Showing posts with label Ceratopsid. Show all posts
Showing posts with label Ceratopsid. Show all posts

Saturday, 26 December 2015

Hualianceratops wucaiwanensis: A new species of Ceratopsid Dinosaur from the Late Jurassic of Xinjiang Province, China.

Ceratopsid Dinosaurs are one of the most diverse and specious groups of herbivorous Ornithischian Dinosaurs, with a large number of species known from the Cretaceous of Asia and North America. The Earliest fossils appear in the Late Jurassic of China, with the earliest known species, Yinlong downsi, thought to have lived between 161.2 and 155.7 million years ago.

In a paper published in the journal PLoS One on 9 December 2015, Fenglu Han of the School of Earth Sciences at the China University of Geosciences and the Institute of Vertebrate Paleontology and Paleoanthropology of the Chinese Academy of Sciences, Catherine Forster and James Clark of the Department of Biological Sciences at The George Washington University and Xing Xu, also of the Institute of Vertebrate Paleontology and Paleoanthropology of the Chinese Academy of Sciences, describe a new species of Ceratopsid from the Late Jurassic Shishugou Formation of the Junggar Basin in  Xinjiang Province, China; the same deposits that produced Yinlong downsi.

The new species is named Hualianceratops wucaiwanensis, where 'Hualianceratops' means 'Ornamental-faced Ceratopsid' and 'wucaiwanensis' means 'from Wucaiwan', the locality which produced both Hualianceratops wucaiwanensis and Yinlong downsi. The species is described from a single fragmentary skull and jaw and a few fragments of post-cranial skeleton. While these remains are somewhat limited, they can be distinguished from Yinlong downsi, indicating the presence of a second species of Ceratopsid living in the same area as Yinlong downsi, and at the same time. The two species are thought to be closely related.

The mandible of Hualianceratops wucaiwanensis. (A) photograph in lateral view, (B) drawing in lateral view, (C) photograph in ventral view, (D) drawing in ventral view. Abbreviations: an, angular; d, dentary; emf, external mandibular fenestra; imf, inner mandibular fenestra; lsp, left splenial; pra, prearticular; pd, predentary; rsp, right splenial; sa, surangular. Han et al. (2015).

See also...

http://sciencythoughts.blogspot.co.uk/2015/06/regaliceratops-peterhewsi-new-species.htmlRegaliceratops peterhewsi: A new species of Chasmosaur from the Late Cretaceous of Alberta.                                                                         Ceratopsids are among the most distinctive and...
Ceratopsian Dinosaurs are thought to have originated in Asia in the Early Cretaceous, spreading to Europe and North America, and becoming the most important and diverse group of herbivorous Dinosaurs in North America by the end of the Period. Unfortunately...
 
Dinosaurs underwent dramatic increases in size over a number of years during their growth, and are presumed to have played a number of different ecological...
Follow Sciency Thoughts on Facebook.

Saturday, 6 June 2015

Regaliceratops peterhewsi: A new species of Chasmosaur from the Late Cretaceous of Alberta.


Ceratopsids are among the most distinctive and easily recognized of Dinosaur groups, due to their large and heavily ornamented skulls, with large neck frills and horns. Despite their ubiquitousness in Dinosaur pop-culture they were a rather short-lived and geographically restricted group, found only in the Late Cretaceous of North America and parts of northeast Asia. The Ceratopsids are split taxonomically into two groups, the Centrosaurs, which went extinct in the Early Maastrichtian, about 5 million years before the end of the Cretaceous, and which tended to have enlarged nasal horns (horns on their noses) and ornate neck frills, and the Chasmosaurs, which survived till the End Cretaceous Extinction, and which tended to have enlarged orbital horns (horns above their eyes) and large but simple frills.

