List of cladograms tested for their correspondence with stratigraphic data. 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
Arthropoda(1) |
7 |
2897 |
396 |
237 |
569 |
86.330687 |
6.75 |
4 |
0.8 |
15.75 |
0.52108 |
Camb-Carb |
Ballard et al. (1992, fig. 3.) |
Arthropoda(2) |
6 |
3089 |
343 |
159 |
343 |
88.896083 |
100 |
2 |
0.5 |
53 |
0 |
Camb-Sil |
Bacetti (1979, fig. 11.4.) |
Arthropoda(3) |
8 |
4113 |
463 |
173 |
463 |
88.74301 |
100 |
4 |
0.8 |
95.5 |
0 |
Camb-Dev |
Boudreaux (1979, implicit in text) |
Arthropoda(4) |
28 |
2953 |
1018 |
220 |
1018 |
65.526583 |
100 |
12 |
0.46154 |
97 |
0 |
Camb-Carb |
Briggs and Fortey (1989, fig. 1. ) |
Arthropoda(5) |
5 |
2454 |
– |
159 |
159 |
93.520782 |
100 |
3 |
1 |
81.5 |
– |
Camb-Sil |
Cisne (1974, fig. 3.) |
Arthropoda(6) |
18 |
4457 |
1444 |
572 |
2208 |
67.601526 |
1 |
8 |
0.5 |
53 |
0.46699 |
Camb-Rec |
Moura and Christoffersen (1996, fig. 1. ) |
Arthropoda(7) |
5 |
2281 |
173 |
173 |
332 |
92.415607 |
20.25 |
3 |
1 |
56.5 |
1 |
Camb-Dev |
Paulus (1979, fig. 6.1.) |
Arthropoda(8) |
5 |
1916 |
– |
159 |
159 |
91.701461 |
100 |
3 |
1 |
82 |
– |
Camb-Sil |
Weygoldt (1979, fig. 3.10.) |
Lobopodia |
8 |
1159 |
346 |
259 |
505 |
70.146678 |
6.75 |
4 |
0.66667 |
63.75 |
0.64634 |
Camb-Carb |
Budd (1993, fig. 4.) |
Onychophora |
9 |
269 |
606 |
572 |
865 |
-125.27881 |
3.5 |
7 |
1 |
1.75 |
0.88396 |
Camb-Rec |
Hou and Bergstrom (1995, fig. 7.) |
Onychophora |
9 |
269 |
572 |
572 |
865 |
-112.63941 |
3.5 |
7 |
1 |
1.75 |
1 |
Camb-Rec |
Monge-Najera (1995, fig. 2. ) |
Atelocerata(1) |
9 |
2305 |
1342 |
413 |
1412 |
41.778742 |
46.5 |
3 |
0.42857 |
39.25 |
0.07007 |
Sil-Rec |
Briggs et al. (1992, fig. 2. (Atelocerata)) |
Atelocerata(2) |
9 |
2305 |
1370 |
413 |
1412 |
40.563991 |
72.25 |
2 |
0.28571 |
92 |
0.04204 |
Sil-Rec |
Wills et al. (1994, fig. 11. (Atelocerata)) |
Atelocerata(3) |
10 |
2381 |
1356 |
413 |
1512 |
43.049139 |
59 |
4 |
0.5 |
94.25 |
0.14195 |
Sil-Rec |
Wills et al. (1998, fig. 2.1. (Atelocerata)) |
Chilopoda(1) |
5 |
804 |
961 |
413 |
1261 |
-19.527363 |
38.25 |
1 |
0.33333 |
57.75 |
0.35377 |
Sil-Rec |
Dohle (1985, fig. 6.) |
Chilopoda(2) |
4 |
804 |
748 |
374 |
848 |
6.965174 |
100 |
1 |
0.5 |
100 |
0.21097 |
Sil-Paleog |
Dohle (1985, fig. 2a.) |
Chilopoda(2) |
4 |
804 |
648 |
374 |
848 |
19.402985 |
36.75 |
1 |
0.5 |
53.25 |
0.42194 |
Sil-Paleog |
Dohle (1985, fig. 2b.) |
Julida(1) |
8 |
134 |
229 |
56 |
314 |
-70.895522 |
62.5 |
2 |
0.33333 |
75.75 |
0.32946 |
Paleog-Rec |
Enghoff (1981, fig. 2.) |
Julida(2) |
6 |
704 |
1174 |
313 |
1174 |
-66.761364 |
100 |
1 |
0.25 |
81.25 |
0 |
Carb-Rec |
Enghoff (1981, fig. 1.) |
Julida(3) |
15 |
134 |
414 |
56 |
706 |
-208.95522 |
89.75 |
6 |
0.46154 |
93.5 |
0.44923 |
Paleog-Rec |
Enghoff (1991, fig. 25.) |
Insecta(3) |
7 |
1792 |
845 |
399 |
1001 |
52.845982 |
60.25 |
3 |
0.6 |
39.5 |
0.25914 |
Dev-Rec |
Stys et al. (1993, fig. 4a.) |
Insecta(3) |
7 |
1792 |
839 |
399 |
1001 |
53.180804 |
40.25 |
3 |
0.6 |
38 |
0.2691 |
Dev-Rec |
Stys et al. (1993, fig. 4b.) |
Insecta(3) |
7 |
1792 |
931 |
399 |
1001 |
48.046875 |
82 |
2 |
0.4 |
68 |
0.11628 |
Dev-Rec |
Stys et al. (1993, fig. 4c.) |
Insecta(1) |
24 |
5876 |
1903 |
399 |
3700 |
67.614023 |
