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 |
Vertebrata(1) |
16 |
721 |
186 |
67 |
783 |
74.202497 |
0.5 |
7 |
0.5 |
0.5 |
0.833799 |
Ord-Dev |
Wilson & Caldwell (1998, fig. 9) |
Agnatha(1) |
8 |
1125 |
719 |
478 |
839 |
36.088889 |
84.25 |
2 |
0.333333 |
100 |
0.33241 |
Camb-Carb |
Halstead (1982, fig. 5) |
Agnatha(2) |
4 |
135 |
149 |
97 |
149 |
-10.37037 |
100 |
1 |
0.5 |
82.75 |
0 |
Camb-Carb |
Janvier (1981, fig. 11) |
Agnatha(3) |
6 |
1039 |
673 |
478 |
719 |
35.226179 |
73.25 |
2 |
0.5 |
88 |
0.19087 |
Camb-Carb |
Janvier (1981, fig. 13a) |
Agnatha(4) |
6 |
1039 |
673 |
478 |
719 |
35.226179 |
71.25 |
2 |
0.5 |
88 |
0.19087 |
Camb-Carb |
Janvier (1981, fig. 13b) |
Agnatha(5) |
6 |
115 |
42 |
21 |
84 |
63.478261 |
20 |
3 |
0.75 |
20 |
0.66667 |
Camb-Carb |
Janvier (1984, fig. 4) |
Agnatha(6) |
8 |
1125 |
645 |
478 |
839 |
42.666667 |
20.5 |
4 |
0.666667 |
3.5 |
0.5374 |
Camb-Carb |
Janvier (1984, fig. 8) |
Agnatha(7) |
7 |
1054 |
636 |
478 |
802 |
39.658444 |
24 |
3 |
0.6 |
10.5 |
0.51235 |
Camb-Carb |
Maisey (1986, fig. 3) |
Agnatha(8) |
7 |
1054 |
673 |
478 |
802 |
36.148008 |
31.25 |
3 |
0.6 |
12 |
0.39815 |
Camb-Carb |
Maisey (1986, fig. 3) |
Agnatha(9) |
11 |
1736 |
683 |
470 |
961 |
60.656682 |
5.25 |
4 |
0.444444 |
29.75 |
0.56619 |
Camb-Carb |
Novitskaya and Talimaa (1989) in Janvier and Blieck (1993, fig. 6) |
Agnatha(10) |
7 |
1056 |
640 |
470 |
754 |
39.393939 |
29 |
1 |
0.2 |
100 |
0.40141 |
Camb-Carb |
Moy-Thomas and Miles (1971) in Janvier and Blieck (1993, fig. 6) |
Agnatha(11) |
12 |
1195 |
794 |
470 |
995 |
33.556485 |
85 |
3 |
0.3 |
100 |
0.38286 |
Camb-Carb |
Halstead (1982) in Janvier and Blieck (1993, fig. 6) |
Agnatha(12) |
10 |
1180 |
752 |
478 |
863 |
36.271186 |
46.25 |
2 |
0.25 |
100 |
0.28831 |
Camb-Carb |
Gagnier (1989) in Janvier and Blieck (1993, fig. 6) |
Agnatha(13) |
10 |
1064 |
637 |
466 |
1239 |
40.131579 |
4 |
6 |
0.75 |
21.75 |
0.77878 |
Camb-Carb |
Forey & Janvier (1993, fig. 4) |
Agnatha: Galeaspida |
8 |
162 |
36 |
21 |
48 |
77.777778 |
5 |
5 |
0.833333 |
11 |
0.44444 |
Sil-Dev |
Janvier (1985, fig. 36) |
Agnatha: Heterostraci |
7 |
749 |
627 |
478 |
802 |
16.288385 |
21 |
4 |
0.8 |
4.5 |
0.54012 |
Sil-Dev |
Janvier (1981, fig. 16) |
Agnatha: Osteostraci |
7 |
162 |
90 |
21 |
90 |
44.444444 |
100 |
0 |
0 |
100 |
0 |
Sil-Dev |
Janvier (1985, fig. 37) |
Osteostraci: Cephalaspidomorphi |
6 |
209 |
466 |
466 |
818 |
-122.96651 |
1.5 |
4 |
1 |
1.5 |
1 |
Ord-Rec |
Janvier & Lund (1983, fig. 5) |
Osteostraci: Cephalaspidomorphi |
5 |
175 |
119 |
119 |
216 |
32 |
9.5 |
3 |
1 |
9.5 |
1 |
Janvier & Lund (1983, fig. 5) |
|
Osteostraci: Thyestidians(1) |
5 |
105 |