In a paper published in the journal Current Biology on 15 June 2015, Caleb Brown and Donald Henderson of the Royal Tyrrell Museum of Palaeontology describe a new species of Chasmosaur from the Late Cretaceous St. Mary River Formation in the Waldron Flats area of Alberta, close to the Oldman River and about 164 km south of Calgary.

The new specimen is named Regaliceratops peterhewsi, where ‘Regaliceratops’ means ‘Royal Ceratopsid’, in reference to both the ornamentation of the frill and the Royal Tyrell Museum, and ‘peterhewsi’ honours Peter Hews, who discovered the specimen from which the species is described, a single skull, complete but for the absence of the rostral bone and the lower jaw; the post cranial skeleton is unknown.

Photographs and Interpretive Line Drawings of the Holotype of Regaliceratops peterhewsi. (A–D) Nearly complete cranium in right lateral (A), left lateral (B), rostral (C), and dorsal (D) views. (A’–D’) Interpretive drawings of photographed views in (A)–(D). Areas in shadow, (C) and (D) left, are fully illustrated at right. Areas in white represent reconstruction (plaster/epoxy putty), and hatched areas indicate matrix. The following abbreviations are used: cvp, caudoventral process of premaxilla; ej, epijugal; en, external naris; isf, interseptal fenestra; itf, infratemporal fenestra; j, jugal; jn, jugal notch; m, maxilla; n, nasal; nhc, nasal horncore; ns, narial strut; ob, orbit; p, parietal; pf, parietal fenestra; phc, postorbital horncore; pm, premaxilla; por, postorbital ridge; pp, palpebral; ps, epiparietosquamosal; P#, epiparietal; s, squamosal; stf, supertemporal fenestra; S#, episquamosal; tp, triangular process. Scale bar represents 10 cm. Brown & Henderson (2015).

The skull morphology of Regaliceratops peterhewsi places it firmly within the Chasmosaurinae, however it shows a number of features common to Centrosaurs, most notably an ornate frill and a large nasal horn. These features have been seen in Chasmosaurs before, but largely in early members of the group, closer to the divergence between the two groups, and never to the extent seen in Regaliceratops peterhewsi.

A phylogenetic analysis of the Chasmosaurs carried out by Brown and Henderson suggests that they can be split into two distinct groups, an earlier Chasmosaurus-like group which were smaller and had features closer to those of Centrosaurs, and a later Triceratops-like group which were larger and had more highly developed Chasmosaur features (such as enlarged orbital horns and large simple frills). These two groups are share a common ancestor more recent than their common ancestor with the Centrosaurs, but before any of the known fossil species appeared, suggesting that a long ghost-lineage (a lineage that can be inferred from the gap in the evolutionary record, but for which no fossils are known) for the Triceratops-like group exists. Importantly the Chasmosaurus-like group appear to go extinct at about the same time as the Centrosaurs, suggesting that a common cause may have been responsible for the demise of the two groups, while the Triceratops-like group diversifies after the disappearance of the other two groups, which may indicate they were moving into ecological niches formerly occupied by Centrosaurs and Chasmosaurus-like Chasmosaurs.

Time-calibrated strict consensus tree of five most parsimonious trees for Chasmosaurinae utilizing the new epiossification homology scheme. Black bars indicate confident stratigraphic occurrence, whereas gray bars indicate less confidence. Bottom right: oblique view of Regaliceratops peterhewsi. Brown & Henderson (2015).

Regaliceratops peterhewsi is situated firmly within the Triceratops-like group, albeit quite early in the known group, and is the first known member of this group to show Centrosaur-like features. Among Mammals convergent evolution of horn ornamentation has been linked to convergent social behaviour. This is impossible to judge in Ceratopsids, an extinct group in which behaviour cannot be directly assessed, however it is possible that a Chasmosaur such as Regaliceratops peterhewsi moving into an ecological niche left vacant by the extinction of the Centrosaurs could also have developed similar social behaviour, resulting in convergent evolution of the skull ornamentation.

