Find research datasets worth reusing

Fig. 11 in Systematic Revision Of The North American Syntropine Vaejovid Scorpions With A Subaculear Tubercle, Konetontli González-Santillán And Prendini, 2013

Fig. 11. Konetontli González-Santillán and Prendini, 2013, metasomal segments I–V, ventral aspect. A. Konetontli acapulco (Armas and Martín-Frías, 2001), holotype ³ (CNAN T0174). B. Konetontli chamelaensis (Williams, 1986), holotype ³ (CAS). C. Konetontli ignes, n. sp., holotype ♀ (CNAN T0885). D. Konetontli ilitchi, n. sp., holotype ♀ (CNAN T0887). E. Konetontli juxtlahuaca, n. sp., holotype ³ (CNAN T0889). Scale bars 5 1 mm.

Fig. 5 in Systematic Revision Of The North American Syntropine Vaejovid Scorpions With A Subaculear Tubercle, Konetontli González-Santillán And Prendini, 2013

Fig. 5. Konetontli González-Santillán and Prendini, 2013, carapaces, dorsal aspect. A. Konetontli acapulco (Armas and Martín-Frías, 2001), holotype ³ (CNAN T0174). B. Konetontli chamelaensis (Williams, 1986), holotype ³ (CAS). C. Konetontli ignes, n. sp., holotype ♀ (CNAN T0885). D. Konetontli ilitchi, n. sp., holotype ♀ (CNAN T0887). Scale bars 5 1 mm (A), 0.5 mm (B, C, D).

Fig. 9 in Systematic Revision Of The North American Syntropine Vaejovid Scorpions With A Subaculear Tubercle, Konetontli González-Santillán And Prendini, 2013

Fig. 9. Konetontli González-Santillán and Prendini, 2013, sternum, genital operculum and pectines, ventral aspect. A. Konetontli ignes, n. sp., holotype ♀ (CNAN T0885). B. Konetontli migrus, n. sp., holotype ³ (CNAN T0891). C. Konetontli kuarapu (Francke and Ponce-Saavedra, 2005), paratype ³ (AMNH). D. Konetontli zihuatanejensis (Baldazo-Monsivaiz, 2003), comb. nov., neotype ³ (CNAN T0893). E. Konetontli chamelaensis (Williams, 1986), holotype ³ (CAS). F. Konetontli pattersoni (Williams and Haradon, 1980), ³ (AMNH). Scale bars 5 0.5 mm.

Fig. 14 in Systematic Revision Of The North American Syntropine Vaejovid Scorpions With A Subaculear Tubercle, Konetontli González-Santillán And Prendini, 2013

Fig. 14. Konetontli González-Santillán and Prendini, 2013, telson, lateral aspect. A. Konetontli acapulco (Armas and Martín-Frías, 2001), holotype ³ (CNAN T0174). B. Konetontli chamelaensis (Williams, 1986), holotype ³ (CAS). C. Konetontli ignes, n. sp., holotype ♀ (CNAN T0885). D. Konetontli ilitchi, n. sp., holotype ♀ (CNAN T0887). E. Konetontli juxtlahuaca, n. sp., holotype ³ (CNAN T0889). F. Konetontli kuarapu (Francke and Ponce-Saavedra, 2005), paratype ³ (AMNH). G. Konetontli migrus, n. sp., holotype ³ (CNAN T0891). H. Konetontli nayarit (Armas and Martín-Frías, 2001), holotype ³ (CNAN T0177). I. Konetontli pattersoni (Williams and Haradon, 1980), ³ (AMNH). J. Konetontli zihuatanejensis (Baldazo-Monsivaiz, 2003), comb. nov., neotype ³ (CNAN T0893). Scale bars 5 1 mm.

Fig. 6 in Systematic Revision Of The North American Syntropine Vaejovid Scorpions With A Subaculear Tubercle, Konetontli González-Santillán And Prendini, 2013

Fig. 6. Konetontli González-Santillán and Prendini, 2013, carapaces, dorsal aspect. A. Konetontli juxtlahuaca, n. sp., holotype ³ (CNAN T0889). B. Konetontli kuarapu (Francke and Ponce-Saavedra, 2005), paratype ³ (AMNH). C. Konetontli migrus, n. sp., holotype ³ (CNAN T0891). D. Konetontli nayarit (Armas and Martín-Frías, 2001), holotype ³ (CNAN T0177). Scale bars 5 0.5 mm.

Fig. 19 in Systematic Revision Of The North American Syntropine Vaejovid Scorpions With A Subaculear Tubercle, Konetontli González-Santillán And Prendini, 2013

Fig. 19. Konetontli acapulco (Armas and Martín-Frías, 2001), holotype ³ (CNAN T0174), dextral pedipalp femur (A), patella (B–E), and chela (F–I). A, B, F. Dorsal aspect. C, G. Retrolateral aspect. D, H. Ventral aspect. E, I. Prolateral aspect. Scale bars 5 0.5 mm.