6 |
6 |
94.28571 |
100 |
2 |
0.666667 |
100 |
Sil-Dev |
Janvier (1985, fig. 40) |
||
Osteostraci: Thyestidians(2) |
11 |
214 |
147 |
21 |
189 |
31.308411 |
50.5 |
3 |
0.333333 |
50.5 |
0.25 |
Sil-Dev |
Forey (1987b, fig. 8) |
Osteostraci: Thyestidians(3) |
11 |
214 |
147 |
21 |
189 |
31.308411 |
52.5 |
3 |
0.333333 |
52.5 |
0.25 |
Sil-Dev |
Forey (1987b, fig. 9a) |
Osteostraci: Thyestidians(4) |
11 |
213 |
166 |
21 |
166 |
22.065728 |
100 |
2 |
0.222222 |
94.75 |
0 |
Sil-Dev |
Forey (1987b, fig. 9b) |
Osteostraci: Thyestidians(5) |
9 |
179 |
109 |
21 |
109 |
39.106145 |
100 |
1 |
0.142857 |
100 |
0 |
Sil-Dev |
Forey (1987b, fig. 10a) |
Osteostraci: Thyestidians(6) |
6 |
107 |
25 |
19 |
25 |
76.635514 |
100 |
3 |
0.75 |
58.75 |
0 |
Sil-Dev |
Forey (1987b, fig. 10b) |
Anaspida/ Petromyzontida |
5 |
417 |
149 |
97 |
149 |
64.268585 |
100 |
2 |
0.666667 |
100 |
0 |
Sil-Carb |
Arsenault & Janvier (1981, fig. 5) |
Gnathostomata(1) |
12 |
2979 |
732 |
376 |
1947 |
75.427996 |
0.25 |
5 |
0.5 |
1.25 |
0.77339 |
Sil-Dev |
Nelson (1969, fig. 25) |
Gnathostomata(2) |
6 |
2152 |
158 |
52 |
182 |
92.657993 |
48.75 |
1 |
0.25 |
70 |
0.18461 |
Dev |
Miles (1977, fig. 158a) |
Gnathostomata(3) |
6 |
2152 |
110 |
52 |
182 |
94.888476 |
16.75 |
2 |
0.5 |
24 |
0.55385 |
Dev |
Miles (1977, fig. 158b) |
Gnathostomata(4) |
8 |
2393 |
343 |
253 |
799 |
85.666527 |
1.5 |
1 |
0.166667 |
100 |
0.83516 |
Dev |
Wiley (1979, fig. 8) |
Gnathostomata(5) |
6 |
2139 |
363 |
216 |
417 |
83.029453 |
51.75 |
1 |
0.25 |
63 |
0.26866 |
Dev |
Wiley (1979, fig. 8) |
Gnathostomata(6) |
6 |
2152 |
104 |
52 |
182 |
95.167286 |
14.25 |
2 |
0.5 |
21.25 |
0.6 |
Dev |
Rosen et al. (1981, fig. 62) |
Gnathostomata(7) |
8 |
2205 |
125 |
52 |
263 |
94.331066 |
8 |
3 |
0.5 |
9 |
0.65403 |
Ord-Dev |
Lauder & Liem (1983, fig. 1) |
Gnathostomata(8) |
10 |
2783 |
609 |
337 |
1327 |
78.11714 |
1.25 |
2 |
0.25 |
100 |
0.72525 |
Ord-Dev |
Bemis (1984, fig. 2) |
Gnathostomata(9) |
10 |
2254 |
176 |
52 |
305 |
92.191659 |
14.5 |
3 |
0.375 |
29.5 |
0.50988 |
Ord-Dev |
Gardiner (1984b, fig. 147) |
Gnathostomata(10) |
10 |
1982 |
716 |
466 |
926 |
63.874874 |
23.25 |
4 |
0.5 |
22.75 |
0.45652 |
Ord-Dev |
Mallatt (1984, fig. 1) |
Gnathostomata(11) |
10 |
2335 |
152 |
52 |
318 |
93.490364 |
5 |
4 |
0.5 |
4.5 |
0.62406 |
Ord-Dev |
Schultze (1987, fig. 9) |
Gnathostomata(12) |
8 |
2367 |
162 |
98 |
529 |
93.155894 |
0.5 |
4 |
0.666667 |
0.75 |
0.85151 |
Ord-Dev |
McAllister (1987, fig. 80) |
Gnathostomata(13) |
6 |
2046 |
110 |
46 |
140 |
94.623656 |
70 |
2 |
0.5 |
58 |
0.31915 |
Ord-Dev |
Schultze (1988, fig. 1) |
Gnathostomata(14) |
23 |
4654 |
1316 |
358 |
2841 |
71.723249 |
21 |
