7|m|ft}} to {{convert|16.6|m|ft}} in length and weighed, for the largest individuals, up to {{convert|16|t|ST}}.<ref>Glut, Donald F. (1997). "Shantungosaurus". Dinosaurs: The Encyclopedia. Jefferson, North Carolina: McFarland & Co. pp. 816–817. {{ISBN|0-89950-917-7}}.</ref><ref>Zhao, X.; Li, D.; Han, G.; Hao, H.; Liu, F.; Li, L.; Fang, X. (2007). "Zhuchengosaurus maximus from Shandong Province". Acta Geoscientia Sinica 28 (2): 111–122. doi:10.1007/s10114-005-0808-x.</ref>
===Early 20th century research===

===Dinosaur renaissance===

===Splitting of ''[[Iguanodon]]''===

===Ichnology===

==Anatomy==
As the name implies, many ankylopollexians possess a conical thumb spike. The purpose of these spikes is still debated. As they are herbivores, ankylopollexians could have used them for foraging or defense. The hadrosauroid ''[[Batyrosaurus]]'' possessed a thumb claw of about {{convert|4|cm|inch}} in length.<ref>Pascal Godefroit, François Escuillié, Yuri L. Bolotsky and Pascaline Lauters (2012). "A New Basal Hadrosauroid Dinosaur from the Upper Cretaceous of Kazakhstan". In Godefroit, P. (eds). Bernissart Dinosaurs and Early Cretaceous Terrestrial Ecosystems. Indiana University Press. pp. 335–358.</ref> They also possess elongated skulls with powerful jaws for grazing. Many had teeth batteries to constantly replace the older teeth.<ref>Palmer, D., ed. (1999). The Marshall Illustrated Encyclopedia of Dinosaurs and Prehistoric Animals. London: Marshall Editions. p. 145. {{ISBN|1-84028-152-9}}.</ref>

===Size===
[[File:Iguanodontian Sizes.svg|thumb|left|Size of three ankylopollexians (''[[Edmontosaurus]]'', ''[[Iguanodon]]'', and ''[[Camptosaurus]]'') compared to other iguanodonts]]
Ankylopollexians varied greatly in size over the course of their evolution.{{citation-needed|date=July 2018}} An early genus, ''[[Camptosaurus]]'' is thought to have reached a maximum size of {{convert|7.9|m|ft}} in length.<ref>Erickson, Bruce R. (2003). Dinosaurs of the Science Museum of Minnesota. St. Paul, Minnesota: The Science Museum of Minnesota. p. 33. {{ISBN|978-0-911338-54-6}}</ref> [[Gregory S. Paul]] contends that ''Camptosaurus'' was smaller, no more than {{convert|5|m|ft}} in length and half a tonne in weight.<ref>Paul, G.S., 2010, The Princeton Field Guide to Dinosaurs, Princeton University Press p. 284</ref> The largest known ankylopollexian, dating to the late [[Campanian]] age (around 70 million years ago), belonged to the hadrosaurid family, and is named ''[[Shantungosaurus]]''. It was around {{convert|14.7|m|ft}} to {{convert|16.6|m|ft}} in length and weighed, for the largest individuals, up to {{convert|16|t|ST}}.<ref>Glut, Donald F. (1997). "Shantungosaurus". Dinosaurs: The Encyclopedia. Jefferson, North Carolina: McFarland & Co. pp. 816–817. {{ISBN|0-89950-917-7}}.</ref><ref>Zhao, X.; Li, D.; Han, G.; Hao, H.; Liu, F.; Li, L.; Fang, X. (2007). "Zhuchengosaurus maximus from Shandong Province". Acta Geoscientia Sinica 28 (2): 111–122. doi:10.1007/s10114-005-0808-x.</ref> An [[Early Cretaceous]] genus from [[England]], ''[[Mantellisaurus]]'', weighed about {{convert|750|kg|lbs}}.<ref name=paul2008>Paul, Gregory S. (2008). "A revised taxonomy of the iguanodont dinosaur genera and species". Cretaceous Research 29 (2): 192–216.doi:10.1016/j.cretres.2007.04.009.</ref>
[[File:Life restoration of Iguanacolossus.jpg|thumb|right|Life restoration of ''[[Iguanacolossus]]'']]
[[File:Life restoration of Iguanacolossus.jpg|thumb|right|Life restoration of ''[[Iguanacolossus]]'']]
Primitive ankylopollexians tended to be smaller as compared to the larger, more derived [[hadrosaur]]s. Of course, there are exceptions to this trend.{{citation-needed|date=July 2018}} A single track from a large ornithopod, likely a relative of ''Camptosaurus'', was reported from the [[Lourinhã Formation]], dating to the [[Jurassic]] in [[Portugal]]. It had an estimated hip height of around {{convert|2.8|m|ft}}, nearly a metre larger than the holotype femur of contemporary relative ''[[Draconyx]]'', estimated by the authors to be {{convert|835|kg|lbs}} in weight.<ref name=mateus2008>{{cite journal | url=https://docentes.fct.unl.pt/omateus/publications/ichnological-evidence-giant-ornithopod-dinosaurs-upper-jurassic-lourinha-format | title=Ichnological evidence for giant ornithopod dinosaurs in the Upper Jurassic Lourinhã Formation, Portugal | last1=Mateus | first1=Octávio | last2=Milàn | first2=Jesper | journal=Oryctos | year=2008 | volume=8 | pages=47-52}}</ref> The primitive styracosternan ''[[Iguanacolossus]]'' was named for its distinct robustness and large size, likely around {{convert|9|m|ft}} in length. Regarding hadrosaurs, one of the more basal members of [[Hadrosauroidea]], the [[China|Chinese]] genus ''[[Bolong]]'', is estimated to have been around {{convert|200|kg|lbs}}.<ref>Wu Wen-hao, Pascal Godefroit, Hu Dong-yu (2010). "Bolong yixianensis gen. et sp. nov.: A new Iguanodontoid dinosaur from the Yixian Formation of Western Liaoning, China". Geology and Resources 19 (2): 127–133.</ref> Another exception of this trend is ''[[Tethyshadros]]'', a more derived genus of Hadrosauroidea. Estimated to have weighed {{convert|350|kg|lbs}}, ''Tethyshadros'' have been found only on certain islands in Italy. Its diminuitive size is explained by [[insular dwarfism]].<ref>Dalla Vecchia, F. M. (2009). "Tethyshadros insularis, a new hadrosauroid dinosaur (Ornithischia) from the Upper Cretaceous of Italy". Journal of Vertebrate Paleontology 29 (4): 1100–1116.</ref>
Primitive styracosternans tended to be smaller as compared to the larger, more derived [[hadrosaur]]s. There are, however, exceptions to this trend. The primitive styracosternan ''[[Iguanacolossus]]'' was named for its distinct robustness and large size, likely around {{convert|9|m|ft}} in length.{{citation needed|date=January 2020}} Conversely, one of the more basal members of [[Hadrosauroidea]], the [[China|Chinese]] genus ''[[Bolong]]'', is estimated to have been around {{convert|200|kg|lbs}}.<ref>Wu Wen-hao, Pascal Godefroit, Hu Dong-yu (2010). "Bolong yixianensis gen. et sp. nov.: A new Iguanodontoid dinosaur from the Yixian Formation of Western Liaoning, China". Geology and Resources 19 (2): 127–133.</ref> Another exception of this trend is ''[[Tethyshadros]]'', a more derived genus of hadrosaur. Estimated to have weighed {{convert|350|kg|lbs}}, ''Tethyshadros'' have been found only on certain islands in Italy. Its diminutive size may be explained by [[insular dwarfism]].<ref>Dalla Vecchia, F. M. (2009). "Tethyshadros insularis, a new hadrosauroid dinosaur (Ornithischia) from the Upper Cretaceous of Italy". Journal of Vertebrate Paleontology 29 (4): 1100–1116.</ref>

