Shoshonius Temporal range: Eocene Early | |
---|---|
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Mammalia |
Order: | Primates |
Suborder: | Haplorhini |
Family: | † Omomyidae |
Subfamily: | † Omomyinae |
Tribe: | † Washakiini |
Genus: | † Shoshonius Granger, 1910 |
Species | |
†S. cooperi Granger, 1910 [1] Contents |
Shoshonius is an extinct genus of omomyid primate that lived during the Eocene (~56-34 million years ago). Specimens identified as Shoshonius have been found exclusively in central Wyoming and the genus currently includes two species, Shoshonius cooperi, described by Granger in 1910, [3] and Shoshonius bowni, described by Honey in 1990. [4]
The type specimen of S. cooperi is AMNH 14664, a right maxillary fragment preserving P3-M3. [3] The type specimen of S. bowni is USGS 2020, a right maxillary fragment preserving M1-3. [4] Based on elements of the postcranial skeleton, Shoshonius is inferred to be a generalized, arboreal quadruped with some affinities for vertical climbing and leaping. [5] Additionally, dental morphology suggests the diet of Shoshonius was primarily insectivorous. [6]
Current research places Shoshonius as the sister group of Tarsius within the suborder Haplorhini, a monophyletic clade which includes tarsiers, monkeys, apes, and humans. [7] Tarsiers and Shoshonius share three unique cranial traits including a basioccipital phlange overlapping with the posteromedial bullar wall, a ventrolateral posterior carotid foramen, and a suprameatal foramen. [8] Among primates, these features are unique to these two taxa, supporting the hypothesis that Shoshonius is the sister group to Tarsius. [8]
Shoshonius has larger eye orbits in proportion to its skull length when compared to other Eocene omomyids and the snout is much smaller, both of these traits are also observed in tarsiers. [8] Shoshonius lacks a postorbital septum, similar to the strepsirrhines Necrolemur and Rooneyia. [8] Noticeably, Shoshonius has a basioccipital phlange that overlaps with the bullar wall. [8] The posterior carotid foramen ventrolaterally intersects the bulla. [8] Shoshonius’ characteristically large orbits as well as the three cranial traits mentioned in the section above, are traits shared with tarsiers, which provides the main line of evidence which unites them taxonomically. [8]
Dental morphology reveals that Shoshonius shares dental features with other omomyids, namely; upper molar mesostyles, a protocone fold on upper molars, and lower molar metastylids. [4] Additionally, Shoshonius retains some dental morphologies that are found in early primitive primates, namely, small lower incisors, indicating their dentition was not specialized for gouging tree bark as seen in other omomoyids. [7]
Analysis of postcranial morphology suggests that Shoshonius, like other omomyids, was quadrupedal with adaptations for leaping. [5] The calcaneus of Shoshonius is elongated, although not to the extent seen in tarsiers, indicating that they may have had an affinity for leaping, but not the exceptional leaping abilities of tarsiers. [5] Other aspects of the lower limb show similarities with modern day vertical clingers and leapers like tarsiers and galagoes, but the morphology of Shoshonius is not specialized to the extent seen in the modern taxa. [5] Additionally, morphology of the upper limb of Shoshonius does not support vertical clinging and leaping as a locomotor behavior and instead shows similarities with other omomyids that were most likely more generalized quadrupeds. [5]
The hypothesis of occasional leaping in Shoshonius was further corroborated in 2002 when Ryan and Ketchum published a bone volume fracture analysis of the femoral head of Shoshonius, Omomys, and multiple extant primate taxa with the hypothesis that the histologic structure of femoral heads could predict locomotor behavior. [9] The results of this analysis showed that the histology of Shoshonius was most similar to that of the leaping galagoes and was significantly different than Omomys. [9] The authors conclude that the histologic structure of the femur suggests Shoshonius was either an occasional or specialized leaper. [9]
Tarsiers are haplorhine primates of the family Tarsiidae, which is, itself, the lone extant family within the infraorder Tarsiiformes. Although the group was, prehistorically, more globally widespread, all of the species living today are restricted to Maritime Southeast Asia, predominantly being found in Brunei, Indonesia, Malaysia and the Philippines.
