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 |
Amniota(1) |
6 |
1233 |
177 |
85 |
189 |
85.644769 |
73 |
2 |
0.5 |
87.5 |
0.11539 |
Tri-Jur |
Gaffney (1980, in Benton 1991, fig. 6) |
Amniota(2) |
6 |
1233 |
189 |
85 |
189 |
84.671533 |
100 |
2 |
0.5 |
88.5 |
0 |
Tri-Jur |
Gardiner (1982, fig. 2) |
Amniota(3) |
12 |
1570 |
333 |
168 |
801 |
78.789809 |
100 |
7 |
0.7 |
0.75 |
0.73934 |
Perm-Cret |
Gardiner (1982, fig. 3) |
Amniota(4) |
5 |
750 |
185 |
156 |
316 |
75.333333 |
2.75 |
2 |
0.666667 |
29.25 |
0.81875 |
Carb-Jur |
Gardiner (1982, fig. 4) |
Amniota(5) |
6 |
1233 |
189 |
85 |
189 |
84.671533 |
100 |
1 |
0.25 |
93.25 |
0 |
Tri-Jur |
Løvtrup (1985, in Benton 1991, fig. 8) |
Amniota(6) |
29 |
1978 |
381 |
101 |
1726 |
80.738119 |
100 |
18 |
0.666667 |
93.25 |
0.82769 |
Carb-Tri |
Gauthier et al. (1988a, fig. 3) |
Amniota(7) |
10 |
986 |
173 |
88 |
362 |
82.454361 |
1.5 |
6 |
0.75 |
3 |
0.68978 |
Carb-Tri |
Gauthier et al. (1988b, fig. 4.4) |
Amniota(8) |
12 |
1284 |
248 |
88 |
500 |
80.685358 |
10 |
7 |
0.7 |
8.5 |
0.61165 |
Carb-Tri |
Benton (1991, fig. 14) |
Amniota(9) |
6 |
1101 |
115 |
107 |
320 |
89.55495 |
3 |
3 |
0.75 |
10.5 |
0.962441 |
Carb-Jur |
Gaffney & Meeker (1983, fig. 2) |
Amniota(10) |
8 |
706 |
107 |
56 |
315 |
84.844193 |
3 |
3 |
0.5 |
16.5 |
0.803089 |
Carb-Perm |
deBraga & Reisz (1996, fig. 3) |
Anapsida-Captorhinidae |
8 |
122 |
55 |
55 |
268 |
54.918033 |
0.5 |
6 |
1 |
0.5 |
1 |
Carb-Perm |
Dodick and Modesto (1995, fig. 15) |
Anapsida-Pareiasauria(1) |
6 |
31 |
11 |
6 |
15 |
64.516129 |
23 |
2 |
0.5 |
42 |
0.444444 |
Perm |
Lee et al. (1997, fig. 9) |
Testudines(1) |
6 |
633 |
231 |
169 |
511 |
63.507109 |
16.25 |
2 |
0.5 |
19.5 |
0.81871 |
Tri-Paleog |
Gaffney (1975, fig. 26) |
Testudines(2) |
18 |
1211 |
652 |
169 |
2323 |
46.160198 |
0.75 |
8 |
0.5 |
6.75 |
0.77577 |
Tri-Paleog |
Gaffney (1984, fig. 1) |
Testudines(3) |
6 |
609 |
193 |
169 |
496 |
68.308703 |
5 |
2 |
0.5 |
42.25 |
0.92661 |
Tri-Paleog |
Moody (1984, fig. 1) |
Testudines(4) |
13 |
944 |
353 |
169 |
1343 |
62.605932 |
5 |
6 |
0.545455 |
0.75 |
0.84327 |
Tri-Paleog |
Gaffney & Meylan (1988, fig. 5.1) |
Testudines(A) |
11 |
846 |
348 |
82 |
518 |
58.865248 |
13.5 |
4 |
0.444444 |
30.5 |
0.389908 |
Cret-Rec |
Shaffer et al. (1997, fig. 1) |
Testudines(B) |
14 |
1033 |
445 |
183 |
1911 |
56.921588 |
2 |
7 |
0.583333 |
14 |
0.84838 |
Tri-Rec |
Shaffer et al. (1997, fig. 2) |
Testudines(C-E) |
13 |
1014 |
276 |
82 |
598 |
72.781065 |
1 |
6 |
0.545455 |
44.5 |
0.624031 |
Cret-Rec |
Shaffer et al. (1997, fig. 3a) |
Testudines(C-E) |
13 |
1014 |
278 |
82 |
598 |
72.583826 |
1 |
5 |
0.454545 |
56.5 |
0.620155 |
Cret-Rec |
Shaffer et al. (1997, fig. 3b) |
Testudines(C-E) |
13 |
1014 |
210 |
82 |
598 |
79.289941 |
1 |
7 |
0.636364 |
32 |
0.751938 |
Cret-Rec |
Shaffer et al. (1997, fig. 3c) |
Testudines(F,G) |
14 |
1033 |
445 |
183 |
1911 |
56.921588 |
2 |
7 |
0.583333 |
14 |
0.84838 |
Tri-Rec |
Shaffer et al. (1997, fig. 3d) |
Testudines(F,G) |
14 |
1033 |
311 |
183 |
1911 |
69.893514 |
2 |
8 |
0.666667 |
5 |
0.925926 |
Tri-Rec |
Shaffer et al. (1997, fig. 4a) |
Testudines(H, J) |
16 |
1206 |
591 |
183 |
2132 |
50.995025 |
0.5 |
7 |
0.5 |
12.5 |
0.790662 |
Tri-Rec |
Shaffer et al. (1997, fig. 4b) |
Testudines(H, J) |
16 |
1206 |
470 |
183 |
2132 |
61.028192 |
0.5 |
8 |
0.571429 |
1 |
0.852745 |
Tri-Rec |
Shaffer et al. (1997, fig. 4c) |
Testudines(I) |
15 |
1132 |
569 |
183 |
1981 |
49.734982 |
1.5 |
7 |
0.538462 |
8.5 |
0.785317 |
Tri-Rec |
Shaffer et al. (1997, fig. 4d) |
Testudines-Baenidae |