===Hand anatomy===


==Classification==
==Classification==
[[File:Iguanodon_manus_1_NHM.jpg|thumb|Hand of ''[[Iguanodon]]'', showing the distinctive thumb of the group]]
[[File:Iguanodon_manus_1_NHM.jpg|thumb|Hand of ''[[Iguanodon]]'', showing the distinctive thumb of the group]]
About 157 million years ago, Ankylopollexia and [[Dryosauridae]] are believed to have split into separate evolutionary branches.<ref name=norman1990 /> Originally named and described in 1986 by Paul Sereno, Ankylopollexia would receive a more formal definition in a later paper by Sereno in 2005.<ref name=sereno1986 /> In the 1986 paper, the groups Camptosauridae and Styracosterna were used to define the clade, but in the 2005 paper, a [[phylogenetic]] definition was given: the last common ancestor of the species ''Camptosaurus dispar'' and ''Parasaurolophus walkeri'' and all its descendants.{{citation-needed|date=June 2018}}


The cladogram below follows the most up-to-date analysis by Andrew McDonald, 2012.<ref name=McDonaldUpdate>{{Cite journal | last1 = McDonald | first1 = A. T. | editor1-last = Farke| editor1-first =Andrew A| title = Phylogeny of Basal Iguanodonts (Dinosauria: Ornithischia): An Update | doi = 10.1371/journal.pone.0036745 | journal = PLoS ONE | volume = 7 | issue = 5 | pages = e36745 | url = http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0036745| year = 2012 | pmid = 22629328| pmc =3358318 }}</ref>
The cladogram below follows the phylogenetic analysis of Bertozzo ''et al.'' (2017).<ref name="bertozzo2017">{{cite journal | title=The Venice specimen of Ouranosaurus nigeriensis (Dinosauria, Ornithopoda) | journal=PeerJ | year=2017 | volume=5 | issue=e3403 | pages=e3403 | doi=10.7717/peerj.3403| pmid=28649466 | pmc=5480399 | last1=Bertozzo | first1=Filippo | last2=Dalla Vecchia | first2=Fabio Marco | last3=Fabbri | first3=Matteo | doi-access=free }}</ref>


{{clade| style=font-size:100%;line-height:80%
{{clade| style=font-size:85%;line-height:85%
|label1=[[Iguanodontia]]
|label1=''[[Ankylopollexia]]''
|1={{clade
|1={{clade
|1=[[Rhabdodontidae]]
|1=''[[Camptosaurus dispar]]''
|2=''[[Owenodon hoggii]]''
|2={{clade
|1=''[[Tenontosaurus]]''
|label3='''Styracosterna'''
|label2=[[Dryomorpha]]
|2={{clade
|1=[[Dryosauridae]]
|label2='''Ankylopollexia'''
|2={{clade
|1=''[[Camptosaurus]]''
|label2=[[Styracosterna]]
|2={{clade
|1=''[[Uteodon]]''
|3={{clade
|3={{clade
|1={{clade
|1={{clade
|1=''[[Hippodraco]]''
|1=''[[Uteodon aphanoecetes]]''
|2=''[[Theiophytalia]]'' }}
|2=''[[Cumnoria prestwichii]]'' }}
|2={{clade
|2={{clade
|1=''[[Iguanacolossus]]''
|1=''[[Cedrorestes crichtoni]]''
|2={{clade
|2=''[[Osmakasaurus depressus]]''
|1=''[[Lanzhousaurus]]''
|3={{clade
|2={{clade
|1=''[[Hippodraco scutodens]]''
|1=''[[Kukufeldia]]''
|2=''[[Theiophytalia kerri]]'' }}
|2={{clade
|4={{clade
|1=''[[Barilium]]''
|1=''[[Iguanacolossus fortis]]''
|label2=[[Hadrosauriformes]]
|2=''[[Planicoxa venenica]]''
|2={{clade
|3=''[[Dakotadon lakotaensis]]''
|1=''[[Iguanodon]]''
|4={{clade
|2=[[Hadrosauroidea]] <small>(including ''[[Mantellisaurus]]'', and ''[[Xuwulong]]'') </small> }} }} }} }} }} }} }} }} }} }} }} }}
|1=''[[Lurdusaurus arenatus]]''
|2=''[[Lanzhousaurus magnidens]]''

|3={{clade
===Potentially Dubious Taxa===
|1=[[NHMUK]] R1831
[[File:Maidstone fossil Iguanodon 1840.jpg|thumb|180px|Holotype specimen of ''Mantellodon'']]
|2=''[[Kukufeldia tilgatensis]]''
A number of styracosternan genera were named in a short period of time, all from material once assigned to the genus ''[[Iguanodon]]''. Some of these, such as ''[[Barilium]]'', ''[[Hypselospinus]]'', and ''[[Mantellisaurus]]'', have seen general acceptance as valid, useful taxa. Several, however, have been questioned and declared by some researchers as ''[[nomina dubia]]'' or otherwise invalid. These include:<ref>{{cite journal |author=David B. Norman |year=2013 |title=On the taxonomy and diversity of Wealden iguanodontian dinosaurs (Ornithischia: Ornithopoda) |journal=Revue de Paléobiologie, Genève |volume=32 |issue=2 |pages=385–404 |url=http://eprints.esc.cam.ac.uk/3039/}}</ref>
|3={{clade
*''[[Darwinsaurus]]''
|1=''[[Barilium dawsoni]]''
*''[[Delapparentia]]''
|2=''[[Fukuisaurus tetoriensis]]''
*''[[Huxleysaurus]]''
|3={{clade
*''[[Kukufeldia]]''
|1=''[[Proa valdearinnoensis]]''
*''[[Mantellodon]]''
|2={{clade
*''[[Proplanicoxa]]''
|1=''[[Iguanodon bernissartensis]]''
*''[[Sellacoxa]]''
|label2=[[Hadrosauroidea]]
|2={{clade
|1=''[[Hypselospinus fittoni]]''
|2={{clade
|1=''[[Mantellisaurus atherfieldensis]]''
|2=[[NHMUK]] R3741 (cf. ''[[Mantellisaurus]]'') }}
|3={{clade
|1=''[[Ouranosaurus nigeriensis]]''
|2={{clade
|1=''[[Altirhinus kurzanovi]]''
|2=''[[Jinzhousaurus yangi]]''
|3=''[[Ratchasimasaurus suranareae]]''
|4={{clade
|1=''[[Penelopognathus weishampeli]]''
|2={{clade
|1=''[[Equijubus normani]]''
|2=''[[Xuwulong yueluni]]'' }}
|3={{clade
|1=''[[Gongpoquansaurus mazongshanensis]]''
|2={{clade
|1={{clade
|1=''[[Jintasaurus meniscus]]''
|2=''[[Probactrosaurus gobiensis]]''
|3=''[[Eolambia caroljonesa]]'' }}
|2='''[[Hadrosauromorpha]]''' }} }} }} }} }} }} }} }} }} }} }} }} }} }} }} }}