4.75 |
11 |
0.5 |
10.5 |
0.54438 |
Dev-Rec |
Brusca and Brusca (1990, fig. 49.) |
Insecta(2) |
29 |
6641 |
2728 |
399 |
4930 |
58.921849 |
19.8 |
9 |
0.333333 |
79.7 |
0.485985 |
Dev-Rec |
Rasnitsyn (1998, fig. 18.1.) |
Hexapoda(1) |
8 |
2358 |
636 |
399 |
834 |
73.02799 |
38.75 |
2 |
0.33333 |
75.75 |
0.45517 |
Dev-Rec |
Kristensen (1975, fig. 1.) |
Hexapoda(2) |
15 |
3510 |
1047 |
290 |
1365 |
70.17094 |
94.5 |
5 |
0.38462 |
96 |
0.29581 |
Carb-Paleog |
Kristensen (1975, fig. 8.) |
Ephemeroptera |
19 |
1715 |
1396 |
210 |
2275 |
18.600583 |
28.75 |
8 |
0.47059 |
98 |
0.42567 |
Jur-Rec |
Edmunds (1962, fig. 1. ) |
Rectracheata |
13 |
888 |
995 |
210 |
1842 |
-12.04955 |
13 |
6 |
0.54546 |
23.5 |
0.519 |
Jur-Rec |
McCafferty (1991, fig. 4. ) |
Setisura |
4 |
163 |
333 |
124 |
333 |
-104.29448 |
100 |
0 |
0 |
100 |
0 |
Cret-Rec |
McCafferty (1991, fig. 2. ) |
Calypterygoidea |
6 |
208 |
400 |
152 |
704 |
-92.307692 |
32.75 |
2 |
0.5 |
29.5 |
0.55073 |
Jur-Rec |
Heymer (1975, fig. 16.) |
Plecoptera |
15 |
1185 |
1262 |
258 |
2685 |
-6.49789 |
17 |
7 |
0.53846 |
11 |
0.58632 |
Perm-Rec |
Nelson (1984, fig. 2c. ) |
Plecoptera |
15 |
1185 |
1363 |
258 |
2685 |
-15.021097 |
38.5 |
7 |
0.53846 |
15.75 |
0.54471 |
Perm-Rec |
Nelson (1984, fig. 3b.) |
Plecoptera |
15 |
1185 |
1352 |
258 |
2685 |
-14.092827 |
32.75 |
7 |
0.53846 |
14.75 |
0.54924 |
Perm-Rec |
Nelson (1984, fig. 3c.) |
Plecoptera |
15 |
1185 |
1127 |
258 |
2685 |
4.894515 |
11.75 |
8 |
0.61538 |
5.75 |
0.64194 |
Perm-Rec |
Nelson (1984, fig. 3d.) |
Plecoptera |
15 |
1185 |
960 |
258 |
2685 |
18.987342 |
4.25 |
8 |
0.61538 |
7.5 |
0.71075 |
Perm-Rec |
Nelson (1984, fig. 3e.) |
Plecoptera |
15 |
1185 |
1084 |
258 |
2685 |
8.523207 |
8.75 |
7 |
0.53846 |
15.75 |
0.65966 |
Perm-Rec |
Nelson (1984, fig. 3f.) |
Blattoneoptera |
7 |
1408 |
834 |
290 |
867 |
40.767045 |
100 |
1 |
0.2 |
100 |
0.05719 |
Carb-Paleog |
Kukalova-Peck and Peck (1993, fig. 23.) |
Dictyoptera |
6 |
665 |
829 |
325 |
1285 |
-24.661654 |
61.75 |
1 |
0.25 |
100 |
0.475 |
Carb-Rec |
Thorne et al. (1992, fig. 2. ) |
Orthoptera |
7 |
1633 |
622 |
179 |
642 |
61.910594 |
100 |
1 |
0.2 |
100 |
0.0432 |
Carb-Cret |
Duncan (1996, @) |
Dermaptera |
8 |
413 |
649 |
157 |
843 |
-57.142857 |
75.75 |
2 |
0.33333 |
95.75 |
0.2828 |
Jur-Rec |
Popham (1965, fig. 49.) |
Forficulina |
9 |
302 |
626 |
157 |
1111 |
-107.28477 |
37 |
1 |
0.14286 |
78 |
0.50839 |
Jur-Rec |
Haas (1955, fig. 7. (Haplodiplatys and above)) |
Hemiptera(1) |
4 |
598 |
350 |
237 |
350 |
41.471572 |
100 |
1 |
0.5 |
83.75 |
0 |
Tri-Rec |
Bourgoin (1986, fig. 12.) |
Hemiptera(1) |
4 |
598 |
350 |
237 |
350 |
41.471572 |
100 |
1 |
0.5 |
84.5 |
0 |
Tri-Rec |
Bourgoin (1986, fig. 13.) |
Hemiptera(1) |
4 |
598 |
350 |
237 |
350 |
41.471572 |
100 |
1 |
0.5 |
82.75 |
0 |
Tri-Rec |
Bourgoin (1986, fig. 14.) |
Hemiptera(2) |
11 |
1611 |
649 |
292 |
1601 |
59.714463 |
0.75 |
7 |
0.77778 |
3.5 |
0.72727 |
Perm-Rec |
von Dohlen (1995, fig. 1. (Thysanoptera and above)) |
Hemiptera(3) |
10 |
1611 |
385 |
253 |
1309 |
76.1018 |
7 |
6 |
0.75 |
7.25 |
0.875 |
Perm-Paleog |
von Dohlen (1995, fig. 6. (superfamily level)) |
Cicadelloidea |
4 |
216 |
146 |
146 |
368 |
32.407407 |
25.25 |
1 |
