Torosaurus Latus

''Torosaurus'' ("perforated lizard", in reference to the large openings in its frill) is a genus of herbivorous ceratopsid dinosaur that lived during the late Maastrichtian stage of the Cretaceous period, between 68 and 66 million years ago, though it is possible that the species range might extend to as far as 69 million years ago.*Hicks, J.F., Johnson, K.R., Obradovich, J. D., Miggins, D.P., and Tauxe, L. 2003. Magnetostratigraphyof Upper Cretaceous (Maastrichtian) to lower Eocene strata of the Denver Basin, Colorado. In K.R. Johnson, R.G. Raynolds and M.L. Reynolds (eds), Paleontology and Stratigraphy of Laramide Strata in the Denver Basin, Pt. II., Rocky Mountain Geology 38: 1-27. Fossils have been discovered across the Western Interior of North America, from Saskatchewan to southern Texas.

''Torosaurus'' possessed one of the largest skulls of any known land animal, with the frilled skull reaching in length. ''Torosaurus'' is thought to have been the same size as the contemporary ''Triceratops'', but is distinguished by an elongated frill with large openings (fenestrae), long squamosal bones of the frill with a trough on their upper surface, and the presence of five or more pairs of hornlets (epoccipitals) on the back of the frill. ''Torosaurus'' also lacked the long nose horn seen in ''Triceratops prorsus'', and instead resembled the earlier and more basal ''Triceratops horridus'' in having a short nose horn. Three species have been named, ''Torosaurus latus'', ''T. gladius'' and ''T. utahensis''. ''T. gladius'' is no longer considered a valid species, however.

In 2010, the validity of ''Torosaurus'' was disputed. A study of fossil bone histology combined with an investigation of frill shape concluded that ''Torosaurus'' probably represented the mature form of ''Triceratops'', with the bones of typical ''Triceratops'' specimens still immature and showing signs of a first development of distinct ''Torosaurus'' frill holes. During maturation, the skull frill would have been greatly lengthened and holes would have appeared in it. In 2011, 2012 and 2013 however, studies of external features of known specimens have claimed that morphological differences between the two genera preclude their synonymy. The main problems are a lack of good transitional forms, the apparent existence of authentic ''Torosaurus'' subadults, different skull proportions independent of maturation, and hole formation at an adult stage not being part of a normal ceratopsian maturation sequence. Consequently, it is still heavily debated whether ''Torosaurus'' truly is an adult ''Triceratops'' or a separate genus; though most researchers favor the latter interpretation currently.

Discovery and species

In 1891, two years after the naming of ''Triceratops'', a pair of ceratopsian skulls with elongated frills bearing holes were found in southeastern Wyoming, Niobrara County, by John Bell Hatcher. Hatcher's employer, palaeontologist Professor Othniel Charles Marsh, coined the genus ''Torosaurus'' for them.O.C. Marsh, 1891, "Notice of new vertebrate fossils", ''The American Journal of Science, series 3'' 42: 265-269

The name ''Torosaurus'' is frequently translated as "bull lizard" from the Latin noun ''taurus'' or Italian and Spanish ''toro'' but much more likely is derived from the Greek verb (''toreo'', "to pierce, perforate"). The allusion is to the ''fenestrae'' or ("window-like") holes in the elongated frill, which have traditionally served to distinguish it from the solid frill of ''Triceratops''. Much of the confusion over etymology of the name results from the fact that Marsh never explicitly explained it in his papers.

Two ''Torosaurus'' species have been identified:
* ''T. latus'' (type species). ''Latus'' means "the wide one" in Latin, in reference to the frill.
* ''T. utahensis'' () Lawson, 1976

Another species was subsequently regarded as identical to ''T. latus'':
* ''T. gladius'' . ''Gladius'' is "sword" in Latin, in reference to the elongated shape of the squamosal.