==Palaeobiology==
==Palaeobiology==
===Locomotion===
As mentioned before, most ankylopollexians were bipedal. There are a few exceptions to this rule, including the ''Mantellisaurus''. Because of its short forelimbs and short body, ''[[Mantellisaurus]]'' was bipedal when moving, but when standing or moving slowly, it used its forelimbs to balance itself.<ref name=paul2008 />

===Social behaviour===

===Diet and chewing===

===Parental behaviour===

===Brain===
===Brain===
[[File:Iguanodon1897.jpg|thumb|left|Brain endocast of an ''Iguanodon'', created in 1897 from specimen NHMUK R2501.]]
[[File:Iguanodon1897.jpg|thumb|left|Brain endocast of an ''Iguanodon'', created in 1897 from specimen NHMUK R2501]]
The [[neurobiology]] of ankylopollexians has been studied as far back as 1871, when a well preserved cranium (specimen [[NHMUK]] R2501<ref name=brasier2017 />) discovered in September of 1869 from the [[Wealden Group]] on the [[Isle of Wight]] and tentatively referred to the genus ''[[Iguanodon]]'' was described by [[John Hulke]]. He noted that due to the lesser correlation of the shape of the brain and wall of cranial cavity in reptiles, any deduction of the shape of the brain of the animal would be approximate.<ref name=hulke1871>{{cite journal|author=Hulke J.W. |year=1871|title= Note on a large reptilian skull from Brooke, Isle of Wight, probably Dinosaurian, referable to the genus ''Iguanodon''|journal=Quart J. Geol Soc|volume=27|pages=199–206|doi=10.1144/GSL.JGS.1871.027.01-02.27 }}</ref> The referral of this skull was reinforced in a later study, published in 1897. It was here inquired that the brain of the dinosaur may have been more closely associated to the cavity than that of modern reptiles, and so an [[endocast]] was created and studied.<ref name="andrews1897">{{cite journal | url=https://www.tandfonline.com/doi/abs/10.1080/00222939708680580?journalCode=tnah12 | title=Note on a cast of the brain-cavity of Iguanodon. | author=Andrews, Chas. W. | journal=Journal of Natural History | year=1897 | volume=19 | issue=114 | pages=585-591 | doi=10.1080/00222939708680580}}</ref> This was not the first endocast of an ankylopolloxian brain, for in 1893, the skull of a ''[[Claosaurus annectens]]'' (today referred to the genus ''[[Edmontosaurus]]''<ref name=BSC07>{{cite book |last=Creisler |first=Benjamin S. |year=2007 |chapter=Deciphering duckbills: a history in nomenclature |editor=Carpenter Kenneth |title=Horns and Beaks: Ceratopsian and Ornithopod Dinosaurs |publisher=Indiana University Press |location=Bloomington and Indianapolis |pages=185–210 |isbn=0-253-34817-X}}</ref>) was used by [[Othniel Charles Marsh]] to create a cast of the brain cavity. Some basics remarks were made, including the small size of the organ, but interpreting minute features of the organ was noted to be difficult.<ref name="marsh1893">{{cite journal | url=http://www.ajsonline.org/content/s3-45/265/83.extract | title=The skull and brain of Claosaurus. | author=Marsh, Othniel Charles | journal=American Journal of Science | year=1893 | volume=265 | pages=83-86}}</ref> The 1897 paper noted the similarity of the two endocasts.<ref name=andrews1897 />
The [[neurobiology]] of ankylopollexians has been studied as far back as 1871, when a well preserved cranium (specimen [[NHMUK]] R2501<ref name=brasier2017 />) discovered in September 1869 from the [[Wealden Group]] on the [[Isle of Wight]] and tentatively referred to the genus ''[[Iguanodon]]'' was described by [[John Hulke]]. He noted that due to the lesser correlation of the shape of the brain and wall of cranial cavity in reptiles, any deduction of the shape of the brain of the animal would be approximate.<ref name=hulke1871>{{cite journal|author=Hulke J.W. |year=1871|title= Note on a large reptilian skull from Brooke, Isle of Wight, probably Dinosaurian, referable to the genus ''Iguanodon''|journal=Quart J. Geol Soc|volume=27|issue=1–2|pages=199–206|doi=10.1144/GSL.JGS.1871.027.01-02.27 |s2cid=130674982}}</ref> The referral of this skull was reinforced in a later study, published in 1897. It was here inquired that the brain of the dinosaur may have been more closely associated to the cavity than that of modern reptiles, and so an [[endocast]] was created and studied.<ref name="andrews1897">{{cite journal | title=Note on a cast of the brain-cavity of Iguanodon. | author=Andrews, Chas. W. | journal=Journal of Natural History | year=1897 | volume=19 | issue=114 | pages=585–591 | doi=10.1080/00222939708680580| url=https://zenodo.org/record/1789648 }}</ref> This was not the first endocast of an ankylopolloxian brain, for in 1893, the skull of a ''[[Claosaurus annectens]]'' (today referred to the genus ''[[Edmontosaurus]]''<ref name=BSC07>{{cite book |last=Creisler |first=Benjamin S. |year=2007 |chapter=Deciphering duckbills: a history in nomenclature |editor=Carpenter Kenneth |title=Horns and Beaks: Ceratopsian and Ornithopod Dinosaurs |publisher=Indiana University Press |location=Bloomington and Indianapolis |pages=185–210 |isbn=978-0-253-34817-3}}</ref>) was used by [[Othniel Charles Marsh]] to create a cast of the brain cavity. Some basics remarks were made, including the small size of the organ, but interpreting minute features of the organ was noted to be difficult.<ref name="marsh1893">{{cite journal | title=The skull and brain of Claosaurus. | author=Marsh, Othniel Charles | journal=American Journal of Science | year=1893 | volume=265 | issue=265 | pages=83–86| doi=10.2475/ajs.s3-45.265.83 | bibcode=1893AmJS...45...83M | s2cid=131740074 | url=https://zenodo.org/record/2198923 }}</ref> The 1897 paper noted the similarity of the two endocasts.<ref name=andrews1897 />