4 |
36 |
92 |
83 |
92 |
-155.55556 |
100 |
1 |
0.5 |
83 |
0 |
Cret-Rec |
Brinkman & Nicholls (1991, fig. 10) |
Testudines-Bataguridae |
26 |
197 |
631 |
56 |
1209 |
-220.30457 |
38.25 |
10 |
0.416667 |
56.75 |
0.5013 |
Paleog-Neog |
Gaffney & Meylan (1988, fig. 5.12) |
Testudines-Chelonioidea |
21 |
368 |
416 |
102 |
958 |
-13.043478 |
4.75 |
8 |
0.421053 |
40.25 |
0.63318 |
Cret-Neog |
Gaffney & Meylan (1988, fig. 5.9) |
Testudines-Cryptodira |
7 |
368 |
220 |
123 |
628 |
40.217391 |
5 |
3 |
0.6 |
12.5 |
0.80792 |
Jur-Cret |
Brinkman & Nicholls (1993, fig. 4) |
Testudines-Emydidae |
10 |
88 |
217 |
56 |
472 |
-146.59091 |
66.25 |
4 |
0.5 |
55.75 |
0.61298 |
Paleog-Neog |
Gaffney & Meylan (1988, fig. 5.11) |
Testudines-Kinosternidae |
9 |
35 |
115 |
56 |
298 |
-228.57143 |
1.5 |
5 |
0.714286 |
4 |
0.756198 |
Eoc-Rec |
Hutchison (1991, fig. 10) |
Testudines-Pleurodira(1) |
15 |
578 |
336 |
112 |
649 |
41.868512 |
2 |
5 |
0.384615 |
72.5 |
0.582868 |
Cret-Rec |
Meylan (1996, fig. 11) |
Testudines-Pleurodira(2) |
18 |
457 |
534 |
225 |
3098 |
-16.849015 |
46.75 |
7 |
0.4375 |
25 |
0.89245 |
Tri-Neog |
Gaffney & Meylan (1988, fig. 5.7) |
Testudines-Protostegidae |
7 |
111 |
45 |
29 |
141 |
59.459459 |
7 |
3 |
0.6 |
12.5 |
0.857143 |
Cret |
Hooks (1998, fig. 1) |
Testudines-Selmacryptodira |
21 |
383 |
751 |
155 |
1559 |
-96.083551 |
0.25 |
10 |
0.526316 |
51.25 |
0.5755 |
Jur-Neog |
Gaffney & Meylan (1988, fig. 5.8) |
Testudines-Testudinidae |
20 |
294 |
282 |
56 |
771 |
4.081633 |
0.75 |
11 |
0.611111 |
2.5 |
0.68392 |
Paleog-Neog |
Gaffney & Meylan (1988, fig. 5.13) |
Testudines-Trionychoidea |
27 |
458 |
857 |
112 |
2125 |
-87.117904 |
2 |
15 |
0.6 |
3.75 |
0.62991 |
Cret-Neog |
Gaffney & Meylan (1988, fig. 5.10) |
Diapsida(1) |
11 |
1102 |
149 |
93 |
624 |
86.479129 |
2 |
4 |
0.444444 |
9.25 |
0.89454 |
Carb-Tri |
Gauthier et al. (1988a, fig. 3) |
Diapsida(2) |
10 |
562 |
201 |
139 |
512 |
64.234875 |
0.5 |
5 |
0.625 |
5.5 |
0.83378 |
Carb-Jur |
Laurin (1991, fig. 11) |
Diapsida(3) |
28 |
1243 |
321 |
133 |
565 |
74.175382 |
19 |
13 |
0.5 |
49 |
0.564815 |
Carb-Cret |
Rieppel (1998, fig. 7B) |
Diapsida-basal(1) |
4 |
94 |
74 |
61 |
90 |
21.276596 |
36 |
1 |
0.5 |
52 |
0.551724 |
Carb-Perm |
Reisz et al. (1984, fig. 5) |
Diapsida-basal(2) |
8 |
124 |
74 |
61 |
241 |
40.322581 |
0.5 |
5 |
0.833333 |
1 |
0.927778 |
Carb-Perm |
deBraga & Reisz (1995, fig. 6) |
Lepidosauromorpha(1) |
12 |
628 |
192 |
187 |
475 |
69.426752 |
4 |
10 |
1 |
84.25 |
0.98264 |
Perm-Paleog |
Benton (1985, fig. 10) |
Lepidosauromorpha(2) |
27 |
392 |
624 |
252 |
1521 |
-59.183673 |
4 |
14 |
0.56 |
4 |
0.70686 |
Perm-Neog |
Evans (1988, fig. 6.2) |
Lepidosauromorpha(3) |
7 |
452 |
96 |
86 |
126 |
78.761062 |
4.25 |
3 |
0.6 |
11.25 |
0.75 |
Perm-Jur |
Gauthier et al. (1988c, fig. 13) |
Lepidosauromorpha(4) |
13 |
497 |
299 |
97 |
399 |
39.839034 |
3.75 |
4 |
0.363636 |
41 |
0.33113 |
Perm-Jur |
Gauthier et al. (1988c, appendix fig. 1) |
Lepidosauromorpha(5) |
14 |
513 |
269 |
100 |
461 |
47.563353 |
0.5 |
7 |
0.583333 |
4.25 |
0.53186 |
Perm-Jur |
Clark & Hernandez (1994, appendix fig.) |
Younginiformes(1) |
6 |
29 |
NAN(000) |
5 |
5 |
82.758621 |
100 |
4 |
1 |
70.5 |
NAN(000) |
Perm-Tri |
Smith & Evans (1996, fig. 9) |
Lepidosauria(1) |
21 |
1481 |
784 |
237 |
3496 |
47.062795 |
4 |
7 |
0.368421 |
84.25 |
0.83216 |
Tri-Neog |
Schwenk (1988, fig. 14) |
Lepidosauria(2) |
23 |
1305 |
1157 |
237 |
3264 |
11.340996 |
1 |
8 |
0.380952 |
19 |
0.696069 |
Tri-Rec |
Evans & Chure (1998, fig. 4) |
Sphenodontia(1) |
