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Electronic Supplementary Information for A New Dromaeosaurid (Dinosauria: Theropoda) with Asian Affinities from the Latest Cretaceous of North America David C. Evans * , Derek W. Larson, and Philip J. Currie * Correspondence and requests for materials about the character list and character-taxon matrix presented below should be addressed to DCE ([email protected]) This file includes: 1. Institutional abbreviations 2. Locality of the specimen 3. X-ray image of Acheroraptor maxilla ROM 63777

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Page 1: link. · Web viewThis character is rescored as a binary character by combining character states 1 and 2, as they form a continuum, following the argumentation of character 239 in Turner

Electronic Supplementary Information for

A New Dromaeosaurid (Dinosauria: Theropoda) with Asian Affinities from the

Latest Cretaceous of North America

David C. Evans*, Derek W. Larson, and Philip J. Currie

* Correspondence and requests for materials about the character list and character-taxon

matrix presented below should be addressed to DCE ([email protected])

This file includes:1. Institutional abbreviations2. Locality of the specimen3. X-ray image of Acheroraptor maxilla ROM 637774. Dromaeosaur maxilla comparison5. Details of morphometric analyses and tables of measurements6. Details of phylogenetic analyses7. References for electronic supplementary information

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1. Institutional Abbreviations

AMNH, American Museum of Natural History, New York, U.S.; IGM, Institute of

Geology, Mongolian Academy of Sciences, Ulaan Baatar, Mongolia; ROM, Royal

Ontario Museum, Toronto, Ontario, Canada; TMP, Royal Tyrrell Museum of

Palaeontology, Drumheller, Alberta, Canada; YPM, Yale Peabody Museum, New Haven,

Connecticut, U.S.

2. Locality

Figure S1. Map of Montana. The red star indicates the general location of the holotype

quarry of Acheroraptor temertyorum gen. et. sp. nov. The holotype specimen (ROM

63777) was collected August 28, 2009 by private interests and subsequently purchased by

the Royal Ontario Museum from a private collector. Locality data for the specimen was

provided by the original collectors of the specimen, including detailed geographic data

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(collected with a GPS) and photographs of the specimen in the ground on the day of

discovery and collection. The referred dentary (ROM 63778) was collected from the

same mixed faunal bonebed several years later by one of the original collectors of the

maxilla. The bonebed reportedly occurs in the upper part of the Hell Creek Formation.

Detailed locality data is on file at the ROM.

3. X-ray image of Acheroraptor maxilla ROM 63777

Figure S2. X-ray image of Acheroraptor temertyorum, gen. et. sp. nov. holotype, ROM

63777. a Maxilla in mediolateral profile. b Isolated maxillary tooth in mediolateral

profile. The specimens were x-rayed at the ROM and recorded digitally with the Kodak

Industrex ACR 2000i under the following settings: 50Kv / 100 mA / 1/4 second.

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4. Dromaeosaur maxilla comparison

Figure S3. Comparison of North American dromaeosaurid (a–c, f) and Asian

velociraptorine (d, e) maxillae. a Saurornitholestes langstoni, TMP 1994.012.0844; b

Bambiraptor feinbergi, AMNH FR 30556 (reflected); c Atrociraptor marshalli, TMP

1995.166.0001; d Velociraptor mongoliensis, AMNH FARB 6515; e Tsaagan mangas,

IGM 100/1015; f Acheroraptor termertorum, gen. et sp. nov., ROM 63777.

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5. Details of Morphometric Analysis and Tables of Measurements

The dentition for ROM 63777 as well as a large sample of isolated small theropod

teeth from the Hell Creek Formation was measured for the variables outlined in Currie

and Varricchio (2004). The measurements were incorporated into an already extensive

small theropod tooth database to compare the dentition of ROM 63777 to other Late

Cretaceous small theropods using canonical variate analysis (Larson and Currie 2013).

Analyses were carried out in the software package JMP Version 5 (2002).

Table S1. Dentition and jaw measurements for holotype maxilla (ROM 63777) and referred dentary (ROM 63778) of Acheroraptor temertyorum. Abbreviations follow Currie and Varricchio (2004). FABL, fore-aft basal length of the crown; BW, basal width; ANT, anterior denticles/mm; POST, posterior denticles/mm; DSDI, denticle serration desnsity index.