0.5 |
51.75 |
1 |
Cret-Rec |
Dietrich and Deitz (1993, fig. 31. (family level)) |
Cimicomorpha |
16 |
870 |
1556 |
178 |
1978 |
-78.850575 |
82.75 |
4 |
0.28571 |
95 |
0.23444 |
Jur-Rec |
Schuh and Stys (1991, fig. 1. (family level)) |
Gerromorpha(1) |
8 |
407 |
467 |
124 |
585 |
-14.742015 |
72.5 |
2 |
0.33333 |
95.75 |
0.25597 |
Cret-Rec |
Spence and Anderson (1994, fig. 1. (family level)) |
Gerromorpha(2) |
8 |
407 |
467 |
124 |
585 |
-14.742015 |
76.5 |
2 |
0.33333 |
95.75 |
0.25597 |
Cret-Rec |
Anderson (1979, fig. 9. ) |
Aphidoidea |
9 |
805 |
509 |
123 |
509 |
36.770186 |
100 |
5 |
0.71429 |
71.25 |
0 |
Cret-Neog |
Heie (1987, @) |
Nepomorpha |
11 |
1202 |
1055 |
237 |
1405 |
12.229617 |
37 |
6 |
0.66667 |
37.5 |
0.29966 |
Tri-Rec |
Rieger (1976, fig. 58.) |
Nepomorpha(2) |
10 |
1202 |
818 |
237 |
1168 |
31.946755 |
22 |
6 |
0.75 |
22.75 |
0.37594 |
Tri-Rec |
Mahner (1993, fig. 6.3.) |
Coccoidea |
5 |
195 |
– |
0 |
0 |
100 |
100 |
3 |
1 |
100 |
– |
Paleog |
Miller and Miller, fig. 8. (family level)) |
Membracoidea |
5 |
259 |
124 |
124 |
361 |
52.123552 |
7 |
2 |
0.66667 |
20.75 |
1 |
Cret-Rec |
Dietrich and Deitz (1993, fig. 31. (family level)) |
Thysanoptera |
8 |
429 |
707 |
157 |
827 |
-64.801865 |
100 |
1 |
0.16667 |
100 |
0.1791 |
Jur-Rec |
Crespi et al. (1996, fig. 1a.) |
Thysanoptera |
8 |
429 |
707 |
157 |
827 |
-64.801865 |
100 |
2 |
0.33333 |
100 |
0.1791 |
Jur-Rec |
Crespi et al. (1996, fig. 1b.) |
Psocodea |
7 |
1577 |
553 |
300 |
768 |
64.933418 |
20 |
4 |
0.8 |
19.75 |
0.4594 |
Carb-Paleog |
Lyal (1985, fig. 1. ) |
Neuroptera(1) |
5 |
841 |
135 |
113 |
344 |
83.947681 |
5.25 |
2 |
0.66667 |
13 |
0.90476 |
Tri-Cret |
Oswald (1995, fig. 1. (Psychopsidae to Ascalaphidae)) |
Neuroptera(2) |
4 |
853 |
268 |
201 |
447 |
68.581477 |
34.25 |
1 |
0.5 |
100 |
0.72764 |
Carb-Cret |
Stys and Bilinsky (1990, fig. 5a) |
Neuroptera(2) |
4 |
853 |
268 |
201 |
447 |
68.581477 |
17.5 |
1 |
0.5 |
50.5 |
0.72764 |
Carb-Cret |
Stys and Bilinsky (1990, fig. 5b) |
Neuroptera(2) |
4 |
853 |
201 |
201 |
447 |
76.436108 |
8.5 |
2 |
1 |
8.5 |
1 |
Carb-Cret |
Stys and Bilinsky (1990, fig. 5c) |
Neuroptera(2) |
4 |
853 |
380 |
201 |
447 |
55.451348 |
100 |
1 |
0.5 |
100 |
0.27236 |
Carb-Cret |
Stys and Bilinsky (1990, fig. 5e) |
Neuroptera(2) |
4 |
853 |
447 |
201 |
447 |
47.596717 |
100 |
0 |
0 |
100 |
0 |
Carb-Cret |
Stys and Bilinsky (1990, fig. 5f) |
Neuroptera(3) |
5 |
853 |
772 |
325 |
772 |
9.495897 |
100 |
0 |
0 |
100 |
0 |
Carb-Rec |
Stys and Bilinsky (1990, fig. 5d) |
Coleoptera(1) |
10 |
1430 |
868 |
208 |
1040 |
39.300699 |
64.75 |
3 |
0.375 |
36.5 |
0.20673 |
Tri-Paleog |
Butler and Leone (1967, fig. 1. ) |
Coleoptera(2) |
15 |
1963 |
857 |
173 |
1217 |
56.342333 |
20.75 |
6 |
0.46154 |
32.25 |
0.34483 |
Tri-Paleog |
Howland and Hewitt (1995, fig. 6.) |
Adephaga(1) |
8 |
1044 |
472 |
237 |
852 |
54.789272 |
2.75 |
3 |
0.5 |
9 |
0.61789 |
Tri-Rec |
Baehr (1979, @) |
Adephaga(2) |
6 |
979 |
412 |
214 |
443 |
57.916241 |
72.75 |
1 |
0.25 |
100 |
0.13537 |
Tri-Neog |
Beutel (1992, fig. 14.) |
Adephaga(3) |
7 |
1044 |
504 |
214 |
615 |
51.724138 |
49 |
2 |
0.4 |
52.25 |
0.27681 |
Tri-Neog |
Beutel (1993, fig. 30.) |
Adephaga(4) |
8 |
1044 |
612 |