12 |
0.571429 |
0.5 |
0.614176 |
Sil-Jur |
Schultze (1990, fig. 7) |
Gnathostomata(15) |
9 |
211 |
79 |
21 |
121 |
62.559242 |
22.5 |
2 |
0.285714 |
55.75 |
0.42 |
Dev |
Forey et al. (1991, fig. 5) |
Gnathostomata(16) |
9 |
211 |
79 |
21 |
121 |
62.559242 |
21.75 |
2 |
0.285714 |
53.5 |
0.42 |
Dev |
Forey et al. (1991, fig. 5, variant) |
Gnathostomata(17) |
8 |
2460 |
114 |
46 |
213 |
95.365854 |
38.5 |
2 |
0.4 |
39 |
0.59281 |
Dev |
Schultze (1994, fig. 2b) |
Gnathostomata(18) |
8 |
2460 |
114 |
46 |
213 |
95.365854 |
39 |
2 |
0.4 |
39 |
0.59281 |
Dev |
Schultze (1994, fig. 3c) |
Placodermi(1) |
8 |
211 |
55 |
31 |
67 |
73.933649 |
41.75 |
4 |
0.666667 |
68.5 |
0.33333 |
Dev |
Miles and Young (1977, fig. 3) |
Placodermi(2) |
8 |
239 |
67 |
31 |
67 |
71.966527 |
100 |
3 |
0.5 |
99 |
0 |
Dev |
Miles and Young (1977, fig. 5) |
Placodermi(3) |
6 |
116 |
42 |
18 |
42 |
63.793103 |
100 |
1 |
0.25 |
100 |
0 |
Dev |
Young (1979, fig. 27a) |
Placodermi(4) |
5 |
168 |
24 |
12 |
24 |
85.714286 |
100 |
2 |
0.666667 |
100 |
0 |
Dev |
Young (1979, fig. 27b) |
Placodermi(5) |
8 |
222 |
89 |
31 |
89 |
59.90991 |
100 |
1 |
0.166667 |
100 |
0 |
Dev |
Young (1979, fig. 27c) |
Placodermi(6) |
10 |
244 |
97 |
31 |
97 |
60.245902 |
100 |
2 |
0.25 |
100 |
0 |
Dev |
Gardiner (1984a, fig. 8) |
Placodermi(7) |
9 |
245 |
79 |
31 |
79 |
67.755102 |
100 |
2 |
0.285714 |
100 |
0 |
Dev |
Goujet (1984, fig. 1) |
Placodermi(8) |
9 |
264 |
48 |
18 |
60 |
81.818182 |
60.75 |
6 |
0.857143 |
73 |
0.28571 |
Dev |
Goujet (1984, fig 12) |
Placodermi(9) |
5 |
126 |
65 |
31 |
65 |
48.412698 |
100 |
1 |
0.333333 |
92.75 |
0 |
Dev |
Long (1984, fig. 26a) |
Placodermi(10) |
5 |
126 |
41 |
31 |
65 |
67.460317 |
8.25 |
2 |
0.666667 |
29.75 |
0.70588 |
Dev |
Long (1984, fig. 26f) |
Placodermi(11) |
5 |
126 |
43 |
31 |
65 |
65.873016 |
17.75 |
2 |
0.666667 |
31.25 |
0.64706 |
Dev |
Long (1984, fig. 27) |
Placodermi(12) |
7 |
201 |
54 |
18 |
54 |
73.134328 |
100 |
2 |
0.4 |
100 |
0 |
Dev |
Forey and Gardiner (1986, fig 4a) |
Placodermi(13) |
7 |
201 |
54 |
18 |
54 |
73.134328 |
100 |
2 |
0.4 |
100 |
0 |
Dev |
Forey and Gardiner (1986, fig 4b) |
Placodermi(14) |
7 |
201 |
54 |
18 |
54 |
73.134328 |
100 |
1 |
0.2 |
100 |
0 |
Dev |
Forey and Gardiner (1986, fig 4c) |
Placodermi(15) |
6 |
197 |
36 |
12 |
36 |
81.725888 |
100 |
1 |
0.25 |
100 |
0 |
Dev |
Forey and Gardiner (1986, fig 4e) |
Placodermi(16) |
10 |
244 |
107 |
31 |
107 |
56.147541 |
100 |
3 |
0.375 |
85.75 |
0 |
Dev |
Forey and Gardiner (1986, fig. 5) |
Placodermi(17) |
8 |
239 |
67 |
31 |
67 |
71.966527 |
100 |
3 |
0.5 |
97.75 |
0 |
Dev |
Young (1986, fig. 18a) |
Placodermi(18) |
8 |
232 |
79 |
31 |
