No. | Character | Character Distribtion | Character status |
| 1. | Scapula very short and deep  Click Image to Enlarge
| 1. Humans: Shortest/deepest 2. Orangutans: Next shortest 3. Chimpanzees: Next shortest 4. Gorilla: Next shortest 5. Gibbons: Next shortest 6. Monkeys: longest/shallow Characters: Proposed coding: 11000 | Presented in Schwartz 1988. Corroborated by Groves (1987: 539). Robust character |
| 2. | Supraspinous fossa (area above scapula spine) 
| 1. Humans: reduced 2. Orangutans: reduced 3. Chimpanzees: moderate reduction 4. Gorilla: moderate reduction 5. Gibbons: little reduction 6. Monkeys: little reduction? Characters: Proposed coding: 11000 | Presented in Schwartz (1988: 197). Accepted by Groves (Grehan, 2006). Robust character |
| 3. | Horizontal orientation of scapula spine
| 1. Humans: most horizontal 2. Orangutans: next most horizontal 3. Chimpanzees: moderatly horizontal 4. Gorilla: moderately horizontal 5. Gibbons: moderately horizontal? 6. Monkeys: most vertical Characters: Proposed coding: 1100000 | Presented in Schwartz 1988. Accepted by Groves (Grehan, 2006). Robust character |
| 4. | Coracoid process of scapula deflected upwards
| 1. Humans: yes 2. Orangutans: yes 3. Chimpanzees: no 4. Gorilla: no 5. Gibbons: no 6. Monkeys: no Characters: Binary Proposed coding: 110000 | Presented in Schwartz 1988. Accepted by Groves (Grehan, 2006). Robust character
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| 5. | Delayed ossification of proximal humerus
 Click Image to Enlarge | 1. Humans: Most delayed 2. Orangutans: Next delayed 3. Chimpanzees: Next delayed 4. Gorilla: Next delayed 5. Gibbons: Next delayed 6. Monkeys: Least delayed Characters: Multistate: Proposed coding: 11000 | Illustrated in Schwartz 1988. Corroborated by Groves (1987: 539) Limited sampling support |
| 6. | Delayed ossification of distal radius  Click Image to Enlarge
| 1. Humans: Most delayed 2. Orangutans: Next delayed 3. Chimpanzees: Next delayed 4. Gorilla: Next delayed 5. Gibbons: Next delayed 6. Monkeys: Least delayed Characters: Multistate: Proposed coding: 11000 | Presented in Schwartz 1988. Corroborated by Groves (1987: 539). Limited sampling support
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7. | Ulna fusion sequence | 1. Humans: Most delayed 2. Orangutans: Next delayed 3. Chimpanzees: Next delayed 4. Gorilla: Next delayed 5. Gibbons: Next delayed 6. Monkeys: Least delayed Characters: Multistate: Proposed coding: 11000 | Presented in Schwartz 1988. Accepted by Groves (Grehan, 2006). Limited sampling support |
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5. | | | Presented in Schwartz 1988. |
7. | Talar tubercle short | 1. Humans: yes 2. Orangutans: yes 3. Chimpanzees: no 4. Gorilla: no 5. Gibbons: no 6. Monkeys: no Characters: Binary Proposed coding: 110000 | Presented in Schwartz 1988. Corroborated by Groves (1987: 539).
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8. | Deep head of flexor digitorum brevis in the lower limb | 1. Humans: rare 2. Orangutans: rare 3. Chimpanzees: common 4. Gorilla: common 5. Gibbons: common 6. Monkeys: common Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. |
9. | Thenar of sole relative to hypothenar pattern | 1. Humans: greater 2. Orangutans: greater 3. Chimpanzees: equal 4. Gorilla: equal 5. Gibbons: equal 6. Monkeys: equal Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988.
