Ana səhifə

Skeletons of Terrestrial Cetaceans and the Relationship of Whales to Artiodactyls Supplementary Information


Yüklə 329 Kb.
səhifə3/3
tarix27.06.2016
ölçüsü329 Kb.
1   2   3
PART V. Apomorphy List for Cetartiodactyla and Artiodactyla Nodes (ACCTRAN and DELTRAN Optimization)

List of characters supporting Cetartiodactyla and Artiodactyla with the number of most parsimonious trees in which the character is transformed at that node.



CETARTIODACTYLA NODE
ACCTRAN DELTRAN

Character Transformation Number of Trees Number of Trees C.I.

1 (01) 38 -- 0.333

6 (01) 10 24 0.167

21 (01) 38 38 0.250

34 (01) 38 19 0.333

38 (10) 14 -- 0.167

40 (01) 14 38 0.250

41 (01) 14 38 0.500

46 (10) 38 38 0.500

51 (01) 14 38 0.500

62 (01) 14 38 0.333

65 (01) 14 38 0.250

66 (01) 14 29 0.250

70 (01) 14 38 0.500

76 (01) -- 10 0.250

77 (01) 14 38 1.000

82 (01) 14 38 0.500

91 (01) 14 38 0.500

94 (01) -- 38 1.000

96 (01) 14 38 1.000

98 (01) 14 38 1.000

99 (01) 14 38 1.000

101 (01) 14 38 1.000

ARTIODACTYLA NODE

ACCTRAN DELTRAN



Character Transformation Number of Trees Number of Trees C.I.

1 (01) -- 38 0.333

7 (10) 28 -- 0.500

8 (10) 38 38 0.500

9 (10) 38 38 0.250

10 (01) 38 38 0.333

25 (10) 38 38 0.500

26 (10) 38 38 0.250

27 (10) 14 -- 0.500

32 (01) 38 -- 1.000

48 (10) 38 36 0.250

64 (01) -- 38 0.333

73 (01) 38 -- 0.500

85 (10) 38 38 0.250




PART VI. Bootstrap Analysis
Bootstrap method with heuristic search:

Number of bootstrap replicates = 100

Starting seed = 1288538431

Optimality criterion = maximum parsimony

Character-status summary:

10 characters are excluded

Of the remaining 95 included characters:

8 characters are of type 'ord' (Wagner)

87 characters are of type 'unord'

All characters have equal weight

All characters are parsimony-informative

Starting tree(s) obtained via stepwise addition

Addition sequence: simple (reference taxon = Arctocyon)

Number of trees held at each step during stepwise addition = 1

Branch-swapping algorithm: tree-bisection-reconnection (TBR)

Steepest descent option not in effect

Initial 'MaxTrees' setting = 14400 (will be auto-increased by 100)

Branches collapsed (creating polytomies) if maximum branch length is zero

'MulTrees' option in effect

Topological constraints not enforced

Trees are unrooted
100 bootstrap replicates completed

Time used = 02:21:01.0


Bootstrap 50% majority-rule consensus tree

(plus other groups compatible with this tree)


/--------------------------------------------------------------------- Arctocyon(1)

|

| /----------- Hyopsodus(2)



| |

| /-------------------------69-------------------------+ /----- Phenacodus(3)

| | \-79--+

| | \----- Meniscotherium(4)

| |

| | /------------------------------------------------ Andrewsarchus(5)



| | |

| | | /----- Pakicetus(15)

| | | /-----------------99-----------------+

| | | | \----- Ambulocetus(16)

| | | |

| | /-26-+ | /---------------- D pakistanensis(17)



| | | | | |

| | | | | | /----- Haplobunodontid(27)

| | | | | /-------9-------+ /-27--+

| | | | | | | | \----- Cebochoerid(28)

| | | | | | \-11-+

\----+ | \-77--+ | \----------- Raoellid(29)

| | | /-12-+

| | | | | /--------------------------- D secans(18)

| | | | | |

| | | | | | /--------------------- Archaeotherium(19)

| | | | \-25-+ |

| | | | | | /---------------- Elomeryx(20)

| /-23-+ | | \-32--+ |

| | | | | | | /----- Hippopotamus(21)

| | | \-48-+ \-47-+ /-62--+

| | | | | | \----- Hexaprotodon(22)

| | | | \-56-+

| | | | \----------- Sus(23)

| | | |

| | | | /----------- Agriochoerus(24)



| | | | |

\-59--+ | \-----------59------------+ /----- Poebrotherium(25)

| | \-34--+

| | \----- Tragulus(26)

| |

| \----------------------------------------------------- Eoconodon(6)



|

| /-------------------------------- Hapalodectes(7)

| |

| | /----- Dissacus(8)