[[Hadrosaurs]] have been noted as having the most complex brains among ankylopollexians, and indeed among [[ornithischian]] dinosaurs as a whole. The brains of a large variety of taxa have been studied. [[John Ostrom]], would, in 1961, provide what was then the most extensive and detailed review and work on hadrosaur neuro-anatomy. This area of hadrosaur study was in its infancy at this point, and only the species known today as ''Edmontosaurus annectens'', ''Edmontosaurus regalis'', and ''Gryposaurus notabilis'' (at that time thought to be a synonym of its relative ''[[Kritosaurus]]'') had specimens suitable at the time to be examined (''Lambeosaurus'' was listed as having a briefly described braincase, but this was a mistake originating in Lull and Wright (1942)).<ref name=evans2009 /><ref name="ostrom1961">{{cite journal | url=http://digitallibrary.amnh.org/handle/2246/1260 | title=Cranial morphology of the hadrosaurian dinosaurs of North America. | author=Ostrom, John H. | journal=Bulletin of the AMNH | year=1961 | volume=122}}</ref> Ostrom supported the view that the brains of hadrosaurs and other dinosaurs would've likely only filled a portion of the cranial cavity, therefore hindering the ability to learn from endocasts, but noted they were still useful. He noted, similar to Marsh, the small predicted size of the organ, but also that it was significantly developed. A number of similarities to the brains of modern reptiles were noted.<ref name=ostrom1961 />
[[Hadrosaurs]] have been noted as having the most complex brains among ankylopollexians, and indeed among [[ornithischian]] dinosaurs as a whole. The brains of a large variety of taxa have been studied. [[John Ostrom]], would, in 1961, provide what was then the most extensive and detailed review and work on hadrosaur neuro-anatomy. This area of hadrosaur study was in its infancy at this point, and only the species known today as ''Edmontosaurus annectens'', ''Edmontosaurus regalis'', and ''Gryposaurus notabilis'' (at that time thought to be a synonym of its relative ''[[Kritosaurus]]'') had specimens suitable at the time to be examined (''Lambeosaurus'' was listed as having a briefly described braincase, but this was a mistake originating in Lull and Wright (1942)).<ref name=evans2009 /><ref name="ostrom1961">{{cite journal | title=Cranial morphology of the hadrosaurian dinosaurs of North America. | author=Ostrom, John H. | journal=Bulletin of the AMNH | year=1961 | volume=122|hdl = 2246/1260}}</ref> Ostrom supported the view that the brains of hadrosaurs and other dinosaurs would've likely only filled a portion of the cranial cavity, therefore hindering the ability to learn from endocasts, but noted they were still useful. He noted, similar to Marsh, noted the small predicted size of the organ, but also that it was significantly developed. A number of similarities to the brains of modern reptiles were noted.<ref name=ostrom1961 />
[[File:Pasta - triceratops brain.jpg|thumb|A 1905 diagram showing the small size of an ''Edmontosaurus annectens'' brain (alongside that of ''Triceratops horridus'') commented on in early sources]]
[[File:Pasta - triceratops brain.jpg|thumb|A 1905 diagram showing the small size of an ''Edmontosaurus annectens'' brain (bottom; alongside that of ''Triceratops horridus'', top) commented on in early sources]]
[[James Hopson]] investigated the [[encephalization quotient]]s (EQs) of various dinosaurs in 1977 study. Three ornithopods for which brain endocasts had previously been produced – ''[[Camptosaurus]]'', ''Iguanodon'', and ''Anatosaurus'' (now known as ''Edmontosaurus annectens''<ref name=BSC07 />) – were investigated. It was found that they had relatively high EQs compared to many other dinosaurs (ranging from 0.8 to 1.5), comparable to that of [[carnosauria]]n [[theropod]]s and of modern [[crocodilian]]s, but far lower than that of [[coelurosauria]]n theropods. The latter two genera, which lived later than ''Camptosaurus'', had somewhat higher EQs than the [[Jurassic]] taxon, which, being at the lower end, was more comparable to the [[ceratopsian]] genus ''[[Protoceratops]]''. Reasonings suggested for their comparably high intelligence were the need for acute senses in the lack of defensive weapons, and more complex [[intraspecific]] behaviours as indicated by their acoustic and visual display structures.<ref name="hopson1977">{{cite journal | url=https://www.annualreviews.org/doi/abs/10.1146/annurev.es.08.110177.002241?journalCode=ecolsys.1 | title=Relative brain size and behavior in archosaurian reptiles. | author=Hopson, James A. | journal=Annual Review of Ecology and Systematics | year=1977 | volume=8 | issue=1 | pages=429-448 | doi=10.1146/annurev.es.08.110177.002241}}</ref>
[[James Hopson]] investigated the [[encephalization quotient]]s (EQs) of various dinosaurs in 1977 study. Three ornithopods for which brain endocasts had previously been produced – ''[[Camptosaurus]]'', ''Iguanodon'', and ''Anatosaurus'' (now known as ''Edmontosaurus annectens''<ref name=BSC07 />) – were investigated. It was found that they had relatively high EQs compared to many other dinosaurs (ranging from 0.8 to 1.5), comparable to that of [[carnosauria]]n [[theropod]]s and of modern [[crocodilian]]s, but far lower than that of [[coelurosauria]]n theropods. The latter two genera, which lived later than ''Camptosaurus'', had somewhat higher EQs than the [[Jurassic]] taxon, which, being at the lower end, was more comparable to the [[ceratopsian]] genus ''[[Protoceratops]]''. Reasonings suggested for their comparably high intelligence were the need for acute senses in the lack of defensive weapons, and more complex [[intraspecific]] behaviours as indicated by their acoustic and visual display structures.<ref name="hopson1977">{{cite journal | title=Relative brain size and behavior in archosaurian reptiles. | author=Hopson, James A. | journal=Annual Review of Ecology and Systematics | year=1977 | volume=8 | issue=1 | pages=429–448 | doi=10.1146/annurev.es.08.110177.002241}}</ref>