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10. | Ethmo-sphenoid contact % | 1. Humans: 97 2. Orangutans: 99 3. Chimpanzees: 77 4. Gorilla: 50 5. Gibbons: less or equal 6. Monkeys: less or equal Characters: Multistate: Proposed coding: 43210 | Presented in Schwartz 1988. |
11. | Subnasal floor smoothness | 1. Humans: smooth 2. Orangutans: variably stepped/smooth 3. Chimpanzees: stepped 4. Gorilla: stepped 5. Gibbons: stepped 6. Monkeys: stepped Characters: Multistate: Proposed coding: 210000 | Presented in Schwartz 1988. |
12. | Adult incisive foramen condition 
| 1. Humans: single foramen 2. Orangutans: single foramen 3. Chimpanzees: weakly double foramena 4. Gorilla: double foramen 5. Gibbons: double fenestrae 6. Monkeys: double fenestrae Characters: Binary: Proposed coding: 332100 | Presented in Schwartz 1983,1988. Corroborated by Groves (1987: 539). > Click here for details |
13. | Juvinile incisive foramen condition | 1. Humans: single foramen 2. Orangutans: single foramen 3. Chimpanzees: double foramena 4. Gorilla: double foramena 5. Gibbons: double fenestrae 6. Monkeys: double fenestrae Characters: Binary: Proposed coding: 221100 | Presented in Schwartz 1988. |
14. | Upper molar lingual shape | 1. Humans: oval 2. Orangutans: oval 3. Chimpanzees: more square 4. Gorilla: more square 5. Gibbons: more square 6. Monkeys: more square Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. |
15. | Molar protocone height relative to paracone of upper anterior deciduous molar | 1. Humans: higher 2. Orangutans: higher 3. Chimpanzees: lower 4. Gorilla: lower 5. Gibbons: lower 6. Monkeys: lower Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. |
16. | Protoconid position on lower anterior deciduous molar | 1. Humans: anterior 2. Orangutans: anterior 3. Chimpanzees: central 4. Gorilla: central 5. Gibbons: central 6. Monkeys: central Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. |
17. | Paracristid orientation on lower anterior deciduous molar | 1. Humans: angled 2. Orangutans: angles 3. Chimpanzees: straight 4. Gorilla: straight 5. Gibbons: straight 6. Monkeys: straight Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. |
18. | Talonid basin condition on lower anterior deciduous molar | 1. Humans: closed 2. Orangutans: closed 3. Chimpanzees: open 4. Gorilla: open 5. Gibbons: open 6. Monkeys: open Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. |
19. | Trigonid of lower posterior deciduous molar | 1. Humans: short 2. Orangutans: short 3. Chimpanzees: moderately short 4. Gorilla: moderatly short 5. Gibbons: moderately short 6. Monkeys: moderately short Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. |
20. | Cerebral asymmetries | 1. Humans: marked 2. Orangutans: marked 3. Chimpanzees: moderate 4. Gorilla: moderate 5. Gibbons: moderate 6. Monkeys: moderate Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. |
21. | Sylvian sulcus asymmetry | 1. Humans: marked 2. Orangutans: marked 3. Chimpanzees: moderate 4. Gorilla: moderate 5. Gibbons: moderate 6. Monkeys: moderate Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. |
22. | Estriol levels high during mensrual cycle | 1. Humans: high 2. Orangutans: high 3. Chimpanzees: low 4. Gorilla: low 5. Gibbons: absent 6. Monkeys: absent Characters: Binary: Proposed coding: 22 1100 | Presented in Schwartz 1988. |
23. | Estriol levels high during pregnancy | 1. Humans: high 2. Orangutans: high 3. Chimpanzees: low 4. Gorilla: low 5. Gibbons: absent 6. Monkeys: absent Characters: Binary: Proposed coding: 221100 | Presented in Schwartz 1988. Corroborated by Groves (1987: 540) for late pregnancy). |
24. | Adrenal gland size in the fetus | 1. Humans: large 2. Orangutans: large 3. Chimpanzees: small 4. Gorilla: small 5. Gibbons: small 6. Monkeys: small Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. |
25. | Estrus cycle | 1. Humans: absent 2. Orangutans: absent 3. Chimpanzees: present 4. Gorilla: present 5. Gibbons: present 6. Monkeys: present Characters: Binary: Proposed coding: 110000 | Variable in monkeys, but inconsistently defined. Questioned by Groves (1987:540) due to zoo orangutans showing mid-cylce proceptivity. > Click here for details |
26. | Gestation period scaled to body weight | 1. Humans: 89.6 2. Orangutans: 87.3 3. Chimpanzees: 81.4 4. Gorilla: 83.8 5. Gibbons: less 6. Monkeys: less Characters: Multistate: Proposed coding: 432100 | Presented in Schwartz 1988. Groves (1987: 540) noted variability for zoo records, but did not identify how they affected the character determination. |
27. | Anogenital tumescence during ovulatory cycle | 1. Humans: absent 2. Orangutans: absent 3. Chimpanzees: present 4. Gorilla: present 5. Gibbons: present 6. Monkeys: sometimes absent? Characters: Binary: Proposed coding: 110000 | Apparently absent in some monkeys, but poorly documented and often overlooked. Treated here as apomorphic for humans and orangutans. > Click here for details |