Strepsirrhini or Strepsirhini is a suborder of primates that includes the lemuriform primates, which consist of the lemurs of Madagascar, galagos ("bushbabies") and pottos from Africa, and the lorises from India and southeast Asia. Collectively they are referred to as strepsirrhines. Also belonging to the suborder are the extinct adapiform primates which thrived during the Eocene in Europe, North America, and Asia, but disappeared from most of the Northern Hemisphere as the climate cooled. Adapiforms are sometimes referred to as being "lemur-like", although the diversity of both lemurs and adapiforms does not support this comparison.
Haplorhini, the haplorhines or the "dry-nosed" primates is a suborder of primates containing the tarsiers and the simians, as sister of the Strepsirrhini ("moist-nosed"). The name is sometimes spelled Haplorrhini. The simians include catarrhines, and the platyrrhines.
Omomyidae is a group of early primates that radiated during the Eocene epoch between about 55 to 34 million years ago (mya). Fossil omomyids are found in North America, Europe & Asia, making it one of two groups of Eocene primates with a geographic distribution spanning holarctic continents, the other being the adapids. Early representatives of the Omomyidae and Adapidae appear suddenly at the beginning of the Eocene in North America, Europe, and Asia, and are the earliest known crown primates.
Tarsiiformes are a group of primates that once ranged across Europe, northern Africa, Asia, and North America, but whose extant species are all found in the islands of Southeast Asia. Tarsiers are the only living members of the infraorder; other members of Tarsiidae include the extinct Tarsius eocaenus from the Eocene, and Tarsius thailandicus from the Miocene. Two extinct genera, Xanthorhysis and Afrotarsius, are considered to be close relatives of the living tarsiers, and are generally classified within Tarsiiformes, with the former grouped within family Tarsiidae, and the latter listed as incertae sedis (undefined). Omomyids are generally considered to be extinct relatives, or even ancestors, of the living tarsiers, and are often classified within Tarsiiformes.
Aegyptopithecus is an early fossil catarrhine that predates the divergence between hominoids (apes) and cercopithecids. It is known from a single species, Aegyptopithecus zeuxis, which lived around 38-29.5 million years ago in the early part of the Oligocene epoch. It likely resembled modern-day New World monkeys, and was about the same size as a modern howler monkey, which is about 56 to 92 cm long. Aegyptopithecus fossils have been found in the Jebel Qatrani Formation of modern-day Egypt. Aegyptopithecus is believed to be a stem-catarrhine, a crucial link between Eocene and Miocene fossils.
Plesiadapis is one of the oldest known primate-like mammal genera which existed about 58–55 million years ago in North America and Europe. Plesiadapis means "near-Adapis", which is a reference to the adapiform primate of the Eocene period, Adapis. Plesiadapis tricuspidens, the type specimen, is named after the three cusps present on its upper incisors.
Necrolemur is a small bodied omomyid with body mass estimations ranging from 114–346 g (4.0–12.2 oz). Necrolemur’s teeth feature broad basins and blunt cusps, suggesting their diet consisted of mostly soft fruit, though examination of microwear patterns suggests that populations from lower latitudes also consumed insects and gums.
Altanius is a genus of extinct primates found in the early Eocene of Mongolia. Though its phylogenetic relationship is questionable, many have placed it as either a primitive omomyid or as a member of the sister group to both adapoids and omomyids. The genus is represented by one species, Altanius orlovi, estimated to weigh about 10–30 g (0.35–1.1 oz) from relatively well-known and complete dental and facial characteristics.
A toothcomb is a dental structure found in some mammals, comprising a group of front teeth arranged in a manner that facilitates grooming, similar to a hair comb. The toothcomb occurs in lemuriform primates, treeshrews, colugos, hyraxes, and some African antelopes. The structures evolved independently in different types of mammals through convergent evolution and vary both in dental composition and structure. In most mammals the comb is formed by a group of teeth with fine spaces between them. The toothcombs in most mammals include incisors only, while in lemuriform primates they include incisors and canine teeth that tilt forward at the front of the lower jaw, followed by a canine-shaped first premolar. The toothcombs of colugos and hyraxes take a different form with the individual incisors being serrated, providing multiple tines per tooth.
