ライフサイエンスコーパス: orang-utan

1 provides a possible function for its use by orang-utans.

2 hile no variation was found for gorillas and orang-utans.

3 ent decisions about captive and free-ranging orang-utans.

4 The geographic distribution of Bornean orang-utans and its overlap with existing land-use categ

5 ces from great apes, chimpanzee, gorilla and orang-utan, and an Old World monkey, Macaca mulatta.

6 ral variation maps in five chimpanzees, five orang-utans, and five rhesus macaques.

7 particularly in light of the ~1500 displaced orang-utans awaiting urgent reintroduction.

8 on content of four primate genomes (macaque, orang-utan, chimpanzee and human) in an effort to unders

9 ographically isolated populations of Bornean orang-utans, consistent with gene flow having occurred b

10 The modelled orang-utan distribution map covers 155,106 km(2) (21% of

11 r of environmental variables, we modelled an orang-utan distribution map.

12 The remaining 24% of the orang-utan distribution range occurs outside of protecte

13 An estimated 49% of the orang-utan distribution will be lost if all forest outsi

14 The overlap of the orang-utan distribution with land-use categories reveals

15 Here we present a Sumatran orang-utan draft genome assembly and short read sequence

16 Orang-utans exist today in small isolated populations on

17 oci were duplicated before the divergence of orang-utans from other Great Apes, that a cytogeneticall

18 ang-utan populations using cellular DNA from orang-utans from two locations in Sumatra and nine locat

19 reveal that, compared to other primates, the orang-utan genome has many unique features.

20 Structural evolution of the orang-utan genome has proceeded much more slowly than ot

21 pecies, emphasizing the gradual evolution of orang-utan genome structure.

22 , bonobo and gorilla genomes, but not in the orang-utan genome.

23 nce data from five Sumatran and five Bornean orang-utan genomes.

24 rts to halt deforestation could mediate some orang-utan habitat loss, but further decline of the most

25 potential decline plantation development in orang-utan habitats must be halted because it infringes

26 e of leaf extracts from Dracaena cantleyi by orang-utan has been observed on several occasions; rubbi

27 differentiation between Sumatran and Bornean orang-utans has reached the level of distinct species.

28 Orang-utans have extremely low energy usage for a euther

29 differentiation between Sumatran and Bornean orang-utans is large, greater than that between the comm

30 'Orang-utan' is derived from a Malay term meaning 'man of

31 an troglodytes (chimpanzee), Pongo pygmaeus (orang-utan), Nomascus nastusus and Hylobates pileatus (g

32 her evaluation of the effects of hybridizing orang-utans of different taxa--particularly in light of

33 e closely related, but more solitary Bornean orang-utans (P. pygmaeus), under the homogeneous environ

34 tes ), the gorilla (Gorilla gorilla) and the orang-utan (Pongo pygmaeus).

35 and Dryopithecus from Eurasia and the living orang-utan (Pongo) from Borneo and Sumatra.

36 em-solving task in a large sample of captive orang-utans (Pongo abelii &P. pygmaeus, N = 103) that ha

37 ared the problem-solving ability of Sumatran orang-utans (Pongo abelii), which are sociable in the wi

38 self-medication in the only Asian great ape, orang-utans (Pongo pygmaeus), and for the first time, to

39 number of non-human primates including eight orang-utans (Pongo pygmaeus), seven gorillas (Gorilla go

40 al characteristics, the Bornean and Sumatran orang-utan populations are generally considered as two s

41 d patterns of molecular genetic variation in orang-utan populations using cellular DNA from orang-uta

42 ic diversity within the Bornean and Sumatran orang-utan populations, suggesting that they have not ex

43 Borneo was suitable habitat within the core orang-utan range; an 18-24% reduction since the 1950s.

44 es and 44 years of data from Camp Leakey, an orang-utan rehabilitation site on Borneo, we determined

45 o, we determined the minimum extent to which orang-utans representing non-native, geographically and

46 tudies and underscores the complexity of the orang-utan speciation process.

47 The orang-utan species, Pongo abelii (Sumatran) and Pongo py

48 level of sequence divergence between the two orang-utan structures was identified.

49 Notably, the orang-utan subject skilfully produced "wookies" - an idi

50 Given that Bornean orang-utan subspecies are thought to have diverged from

51 Based on an extensive orang-utan survey dataset and a number of environmental

52 In the orang-utan, two alleles with different structures were i

53 hibiting a unique spectral profile among the orang-utan vocal repertoire.

54 Using a case study of the endangered Bornean orang-utan, we identify environmental refuges by integra

55 t probably represent the proximal end of the orang-utan Xp/Yp telomere.