List of cladograms tested for their correspondence with stratigraphic data. Cladograms are listed alphabetically. For each group, data are listed in order, as follows:
- Group name
- Tree size (number of terminals)
- SRL, Standard range length, the total time represented by known fossil ranges
- MIG, Minimum implied gap or ‘ghost range’
- Gmin, the minimum possible ghost range when cladogram branches are rearranged
- Gmax, the maximum possible ghost range when cladogram branches are rearranged
- RCI, the Relative completeness index (Benton, 1994)
- RCI and GER Sig., significance of the RCI and GER measures
- No. consistent nodes, the number of stratigraphically consistent nodes
- SCI, the Stratigraphic consistency index (Huelsenbeck, 1994)
- SCI Sig., significance of the SCI measure
- GER, the Gap excess ratio (Wills, 1999)
- Range, the broad stratigraphic range of the cladogram
- Reference, the source of the cladogram assessed
Group |
No. terminals |
SRL |
MIG |
Gmin |
Gmax |
RCI |
RCI & GER Sig |
Consistent nodes |
SCI |
SCI Sig. |
GER |
Range of O |
Reference |
Mammalia(1) |
26 |
1443 |
358 |
102 |
1330 |
75.190575 |
2.25 |
10 |
0.43478 |
42.75 |
0.79153 |
Cret-Neog |
Shoshani (1986, fig. 3) |
Mammalia(2) |
20 |
1198 |
389 |
102 |
1042 |
67.529215 |
2 |
6 |
0.33333 |
38.75 |
0.69468 |
Cret-Neog |
Novacek et al. (1988, fig. 3.3) |
Mammalia(3) |
20 |
1198 |
302 |
102 |
1042 |
74.791319 |
0.5 |
8 |
0.44444 |
51.5 |
0.78723 |
Cret-Neog |
Novacek (1989, fig. 3) |
Mammalia(4) |
6 |
465 |
119 |
59 |
119 |
74.408602 |
100 |
0 |
0 |
100 |
0 |
Tri-Jur |
Butler (1997, fig. 3) |
Mammalia(5) |
9 |
519 |
259 |
146 |
741 |
50.096339 |
100 |
4 |
0.571429 |
14.5 |
0.810084 |
Tri-Cret |
Greenwald (1988, fig. 4) |
Mammalia(6) |
9 |
427 |
172 |
128 |
526 |
59.71897 |
2 |
4 |
0.571429 |
9 |
0.889447 |
Tri-Rec |
Wang et al. (1998, fig. 7) |
Mammalia-Paurodontidae |
5 |
113 |
11 |
11 |
44 |
90.265487 |
17 |
3 |
1 |
17 |
1 |
Jur |
Ensom & Sigogneau-Russell (1998, fig. 14) |
Marsupialia(1) |
17 |
568 |
364 |
139 |
1567 |
35.915493 |
2 |
6 |
0.4 |
3 |
0.842437 |
Cret-Pleist |
Szalay & Trofimov (1996, fig. 25) |
Marsupialia(2) |
9 |
320 |
56 |
47 |
266 |
82.5 |
1 |
6 |
0.857143 |
1 |
0.958904 |
Cret-Paleoc |
Wible (1990, fig. 6) |
Marsupialia-Phalangeriformes |
8 |
150 |
69 |
24 |
82 |
54 |
51 |
1 |
0.166667 |
100 |
0.224138 |
Olig-Rec |
Springer & Woodburne (1989, fig. 3A) |
Marsupialia-Phalangeriformes |
8 |
150 |
82 |