5 |
278 |
203 |
82 |
203 |
26.978417 |
100 |
0 |
0 |
100 |
0 |
Tri-Jur |
Gauthier et al. (1988c, fig. 12) |
Sphenodontia(2) |
10 |
305 |
350 |
85 |
350 |
-14.754098 |
100 |
2 |
0.25 |
94.5 |
0 |
Tri-Jur |
Sues et al. (1994, fig. 8) |
Sphenodontia(3) |
14 |
130 |
434 |
237 |
871 |
-233.84615 |
20 |
2 |
0.166667 |
100 |
0.689274 |
Tri-Rec |
Reynoso (1996, fig. 9) |
Sphenodontia(4) |
9 |
329 |
382 |
125 |
587 |
-16.109422 |
21 |
1 |
0.142857 |
75 |
0.443723 |
Tri-Cret |
Reynoso (1997, fig. 7) |
Sphenodontia(5) |
20 |
229 |
700 |
237 |
1192 |
-205.67686 |
0.5 |
5 |
0.277778 |
97.5 |
0.515183 |
Tri-Rec |
Reynoso & Clark (1998, fig. 4) |
Squamata(1) |
18 |
1157 |
479 |
112 |
859 |
58.599827 |
17.25 |
6 |
0.375 |
92 |
0.5087 |
Cret-Paleog |
Camp (1923; in Estes et al. 1988, fig. 7) |
Squamata(2) |
18 |
1055 |
559 |
112 |
961 |
47.014218 |
79 |
7 |
0.4375 |
77.5 |
0.4735 |
Cret-Paleog |
Underwood (1957; in Presch 1988, fig. 3) |
Squamata(3) |
21 |
1057 |
687 |
112 |
1295 |
35.00473 |
49 |
9 |
0.473684 |
73.75 |
0.51395 |
Cret-Paleog |
Underwood (1971; in Presch 1988, fig. 4) |
Squamata(4) |
24 |
1225 |
568 |
112 |
1463 |
53.632653 |
35.25 |
7 |
0.466667 |
71.5 |
0.66247 |
Cret-Paleog |
Northcutt (1978; in Presch 1988, fig. 2) |
Squamata(5) |
25 |
1225 |
519 |
112 |
1575 |
57.632653 |
16.5 |
7 |
0.466667 |
81.25 |
0.7218 |
Cret-Paleog |
Estes et al. (1988, fig. 5A) |
Squamata(6) |
16 |
958 |
470 |
112 |
834 |
50.939457 |
43.5 |
6 |
0.428571 |
74.75 |
0.50416 |
Cret-Paleog |
Estes et al. (1988, fig. 5B) |
Squamata(7) |
16 |
958 |
450 |
112 |
834 |
53.02714 |
40.25 |
5 |
0.357143 |
95.75 |
0.53186 |
Cret-Paleog |
Estes et al. (1988, fig. 5C) |
Squamata(8) |
25 |
1225 |
665 |
112 |
1575 |
45.714286 |
17.75 |
7 |
0.411765 |
63.25 |
0.62201 |
Cret-Paleog |
Estes et al. (1988, fig. 6) |
Squamata(9) |
16 |
1032 |
396 |
112 |
760 |
61.627907 |
47.75 |
6 |
0.428571 |
79.25 |
0.56173 |
Cret-Paleog |
Presch (1988, fig. 5) |
Squamata(10) |
16 |
1032 |
376 |
112 |
760 |
63.565891 |
32 |
6 |
0.428571 |
74.25 |
0.59259 |
Cret-Paleog |
Rieppel (1988, fig. 7.1) |
Squamata(11) |
25 |
1225 |
680 |
112 |
1575 |
44.489796 |
31 |
6 |
0.352941 |
91.75 |
0.61176 |
Cret-Paleog |
Schwenk (1988, fig. 12) |
Squamata(12) |
6 |
392 |
133 |
101 |
373 |
66.071429 |
18 |
1 |
0.25 |
68 |
0.882353 |
Jur-Eoc |
Zaher (1998, fig. 1) |
Squamata-Anguimorpha(1) |
6 |
407 |
332 |
92 |
360 |
18.427518 |
61 |
1 |
0.25 |
66 |
0.104478 |
Jur-Cret |
Evans (1994, fig. 16) |
Squamata-Anguimorpha(2) |
10 |
428 |
474 |
157 |
777 |
-10.747664 |
15 |
4 |
0.5 |
9.5 |
0.48871 |
Jur-Rec |
Carroll & deBraga (1992, fig. 14) |
Squamata-Anolinae |
8 |
25 |
117 |
23 |
159 |
-368 |
100 |
1 |
0.166667 |
100 |
0.30882 |
Neog |
Etheridge & de Queiroz (1988, fig. 9) |
Squamata-Gekkota |
18 |
2 |
10 |
2 |
34 |
-400 |
59.75 |
12 |
0.75 |
59.75 |
0.75 |
Cret-Neog |
Grismer (1988, fig. 4) |
Squamata-Gerrhonotinae |
8 |
34 |
81 |
23 |
146 |
-138.23529 |
33 |
1 |
0.166667 |
66.5 |
0.528455 |
Mioc-Rec |
Good (1988, fig. 1) |
Squamata-Glyptosaurinae |
12 |
109 |
99 |
48 |
378 |
9.174312 |
1.5 |
6 |
0.6 |
5.5 |
0.845455 |
Cret-Olig |
Sullivan (1986, fig. 7) |
Squamata-Iguaninae |
8 |
29 |
48 |
23 |
155 |
-65.517241 |
17.25 |
3 |
0.5 |
25.5 |
0.81061 |
Neog |
Etheridge & de Queiroz (1988, fig. 13) |
Squamata-Mosasauridae |
9 |
129 |
50 |
16 |
69 |
61.24031 |
23.5 |
4 |
0.571429 |
13 |
0.358491 |
Cret |
Soliar (1988, fig. 8) |
Squamata-Plioplatecarpus |
5 |
49 |
13 |
13 |
52 |
73.469388 |
17.5 |
3 |
1 |
17.5 |
1 |
Cret |
Holmes (1996, fig. 18) |
Squamata-Sceloporinae |