See also…

Ceratopsian Dinosaurs are thought to have originated in Asia in the Early Cretaceous, spreading to Europe and North America, and becoming the most important and diverse group of herbivorous Dinosaurs in North America by the end of the Period. Unfortunately...

Dinosaurs underwent dramatic increases in size over a number of years during their growth, and are presumed to have played a number of different ecological roles during this growth period. Numerous examples...


Ceratopsid Dinosaurs were a speciose group of large, herbivorous Dinosaurs from the Late Cretaceous of Asia and North America...


Follow Sciency Thoughts on Facebook.

Tuesday, 16 December 2014

A Ceratopsian Dinosaur from the Early Cretaceous of Montana.


Ceratopsian Dinosaurs are thought to have originated in Asia in the Early Cretaceous, spreading to Europe and North America, and becoming the most important and diverse group of herbivorous Dinosaurs in North America by the end of the Period. Unfortunately, while the group are well known from Latest Cretaceous fossils in North America, for much of the period they are only known from isolated teeth and bone fragments. It is not certain when they first reached North America, nor whether they got their via northeast Asia and Alaska or via Europe.

In a paper published in the journal PLoS One on 10 December 2014, Andrew Farke of the Raymond M. Alf Museum of Paleontology and the Sam Noble Oklahoma Museum of Natural History, Desmond Maxwell of the Department of Biological Sciences at the University of the Pacific and the Sam Noble Oklahoma Museum of Natural History, Richard Cifellialso of the Sam Noble Oklahoma Museum of Natural History and Mathew Wedel of the College of Podiatric Medicine at the Western University of Health Sciences and of the Sam Noble Oklahoma Museum of Natural History describe a new species of Ceratopsid Dinosaur from the Early Cretaceous Cloverly Formation of Carbon County in southern Montana.

The new species is named Aquilops americanus, where ‘Aquilops’ means ‘Eagle-face’, a reference to the Dinosaur’s hoked beak, and ‘americanus’ means ‘American’. The specimen comprises a partial skull 84.2 mm in length, with an accompanying left lower jaw in three fragments. The skull is slightly compressed mediolaterally and dorsoventrally, leading to some deformation, particularly at the rear, and the right side is better preserved than the left.

Cranium of Aquilops americanus. (A) Right lateral and (B) left lateral views. Farke et al. (2014).

Aquilops americanusis about 60% of the size of specimens of the early Ceratopsians Liaoceratops yanzigouensis and Archaeoceratops oshimai, both of which are presumed to be adults, and pf a similar size to a presumed juvenile specimen of Liaoceratops yanzigouensis. Developmentally it shows a mixture of features associated with juvenile and adult Ceratpsians, and Farke et al. suggest that the specimen is a subadult (i.e. an animal that had almost reached adult size).

Cranial reconstruction of Aquilops americanus in (A) right lateral and (B) dorsal views. Farke et al. (2014).

Aquilops americanus is the earliest described Ceratopsian from North America, dating from about 104–109 million years ago. This suggests that Ceratopsians had reached the continent much earlier than previously supposed; however as we currently understand the phylogeny of Ceratpsian Dinosaurs it occupies a position very close to the base of the group’s family tree, with the more derived Ceratopsians of Late Cretaceous North America emerging from a group of Dinosaurs that were apparently still in Asia much later the period, suggesting that Aquilops americanus is the result of an earlier, separate invasion of the continent, and has little bearing on the origins of these later animals.

Hypothesis of phylogeny and biogeography for Neoceratopsia. Some terminal taxa have been combined for space considerations, and the range bars for each taxon indicate uncertainty rather than known geological ranges. Continent icons indicate the ancestral areas reconstructed by DEC modeling. Silhouettes depict representative members of major clades and grades. Farke et al. (2014).

Life restoration of Aquilops americanus. Brian Engh in Farke et al. (2014).

See also…

Ceratopsid Dinosaurs were a speciose group of large, herbivorous Dinosaurs from the Late Cretaceous of...