79 |
65.948276 |
100 |
1 |
0.166667 |
100 |
0 |
Dev |
Young (1986, fig. 18b) |
Placodermi(19) |
8 |
239 |
67 |
31 |
67 |
71.966527 |
100 |
3 |
0.5 |
97.75 |
0 |
Dev |
Young (1986, fig. 18c) |
Placodermi(20) |
11 |
316 |
70 |
31 |
165 |
77.848101 |
0.75 |
6 |
0.666667 |
3.5 |
0.70896 |
Dev |
Carr (1995, fig. 4) |
Placodermi: Arthrodira(1) |
9 |
144 |
41 |
31 |
173 |
71.527778 |
0.25 |
6 |
0.857143 |
0.25 |
0.92958 |
Dev |
Miles and Dennis (1979, fig. 15) |
Placodermi: Arthrodira(2) |
11 |
207 |
41 |
31 |
197 |
80.193237 |
1.75 |
8 |
0.888889 |
83.75 |
0.93976 |
Dev |
Dennis and Miles (1980, fig. 22) |
Placodermi: Arthrodira(3) |
8 |
112 |
39 |
29 |
92 |
65.178571 |
0.25 |
3 |
0.5 |
30.5 |
0.84127 |
Dev |
Carr (1991, fig. 19a) |
Placodermi: Arthrodira(4) |
10 |
122 |
47 |
29 |
127 |
61.47541 |
1.75 |
3 |
0.428571 |
83.75 |
0.81633 |
Dev |
Carr (1991, fig. 19c) |
Placodermi: Arthrodira(5) |
16 |
313 |
59 |
31 |
340 |
81.15016 |
100 |
11 |
0.785714 |
100 |
0.90938 |
Dev |
Gardiner and Miles (1994, fig. 19) |
Placodermi: Arthrodira(6) |
12 |
250 |
53 |
31 |
228 |
78.8 |
100 |
7 |
0.7 |
100 |
0.88832 |
Dev |
Gardiner and Miles (1994, fig. 30) |
Placodermi: Euarthrodira |
7 |
168 |
28 |
22 |
76 |
83.333333 |
5 |
4 |
0.8 |
7.25 |
0.88889 |
Dev |
Young (1979, fig. 18) |
Placodermi: Antiarcha(1) |
5 |
82 |
27 |
27 |
99 |
67.073171 |
5.75 |
3 |
1 |
5.75 |
1 |
Dev |
Young (1984, fig. 2) |
Placodermi: Antiarcha(2) |
6 |
98 |
32 |
27 |
76 |
67.346939 |
7.5 |
3 |
0.75 |
78.5 |
0.897959 |
Dev |
Zhu, M. & Janvier, P. (1996, fig. 12) |
Acanthodii(1) |
8 |
466 |
125 |
46 |
189 |
73.175966 |
30.25 |
4 |
0.666667 |
13.5 |
0.44755 |
Sil-Dev |
Long (1986, fig. 8b) |
Acanthodii(2) |
8 |
376 |
143 |
52 |
262 |
61.968085 |
16.5 |
3 |
0.5 |
31.5 |
0.56667 |
Sil-Dev |
Long (1986, fig. 9) |
Chondrichthyes(1) |
8 |
952 |
510 |
232 |
784 |
46.428571 |
8 |
1 |
0.166667 |
100 |
0.49638 |
Dev-Jur |
Maisey (1984a, fig. 1) |
Chondrichthyes(2) |
4 |
821 |
65 |
37 |
65 |
92.082826 |
100 |
0 |
0 |
100 |
0 |
Dev-Carb |
Maisey (1986, fig. 6) |
Chondr.: Elasmobranchii(1) |
7 |
1024 |
328 |
142 |
328 |
67.96875 |
100 |
0 |
0 |
100 |
0 |
Dev-Jur |
Schaeffer and Williams (1977, fig. 2) |
Chondr.: Elasmobranchii(2) |
6 |
987 |
200 |
178 |
342 |
79.736575 |
13.75 |
1 |
0.25 |
100 |
0.86585 |
Dev-Jur |
Schaeffer (1981, fig. 26b) |
Chondr.: Elasmobranchii(3) |
6 |
581 |
214 |
209 |
732 |
63.166954 |
8 |
3 |
0.75 |
3.5 |
0.99044 |
Dev-Jur |
Maisey (1984b, fig. 2) |
Chondr.: Elasmobranchii(4) |
4 |
744 |
179 |
174 |
445 |
75.94086 |
25 |
1 |
0.5 |
48.75 |
0.98155 |
Dev-Jur |
Maisey (1986, fig. 7) |
Chondr.: Carcharinoidea |
4 |
477 |
111 |
106 |
187 |
76.72956 |