24 |
82 |
45.333333 |
100 |
0 |
0 |
100 |
0 |
Olig-Rec |
Springer & Woodburne (1989, fig. 3B) |
Marsupialia-Phalangeriformes |
8 |
150 |
82 |
24 |
82 |
45.333333 |
100 |
0 |
0 |
100 |
0 |
Olig-Rec |
Springer & Woodburne (1989, fig. 3C) |
Marsupialia-Phalangeriformes |
8 |
150 |
82 |
24 |
82 |
45.333333 |
100 |
2 |
0.333333 |
64 |
0 |
Olig-Rec |
Springer & Woodburne (1989, fig. 3D) |
Marsupialia-Thylacinidae |
12 |
61 |
92 |
21 |
131 |
-50.819672 |
27 |
5 |
0.5 |
26.5 |
0.354545 |
Mioc-Rec |
Muirhead & Wroe (1998, fig. 5) |
Eutheria(1) |
17 |
936 |
236 |
73 |
475 |
74.786325 |
28.75 |
7 |
0.46667 |
78.5 |
0.59453 |
Paleog-Neog |
Gregory (1910; in Novacek et al. 1988, fig. 3.1(a)) |
Eutheria(2) |
16 |
926 |
219 |
48 |
402 |
76.349892 |
45.25 |
4 |
0.28571 |
86.25 |
0.51695 |
Paleog-Neog |
Simpson (1945; in Novacek et al. 1988, fig. 3.1(b)) |
Eutheria(3) |
18 |
996 |
275 |
73 |
498 |
72.389558 |
32.75 |
8 |
0.47059 |
36.25 |
0.52471 |
Paleog-Neog |
McKenna (1975; in Novacek et al. 1988, fig. 3.2(a)) |
Eutheria(4) |
18 |
996 |
298 |
73 |
498 |
70.080321 |
71 |
4 |
0.25 |
100 |
0.47059 |
Paleog-Neog |
Novacek (1982; in Novacek et al. 1988, fig. 3.2(b)) |
Eutheria(5) |
18 |
996 |
291 |
73 |
498 |
70.783133 |
58.5 |
4 |
0.25 |
98.25 |
0.48706 |
Paleog-Neog |
Novacek & Wyss (1986; in Novacek et al. 1988, fig. 3.4A) |
Eutheria(6) |
24 |
1241 |
329 |
73 |
612 |
73.489122 |
79.75 |
8 |
0.38095 |
88.25 |
0.52505 |
Paleog-Neog |
Shoshani (1986, fig. 3) |
Eutheria(7) |
18 |
986 |
395 |
73 |
473 |
59.939148 |
78 |
4 |
0.25 |
96 |
0.195 |
Paleog-Neog |
Novacek et al. (1988, fig. 3.3) |
Eutheria(8) |
18 |
996 |
273 |
73 |
498 |
72.590361 |
72.5 |
6 |
0.375 |
98.5 |
0.52941 |
Paleog-Neog |
Novacek (1989, fig. 3) |
Edentata |
5 |
217 |
31 |
31 |
41 |
85.714286 |
7.25 |
3 |
1 |
7.25 |
1 |
Paleog-Neog |
Gaudin (1995, fig. 1) |
Edentata-Tardigrada |
21 |
83 |
257 |
35 |
531 |
-209.63855 |
18 |
10 |
0.52632 |
25.5 |
0.55242 |
Paleog-Neog |
Gaudin (1995, fig. 2) |
Insectivora |
15 |
476 |
273 |
72 |
470 |
42.647059 |
22 |
5 |
0.41667 |
25.75 |
0.49497 |
Paleog-Neog |
Butler (1988, fig. 5.6) |
Mesonychia |
10 |
73 |
15 |
15 |
84 |
79.452055 |
6.75 |
8 |
1 |
16.5 |
1 |
Paleog |
Zhou et al. (1995, fig. 7) |
Pantodonta-Coryphodontidae |
5 |
66 |
4 |
4 |
16 |
93.939394 |
22.5 |
3 |
1 |
22.5 |
1 |
Paleoc-Eoc |
Lucas & Tong (1987, fig. 7) |
Plesiadapiformes-Micromomyini |
5 |
28 |
NAN(000) |
4 |
4 |
85.714286 |
100 |
3 |
1 |
