Plesiadapis (near Adapis)[2] is an extinct genus of mammal closely related to primates, found in North America and western Europe. The type species, P. tricuspidens, was described in 1877 by François Louis Paul Gervaise, based on a partial left mandible (lower jaw) uncovered in France. Fourteen valid species have since been named.
Taxonomy
The first discovery of Plesiadapis was made by François Louis Paul Gervaise in 1877, who first discovered Plesiadapis tricuspidens in France. The type specimen is MNHN Crl-16, and is a left mandibular fragment dated to the early Eocene epoch.
This genus probably arose in North America and colonized Europe on a land bridge via Greenland. Thanks to the abundance of the genus and to its rapid evolution, species of Plesiadapis play an important role in the zonation of Late Paleocene continental sediments and in the correlation of faunas on both sides of the Atlantic. Two remarkable skeletons of Plesiadapis, one of them nearly complete, have been found in lake deposits at Menat, France.[3] Although the preservation of the hard parts is poor, these skeletons still show remains of skin and hair as a carbonaceous film, something unique among Paleocene mammals. Details of the bones are better preserved in fossils from Cernay, also in France, where Plesiadapis is one of the most common mammals.
Classification

The following are possible shared derived features of Plesiadapiformes: maxillary-frontal contact in orbit, the presence of a suboptic foramen, an ossified external auditory meatus, the absence of a promontory artery, the absence of a stapedial artery, and a strong mastoid tubercle.[4]
Although the placement of the Plesiadapis lineage is still up for debate, the consensus in the 1970s was that they were closest to early tarsier-like primates.[5] Plesiadapiformes have also been proposed as a nonprimate sister group to Eocene-Recent primates. A study done in 1987 linked Plesiadapiformes with adapids and omomyids through nine shared-derived features, six of which are cranial or dental: (1) auditory bulla inflated and formed by the petrosal bone, (2) ectotympanic expanded laterally and fused medially to the wall of the bulla, (3) promontorium centrally positioned in the bulla, and large hypotympanic sinus widely separating promontorium from the basisphenoid, (4) internal carotid entering the bulla posteriolaterally and enclosed in a bony tube, (5) nannopithex fold on the upper molars, and (6) loss of one pair of incisors.[4]
In 2013, a phylogenetic analysis that includes also the basal primate Archicebus positions Plesiadapis firmly outside of the Primates, as a sister group to both Primates and Dermoptera.[6]
Species
Fifteen species of Plesiadapis recognised by Fredrick S. Szalay and Eric Delson in 1979. The following table is based on that work:[7]
| Species[7] | Synonyms | Localities |
|---|---|---|
| P. anceps Simpson, 1936 |
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| P. churchilli Gingerich, 1974 |
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| P. cookei Jepsen, 1930 |
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| P. dubius Matthew, 1915 |
|
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| P. intermedius Gazin, 1971 |
|
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| P. fodinatus Jepsen, 1930 |
|
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| P. gidleyi Matthew, 1917 |
|
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| P. insignis Piton, 1940 |
|
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| P. remensis Lemoine, 1887 |
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| P. rex Gidley, 1923 |
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| P. russelli Gingerich, 1974 |
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| P. simonsi Gingerich, 1974 |
| |
| P. simpsoni Gazin, 1956 |
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| P. tricuspidens (type species) Gervais, 1877 |
|
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| P. walbeckensis Russel, 1964 |
|
Description

Plesiadapis is one of the most completely known early primatomorphs, with a significant amount of the skeleton known, unlike most other plesiadapids which are quite fragmentary.[7] In 1988, John Fleagle estimated its body mass at about 2.1 kg (4.6 lb).[8] In 2006, Philip D. Gingerich and Gregg F. Gunnel estimated the body mass of P. cookei at around 2.176 kg (4.80 lb), though recovered ranges from 1.845–3.621 kg (4.07–7.98 lb) depending on the methodology used. For example, an estimate of 3.067 kg (6.76 lb) based on ratios between tooth weight and body size in modern primates, and regression of body weight versus skull length, using a dataset of insectivorous mammals, yielded a mass of 2.299 kg (5.07 lb). In 2014, Maeva J Orliac and colleagues estimated the body mass of P. tricuspidens at 2.039 kg (4.50 lb) and estimated P. cookei‘s mass at 2.2 kg (4.9 lb).[9]
Skull
The skull of Plesiadapis is relatively broad and flat, with a long snout with rodent-like jaws and teeth and long, gnawing incisors separated by a gap from its molars. Orbits are still directed to the side, unlike the forward-facing eyeballs of modern primates that enable three-dimensional vision.[7] The skull is reminiscent of a lemur’s, though it lacks the postorbital bars (vertical bars bordering the posterior, or rear, margin of the eye socket).[7] Plesiadapis‘ brain was very small, around one-quarter the size expected for a mammal of its size.[10]
Dentition
Plesiadapis’ dentition shows a functional shift toward grinding and crushing in the cheek teeth as an adaptation towards increasing omnivory and herbivory.[11] The dental formula is usually 2.1.3.31.1.3.3, with two incisors, one canine, three premolars, and three molars in either half of the upper jaw; and one incisor, one canine, three premolars, and one molar in either half of the lower jaw. The incisors are quite long. Already, Plesiadapis had lost the first premolar from the mammalian common ancestor, but later primatomorphs would lose the second premolar as well. P. dubius consistently lacks the lower second premolar, and about half of P. rex specimens lack it too. P. gidleyi and European Plesiadapis lack the lower canines.[7]