In a first for any terrestrial fossil [[vertebrate]], Brasier ''et al.'' (2017) reported mineralized soft tissues from the brain of an iguanodontian dinosaur, from the [[Valanginian]] age (around 133 million years ago) [[Tunbridge Wells Sand Formation|Upper Tunbridge Wells Formation]] at [[Bexhill-on-Sea|Bexhill]], [[Sussex]]. Fragmentary [[ornithopod]] remains were associated with the fossil, and though assigning the specimen to any one taxon with certainty wasn't possible, ''[[Barilium]]'' or ''[[Hypselospinus]]'' were put forward as likely candidates. The specimen compared well to endocasts of similar taxa, such as one from a ''[[Mantellisaurus]]'' on display at the [[Oxford University Museum of Natural History]]. Detailed observations were made with the use of a [[scanning electron microscope]]. Only some parts of the brain were preserved; the [[cerebellum|cerebellar]] and [[cerebrum|celebral expansion]]s were best preserved, whereas the [[olfactory lobes]] and [[medulla oblongata]] were missing or nearly so. The [[neural tissue]]s seemed to be very tightly packed, indicating an EC closer to five (with hadrosaurs having even higher ECs), nearly matching that of the most intelligent non-avian theropods. Though it was noted this was in-line with their complex behaviour, as had been noted by Hopson, it was cautioned the dense packing may have been an artifact of preservation, and the original lower estimates were considered more accurate. Some of the complex behaviours ascribed can be seen to some extent in modern crocodilians, who fall near the original numbers.<ref name="brasier2017">{{cite journal | url=http://sp.lyellcollection.org/content/448/1/383.short | title=Remarkable preservation of brain tissues in an Early Cretaceous iguanodontian dinosaur. | author=Brasier, Martin D. ''et al.'' | journal=Geological Society, London, Special Publications | year=2017 | volume=448 | issue=1 | pages=383-398 | doi=10.1144/SP448.3}}</ref>
In a first for any terrestrial fossil [[vertebrate]], Brasier ''et al.'' (2017) reported mineralized soft tissues from the brain of an iguanodontian dinosaur, from the [[Valanginian]] age (around 133 million years ago) [[Tunbridge Wells Sand Formation|Upper Tunbridge Wells Formation]] at [[Bexhill-on-Sea|Bexhill]], [[Sussex]]. Fragmentary [[ornithopod]] remains were associated with the fossil, and though assigning the specimen to any one taxon with certainty wasn't possible, ''[[Barilium]]'' or ''[[Hypselospinus]]'' were put forward as likely candidates. The specimen compared well to endocasts of similar taxa, such as one from a ''[[Mantellisaurus]]'' on display at the [[Oxford University Museum of Natural History]]. Detailed observations were made with the use of a [[scanning electron microscope]]. Only some parts of the brain were preserved; the [[cerebellum|cerebellar]] and [[cerebrum|cerebral expansion]]s were best preserved, whereas the [[olfactory lobes]] and [[medulla oblongata]] were missing or nearly so. The [[neural tissue]]s seemed to be very tightly packed, indicating an EC closer to five (with hadrosaurs having even higher ECs), nearly matching that of the most intelligent non-avian theropods. Though it was noted this was in-line with their complex behaviour, as had been noted by Hopson, it was cautioned the dense packing may have been an artifact of preservation, and the original lower estimates were considered more accurate. Some of the complex behaviours ascribed can be seen to some extent in modern crocodilians, who fall near the original numbers.<ref name="brasier2017">{{cite journal | url=http://sp.lyellcollection.org/content/448/1/383.short | title=Remarkable preservation of brain tissues in an Early Cretaceous iguanodontian dinosaur. | author=Brasier, Martin D.|display-authors=et al | journal=Geological Society, London, Special Publications | year=2017 | volume=448 | issue=1 | pages=383–398 | doi=10.1144/SP448.3| bibcode=2017GSLSP.448..383B | doi-access=free }}</ref>
[[File:Amurosaurus endocast.png|left|thumb|Endocast of an ''Amurosaurus'' brain in right lateral (A), dorsal (B), and ventral (C) views]]
[[File:Hypacrosaurus altispinus, head.jpg|thumb|left|Skull of ''Hypacrosaurus'', a genus whose brain has been studied]]
The advent of [[CT scanning]] for use in palaeontology has allowed for more widespread application of this without the need for specimen destruction. Modern research using these methods has focused largely on hadrosaurs. In a 2009 study by palaeontologist David C. Evans and colleagues, the brains of various [[lambeosaurine]] hadrosaur genera were scanned and compared to each other, related taxa, and previous predictions. Contra the early works, Evans' studies indicate that only some regions of the hadrosaur brain were loosely correlated to the brain wall. As with previous studies, EQ values were investigated; even the lowest end of the determined EQ range was still higher than that of modern reptiles and most non-[[maniraptoran]] dinosaurs, though fell well short of maniraptorans themselves. The size of the [[cerebral hemispheres]] was, for the first time, remarked upon, being far larger than in other ornithischians and all large [[saurischian]] dinosaurs; maniraptorans ''[[Conchoraptor]]'' and ''[[Archaeopteryx]]'' had very similar proportions. This lends further support to the idea of complex behaviours and relatively high intelligence, for non-avian dinosaurs, in hadrosaurids.<ref name="evans2009">{{cite journal | title=Endocranial Anatomy of Lambeosaurine Hadrosaurids (Dinosauria: Ornithischia): A Sensorineural Perspective on Cranial Crest Function | author=Evans, David C.|display-authors=et al | journal=The Anatomical Record | year=2009 | volume=292 | issue=9 | pages=1315–1337 | doi=10.1002/ar.20984|pmid = 19711466| s2cid=15177074| doi-access=free }}</ref> Lambeosaurine ''[[Amurosaurus]]'' was the subject of a 2013 paper once again looking into a cranial endocast. A once again high EQ range was found, higher than that of living reptiles, [[sauropod]]s and other ornithischians, but different EQ estimates for theropods were cited, placing the hadrosaur numbers significantly below the majority of theropods. Additionally, the relative cerebral volume was only 30% in ''Amurosaurus'', significantly lower than in ''Hypacrosaurus'', closer to that of theropods like ''Tyrannosaurus'', though still distinctly larger than previously estimated numbers for more primitive iguanodonts. This demonstrated a previously unrecognized level of variation in neuro-anatomy within Hadrosauridae.<ref name="lauters2013">{{cite journal | title=Cranial Endocast of the Lambeosaurine Hadrosaurid Amurosaurus riabinini from the Amur Region, Russia | author=Lauters, Pascaline|display-authors=et al | journal=PLOS ONE | year=2013 | volume=8 | issue=11 |pages = e78899| doi=10.1371/journal.pone.0078899| pmid=24236064 | pmc=3827337 | bibcode=2013PLoSO...878899L| doi-access=free}}</ref>
The advent of [[CT scanning]] for use in palaeontology has allowed for more widespread application of this without the need for specimen destruction. Modern research using these methods has focused largely on hadrosaurs. In a 2009 study by palaeontologist David C. Evans and colleagues, the brains of [[lambeosaurine]] hadrosaur genera ''[[Hypacrosaurus]]'' (adult specimen [[Royal Ontario Museum|ROM]] 702), ''[[Corythosaurus]]'' (juvenile specimen ROM 759 and subadult specimen [[Canadian Museum of Nature|CMN]] 34825), and ''[[Lambeosaurus]]'' (juvenile specimen ROM 758) were scanned and compared to each other (on a [[phylogenetic]] and [[ontogenetic]] level), related taxa, and previous predictions, the first such large-scale look into the neurology of the subfamily. Contra the early works, Evans' studies indicate that only some regions of the hadrosaur brain (the dorsal portion and much of the hindbrain) were loosely correlated to the brain wall, like modern reptiles, with the ventral and lateral regions correlating fairly closely. Also unlike modern reptiles, the brains of the juveniles did not seem to correlate any closer to the brain wall than those of adults. It was cautioned, however, that very young individuals were not included in the study.<ref name=evans2009 />


