Forstercooperia
| Forstercooperia Temporal range: Middle to Late Eocene, 40–34 Ma | |
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| Life restoration of F. minuta | |
Scientific classification  | |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Mammalia |
| Order: | Perissodactyla |
| Family: | †Hyracodontidae |
| Subfamily: | †Indricotheriinae |
| Genus: | †Forstercooperia Wood, 1939 |
| Type species | |
| Cooperia totadentata Wood, 1938 | |
| Species | |
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| Location of finds of Forstercooperia | |
| Synonyms[1] | |
Species synonymy
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Forstercooperia is an extinct genus of indricotheriine hyracodontid rhinoceros from the Middle to Late Eocene of Eurasia.
Description
Forstercooperia is known from a vast amount of cranial material, although only some scant postcranial remains. The largest species is F. totadentata, followed by F. confluens and finally F. minuta.[1] The average size of all species, is about equal with a large dog, even though later genera like Juxia and Paraceratherium reached sizes of a cow and even much larger.[2] Each species is distinguished by cheek tooth morphology, with the remaining skull quite similar.[1] Like primitive rhinocerotoids, Forstercooperia possesses blunt ends on the tips of its nasals, above the nasal incision. Unlike all modern rhinoceroses, the nasals of Forstercooperia, as well as many related genera, lack rugosities, which suggests that they lacked any form of horn. The nasal incision extends fairly far into the upper jaw, ending just posterior to the canine. Forstercooperia possesses a small post-insicor diastema, not as large as its descendants, and similar in size to that of Hyracodon.[3]
Distribution and habitat
Remains of Forstercooperia have been found all across Asia. Most important remains are from the Middle to Late Eocene Irdin Manha Formation of Inner Mongolia (China).[1] In 1938, the holotype of F. totadentata was described, from the Irdin Manha Formation.[3] Later in 1963, the species Pappaceras confluens (now Forstercooperia) was described from the same region, probably within the same formation.[4] The most recent valid species, F. minuta, is based off a maxilla from the Irdin Manha Formation as well.[1] However, many specimens from across other parts of Asia have also been assigned to Forstercooperia. The only non-holotypic specimen of F. totadentata is that of F. shiwopuensis, which comes from the Lunan Formation of China.[1] F. confluens, now including the Asian material of F. grandis,[5] is known from Shara Murun Formation, Ulan Shireh Formation and Houldjin Formation, as well as the Irdin Manha Formation. Finally, F. minuta is known from specimens only from the Irdrin Manha Formation and possibly the Shara Murun Formation of China,[1] and the Kolpak Formation of Kazakhstan,[6] now that its North American material has been reassigned.[5]
Taxonomy
Forstercooperia is considered to be a primitive rhinocerotoid, and as a result, many unrelated species were lumped into it. Species have also been oversplit based on small or insignificant features. In the most inclusive review of the genus yet, it was identified that many of the species are junior synonyms of previous names, not in the genus, or are potentially invalid in some other way. Many specimens, ranging in age from the Middle Eocene to Late Eocene, and in location from eastern Asia to Kazhakstan, and as far west as USA, have at some time been included in Forstercooperia. Material of many different genera as well have been at some time included in Forstercooperia, such as that of Juxia[1] and Uintaceras[5]
In 1923, a mostly complete skull of an early rhinoceros relative was unearthed. This skull came from the Late Eocene of the Mongolian Irdin Manha Formation. The material, including the "front of skull with all premolars and some front teeth", was given the specimen number AMNH 20116. It was first discovered in the formation by George Olsen, and in 1938 in was described as a new genus and species by Horace Elmer Wood II. Wood named the binomial Cooperia totadentata to contain the skull. The generic name was to honor Clive Forster-Cooper, who had major contributions to the knowledge of indricotheres.[3] In 1939 Wood corrected the genus name to Forstercooperia, because he was informed that the name Cooperia was preoccupied.[7] The species Forstercooperia totadentata is currently retained as type species, and Wood's original species Cooperia totadentata is now its junior synonym.[1][4][6] The species is also the first named that has been included in Forstercooperia that is still valid.[5] It is also the senior synonym of F. shiwopuensis, a species named in 1974 by Chow et al..[1][8]