237 |
852 |
41.37931 |
19 |
1 |
0.16667 |
78.25 |
0.39024 |
Tri-Rec |
Beutel (1995, @) |
Adephaga(5) |
16 |
1361 |
1455 |
237 |
1694 |
-6.906686 |
24.5 |
7 |
0.466667 |
17.5 |
0.164036 |
Tri-Rec |
Kavanaugh (1986, fig. 22.) |
Geadephaga |
6 |
268 |
556 |
206 |
968 |
-107.46269 |
23.75 |
2 |
0.5 |
46.5 |
0.54068 |
Jur-Rec |
Regenfu_ (1975, fig. 2.) |
Scarabaeoidea |
13 |
330 |
635 |
210 |
2400 |
-92.424242 |
13.25 |
5 |
0.45455 |
40 |
0.80594 |
Jur-Rec |
Browne and Scholtz (1995, fig. 10. (Glaresidae and above)) |
Salpingid group |
6 |
198 |
546 |
124 |
546 |
-175.75758 |
100 |
0 |
0 |
100 |
0 |
Cret-Rec |
Pollock (1994, fig. 29.) |
Mecoptera |
15 |
1207 |
1294 |
252 |
1684 |
-7.207954 |
17.75 |
7 |
0.53846 |
6.75 |
0.27235 |
Perm-Rec |
Willman (1987, fig. 1. ) |
Mecopteroidea |
4 |
1027 |
120 |
86 |
141 |
88.315482 |
100 |
1 |
0.5 |
100 |
0.38182 |
Perm-Jur |
Griffiths (1976, fig. 2. ) |
Lepidoptera(1) |
5 |
205 |
45 |
15 |
45 |
78.04878 |
100 |
1 |
0.33333 |
91.5 |
0 |
Paleog |
de Jong (1996, fig. 4. (groups of genera recoded into families)) |
Lepidoptera(2) |
11 |
1429 |
952 |
292 |
1783 |
33.379986 |
4.5 |
3 |
0.33333 |
51 |
0.55734 |
Perm-Rec |
Friedlander et al. (1996, fig. 6a.) |
Lepidoptera(2) |
11 |
1429 |
952 |
292 |
1783 |
33.379986 |
4.5 |
3 |
0.33333 |
51 |
0.55734 |
Perm-Rec |
Friedlander et al. (1996, fig. 6b.) |
Lepidoptera(2) |
11 |
1429 |
952 |
292 |
1783 |
33.379986 |
4.5 |
3 |
0.33333 |
51 |
0.55734 |
Perm-Rec |
Friedlander et al. (1996, fig. 6c.) |
Lepidoptera & Trichoptera |
6 |
668 |
502 |
271 |
958 |
24.850299 |
18.25 |
2 |
0.5 |
31.75 |
0.66376 |
Perm-Rec |
Kobayashi and Ando (1988, fig. 1. ) |
Heteroneura |
8 |
196 |
353 |
157 |
1060 |
-80.102041 |
15.5 |
4 |
0.66667 |
22 |
0.78295 |
Jur-Rec |
Nielsen et al. (1989, fig. 2. (Nepticulidae to Prodoxidae)) |
Incurvarioidea |
6 |
78 |
39 |
39 |
156 |
50 |
7.5 |
4 |
1 |
7.5 |
1 |
Paleog-Rec |
Schmidt Nielsen and Davis (1985, fig. 29) |
Noctuoidea |
6 |
98 |
171 |
83 |
400 |
-74.489796 |
26 |
2 |
0.5 |
60.5 |
0.7224 |
Cret-Rec |
Weller et al. (1994, fig. 1. (Noctuidae treated as single terminal)) |
Papilionoidea |
7 |
240 |
65 |
50 |
110 |
72.916667 |
15 |
4 |
0.8 |
15 |
0.75 |
Paleog-Rec |
Martin and Pashley (1992, fig. 4., tree 1.) |
Rhopalocera |
5 |
205 |
45 |
15 |
45 |
78.04878 |
100 |
1 |
0.33333 |
91.75 |
0 |
Paleog |
Kristensen (1976, fig. 1. ) |
Mecopteroidea |
6 |
1003 |
195 |
195 |
749 |
80.558325 |
1.75 |
4 |
1 |
1.75 |
1 |
Perm-Cret |
King (1991, fig. 2. (polytomies collapsed)) |
Strepsiptera |
9 |
130 |
322 |
56 |
339 |
-147.69231 |
100 |
1 |
0.14286 |
100 |
0.06007 |
Paleog-Rec |
Kinzelbach and Pohl (1994, fig. 2. ) |
Trichoptera |
16 |
1113 |
1348 |
237 |
2679 |
-21.114106 |
64.25 |
5 |
0.357143 |
100 |
0.545045 |
Tri-Rec |
Wiggins and Wichard (1989, fig. 19.) |
Diptera |
9 |
652 |
355 |
146 |
662 |
45.552147 |
3.75 |
3 |
0.42857 |
92.75 |
0.59496 |
Cret-Rec |
Wada (1991, fig. 17.) |
Aschiza |
7 |
652 |
258 |
146 |
370 |
60.429448 |
24.5 |
3 |
0.6 |
43.25 |
0.5 |
Cret-Rec |
McAlpine (1989, fig. 116.1. (Aschiza only)) |
Asiloidea |
6 |
461 |
302 |
178 |
607 |
34.490239 |
10.75 |
3 |
0.75 |
12.75 |
0.71096 |
Jur-Rec |
Woodley (1989, fig. 115.5.) |
Bibionomorpha |
5 |