9 |
57 |
122 |
23 |
150 |
-114.03509 |
89.75 |
2 |
0.285714 |
84.25 |
0.22047 |
Neog |
Etheridge & de Queiroz (1988, fig. 16) |
Squamata-Teiidae |
14 |
134 |
282 |
83 |
676 |
-110.44776 |
0.25 |
5 |
0.416667 |
100 |
0.66442 |
Cret-Neog |
Denton & O’Neill (1995, fig. 14) |
Squamata-Tropidurinae |
13 |
23 |
46 |
23 |
276 |
-100 |
17 |
10 |
0.909091 |
17 |
0.90909 |
Neog |
Etheridge & de Queiroz (1988, fig. 12) |
Squamata-Varanidae |
6 |
87 |
166 |
83 |
166 |
-90.804598 |
100 |
2 |
0.5 |
100 |
0 |
Cret-Neog |
Clos (1995, fig. 5) |
Squamata-Varanoidea |
8 |
72 |
125 |
97 |
213 |
-73.611111 |
1.5 |
2 |
0.333333 |
64 |
0.75862 |
Cret-Neog |
Caldwell et al. (1995, fig. 4A) |
Archosauromorpha(1) |
12 |
829 |
143 |
80 |
658 |
82.750302 |
4 |
5 |
0.5 |
7.25 |
0.891 |
Carb-Tri |
Benton (1985, fig. 4) |
Archosauromorpha(2) |
15 |
626 |
209 |
45 |
261 |
66.613419 |
49 |
3 |
0.230769 |
33.75 |
0.24074 |
Perm-Tri |
Evans (1988, fig. 6.1) |
Archosauromorpha(3) |
8 |
604 |
45 |
20 |
84 |
92.549669 |
10.25 |
4 |
0.666667 |
2.25 |
0.60938 |
Perm-Tri |
Clark et al. (1993, fig. 1) |
Archosauromorpha(4) |
5 |
598 |
30 |
20 |
40 |
94.983278 |
32.5 |
1 |
0.333333 |
100 |
0.5 |
Perm-Tri |
Chatterjee (1986, fig. 9) |
Prolacertiformes(1) |
17 |
409 |
233 |
32 |
233 |
43.031785 |
100 |
0 |
0 |
100 |
0 |
Perm-Tri |
Jalil (1997, fig. 21) |
Prolacertiformes(2) |
8 |
75 |
40 |
20 |
102 |
46.666667 |
3 |
4 |
0.666667 |
13.5 |
0.756098 |
Perm-Tri |
Chatterjee (1986, fig. 10) |
Prolacertiformes(3) |
17 |
138 |
252 |
33 |
351 |
-82.608696 |
1.5 |
3 |
0.2 |
19 |
0.311321 |
Perm-Tri |
Benton & Allen (1997, fig. 16A) |
Prolacertiformes(4) |
12 |
95 |
205 |
33 |
238 |
-115.78947 |
74 |
3 |
0.3 |
49.5 |
0.160976 |
Perm-Tri |
Benton & Allen (1997, fig. 16B) |
Prolacertiformes(5) |
13 |
393 |
104 |
32 |
193 |
73.536896 |
5.5 |
6 |
0.545455 |
3 |
0.552795 |
Perm-Tri |
Jalil (1997, fig. 22) |
Prolacertiformes(6) |
16 |
125 |
169 |
33 |
318 |
-35.2 |
19.5 |
6 |
0.428571 |
29 |
0.522807 |
Perm-Tri |
Benton & Allen (1997, fig. 17) |
Rhynchosauria(1) |
6 |
39 |
10 |
10 |
28 |
74.358974 |
1.5 |
4 |
1 |
1.5 |
1 |
Tri |
Dilkes, D. W. (1995, fig. 8) |
Archosauria(1) |
12 |
795 |
64 |
27 |
141 |
91.949686 |
4.5 |
4 |
0.4 |
24 |
0.67544 |
Perm-Tri |
Gauthier (1986, fig. 7) |
Archosauria(2) |
15 |
621 |
66 |
42 |
227 |
89.371981 |
4.5 |
9 |
0.692308 |
24 |
0.87027 |
Perm-Tri |
Benton & Clark (1988, fig. 8.1) |
Archosauria(3) |
20 |
693 |
84 |
40 |
242 |
87.878788 |
0.25 |
8 |
0.444444 |
5.25 |
0.78218 |
Perm-Tri |
Parrish (1993, fig. 1) |
Archosauria(4) |
11 |
740 |
59 |
40 |
151 |
92.027027 |
0.25 |
7 |
0.777778 |
5.25 |
0.82883 |
Perm-Tri |
Sereno (1991, fig. 26) |
Archosauria(5) |
5 |
650 |
23 |
18 |
26 |
96.461538 |
26.25 |
2 |
0.666667 |
25.5 |
0.375 |
Tri |
Sereno & Arcucci (1993, fig. 6) |
Archosauria(6) |
5 |
281 |
174 |
164 |
194 |
38.078292 |
58.5 |
1 |
0.333333 |
100 |
0.666667 |
Tri-Cret |
Paul (1984, fig. 5, version 1) |
Archosauria(6) |
5 |
281 |
174 |
164 |
194 |
38.078292 |
62.5 |
2 |
0.666667 |
49 |
0.666667 |
Tri-Cret |
Paul (1984, fig. 5, version 2) |
Archosauria(7) |
12 |
293 |
467 |
160 |
1072 |
-59.385666 |
0.5 |
4 |
0.4 |
7.5 |
0.663377 |
Tri-Cret |
Buscalioni et al. (1996, fig. 3) |
Archosauria(8) |
10 |
321 |
10 |
10 |
30 |
96.884735 |
62.5 |
8 |
1 |
6 |
1 |
Tri |
Gower & Sennikov (1996, fig. 7) |
Archosauria(9) |
7 |
35 |
41 |
37 |
41 |
-17.142857 |
100 |
5 |
1 |
58 |
0 |
Tri-Jur |
Gower & Sennikov (1997, fig. 11) |
Archosauria(10) |
6 |
31 |
41 |
37 |
41 |
-32.258065 |
100 |
3 |
0.75 |
96 |
0 |
