Evidence for the Orangutan Relationship
Evidence for the orangutan being the closest living relative of modern humans is based on at least 35 known characters that appear to be either exclusive to humans and orangutans or largely absent in outgroups.
| Taxon comparaison: humans, orangutan, chimpanzee, gorilla (outgroups gibbon, monkeys) Characters and states from Grehan and Schwartz (2009) Evolution of the second orangutan: phylogeny and biogeography of hominid origins. Journal of Biogeography 36: 1823-1844. |
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No. |
Character |
Character Distribtion |
Character status |
| 1. | Scapula short and deep
|
Humans and orangutans: Shortest/deepest Coding:11000 |
Schwartz (1988), Groves (1987: 539). |
| 2. |
Supraspinous fossa |
Humans and orangutans: most reduced |
Schwartz (1988: 197). Accepted by Groves (Grehan, 2006). |
| 3. | Orientation of scapula spine![]() |
Humans and orangutans: most horizontal Coding: 11000 |
Schwartz 1988. Accepted by Groves (Grehan, 2006). Robust Grehan and Schwartz 2009 |
4. |
Upward deflection of coracoid process
![]() |
Humans and orangutans: Greatest Coding: 11000 |
Schwartz 1988. Accepted by Groves (Grehan, 2006). Robust Grehan and Schwartz 2009 Click here for scapula images |
5. |
Ethmo-sphenoid contact |
Humans: 97%, Orangutans: 99% Chimpanzees: 77%, Gorilla: 50% Gibbons and monkeys: less or equal Coding: 11000 |
Presented in Schwartz 1988. Robust |
6. |
Juvenile incisive foramen |
Humans and orangutans: single |
Presented in Schwartz 1983,1988. |
7. |
Foramen lacerum |
Humans and orangutans: present |
Robust |
8. |
Posterior palate thick |
Humans and orangutans: thick |
Robust |
9. |
Upper posterior deciduous molar protocone taller than paracone |
Humans and orangutans: yes |
Robust |
10. |
Lower posterior deciduous molar trigonid shortest |
Humans and orangutans: yes |
Robust |
11. |
Upper molar lingual shape |
Humans and orangutans: oval
Coding: 11000 |
Moderate |
12. |
lower anterior deciduous molar protoconid anteriorly placed | Humans and orangutans: yes Coding: 11000 |
Robust |
13. |
lower anterior deciduous molar mesially angled |
Robust |
|
14. |
lower anterior deciduous molar talonid basin closed |
Humans and orangutans: yes
Coding: 11000 |
Robust |
15. |
Molar enamel thick |
Humans and orangutans: yes Coding: 11000 |
Robust |
16. |
Ischial callosities |
Humans: and orangtuans: never Coding: 11000 |
Robust |
17. |
Mamary gland/nipple distance between right and left gland as a percentage of chest breadth |
Humans: 71%, Orangutans: 90% Chimpanzees: 52%, Gorilla: 46% Gibbons: 32%, Monkeys: 40% (narrow thorax) |
Robust |
18. |
Hairline receeded | Humans and orangutans: yes Coding: 11000 |
Robust |
19. |
Hair orientation | Humans and orangutans: forward Coding: 11000 |
Robust |
20. |
Beard and mustache developed | Humans and orangutans: yes Coding: 11000 |
Robust |
21. |
Longest hair | Humans (head) and orangutans (body) yes Coding: 11000 |
Robust |
22. |
Smile with closed lips | Humans and orangutans: yes Coding: 11000 |
Robust |
23. |
estrogen production | Humans and orangutans: highest Coding: 11000 |
Robust |
24. |
Estriol levels during mensrual cycle |
Humans and orangutans highest Coding: 11000 |
Robust |
25. |
Female initiated mounting |
Humans and orangutans yes Coding: 11000 |
Robust |
26. |
Radial vein present in forearm |
Humans and orangutans yes Coding: 11000 |
Robust |
27. |
Mechanical aptitude |
Humans and orangutans: highest |
Robust |
28. |
External ear helicies |
Humans and orangutans: close |
Robust |
| Derived (but not unique) features | |||
|
. |
Estrus cycle |
1. Humans: absent 2. Orangutans: absent 3. Chimpanzees: present 4. Gorilla: present 5. Gibbons: present 6. Monkeys: present |
Variable in monkeys, but inconsistently defined. |
|
|
Anogenital tumescence during ovulatory cycle |
1. Humans: absent 2. Orangutans: absent 3. Chimpanzees: present 4. Gorilla: present 5. Gibbons: present 6. Monkeys: sometimes absent? |
Apparently absent in some monkeys, but poorly documented and often overlooked. Treated here as apomorphic for humans and orangutans. |




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