''T. latus'' was based on holotype YPM 1830, a partial skull. The holotype of ''T. gladius'' was specimen YPM 1831, a larger skull. Both fossils were found in the Lance Formation, dating from the Maastrichtian. Similar specimens found in Wyoming, Montana, South Dakota, North Dakota, Colorado, Utah and Saskatchewan have since been referred to ''Torosaurus''. Those that can be identified with some certainty include: ANSP 15192, a smaller individual in South Dakota uncovered by Edwin Harris Colbert in 1944; MPM VP6841, a partial skeleton with skull, now mounted at Milwaukee Public Museum; SMM P97.6.1, a skull lacking the snout; and two partial skulls from the Hell Creek Formation reported in 2002: MOR 981, discovered in 1998, and MOR 1122, from 2001. Fragmentary remains that could possibly be identified with the genus have been found in the Big Bend Region of Texas and in the San Juan Basin of New Mexico. Paleontologists have observed that ''Torosaurus'' specimens are uncommon in the fossil record; specimens of ''Triceratops'' are much more abundant.

''Torosaurus utahensis'' was originally described as ''Arrhinoceratops utahensis'' by Charles Whitney Gilmore in 1946, based on specimen USNM 15583, a frill fragment from Emery County, Utah. In 1976 it was renamed ''Torosaurus utahensis'' by Douglas Lawson. Review by Robert Sullivan ''et al.'' in 2005 left it as ''Torosaurus utahensis'' and somewhat older than ''T. latus''. In 2008 Rebecca Hunt referred considerable additional material to this species. Research has not yet been published on whether ''T. utahensis'' should be regarded as a new genus or, as has been suggested for ''T. latus'', the mature growth stage of some species of ''Triceratops''.

Description

The individuals referred to as ''Torosaurus'' are all large, comparable to the largest ''Triceratops'' specimens. Due to the elongated frill, especially the skull length is considerable. Hatcher estimated the skull of YPM 1830 at 2.2 metres, of YPM 1831 at 2.35 metres. In 1933 Richard Swann Lull increased this to 2.4 metres and 2.57 metres respectively. Based on this, ''Torosaurus'' was seen as having the longest skull of any known land animal. However, in 1998 Thomas Lehman claimed that a ''Pentaceratops'' specimen possessed a partial skull that would have been 2.9 metres long in life. This was again doubted by Nicholas Longrich who in 2011 named this exemplar as a separate genus ''Titanoceratops'' and concluded its skull had been reconstructed as too long. Furthermore, in 2006 Andrew Farke had pointed out that the new skulls described by him were on average even longer than Hatcher's original two: MOR 1122 has a length of 252 centimetres and MOR 981 of 277 centimetres.

Farke in 2006 established some diagnostic traits of ''Torosaurus''. The frill is extremely long in comparison to the remainder of the skull. The rear, parietal, edge of the frill bears ten or more epiparietals, triangular osteoderms. A midline epiparietal is absent; likewise no osteoderm straddles the parietal-squamosal boundary. The parietal bone is thin. It is pierced by parietal ''fenestrae'' in the form of circular or transversely oval openings. The parietal bone is about 20% wider than long. Farke identified a single trait in which ''T. latus'' differed from both ''Triceratops horridus'' and ''T. utahensis'': its squamosal bore a conspicuous ridge on the edge with the parietal combined with a deep longitudinal trough parallel to it.

Farke pointed out that the known ''Torosaurus'' specimens are rather variable. The orbital "brow" horns are sometimes large and curved to the front, as with MOR 981, sometimes short and straight as shown by MOR 1122 and ANSP 15191. Also the position of these horns differs: often they are located directly on top of the eye socket but with YPM 1831 they originate at the rear edge of the orbit. Likewise there is a variation in the form of the nose horn. YPM 1831 and to a lesser extent YPM 1830 have a straight upright nasal horn but MOR 981, ANSP 15192 and especially MOR 1122 at most possess a low bump. The frill too differs. ANSP 15192 and YPM 1830 have a shield curving upwards at the rear, but the frill of YPM 1831 is nearly flat, though this could be an artefact of restoration. The frill of YPM 1831 is also heart-shaped, with a clear midline notch, whereas the rear edge of the other specimens is straight. The frill proportions are quite variable: with YPM 1831 the length-width ratio is 1.26 but MOR 981 has a shield 2.28 times longer than wide. The number of epiparietals is difficult to assess as most fossils seem to have lost them. MOR 981 and MOR 1122 have ten and twelve epiparietals respectively. YPM 1831 has been restored with a fontanelle in the skull roof, which possibly is authentic. Farke also concluded that the degree of variability did not exceed that shown by related genera.