28. | Mamary gland/nipple distance between right and left gland as a percentage of chest bredth | 1. Humans: 71% 2. Orangutans: 90% 3. Chimpanzees: 52% 4. Gorilla: 46% 5. Gibbons: 32% 6. Monkeys: 40% or less? Characters: Multistate: Proposed coding: 342100 | Presented in Schultz (1936: pages 281, 444). Variable according to Groves (1987: 540), but no data provided. |
29. | Gall bladder shape | 1. Humans: slight bend 2. Orangutans: straight 3. Chimpanzees: bent 4. Gorilla: bent 5. Gibbons: bent 6. Monkeys: bent Characters: Multistate: Proposed coding: 120000 | Presented in Schwartz 1988. |
30. | Accessory lobe size on parotid gland | 1. Humans: slight 2. Orangutans: small 3. Chimpanzees: none 4. Gorilla: none 5. Gibbons: none 6. Monkeys: none Characters: Binary: Proposed coding: 120000 | Presented in Schwartz 1988. |
31. | Hair length | 1. Humans: longest (head) 2. Orangutans: next longest (body) 3. Chimpanzees: moderate 4. Gorilla: moderate 5. Gibbons: moderate 6. Monkeys: moderate Characters: Multistate: Proposed coding: 21000 | Presented in Schwartz 1988. |
32. | Ischial callosities absent (unkeratinized) | 1. Humans: absent 2. Orangutans: absent 3. Chimpanzees: variably present 4. Gorilla: present 5. Gibbons: present 6. Monkeys: present Characters: Multistate: Proposed coding: 221000 | Presented in Schwartz 1988. Homology of character in monkeys questioned by Groves (1987: 539). Groves also notes absence of callosities in some individuals of African apes but this does not contradict the complete absence of keratinized callosities in orangutans. |
33. | Vallate paillae number | 1. Humans: 8-12 2. Orangutans: 7-12 3. Chimpanzees: 6-8 4. Gorilla: 3-8 5. Gibbons: less 6. Monkeys: less Characters: Binary: Proposed coding: 432100 | Presented in Schwartz 1988. |
34. | Foramen lacerum | 1. Humans: present 2. Orangutans: present 3. Chimpanzees: absent 4. Gorilla: absent 5. Gibbons: absent 6. Monkeys: absent Characters: Binary: Proposed coding: 110000 | Presented in Schwartz 1988. Corroborated by Groves (1987: 539) although apparent absence of this character in australopithecines was questioned. Schwartz (pers. comm.) has since confirmed the presence of this character in australopithecines. |
35. | Thick molar enamel | 1. Humans: present 2. Orangutans: present 3. Chimpanzees: absent 4. Gorilla: absent 5. Gibbons: absent 6. Monkeys: rare Characters: Binary: Proposed coding: 110000 | Presented in Schwartz (1988b, 2001). > Click here for details |
36. | Hair on forehead 
| 1. Humans: vestigial 2. Orangutans: vestigial 3. Chimpanzees: similar to body 4. Gorilla: similar to body 5. Gibbons: similar to body 6. Monkeys: similar to body Characters: Binary: Proposed coding: 110000 | Two monkey species have a receded hairline. It is therefore suggested here that the human-orangutan condition represents a potential synapomorphy. > Click here for details |
37. | Leading edge of cranial hair with a anterior (forward) orientation. 
| 1. Humans: yes 2. Orangutans: yes 3. Chimpanzees: no (posterio-lateral) 4. Gorilla: no (posterior) 5. Gibbons: no (posterior) 6. Monkeys: extremely rare Characters: Binary: Proposed coding: 110000 | Anterior orientatoin of cranial hair found in eight New World monkey species, sometimes in combination with vestigial forehead hair > Click here for details
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38. | Prescence of a well-developed beard and mustache in the male | 1. Humans: present 2. Orangutans: present 3. Chimpanzees: absent 4. Gorilla: absent 5. Gibbons: absent 6. Monkeys: absent Characters: Binary: Proposed coding: 110000 | Some monkeys have beards or mustaches, but none have both well developed. The closest similairty in monkeys would be the New World species Saguinus imperator > See Rowe (1996). The Pictorial Guide to the Living Primates. |
39. | Sustained copulation | 1. Humans: Long 2. Orangutans: Long (5-45 minutes) 3. Chimpanzees: brief 4. Gorilla: brief 5. Gibbons: brief 6. Monkeys: brief Characters: Binary: Proposed coding: 110000 | |
40. | Proximal end of ulna is the second element to fuse in the elbow | 1. Humans: yes 2. Orangutans: yes 3. Chimpanzees: no 4. Gorilla: no 5. Gibbons: no 6. Monkeys: no Characters: Binary: Proposed coding: 110000 | In other primates it is either the epicondyle or the proximal end of the radius. See Shultz (1968: 181) |
41. | Head of the humerus fuses after fusion of the epicondyle in the elbow-hip-annkle joints | 1. Humans: yes 2. Orangutans: yes 3. Chimpanzees: no 4. Gorilla: no 5. Gibbons: no 6. Monkeys: no Characters: Binary: Proposed coding: 110000 | In other primates the humerus fuses after the proximal radius, trochanter of femur, or proximal ulna (See Shultz 1968: 181) 42 Radial cross vein in forearm |
| | | 1. Humans: yes 2. Orangutans: yes 3. Chimpanzees: no 4. Gorilla: no 5. Gibbons: no 6. Monkeys: no Characters: Binary: Proposed coding: | |