Pongo hooijeri

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Pongo hooijeri
Temporal range: Pleistocene
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Primates
Suborder: Haplorhini
Infraorder: Simiiformes
Family: Hominidae
Genus: Pongo
Species:
P. hooijeri
Binomial name
Pongo hooijeri
Schwartz et al. 1995

Pongo hooijeri is an extinct species of orangutan from the Pleistocene of Vietnam. [1] It was named in honor of paleontologist Dirk Albert Hooijer. Fossils of the ape were found in the Tham Hai Cave. [2]

Contents

Description

Pongo hooijeri is only known from isolated teeth. In its initial description, it was distinguished from other orangutan species by its generally larger tooth size than living orangutans, as well as a number of morphological characters of the teeth, differing from Pongo pygmaeus "in lacking significant crenelation on the occlusal surfaces of the molars and upper premolars, and on the basins of the lower premolars. Incisors are not known. Molar cusp disposition similar to that of P. pygmaeus, but the cusps themselves are puffier and more rounded occlusally as well as on their external slopes. The occlusal surfaces are thus more poorly defined, and the occlusal basins are more constricted." [2]

Taxonomy

Harrison et al. 2014 argued that the species should be considered a junior synonym of the more widespread extinct species Pongo weidenreichi. [3]

Related Research Articles

<span class="mw-page-title-main">Orangutan</span> Genus of Asian apes

Orangutans are great apes native to the rainforests of Indonesia and Malaysia. They are now found only in parts of Borneo and Sumatra, but during the Pleistocene they ranged throughout Southeast Asia and South China. Classified in the genus Pongo, orangutans were originally considered to be one species. From 1996, they were divided into two species: the Bornean orangutan and the Sumatran orangutan. A third species, the Tapanuli orangutan, was identified definitively in 2017. The orangutans are the only surviving species of the subfamily Ponginae, which diverged genetically from the other hominids between 19.3 and 15.7 million years ago.

Ferugliotherium is a genus of fossil mammals in the family Ferugliotheriidae from the Campanian and/or Maastrichtian period of Argentina. It contains a single species, Ferugliotherium windhauseni, which was first described in 1986. Although originally interpreted on the basis of a single brachydont (low-crowned) molar as a member of Multituberculata, an extinct group of small, rodent-like mammals, it was recognized as related to the hypsodont (high-crowned) Sudamericidae following the discovery of additional material in the early 1990s. After a jaw of the sudamericid Sudamerica was described in 1999, these animals were no longer considered to be multituberculates and a few fossils that were previously considered to be Ferugliotherium were assigned to unspecified multituberculates instead. Since 2005, a relationship between gondwanatheres and multituberculates has again received support. A closely related animal, Trapalcotherium, was described in 2009 on the basis of a single tooth.

<i>Gigantopithecus</i> Genus of primate

Gigantopithecus is an extinct genus of ape that lived in southern China from 2 million to approximately 300,000-200,000 years ago during the Early to Middle Pleistocene, represented by one species, Gigantopithecus blacki. Potential identifications have also been made in Thailand, Vietnam, and Indonesia. The first remains of Gigantopithecus, two third molar teeth, were identified in a drugstore by anthropologist Ralph von Koenigswald in 1935, who subsequently described the ape. In 1956, the first mandible and more than 1,000 teeth were found in Liucheng, and numerous more remains have since been found in at least 16 sites. Only teeth and four mandibles are known currently, and other skeletal elements were likely consumed by porcupines before they could fossilise. Gigantopithecus was once argued to be a hominin, a member of the human line, but it is now thought to be closely allied with orangutans, classified in the subfamily Ponginae.

<span class="mw-page-title-main">Carnassial</span> Mammal tooth type

Carnassials are paired upper and lower teeth modified in such a way as to allow enlarged and often self-sharpening edges to pass by each other in a shearing manner. This adaptation is found in carnivorans, where the carnassials are the modified fourth upper premolar and the first lower molar. These teeth are also referred to as sectorial teeth.