Farke stressed that, apart from the frill, no systematic differences could be found between ''Torosaurus'' and ''Triceratops''. All ''Torosaurus'' specimens are similar in that they lack a truly long nasal horn and a horizontal arterial groove at the front base of that horn, but ''Triceratops'' fossils with the same combination of traits are not uncommon. Hunt in 2008 concluded that ''T. utahensis'', contrary to ''T. latus'' but similar to ''Triceratops'', possessed a midline epiparietal.

Classification

Ceratopsid cladogram based on the phylogenetic analysis conducted by Sampson ''et al.'', in 2010:

In 1891, Marsh placed ''Torosaurus'' in the Ceratopsidae family of the Ceratopsia (Greek: "horned faces"), a group of herbivorous dinosaurs with parrot-like beaks which thrived in North America and Asia during the Jurassic and Cretaceous Periods.

''Torosaurus'' has, with its long frill, traditionally been classified in the Chasmosaurinae. It was seen as a late member of a line descending from ''Anchiceratops'' or ''Arrhinoceratops''. It was thus placed in a different branch from ''Triceratops'' which well into the 1980s was seen as a member of the Centrosaurinae because of its short frill. However, in the 1990s exact cladistic analysis showed that both genera were chasmosaurines. Recent analyses invariably show a close relationship between ''Torosaurus'' and ''Triceratops''.Farke, A. A. "Cranial osteology and phylogenetic relationships of the chasmosaurine ceratopsid ''Torosaurus latus''", pp. 235-257. In K. Carpenter (ed.). ''Horns and Beaks: Ceratopsian and Ornithopod Dinosaurs''. Indiana Univ. Press (Bloomington), 2006.

Possible synonymy with ''Triceratops''

A debate has sparked over the possibility that ''Torosaurus'' might be identical to ''Triceratops''. In the Maastrichtian of Laramidia two closely related chasmosaurine genera shared the same habitat. The only discernible difference between them was the form of the frill. No ''Torosaurus'' juveniles are known but a considerable number of ''Triceratops'' juveniles have been found. ''Triceratops'' differs from other chasmosaurines in the retention as an adult of a juvenile trait: the short squamosals, a case of paedomorphosis. In 2009 John Scannella, investigating dinosaur ontogeny in the Hell Creek Formation of Montana, concluded that this situation could be best explained by the hypothesis that ''Triceratops'' and ''Torosaurus'' were growth stages of a single genus. The ''Torosaurus'' specimens would be fully mature individuals of ''Triceratops''. ''Torosaurus'' would be a junior synonym of ''Triceratops'', the latter name having priority.

In 2010 Scanella and Jack Horner, Scannella's mentor at Montana State University, published research on the growth patterns in thirty-eight skull specimens (twenty-nine of ''Triceratops'', nine of ''Torosaurus'') from the Hell Creek formation. They concluded that ''Torosaurus'' indeed represents the mature form of ''Triceratops''.Scannella, J. and Horner, J.R. (2010). "''Torosaurus'' Marsh, 1891, is ''Triceratops'' Marsh, 1889 (Ceratopsidae: Chasmosaurinae): synonymy through ontogeny ." ''Journal of Vertebrate Paleontology'', 30(4): 1157–1168. Horner stressed that the frill of ceratopsian skulls consisted of metaplastic bone. A characteristic of metaplastic bone is that it can lengthen and shorten over time, extending and resorbing to form new shapes. Significant development is seen even in those skulls already identified as ''Triceratops'', Horner observed, "where the horn orientation is backwards in juveniles and forward in adults". Approximately 50% of all subadult ''Triceratops'' skulls have two thin areas in the frill that correspond with the placement of the "holes" in ''Torosaurus'' skull frills which are surrounded by mature granular bone, suggesting that these developed to offset the weight that would otherwise have been added as maturing ''Triceratops'' individuals grew longer frills. Horner made this part of a larger argument that in general many purported dinosaur species might have been growth stages of other known species. With old ''Triceratops'' individuals the frill would have begun to lengthen considerably, causing it to flatten and widen at its rear edge. At the same time parietal ''fenestrae'' would have appeared, resulting in the typical chasmosaurine frill shape.