Tooth Postion FABL CH BW ANT POST DSDIMx-1 6.125* 3.375*Mx-2 7.625* 3.625*Mx-3 7.5 13.125 3.375 7.8 4.6 1.70Mx-4 7.75* 3.375*Mx-5 7.375 12 3 6.6 4.7 1.40Mx-6 7.5* 7.875+ 3.375* 7 4.8 1.46Mx-7 6.375 10.125 3 7.6e 4.8 1.58Mx-8 5.625 6.375+ 2.75 5Mx-9 5.25* 2.125*Isolated 7.125 12 3.25 4.4D-1 3.2* 2.5*D-2 5.2* 2.6*D-3 6.2* 2.7*D-4 6.5* 2.7*D-5 6.7* 2.3*D-6 6.9* 2.7*D-7 6.9* 2.4*D-8 7.5* 2.1*D-9 6.7* 2.4*D-10 6.5* 2.4*D-11 6.5* 2*D-12 6.4* 1.6*D-13 5.8* ?D-14 5.6* ?D-15 3.4+* ?* indicates an alveolar measurement where actual tooth measurements are not available, +, minimum measurement, e, estimate.

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Figure S4. Canonical variate analyses comparing the complete teeth of ROM 63777 to isolated teeth from the Lance and Hell Creek formations (a), and named dromaeosaurid teeth from the Campanian and Maastrichtian of North America (b).

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Table S2. Published ranges of anterior and posterior denticle densities in dromaeosaurid holotype specimens with preserved teeth. Denticle measurements follow Currie and Varricchio (2004).

Taxon ANT POST ReferenceAcheroraptor temertyorum 6.6–7.8 4.4–5.0 this studyAchillobator giganticus 3.4–4.0 3.0–3.6 Perle et al. (1999)Atrociraptor marshalli 2.7–8.0 2.3–5.0 Currie and Varricchio

(2004)Austroraptor cabazai none none Novas et al. (2008)Bambiraptor feinbergi 6.0–6.5** 3.0–6.5 Burnham et al. (2000);

Smith et al. (2005)Buitreraptor gonzalezorum none none Novas et al. (2008)Deinonychus antirrhopus 4.0–5.9 3.0–3.5 Smith et al. (2005)Dromaeosaurus albertensis 1.8–3.5 3.0–5.0 Smith et al. (2005)Linheraptor exquisitus none not reported Xu et al. (2010)Graciliraptor lujiatunensis present but not

measured*present but not measured*

Xu and Wang (2004)

Microraptor zhaoianus none present but not measured*

Xu et al. (2000)

Saurornitholestes langstoni 6.5–7.0 4.0–5.0 Currie and Varricchio (2004)

Shanag ashile none 12.4* Turner et al. (2007)Sinornithosaurus millenii 9.0–13.0* 7.0–14.0* Xu and Wu (2001)Tianyuraptor ostromi present but not

measuredpresent but not measured

Zheng et al. (2009)

Tsaagan mangas none 3.0–3.5 Norell et al. (2006)Utahraptor ostrommaysorum 2.2–2.3 2.4–2.5 Kirkland et al. (1993)Velociraptor mongoliensis 5.0–8.0 5.0–6.0 Smith et al. (2005)Velociraptor osmolskae none present but not

measuredGodefroit et al. (2008)

*, anterior teeth lack denticles. **, denticles absent on dentary teeth and some maxillary teeth.

6. Details of Phylogenetic Analyses

In order to assess the systematic relationships of Acheroraptor temertyorum

within Dromaeosauridae, both the holotype and referred dentary were scored in two

recent dromaeosaurid character-taxon matrices. The specimens were coded as a single

OTU into the character-taxon matrix used for the reduced consensus tree of Turner et al.

(2012), a large-scale maniraptoran data matrix with wild-card taxa removed. This matrix

consists of 477 characters and 110 (108 ingroup) taxa. Phylogenetic analyses were

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conducted in TNT v. 1.0 (Goloboff et al. 2003, 2008) using a heuristic tree search with

1000 random sequence addition replicate Wagner trees with tree bisection-reconnection

(TBR) branch-swapping, holding ten trees per replicate, followed by an additional round

of TBR branch-swapping. Ordered characters were run as ordered as per the original

analysis. The resulting strict consensus tree of most-parsimonious trees (Fig. S5) places

Acheroraptor termertyorum, gen. et sp. nov., within a largely unresolved

Dromaeosauridae. This confirms its identification as a probable eudromaeosaur, but fails

to resolve its systematic position relative to many other members within this clade.

For potentially greater in-group resolution, the specimens were also scored in a

data matrix modified from Longrich and Currie (2009), a dromaeosaur-specific dataset.

This matrix was updated to include the holotype of Linheraptor exquisitus (Xu et al.