Tri-Jur |
Gower & Sennikov (1997, fig. 12) |
Archosauria(11) |
8 |
89 |
37 |
37 |
57 |
58.426966 |
1 |
5 |
0.833333 |
60.5 |
1 |
Tri-Jur |
Gower & Sennikov (1997, fig. 13) |
Archosauria-Erythrosuchidae |
7 |
30 |
NAN(000) |
0 |
0 |
100 |
100 |
5 |
1 |
100 |
NAN(000) |
Tri |
Parrish (1992, fig. 1) |
Archos.-Rauisuchiformes |
10 |
162 |
43 |
18 |
85 |
73.45679 |
2.5 |
5 |
0.625 |
5.75 |
0.62687 |
Tri |
Parrish (1994, fig. 7) |
Crocodylomorpha(1) |
22 |
801 |
743 |
198 |
1892 |
7.240949 |
4.75 |
7 |
0.35 |
1.25 |
0.67828 |
Tri-Paleog |
Benton & Clark (1988, figs 8.6, 8.7B, 8.9B, 8.10A, 8.11B) |
Crocodylomorpha(2) |
22 |
801 |
709 |
198 |
1892 |
11.485643 |
0.5 |
8 |
0.4 |
2 |
0.69835 |
Tri-Paleog |
Benton & Clark (1988, figs 8.6, 8.7A, 8.9A, 8.10C) |
Crocodylomorpha(3) |
11 |
353 |
97 |
37 |
216 |
72.521246 |
1 |
3 |
0.333333 |
49 |
0.6648 |
Tri-Jur |
Wu & Chatterjee (1993, fig. 21 rev.) |
Crocodylomorpha(4) |
10 |
366 |
364 |
160 |
726 |
0.546448 |
2.75 |
4 |
0.5 |
14 |
0.63958 |
Tri-Cret |
Wu et al. (1994, fig. 10A) |
Crocodylomorpha(5) |
6 |
281 |
17 |
15 |
43 |
93.950178 |
8 |
2 |
0.5 |
100 |
0.928571 |
Tri-Jur |
Sereno & Wild (1992, fig. 12A) |
Crocodylomorpha(6) |
7 |
295 |
58 |
15 |
58 |
80.338983 |
100 |
3 |
0.6 |
65.5 |
0 |
Tri-Jur |
Sereno & Wild (1992, fig. 12B) |
Crocodylomorpha(7) |
31 |
1058 |
966 |
173 |
2114 |
8.695652 |
0.5 |
10 |
0.344828 |
70 |
0.591448 |
Tri-Rec |
Wu et al. (1997, fig. 6) |
Crocodylomorpha(7) |
31 |
1058 |
1240 |
173 |
2114 |
-17.202268 |
0.5 |
7 |
0.241379 |
89.5 |
0.450283 |
Tri-Rec |
Wu et al. (1997, fig. 7) |
Crocodylomorpha(7) |
31 |
1058 |
996 |
173 |
2114 |
5.860113 |
0.5 |
10 |
0.344828 |
68.5 |
0.575992 |
Tri-Rec |
Wu et al. (1997, fig. 8) |
Crocodylomorpha(8) |
16 |
459 |
588 |
127 |
1316 |
-28.104575 |
7 |
4 |
0.285714 |
62.5 |
0.612279 |
Jur-Rec |
Wu & Sues (1996, fig. 9) |
Mesosuchia(1) |
8 |
140 |
186 |
95 |
406 |
-32.857143 |
3 |
4 |
0.666667 |
4 |
0.707395 |
Jur-Paleoc |
Gomani (1997, fig. 6A) |
Mesosuchia(1) |
8 |
140 |
142 |
95 |
406 |
-1.428571 |
3 |
5 |
0.833333 |
1.5 |
0.848875 |
Jur-Paleoc |
Gomani (1997, fig. 6B) |
Mesosuchia(2) |
10 |
194 |
208 |
95 |
468 |
-7.216495 |
3 |
4 |
0.5 |
11.5 |
0.697051 |
Jur-Paleoc |
Gomani (1997, fig. 6C) |
Mesosuchia(3) |
8 |
239 |
191 |
75 |
299 |
20.083682 |
17 |
2 |
0.333333 |
100 |
0.482143 |
Cret-Eoc |
Gasparini et al. (1991, fig. 7) |
Mesosuchia-Atoposauridae |
4 |
28 |
9 |
9 |
18 |
67.857143 |
30.5 |
1 |
0.5 |
100 |
1 |
Jur-Cret |
Buscalioni & Sanz (1990, fig. 10A) |
Mesosuchia-Atoposauridae |
4 |
28 |
18 |
9 |
18 |
35.714286 |
100 |
0 |
0 |
100 |
0 |
Jur-Cret |
Buscalioni & Sanz (1990, fig. 10B) |
Neosuchia |
7 |
330 |
212 |
92 |
298 |
35.757576 |
16 |
2 |
0.4 |
33.5 |
0.41748 |
Jur-Cret |
Wu & Brinkman (1993, fig. 10) |
Eusuchia(1) |
16 |
157 |
593 |
132 |
1276 |
-277.70701 |
21 |
7 |
0.5 |
16 |
0.597028 |
Cret-Rec |
Wu et al. (1996, fig. 4) |
Eusuchia(2) |
61 |
444 |
825 |
196 |
9674 |
-85.810811 |
21 |
41 |
0.694915 |
16 |
0.933636 |
Jur-Rec |
Brochu (1997, fig. 8) |
Eusuchia(3) |
62 |
492 |
843 |
196 |
9787 |
-71.341463 |
21 |
41 |
0.683333 |
16 |
0.932541 |
Jur-Rec |
Brochu (1997, fig. 9) |
Eusuchia-Alligatoridae |
8 |
87 |
275 |
157 |
663 |
-216.09195 |
8.5 |
3 |
0.5 |
36 |
0.766798 |
Jur-Rec |
Williamson (1996, fig. 10) |
Ornithodira(1) |
10 |
792 |
22 |
17 |
47 |
97.222222 |
5 |
7 |
0.875 |
5.5 |
0.833333 |
Tri |
Novas (1996, fig. 10) |
Dinosauriformes(1) |
5 |
431 |
5 |
5 |
15 |
98.839907 |
12 |
3 |
1 |
12 |
1 |
Tri |
Novas (1992, fig. 6) |
Dinosauria |
31 |
1709 |
825 |
150 |