42.5 |
NAN(000) |
Paleoc-Eoc |
Beard & Houde (1989, fig. 7) |
Primates(1) |
7 |
218 |
114 |
60 |
147 |
47.706422 |
27 |
3 |
0.6 |
4.5 |
0.37931 |
Paleog-Neog |
Pocock (1918; in Andrews 1988, fig. 6.2B) |
Primates(2) |
5 |
157 |
106 |
56 |
123 |
32.484076 |
100 |
1 |
0.33333 |
100 |
0.25373 |
Paleog-Neog |
Simpson (1945; in Andrews 1988, fig. 6.2A) |
Primates(3) |
7 |
209 |
112 |
65 |
156 |
46.411483 |
24 |
2 |
0.4 |
100 |
0.48352 |
Paleog-Neog |
Gingerich (1975; in Andrews 1988, fig. 6.2C) |
Primates(4) |
6 |
187 |
133 |
65 |
168 |
28.877005 |
56.75 |
2 |
0.5 |
52.75 |
0.33981 |
Paleog-Neog |
Schwartz & Tattersall (1987; in Andrews 1988, fig. 6.2D) |
Primates(5) |
6 |
187 |
133 |
65 |
168 |
28.877005 |
56.75 |
2 |
0.5 |
52.75 |
0.33981 |
Paleog-Neog |
Andrews (1988, figs. 6.3, 6.4) |
Primates(6) |
11 |
342 |
167 |
65 |
254 |
51.169591 |
14.75 |
3 |
0.33333 |
68.25 |
0.46032 |
Paleog-Neog |
Andrews (1988, figs. 6.3, 6.4) |
Primates-Washakiini |
14 |
129 |
20 |
14 |
20 |
84.496124 |
100 |
12 |
1 |
27.5 |
0 |
Eoc |
Honey (1990, fig. 6) |
Primates-Platyrrhini(1) |
16 |
0 |
NAN(000) |
0 |
0 |
NAN(000) |
26 |
14 |
1 |
100 |
NAN(000) |
Hol-Rec |
Ford & Morgan (1986, fig. 3) |
Primates-Platyrrhini(2) |
16 |
0 |
NAN(000) |
0 |
0 |
NAN(000) |
26 |
14 |
1 |
100 |
NAN(000) |
Hol-Rec |
Ford & Morgan (1986, fig. 3) |
Rodentia(1) |
5 |
202 |
27 |
21 |
39 |
86.633663 |
60.5 |
2 |
0.66667 |
51.5 |
0.66667 |
Paleog |
Jaeger (1988, fig. 7.2) |
Rodentia(2) |
5 |
191 |
8 |
4 |
8 |
95.811518 |
100 |
2 |
0.66667 |
29.75 |
0 |
Paleog |
Jaeger (1988, fig. 7.3A) |
Rodentia(3) |
5 |
191 |
8 |
4 |
8 |
95.811518 |
100 |
2 |
0.66667 |
66.75 |
0 |
Paleog |
Jaeger (1988, fig. 7.3C) |
Rodentia(4) |
7 |
276 |
35 |
25 |
43 |
87.318841 |
11.25 |
3 |
0.6 |
26.75 |
0.44444 |
Paleog |
Jaeger (1988, fig. 7.3B) |
Rodentia-Geomorpha(1) |
5 |
165 |
17 |
7 |
17 |
89.69697 |
100 |
1 |
0.33333 |
91.5 |
0 |
Paleog |
Korth (1993, fig. 3) |
Rodentia-Geomorpha(2) |
5 |
182 |
47 |
21 |
47 |
74.175824 |
100 |
1 |
0.333333 |
91.5 |
0 |
Eoc-Olig |
Korth et al. (1991, fig. 3) |
Rodentia-Hydrochoeridae |
13 |
41 |
98 |
23 |
210 |
-139.02439 |
8 |
5 |
0.454545 |
16.5 |
0.59893 |
Mioc-Rec |
Prado et al. (1998, fig. 9A) |
Rodentia-Hydrochoeridae |
13 |
41 |
98 |
23 |
210 |
-139.02439 |
10 |
5 |
0.454545 |
17 |
0.59893 |
Mioc-Rec |
Prado et al. (1998, fig. 9B) |
Rodentia-Hydrochoeridae |
13 |
41 |
98 |
23 |
210 |
-139.02439 |
9 |
5 |
0.454545 |
17 |
0.59893 |