\-----------68------------+ /---------34----------+

| | \----- Sinonyx(10)

| |

\-20-+ /--------------------- Ankalagon(9)



| |

| | /----------- Pachyaena(11)

\-22--+ |

| /-36-+ /----- Mesonyx(12)

| | \-51--+

\-27-+ \----- Harpagolestes(14)

|

\---------------- Synoplotherium(13)


Bipartitions found in one or more trees and frequency of occurrence (bootstrap support

values):
1 2 2

12345678901234567890123456789 Freq

---------------------------------------

..............**............. 99.00

..**......................... 78.55

..............*************** 76.91

.***......................... 69.27

......********............... 68.27

....................**....... 61.64

....************************* 59.34

.......................***... 59.19

....................***...... 56.40

...........*.*............... 51.38

................************* 48.00

...................****...... 46.66

..........**.*............... 35.72

........................**... 34.12

.......................*.*... 34.06

.......*.*................... 33.85

..................*****...... 32.39

..........................**. 27.04

..........****............... 27.01

....*.........*************** 26.39

.................******...... 25.18

....**........*************** 23.32

....*.*********************** 22.46

........*.****............... 21.91

.......*******............... 20.37

......*********************** 19.62

.**.......................... 19.61

......******.*............... 19.20

.....*........*************** 17.90

..............**............* 17.28

..........*..*............... 17.25

.......................**.... 16.51

....*.********............... 16.44

..*************************** 15.49

...................*..*...... 14.66

..........................*.* 14.60

...................*...***... 14.20

.***.*........*************** 13.96

..................*.....*.... 12.71

................**........... 12.39

.....................**...... 11.87

.....************************ 11.82

................*******...*** 11.69

......**.*................... 11.46

.................**.......... 11.26

..........................*** 10.95

................*.........**. 10.92

.................**.***...... 10.58

......**..................... 10.52

.................************ 9.88

.***.************************ 9.77

....................*.*...... 9.33

..............**************. 9.09

.......................****.. 8.96

......****................... 8.88

.......***................... 8.72

................*.........*.. 8.71

..................*.....**... 8.71

................*.........*** 8.68

.....*********............... 8.64

...........***............... 8.56

......***.****............... 8.50

.......**.................... 8.48

......***.*..*............... 8.28

..................*....***... 8.22

......***.................... 8.18

..................*.***...... 8.08

.***..........*************** 8.08

....**********............... 7.93

.***.*....................... 7.68

................************. 7.68

...................****....*. 7.67

..............*****....****** 7.50

......*.*.................... 7.41

.........*.*................. 7.40

.......................*****. 7.12

......*****.................. 7.10

..............****.....****** 6.94

..............***............ 6.68

..............******..******* 6.60

...................*.**...... 6.50

..............*******.******* 6.50

.*****........*************** 6.47

..............**.......***... 6.41

.......................*.**.. 6.36

................*.........*.* 6.31

........*.*..*............... 6.30

........*.*.................. 6.29

........******............... 6.15

......*****..*............... 6.10

......*****.**............... 6.09

......***.**.*............... 6.07

..................*.........* 6.02

..............***..*...****** 6.00

........*.**.*............... 5.99

..........*.*................ 5.76

......*.*.****............... 5.71

...........**................ 5.69

......*.......*************** 5.57

..............******...****** 5.50