15.5 |
1 |
0.5 |
49.75 |
0.93827 |
Dev-Jur |
Maisey (1984b, fig. 3) |
Chondr.: Petalodontiformes |
4 |
225 |
27 |
27 |
54 |
88 |
21 |
2 |
1 |
21 |
1 |
Carb |
Lund (1989, fig. 18) |
Osteichthyes(1) |
6 |
1248 |
168 |
168 |
292 |
86.538462 |
0.25 |
4 |
1 |
0.25 |
1 |
Dev-Carb |
Lund & Lund (1985, fig. 77a) |
Osteichthyes(2) |
6 |
1266 |
172 |
168 |
302 |
86.413902 |
2.75 |
3 |
0.75 |
7.5 |
0.97015 |
Dev-Carb |
Lund & Lund (1985, fig. 77b) |
Osteichthyes: Actinopterygii(1) |
12 |
1476 |
340 |
123 |
817 |
76.96477 |
0.5 |
6 |
0.6 |
19.5 |
0.68732 |
Tri-Cret |
Patterson (1976, fig. 19) |
Osteichthyes: Actinopterygii(2) |
6 |
809 |
105 |
105 |
389 |
87.021014 |
0.25 |
4 |
1 |
0.25 |
1 |
Tri-Cret |
Patterson and Rosen (1977, fig. 38) |
Osteichthyes: Actinopterygii(3) |
6 |
609 |
513 |
315 |
775 |
15.763547 |
19.5 |
2 |
0.5 |
19.5 |
0.56956 |
Dev-Carb |
Patterson (1982, fig. 3B) |
Osteichthyes: Actinopterygii(4) |
18 |
1720 |
531 |
177 |
2288 |
69.127907 |
0.25 |
9 |
0.5625 |
1.5 |
0.83231 |
Tri-Cret |
Rosen (1982, fig. 6) |
Osteichthyes: Actinopterygii(5) |
16 |
1392 |
963 |
333 |
2769 |
30.818966 |
1.75 |
8 |
0.571429 |
4.5 |
0.74138 |
Dev-Jur |
Lauder and Liem (1983, fig. 6) |
Osteichthyes: Actinopterygii(6) |
16 |
1514 |
1151 |
315 |
1950 |
23.976222 |
1.75 |
4 |
0.285714 |
20.75 |
0.48869 |
Dev-Jur |
Gardiner (1984b, fig. 146) |
Osteichthyes: Actinopterygii(7) |
16 |
1514 |
1151 |
315 |
1950 |
23.976222 |
3.5 |
4 |
0.285714 |
22.5 |
0.48869 |
Dev-Jur |
Gardiner (1984b, fig. 146) |
Osteichthyes: Actinopterygii(8) |
11 |
1029 |
252 |
101 |
338 |
75.510204 |
19.25 |
4 |
0.444444 |
48.25 |
0.36287 |
Tri-Jur |
Olsen (1984, fig. 19) |
Osteichthyes: Actinopterygii(9) |
5 |
882 |
303 |
181 |
303 |
65.646259 |
100 |
0 |
0 |
100 |
0 |
Carb-Jur |
Maisey (1986, fig. 10) |
Osteichthyes: Actinopterygii(10) |
16 |
952 |
593 |
315 |
1801 |
37.710084 |
8.5 |
9 |
0.642857 |
0.5 |
0.81292 |
Carb-Jur |
Gardiner and Schaeffer (1989, fig. 10) |
Osteichthyes: Actinopterygii(11) |
13 |
839 |
735 |
315 |
1961 |
12.395709 |
0.5 |
8 |
0.727273 |
0.25 |
0.74484 |
Carb-Jur |
Gardiner and Schaeffer (1989, fig. 11) |
Osteichthyes: Actinopterygii(12) |
26 |
1466 |
929 |
315 |
2952 |
36.630286 |
0.25 |
14 |
0.583333 |
0.25 |
0.76716 |
Carb-Jur |
Gardiner and Schaeffer (1989, fig. 12) |
Osteichthyes: Actinopterygii(13) |
11 |
803 |
271 |
183 |
1188 |
66.251557 |
0.75 |
1 |
0.111111 |
83.25 |
0.91244 |
Perm-Jur |
Rieppel (1992, fig. 12) |
Actinopterygii: Neopterygii(1) |
5 |
729 |
213 |
112 |
249 |
70.781893 |
30.5 |
2 |
0.666667 |
16.75 |
0.26277 |
Tri-Jur |
Wiley and Schultze (1984, fig. 2) |
Actinopterygii: Neopterygii(2) |
8 |
1221 |
311 |