<span class="mw-page-title-main">Mandibular second premolar</span> Human tooth

The mandibular second premolar is the tooth located distally from both the mandibular first premolars of the mouth but mesial from both mandibular first molars. The function of this premolar is assist the mandibular first molar during mastication, commonly known as chewing. Mandibular second premolars have three cusps. There is one large cusp on the buccal side of the tooth. The lingual cusps are well developed and functional. Therefore, whereas the mandibular first premolar resembles a small canine, the mandibular second premolar is more alike to the first molar. There are no deciduous (baby) mandibular premolars. Instead, the teeth that precede the permanent mandibular premolars are the deciduous mandibular molars.

<span class="mw-page-title-main">Mandibular first molar</span> Human tooth

The mandibular first molar or six-year molar is the tooth located distally from both the mandibular second premolars of the mouth but mesial from both mandibular second molars. It is located on the mandibular (lower) arch of the mouth, and generally opposes the maxillary (upper) first molars and the maxillary 2nd premolar in normal class I occlusion. The function of this molar is similar to that of all molars in regard to grinding being the principal action during mastication, commonly known as chewing. There are usually five well-developed cusps on mandibular first molars: two on the buccal, two lingual, and one distal. The shape of the developmental and supplementary grooves, on the occlusal surface, are described as being M-shaped. There are great differences between the deciduous (baby) mandibular molars and those of the permanent mandibular molars, even though their function are similar. The permanent mandibular molars are not considered to have any teeth that precede it. Despite being named molars, the deciduous molars are followed by permanent premolars.

<span class="mw-page-title-main">Cusp (anatomy)</span> Pointed, projecting, or elevated anatomical feature

A cusp is a pointed, projecting, or elevated feature. In animals, it is usually used to refer to raised points on the crowns of teeth. The concept is also used with regard to the leaflets of the four heart valves. The mitral valve, which has two cusps, is also known as the bicuspid valve, and the tricuspid valve has three cusps.

<span class="mw-page-title-main">Postcanine megadontia</span> Relative enlargement of pre-molars and molars compared with other teeth.

Post-canine megadontia is a relative enlargement of the molars and premolars compared to the size of the incisors and canines. This phenomenon is seen in some early hominid ancestors such as Paranthropus aethiopicus.

Chororapithecus is an extinct great ape from the Afar region of Ethiopia roughly 8 million years ago during the Late Miocene, comprising one species, C. abyssinicus. It is known from 9 isolated teeth discovered in a 2005–2007 survey of the Chorora Formation. The teeth are indistinguishable from those of gorillas in terms of absolute size and relative proportions, and it has been proposed to be an early member of Gorillini. However, this is controversial given the paucity of remains, and notable anatomical differences between Chororapithecus and gorilla teeth. The Kenyan ape Nakalipithecus has been proposed to be an ancestor of Chororapithecus or at least closely related. If correct, they would be the only identified fossil members of any modern non-human great ape lineage, and would push the gorilla–human last common ancestor from 8 million years ago to 10 million years ago. The teeth are adapted for processing tough plant fibres as well as hard, brittle food, and the formation is thought to represent a forested lakeside habitat.

<i>Nakalipithecus</i> Extinct species of ape

Nakalipithecus nakayamai, sometimes referred to as the Nakali ape, is an extinct species of great ape from Nakali, Kenya, from about 9.9–9.8 million years ago during the Late Miocene. It is known from a right jawbone with 3 molars and from 11 isolated teeth. The jawbone specimen is presumed female as the teeth are similar in size to those of female gorillas and orangutans. Compared to other great apes, the canines are short, the enamel is thin, and the molars are flatter. Nakalipithecus seems to have inhabited a sclerophyllous woodland environment.