2010), whose codings were added to the Tsaagan mangas OTU following Turner et al.

(2012), as well as Velociraptor osmolskae (Godefroit et al. 2008) and Balaur bondoc

(Csiki et al. 2010), which were not included in the original analysis. Additionally,

following the discussion in Turner et al. (2012), the codings for Adasaurus mongoliensis

in Longrich and Currie (2009) were separated into Adasaurus mongoliensis based on the

holotype specimen from the Nemegt Formation, and an additional OTU based on the

skull of IGN 100/23, which represents a new taxon from the Bayanshiree Formation

(Turner et al. 2012). Scorings for IGN 100/23 were originally incorporated into the

Adasaurus mongoliensis OTU in Longrich and Currie (2009), and we have used these

codings for the Bayanshiree sp. nov. OTU in this analysis, and verified the scorings based

on personal observation of the specimen (PJC). Itemirus was excluded from the analysis

due to its identification as a tyrannosauroid following Miyashita and Currie (2009).

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Several characters were also rescored or modified (as noted in the following character

descriptions), and two maxillary characters from Turner et al. (2012) were added to the

matrix. The final analysis included 116 characters scored for 26 in-group taxa. Four

outgroup taxa were included and Archaeopteryx was used to root the tree as per the

original analysis (Longrich and Currie 2009). All of the multistate characters were treated

as unordered and were equally weighted for this analysis, except character 90, as per the

original analysis. The data matrix was analyzed and tree statistics were calculated using

TNT v. 1.0 (Goloboff et al. 2003, 2008). A heuristic tree search was conducted with 1000

random sequence addition replicate Wagner trees with tree bisection-reconnection

branch-swapping, holding ten trees per replicate. Unambiguous synapomorphies were

obtained using the list synapomorphies function and mapped onto the strict consensus

tree (Fig. S6). A separate analysis was run, under the same parameters, using only

character scorings derived from the holotype maxilla (ROM 63777).

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Figure S5. Hypothesis of phylogenetic relationships of Acheroraptor temertyorum (highlighted in bold type) based on data matrix for reduced consensus tree from Turner et al. (2012). Strict consensus of the 9600 most parsimonious trees, each with a tree length of 2042 steps.

UCharacter codings for Acheroraptor termertyorum , gen. et sp. nov., in Turner et al. (2012) character-taxon matrix

Acheroraptor temertyorum????????????????????????10111???????????????????????????????????000?010??????????010010100????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????0????0????????????????11100000??000??1?????????????????00????????????????????????????????00??0?????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????

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Figure S6. Hypothesis of dromaeosaurid phylogenetic relationships based on a character-

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taxon matrix modified from Longrich and Currie (2009; see below). Strict consensus of

the 90 most parsimonious trees, each with a tree length of 237 steps, CI=0.523, RI=0.705,

RC=0.369. Unambiguous synapomorphies (with states) are mapped onto branches.

Boldface numbers indicates those characters that can be assessed in the holotype and

referred material of Acheroraptor temertyorum, gen. et sp. nov.

UCharacter list for modified Longrich and Currie (2009) character-taxon matrix

Characters 1–114 were taken from Longrich and Currie (2009). Characters 115–116 are taken from Turner et al (2012). All characters were treated as unordered.

1. Premaxilla, maxilla, and dentary bearing distinct interdental plates [0], interdental

plates fused [1], or interdental plates absent [2]

This character is modified from Longrich and Currie (2009) with the addition of

one character state [2] that distinguishes troodontids, which lack interdental plates,

from dromaeosaurids, in which they are fused to the dentigerous bones Currie and

Varricchio (2004).

2. Premaxilla elongate [0], or body of premaxilla short, no more than 15% length of

maxilla [1]

3. Premaxilla with short maxillary process [0] or elongate maxillary process separating

nasal and maxilla [1]

4. Premaxilla: body of premaxilla longer than tall [0] or at least as tall as long [1]

5. Nasal process of premaxilla projecting posterodorsally [0] or posteriorly [1]

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6. Premaxilla with limited exposure of narial fossa on lateral surface [0] or with

prominent anteroventral extension of narial fossa onto lateral surface of premaxilla

[1]

7. Maxilla does not contribute to narial fossa [0] or narial fossa expanded onto anterior

ramus of maxilla [1]

8. Maxilla, postantral wall concealed in lateral view [0] or posteriorly projecting into

antorbital fenestra and exposed in lateral view [1]

9. Maxilla, palatal shelf concealed in lateral view [0], or palatal shelf projecting dorsally

into the antorbital fenestra and visible in lateral view [1]

10. Maxilla, promaxillary fenestra subcircular and broadly exposed in lateral view [0] or

slitlike, largely concealed in the anteroventral margin of antorbital fossa [1]

11. Maxilla, anterior ramus elongate, 25% or more of the length of maxilla [0] or short,

less than 25% length of maxilla [1]

This character is scored for Bayanshiree new taxon based on IGB 100/23.