Ceratopsid Dinosaurs were a speciose group of large, herbivorous Dinosaurs from the Late Cretaceous of Asia and North America. They were large, quadruped Dinosaurs with distinctive neck-frills and horns, and...

Ceratopsid dinosaurs changed considerably during growth, which caused early palaeontologists to name different growth stages of the same animal as different species, or even genera. The Maastrichtian (Latest Cretaceous, 70.6-65.5 million years ago) Ceratopsids of North America were at one point divided into 22 species...



Follow Sciency Thoughts on Facebook.

Saturday, 21 September 2013

A short-snouted Ceratopsid Dinosaur from the Late Cretaceous of southern Utah.

Ceratopsid Dinosaurs were a speciose group of large, herbivorous Dinosaurs from the Late Cretaceous of Asia and North America. They were large, quadruped Dinosaurs with distinctive neck-frills and horns, and many vertebrate paleaontologists have speculated that the large number of species may have been the result of sexual selection, as in many modern Mammals. The group do not show any great ecological diversity, but each species has a distinctive arrangement of horns and frill-ornaments; if this is a result of sexual selection it is likely that the males and females of many species have been described separately.

In a paper published in the Proceedings of the Royal Society Series B Biological Sciences on 17 July 2013, a team of scientists led by Scott Sampson of the Denver Museum of Nature and Science, the Department of Geology and Geophysics at the University of Utah and the Natural History Museum of Utah, describe a new species of Ceratopsid Dinosaur from the Late Cretaceous Kaiparowits Formation in southern Utah’s Grand Staircase-Escalante National Monument.

The new species is named Nasutoceratops titusi, where 'Nasutoceratops' means 'large-nosed Ceratopsid' and 'titusi' honours Alan Titus a palaeontologist at Grand Staircase-Escalante National Monument for his assistance in work at the site. The species is described from a specimen comprising a nearly complete 1.8 m skull plus three fragmentary dorsal vertebrae and parts of both forelimbs, plus a second specimen comprising a disarticulated skull and jaw elements, and an isolated squamosal bone from a third specimen.

Nasutoceratops titusi,  skull in dorsal (a) and lateral (b) views. Scale bar represents 50 cm and the naris and maxilla are photoreversed in (b). Squamosal in lateral view (c). Note lateral squamosal ridge in (b) and (c). Epijugal in anterior view (d ). Nasal in medial (e) and lateral ( f ) view. Nasal (g,h), premaxilla (h), and maxilla (i) in caudal (g) and lateral (i) views ( photoreversed). Scale bars for (c–i) represent 10 cm. Abbreviations (autapomorphies noted with an asterisk (*)): cns, caudal nasal septum*; f, frontal; ff, frontoparietal fontanelle; ins, internarial suture; j, jugal; js, jugal suture; la, lacrimal; m, maxilla; md, maxillary diastema; n, nasal; na, naris; nh, nasal horncore; np, nasal pneumatopore*; ns, narial septum; nsp, narial spine; o, orbit; on, otic notch; p, parietal; p0–p7, epiparietals; pf, parietal fenestra; epiparietals; pm, premaxilla; pms, premaxillary suture*; poh, postorbital horncore*; pts, pterygoid-epipterygoid suture; rs, rostral suture; sq, squamosal; sqr, lateral squamosal ridge; va, ventral angle. Sampson et al. (2013).


Nasutoceratops titusi is an unusual Ceratopsid; it has a shorter snout than any other known member of the group, but it's narial region (nose) is extremely inflated and dominates the face. The supraorbital horns (horns above the eyes) are elongated and twisted, and have grooves running along their entire length. The frill is large but not outstandingly so and not otherwise unusual.

Nasutoceratops titusi,  skull reconstruction in (a) dorsal and (b) lateral views. (c) Skeletal reconstruction with elements presently known in white. (a,b) Scale bars, 50 cm and (c) 1 m. Sampson et al. (2013).