........**................... 5.46

.........*....**............. 5.31

................*......*****. 5.25

...................*....*.... 5.25

......*...*.................. 5.18

......***.*.................. 5.18

.....*..........************* 5.08

......**********............. 5.00

..............*****....***..* 5.00

..............*****....****.* 5.00


782 groups at (relative) frequency less than 5% not shown


REFERENCES
Cifelli, R.L. The petrosal structure of Hyopsodus with respect to that of some other ungulates, and its phylogenetic implications. Jour. Paleontol. 56, 795-805 (1982).
Geisler, J.H., and Luo, Z. in The Emergence of Whales: Evolutionary Patterns in the Origin of Cetacea (ed. Thewissen, J.G.M.) 163-212 (1998).
Gentry, A.W., and Hooker, J.J. in The Phylogeny and Classification of the Tetrapods, Volume 2: Mammals (ed. Benton, M.J.) 235-272 (Clarendon Press, Oxford, 1988).
Gingerich, P.D, Arif, M., and Clyde, W.C. New archaeocetes (Mammalia, Cetacea) form the middle Eocene Domanda Formation of the Sulaiman Range, Punjab (Pakistan). Contrib. Mus. Paleontol. Univ. Michigan 29, 291-230 (1995)
Luckett, W.P., and Hong, N. Phylogenetic relationships between the orders Artiodactyla and Cetacea: a combined assessment of morphological and molecular evidence. Jour. Mamm. Evol. 5, 127-182 (1998).
Luo, Z., and Gingerich, P.D. Terrestrial Mesonychia to aquatic Cetacea: transformation of the basicranium and evolution of hearing in whales. Univ. Mich. Papers Paleontol. 31, 1-98 (1999).
MacLeod, N., and Rose, K.D. Inferring locomotor behavior in Paleogene mammals via eigenshape analysis. Am. Jour. Sci. 293-A, 300-355 (1993).
MacPhee, R.D.E. Morphology, adaptations, and relationships of Plesiorycteropus, and a diagnosis of a new order of eutherian mammal. Bull. Am. Mus. Nat. Hist. 220, 1-214 (1994).
Novacek M.J. The skull of lepticdid insectivorans and the higher-level classification of eutherian mammals. Bull. Am. Mus. Nat. Hist. 183, 1-111 (1986).
O’Leary, M.A. in The Emergence of Whales: Evolutionary Patterns in the Origin of Cetacea (ed Thewissen, J.G.M.) 133-161 (Plenum Press, New York, 1998).
O’Leary, M.A., and Rose, K.D. Postcranial skeleton of the early Eocene mesonychid Pachyaena (Mammalia; Mesonychia). Jour. Vert. Paleontol. 15, 401-430 (1995).
O’Leary, M.A., and Geisler, J.H. The position of Cetacea within Mammalia: phylogenetic analysis of morphological data from extinct and extant taxa. Syst. Biol. 48, 455-490 (1999).
Schaeffer, B. Notes on the origin and function of the artiodactyl tarsus. Am. Mus. Nov. 1356, 1 24 (1947).
Shoshani, J. Mammalian phylogeny: comparison of morphological and molecular results. Mol. Biol. Evol. 3, 222-242 (1986).
Swofford, D.L. PAUP 4.0b8: Phylogenetic Analysis Using Parsimony (and other methods) (Sinauer Associates, Sunderland, Massachusetts, 1998).
Theodor, J.M. Phylogeny, locomotor evolution and diversity patterns in Eocene Artiodactyla (Unpublished Dissertation, University of California at Berkeley, 1996).
Thewissen, J.G.M. Phylogenetic aspects of cetacean origins: a morphological perspective. Jour. Mamm. Evol. 2, 157-183 (1994).
Thewissen, J.G.M., and Domning, D.P. The role of phenacodontids in the origin of the modern orders of ungulate mammals. Jour. Vert. Paleontol. 12, 494-504 (1992).
Thewissen, J.G.M., and Madar, S.I. Ankle morphology of the earliest cetaceans and its implications for the phylogenetic relations among ungulates. Syst. Biol. 48(1),21-30 (1999).
Webb, S.D., and Taylor, B.E. The phylogeny of hornless ruminants and a description of the cranium of Archeomeryx. Bull. Am. Mus. Nat. Hist. 167, 117-158 (1980).
Wible, J.R. Petrosals of the late Cretaceous marsupials from North America, and a cladistic analysis of the petrosal in therian mammals. Jour. Vert. Paleontol. 10, 183-205 (1990).
Zhou, X, Zhai, R., Gingerich, P.D., and Chen, L. Skull of a new mesonychid (Mammalia: Mesonychia) from the late Paleocene of China. Jour. Vert. Paleontol. 15,387-400 (1995).


1   2   3


Verilənlər bazası müəlliflik hüququ ilə müdafiə olunur ©atelim.com 2016
rəhbərliyinə müraciət