Skeleton
The skeletal adaptations are consistent with a largely arboreal lifestyle in the trees. The sacrum of P. gidleyi is similar to that of the eastern gray squirrel, though lacking the strong spines. The humerus is robust and features a strong S-curve.[7] Plesiadapis had mobile limbs that terminated in strongly curved claws, and it sported a long bushy tail which is preserved in the Menat skeletons. The way of life of Plesiadapis has been much debated in the past. Climbing habits could be expected in a relative of the primates, but tree-dwelling animals are rarely found in such high numbers. Based on this and other evidence, some paleontologists have concluded that these animals were mainly living on the ground, like today’s marmots and ground squirrels.[3] However, more recent investigations have confirmed that the skeleton of Plesiadapis is that of an adept climber, which can be best compared to tree squirrels or to tree-dwelling marsupials such as possums.[7] The short, robust limbs, the long, laterally compressed claws, and the long, bushy tail indicate that it was an arboreal quadruped.[8]
Palaeoecology
Remains belonging to Plesiadapis have been discovered in the Rocky Mountains region of North America and parts of western Europe.[7] The teeth of P. russelli and P. cookei indicate these species were adapted to eat leaves.[12] Large Plesiadapis species in Europe evolved to become increasingly adapted for folivory across the Palaeocene–Eocene boundary, although they were not as adapted for a folivorous diet as Platychoerops daubrei.[13]
References
- ^ McKenna, M. C & S. K. Bell (1997). Classification of Mammals Above the Species Level. Columbia University Press. ISBN 0-231-11012-X.
- ^ Silcox, Mary T.; Bloch, Jonathan I.; Boyer, Doug M.; Chester, Stephen G. B.; López‐Torres, Sergi (2017). “The evolutionary radiation of plesiadapiforms”. Evolutionary Anthropology: Issues, News, and Reviews. 26 (2): 74–94. doi:10.1002/evan.21526. ISSN 1060-1538. Archived from the original on 2023-04-23.
- ^ a b Gingerich, P.D. (1976). “Cranial anatomy and evolution of early Tertiary Plesiadapidae (Mammalia, Primates)”. University of Michigan Papers on Paleontology. 15: 1–141. hdl:2027.42/48615.
- ^ a b Kay, Richard F.; Thewissen, J. G.; Yoder, Anne D. (1992). “Cranial anatomy of Ignacius graybullianus and the affinities of the Plesiadapiformes”. American Journal of Physical Anthropology. 89 (4): 477–498. doi:10.1002/ajpa.1330890409.
- ^ Gingerich, Philip D. (1975). New North American Plesiadapidae (mammalia, primates) and a biostratigraphic zonation of the Middle and Upper Paleocene. Ann Arbor: University of Michigan Museum of Paleontology.
- ^ Ni, X.; Gebo, D. L.; Dagosto, M.; Meng, J.; Tafforeau, P.; Flynn, J. J.; Beard, K. C. (2013). “The oldest known primate skeleton and early haplorhine evolution”. Nature. 498 (7452): 60–64. Bibcode:2013Natur.498…60N. doi:10.1038/nature12200. PMID 23739424. S2CID 4321956.
- ^ a b c d e f g h i Szalay, F. S. & Delson, E. (1979). Evolutionary history of the Primates. Academic Press. ISBN 978-0-12-680150-7.
- ^ a b Fleagle, J. G. (1988). Primate Adaptation and Evolution. San Diego: Academic Press. ISBN 0-12-260340-0.
- ^ Orliac, Maeva J.; Ladevèze, Sandrine; Gingerich, Philip D.; Lebrun, Renaud; Smith, Thierry (2014-04-22). “Endocranial morphology of Palaeocene Plesiadapis tricuspidens and evolution of the early primate brain”. Proceedings. Biological Sciences. 281 (1781) 20132792. doi:10.1098/rspb.2013.2792. ISSN 1471-2954. PMC 3953834. PMID 24573845.
- ^ Gingerich, Philip D.; Gunnell, Gregg F. (2006). “Brain of Plesiadapis cookei (Mammalia, Proprimates): surface morphology and encephalization compared to those of Primates and Dermoptera”. Contributions from the Museum of Paleontology, University of Michigan. 31 (8): 185–195 – via ResearchGate.
- ^ Fleagle, K. D. (1987). “The First Radiation—Plesiadapiform Primates”. In Ciochon, R. L.; Fleagle, J. G. (eds.). Primate Evolution and Human Origins. Hawthorne: Aldine de Gruyter. pp. 41–51. ISBN 0-202-01175-5.
- ^ Boyer, Doug M.; Evans, Alistair R.; Jernvall, Jukka (23 December 2009). “Evidence of dietary differentiation among late Paleocene–early Eocene plesiadapids (Mammalia, primates)”. American Journal of Physical Anthropology. 142 (2): 194–210. doi:10.1002/ajpa.21211. ISSN 0002-9483. Retrieved 25 December 2025 – via Wiley Online Library.
- ^ Jehle, Martin; Godinot, Marc; Delsate, Dominique; Phélizon, Alain; Pellouin, Jean-Louis (18 August 2018). “Evolution of plesiadapid mammals (Eutheria, Euarchonta, Plesiadapiformes) in Europe across the Paleocene/Eocene boundary: implications for phylogeny, biochronology and scenarios of dispersal”. Palaeobiodiversity and Palaeoenvironments. 99 (2): 293–351. doi:10.1007/s12549-018-0331-6. ISSN 1867-1594. Retrieved 6 August 2025 – via Springer Nature Link.