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Fig. 17 in Phylogenetic Studies On Didelphid Marsupials Ii. Nonmolecular Data And New Irbp Sequences: Separate And Combined Analyses Of Didelphine Relationships With Denser Taxon Sampling

Fig. 17. Strict consensus of 2161 equally mostparsimonious trees obtained by a heuristic analysis of nonmolecular characters described in this report (see table 4 for summary dataset characteristics and tree statistics). Bremer support and bootstrap values are provided above and below each branch, respectively. Outgroup taxa are indicated with asterisks.

Fig. 18 in Phylogenetic Studies On Didelphid Marsupials Ii. Nonmolecular Data And New Irbp Sequences: Separate And Combined Analyses Of Didelphine Relationships With Denser Taxon Sampling

Fig. 18. Strict consensus of 252 equally mostparsimonious trees obtained by a heuristic analysis of IRBP sequences described in this report (see table 4 for summary dataset characteristics and tree statistics). Bremer support and bootstrap values are provided above and below each branch, repectively. For simplicity, conspecific sequences (analyzed separately in PAUP*) have been condensed to single terminals in this diagram. Outgroup taxa are indicated with asterisks. All parsimonyequivalent resolutions of the basal ingroup polytomy are shown in figure 19A–E.

Fig. 19 in Phylogenetic Studies On Didelphid Marsupials Ii. Nonmolecular Data And New Irbp Sequences: Separate And Combined Analyses Of Didelphine Relationships With Denser Taxon Sampling

Fig. 19. All equally mostparsimonious resolutions of the basal didelphine polytomy in figures 18 and 21. A, Resolution supported by 72 mostparsimonious trees (MPTs) from the IRBP1 analysis and 6 MPTs from the IRBP2 analysis; B, resolution supported by 72 MPTs from the IRBP1 analysis and 6 MPTs from the IRBP2 analysis; C, resolution supported by 36 MPTs from the IRBP1 analysis and 3 MPTs from the IRBP2 analysis; D, resolution supported by 36 MPTs from the IRBP1 analysis, 6 MPTs from the IRBP2 analysis, and 8 MPTs from the combined analysis; E, resolution supported by 36 MPTs from the IRBP1 analysis, 6 MPTs from the IRBP2 analysis, and 8 MPTs from the combined analysis; F, resolution supported by 18 MPTs from the combined analysis only.

Fig. 13 in Phylogenetic Studies On Didelphid Marsupials Ii. Nonmolecular Data And New Irbp Sequences: Separate And Combined Analyses Of Didelphine Relationships With Denser Taxon Sampling

Fig. 13. Anterolingual views of left M3 illustrating taxonomic differences in cingular morphology. Left, Marmosa murina (AMNH 272870) with preprotocrista and anterolabial cingulum joined to form a continuous shelf along the anterior margin of the tooth crown. Right, Monodelphis adusta (AMNH 272781) with separate crista and cingulum (no continuous shelf).

FIG. 4. — A, B, Sphaerocypraea tardivelae n in Nouveaux taxons et discussion de la systématique des genres correspondants d'Ovulidae (Mollusca, Caenogastropoda) de l'Éocène inférieur de Gan (France)

FIG. 4. — A, B, Sphaerocypraea tardivelae n. sp., vue ventrale et vue latérale externe, holotype (déformé) MNHN-LP n° R63014 (coll. D. Ledon), h. 48,8 mm, Gan (La Tuilerie); C, D, Sphaerocypraea incomparabilis (Briano, 1993), vue ventrale et détail du pli terminal, spécimen USNM, h. 80,3 mm, « off Somalia » (« north-western Indian Ocean »); E, Sphaerocypraea jacksonensis (Johnson, 1899), détail du pli terminal, spécimen MNHN-BIMM (coll. L. & C. Dolin), h. 85 mm, Jackson (Town Creek), Hinds County (Mississippi), détail. Échelles: 5 mm.