Scanella and Horner recognised that not all data were easily explained by their hypothesis. For these they advanced auxiliary hypotheses. One problem was that if ''Torosaurus'' were the normal last maturation phase of ''Triceratops'', which phase they called the "toromorph", it would be expected that ''Torosaurus'' fossils were quite common, whereas in fact they are rather rare. This they explained by a high mortality of subadults and the possibility that old animals preferentially lived on heights, where erosion prevented fossilisation. A second problem was the size range of ''Torosaurus'' specimens which seems to suggest the existence of authentic ''Torosaurus'' subadults. Of these they claimed that the bone structure indicated a fully mature age, the size difference being the apparent result of individual variation. A third possible objection was the seeming lack of transitional forms between individuals with and without parietal holes; these ''fenestrae'' are always perfectly shaped, not like incipient perforations. To counter it, they pointed to specimen USNM 2412, the holotype of the contentious ''Nedoceratops'', as an example of precisely such a transitional form. The problematic traits of this genus would simply reflect its being in the first stages of transforming into a "toromorph". A last problem was offered by the number of epoccipitals, the osteoderms on the frill edge. With ''Triceratops'' there are typically five epiparietals, including a midline osteoderm; with ''Torosaurus'' there are ten or twelve, a midline epiparietal being absent. Also the number of episquamosals on the side edge of the frill differs: five with ''Triceratops'', six or seven with ''Torosaurus''. This was explained by the assumption that the number of epoccipitals increased during maturation. Also it was pointed out that both number and position of the osteoderms are variable with ''Triceratops'' as shown by specimen MOR 2923, having six epiparietals but lacking a midline one.

Scannella and Horner's conclusions have not been unanimously accepted. Several experts, though admitting the possibility that the "toromorph" hypothesis is correct, have denied this is probable. The hypothesis was directly challenged by a 2011 paper by Andrew Farke and a 2012 one by Nicholas Longrich. Farke in 2011 redescribed the problematic ''Nedoceratops hatcheri'' as an aged or diseased individual of its own genus, against Scannella and Horner who argued for its identification with ''Triceratops''. Farke pointed out that the irregular holes in the ''Nedoceratops'' frill, far from piercing thinning bone, were surrounded by thick swellings. Farke further concluded that several facts were difficult to reconcile with the proposed development of a ''Triceratops'' into a ''Torosaurus''. In general, with ceratopids the number of epoccipitals does not increase when the frill grows. Even though the number of episquamosals is often variable, there seems to be no relation with size, because sometimes juveniles already show the maximum number; apparently this is a matter of individual variation, not ontogeny. Likewise, with Ceratopia in general, the formation of holes in the frill is not related to age, even the youngest individuals often possessing the parietal ''fenestrae''. The thin bone areas on the frill of ''Triceratops'', the purported location of incipient holes, Farke explained as muscle attachment sites. There would be no consistent relation between holes and a granular bone structure. Many ''Triceratops'' specimens have frills with a deeply veined surface, indicating considerable age; the bone of their frills would have to be rejuvenated and then become granulated again in order for hole formation to begin, which Farke considered an unlikely sequence. Finally, Farke pointed out that specimen YPM 1831, despite its enormous size, was apparently not yet full-grown, as shown by its unfused sutures and smooth bone texture, and thus seemed to represent an authentic ''Torosaurus'' subadult.Farke, A. A. (2011)
Anatomy and taxonomic status of the chasmosaurine ceratopsid ''Nedoceratops hatcheri'' from the Upper Cretaceous Lance Formation of Wyoming, U.S.A..
''PLoS ONE'' 6 (1): e16196.

The same year Scanella and Horner responded to some of Farke's critique. They admitted that USNM 2412, in view of its pathologies, was not an ideal candidate for a transitional form, but stressed that, apart from swellings, the holes in its frill were also bordered by granular and thinning bone. Taking all the evidence into consideration, they thought it much more likely that ''Nedoceratops'' represented a diseased individual of ''Triceratops'', than a genus of its own. They also pointed to ''Triceratops'' specimens showing precisely the combination of veined, granular and young striated bone that Farke had considered improbable. That the thin areas on ''Triceratops'' frills were muscle attachment sites was rejected by them because the bone at these points did not show the rugose surface typical for such an attachment. For the difference in the number of epoccipitals they offered two additional explanations. The osteoderm tips of old individuals might during life have eroded in such a way that each osteoderm gave the impression of two being present. This way the normal number of five or six ''Triceratops'' epiparietals could have doubled to ten or twelve, precisely the amount seen with the ''Torosaurus'' specimens. Alternatively, the ''Torosaurus latus'' specimens, having been found in older layers, might, in a process of anagenesis, represent an early stage of ''Triceratops'' evolution. The oldest specimen that can be dated, MOR 1122, has twelve epiparietals, the younger MOR 981 possesses ten, seeming to indicate an evolutionary sequence in which the number of epiparietals gradually decreased.