Mioc-Rec |
Prado et al. (1998, fig. 9C) |
Rodentia-Hystricomorpha |
9 |
282 |
87 |
46 |
138 |
69.148936 |
3.25 |
4 |
0.57143 |
28.5 |
0.55435 |
Paleog-Neog |
Jaeger (1988, fig. 7.1) |
Rodentia-Microtus |
10 |
24 |
14 |
5 |
26 |
41.666667 |
52 |
6 |
0.75 |
39 |
0.571429 |
Pli-Rec |
Martin (1987, fig. 4) |
Rodentia-Mimomys |
7 |
26 |
5 |
5 |
30 |
80.769231 |
13.5 |
5 |
1 |
13.5 |
1 |
Mioc-Pli |
Mou (1997, fig. 5) |
Rodentia-Phyllotini |
20 |
9 |
47 |
5 |
89 |
-422.22222 |
79 |
8 |
0.444444 |
80.5 |
0.5 |
Pli-Rec |
Steppan & Pardiñas (1998, fig. 5) |
Rodentia-Pleurolocus |
4 |
28 |
NAN(000) |
0 |
0 |
100 |
100 |
2 |
1 |
100 |
NAN(000) |
Mioc |
Korth (1996, fig. 2) |
Rodentia-Sciuridae |
5 |
33 |
30 |
23 |
30 |
9.090909 |
100 |
2 |
0.666667 |
100 |
0 |
Mioc-Rec |
Pratt & Morgan (1989, fig. 2) |
Rodentia-Sigmodontinae |
8 |
4 |
8 |
2 |
12 |
-100 |
47.5 |
3 |
0.5 |
57 |
0.4 |
Pleist-Rec |
Steppan (1996, fig. 4A) |
Rodentia-Sigmodontinae |
8 |
4 |
6 |
2 |
12 |
-50 |
22 |
3 |
0.5 |
22 |
0.6 |
Pleist-Rec |
Steppan (1996, fig. 4B) |
Rodentia-Thryonomyoidea |
11 |
77 |
53 |
33 |
189 |
31.168831 |
2 |
5 |
0.555556 |
6 |
0.871795 |
Olig-Rec |
Winkler (1992, fig. 6) |
Arctocyonidae |
7 |
54 |
54 |
18 |
54 |
0 |
100 |
2 |
0.4 |
96 |
0 |
Cret-Eoc |
Luo (1991, fig. 15A) |
Arctocyonidae |
7 |
54 |
45 |
18 |
54 |
16.666667 |
64.5 |
3 |
0.6 |
26 |
0.25 |
Cret-Eoc |
Luo (1991, fig. 15B) |
Arctocyonidae |
7 |
54 |
54 |
18 |
54 |
0 |
100 |
2 |
0.4 |
91 |
0 |
Cret-Eoc |
Luo (1991, fig. 15C) |
Creodonta-Hyaenodontidae |
16 |
206 |
117 |
42 |
274 |
43.203883 |
0.5 |
9 |
0.642857 |
3.5 |
0.676724 |
Paleoc-Mioc |
Polly (1996, fig. 10) |
Creodonta-Proviverrini |
13 |
153 |
112 |
49 |
287 |
26.797386 |
0.5 |
8 |
0.727273 |
1 |
0.735294 |
Paleoc-Mioc |
Barry (1988, fig. 5) |
Creodonta-Proviverrini |
13 |
153 |
142 |
49 |
287 |
7.189542 |
3 |
5 |
0.454545 |
26.5 |
0.609244 |
Paleoc-Mioc |
Barry (1988, fig. 6) |
Creodonta-Proviverrini |
13 |
153 |
112 |
49 |
287 |
26.797386 |
0.5 |
8 |
0.727273 |
26.5 |
0.735294 |
Paleoc-Mioc |
Barry (1988, fig. 7A) |
Creodonta-Proviverrini |
13 |
153 |
118 |
49 |
287 |
22.875817 |
0.5 |
7 |
0.636364 |
2.5 |
0.710084 |
Paleoc-Mioc |
Barry (1988, fig. 7B) |
Carnivora(1) |
16 |
465 |
161 |
37 |
360 |
65.376344 |
0.5 |
5 |
0.35714 |
29.75 |
0.6161 |
Paleog-Neog |
Flynn et al. (1988, fig. 4.2) |
Carnivora(2) |
6 |
222 |
56 |
25 |
98 |
74.774775 |
13 |
2 |
0.5 |
55.5 |
0.57534 |
Paleog |