Fig. 3 in Systematic Revision Of The North American Syntropine Vaejovid Scorpions With A Subaculear Tubercle, Konetontli González-Santillán And Prendini, 2013

Fig. 3. Map of central Mexico, plotting known locality records for four species in the vaejovid scorpion genus Konetontli González-Santillán and Prendini, 2013, based on data collected in the present study: Konetontli kuarapu (Francke and Ponce-Saavedra, 2004) (squares), Konetontli migrus, n. sp. (triangle), Konetontli nayarit (Armas and Martín-Frías, 2001) (circles), and Konetontli zihuatanejensis (Baldazo- Monsivaiz, 2003), comb. nov. (crosses).

Fig. 30. Konetontli migrus, n in Systematic Revision Of The North American Syntropine Vaejovid Scorpions With A Subaculear Tubercle, Konetontli González-Santillán And Prendini, 2013

Fig. 30. Konetontli migrus, n. sp., holotype ³ (CNAN T0891), dextral pedipalp femur (A), patella (B– E), and chela (F–I). A, B, F. Dorsal aspect. C, G. Retrolateral aspect. D, H. Ventral aspect. E, I. Prolateral aspect. Scale bars 5 0.5 mm.

Fig. 1 in Systematic Revision Of The North American Syntropine Vaejovid Scorpions With A Subaculear Tubercle, Konetontli González-Santillán And Prendini, 2013

Fig. 1. Konetontli acapulco (Armas and Martín-Frías, 2001), adult female from Cumbres de Llano Largo, Guerrero, Mexico, habitus in life.

Fig. 2 in Systematic Revision Of The North American Syntropine Vaejovid Scorpions With A Subaculear Tubercle, Konetontli González-Santillán And Prendini, 2013

Fig. 2. Map of central Mexico, plotting known locality records for five species in the vaejovid scorpion genus Konetontli González-Santillán and Prendini, 2013, based on data collected in the present study: Konetontli acapulco (Armas and Martín-Frías, 2001) (circles), Konetontli chamelaensis (Williams, 1986) (square), Konetontli ignes, n. sp. (triangle), Konetontli ilitchi, n. sp. (pentagons), and Konetontli juxtlahuaca, n. sp. (cross).

Fig. 82. Character changes associated with avialan shoulder girdle evolution. A in A Review Of Dromaeosaurid Systematics And Paravian Phylogeny

Fig. 82. Character changes associated with avialan shoulder girdle evolution. A, right coracoid of Deinonychus antirrhopus (YPM 5236; top) and Sinovenator changii (IVPP 12583; bottom); B, Sapeornis chaoyangensis (IVPP V13396) in ventral view; C, Jeholornis prima (IVPP V13274) in ventral view; D, Jixiangornis orientalis (CAGS uncataloged) in dorsal view.

Fig. 81 in A Review Of Dromaeosaurid Systematics And Paravian Phylogeny

Fig. 81. Strict consensus cladogram of Coelurosauria based on the Xu et al. (2011) matrix having modified the scorings for their characters 322 and 366. Percentages indicate the frequencies of occurrence in the set of most parsimonious trees for the positions indicted by the arrows.

Fig. 78 in A Review Of Dromaeosaurid Systematics And Paravian Phylogeny

Fig. 78. Adam's consensus cladogram of exploratory phylogenetic analysis including Pedopenna daohugouensis and Epidendrosaurus ningchengensis.

Fig. 79 in A Review Of Dromaeosaurid Systematics And Paravian Phylogeny

Fig. 79. Reduced strict consensus cladogram of Paraves showing the number of extra steps required to place Rahonavis as basal within Avialae (7 steps longer), or to place it within Avialae in a position more derived than Archaeopteryx (11 extra steps).

Fig. 73 in A Review Of Dromaeosaurid Systematics And Paravian Phylogeny

Fig. 73. Simplified cladogram showing manipulated paravian relationships. Constraining Troodontidae to be sister group of Avialae requires 1 additional step.

Fig. 72 in A Review Of Dromaeosaurid Systematics And Paravian Phylogeny

Fig. 72. Simplified cladogram showing manipulated paravian relationships. Constraining Dromaeosauridae to be sister group of Avialae requires 4 additional steps.

Fig. 76. Results from exploratory phylogenetic analysis including Epidendrosaurus ningchengensis. A, reduced strict consensus cladogram. B in A Review Of Dromaeosaurid Systematics And Paravian Phylogeny

Fig. 76. Results from exploratory phylogenetic analysis including Epidendrosaurus ningchengensis. A, reduced strict consensus cladogram. B, detail of the base of Avialae showing the number of additional steps required to constrain Epidendrosaurus and Epidexipteryx are sister taxa.

Fig. 74 in A Review Of Dromaeosaurid Systematics And Paravian Phylogeny

Fig. 74. Modified cladogram showing manipulated paravian relationships. Constraining Troodontidae to be paraphyletic relative to Avialae with Xiaotingia + Anchiornis and Jinfengopteryginae as successive sister taxa to Avialae requires 12 additional steps.

Fig. 77 in A Review Of Dromaeosaurid Systematics And Paravian Phylogeny

Fig. 77. Reduced strict consensus cladogram of exploratory phylogenetic analysis including Pedopenna daohugouensis and Epidendrosaurus ningchengensis.

Fig. 69 in A Review Of Dromaeosaurid Systematics And Paravian Phylogeny

Fig. 69. Bremer analysis. Strict consensus cladogram of basal coelurosaurs. Values indicate Bremer support derived from the BREMER.RUN script supplied by TNT.