In 2012, Longrich investigated the problem by applying the principle of falsification. From any valid scientific hypothesis predictions can be derived by which it can be tested. Longrich argued that the "toromorph" hypothesis implied three such predictions. Firstly, if ''Torosaurus'' were identical to ''Triceratops'', their fossils should be found in the same locations. In fact, their geographical ranges do not perfectly coincide: in the very north no ''Torosaurus'' fossils have been found, while from the south only ''Torosaurus utahensis'' is known. However, this situation could be an artefact of the relative scarcity of ''Torosaurus'' remains and imperfect sampling. Longrich therefore concluded that the hypothesis was corroborated by the first prediction. Secondly, the hypothesis predicted that all ''Torosaurus'' specimens would be adults, while no ''Triceratops'' specimens would be very old. According to Longrich, this last point had not yet been established. Admittedly, in 2011 Horner had published an histological study showing that all ''Triceratops'' specimens investigated possessed a subadult bone structure, but the sample had been too small to allow for a valid generalisation to all ''Triceratops'' fossils. To better test the prediction, Longrich proposed a list of twenty-four external skull traits, by which specimens could be checked regarding their level of skull element fusion and thus maturation. Thirty-six specimens were investigated applying these criteria. It transpired that the fusion typically took place in a certain sequence, providing additional information about their age. Indeed, by these criteria most ''Torosaurus'' specimens were very old. However, there were two exceptions. The small individual ANSP 15192 was, though adult, still relatively young as shown by the lack of fusion of the snout bones. The youngest specimen was YPM 1831, with an unfused snout, epijugal and occipital condyle; furthermore, it had lost all of its frill osteoderms, apparently because they had not been fused yet, while the frill edge had the external appearance of growing, young, bone. On the other hand, Longrich found that ten of the ''Triceratops'' skulls investigated had attained the same level of maturation as the most aged ''Torosaurus'' specimens. Longrich concluded that the test of the second prediction refuted the hypothesis. The third prediction was that transitional forms could be found between ''Torosaurus'' and ''Triceratops''. Longrich considered the claim that the thin areas on ''Triceratops'' frills were precursors of parietal ''fenestrae'', as the strongest proof of a transitional phase. However, he pointed out that these structures differed in position: the ''Triceratops'' depressions are partly located on the squamosal while the ''Torosaurus'' holes are fully surrounded by the parietal. Furthermore, the depressions are bordered by much thicker bone, while the ''Torosaurus'' holes are surrounded by thin bone. Longrich concluded that the hypothesis failed regarding the third prediction. Being refuted in two of the three predictions, the hypothesis should be rejected.

Longrich also suggested some additional objections to the "toromorph" hypothesis. There are no transitional forms known regarding the number of epiparietals. Also, it is hard to see how their number could have increased as they occupied the full frill edge and would, in a metaplastic growth process, simply have increased their size along with the remainder of the frill. The proposed splitting of osteoderms by erosion has only been established with episquamosals, never with epiparietals. ''Torosaurus'' has a squamosal that is thickened at the inner side and concave at the outer surface while the ''Triceratops'' squamosal is concave at the inner side and flat on top; transitional forms are unknown. The ''Torosaurus'' squamosal is also, independent from absolute size, more elongated. Longrich pointed out that when ''Torosaurus'' and ''Triceratops'' specimens are combined to create a single growth sequence, as Scanella and Horner had done, ''Torosaurus'' specimens ANSP 15192 and YPM 1831 were outliers relative to the regression line because their squamosals were more elongated than could be explained by allometry. Longrich admitted that the fact that Horner in his histological study could only find ''Triceratops'' subadults was suggestive, but offered the alternative explanation that ''Triceratops'' differed from its relatives in retaining a relative young bone structure until old age. On the other hand, bone remodelling is not a reliable estimator of maturity, in view of experimental studies demonstrating that differences in the mechanical strain conditions of various bones can significantly alter the rate or degree of such remodelling and may generate the illusion of old bone tissue. Longrich foresaw that Scanella and Horner would respond to his second test of their hypothesis by claiming that its results were caused by individual variation. According to Longrich, the importance of this factor was limited however: e.g. the size difference between ANSP 15192 and YPM 1831 had better been explained by sexual dimorphism, the former possibly being a young adult female, the latter a subadult male.