Follow Sciency Thoughts on Facebook.

Wednesday, 7 March 2012

Torosaurus and Triceratops; one dinosaur or two?

Ceratopsid dinosaurs changed considerably during growth, which caused early palaeontologists to name different growth stages of the same animal as different species, or even genera. The Maastrichtian (Latest Cretaceous, 70.6-65.5 million years ago) Ceratopsids of North America were at one point divided into 22 species in 10 genera, but as palaeontologists have uncovered intermediate forms this has been consolidated into three species in two genera, Torosaurus and Triceratops.

In 2010 John Scannella and Jack Horner of Montana State University published a paper in the Journal of Vertebrate Paleontology in which they propose that the small-frilled Triceratops is an immature form of the large-frilled Torosaurus, so that there should only be a single genus, Triceratops (when species or genera are combined the older name takes preference, in this case Triceratops which was first named in 1889, two years ahead of Torosaurus in 1891).

In a paper published in the journal PLoS ONE on 29 February 2012, Nicholas Longrich and Daniel Field of the Department of Geology and Geophysics at Yale University discuss the results of a study of both the physical and chronological distribution of Torosaurus and Triceratops, and a study of a large number of individual specimens to look for intermediate characters.

The skulls of (A) Triceratops and (B) Torosaurus. (B) has a larger crest than (A), with two promanent openings, but this might be a later developmental stage. From Longrich and Field (2012).

Longrich and Field found that Triceratops and Torosaurus did overlap closely in both chronological and physical distribution, with the majority of locations that produced fossils of one also producing fossils of the other, and those sights which produced only one or the other being otherwise fossil-poor. This leaves open the possibility that the two dinosaurs might be members of the same species.

The distribution of Triceratops and Torosaurus. (1) Scollard Formation, Alberta; (2) Frenchman Formation, Saskatchewan, (3) Hell Creek Formation, Montana; (4) Hell Creek Formation, North Dakota; (5) Hell Creek Formation, South Dakota; (6) Lance Formation, Wyoming; (7) Denver Formation, Colorado; (8) North Horn Formation, Utah; (9) Javelina Formation, Texas. From Longrich and Field (2012).

After this Longrich and Field looked at the skulls of a large number of Triceratops and Torosaurus specimens, examining both the morphological development and the age based upon bone tissue development. They found that a full range of ages were present in both dinosaurs, strongly implying that they were not the same species.

Scanella and Horner had reported depressions in the crests of some Triceratops, which they argued were analogous to the gaps in the crest of Torosaurus, but Longrich and Field argue that these do not form on the same bones, and therefore cannot develop from one to another.

The frills of (A) Triceratops and (B) Torosaurus; fen, fenestra; fos, parietal-squamosal fossa; par, parietal; sq, squamosal. P0, midline epiparietal; p1–p5 epiparietals 1–5; eps, epoccipital crossing the parietal-squamosal suture. From Longrich and Field (2012).

They also found that two forms of Torosaurus previously thought to be different developmental stages did not appear to be sequential when assessed by tissue development, the larger, apparently more developed, form often (but not always) being younger than the smaller, less developed form. Longrich and Field examined several possibilities for this. Firstly our understanding of bone tissue development in Ceratopsid Dinosaurs might be inaccurate. This would have implications for the wider study of the group, so Longrich and Field suggest this needs to be investigated further. Then there is the possibility that development in Torosaurus was variable, either between populations or in response to climatic variations, so that individuals of the same age might be at different developmental stages. Finally they examined the possibility that Torosaurus might be sexually dimorphic, so that the different forms could represent the two sexes of a single species.

The two morphotypes of Torosaurus. B was formerly thought to grow into A, but tissue development suggests A is younger than B. From Longrich and Field (2012).