12. Maxilla, accessory antorbital fenestra large and subcircular [0] or small and

subcircular [1] or anteroposteriorly elongate [2]

13. Maxilla, accessory antorbital fenestra positioned low in antorbital fossa [0] or placed

dorsally in antorbital fossa [1]

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This character is scored “1” for the Bayanshiree Formation new taxon based on

IGB 100/23. The preserved portion of the maxilla in this specimen allows inference

of a dorsally positioned accessory antorbitabl fenestra. Acheroraptor temertyorum

has an accessory antorbital fenestra positioned very low in the antorbital fossa

compared to other dromaeosaurids, and is scored as [0].

14. Maxilla, accessory antorbital fenestra developed as a simple perforation [0] or located

in distinct fossa [1] or located in a fossa containing a deep and pit-like excavation

posterodorsal to the accessory antorbital fenestra [2] [Modified]

This character is rescored as a binary character by combining character states 1 and

2, as they form a continuum, following the argumentation of character 239 in

Turner et al. (2012).

15. Maxilla, lateral margin smooth [0] or maxilla with a distinct lip (ridge) bounding the

ventral margin of the antorbital fossa [1]

Character definition modified to point out that the ridge at the margin of the fossa

protrudes from the lateral surface of the maxilla. Scoring remains the same for all

taxa in the original analysis.

16. Maxilla, anterior ramus longer than tall [0] or short, at least as tall as long [1]

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17. Maxilla, interfenestral bar separating maxillary fenestra and antorbital fenestra:

narrow [0] or broad [1]

Velociraptor spp. and Tsaagan have relatively broad interfenestral bars.

18. Nasals concave in lateral view [0] or straight to convex in lateral view [1]

19. Frontal, orbital margin straight or smoothly concave in dorsal view [0] or postorbital

process sharply offset, and orbital margin L-shaped in dorsal view [1]

20. Frontal notched to receive lacrimal: absent [0] or present [1]

21. Frontal, supratemporal fossa smooth [0] or supratemporal fossa with a distinct pit [1]

22. Frontal, supratemporal fossa restricted to the lateral half of the frontal [0] or

supratemporal fossa extends medially [1]

23. Jugal, suborbital ramus slender [0] or dorsoventrally deep and robust [1]

24. Jugal, postorbital process slender; jugal triradiate [0] or postorbital process broad, and

jugal triangular [1]

25. Quadratojugal with straight ascending ramus [0] or ascending ramus bowed anteriorly

[1]

26. Quadrate shaft pierced by large foramen: present [0] or absent [1]

27. Quadrate shaft straight or weakly curved in lateral view [0] or strongly bowed

anteriorly in lateral view [1]

28. Exoccipital, caudal surface with a bowl-like depression containing the exits of cranial

nerves X and XII: absent [0], or present [1]

29. Exoccipital, paroccipital processes of exoccipital project ventrolaterally [0] or

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laterally [1]

30. Basioccipital tubera, caudal surfaces flat or smoothly concave [0] or basioccipital

tubera with distinct, ovoid depressions on the caudal surface [1]

31. Basioccipital tubera separated by weak notch [0] or separated by a deep, broad, U-

shaped ventral notch [1]

32. Basisphenoid recess with paired openings: absent [0] or present [1]

33. Prominent lateral depression of braincase bounded by otosphenoidal crest: absent [0]

or present [1]

34. Foramen magnum subcircular [0] or distinctly taller than wide [1]

35. Dentary subtriangular, with dorsal and ventral margins diverging posteriorly [0] or

dentary dorsal and ventral margins subparallel [1]

Velociraptor mongoliensis is considered to have subparallel dentary margins in

lateral view, and is scored as [1]

36. Dentary with prominent groove along the length of the lateral surface [0] or lateral

groove reduced anteriorly or absent [1]

37. Dentary straight or weakly curved in lateral view [0] or strongly bowed, with curved

dorsal and ventral margins [1]

In this analysis, Shanag and Deinonychus are considered to have relatively straight

dentaries, and are thus scored as [0], rather than the derived state in the original

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analysis.