FIG. 2 in Nouveaux taxons et discussion de la systématique des genres correspondants d'Ovulidae (Mollusca, Caenogastropoda) de l'Éocène inférieur de Gan (France)

FIG. 2. — Analyse biométrique du rapport entre hauteur et diamètre maximal (A) et du rapport entre hauteur/diamètre maximal et diamètre maximal/nombre de dents labrales (B) chez Cypraea kerniana (Anderson & Hanna, 1925) synonyme junior de Prionovolva (Grovesia) mathewsonii (Gabb, 1869) () et chez P. (G.) ganensis n. sp. ().

FIG. 1. — A-D in Nouveaux taxons et discussion de la systématique des genres correspondants d'Ovulidae (Mollusca, Caenogastropoda) de l'Éocène inférieur de Gan (France)

FIG. 1. — A-D, Prionovolva (Grovesia) ganensis n. sp.; A, B, vue ventrale et vue latérale externe, holotype MNHN-LP n° R63009 (coll. L. & T. Dolin), h. 13,4 mm, Gan (La Tuilerie); C, D, vue ventrale et détail du pli teminal, paratype MNHN-LP n° R63011a (coll. D. Merle), h. 13 mm, Gan (La Tuilerie); E, F, Prionovolva (Prionovolva) nubeculata (Adams, 1854), vue ventrale et détail du pli terminal, spécimen MNHN-BIMM (coll. L. Dolin), h. 18,6 mm, Nouméa (chenal îlot Maître), Nouvelle-Calédonie; G, Habuprionovolva umbilicata (Sowerby, 1849), vue ventrale, spécimen MNHN-BIMM (coll. L. Dolin), h. 9,5 mm, Honshu Isl. (Kii channel), Wakayama Prefecture (Japon). Échelles: 5 mm.

FIG. 5. — A, B, Simnia pacaudi n in Nouveaux taxons et discussion de la systématique des genres correspondants d'Ovulidae (Mollusca, Caenogastropoda) de l'Éocène inférieur de Gan (France)

FIG. 5. — A, B, Simnia pacaudi n. sp., vue ventrale et vue latérale externe, holotype MNHN-LP n° R63015 (coll. J.-M. Pacaud), h. 18,9 mm, Gan (La Tuilerie); C, D, Sandalia vibrayana (Raincourt, 1870), vue ventrale et détail du pli terminal, spécimen MNHN-BIMM (coll. L. Staadt), h. 10,2 mm, Mons-en-Laonnois (hameau des Creuttes), Aisne (France); E, F, Simnia brevirostris (Schumacher, 1817), vue ventrale et détail du pli terminal, spécimen MNHN-BIMM (coll. L. Dolin), h. 21,3 mm, Cebu Isl. (off Punta Engaño), Philippines; G, Phenacovolva angasi (Reeve, 1865), vue ventrale, spécimen MNHN-BIMM (coll. L. Dolin), h. 15,9 mm, Cebu Isl. (off Punta Engaño), Philippines. Échelles: 5 mm.

FIG. 3. — A-C, Luponovula merlei n in Nouveaux taxons et discussion de la systématique des genres correspondants d'Ovulidae (Mollusca, Caenogastropoda) de l'Éocène inférieur de Gan (France)

FIG. 3. — A-C, Luponovula merlei n. sp.; A, B, vue ventrale et vue latérale externe, holotype MNHN-LP n° R63012 (coll. L. & T. Dolin), h. 39 mm, Gan (La Tuilerie); C, vue ventrale reconstituant (tirés) le galbe initial, paratype (comprimé latéralement) MNHN-LP n° R63013 (coll. J.-M. Pacaud), h. 45,5 mm, Gan (La Tuilerie); D, E, Luponovula normalis (Gregorio, 1880), vue ventrale et détail du pli terminal, spécimen (incomplet, pédomorphisé) MNHN-LP n°J 03872 (coll. E. Hébert & E. Munier-Chalmas), h. 46,4 mm, San Giovanni Ilarione (Bosco del Prete), Vicenza (Italie). Échelles: 5 mm.