In 1963, material including a partial skull containing cheek teeth was unearthed in Late Eocene deposits of Mongolia. These remains were identified as from a true rhinoceros by Wood, who found them an important discovery with the scant amount of previous cranial material of early rhinocerotids available. On July 25, the same year, a paper was published by Wood concerning the taxonomy and osteology of these remains, in which he named them a new genus and species (or binomial) as well as re-ranking a previously named family as a subfamily containing the new taxon. The binomial created was Pappaceras confluens, classified as a close relative of Forstercooperia within Forstercooperiinae (before Forstercooperiidae, named in 1940 by Kretzoi). Wood noted that the generic name is derived from the Latin word πaππos, "grandfather", and the Greek words alpha, "without", and keras, "horn", translating as "Grandfather without horn". The species name is based on the confluent morphology of the teeth. The catalogue number for the skull is AMNH 26660, and it specifically preserved a "front half of the skull and a complete lower jaw, with most of the teeth and remaining alveoli, totaling a full placental series". Other remains included a portion of the mandible and a premolar. All of these specimens were from the lame locality, the Upper Gray Clays, of the Irdin Manha Formation in Inner Mongolia.[4] In the revision by Radnisky, it was found that this species was assignable to Forstercooperia, and the new combination F. confluens was erected.[9] This species is well known, although in the 1981 review of Forstercooperia, it was identified that this species could not be validly distinguished from F. grandis. Therefore, and since the latter species has priority, F. confluens was no longer considered a valid species, in fact a junior synonym of F. grandis.[1][6] However, the description of Uintaceras found F. grandis invalid, and in the new genus, and F. confluens to be a valid species including the Asian material of F. grandis.[5]
In the 1960s, newly uncovered material from the Irdin Manha Formation was identified as belonging to a new species of rhinocerotoid. Originally, they were found to be from F. confluens, as they were in the same location as that species holotype. They were later assigned to Forstercooperia sp., with no new name being given. The material included an almost complete skull, an almost complete lower jaw, an anterior portion of the skull, and an astragalus. These bones were first assigned a new species by Lucas et al., Forstercooperia minuta. They were found to be a unique species based on their size and the anatomy of their teeth. The species has been retained in the species complex of Forstercooperia throughout major revisions, by Lucas et al. in 1981,[1] Lucas and Sobus in 1989,[8] and Holbrook and Lucas in 1997. However, Holbrook and Lucas identified that the only North American material of F. minuta, F:AM 99662, had no features justifying its inclusion with the species, and reassigned it to their new binomial, Uintaceras radinskyi.[5]
An upper tooth row of an indricothere from the Eocene was first described in 1974. It was analysed by Chow, Chang and Ding, who published a new species for it, Forstercooperia shiwopuensis. The authors noted that it was from the same region and in the same size range as F. totadentata, which Lucas et al. (1981) found it to tentatively represent. The holotype of F. totadentata lacked an upper tooth row, and as it was presumably the right size to represent the missing teeth, Lucas et al. predicted it was of the same size and morphology as would have been predicted for the species.[1]
In 1977, some the first description of a dentary from Kazakhstan's Sargamys Formation was published. Authored by Gabunia, the paper figured the dentary, as well as some other material. In the images caption, the dentary was assigned to as Forstercooperia sp. although the text used a different name. In the text, the dentary and its teeth were assigned to Forstercooperia crudus, although no size was mentioned. As the text did not have a description in it of F. crudus, the name is now considered a nomen nudum. Its material is possibly assignable to F. minuta, however.[1] In 1997, other material from Kazakhstan, specifically the Kolpak Formation, was assigned to F. minuta, meaning that it certainly lived in Kazakhstan at the same time as F. crudus.[6]
Species and synonyms
Forstercooperia has been represented by many different species in the different reviews of the genus.[1][5][8][9] In the first significant review, authored by Leonard Radinsky and published in 1967, found that many previous species were junior synonyms, and that only four species certainly in the genus were valid. Radinsky noted that of all published species, F. totadentata, F.? grandis, F. confluens, F. sharamurense, and F. borissiaki were the only valid ones, creating new combinations from Juxia sharamurense, Hyrachyus grandis, and Pappaceras borissiaki. He also synonymized the genera Pappaceras and Juxia with Forstercooperia.[9]
In a more recent review focused purely on the genus Forstercooperia, it was found that there was very little diversity in the species found valid by Radinsky. This paper, authored by Spencer G. Lucas and Robert Schoch and Earl Manning and published in 1981 reviewed all currently-named species of Forstercooperia, and named the new species F. minuta. Unlike Radinsky, their paper found Juxia to be separate, with F. borissiaki inside the genus, and F. grandis to be a definite species. F. confluens, named in 1963 by Wood, was found to be a synonym of F. grandis; F. sharamurunense, named in 1964 by Chow and Chiu, was found to be a synonym of F. borisiaki; F. jigniensis, named in 1973 by Sahni and Khare, was found to be an indeterminate species; F. shiwopuensis, named in 1974 by Chow, Chang and Ding, was found to be a synonym of F. totadentata; F. ergiliinensis, named in 1974 by Gabunia and Dashzeveg, was found to be a synonym of Juxia borissiaki; and F. crudus, named in 1977 by Gabunia, was found to be a nomen nudum.[1] In 1989, Lucas and Jay Sobus, it was noted that no new material of the genus had been identified, and that therefore, the conclusions were not changed.[8]