Flynn et al. (1988, fig. 4.6A) |
Carnivora(3) |
6 |
222 |
56 |
25 |
98 |
74.774775 |
19.75 |
1 |
0.25 |
68.25 |
0.57534 |
Paleog |
Flynn et al. (1988, fig. 4.6B) |
Carnivora-Barbourfelinae |
8 |
45 |
13 |
13 |
72 |
71.111111 |
1.5 |
6 |
1 |
1.5 |
1 |
Mioc |
Geraads & Güleç (1997, fig. 2) |
Carnivora-Caniformia |
5 |
159 |
26 |
16 |
36 |
83.647799 |
29.75 |
2 |
0.66667 |
17.5 |
0.5 |
Paleog-Neog |
Flynn et al. (1988, fig. 4.4) |
Carnivora-Chasmaporthetes |
5 |
28 |
5 |
5 |
20 |
82.142857 |
15.5 |
3 |
1 |
15.5 |
1 |
Mioc-Pleist |
Berta (1981, fig. 12) |
Carnivora-Felinae |
6 |
9 |
15 |
5 |
21 |
-66.666667 |
50.5 |
2 |
0.5 |
35.5 |
0.375 |
Pli-Rec |
Van Valkenburgh et al. (1990, fig. 15) |
Carnivora-Musteloidea |
4 |
71 |
42 |
30 |
67 |
40.84507 |
16 |
1 |
0.5 |
53 |
0.675676 |
Olig-Pli |
Wang (1997, fig. 9) |
Carnivora-Pinnipedia(1) |
5 |
71 |
26 |
13 |
38 |
63.380282 |
46.75 |
1 |
0.33333 |
63 |
0.48 |
Paleog-Neog |
Berta (1994, fig. 6) |
Carnivora-Pinnipedia(2) |
9 |
71 |
26 |
19 |
127 |
63.380282 |
46.75 |
6 |
0.85714 |
63 |
0.93518 |
Paleog-Neog |
Kohno (1994, fig. 5) |
Carnivora-Pinnipedia(3) |
5 |
87 |
32 |
13 |
32 |
63.218391 |
100 |
1 |
0.333333 |
69 |
0 |
Olig-Mioc |
Berta & Ray (1990, fig. 6) |
Carnivora-Procyoninae(1) |
10 |
92 |
40 |
23 |
95 |
56.521739 |
1.5 |
8 |
1 |
1 |
0.763889 |
Mioc-Rec |
Baskin (1982, fig. 14) |
Carnivora-Procyoninae(2) |
8 |
70 |
26 |
13 |
60 |
62.857143 |
6 |
4 |
0.666667 |
19.5 |
0.723404 |
Mioc-Rec |
Baskin (1989, fig. 3) |
Ungulata(1) |
12 |
243 |
59 |
36 |
114 |
75.720165 |
4 |
7 |
0.7 |
20 |
0.705128 |
Paleoc-Olig |
Thewissen & Domning (1992, fig. 1) |
Ungulata(2) |
11 |
367 |
61 |
36 |
107 |
83.378747 |
1 |
3 |
0.333333 |
48.5 |
0.647887 |
Paleoc-Olig |
Thewissen & Domning (1992, fig. 2) |
Ungulata(3) |
6 |
310 |
51 |
15 |
51 |
83.548387 |
100 |
0 |
0 |
100 |
0 |
Paleoc-Eoc |
Court (1990, fig. 4A) |
Ungulata(3) |
6 |
310 |
42 |
15 |
51 |
86.451613 |
100 |
1 |
0.25 |
100 |
0.25 |
Paleoc-Eoc |
Court (1990, fig. 4B) |
Ungulata(4) |
21 |
674 |
111 |
32 |
369 |
83.531157 |
0.25 |
15 |
0.78947 |
17 |
0.76558 |
Paleog |
Prothero et al. (1988, fig. 8.1) |
Toxodontia-Notohippidae |
18 |
170 |
91 |
37 |
493 |
46.470588 |
3.5 |
9 |
0.6 |
3 |
0.881579 |
Paleoc-Mioc |
Shockey (1997, fig. 7) |
Notoungulata-Pachyrukhinae |
8 |
80 |
35 |
30 |
135 |
56.25 |
2.5 |
3 |
0.5 |
85.5 |
0.952381 |
Olig-Pleist |
Cerdeño & Bond (1998, fig. 11A) |
Notoungulata-Pachyrukhinae |
8 |
80 |
35 |