38. Dentary with distinct midlength constriction and terminal expansion: absent [0] or

present [1]

39. Articular with tall, columnar process on retroarticular process: absent [0] or present

[1]

40. Skull short [0] or elongate, at least 125% length of femur [1]

41. Teeth constricted between crown and root [0] or constriction absent [1]

42. Premaxillary and anterior dentary teeth unserrated [0] or bearing denticles on

posterior carina [1]

43. Premaxillary teeth 2–4 subequal in size [0] or second premaxillary tooth larger than

third and fourth [1]

44. Maxillary teeth number fewer than 20 [0] or numbering at least 20 [1]

45. Maxillary teeth strongly raked posteriorly: absent [0] or present [1]

46. Maxillary teeth subequal in length along the jaw [0] or posterior maxillary teeth

elongate and fanglike, approximately 200% the length of anteriormost maxillary

teeth [1]

47. Maxillary and posterior dentary teeth unserrated [0] or bearing denticles on posterior

carina only [1] or bearing denticles on anterior and posterior carina [2]

48. Maxillary and posterior dentary teeth, denticles: anterior denticles smaller (or absent)

than posterior denticles [0] or anterior and posterior denticles subequal in size [1]

(Modified character definition.)

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49. Anterior dentary teeth closely packed: absent [0] or present [1]

50. Vertebral, Axis bearing short epipophyses [0] or elongate axial epipophyses that

project laterally beyond postzygapophyses [1]

51. Vertebral, cervical, carotid processes present [0] or carotid processes absent [1]

52. Vertebral, cervical, with low neural spines [0] or cervical neural spines at least as tall

as long anteroposteriorly [1]

53. Vertebral, dorsal, parapophyses short [0] or borne on elongate pedicels [1]

54. Vertebral, dorsal, pneumatopores absent [0] or present on dorsal centra [1]

55. Vertebral, dorsal, neural spines low, height does not exceed anteroposterior length [0]

or taller than long anteroposteriorly [1]

56. Vertebral, dorsal, neural arch bearing prominent anterior fossae on either side of

neural canal: absent [0] or present [1]

57. Vertebral, dorsal, centra of posterior dorsals elongate [0] or short and massive, length

of centrum less than diameter [1]

58. Vertebral, dorsal, distal end of neural spines transversely expanded by at least 200%

to form a distinct spine table: absent [0] or present [1]

59. Vertebral, sacral, 5 vertebrae incorporated into sacrum [0] or sacrum incorporating at

least 6 vertebrae [1]

60. Vertebral, sacral, lack pneumatopores [0] or pneumatopores present in one or more

sacral vertebrae [1]

61. Vertebral, caudal, distal caudal centra bearing prominent lateral depressions [0] or

lateral surfaces of centra flat or convex [1]

62. Vertebral, caudal, distal caudals greatly elongated, more than 200% the length of

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proximal caudals [0] or moderately elongate, no more than 200% the length of the

proximal caudals [1]

63. Vertebral, caudal, distal caudal vertebrae with a convex or flat dorsal surface [0] or

bearing a prominent dorsal groove [1]

64. Vertebral, caudal, prezygapophyses short [0] or elongate [1] or extended by ossified

tendons of caudal epaxial muscles [2]

65. Sternal plates unossified [0] or ossified [1]

66. Furcula, interclavicular angle less than 90° [0] or at least 90° [1]

67. Coracoid highly flexed in lateral view, with dorsal and ventral rami of coracoid

forming an angle of 90°–100° [0] or coracoids weakly flexed, forming an angle

larger than 100° [1]

68. Coracoid elongate, taller than wide [0] or short, at least as wide as tall [1]

69. Humerus elongate, at least 75% length of femur [0] or shortened, humerus less than

75% length of the femur [1]

70. Humerus, internal tuberosity proximodistally short [0] or proximodistally elongate,

about 50% the length of deltopectoral crest [1]

71. Humerus, proximal shaft with prominent longitudinal ridge on posterior surface:

absent [0] or present [1]

72. Manual phalanx I-1 strongly bowed in medial view [0], weakly curved or straight [1]

73. Manual phalanx III-1 elongate, at least 75% length of III-3: absent [0] or present [1]

74. Metacarpal I no more than 33% length of mtc II [0] or metacarpal I more than 33%

length of MC II [1]

75. Manual phalanx I-1 elongate [0] or short, combined length of metacarpal I and

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manual phalanx I-1 <MC II [1]

76. Ilium, anterior wing 200% length of posterior wing [0] or short, less than twice length

of posterior blade [1]

77. Ilium, end of anterior wing rounded or straight [0], or with notched cranial margin [1]

78. Ilium, cuppedicus ridge ends on pubic peduncle [0] or extends posteriorly to

acetabulum [1]