757 |
213 |
82 |
273 |
71.862616 |
49 |
1 |
0.33333 |
58.5 |
0.31414 |
Jur-Cret |
Wood and Borkent (1989, fig. 114.2.) |
Blephariceromorpha and related Diptera |
8 |
905 |
684 |
237 |
991 |
24.41989 |
13.5 |
3 |
0.5 |
17.5 |
0.40716 |
Tri-Rec |
Courtney (1990, fig. 43. (Blephariceridae coded rather than subfamilies)) |
Calyptratae |
14 |
358 |
489 |
97 |
1000 |
-36.592179 |
77.5 |
6 |
0.5 |
75.75 |
0.56589 |
Cret-Rec |
McAlpine (1989, fig. 116.8.) |
Carnoidea |
9 |
295 |
388 |
97 |
578 |
-31.525424 |
59.25 |
4 |
0.57143 |
91 |
0.39501 |
Cret-Rec |
McAlpine (1989, fig. 116.6.) |
Culicimorpha(1) |
8 |
1040 |
544 |
210 |
640 |
47.692308 |
63 |
2 |
0.33333 |
94.5 |
0.22326 |
Jur-Rec |
Pawloski et al. (1996, fig. 3.) |
Culicimorpha(1) |
8 |
1040 |
608 |
210 |
640 |
41.538462 |
84.5 |
2 |
0.33333 |
94.5 |
0.07442 |
Jur-Rec |
Pawloski et al. (1996, fig. 5.) |
Culicimorpha(2) |
8 |
1040 |
640 |
210 |
640 |
38.461538 |
100 |
2 |
0.33333 |
96.25 |
0 |
Jur-Rec |
Wood and Borkent (1989, fig. 114.2. (right eight taxa)) |
Cyclorrhapha(1) |
10 |
809 |
512 |
157 |
761 |
36.71199 |
15 |
4 |
0.5 |
19.25 |
0.41225 |
Jur-Rec |
Cumming et al. (19@@, fig. 2.) |
Cyclorrhapha(2) |
4 |
127 |
81 |
65 |
133 |
36.220472 |
23.25 |
1 |
0.5 |
50 |
0.76471 |
Paleog-Rec |
Soto (1994, fig. 2a.) |
Cyclorrhapha(2) |
4 |
127 |
81 |
65 |
133 |
36.220472 |
23.25 |
1 |
0.5 |
46 |
0.76471 |
Paleog-Rec |
Soto (1994, fig. 2b.) |
Cyclorrhapha(2) |
4 |
127 |
65 |
65 |
133 |
48.818898 |
7 |
2 |
1 |
7 |
1 |
Paleog-Rec |
Soto (1994, fig. 2c.) |
Diopsoidea |
8 |
117 |
156 |
39 |
195 |
-33.333333 |
83.5 |
4 |
0.66667 |
83.25 |
0.25 |
Paleog-Rec |
McAlpine (1989, fig. 116.2. (Diopsoidea only)) |
Ephydroidea |
5 |
156 |
– |
39 |
39 |
75 |
100 |
2 |
0.66667 |
100 |
– |
Paleog-Rec |
McAlpine (1989, fig. 116.7. (Ephydroidea only)) |
Eremoneura+ |
4 |
638 |
74 |
32 |
74 |
88.401254 |
100 |
0 |
0 |
100 |
0 |
Jur-Cret |
Sinclair (1992, fig. 2. (rh four taxa)) |
Lauxanioidea |
4 |
95 |
73 |
56 |
129 |
23.157895 |
16.5 |
1 |
0.5 |
50 |
0.76712 |
Paleog-Rec |
McAlpine (1989, fig. 116.4. (lauxanioidea only)) |
Opomyzoidea |
13 |
387 |
175 |
50 |
263 |
54.780362 |
64 |
7 |
0.63636 |
51.5 |
0.41315 |
Paleog-Rec |
McAlpine (1989, fig. 116.5. (Pachyneuridae to Cecidomiidae)) |
Orthorrhapha |
7 |
1035 |
382 |
210 |
435 |
63.091787 |
82.5 |
1 |
0.2 |
100 |
0.23556 |
Jur-Rec |
Nagatomi et al. (1991, fig. 54.) |
Orthorrhapha |
7 |
1035 |
274 |
210 |
435 |
73.52657 |
8.5 |
3 |
0.6 |
25.5 |
0.71556 |
Jur-Rec |
Nagatomi et al. (1991, fig. 55a.) |
Orthorrhapha |
7 |
1035 |
274 |
210 |
435 |
73.52657 |
7.5 |
3 |
0.6 |
27.25 |
0.71556 |
Jur-Rec |
Nagatomi et al. (1991, fig. 55b.) |
Psychodomorpha |
6 |
922 |
274 |
210 |
338 |
70.281996 |
24.5 |
2 |
0.5 |
40.5 |
0.5 |
Jur-Rec |
Wood and Borkent (1989, fig. 114.2.) |
Sciomyzoidea |
6 |
250 |
519 |
146 |
626 |
-107.6 |
80 |
1 |
0.25 |
100 |
0.22292 |
Cret-Rec |
McAlpine (1989, fig. 116.4. (Sciomyzoidea only)) |
Sphaeroceratoidea |
6 |
152 |
78 |
39 |
82 |
48.684211 |
41.25 |
3 |
0.75 |
69.5 |
0.09302 |
Paleog-Rec |
McAlpine (1989, fig. 116.7. (Sphaeroceratoidea only)) |
Tabanomorpha |
4 |
390 |
278 |
210 |
450 |
28.717949 |
26 |
1 |
0.5 |
50 |
0.71667 |
Jur-Rec |