For some reason Longrich and Field did not discuss the possibility that the two morphotypes of Torosaurus might tie in with the two 'species' of Triceratops, to give two sexually dimorphic species, each with a large and small crested form, though it seems unlikely that this did not occur to them.

Wednesday, 7 December 2011

New dinosaurs from old draws.

In 1916 the father and son dinosaur hunting team Charles and Levi Sternberg mounted an expedition to the Steveville Badlands of Alberta, Canada to collect dinosaur bones for the Natural History Museum in London. The area had proven a bountiful source of dinosaur bones for previous expeditions, having first been worked by Lawrence Lamb in 1898, and has remained a centre for dinosaur hunting to this day, forming part of Dinosaur Provincial Park, an area so rich in dinosaur bones that palaeontologists have attempted to erect stratigraphic biozones based upon them. Erecting biozones is a method of using fossils to date rocks; this uses fossils with known chronological ranges to establish the maximum and minimum age of rocks containing them; usually biozones are erected using shellfish, micro-organisms, pollen, rodents' teeth or other such small widespread fossils.

Alberta proved to be a productive area for the Sternbergs, but failed to impress the Museum; the then Keeper of Geology, Arthur Smith Woodward, described the fossils returned as 'rubbish'. Woodward was a powerful and influential figure at the time, though not a wise one. He gained a reputation for using his influence to marginalize promising younger palaeontologists who he saw as a threat to his status, and had an unscientific tendency towards self promotion, attaching himself to newsworthy discoveries and burying others. He was eventually discredited by the Piltdown forgery.

The items sent by the Sternbergs to Woodward did not contain large, complete fossil dinosaurs that would make good displays in the Museum, so they were stored away and forgotten, and never really assessed for their scientific interest. The Sternbergs were apparently unconcerned by this; they were veteran fossil hunters, and if the British Museum was not interested in their fossils, then there were plenty of other museums that were.

Ninety years later the specimens were re-examined by modern scientists, who realized the significance of the fossils. Amongst other treasures were two partial skulls from a previously unknown Ceratopsid Dinosaur, which has now been formerly described by a team lead by Andrew Farke of the Raymond M. Alf Museum of Paleontology in California in a paper in the journal Acta Palaeontologica Polonica.

The new dinosaur has been given the name Sinops sternbergorum (Spinops meaning 'spineface' and sternbergorum in honor of its' discoverers. Sinops lived about 76 million years ago, in the Late Cretaceous. It is thought to have been about six meters long in life, and to have weighed about two tonnes. Like other Ceratopsid Dinosaurs it had a prominent facial shield, with several horns.
Artist's rendering of the skull bones of Sinops sterbergorum. Copyright Lukas Panzrin, courtesy of the Raymond M. Alf Museum of Paleontology.

This is where things got interesting. When Farke et al. examined the nasal horn of Sinops they realized that it erupted from a different part of the skull to that of better described Ceratopsid Dinosaurs. This was not entirely unexpected; it had been suggested of some other species, but in these cases the fossils had been imperfect and somewhat ambivalent. In the case of Sinops there was no doubt; the horn was sufficiently different from that of other ceratopsids that it must have arisen separately.

Sinops is a member of a group of ceratopsids called the Centrosaurinae. This group are considered basal or (misleadingly) primitive within the ceratopsid group. What this actually means is that the group divided from the other Ceratopsid Dinosaurs early in the family's history; it is not closely related to the most familiar ceratopsid, Triceratops.

The earliest known centrosaur derives from Late Cretaceous Oldman Formation of Alberta the is Albertaceratops nesmoi; it is about a million and a half years older than Sinops at roughly 77.5 million years old. It is known from a single skull and a few fragmentary bones from the rest of the body. Albertaceratops is bore long brow horns and a bony ridge on its nose where most ceratopsids have a horn, which suggests that it came from a lineage in which the horn had not yet arisen, this supports the idea that the nasal horn subsequently evolved in separate lineages. Albertaceratops also had two small, hook-like horns pointing outward at the top of it's crest.
An impression of Albertaceratops nesmoi by paleoartist Nobu Tamura.