==Palaeobiogeography==
As with previous studies, EQ values were investigated, although a wider number range was given to account for uncertainty in brain and body mass. The range for the adult ''Hypacrosaurus'' was 2.3 to 3.7; the lowest end of this range was still higher than modern reptiles and most non-[[maniraptoran]] dinosaurs (nearly all having EQs below two), but fell well short of maniraptorans themselves, which had quotients higher than four. The size of the [[cerebral hemispheres]] was, for the first time, remarked upon. It was found to taking up around 43% of endocranial volume (not considering [[olfactory bulbs]]) in ROM 702. This is comparable to their size in [[saurolophine]] hadrosaurs, but far larger than in any ornithischians outside of Hadrosauriformes, and all large [[saurischian]] dinosaurs; maniraptors ''[[Conchoraptor]]'' and ''[[Archaeopteryx]]'', an early bird, had very similar proportions. This lends further support to the idea of complex behaviours and relatively high intelligence, for non-avian dinosaurs, in hadrosaurids.<ref name="evans2009">{{cite journal | url=https://onlinelibrary.wiley.com/doi/full/10.1002/ar.20984 | title=Endocranial Anatomy of Lambeosaurine Hadrosaurids (Dinosauria: Ornithischia): A Sensorineural Perspective on Cranial Crest Function | author=Evans, David C. ''et al.'' | journal=The Anatomical Record | year=2009 | volume=292 | issue=9 | pages=1315-1337 | doi=10.1002/ar.20984}}</ref>
[[File:Camptosaurus.jpg|thumb|Life restoration of ''[[Camptosaurus]]'']]
[[File:Amurosaurus endocast.png|thumb|Endocast of an ''Amurosaurus'' brain in right lateral (A), dorsal (B), and ventral (C) views]]
Ankylopollexians would in the Cretaceous become one of the most successful groups on the planet, being both widespread and numerous in nature.<ref name=MacDonald2010>{{cite journal | title=New Basal Iguanodonts from the Cedar Mountain Formation of Utah and the Evolution of Thumb-Spiked Dinosaurs | author=MacDonald, Andrew|display-authors=et al | journal=PLOS ONE | year=2010 | volume=5 | issue=11 |pages = e14075| doi=10.1371/journal.pone.0014075| pmid=21124919 | pmc=2989904 | bibcode=2010PLoSO...514075M| doi-access=free}}</ref> Around this time, styracosternans spread to [[Asia]] and [[Europe]]. An early example is the [[China|Chinese]] genus ''[[Bayannurosaurus]]'', from the [[Berriasian]].<ref name=xing2018>{{cite journal | title=A large-sized basal ankylopollexian from East Asia, shedding light on early biogeographic history of Iguanodontia | author=Xu, Xing|display-authors=et al | journal=Science Bulletin | year=2018 | volume=63 | issue=9 | pages=556–563 | doi=10.1016/j.scib.2018.03.016| pmid=36658842| bibcode=2018SciBu..63..556X| doi-access= }}</ref>
''[[Amurosaurus]]'', a close relative of the taxa from the 2009 study, was the subject of a 2013 paper once again looking into a cranial endocast. A nearly identical EQ range of 2.3 to 3.8 was found, and it was again noted this was higher than that of living reptiles, [[sauropod]]s and other ornithischians, but different EQ estimates for theropods were cited, placing the hadrosaur numbers significantly below even more basal theropods like ''[[Ceratosaurus]]'' (with an EQ range of 3.31 to 5.07) and ''[[Allosaurus]]'' (with a range of 2.4 to 5.24, compared to only 1.6 in the 2009 study<ref name=evans2009 /><ref name=lauters2013 />); more bird-like coelurosaurians theropods such as ''Troodon'' had stated EQs higher than seven. Additionally, the relative cerebral volume was only 30% in ''Amurosaurus'', significantly lower than in ''Hypacrosaurus'', closer to that of theropods like ''Tyrannosaurus'' (with 33%), though still distinctly larger than previously estimated numbers for more primitive iguanodonts like ''Lurdusaurus'' and ''Iguanodon'' (both at 19%). This demonstrated a previously unrecognized level of variation in neuro-anatomy within Hadrosauridae.<ref name="lauters2013">{{cite journal | url=http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0078899 | title=Cranial Endocast of the Lambeosaurine Hadrosaurid Amurosaurus riabinini from the Amur Region, Russia | author=Lauters, Pascaline ''et al.'' | journal=PLoS One | year=2013 | volume=8 | issue=11 | doi=10.1371/journal.pone.0078899}}</ref>


==Palaeoecology==
==References==
{{Reflist}}
===Distribution===
[[File:Camptosaurus.jpg|thumb|left|180px|Life restoration of ''[[Camptosaurus]]'']]
Ankylopollexians would in the Cretaceous become one of the most successful groups on the planet, being both widespread and numerous in nature.<ref name=MacDonald2010>{{cite journal | url=http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0014075 | title=New Basal Iguanodonts from the Cedar Mountain Formation of Utah and the Evolution of Thumb-Spiked Dinosaurs | author=MacDonald, Andrew ''et al.'' | journal=PLoS One | year=2010 | volume=5 | issue=11 | doi=10.1371/journal.pone.0014075}}</ref> Around this time, ankylopollexians spread to [[Asia]] and [[Europe]]. An early example is the [[China|Chinese]] genus ''[[Bayannurosaurus]]'', from the [[Berriasian]].<ref name=xing2018>{{cite journal | url=https://www.sciencedirect.com/science/article/pii/S2095927318301580?via%3Dihub | title=A large-sized basal ankylopollexian from East Asia, shedding light on early biogeographic history of Iguanodontia | author=Xu, Xing ''et al.'' | journal=Science Bulletin | year=2018 | volume=63 | issue=9 | pages=556-563 | doi=10.1016/j.scib.2018.03.016}}</ref> The earliest known member of the clade Styracosterna, ''[[Cumnoria]]'', was from [[England]].<ref name=McDonald>{{Cite journal|author=Andrew T. McDonald |year=2011 |title=The taxonomy of species assigned to ''Camptosaurus'' (Dinosauria: Ornithopoda) |url=http://www.mapress.com/zootaxa/2011/f/z02783p068f.pdf |journal=Zootaxa |volume=2783 |issue= |pages=52–68 |doi= }}</ref> The oldest genus, found in [[Wyoming]], is ''[[Camptosaurus dispar]]'', which dates to around the [[Callovian]]-[[Oxfordian (stage)|Oxfordian]], about 156-157 million years ago.<ref>Carpenter, K. and Wilson, Y. (2008). "A new species of Camptosaurus (Ornithopoda: Dinosauria) from the Morrison Formation (Upper Jurassic) of Dinosaur National Moument, Utah, and a biomechanical analysis of its forelimb". Annals of the Carnegie Museum 76: 227–263. doi:10.2992/0097-4463(2008)76[227:ansoco]2.0.co;2.</ref>


==External links==
===Palaeobiogeography===
[[Hadrosauridae]] are thought to originate in Asia around 122 million years ago.<ref name=norman1990>Norman, David B.; Weishampel, David B. (1990). "Iguanodontidae and related ornithopods". In Weishampel, David B.; Dodson, Peter; and Osmólska, Halszka (eds.). The Dinosauria. Berkeley: University of California Press. pp. 510–533. {{ISBN|0-520-06727-4}}.</ref> They would spread throughout Europe, Asia, and North America where they would live until 65.5 million years ago with the [[Cretaceous–Paleogene extinction event|mass extinction of dinosaurs]].<ref name=sereno1999>Sereno, P. C. (1999). The Evolution of Dinosaurs. (cover story). Science, 284(5423), 2137</ref>