<span class="mw-page-title-main">Wushan Man</span> Fossil of an extinct non-hominin ape of central China from 2 mya

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<i>Lufengpithecus</i> Extinct genus of primates

Lufengpithecus is an extinct genus of ape, known from the Late Miocene of East Asia. It is known from thousands of dental remains and a few skulls and probably weighed about 50 kg (110 lb). It contains three species: L. lufengensis, L. hudienensis and L. keiyuanensis. Lufengpithecus lufengensis is from the Late Miocene found in China, named after the Lufeng site and dated around 6.2 Ma. Lufengpithecus is either thought to be the sister group to Ponginae, or the sister to the clade containing Ponginae and Homininae.

<span class="mw-page-title-main">Hominidae</span> Family of primates

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<i>Ektopodon</i> Extinct genus of marsupials

Ektopodon is an extinct genus of marsupial, and is the type genus of the family Ektopodontidae which occurred in forested environments in South Australia, Queensland and Victoria. The last species of this group went extinct in the early Pleistocene. Its body mass was estimated around 1300 grams. Scientists believe that ektopodontids were highly specialised seed-eating possums.

<i>Eritherium</i> Extinct genus of mammals

Eritherium is an extinct genus of early Proboscidea found in the Ouled Abdoun basin, Morocco. It lived about 60 million years ago. It was first named by Emmanuel Gheerbrant in 2009 and the type species is Eritherium azzouzorum. Eritherium is the oldest, smallest and most primitive known elephant relative.

<i>Hipposideros besaoka</i> Extinct species of bat

Hipposideros besaoka is an extinct bat from Madagascar in the genus Hipposideros. It is known from numerous jaws and teeth, which were collected in a cave at Anjohibe in 1996 and described as a new species in 2007. The site where H. besaoka was found is at most 10,000 years old; other parts of the cave have yielded H. commersoni, a living species of Hipposideros from Madagascar, and some material that is distinct from both species. H. besaoka was larger than H. commersoni, making it the largest insectivorous bat of Madagascar, and had broader molars and a more robust lower jaw. As usual in Hipposideros, the second upper premolar is small and displaced from the toothrow, and the second lower premolar is large.

<i>Hispanopithecus</i> Genus of apes from Miocene Europe

Hispanopithecus is a genus of apes that inhabited Europe during the Miocene epoch. It was first identified in a 1944 paper by J. F. Villalta and M. Crusafont in Notas y Comunicaciones del Instituto Geologico y Minero de España. Anthropologists disagree as to whether Hispanopithecus belongs to the subfamily Ponginae or Homininae.

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The Chinese orangutan is an extinct species of orangutan from the Pleistocene of South China. It is known from fossil teeth found in the Sanhe Cave, and Baikong, Juyuan and Queque Caves in Chongzuo, Guangxi. Its dental dimensions are 20% bigger than those of living orangutans. The youngest remains of the species date to between 57,000-66,000 years ago in Yincun Cave, Guangxi.

Altitypotherium is an extinct genus of Notoungulate, belonging to the suborder Typotheria. It lived during the Early Miocene, and its fossilized remains were discovered in South America.

References

  1. Grehan; Schwartz (2009). "Evolution of the second orangutan: phylogeny and biogeography of hominid origins". Journal of Biogeography. 36 (10): 1823–1844. Bibcode:2009JBiog..36.1823G. doi:10.1111/j.1365-2699.2009.02141.x. S2CID   26154219.
  2. 1 2 Schwartz, J.H.; Vu The Long; Nguyen Lan Cuong; Le Trung Kha; Tattersall, I (1995). "A review of the Pleistocene hominoid fauna of the Socialist Republic of Vietnam (excluding Hylobatidae)". Anthropological Papers of the American Museum of Natural History (76): 1–24. hdl:2246/259.
  3. Harrison, Terry; Jin, Changzhu; Zhang, Yingqi; Wang, Yuan; Zhu, Min (December 2014). "Fossil Pongo from the Early Pleistocene Gigantopithecus fauna of Chongzuo, Guangxi, southern China". Quaternary International. 354: 59–67. Bibcode:2014QuInt.354...59H. doi:10.1016/j.quaint.2014.01.013. ISSN   1040-6182.