2184 |
51.726156 |
0.5 |
20 |
0.689655 |
5.5 |
0.66814 |
Tri-Cret |
Benton (1990, fig. 1.5) |
Theropoda(1) |
9 |
468 |
323 |
154 |
881 |
30.982906 |
3.75 |
3 |
0.428571 |
3.25 |
0.76754 |
Tri-Cret |
Gauthier (1986, fig. 9) |
Theropoda(2) |
7 |
505 |
279 |
150 |
683 |
44.752475 |
6 |
2 |
0.4 |
16.5 |
0.75797 |
Tri-Cret |
Benton (1990, fig. 1.5) |
Theropoda(3) |
15 |
585 |
456 |
154 |
1565 |
22.051282 |
0.25 |
8 |
0.615385 |
0.75 |
0.78597 |
Tri-Cret |
Holtz (1994, fig. 9A) |
Theropoda(4) |
15 |
585 |
340 |
154 |
1565 |
41.880342 |
0.25 |
7 |
0.538462 |
1.5 |
0.86818 |
Tri-Cret |
Holtz (1994, fig. 9B) |
Theropoda(5) |
7 |
254 |
165 |
74 |
377 |
35.03937 |
24 |
2 |
0.4 |
47.5 |
0.69967 |
Jur-Cret |
Sues (1997, fig. 11) |
Theropoda-Coelurosauria(1) |
8 |
334 |
252 |
69 |
314 |
24.550898 |
50 |
1 |
0.166667 |
73.5 |
0.253061 |
Jur-Cret |
Novas (1997, fig. 32A) |
Theropoda-Coelurosauria(1) |
8 |
334 |
218 |
69 |
314 |
34.730539 |
41 |
2 |
0.333333 |
65.5 |
0.391837 |
Jur-Cret |
Novas (1997, fig. 32B) |
Theropoda-Carnosauria |
7 |
127 |
124 |
87 |
227 |
2.362205 |
2 |
4 |
0.8 |
2 |
0.73571 |
Jur-Cret |
Molnar et al. (1990, fig. 6.13) |
Theropoda-Ceratosauria |
7 |
89 |
234 |
82 |
234 |
-162.92135 |
100 |
0 |
0 |
100 |
0 |
Tri-Jur |
Rowe & Gauthier (1990, fig. 5.1) |
Thero.-Ornithomimosauria |
8 |
120 |
81 |
81 |
458 |
32.5 |
0.75 |
5 |
0.833333 |
0.75 |
1 |
Cret |
Barsbold & Osmólska (1990, fig. 8.10) |
Aves(1) |
23 |
1069 |
436 |
129 |
2147 |
59.214219 |
9.25 |
9 |
0.428571 |
1.5 |
0.84787 |
Jur-Neog |
Cracraft (1988, fig. 9.1) |
Aves(2) |
6 |
200 |
94 |
48 |
186 |
53 |
20 |
2 |
0.5 |
21.75 |
0.66667 |
Cret |
Chiappe & Calvo (1994, fig. 9) |
Aves(3) |
6 |
402 |
147 |
147 |
561 |
63.432836 |
0.5 |
4 |
1 |
0.5 |
1 |
Tri-Cret |
Sanz & Buscalioni (1992, fig. 9) |
Aves(4) |
8 |
469 |
167 |
147 |
791 |
64.392324 |
0.5 |
5 |
0.833333 |
0.5 |
0.968944 |
Tri-Cret |
Sanz & Buscalioni (1992, fig. 10A) |
Aves(4) |
8 |
469 |
147 |
147 |
791 |
68.656716 |
0.5 |
6 |
1 |
0.5 |
1 |
Tri-Cret |
Sanz & Buscalioni (1992, fig. 10B) |
Enantiornithes |
6 |
46 |
51 |
14 |
61 |
-10.869565 |
58.25 |
1 |
0.25 |
65.75 |
0.21277 |
Cret |
Varicchio & Chiappe (1995, fig. 2) |
Anseriformes-Anatidae |
6 |
10 |
50 |
10 |
50 |
-400 |
100 |
0 |
0 |
100 |
0 |
Mioc-Rec |
Livezey & Martin (1988, fig. 10) |
Ciconiiformes-Vulturidae |
9 |
68 |
54 |
50 |
382 |
20.588235 |
0.5 |
4 |
0.571429 |
14.5 |
0.987952 |
Eoc-Rec |
Emslie (1988, fig. 10) |
Sauropodomorpha |
8 |
472 |
132 |
82 |
364 |
72.033898 |
1 |
4 |
0.666667 |
1.25 |
0.8227 |
Tri-Jur |
Benton (1990, fig. 1.5) |
Prosauropoda |
12 |
138 |
99 |
41 |
219 |
28.26087 |
10.75 |
7 |
0.7 |
8 |
0.67416 |
Tri-Jur |
Galton (1990, fig. 15.9) |
Sauropoda |
13 |
220 |
139 |
55 |
611 |
36.818182 |
4.25 |
7 |
0.636364 |
9 |
0.84892 |
Jur |
McIntosh (1990, fig. 16.20) |
Ornithischia(1) |
18 |
750 |
374 |
136 |
1402 |
50.133333 |
16 |
10 |
0.625 |
0.25 |
0.81201 |
Jur-Cret |
Sereno (1984, fig. 1) |
Ornithischia(2) |
11 |
634 |
240 |
113 |
486 |
62.14511 |
1.5 |
8 |
0.888889 |
0.25 |
0.65952 |
Jur-Cret |
Cooper (1995; in Benton 1990, fig. 1.6b) |
Ornithischia(3) |
6 |
489 |
131 |
78 |
250 |
73.210634 |
8.75 |
2 |
0.5 |
24.25 |
0.69186 |
Jur-Cret |
Maryanska & Osmólska (1985; in Benton 1990, fig. 1.6a) |
Ornithischia(4) |
11 |
646 |
240 |
113 |
486 |
62.848297 |
1.25 |
7 |
0.777778 |
0.5 |
0.65952 |
Jur-Cret |
Sereno (1986; in Benton 1990, fig. 1.6d) |
Ornithischia(5) |
13 |
685 |
247 |
120 |
646 |
63.941606 |
1.25 |
9 |
0.818182 |
0.5 |
0.75855 |
Jur-Cret |
Benton (1990, fig. 1.5) |