In the most recent review of the genus, focusing on the North American material, it was found that some earlier conclusions were no longer valid. This paper, published in 1997 by Luke Holbrook and Lucas, named a new genus, Uintaceras for all the North American material of Forstercooperia. Holbrook and Lucas named a new species, U. radinskyi, assigning the North American material of F. minuta and F. grandis to it. They found that the features uniting F. grandis with Forstercooperia were plesiomorphic, and that F. grandis was actually not a hyracodontid, instead the closest non-rhinocerotid relative of Rhinocerotidae. They concluded that F. grandis was a nomen dubium, its Asian material was assignable to F. confluens, Indricotheriinae was therefore only a Eurasian subfamily, and F. confluens was a valid species.[5] More recent mentions of Forstercooperia found no reason to contradict these conclusions.[10]
Evolution
The superfamily Rhinocerotoidea can be traced back to the early Eocene—about 50 million years ago—with early precursors such as Hyrachyus. Rhinocerotoidea contains three families; the Amynodontidae, the Rhinocerotidae ("true rhinoceroses"), and the Hyracodontidae. The diversity within the rhinoceros group was much larger in prehistoric times; sizes ranged from dog-sized to the size of Paraceratherium. There were long-legged, cursorial forms and squat, semi aquatic forms. Most species did not have horns. Rhinoceros fossils are identified as such mainly by characteristics of their teeth, which is the part of the animals most likely to be preserved. The upper molars of most rhinoceroses have a pi (π) shaped pattern on the crown, and each lower molar has paired L-shapes. Various skull features are also used for identification of fossil rhinoceroses.[2]
The Indricotherinae subfamily, to which Forstercooperia belongs, is considered part of the Hyracodontidae, a group containing long-legged members adapted to running, such as Hyracodon. Indricotheres are distinguished by their larger size and the derived structure of their snouts, incisors and canines. The earliest known indricothere is the dog-sized Forstercooperia from the middle and late Eocene of western North America and Asia. The cow-sized Juxia is known from the middle Eocene; by the late Eocene the genus Urtinotherium of Asia had almost reached the size of the largest genus Paraceratherium.[8][2] Forstercooperia is by far the earliest genus, surviving from the Middle Eocene until the Late Eocene throughout Eurasia.[1][5][8][2] The genus is distinct because of features of its nasal incision, dentition, tooth anatomy, and tooth proportions and size.[1] It retained the relatively primitive features of possessing three incisors, lower canines, and lower first premolars.[2]
Below is a phylogenetic analysis conducted by Lucas and Sobus in their 1989 revision of Indricotheriinae:[8]
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In a 1999 study, Holbrook instead found the indricotheres to be outside the hyracodontid group and wrote that the indricotheres may not be a monophyletic grouping. He performed a phylogenetic analysis which placed Uintaceras, then amynodontids, then Paraceratherium, then Juxia and Forstercooperia, and finally hyracodontids as the successive outgroups of Rhinocerotidae within Rhinocerotoidea. The analysis however, did not include the genus Urtinotherium.[11]
References
- 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Lucas, S.G.; Schoch, R.M.; Manning, E. (1981). "The Systematics of Forstercooperia, a Middle to Late Eocene Hyracodontid (Perissodactyla: Rhinocerotoidea) from Asia and Western North America". Journal of Paleontology 55 (4): 826–841. JSTOR 1304430.
- 1 2 3 4 5 Prothero, D.R. (2013). Rhinoceros Giants: The Palaeobiology of Indricotheres. Indiana University Press. pp. 1–160. ISBN 978-0-253-00819-0.
- 1 2 3 Wood, H.E. (1938). "Cooperia totadentata, a remarkable rhinoceros from the Eocene of Mongolia" (PDF). American Museum Novitates 1012: 1–20.
- 1 2 3 Wood, H.E. (1963). "A Primitive Rhinoceros from the Late Eocene of Mongolia". American Museum Novitates (2146): 1–12.
- 1 2 3 4 5 6 7 8 9 Holbrook, L.T.; Lucas, S.G. (1997). "A New Genus of Rhinocerotoid from the Eocene of Utah and the Status of North American "Forstercooperia"". Journal of Vertebrate Paleontology 17 (2): 384–396. doi:10.1080/02724634.1997.10010983. JSTOR 4523815.
- 1 2 3 4 Lucas, S.G.; Emry, R.J.; Bayshashanov, B.U. (1997). "Eocene Perissodactyla from the Shinzhaly River, Eastern Kazakhstan". Journal of Vertebrate Paleontology 17 (1): 235–246. doi:10.1080/02724634.1997.10010967. JSTOR 4523800.
- ↑ Wood, H.E. (1939). "Addendum to American Museum Novitates No. 1012" (PDF). American Museum Novitates 1012: 1.
- 1 2 3 4 5 6 7 Lucas, S.G.; Sobus, J.C. (1989). "The Systematics of Indricotheres". In Prothero, Donald R.; Schoch, Robert M. The Evolution of Perissodactyls. Oxford University Press. pp. 358–378. ISBN 978-0-19-506039-3. OCLC 19268080.
- 1 2 3 Radinsky, L.B. (1967). "A Review of the Rhinocerotoid Family Hyracodontidae (Perissodactyla)". Bulletin of the American Museum of Natural History 136 (1): 1–46.
- ↑ Prothero, D.R. (2005). The Evolution of North American Rhinoceroses. Cambridge University Press. pp. 1–218. ISBN 0-521-83240-3.
- ↑ Holbrook, L.T. (1999). "The Phylogeny and Classification of Tapiromorph Perissodactyls (Mammalia)". Cladistics 15 (3): 331–350. doi:10.1006/clad.1999.0107.