30 |
135 |
56.25 |
2.5 |
3 |
0.5 |
85.5 |
0.952381 |
Olig-Pleist |
Cerdeño & Bond (1998, fig. 11B) |
Notoungulata-Pachyrukhinae |
8 |
80 |
60 |
30 |
135 |
25 |
10 |
3 |
0.5 |
90 |
0.714286 |
Olig-Pleist |
Cerdeño & Bond (1998, fig. 11C) |
Perissodactyla(1) |
18 |
421 |
35 |
21 |
35 |
91.686461 |
100 |
16 |
1 |
6.5 |
0 |
Paleog |
Hooker (1989, figs. 6.5, 6.6) |
Perissodactyla(2) |
16 |
397 |
39 |
21 |
45 |
90.176322 |
31.75 |
10 |
0.71429 |
99.25 |
0.25 |
Paleog |
Prothero & Schoch (1989, fig. 28.2) |
Perissodactyla(3) |
6 |
132 |
60 |
45 |
129 |
54.545455 |
10.5 |
3 |
0.75 |
12.5 |
0.821429 |
Eoc-Pli |
Hermanson & MacFadden (1996, fig. 5) |
Perisso.-Brontotheriidae |
12 |
68 |
37 |
21 |
154 |
45.588235 |
38.25 |
9 |
0.9 |
56.75 |
0.8797 |
Paleog |
Mader (1989, fig. 25.3) |
Perisso.-Chalicotheriidae |
11 |
103 |
63 |
37 |
166 |
38.834951 |
100 |
6 |
0.66667 |
2.5 |
0.79845 |
Paleog-Neog |
Coombs (1989, fig. 24.1) |
Perisso.-Chalicotheriinae |
8 |
59 |
24 |
18 |
52 |
59.322034 |
1 |
4 |
0.66667 |
5.5 |
0.82353 |
Neog |
Coombs (1989, fig. 24.3) |
Perisso.-Equidae(1) |
4 |
47 |
13 |
13 |
20 |
72.340426 |
15 |
2 |
1 |
15 |
1 |
Mioc |
Hermanson & MacFadden (1992, fig. 5) |
Perisso.-Equidae(2) |
19 |
197 |
77 |
51 |
614 |
60.913706 |
58.25 |
14 |
0.82353 |
65.75 |
0.95382 |
Paleog-Neog |
Evander (1989, fig. 8.1) |
Perisso.-Equinae(1) |
13 |
123 |
30 |
18 |
107 |
75.609756 |
7.75 |
10 |
0.90909 |
2.25 |
0.86517 |
Neog |
Matthew (1926; in Hulbert 1989, fig. 11.1A) |
Perisso.-Equinae(2) |
16 |
143 |
30 |
18 |
134 |
79.020979 |
2.5 |
13 |
0.92857 |
2.5 |
0.89655 |
Neog |
Stirton (1940; in Hulbert 1989, fig. 11.1B) |
Perisso.-Equinae(3) |
14 |
131 |
35 |
11 |
35 |
73.282443 |
100 |
11 |
0.91667 |
17 |
0 |
Neog |
Quinn (1955; in Hulbert 1989, fig. 11.1C) |
Perisso.-Equinae(4) |
24 |
216 |
94 |
18 |
196 |
56.481481 |
18 |
17 |
0.77273 |
20.5 |
0.57303 |
Neog |
Hulbert (1989, fig. 11.2) |
Perisso.-Equini(1) |
5 |
14 |
10 |
10 |
31 |
28.571429 |
8 |
2 |
0.666667 |
22.5 |
1 |
Mioc-Rec |
MacFadden & Azzaroli (1987, fig. 6) |
Perisso.-Equini(2) |
15 |
62 |
35 |
14 |
121 |
43.548387 |
3.5 |
10 |
0.769231 |
1.5 |
0.803738 |
Mioc-Pleist |
Prado & Alberdi (1996, fig. 7) |
Perisso.-Equini(3) |
8 |
40 |
13 |
8 |
23 |
67.5 |
14.5 |
6 |
1 |
3.5 |
0.666667 |
Mioc-Pleist |
MacFadden (1997, fig. 15) |
Perisso.-Hipparionini |
11 |
61 |
6 |
6 |
60 |
90.163934 |
12 |
9 |
1 |
12 |
1 |
Mioc |
Bernor et al. (1988, fig. 10) |