===Habitat preference===

===Predation===

===Diet===

==External Links==
*{{Wikispecies-inline|Iguanodontia}}
*{{Wikispecies-inline|Iguanodontia}}


{{Portal bar|Dinosaurs}}
==References==
{{Reflist}}
{{Portalbar|Dinosaurs|Jurassic|Cretaceous}}
{{Ornithopoda|O.}}
{{Ornithopoda|O.}}
{{Taxonbar|from=Q2490737}}
{{Taxonbar|from=Q2490737}}

Latest revision as of 03:15, 27 April 2024

LittleLazyLass/Ankylopollexia
Temporal range: Late JurassicLate Cretaceous, 156.3–66 Ma
Mantellisaurus skeleton, Natural History Museum, London
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Ornithischia
Clade: Ornithopoda
Clade: Ankylopollexia
Clade: Styracosterna
Sereno, 1986
Subgroups

Styracosterna is an extinct clade of ornithischian dinosaurs that lived from the Late Jurassic to the Late Cretaceous. It is a derived clade of ornithopods and contains thumb spiked animals such as Iguanodon, the crested hadrosaurs, and their many relatives.[1]

Likely first appearing during the Jurassic, Styracosterna became an extremely successful and widespread clade during the Cretaceous, and were found around the world. The group died out at the end of the Maastrichtian.[1] They grew to be quite large, comparable to some carnivorous dinosaurs and they were universally herbivorous.[2]

Size[edit]

Size of three ankylopollexians (Edmontosaurus, Iguanodon, and Camptosaurus) compared to other ornithopods

Ankylopollexians varied greatly in size over the course of their evolution.[citation needed]. The largest known ankylopollexian, dating to the late Campanian age (around 70 million years ago), belonged to the hadrosaurid family, and is named Shantungosaurus. It was around 14.7 metres (48 ft) to 16.6 metres (54 ft) in length and weighed, for the largest individuals, up to 16 tonnes (18 short tons).[3][4]

Life restoration of Iguanacolossus

Primitive styracosternans tended to be smaller as compared to the larger, more derived hadrosaurs. There are, however, exceptions to this trend. The primitive styracosternan Iguanacolossus was named for its distinct robustness and large size, likely around 9 metres (30 ft) in length.[citation needed] Conversely, one of the more basal members of Hadrosauroidea, the Chinese genus Bolong, is estimated to have been around 200 kilograms (440 lb).[5] Another exception of this trend is Tethyshadros, a more derived genus of hadrosaur. Estimated to have weighed 350 kilograms (770 lb), Tethyshadros have been found only on certain islands in Italy. Its diminutive size may be explained by insular dwarfism.[6]

Classification[edit]

Hand of Iguanodon, showing the distinctive thumb of the group

The cladogram below follows the phylogenetic analysis of Bertozzo et al. (2017).[7]

Ankylopollexia

Palaeobiology[edit]

Brain[edit]

Brain endocast of an Iguanodon, created in 1897 from specimen NHMUK R2501

The neurobiology of ankylopollexians has been studied as far back as 1871, when a well preserved cranium (specimen NHMUK R2501[8]) discovered in September 1869 from the Wealden Group on the Isle of Wight and tentatively referred to the genus Iguanodon was described by John Hulke. He noted that due to the lesser correlation of the shape of the brain and wall of cranial cavity in reptiles, any deduction of the shape of the brain of the animal would be approximate.[9] The referral of this skull was reinforced in a later study, published in 1897. It was here inquired that the brain of the dinosaur may have been more closely associated to the cavity than that of modern reptiles, and so an endocast was created and studied.[10] This was not the first endocast of an ankylopolloxian brain, for in 1893, the skull of a Claosaurus annectens (today referred to the genus Edmontosaurus[11]) was used by Othniel Charles Marsh to create a cast of the brain cavity. Some basics remarks were made, including the small size of the organ, but interpreting minute features of the organ was noted to be difficult.[12] The 1897 paper noted the similarity of the two endocasts.[10]

Hadrosaurs have been noted as having the most complex brains among ankylopollexians, and indeed among ornithischian dinosaurs as a whole. The brains of a large variety of taxa have been studied. John Ostrom, would, in 1961, provide what was then the most extensive and detailed review and work on hadrosaur neuro-anatomy. This area of hadrosaur study was in its infancy at this point, and only the species known today as Edmontosaurus annectens, Edmontosaurus regalis, and Gryposaurus notabilis (at that time thought to be a synonym of its relative Kritosaurus) had specimens suitable at the time to be examined (Lambeosaurus was listed as having a briefly described braincase, but this was a mistake originating in Lull and Wright (1942)).[13][14] Ostrom supported the view that the brains of hadrosaurs and other dinosaurs would've likely only filled a portion of the cranial cavity, therefore hindering the ability to learn from endocasts, but noted they were still useful. He noted, similar to Marsh, noted the small predicted size of the organ, but also that it was significantly developed. A number of similarities to the brains of modern reptiles were noted.[14]

A 1905 diagram showing the small size of an Edmontosaurus annectens brain (bottom; alongside that of Triceratops horridus, top) commented on in early sources

James Hopson investigated the encephalization quotients (EQs) of various dinosaurs in 1977 study. Three ornithopods for which brain endocasts had previously been produced – Camptosaurus, Iguanodon, and Anatosaurus (now known as Edmontosaurus annectens[11]) – were investigated. It was found that they had relatively high EQs compared to many other dinosaurs (ranging from 0.8 to 1.5), comparable to that of carnosaurian theropods and of modern crocodilians, but far lower than that of coelurosaurian theropods. The latter two genera, which lived later than Camptosaurus, had somewhat higher EQs than the Jurassic taxon, which, being at the lower end, was more comparable to the ceratopsian genus Protoceratops. Reasonings suggested for their comparably high intelligence were the need for acute senses in the lack of defensive weapons, and more complex intraspecific behaviours as indicated by their acoustic and visual display structures.[15]

In a first for any terrestrial fossil vertebrate, Brasier et al. (2017) reported mineralized soft tissues from the brain of an iguanodontian dinosaur, from the Valanginian age (around 133 million years ago) Upper Tunbridge Wells Formation at Bexhill, Sussex. Fragmentary ornithopod remains were associated with the fossil, and though assigning the specimen to any one taxon with certainty wasn't possible, Barilium or Hypselospinus were put forward as likely candidates. The specimen compared well to endocasts of similar taxa, such as one from a Mantellisaurus on display at the Oxford University Museum of Natural History. Detailed observations were made with the use of a scanning electron microscope. Only some parts of the brain were preserved; the cerebellar and cerebral expansions were best preserved, whereas the olfactory lobes and medulla oblongata were missing or nearly so. The neural tissues seemed to be very tightly packed, indicating an EC closer to five (with hadrosaurs having even higher ECs), nearly matching that of the most intelligent non-avian theropods. Though it was noted this was in-line with their complex behaviour, as had been noted by Hopson, it was cautioned the dense packing may have been an artifact of preservation, and the original lower estimates were considered more accurate. Some of the complex behaviours ascribed can be seen to some extent in modern crocodilians, who fall near the original numbers.[8]

Endocast of an Amurosaurus brain in right lateral (A), dorsal (B), and ventral (C) views