Woodley (1989, fig. 115.2.) |
Tephritoidea |
9 |
245 |
106 |
39 |
106 |
56.734694 |
100 |
3 |
0.42857 |
93.75 |
0 |
Paleog-Rec |
McAlpine (1989, fig. 116.3. (Tephritoidea only)) |
Hymenoptera |
5 |
680 |
123 |
91 |
204 |
81.911765 |
19 |
2 |
0.66667 |
21 |
0.71681 |
Tri-Cret |
Zessin (1985, fig. 4. ) |
Hymenoptera (aculeate) |
10 |
907 |
482 |
146 |
553 |
46.857773 |
40.5 |
4 |
0.5 |
94 |
0.17445 |
Cret-Rec |
Brothers (1975) |
Chrysidoidea |
7 |
477 |
545 |
146 |
545 |
-14.255765 |
100 |
2 |
0.4 |
100 |
0 |
Cret-Rec |
Carpenter (1986, fig. 4. ) |
Siricidae |
5 |
187 |
148 |
124 |
433 |
20.855615 |
20.5 |
1 |
0.333333 |
42.5 |
0.92233 |
Cret-Rec |
? |
Marrellomorpha |
4 |
63 |
– |
139 |
139 |
-120.63492 |
100 |
2 |
1 |
51.75 |
– |
Camb-Dev |
Wills et al. (1998, fig. 2.1. (Marrellomorph clade)) |
Arachnomorpha(1) |
16 |
2146 |
369 |
131 |
403 |
82.805219 |
87.5 |
8 |
0.57143 |
100 |
0.125 |
Camb-Sil |
Briggs et al. (1992, fig. 2. (Arachnomorpha)) |
Arachnomorpha(2) |
16 |
2069 |
369 |
131 |
480 |
82.165297 |
19.75 |
8 |
0.57143 |
87.75 |
0.31805 |
Camb-Sil |
Wills et al. (1994, fig. 11. (Arachnomorpha)) |
Arachnomorpha(3) |
20 |
2367 |
561 |
173 |
903 |
76.299113 |
1 |
10 |
0.55556 |
74.5 |
0.46849 |
Camb-Dev |
Wills et al. (1998, fig. 2.1. (Arachnomorpha)) |
Chelicerata(2) |
18 |
1654 |
522 |
173 |
1591 |
68.440145 |
0.1 |
11 |
0.6875 |
1 |
0.753879 |
Camb-Dev |
Dunlop and Selden (1998, fig. 17.3.) |
Chelicerata(1) |
13 |
4346 |
1148 |
490 |
2089 |
73.584906 |
4.25 |
5 |
0.45455 |
96.25 |
0.58849 |
Ord-Neog |
Brusca and Brusca (1990, fig. 31.) |
Arachnida(3) |
12 |
3647 |
1391 |
466 |
2293 |
61.859062 |
26.75 |
4 |
0.4 |
100 |
0.49371 |
Ord-Paleog |
Selden (1993, fig. 3b.) |
Arachnida(4) |
12 |
4094 |
1543 |
466 |
1846 |
62.310699 |
67.5 |
3 |
0.3 |
97.75 |
0.21956 |
Ord-Paleog |
Selden (1993, fig. 3c.) |
Arachnida(2) |
11 |
3109 |
1255 |
436 |
1742 |
59.633323 |
36 |
4 |
0.44444 |
46.75 |
0.37289 |
Sil-Neog |
Selden (1993, fig. 3a.) |
Arachnida(1) |
8 |
1178 |
590 |
384 |
1083 |
49.91511 |
2.25 |
5 |
0.83333 |
1 |
0.70529 |
Sil-Paleog |
Selden (1991, fig. 3.) |
Acarida |
8 |
909 |
890 |
399 |
2283 |
2.090209 |
11 |
2 |
0.33333 |
100 |
0.73938 |
Dev-Rec |
Bernini (1986, fig. 5.) |
Ricinulei |
3 |
345 |
– |
325 |
325 |
5.797101 |
100 |
0 |
0 |
100 |
– |
Carb-Rec |
Selden (1992, fig. 2. (genera collapsed to families)) |
Scorpionida |
5 |
652 |
107 |
107 |
315 |
83.588957 |
2 |
3 |
1 |
2 |
1 |
Sil-Carb |
Jeram (1994, fig. 1. (group A and group B collapsed)) |
Scorpionoidea |
5 |
35 |
140 |
35 |
140 |
-300 |
100 |
0 |
0 |
100 |
0 |
Paleog-Rec |
Stockwell (1989, fig. 251.) |
Araneoidea |
11 |
575 |
797 |
161 |
1196 |
-38.608696 |
70 |
3 |
0.33333 |
100 |
0.38551 |
Jur-Rec |
Heimer and Nentwig (1982, fig. 4. (nodes collapsed to the family level)) |
Haplogynae |
17 |
285 |
210 |
35 |
310 |
26.315789 |
16.75 |
11 |
0.73333 |
7.25 |
0.36364 |
Paleog-Rec |
Coddington and Levi (1991, fig. 2. (Haplogynae only)) |
Lycosoidea |
10 |
204 |
146 |
35 |
146 |
28.431373 |
100 |
6 |
0.75 |
60.75 |
0 |
Paleog-Rec |
Coddington and Levi (1991, fig. 1) |
Mygalomorphae |
15 |
603 |
802 |
243 |
3042 |
-33.001658 |
1.25 |
8 |
0.61538 |
4 |
0.80029 |
Tri-Rec |
Raven (1985, fig. 1.) |