Ornithischia(6) |
6 |
237 |
90 |
86 |
198 |
62.025316 |
1.5 |
4 |
1 |
5.5 |
0.964286 |
Jur-Cret |
Forster (1990, fig. 24) |
Ornithopoda(1) |
12 |
260 |
416 |
136 |
925 |
-60 |
14 |
4 |
0.4 |
68.5 |
0.64512 |
Jur-Cret |
Norman (1984, fig. 7) |
Ornithopoda(2) |
7 |
281 |
100 |
78 |
231 |
64.412811 |
14 |
3 |
0.6 |
17.5 |
0.85621 |
Jur-Cret |
Norman (1990, fig. 25.36) |
Ornithopoda(3) |
6 |
269 |
167 |
136 |
376 |
37.918216 |
3 |
2 |
0.5 |
28 |
0.870833 |
Jur-Cret |
Coria & Salgado (1996, fig. 13) |
Ornithopoda(4) |
11 |
206 |
332 |
136 |
936 |
-61.165049 |
6 |
5 |
0.555556 |
16 |
0.755 |
Jur-Cret |
Winkler et al. (1997, fig. 19A) |
Ornithopoda(4) |
11 |
206 |
332 |
136 |
936 |
-61.165049 |
3 |
5 |
0.555556 |
6 |
0.755 |
Jur-Cret |
Winkler et al. (1997, fig. 19B) |
Ornithopoda-Hadrosauridae(1) |
14 |
173 |
102 |
67 |
749 |
41.040462 |
0.5 |
10 |
0.833333 |
1.5 |
0.94868 |
Cret |
Weishampel et al. (1993, fig. 7) |
Ornithopoda-Hadrosauridae(2) |
7 |
108 |
25 |
25 |
128 |
76.851852 |
2 |
4 |
0.8 |
4.5 |
1 |
Cret |
Head (1998, fig. 16) |
Ornithopoda-Hadrosauridae(3) |
17 |
215 |
106 |
23 |
239 |
50.697674 |
9.5 |
8 |
0.533333 |
55 |
0.61574 |
Cret |
Weishampel & Horner (1990, fig. 26.12) |
Ornithopoda-Hadrosauridae(4) |
10 |
88 |
48 |
16 |
90 |
45.454545 |
61 |
5 |
0.625 |
60 |
0.56757 |
Cret |
Weishampel & Horner (1990, fig. 26.12) |
Ceratopsia(1) |
10 |
142 |
55 |
41 |
299 |
61.267606 |
1.5 |
7 |
0.875 |
1 |
0.945736 |
Cret |
Chinnery & Weishampel (1998, fig. 10) |
Ceratopsia(2) |
18 |
225 |
77 |
50 |
751 |
65.777778 |
1 |
13 |
0.8125 |
2.75 |
0.96148 |
Cret |
Dodson & Currie (1990, fig. 29.9) |
Ceratopsia-Centrosaurinae |
6 |
72 |
9 |
9 |
36 |
87.5 |
7 |
3 |
0.75 |
41 |
1 |
Cret |
Sampson (1995, fig. 9) |
Ceratopsia-Triceratops |
6 |
54 |
NAN(000) |
0 |
0 |
100 |
100 |
4 |
1 |
100 |
NAN(000) |
Cret |
Forster (1996, fig. 5) |
Pachycephalosauria |
10 |
107 |
107 |
58 |
459 |
0 |
1 |
7 |
0.875 |
3 |
0.8778 |
Cret |
Maryanska (1990, fig. 27.5) |
Thyreophora(1) |
6 |
278 |
111 |
49 |
155 |
60.071942 |
24 |
1 |
0.25 |
72 |
0.415094 |
Jur-Cret |
Sereno & Dong (1992, fig. 14) |
Ankylosauria(1) |
9 |
175 |
135 |
123 |
832 |
22.857143 |
0.5 |
6 |
0.857143 |
1 |
0.983075 |
Jur-Cret |
Lee (1996, fig. 14A) |
Ankylosauria(1) |
9 |
175 |
135 |
123 |
832 |
22.857143 |
0.5 |
6 |
0.857143 |
1 |
0.983075 |
Jur-Cret |
Lee (1996, fig. 14B) |
Ankylosauria |
14 |
254 |
203 |
67 |
594 |
20.07874 |
1.5 |
8 |
0.666667 |
0.75 |
0.74193 |
Cret |
Coombs & Maryanska (1990, fig. 22.14) |
Sauropterygia(1) |
5 |
394 |
109 |
86 |
220 |
72.335025 |
20.5 |
2 |
0.666667 |
27 |
0.828358 |
Tri-Jur |
Brown & Cruickshank (1994, fig. 7) |
Sauropterygia(2) |
8 |
98 |
17 |
5 |
17 |
82.653061 |
100 |
4 |
0.666667 |
78.5 |
0 |
Tri |
Rieppel & Werneburg (1998, fig. 5) |
Sauropt.-Pachypleurosauria |
9 |
30 |
1 |
1 |
4 |
96.666667 |
1 |
7 |
1 |
4 |
1 |
Tri |
Rieppel (1998, fig. 7A) |
Synapsida(1) |
21 |
630 |
153 |
101 |
1174 |
75.714286 |
32 |
15 |
0.789474 |
74.25 |
0.95154 |
Carb-Tri |
Kemp (1982, fig. 115) |
Synapsida(2) |
16 |
610 |
144 |
101 |
897 |
76.393443 |
1 |
12 |
0.857143 |
74.25 |
0.94598 |
Carb-Tri |
Gauthier et al. (1988a, fig. 3) |
Synapsida(3) |
19 |
834 |
311 |
223 |
1577 |
62.709832 |
1 |
14 |
0.823529 |
74.25 |
0.93501 |
Carb-Cret |
Rowe (1988, figs. 2, 3) |
Synapsida(4) |
15 |
1095 |
364 |
223 |
1935 |
66.757991 |
1 |
8 |
0.615385 |
74.25 |
0.91764 |
Carb-Cret |
Desui (1991, fig. 1) |
Synapsida(5) |
22 |
451 |
374 |
101 |
1088 |
17.073171 |
1 |
15 |
0.714286 |
74.25 |
0.7234 |
Carb-Tri |
Hopson (1991, figs. 7, 22, 32) |
