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1 ely with any extant crown hominid, including Pongo.
2 the relationships between Lufengpithecus and Pongo.
3 sk in a large sample of captive orang-utans (Pongo abelii &P. pygmaeus, N = 103) that had experienced
4                      The orang-utan species, Pongo abelii (Sumatran) and Pongo pygmaeus (Bornean), ar
5 ion of information in 15 captive orangutans (Pongo abelii and Pongo pygmaeus) using a simulated food-
6 ene repertoire in the two orangutan species, Pongo abelii and Pongo pygmaeus, is presented in this ar
7 himpanzees (Pan troglodytes) and orangutans (Pongo abelii) either had to determine the location of a
8 lem-solving ability of Sumatran orang-utans (Pongo abelii), which are sociable in the wild, with that
9 nd fossil members of a proposed Sivapithecus/Pongo clade, but which now appear to be primitive featur
10 ecus from Eurasia and the living orang-utan (Pongo) from Borneo and Sumatra.
11 able ages at M1 emergence for the orangutan, Pongo pygmaeus (4.6 y), and the gorilla, Gorilla gorilla
12 ng-utan species, Pongo abelii (Sumatran) and Pongo pygmaeus (Bornean), are the most phylogenetically
13 lla (gorilla), Pan troglodytes (chimpanzee), Pongo pygmaeus (orang-utan), Nomascus nastusus and Hylob
14 luate the extent to which Bornean orangutans Pongo pygmaeus come down from the trees to travel terres
15 differentiate these teeth from more numerous Pongo pygmaeus elements.
16 lations on the islands of Borneo (subspecies Pongo pygmaeus pygmaeus) and Sumatra (subspecies P. p. a
17  and memory to determine whether orangutans (Pongo pygmaeus x P. abelii) would show evidence of subje
18  adequate habitat for the Bornean orangutan (Pongo pygmaeus) and Bornean elephant (Elephas maximus bo
19 lactoside binding sites from both orangutan (Pongo pygmaeus) and murine (Mus musculus) genomic DNAs,
20               The authors tested orangutans (Pongo pygmaeus) and squirrel monkeys (Saimiri sciureus)
21 (Gorilla gorilla) and 19 captive orangutans (Pongo pygmaeus) and were compared with chimpanzee (Pan t
22  paniscus, Pan troglodytes, Gorilla gorilla, Pongo pygmaeus) by varying whether apes were endowed wit
23 n in 15 captive orangutans (Pongo abelii and Pongo pygmaeus) using a simulated food-processing task.
24 s study, the authors presented 2 orangutans (Pongo pygmaeus) with a quantity judgment task.
25 las (Gorilla gorilla gorilla), 4 orangutans (Pongo pygmaeus), 14 chimpanzees (Pan troglodytes), and 4
26 the critically endangered Bornean orangutan (Pongo pygmaeus), allowing a deeper understanding of the
27 troglodytes), a group of 2 adult orangutans (Pongo pygmaeus), and a group of 36 children (between 2 a
28 on in the only Asian great ape, orang-utans (Pongo pygmaeus), and for the first time, to our knowledg
29 chimpanzees (Pan troglodytes), an orangutan (Pongo pygmaeus), and human infants (Homo sapiens) were i
30 -human primates including eight orang-utans (Pongo pygmaeus), seven gorillas (Gorilla gorilla), seven
31 tudied for the two subspecies of orangutans (Pongo pygmaeus), which are located in Borneo (P. p. pygm
32  two human-reared (enculturated) orangutans (Pongo pygmaeus).
33 impanzees (Pan troglodytes), and orangutans (Pongo pygmaeus).
34 orilla (Gorilla gorilla) and the orang-utan (Pongo pygmaeus).
35 s), gorilla (Gorilla gorilla) and orangutan (Pongo pygmaeus).
36  the two orangutan species, Pongo abelii and Pongo pygmaeus, is presented in this article.
37 m EDN from sequences derived from orangutan (Pongo pygmaeus, oEDN) and Old World monkey (Macaca fasci
38 orilla (Gorilla gorilla, GGO) and orangutan (Pongo pygmaeus, PPY).
39 ed to be a relative of the extant orangutan, Pongo pygmaeus.
40        From the population perspective, both Pongo species are deeply diverse; however, Sumatran indi
41 ate polymorphic neocentromere, found in both Pongo species, emphasizing the gradual evolution of oran
42  daily energy use in free-living orangutans (Pongo spp.) and test whether observed differences in ene
43 n biodiversity [1, 4, 5], and on orangutans (Pongo spp.) in particular, have been well documented [6,
44 xible properties was explored in orangutans (Pongo spp.) through an extension of D.J. Povinelli, J.E.
45 e species (Pan troglodytes, Gorilla gorilla, Pongo spp., and Pan pansicus).
46 hecus) with clear craniofacial affinities to Pongo suggests both more diversity among Asian Late Mioc
47                             The new species, Pongo tapanuliensis, encompasses the Batang Toru populat
48  is particularly true for orangutans (genus: Pongo), the only Asian great apes and phylogenetically o

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