Mygalomorphae(2) |
21 |
2028 |
1318 |
413 |
6348 |
35.009862 |
16.75 |
12 |
0.63158 |
0.25 |
0.84752 |
Sil-Rec |
Coddington and Levi (1991, fig. 1. ) |
Orbiculariae |
13 |
408 |
695 |
146 |
1490 |
-70.343137 |
34.75 |
5 |
0.45455 |
60.75 |
0.59152 |
Cret-Rec |
Coddington and Levi (1991, fig. 1) |
Palpimanoidea |
9 |
196 |
854 |
161 |
1253 |
-335.71429 |
79.25 |
2 |
0.28571 |
100 |
0.36538 |
Jur-Rec |
Coddington and Levi (1991, fig. 2. (Palpimanoidea only)) |
Trilobita(1) |
7 |
1209 |
– |
0 |
0 |
100 |
100 |
5 |
1 |
100 |
– |
Camb |
Fortey (1990, fig. 14.) |
Trilobita(2) |
5 |
1902 |
– |
173 |
173 |
90.904311 |
100 |
3 |
1 |
35.25 |
– |
Camb-Dev |
Fortey and Whittington (1989, fig. 1a.) |
Crozonaspis |
7 |
70 |
20 |
12 |
48 |
71.428571 |
1.75 |
4 |
0.8 |
10.25 |
0.77778 |
Ord |
Henry (1984, fig. 3.) |
Echinolichinae |
4 |
31 |
20 |
10 |
20 |
35.483871 |
100 |
2 |
1 |
69.25 |
0 |
Dev |
Thomas and Holloway (1988, fig. 361.) |
Homolichinae |
9 |
306 |
96 |
67 |
352 |
68.627451 |
34.25 |
5 |
0.71429 |
3.5 |
0.89825 |
Ord |
Thomas and Holloway (1988, fig. 362.) |
Lichinae |
8 |
109 |
85 |
59 |
243 |
22.018349 |
8.75 |
5 |
0.83333 |
2.75 |
0.8587 |
Ord-Dev |
Thomas and Holloway (1988, fig. 360.) |
Tetralichinae |
4 |
109 |
79 |
54 |
108 |
27.522936 |
34.25 |
1 |
0.5 |
50.5 |
0.53704 |
Ord-Sil |
Thomas and Holloway (1988, fig. 363.) |
Trochurinae |
12 |
241 |
274 |
56 |
302 |
-13.692946 |
59.75 |
5 |
0.5 |
75.75 |
0.11382 |
Ord-Dev |
Thomas and Holloway (1988, fig. 364.) |
Crustacea(1) |
18 |
3390 |
1935 |
572 |
2663 |
42.920354 |
11.25 |
7 |
0.4375 |
98 |
0.34816 |
Camb-Rec |
Briggs et al. (1992, fig. 2. (Crustacea/Crustacenomorpha)) |
Crustacea(2) |
7 |
2217 |
1787 |
572 |
1787 |
19.39558 |
100 |
1 |
0.2 |
94 |
0 |
Camb-Rec |
Sanders (1965, fig. 9.) |
Crustacea(3) |
14 |
2850 |
2035 |
384 |
2268 |
28.596491 |
55 |
5 |
0.41667 |
29.5 |
0.12367 |
Dev-Rec |
Schram (1986, fig. 1. ) |
Crustacea(4) |
20 |
3929 |
2265 |
572 |
3359 |
42.351743 |
4 |
9 |
0.5 |
70.5 |
0.39254 |
Camb-Rec |
Wills et al. (1994, fig. 11. (Crustacean/crustaceanomorph clade)) |
Crustacea(5) |
22 |
2827 |
3509 |
572 |
4322 |
-24.124514 |
33.75 |
9 |
0.45 |
65 |
0.2168 |
Camb-Rec |
Wills et al. (1998, fig. 2.1. (Crustacean/crustaceanomorph clade)) |
Phyllopod Biantennata |
8 |
1055 |
287 |
179 |
667 |
72.796209 |
4.5 |
2 |
0.33333 |
91.75 |
0.77869 |
Camb-Dev |
Bousfield (1995, fig. 9. (Phyllopod Biantennata)) |
Eumalacostraca(4) |
23 |
3625 |
3336 |
370 |
4030 |
7.972414 |
57.5 |
8 |
0.38095 |
49 |
0.18962 |
Dev-Rec |
Wills (1998, fig. 15.3b.) |
Eumalacostraca(1) |
8 |
2116 |
821 |
370 |
844 |
61.200378 |
72.5 |
2 |
0.33333 |
71.75 |
0.04852 |
Dev-Rec |
Nylund et al. (1987, fig. 5.) |
Eumalacostraca(2) |
24 |
3642 |
3579 |
370 |
4048 |
1.729819 |
80 |
6 |
0.27273 |
95.75 |
0.12751 |
Dev-Rec |
Schram (1986, fig. 43-3.) |
Eumalacostraca(3) |
12 |
2955 |
1385 |
370 |
1485 |
53.130288 |
51.75 |
4 |
0.4 |
32 |
0.08969 |
Dev-Rec |
Watling (1983, fig. 4. ) |
Peracarida |
8 |
1759 |
1148 |
365 |
1161 |
34.735645 |
100 |
3 |
0.5 |
88.25 |
0.01633 |
Carb-Rec |
Pires (1987, fig. 23.) |
Isopoda |
4 |
490 |
494 |
247 |
498 |
-0.816327 |
53 |
1 |
0.5 |
53 |
0.01594 |
Tri-Rec |
Brandt (1992, fig. 3a.) |