219 |
1088 |
74.529075 |
0.5 |
4 |
0.666667 |
3 |
0.894131 |
Carb-Cret |
Olsen & McCune (1991, fig. 16) |
Actinopterygii: Neopterygii(3) |
8 |
1221 |
311 |
219 |
1088 |
74.529075 |
1 |
4 |
0.666667 |
2 |
0.894131 |
Carb-Cret |
Olsen & McCune (1991, fig. 17A) |
Actinopterygii: Chondrostei |
11 |
852 |
479 |
202 |
668 |
43.779343 |
17.75 |
3 |
0.333333 |
98.5 |
0.40558 |
Carb-Jur |
Schaeffer (1973, fig. 14) |
Actinopt.: Semionotiformes(1) |
7 |
780 |
169 |
101 |
267 |
78.333333 |
9 |
5 |
1 |
1.25 |
0.59036 |
Carb-Jur |
Olsen and McCune (1991, fig 17A) |
Actinopt.: Semionotiformes(2) |
7 |
780 |
181 |
101 |
267 |
76.794872 |
19 |
4 |
0.8 |
4.25 |
0.51807 |
Carb-Jur |
Olsen and McCune (1991, fig. 17B) |
Actinopterygii: Amiidae |
9 |
236 |
189 |
74 |
211 |
19.915254 |
41 |
3 |
0.428571 |
97 |
0.160584 |
Jur-Cret |
Chalifa & Tchernov (1982, fig. 14) |
Actinopterygii: Teleostei(1) |
4 |
590 |
25 |
25 |
38 |
95.762712 |
6.5 |
2 |
1 |
6.5 |
1 |
Jur-Cret |
Patterson and Rosen (1977, fig. 22) |
Actinopterygii: Teleostei(2) |
13 |
1248 |
388 |
177 |
1324 |
68.910256 |
0.75 |
7 |
0.636364 |
0.75 |
0.81604 |
Jur-Cret |
Patterson and Rosen (1977, fig. 54) |
Actinopterygii: Teleostei(3) |
28 |
2066 |
1166 |
145 |
1801 |
43.562439 |
0.25 |
15 |
0.535714 |
0.25 |
0.38345 |
Tri-Cret |
Rosen (1982, fig. 5) |
Teleostei: Acanthopterygii |
11 |
695 |
155 |
33 |
218 |
77.697842 |
14 |
3 |
0.333333 |
46.75 |
0.34054 |
Cret-Eoc |
Lauder and Liem (1983, fig. 50) |
Teleostei: Atherinomorpha |
4 |
211 |
47 |
47 |
121 |
77.725118 |
25.25 |
2 |
1 |
18.25 |
1 |
Cret-Eoc |
Lauder and Liem (1983, fig. 47) |
Teleostei: Beloniformes |
5 |
168 |
67 |
40 |
82 |
60.119048 |
61.5 |
1 |
0.333333 |
100 |
0.35714 |
Eoc-Olig |
Boughton et al. (1991, fig. 1) |
Teleostei: Caproidae |
4 |
263 |
125 |
47 |
125 |
52.471483 |
100 |
0 |
0 |
100 |
0 |
Eoc-Olig |
Zehren (1987, fig. 1) |
Teleostei: Clupeomorpha |
4 |
373 |
111 |
111 |
211 |
70.241287 |
8.5 |
2 |
1 |
8.5 |
1 |
Cret-Eoc |
Grande (1985, fig. 1a) |
Teleostei: Cyprinodontiformes |
4 |
121 |
94 |
50 |
119 |
22.31405 |
50.25 |
1 |
0.5 |
50.25 |
0.36232 |
Paleoc-Eoc |
Parenti (1981, fig. 9) |
Teleostei: Elopomorpha |
7 |
454 |
124 |
62 |
198 |
72.687225 |
15 |
4 |
0.8 |
9 |
0.54412 |
Cret-Eoc |
Lauder and Liem (1983, fig. 24) |
Teleostei: Euteleostei(1) |
7 |
629 |
214 |
82 |
295 |
65.977742 |
27.75 |
2 |
0.4 |
43 |
0.38028 |
Cret-Paleoc |
Lauder and Liem (1983, fig. 28) |
Teleostei: Euteleostei(2) |
12 |
925 |
503 |
136 |
827 |
45.621622 |
24 |
4 |
0.4 |
63.75 |
0.46889 |
Cret-Paleoc |
Schaeffer and Lauder (1986, fig. 1) |
Teleostei: Osmeridae |
8 |
16 |
248 |
60 |
408 |
-1450 |
52 |
2 |
0.333333 |
61 |