Synapsida(6) |
13 |
562 |
107 |
61 |
462 |
80.960854 |
0.5 |
8 |
0.727273 |
97.5 |
0.885287 |
Carb-Perm |
Modesto (1995, fig. 19A) |
Synapsida(7) |
14 |
485 |
144 |
101 |
699 |
70.309278 |
0.5 |
10 |
0.833333 |
97.5 |
0.928094 |
Carb-Tri |
Rowe (1988, fig. 2) |
Pelycosauria(1) |
8 |
467 |
113 |
55 |
187 |
75.802998 |
8.5 |
4 |
0.666667 |
8.25 |
0.56061 |
Carb-Perm |
Rowe (1986; in Hopson 1991, fig. 7) |
Pelycosauria(2) |
6 |
201 |
74 |
42 |
124 |
63.18408 |
9.25 |
2 |
0.5 |
55 |
0.60976 |
Carb-Perm |
Rowe (1986; in Kemp 1988, fig. 1.2) |
Pelycosauria(3) |
11 |
264 |
85 |
56 |
261 |
67.80303 |
0.25 |
6 |
0.666667 |
4.5 |
0.85854 |
Carb-Perm |
Laurin (1993, fig. 22) |
Pelycosauria(4) |
8 |
127 |
160 |
56 |
301 |
-25.984252 |
17.5 |
3 |
0.5 |
20.5 |
0.57551 |
Carb-Perm |
Reisz et al. (1998, fig. 3) |
Pelycosauria(5) |
19 |
340 |
499 |
68 |
936 |
-46.764706 |
0.5 |
12 |
0.705882 |
97.5 |
0.503456 |
Carb-Perm |
Reisz et al. (1998, fig. 4) |
Pelycosauria(6) |
8 |
158 |
135 |
51 |
212 |
14.556962 |
46.5 |
4 |
0.666667 |
9 |
0.478261 |
Carb-Perm |
Modesto (1994, fig. 3) |
Pelycosauria-Edaphosauridae |
6 |
80 |
74 |
35 |
113 |
7.5 |
42.5 |
2 |
0.5 |
39 |
0.5 |
Carb-Perm |
Modesto (1995, fig. 19B) |
Therapsida(1) |
16 |
497 |
53 |
46 |
164 |
89.336016 |
4 |
10 |
0.714286 |
25 |
0.94068 |
Perm-Tri |
Hopson & Barghusen (1986, figs. 1, 12) |
Therapsida(2) |
6 |
332 |
7 |
6 |
8 |
97.891566 |
20.25 |
3 |
0.75 |
20.25 |
0.5 |
Perm |
Rowe (1986, 1988; in Hopson 1991, fig. 21) |
Therapsida(3) |
6 |
332 |
7 |
6 |
8 |
97.891566 |
35.75 |
3 |
0.75 |
69 |
0.5 |
Perm |
Kemp (1988, fig. 1.3) |
Therapsida(4) |
7 |
337 |
8 |
6 |
9 |
97.626113 |
27.75 |
3 |
0.6 |
25.75 |
0.33333 |
Perm |
Hopson (1991, fig. 22) |
Therapsida(5) |
10 |
228 |
52 |
46 |
183 |
77.192982 |
27.75 |
6 |
0.75 |
0.25 |
0.9562 |
Perm-Tri |
Luo & Crompton (1994, fig. 1A) |
Therapsida(6) |
10 |
228 |
52 |
46 |
183 |
77.192982 |
27.75 |
6 |
0.75 |
0.25 |
0.9562 |
Perm-Tri |
Luo & Crompton (1994, fig. 1B) |
Dinocephalia(1) |
5 |
37 |
1 |
1 |
3 |
97.297297 |
8 |
2 |
0.666667 |
91 |
1 |
Perm |
Rubidge (1991, fig. 4) |
Dinocephalia-Anteosauridae |
4 |
26 |
6 |
6 |
18 |
76.923077 |
18.5 |
2 |
1 |
18.5 |
1 |
Perm |
Rubidge (1994, fig. 9) |
Cynodontia(1) |
11 |
106 |
24 |
9 |
39 |
77.358491 |
18.25 |
6 |
0.666667 |
20.75 |
0.5 |
Perm-Tri |
Battail (1982; in Hopson 1991, fig. 30) |
Cynodontia(2) |
11 |
388 |
66 |
40 |
134 |
82.989691 |
1 |
6 |
0.666667 |
7.5 |
0.7234 |
Perm-Tri |
Kemp (1988, fig. 1.4) |
Cynodontia(3) |
10 |
369 |
41 |
40 |
114 |
88.888889 |
1 |
6 |
0.75 |
2.25 |
0.98649 |
Perm-Tri |
Hopson (1991, fig. 32) |
Cynodontia(4) |
12 |
561 |
387 |
135 |
572 |
31.016043 |
0.75 |
3 |
0.3 |
4.5 |
0.42334 |
Tri-Cret |
Lucas & Luo (1993, fig. 14A) |
Cynodontia(5) |
12 |
561 |
487 |
135 |
572 |
13.190731 |
3 |
2 |
0.2 |
28.25 |
0.19451 |
Tri-Cret |
Lucas & Luo (1993, fig. 14B) |
Cynodontia(6) |
10 |
285 |
42 |
35 |
134 |
85.263158 |
0.5 |
5 |
0.625 |
1.5 |
0.929293 |
Tri |
Martinez et al. (1996, fig. 5) |
Cynodontia(7) |
8 |
591 |
150 |
150 |
580 |
74.619289 |
0.5 |
6 |
1 |
1.5 |
1 |
Tri-Cret |
Wible (1991, fig. 3) |
Cynodontia(8) |
16 |
873 |
386 |
150 |
875 |
55.784651 |
0.5 |
7 |
0.5 |
1.5 |
0.674483 |
Tri-Cret |
Wible (1991, fig. 4) |
Cynodontia(9) |
7 |
479 |
247 |
150 |
445 |
48.434238 |
0.5 |
5 |
1 |
0.5 |
0.671186 |
Tri-Cret |
Rowe (1988, fig. 3) |
Cynodontia(10) |
9 |
715 |
174 |
146 |
608 |
75.664336 |
0.5 |
4 |
0.571429 |
3.5 |
0.939394 |
Tri-Cret |
Rowe (1988, fig. 4) |
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