79. Ilium, medial antiliac shelf short [0] or elongate, approaching length of posterior wing

[1]

80. Ilium, posterior wing of ilium slender, shallower than anterior wing [0] or posterior

wing as deep or deeper than anterior wing [1]

81. Ilium, posterior wing longer than tall [0] or posterior wing at least as tall as long [1]

82. Ilium with acuminate caudal margin [0] or brevis shelf lobate and projecting

posteriorly beyond postacetabular lamina [1] or brevis shelf notched in lateral view

[2]

83. Ilium, posterior wing with straight or convex dorsal margin [0] or concave dorsal

margin [1]

84. Ilium, pubic peduncle narrow in lateral view [0] or broad, anteroposterior width

approximately 200% of height [1]

85. Pubis, distal end with prominent posterior expansion [0] distal end spatulate, both

anterior and posterior expansions absent [1] or with prominent anterior and

posterior expansions [2]

86. Pubis, shaft straight or gently curved [0] or distal end of shaft strongly bent

posteriorly [1]

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87. Pubis, lateral surface of shaft smooth or bearing a ridge [0] or with enlarged tubercles

or processes [1]

88. Pubis, Pubic apron extends less than 50% length of pubis [0] or pubic apron elongate,

at least 50% length of pubis [1]

89. Ischium short, no more than 50% length of pubis [0] or elongate, more than 50%

length of pubis [1]

90. Ischium, obturator process located at distal end of shaft [0] or located at midshaft [1]

or proximally located [2]

91. Ischium, proximodorsal process present [0] or absent [1] or hypertrophied [2]

92. Ischium with distal dorsal process prominent [0] or highly reduced or absent [1]

93. Ischium, lateral ridge on shaft absent [0] or present [1]

94. Ischium, obturator process elongate and spur-like [0] or broad and flange-like [1]

95. Ischium with obturator process separated from ischial shaft by caudal notch [0] or

confluent [1]

96. Ischium, distal end tapers to a narrow point [0] or broadly expanded, blunt or

spatulate end [1]

97. Ischium, shaft mediolaterally compressed [0] or subcircular in section [1]

98. Ischium, ridge on medial surface connecting proximodorsal process and iliac

peduncle: absent [0], or present [1]

99. Femur with femoral head projecting dorsomedially or medially relative to shaft [0] or

femoral head projects ventromedially [1]

100. Metatarsal II and phalanx II-1 articulate via ginglymoid articulation: absent [0] or

present [1]

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101. Metatarsal II, subequal to IV in length [0] or markedly shorter than IV [1]

102. Metatarsal II, distal condyles broad, subequal to III in width: absent [0] or present

[1]

103. Metatarsal III, plantar surface broadly exposed [0] or metatarsal III largely covered

by metatarsal III and IV in ventral view [1]

104. Metatarsal III, dorsal surface of shaft flat or rounded [0] or with prominent

longitudinal sulcus [1]

105. Metatarsal IV, distal surface trochlear to planar [0] or condyle strongly ball-shaped

[1]

106. Metatarsal IV, prominent flange on caudolateral surface of shaft: present [0] or

highly reduced or absent [1]

107. Metatarsal IV, lateral flange on proximal end of shaft: absent [0] or present [1]

108. Metatarsal IV, ventral surface with a prominent tuber proximal to distal articular

surface: absent [0] or present [1]

109. Pedal phalanx II-1 elongate [0] or short and robust, shaft length does not exceed

200% the diameter of the distal condyle [1]

110. Pedal phalanx II-2 proximoventral heel: short [0] or with elongate caudal projection

[1]

111. Pedal phalanx II-2 slender to moderately robust [0] or extremely massive, shaft

diameter at least 50% of shaft length [1]

112. Pedal phalanx II-2 subequal to or longer than, II-1 [0] or significantly shorter than

II-1 [1]

113. Pedal phalanx II-2 with deep collateral ligament pits [0] or ligament pits reduced [1]

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114. Pedal phalanx II-3; lateral and medial vascular grooves at same level [0] or lateral

groove dorsally displaced and medial groove ventrally displaced [1]

115. Maxilla, accessory antorbital fossa situated posterior to anterior border of antorbital

fossa [0] or situated close to anterior border [1] [from Turner et al. (2012):

character 28, reversed polarity]

116. Maxilla, jugal process, ventral to the external antorbital fenestra dorsoventrally

narrow [0] or dorsoventrally wide [1] [from Turner et al. (2012): character 238]

UCharacter codings for modified Longrich and Currie (2009) character-taxon matrix

Archaeopteryx

000000000000000000000000??000???0?1000000000000100?0000?0000

000000000000000000?000000000000000000?001100??0?00000000

Sinovenator changii

?1000010000200000?0?0000?100000?010010??000100111???000?0000

??????11??????????0??0?0?001000001??000010100010?00?0000

Byronosaurus jaffei

2100111????2000010???????????00?110010??00?101011??000??????