0.45977 |
Paleoc-Rec |
Wilson & Williams (1991, fig. 12) |
Teleostei: Ostariophysi(1) |
5 |
320 |
221 |
136 |
410 |
30.9375 |
23.5 |
1 |
0.333333 |
59 |
0.68978 |
Cret-Paleoc |
Fink and Fink (1981, fig. 1) |
Teleostei: Ostariophysi(2) |
5 |
427 |
261 |
136 |
303 |
38.875878 |
39.5 |
1 |
0.333333 |
64 |
0.2515 |
Cret-Paleoc |
Lauder and Liem (1983, fig. 30) |
Teleostei: Osteoglossidae(1) |
11 |
102 |
193 |
97 |
510 |
-89.215686 |
15 |
7 |
0.777778 |
7 |
0.767554 |
Cret-Rec |
Li & Wilson (1996, fig. 7) |
Teleostei: Osteoglossidae(2) |
18 |
188 |
440 |
97 |
982 |
-134.04255 |
3.5 |
10 |
0.625 |
5 |
0.612429 |
Cret-Rec |
Li et al. (1997, fig. 9) |
Teleostei: Paracanthopterygii |
11 |
714 |
570 |
154 |
1269 |
20.168067 |
13 |
3 |
0.333333 |
8.5 |
0.626906 |
Cret-Rec |
Grande (1988, fig. 7) |
Teleostei: Pimelodidae |
6 |
42 |
38 |
16 |
54 |
9.52381 |
37.5 |
2 |
0.5 |
90.5 |
0.421053 |
Mioc-Rec |
Lundberg et al. (1988, fig. 4) |
Teleostei: Pleuronectiformes |
7 |
330 |
56 |
33 |
62 |
83.030303 |
29 |
3 |
0.6 |
19.5 |
0.2069 |
Paleoc-Eoc |
Lauder and Liem (1983, fig. 63) |
Teleostei: Salmoniformes(1) |
5 |
277 |
115 |
73 |
138 |
58.483755 |
41.25 |
1 |
0.333333 |
60 |
0.35385 |
Paleoc-Eoc |
Rosen (1974, fig. 38) |
Teleostei: Salmoniformes(2) |
5 |
277 |
73 |
73 |
138 |
73.646209 |
2.25 |
3 |
1 |
2.25 |
1 |
Paleoc-Eoc |
Rosen (1974, fig. 39) |
Teleostei: Tetraodontiformes |
4 |
112 |
88 |
40 |
88 |
21.428571 |
100 |
0 |
0 |
100 |
0 |
Eoc-Olig |
Lauder and Liem (1983, fig. 52) |
Sarcopterygii(1) |
4 |
1303 |
70 |
31 |
70 |
94.627782 |
100 |
0 |
0 |
100 |
0 |
Dev |
Rosen et al. (1981, fig. 4C) |
Sarcopterygii(2) |
4 |
1303 |
70 |
31 |
70 |
94.627782 |
100 |
0 |
0 |
100 |
0 |
Dev |
Rosen et al. (1981, fig. 4D) |
Sarcopterygii(3) |
7 |
1431 |
87 |
56 |
222 |
93.920335 |
15 |
2 |
0.4 |
39.5 |
0.81325 |
Dev |
Long (1985, fig. 14a) |
Sarcopterygii(4) |
6 |
1328 |
40 |
19 |
50 |
96.987952 |
36 |
1 |
0.25 |
100 |
0.32258 |
Dev |
Maisey (1986, fig. 14) |
Sarcopterygii(5) |
7 |
1651 |
112 |
46 |
187 |
93.216233 |
16 |
1 |
0.2 |
65 |
0.53192 |
Dev |
Forey (1987a, fig. 2) |
Sarcopterygii(6) |
6 |
1357 |
73 |
29 |
73 |
94.620486 |
100 |
0 |
0 |
100 |
0 |
Dev |
Ahlberg (1989, fig. 16a) |
Sarcopterygii(7) |
6 |
1357 |
73 |
29 |
73 |
94.620486 |
100 |
0 |
0 |
100 |
0 |
Dev |
Ahlberg (1989, fig. 16b) |
Sarcopterygii(8) |
9 |
1787 |
85 |
46 |
239 |
95.243425 |
1.75 |
4 |
0.571429 |
23 |
0.79793 |
Dev |
Gee (1990, fig. 1) |
Sarcopterygii(9) |
10 |
1414 |
176 |
98 |
247 |
87.553041 |
17 |
3 |
0.375 |
71 |
0.47651 |
Dev |
Ahlberg (1991, fig. 14) |
Sarcopterygii(10) |
8 |
1406 |
88 |
31 |
149 |
93.74111 |
23.25 |
3 |
0.5 |
12 |
0.51695 |
Dev |