Adapis is an extinct adapiform primate from the Eocene of Europe. While this genus has traditionally contained five species, recent research has recognized at least six morphotypes that may represent distinct species. Adapis holds the title of the first Eocene primate ever discovered. In 1821, Georges Cuvier, who is considered to be the founding father of paleontology, discovered Adapis in fissure fillings outside of Paris, France. Given its timing and appearance in the fossil record, Cuvier did not recognize the primate affinities of Adapis and first described it as a small extinct pachyderm; only later in the 19th century was Adapis identified as a primate.
Rooneyia viejaensis is a relatively small primate belonging to the extinct monotypic genus Rooneyia. Rooneyia viejaensis is known from the North American Eocene of the Sierra Vieja of West Texas; the species is only known from the type specimen. The lack of additional fossils at this time makes it difficult to hypothesize where and how Rooneyia may have evolved. The minimal wear upon the molar teeth of the specimen has led to the assumption that the type specimen is that of a young adult. Rooneyia does not consistently fall within any one group of fossil or extant primates.
Vertical clinging and leaping (VCL) is a type of arboreal locomotion seen most commonly among the strepsirrhine primates and haplorrhine tarsiers. The animal begins at rest with its torso upright and elbows fixed, with both hands clinging to a vertical support, such as the side of a tree or bamboo stalk. To move from one support to another, it pushes off from one vertical support with its hindlimbs, landing on another vertical support after an extended period of free flight. Vertical clinging and leaping primates have evolved a specialized anatomy to compensate for the physical implications of this form of locomotion. These key morphological specializations have been identified in prosimian fossils from as early as the Eocene.
Anaptomorphinae is a pre-historic group of primates known from Eocene fossils in North America and Europe and later periods of Paleocene Asia, and are a sub-family of omomyids. The anaptomorphines is a paraphyletic group consisting of the two tribes Trogolemurini and Anaptomorphini. Anaptomorphine radiation in Wyoming, one of the most detailed records of changes within populations and between species in the fossil record, has provided remarkable evidence of transitional fossils.
Afrotarsius is a primate found in the Paleogene of Africa.
Archicebus is a genus of fossil primates that lived in the early Eocene forests of what is now Jingzhou in the Hubei Province in central China, discovered in 2003. The only known species, A. achilles, was a small primate, estimated to weigh about 20–30 grams (0.7–1.1 oz), and is the only known member of the family Archicebidae. When discovered, it was the oldest fossil haplorhine primate skeleton found, appearing to be most closely related to tarsiers and the fossil omomyids, although A. achilles is suggested to have been diurnal, whereas tarsiers are nocturnal. Resembling tarsiers and simians, it was a haplorhine primate, and it also may have resembled the last common ancestor of all haplorhines.
Sivaladapis is a genus of adapiform primate that lived in Asia during the middle Miocene.
Afradapis is a genus of adapiform primate that lived during the Late Eocene. The only known species, Afradapis longicristatus, was discovered in the Birket Qarun Formation in northern Egypt in 2009. While its geographic distribution is confined to Afro-Arabia, Afradapis belongs to the predominantly European adapiform family Caenopithecinae. This taxonomic placement is supported by recent phylogenetic analyses that recover a close evolutionary relationship between Afradapis and adapiforms, including Darwinius. While adapiforms have been noted for their strepsirrhine-like morphology, no adapiform fossil possesses the unique anatomical traits to establish an ancestor-descent relationship between caenopithecids and living strepsirrhines. It ate leaves and moved around slowly like lorises.
Microsyops is a plesiadapiform primate found in Middle Eocene in North America. It is in the family Microsyopidae, a plesiadapiform family characterized by distinctive lanceolate lower first incisors. It appears to have had a more developed sense of smell than other early primates. It is believed to have eaten fruit, and its fossils show the oldest known dental cavities in a mammal.
Nanotitanops is an extinct genus of Brontothere from the middle Eocene of China. It contains a single species, N. shanghuangensis. It is known only from isolated teeth, the smallest of any known Brontothere.