In 2013, Farke and Leonardo Maiorino published morphometric research, a statistical analysis of the morphospace (shape space) describing the variation of the ''Torosaurus'', ''Triceratops horridus'', ''Triceratops prorsus'' and ''Nedoceratops'' skulls correlated with maturation. They concluded that ''Torosaurus latus'' skulls throughout maturation retained a different form from ''T. horridus'' and ''T. prorsus'', the last two species showing an overlapping in their proportions. This is even true when the frill shape is disregarded. ''Nedoceratops'' proved, except for size, not to be a plausible transitional form between ''Torosaurus'' and ''Triceratops horridus''. Farke and Maiorino admitted that the low number of ''Torosaurus'' specimens reduced the reliability of these results but concluded that ''Torosaurus'' and ''Triceratops'' were separate taxa, though allowing for the possibility of anagenesis, i.e. the several taxa forming a single chronospecies line of descent, given the lack of good stratigraphic data.Maiorino L., Farke A.A., Kotsakis T., Piras P.,2013, "Is ''Torosaurus'' ''Triceratops''? Geometric Morphometric Evidence of Late Maastrichtian Ceratopsid Dinosaurs", ''PLoS ONE'' 8(11): e81608. doi:10.1371/journal.pone.0081608

The hypothesis that the ''Torosaurus latus'' specimens might represent a "toromorph" phase of ''Triceratops'' maturation has raised the question of whether the second ''Torosaurus'' species, ''Torosaurus utahensis'', is a "toromorph" as well. This issue has been complicated by the lack of good fossil material, most specimens consisting of isolated bones. ''T. utahensis'' was largely referred to ''Torosaurus'' because of elongated squamosals, indicating a long frill. The number of epiparietals and the size, location or even existence of parietal ''fenestrae'' are unknown. Researchers have claimed that distinct juvenile torosaurs have been excavated from a bonebed in the Javelina Formation of Big Bend National Park, basing their identification as ''Torosaurus'' cf. ''utahensis'' on their proximity to an adult with a characteristic ''Torosaurus'' parietal.Hunt, Rebecca K. and Thomas M. Lehman. 2008. Attributes of the ceratopsian dinosaur ''Torosaurus'', and new material from the Javelina Formation (Maastrichtian) of Texas. Journal of Paleontology 82(6): 1127–1138. Scanella and Horner concluded that only future finds could solve this problem. They suggested that this taxon, which extends the ''Torosaurus'' range southwards of that of ''Triceratops'', might represent a separate chasmosaurine genus or a third ''Triceratops'' species. Farke's 2013 morphometric study was inconclusive on this point, ''T. utahensis'' morphospace falling in between ''Triceratops'' and ''Torosaurus latus'' and not well separated from either.

In 2022 Mallon et al. argued that two specimens found in Canada's Frenchman and Scollard Formations, EM P16.1. at Eastend Historical Museum in Saskatchewan and UALVP 1646 at the University of Alberta, are subadults and can be referred to ''Torosaurus'', indicating it was a valid taxon. The same study also noted that ''Torosaurus'' indeed lived during the Upper Maastrichtian.Jordan C. Mallon, Robert B. Holmes, Emily L. Bamforth, Dirk Schumann, 2022,
The record of ''Torosaurus'' (Ornithischia: Ceratopsidae) in Canada and its taxonomic implications
, ''Zoological Journal of the Linnean Society'', 2022: zlab120

See also

* Timeline of ceratopsian research

References

* Dodson, P. (1996). ''The Horned Dinosaurs''. Princeton University Press, Princeton, New Jersey, pp. xiv-346

External links

Kids Zone - ''Torosaurus''

{{Taxonbar, from=Q14491

Chasmosaurines
Late Cretaceous dinosaurs of North America
Maastrichtian life
Hell Creek fauna
Fossil taxa described in 1891
Taxa named by Othniel Charles Marsh
Ornithischian genera