Ahlberg (1991, fig. 15a) |
Sarcopterygii(11) |
7 |
1337 |
82 |
31 |
116 |
93.866866 |
39.75 |
2 |
0.4 |
55.5 |
0.4 |
Dev |
Ahlberg (1991, fig. 15b) |
Sarcopterygii(12) |
9 |
1667 |
115 |
46 |
244 |
93.10138 |
15.75 |
3 |
0.428571 |
26 |
0.65151 |
Dev |
Chang (1991, fig. 35) |
Sarcopterygii(13) |
9 |
1688 |
139 |
46 |
244 |
91.765403 |
16.75 |
3 |
0.428571 |
41.75 |
0.5303 |
Dev |
Forey et al. (1991, fig. 5) |
Sarcopterygii(14) |
9 |
1688 |
139 |
46 |
244 |
91.765403 |
14.5 |
2 |
0.285714 |
56.5 |
0.5303 |
Dev |
Forey et al. (1991, fig. 5, variant 1) |
Sarcopterygii(15) |
9 |
1688 |
112 |
46 |
244 |
93.364929 |
9.25 |
4 |
0.571429 |
33.5 |
0.66667 |
Dev |
Forey et al. (1991, fig. 5, variant 2) |
Sarcopterygii(16) |
6 |
1248 |
168 |
168 |
292 |
86.538462 |
1.5 |
4 |
1 |
1.5 |
1 |
Dev-Carb |
Lund & Lund (1985, fig. 77a) |
Sarcopterygii(17) |
6 |
1266 |
172 |
168 |
302 |
86.413902 |
1.5 |
3 |
0.75 |
4.75 |
0.97015 |
Dev-Carb |
Lund & Lund (1985, fig. 77b) |
Sarcopterygii: Dipnoi(1) |
10 |
829 |
406 |
325 |
797 |
51.025332 |
0.25 |
5 |
0.625 |
3.75 |
0.82839 |
Dev-Carb |
Miles (1977, fig. 157) |
Sarcopterygii: Dipnoi(2) |
7 |
468 |
167 |
152 |
177 |
64.316239 |
31.75 |
4 |
0.8 |
55.75 |
0.4 |
Dev-Carb |
Bemis (1984, fig. 6) |
Sarcopterygii: Dipnoi(3) |
9 |
594 |
433 |
343 |
875 |
27.104377 |
31.75 |
4 |
0.571429 |
96.5 |
0.83083 |
Dev-Carb |
Bemis (1984, fig. 8) |
Sarcopterygii: Dipnoi(4) |
7 |
375 |
192 |
164 |
278 |
48.8 |
1.25 |
4 |
0.8 |
2 |
0.75439 |
Dev-Carb |
Maisey (1986, fig. 12) |
Sarcopterygii: Dipnoi(5) |
29 |
695 |
148 |
86 |
626 |
78.705036 |
31.75 |
23 |
0.851852 |
96.5 |
0.88518 |
Dev-Carb |
Campbell and Barwick (1990, fig. 1) |
Sarcopterygii: Dipnoi(6) |
5 |
494 |
24 |
12 |
24 |
95.1417 |
100 |
2 |
0.666667 |
100 |
0 |
Dev |
Chang & Smith (1992, fig. 11) |
Sarcopterygii: Dipnoi(7) |
8 |
568 |
34 |
22 |
58 |
94.014085 |
25.5 |
4 |
0.8 |
39 |
0.666667 |
Dev |
Yu (1998, fig. 8) |
Sarcopterygii: Rhipidistia |
6 |
570 |
61 |
47 |
130 |
89.298246 |
3 |
3 |
0.75 |
5.5 |
0.83132 |
Dev |
Vorobyeva and Schultze (1991, fig. 39) |
Sarcopt.: Tristichopteridae |
7 |
49 |
14 |
14 |
54 |
71.428571 |
0.5 |
5 |
1 |
0.5 |
1 |
Dev |
Ahlberg & Johanson (1997, fig. 16) |
Sarcopterygii: tetrapods(1) |
7 |
149 |
113 |
113 |
187 |
24.161074 |
0.75 |
5 |
1 |
0.75 |
1 |
Dev |
Lebedev & Coates (1995, fig. 19b) |
Sarcopterygii: tetrapods(2) |
7 |
406 |
32 |
32 |
82 |
92.118227 |
0.25 |
5 |
1 |
0.75 |
1 |
Dev |
Ahlberg (1995, fig. 4) |
Sarcopterygii: tetrapods(3) |
11 |
905 |
37 |
37 |
275 |
95.911602 |
0.25 |
9 |
1 |
0.75 |
1 |
Dev-Carb |
Ahlberg & Milner (1994, fig. 3) |
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