0?1???????????????????????????????????????????????????00

Troodon

2?0???10010210001?[01]000???0100000110000??01?100211?000010?1?0

1?11?????00?????????????2000?1110110000010100000011100?0

Mahakala omnogovae

Page 25: link. · Web viewThis character is rescored as a binary character by combining character states 1 and 2, as they form a continuum, following the argumentation of character 239 in Turner

??????????????????0000????0?0???00???????????????0????????10

?100?????????????0??0000??????????????01?001?????00?01??

Rahonavis ostromi

????????????????????????????????????????????????????11000011

0001????0??????0011000110000002?00??000111011000000101??

Unenlagia comahuensis

????????????????????????????????????????????????????111101??

????????111????0011011110101012?01??001?????????????????

Unenlagia paynemili

????????????????????????????????????????????????????????0???

?????????11?????????111?2101????????????????????0???????

Buitreraptor gonzalezorum

1??????10??20?0?001?0?00?00???????0001?110??0?010?0?100?00??

0?01?00?011?????????011??1???10110000?11011??00???????00

Neuquenraptor argentinus

????????????????????????????????????????????????????????????

???????????????????????????????????????10?11?00000010???

Austroraptor cabazai

0?0???010002000010110100??????????0011?110?100010?0?11??01??

????????11???????????????????????????????????????01?0?00

Microraptor

101100????1???1???????????????????1110?0101001110?00100?000?

00?21[01]??00001011?0?000?01110000000000?01111?100?00000?00

Page 26: link. · Web viewThis character is rescored as a binary character by combining character states 1 and 2, as they form a continuum, following the argumentation of character 239 in Turner

Graciliraptor lujiatensis

?????????????????????????????????????????0????20????????0???

0?02????????101????????????????????????1111?????00000???

Shanag ashile

1?1???000?1111100?????????????????0000??10??01110???????????

??????????????????????????????????????????????????????00

Sinornithosaurus millennii

1011??0???11111??00111??0?????????101010101001200????0??000?

???21?0001?010111?0??0??1110000000000??1??1?100??0000??0

Hesperonychus elizabethae

????????????????????????????????????????????????????????????

?????????????????0???0001110????????????????????????????

Saurornitholestes langstoni

1?11?000110111010?1111??110???????1110101?1000200???11111?[01]1

1?021?11010??????????????????00111100101?0001000110?0100

Atrociraptor marshalli

10110000110111010?????????????????1100??111010200???????????

??????????????????????????????????????????????????????11

Bambiraptor feinbergi

101100000011110101?0?1001110?010??1110?01??010110?1111111001

10021111010110010000000000010001111001011000100011000100

Deinonychus antirrhopus

1011000001011101011?11100??1??????11001?11?010200111111011??

Page 27: link. · Web viewThis character is rescored as a binary character by combining character states 1 and 2, as they form a continuum, following the argumentation of character 239 in Turner

1102??11110101011000000020010111111100011000110011010100

Dromaeosaurus albertensis

1?1???0?001???01??110110010010000011001?11?000210???????????

???????????????????????????????????????1?0??1?1111111?01

Utahraptor ostrommaysorum

???100??????????????????????????????????111????1????11101???

1?02??11?????????00?0200?????201011?1001?000?1111????1??

Achillobator giganticus

1?1???0?0?0???010???????????????????????1??00021??11111?1???

1?01???????????1100112002001120101111001?0?0?????11?1?01

Velociraptor mongoliensis

10101101010101001011111010011111001110?01110002001111[01]1?1110

11021111110101011001000020011111111100011000111111000100

Velociraptor osmolskae

1?????0?000101001???????????????????????1??00010????????????

??????????????????????????????????????????????????????10

Tsaagan mangas

?010110101010?00101?011100110011010110101110001101?1??1?????

?1?21???1????????????????00???????????????????????????11

Adasaurus mongoliensis

??????????????????????11??1???????????????????????????1?1???

???????????????110010?00200?1111?110????????????11?1????