The advent of CT scanning for use in palaeontology has allowed for more widespread application of this without the need for specimen destruction. Modern research using these methods has focused largely on hadrosaurs. In a 2009 study by palaeontologist David C. Evans and colleagues, the brains of various lambeosaurine hadrosaur genera were scanned and compared to each other, related taxa, and previous predictions. Contra the early works, Evans' studies indicate that only some regions of the hadrosaur brain were loosely correlated to the brain wall. As with previous studies, EQ values were investigated; even the lowest end of the determined EQ range was still higher than that of modern reptiles and most non-maniraptoran dinosaurs, though fell well short of maniraptorans themselves. The size of the cerebral hemispheres was, for the first time, remarked upon, being far larger than in other ornithischians and all large saurischian dinosaurs; maniraptorans Conchoraptor and Archaeopteryx had very similar proportions. This lends further support to the idea of complex behaviours and relatively high intelligence, for non-avian dinosaurs, in hadrosaurids.[13] Lambeosaurine Amurosaurus was the subject of a 2013 paper once again looking into a cranial endocast. A once again high EQ range was found, higher than that of living reptiles, sauropods and other ornithischians, but different EQ estimates for theropods were cited, placing the hadrosaur numbers significantly below the majority of theropods. Additionally, the relative cerebral volume was only 30% in Amurosaurus, significantly lower than in Hypacrosaurus, closer to that of theropods like Tyrannosaurus, though still distinctly larger than previously estimated numbers for more primitive iguanodonts. This demonstrated a previously unrecognized level of variation in neuro-anatomy within Hadrosauridae.[16]

Palaeobiogeography[edit]

Life restoration of Camptosaurus

Ankylopollexians would in the Cretaceous become one of the most successful groups on the planet, being both widespread and numerous in nature.[17] Around this time, styracosternans spread to Asia and Europe. An early example is the Chinese genus Bayannurosaurus, from the Berriasian.[18]

References[edit]

  1. ^ a b McDonald, A. T. (2012). Farke, Andrew A (ed.). "Phylogeny of Basal Iguanodonts (Dinosauria: Ornithischia): An Update". PLOS ONE. 7 (5): e36745. Bibcode:2012PLoSO...736745M. doi:10.1371/journal.pone.0036745. PMC 3358318. PMID 22629328.
  2. ^ Foster, J. (2007). Camptosaurus dispar. Jurassic West: The Dinosaurs of the Morrison Formation and Their World. Indiana University Press. p. 219-221
  3. ^ Glut, Donald F. (1997). "Shantungosaurus". Dinosaurs: The Encyclopedia. Jefferson, North Carolina: McFarland & Co. pp. 816–817. ISBN 0-89950-917-7.
  4. ^ Zhao, X.; Li, D.; Han, G.; Hao, H.; Liu, F.; Li, L.; Fang, X. (2007). "Zhuchengosaurus maximus from Shandong Province". Acta Geoscientia Sinica 28 (2): 111–122. doi:10.1007/s10114-005-0808-x.
  5. ^ Wu Wen-hao, Pascal Godefroit, Hu Dong-yu (2010). "Bolong yixianensis gen. et sp. nov.: A new Iguanodontoid dinosaur from the Yixian Formation of Western Liaoning, China". Geology and Resources 19 (2): 127–133.
  6. ^ Dalla Vecchia, F. M. (2009). "Tethyshadros insularis, a new hadrosauroid dinosaur (Ornithischia) from the Upper Cretaceous of Italy". Journal of Vertebrate Paleontology 29 (4): 1100–1116.
  7. ^ Bertozzo, Filippo; Dalla Vecchia, Fabio Marco; Fabbri, Matteo (2017). "The Venice specimen of Ouranosaurus nigeriensis (Dinosauria, Ornithopoda)". PeerJ. 5 (e3403): e3403. doi:10.7717/peerj.3403. PMC 5480399. PMID 28649466.
  8. ^ a b Brasier, Martin D.; et al. (2017). "Remarkable preservation of brain tissues in an Early Cretaceous iguanodontian dinosaur". Geological Society, London, Special Publications. 448 (1): 383–398. Bibcode:2017GSLSP.448..383B. doi:10.1144/SP448.3.
  9. ^ Hulke J.W. (1871). "Note on a large reptilian skull from Brooke, Isle of Wight, probably Dinosaurian, referable to the genus Iguanodon". Quart J. Geol Soc. 27 (1–2): 199–206. doi:10.1144/GSL.JGS.1871.027.01-02.27. S2CID 130674982.
  10. ^ a b Andrews, Chas. W. (1897). "Note on a cast of the brain-cavity of Iguanodon". Journal of Natural History. 19 (114): 585–591. doi:10.1080/00222939708680580.
  11. ^ a b Creisler, Benjamin S. (2007). "Deciphering duckbills: a history in nomenclature". In Carpenter Kenneth (ed.). Horns and Beaks: Ceratopsian and Ornithopod Dinosaurs. Bloomington and Indianapolis: Indiana University Press. pp. 185–210. ISBN 978-0-253-34817-3.
  12. ^ Marsh, Othniel Charles (1893). "The skull and brain of Claosaurus". American Journal of Science. 265 (265): 83–86. Bibcode:1893AmJS...45...83M. doi:10.2475/ajs.s3-45.265.83. S2CID 131740074.
  13. ^ a b Evans, David C.; et al. (2009). "Endocranial Anatomy of Lambeosaurine Hadrosaurids (Dinosauria: Ornithischia): A Sensorineural Perspective on Cranial Crest Function". The Anatomical Record. 292 (9): 1315–1337. doi:10.1002/ar.20984. PMID 19711466. S2CID 15177074.
  14. ^ a b Ostrom, John H. (1961). "Cranial morphology of the hadrosaurian dinosaurs of North America". Bulletin of the AMNH. 122. hdl:2246/1260.
  15. ^ Hopson, James A. (1977). "Relative brain size and behavior in archosaurian reptiles". Annual Review of Ecology and Systematics. 8 (1): 429–448. doi:10.1146/annurev.es.08.110177.002241.
  16. ^ Lauters, Pascaline; et al. (2013). "Cranial Endocast of the Lambeosaurine Hadrosaurid Amurosaurus riabinini from the Amur Region, Russia". PLOS ONE. 8 (11): e78899. Bibcode:2013PLoSO...878899L. doi:10.1371/journal.pone.0078899. PMC 3827337. PMID 24236064.
  17. ^ MacDonald, Andrew; et al. (2010). "New Basal Iguanodonts from the Cedar Mountain Formation of Utah and the Evolution of Thumb-Spiked Dinosaurs". PLOS ONE. 5 (11): e14075. Bibcode:2010PLoSO...514075M. doi:10.1371/journal.pone.0014075. PMC 2989904. PMID 21124919.
  18. ^ Xu, Xing; et al. (2018). "A large-sized basal ankylopollexian from East Asia, shedding light on early biogeographic history of Iguanodontia". Science Bulletin. 63 (9): 556–563. Bibcode:2018SciBu..63..556X. doi:10.1016/j.scib.2018.03.016. PMID 36658842.

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