Tanaidacea |
12 |
665 |
391 |
352 |
3559 |
41.203008 |
1.25 |
9 |
0.9 |
1.25 |
0.98784 |
Carb-Rec |
Sieg (1988, fig. 1. ) |
Caridea |
8 |
91 |
189 |
56 |
357 |
-107.69231 |
25 |
3 |
0.5 |
30 |
0.55814 |
Paleog-Rec |
Christoffersen (1990, fig. 1.(?)) |
Brachyura |
7 |
583 |
313 |
91 |
404 |
46.312178 |
47 |
1 |
0.2 |
100 |
0.29073 |
Cret-Paleog |
Spears (1992, fig. 2. (Raninidae and above)) |
Hoplocarida |
4 |
290 |
226 |
213 |
256 |
22.068966 |
16 |
1 |
0.5 |
48.75 |
0.69767 |
Carb-Jur |
Schram (1986, fig. 43-4.) |
Maxillopoda(1) |
10 |
1735 |
2705 |
572 |
3985 |
-55.907781 |
44.25 |
3 |
0.375 |
71.25 |
0.37504 |
Camb-Rec |
Schram (1986, fig. 43-6.) |
Maxillopoda(2) |
11 |
1788 |
1810 |
572 |
2456 |
-1.230425 |
31.75 |
5 |
0.55556 |
24.75 |
0.34289 |
Camb-Rec |
Wills (1998, fig. 15.4. (Maxillopod clade)) |
Copepoda(3) |
8 |
156 |
604 |
124 |
836 |
-287.17949 |
53.25 |
2 |
0.33333 |
46.5 |
0.32584 |
Cret-Rec |
Huys and Boxshall (1991, fig. 4.3.2.) |
Copepoda(1) |
10 |
156 |
836 |
124 |
1084 |
-435.89744 |
89 |
2 |
0.25 |
88 |
0.25833 |
Cret-Rec |
Ho (1994, fig. 4.) |
Copepoda(4) |
10 |
156 |
728 |
124 |
1084 |
-366.66667 |
91.5 |
3 |
0.375 |
89.25 |
0.37083 |
Cret-Rec |
Ho (1990, fig. 4.1.6.) |
Copepoda(2) |
10 |
156 |
960 |
124 |
1084 |
-515.38462 |
93.5 |
1 |
0.125 |
100 |
0.12917 |
Cret-Rec |
Ho (1994, fig. 1.) |
Copepoda(5) |
10 |
156 |
512 |
124 |
1084 |
-228.20513 |
23.75 |
3 |
0.375 |
38.75 |
0.59583 |
Cret-Rec |
Wills (1998, fig. 15.4. (Copepod clade)) |
Myodocopina |
7 |
1851 |
408 |
317 |
566 |
77.957861 |
6.75 |
3 |
0.6 |
37 |
0.63454 |
Sil-Cret |
Vannier and Abe (1992, fig. 8.) |
Phyllopoda |
10 |
1848 |
1525 |
572 |
2782 |
17.478355 |
28.5 |
1 |
0.16667 |
100 |
0.56878 |
Camb-Rec |
Schram (1986, fig. 43-5.) |
Branchiopoda(2) |
5 |
960 |
811 |
372 |
917 |
15.520833 |
100 |
1 |
0.33333 |
100 |
0.19449 |
Dev-Paleog |
Wills (1998, fig. 15.4. (Branchiopod clade)) |
Branchiopoda(1) |
8 |
1545 |
1080 |
533 |
1948 |
30.097087 |
6.5 |
4 |
0.66667 |
3.5 |
0.61343 |
Camb-Paleog |
Walossek (1993, fig. 41.) |
Cladocera |
7 |
557 |
557 |
411 |
2320 |
0 |
5.75 |
4 |
0.8 |
12.5 |
0.92352 |
Dev-Rec |
Martin and Cash-Clark (1995, fig. 23.) |
References for tested cladograms
- Andersen, N.M. (1979) Phylogenetic inference as applied to the study of evolutionary diversification of semiaquatic bugs (Hemiptera: Gerromorpha). Systematic Zoology, 28, 554-578.
- Baccetti, B. (1979) Ultrastructure of sperm and its bearing on arthropod phylogeny. Pp. 609-644 in Gupta, A. P. (ed.), Arthropod Phylogeny. Van Nostrand Reinhold Company, New York.
- Baehr, M. (1979) Vergleichende Untersuchungen am Skelett und an der Coxalmuskulatur des Prothorax der Coleoptera. Ein Beitrag zur Kldrung der phylogenetischen Beziehungen der Adephaga (Coleoptera, Insecta). Zoologica 44, 1-76. http://phylogeny.arizona.ed
- Ballard, J.W.O., Olsen, G.J., Faith, D.P, Odgers, W.A., Rowell, D.M. and Atkinson, P. W. (1992) Evidence from 12S ribosomal RNA that onychophorans are modified arthropods. Science, 258: 1345-1348.
- Bernini, F. (1986) Current ideas on the phylogeny and the adaptive raditions of Acarida. Bollettino di Zoologia, 53, 279-313.
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