Acheroraptor temertyorum

Page 28: link. · Web viewThis character is rescored as a binary character by combining character states 1 and 2, as they form a continuum, following the argumentation of character 239 in Turner

1?????01?10101000?????????????????1110??1??00020????????????

??????????????????????????????????????????????????????01

Bayanshiree Fm

1010?10?0?1?1?01??????????????????1110??1?1000?10???????????

??????????????????????????????????????????????????????01

Balaur bondoc

????????????????????????????????????????????????????111??1?0

????1?????01010??1???????1011???0??????00???1?1?1?001???

Page 29: link. · Web viewThis character is rescored as a binary character by combining character states 1 and 2, as they form a continuum, following the argumentation of character 239 in Turner

7. References for Electronic Supplementary Material

Burnham DA, Derstler KL, Currie PJ, Bakker RT, Zhou Z-H, Ostrom JH (2000)

Remarkable new birdlike dinosaur (Theropoda: Mantraptora) from the Upper

Cretaceous of Montana. U Kans Paleontol Cont 13:1–14

Csiki Z, Vremir M, Brusatte SL, Norell MA (2010) An aberrant island-dwelling theropod

dinosaur from the Late Cretaceous of Romania. PNAS 107:15357–15361

Currie PJ, Varricchio DJ (2004) A new dromaeosaurid from the Horseshoe Canyon

Formation (Upper Cretaceous) of Alberta, Canada. In: Currie PJ, Koppelhus EB,

Shugar MA, Wright JL (eds) Feathered dragons. Indiana University Press,

Bloomington, IN, pp 112 –132

Godefroit P, Currie PJ, Hong L, Yong SC, Dong Z (2008) A new species of Velociraptor

(Dinosauria: Dromaeosauridae) from the Upper Cretaceous of northern China. J

Vert Paleontol 28:432–438

Goloboff PA, Farris JS, Nixon KC (2003) TNT: Tree analysis using new technologies.

http://www.zmuc.dk/public/phylogeny

Goloboff PA, Farris JS, Nixon KC (2008) TNT, a free program for phylogenetic analysis.

Cladistics 24:774-786

JMP. JMP Version 5. 2002 SAS Institute Inc., Cary, North Carolina, USA.

Kirkland JI, Burge D, Gaston R (1993) A large dromaeosaur (Theropoda) from the Lower

Cretaceous of eastern Utah. Hunteria 2(10):1–16

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Larson DW, Currie PJ (2013) Multivariate analyses of small theropod dinosaur teeth and

implications for paleoecological turnover through time. PLoS ONE 8(1): e54329.

doi: 10.1371/journal.pone.0054329

Longrich NR, Currie PJ (2009) A microraptorine (Dinosauria–Dromaeosauridae) from

the Late Cretaceous of North America. PNAS 106:5002–5007

Miyashita, T, Currie PJ (2009) A new phylogeny of the Tyrannosauroidea (Dinosauria,

Theropoda). J Vert Paleont 29(3): 149A

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dromaeosaurid theropod from Ukhaa Tolgod (Ömnögov, Mongolia). Am Mus

Novit 3545:1–50

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Soc B 276:1101–1107

Perle A, Norell MA, Clark JM (1999) A new maniraptoran theropod—Achillobator

giganticus (Dromaeosauridae)—from the Upper Cretaceous of Burkhant,

Mongolia. Ulaan Baatar. Contrib Dept Geol Natl Univ Mongolia 101:1–105

Smith JB, Vann DR, Dodson P (2005) Dental morphology and variation in theropod

dinosaurs: implications for the taxonomic identification of isolated teeth. Anat Rec

Part A 285A:699–736

Turner AH, Hwang SH, Norell MA (2007) A small derived theropod from Öösh, Early

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Cretaceous, Baykhangor Mongolia. Am Mus Novit 3557:1–27

Turner AH, Makovicky PJ, Norell MA (2012) A review of dromaeosaurid systematics

and paravian phylogeny. B Am Mus Nat Hist 371:1–206

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Cretaceous Yixian Formation of western Liaoning. Vertebrat PalAsiatic 42(2):11–

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(Dinosauria: Theropoda: Dromaeosauridae) from the Yixian Formation of

Liaoning, China. Can J Earth Sci 38:1739–1752

Xu X, Wang X-L, Wu X-C (2000) A dromaeosaurid dinosaur with a filamentous

integument from the Yixian Formation of China. Nature 401:262–266

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Theropoda) from the Upper Cretaceous Wulansuhai Formation of Inner Mongolia,

China. Zootaxa 2403:1–9

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Jehol Group of China with implications for early dromaeosaurid evolution. Proc R

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