YPM VPPU 17053
Zygodactylus ochlurus n.sp.
Holotype
|
21.0
|
~ 8.7/
~ 8.7
|
12.5/
|
~ 13.2/
14.7
|
6.7/
|
/
10.3
|
/
~ 21.4
|
15.6/
15.4
|
3.8/
|
2.0/
|
3.2/
|
3.0/
|
3.3/
|
/
2.8
|
/
3.3
|
/
3.0
|
/
2.0
|
12.6
|
0.82
|
0.53
|
0.23
|
0.17
|
SMF Av 519a
Zygodactylus luberonensis
Holotype
|
35.0
|
14.7/
|
17.2/
17.2
|
18.1/
|
/
8.6
|
~ 19.5/
|
34.8/
34.7
|
24.6/
24.5
|
/
4.6
|
/
2.1
|
/
6.5
|
/
4.6
|
/
2.7
|
/
7.1
|
/
6.5
|
/
5.4
|
/
3.1
|
18.8
|
1.04
|
0.46
|
0.16
|
0.25
|
FMNH PA 726b
Zygodactylus grandei
Holotype
|
21.1
|
13.7/
|
18.3/18.6
|
19.3/
|
~ 8.5
|
15.1/
|
33.0/33.6
|
21.4/20.4
|
4.6/4.3
|
2.6/2.7
|
/5.2
|
4.7/4.6
|
3.0
|
6.0/5.8
|
5.0/5.2
|
4.2/4.4
|
3.8/3.9
|
17.9
|
0.84
|
0.47
|
0.17
|
0.22
|
USNM 299821c
Eozygodactylus americanus
|
~ 19
| |
16.8/
16.8
|
~ 19/
19.1
|
/
8.8
| | | | | | | | | | | | | | | | | |
WDC-CGR-014c
Eozygodactylus americanus
| |
13.8/
~ 13.1
|
/
~ 17.2
|
~ 18.2/
|
8.8/
|
19.7/
|
/
30.6
|
21.7/
21.8
|
5.4/
~ 5.6
|
2.5/
~ 2.0
|
/
5.9
|
5.1/
5.2
|
2.9/
~ 2.2
|
~ 6.0/
~ 4.6
|
5.7/
5.7
|
4.7/
4.8
|
~ 2.7/
3.3
|
18.2
|
1.08
|
0.48
|
0.21
|
0.20
|
SMF-ME 1758a + bd
Primozygodactylus major
Holotype
| | |
~ 28.4/
|
~ 31.1/
|
~ 12.0/
|
24.6/
|
39.0/
39.8
|
28.0/
| | | | | | | | | |
25.7
|
0.96
|
0.47
| | |
SMF-ME 2108d
Primozygodactylus ballmanni
Holotype
| | |
21.0/
20.5
|
22.9/
22.9
|
~ 9.0
/~ 9.5
|
20.8/
|
33.0/
|
24.6/
| | | | | | | | | |
20.5
|
1.02
|
0.45
| | |
SMF-ME 2522a + bd
Primozygodactylus danielsi
Holotype
| | |
16.5/
16.4
|
18.3/
~ 17.4
|
8.2/
8.1
|
/
16.5
|
27.4/
27.3
|
19.6/
~ 18.3
|
4.0/
|
2.4/
|
4.8/
|
4.3/
|
2.4/
|
5.7/
|
4.9/
|
4.3/
|
2.6/
|
16.5
|
1.00
|
0.49
|
0.17
|
0.24
|
SMF-ME 1074d
Primozygodactylus eunjooae
Holotype
| | | | | |
17.5/
|
29.8/
|
~ 21.7
/~ 21.7
| | | | | | | | | | | | | | |
SMF-ME 11091a + bd
Primozygodactylus quintus
Holotype
| | |
19.7/ 20.0
|
20.7/20.7
|
9.5/9.5
| |
32.5/32.5
|
22.8/23.1
| | | | | | | | | | | | | | |
SMF-ME 11171a + bd
Primozygodactylus longibrachium
Holotype
| | |
> 19/ 19.6
|
21.4/> 21
|
9.6/
| |
29.5/29.5
|
/19.0
| | | | | | | | | | | | | | |