Perisso.-Hyracodontidae |
5 |
84 |
27 |
27 |
71 |
67.857143 |
1.75 |
3 |
1 |
1.75 |
1 |
Paleog |
Lucas & Sobus (1989, fig. 19.8) |
Perisso.-Rhinocerotoidea(1) |
4 |
94 |
35 |
27 |
35 |
62.765957 |
100 |
1 |
0.5 |
86 |
0 |
Eoc |
Holbrook & Lucas (1997, fig. 10) |
Perisso.-Rhinocerotoidea(2) |
5 |
148 |
24 |
8 |
24 |
83.783784 |
100 |
2 |
0.66667 |
78 |
0 |
Paleog |
Heissig (1989, fig. 21.3) |
Perisso.-Tapiridae |
10 |
119 |
45 |
33 |
221 |
62.184874 |
0.5 |
7 |
0.875 |
0.5 |
0.93617 |
Eoc-Mioc |
Albright (1998, fig. 12) |
Perisso.-Tapiroidea |
16 |
206 |
82 |
56 |
228 |
60.194175 |
1 |
10 |
0.71429 |
0.5 |
0.84884 |
Paleog-Neog |
Schoch (1989, fig. 15.1) |
Artiodactyla |
26 |
683 |
187 |
40 |
288 |
72.620791 |
9.25 |
16 |
0.66667 |
13 |
0.40726 |
Paleog-Neog |
Gentry & Hooker (1988, fig. 9.8) |
Artiodactyla-Camthumerycini |
5 |
48 |
7 |
7 |
21 |
85.416667 |
9.5 |
3 |
1 |
9.5 |
1 |
Mioc |
Bonis et al. (1997, fig. 5) |
Artiodactyla-Lagomerycidae |
6 |
209 |
466 |
466 |
818 |
-122.96651 |
9.5 |
4 |
1 |
9.5 |
1 |
Olig-Mioc |
Azanza & Ginsburg (1997, fig. 13) |
Artiodactyla-Protoceratidae |
6 |
45 |
34 |
34 |
98 |
24.444444 |
20.5 |
4 |
1 |
17.5 |
1 |
Eoc-Pli |
Webb (1981, fig. 5) |
Artiodactyla-Ruminantia(1) |
19 |
387 |
129 |
40 |
376 |
66.666667 |
0.2 |
10 |
0.588235 |
0.4 |
0.735119 |
Eoc-Mioc |
Janis & Scott (1988, fig. 10.1) |
Artiodactyla-Ruminantia(2) |
13 |
37 |
52.56 |
6.5 |
0.5 |
10.5 |
Paleog-Neog |
Gentry & Hooker (1988, fig. 9.10) |
|||||
Artiodactyla-Ruminantia(3) |
13 |
221 |
84 |
21 |
188 |
61.99095 |
8 |
5 |
0.454545 |
12.5 |
0.622754 |
Eoc-Olig |
Janis (1987, fig. 10) |
Cetacea(1) |
18 |
176 |
101 |
50 |
547 |
42.613636 |
8 |
9 |
0.5625 |
4 |
0.897384 |
Eoc-Rec |
Luo & Marsh (1996, fig. 2) |
Desmostylia |
8 |
62 |
26 |
13 |
38 |
58.064516 |
17 |
5 |
0.833333 |
15.5 |
0.48 |
Olig-Mioc |
Clark (1991, fig. 6) |
Sirenia(1) |
13 |
106 |
49 |
42 |
227 |
53.773585 |
0.5 |
9 |
0.818182 |
0.5 |
0.962162 |
Eoc-Rec |
Bajpaj & Domning (1997, fig. 6) |
Sirenia-Rytiodontinae |
6 |
53 |
12 |
6 |
24 |
77.358491 |
23.5 |
3 |
0.75 |
23.5 |
0.666667 |
Olig-Mioc |
Domning (1989, fig. 6) |
Proboscidea(1) |
18 |
178 |
98 |
48 |
504 |
44.94382 |
56.75 |
10 |
0.625 |
52.75 |
0.89035 |
Paleog-Neog |
Tassy & Shoshani (1988, figs. 11.5, 11.8) |
Proboscidea(2) |
5 |
93 |
32 |
16 |
32 |
65.591398 |
100 |
2 |
0.66667 |
67.75 |
0 |
Paleog-Neog |
Court (1995, fig. 8) |
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