The next centrosaur to appear in the fossil record is Centrosuarus, which first appears in the Oldman Formation of Alberta, about 65.5 million years ago, and continues into the overlying Dinosaur Park Formation. The genus after which the group is named. Centrosaurus had a large nasal horn, small brow horns and a row of small horns around the frill. Centrosaurus could be up to six meters long, but was not especially heavily built. There are two described species, C. apertus, in which the small brow horns curve upwards, and C. brinkmani, in which they curve to the side. It has a much better record than most other species, with several vast bone beads known. These are though to have formed where large numbers of individuals gathered around drying water holes and eventually perished.

A reconstruction of the head of Centrosaurus brinkmani by Julius Csotonyi of the Royal Tyrell Museum in Alberta.

The beds immediately overlying those containing Centrosaurus contain another species of centrosaur, Styracosaurus albertensis. This was a slightly shorter animal from tip to tail, but was much heavier built, reaching 1.8 m at the shoulder, and being loner in the body and shorter in the tail; it could probably weigh nearly 3 tonnes. Like Centrosaurus, Styracosaurus has been found in large bone beds, thought to have formed in mass death events around drying water holes in times of draught. Styracosaurus had a large, straight, nasal horn and almost non-existent brow horns. The edge of the frill bore a number of large horns rivaling the nasal horn in length. The nasal horn has not been found intact, so the exact size and development pattern of this horn is unclear.
A reconstruction of Styracosaurus albertensis by Nobu Tamura.

Diabloceratops eatoni lived 75 million years ago in what is now Utah. It is known only from a partial skull, with a pair of large spikes on the top of its neck frill, small brow horns and one or two small nasal horns (again this part of the skull is not well preserved). Diabloceratops is considered to be from a lineage that derived from the earliest centrosaurs separately; all other known centrosaurs are thought to be more clesely related to one-another than to Diabloceratops.
A reconstruction of Diabloceratops eatoni, by natural history illustrator Andrey Atuchin.

Einiosuarus procurvicornis is known from a number of bone beds from Montana, between 74.5 and 74 million years old. It reached about six meters in length, had a forward curving nasal horn, brow horns reduced to a pair of knobs, and a pair of horns on the top of its small neck frill.
Reconstruction of Einiosaurus procurvicornis by illustrator Sergey Krasovskiy.

From the same time in Montana came Rubeosaurus ovatus, known only from two partial skulls. Rubeosaurus appears to have had a large nasal horn, and at least two pairs of horns on the neck frill. Some juvenile fossils attributed to the genus Brachyceratops may also belong to this species.

Above these species in the same deposits in Montana, the species Achelousaurus horneri dates from about 74 million years ago, and is known from three skulls and a partial skeleton. It appears to have been about six meters in length, and to have had boney ridges in the place of the nasal and brow horns, though it did have a pair of horns on the top of the neck frill.
An illustration of Achelousaurus horneri by Sergey Krasovskiy.

The latest surviving genus of centrosaur appears to have been Pachyrhinosaurus. Two species of this are known from Alberta, P. lakustai dating from between 73.5 and 72.5 million year ago and P. canadensis from about 71.5 to 71 million years ago. A third species, P. perotorum has been found in Alaska, and is even younger, at between 70 and 69 million years old, making it the last known surviving centrosaur. Pachyrhinosaurus was about eight meters long when fully grown, and weighed about eight tonnes. The nose and brow horns were replaced by bony ridges, and the neck frill bore a single pair of small horns in P. canadensis and some specimens of P. lakustai. P. perotorum and some specimens of P. lakstai lacked these horns. In P. Canadensis and P. perotorum the brow ridges were close together, but in P. lakustai they were further apart.
Pachyrhinosaurus canadensis by Nobu Tamura.