Figure 6 in Variation in elasmoid fish scale patterns is informative with regard to taxon and swimming mode

Figure 6. Scaled body section of slices (in grey) in the different longitudinal (A, C, and P) and transversal zones (1, 2, and 3). Angles increase from the central areas to the extremes. The lower insets show the transformations between the overall scale consensus shape (reference) and the shapes represented by the extremes of principal component 1 (PC1) (targets; leftmost = -ve PC1 scores; rightmost = +ve PC1 scores; see Fig. 4), which broadly reflect anterior–posterior variation in scale shape.

Figure 4 in Variation in elasmoid fish scale patterns is informative with regard to taxon and swimming mode

Figure 4. First two principal components (PCs) of shape labelled by species. Thin plate spline transformation grids for the extreme points of each PC are shown; these are superimposed on the shapes predicted when the average landmark configuration of all specimens is deformed into that of a hypothetical specimen positioned at the extreme of the PC of interest.

Figure 3 in Variation in elasmoid fish scale patterns is informative with regard to taxon and swimming mode

Figure 3. First two principal components of scale shape. A, labelled by longitudinal zones. B, labelled by transverse zones.

Figure 6 in High molecular and phenotypic diversity in the Merodon avidus complex (Diptera, Syrphidae): cryptic speciation in a diverse insect taxon

Figure 6. Scatterplot of individual scores from the canonical variate analysis (CVA) of female specimens of: A, sympatric populations of Merodon avidus A and M. avidus B from Dubašnica Mt (ADUB, BDUB) and Greece (AGRE, BGRE) (Wilks' L = 0.003; F(48,30) = 3.64; P <0.001); B, allopatric populations of M. avidus A from FYR MACEDONIA (AMKD), Morinj (AMOR), and the Pannonian region (APAN) (Wilks' L = 0.09; F(32,48) = 3.59; P <0.0001); C, allopatric populations of M. avidus B from Durmitor Mt (BDUR), Stara Mt (BSPL), Kopaonik Mt (BKOP), and FYR MACEDONIA (BMKD) (Wilks' L = 0.36; F(32,32) = 0.66; P <0.879); D, allopatric populations of M. avidus A and M. avidus B (Wilks' L = 0.09; F(80,245) = 1.94; P <0.0001). The amount of variation explained by each canonical axis is in parentheses.

Figure 5 in High molecular and phenotypic diversity in the Merodon avidus complex (Diptera, Syrphidae): cryptic speciation in a diverse insect taxon

Figure 5. Scatterplot of individual scores from the canonical variate analysis (CVA) of all specimens (both sexes) of metapopulations: A, Merodon avidus A from Dubašnica Mt (ADUB) (Wilks' L = 0.04; F(48,72) = 3.06; P <0.000); B, M. avidus B from Dubašnica Mt (BDUB) (Wilks' L = 0.10; F(64,174) = 2.18; P <0.000); C, M. avidus B from Durmitor Mt (BDUR) (Wilks' L = 0.10; F(64,174) = 2.21; P <0.000); D, M. avidus A from FYR MACEDONIA (AMKD) (Wilks' L = 0.002; F(112,171) = 2.40; P <0.000); E, M. avidus A from Greece (AGRE) (Wilks' L = 0.009; F(64,53) = 1.93; P <0.007). The amount of variation explained by each canonical axis is in parentheses. The number of misclassified specimens/total number of analysed

Figure 1 in High molecular and phenotypic diversity in the Merodon avidus complex (Diptera, Syrphidae): cryptic speciation in a diverse insect taxon

Figure 1. Origin of the analysed populations using wing geometric morphometrics from the Balkan Peninsula: 1, Pannonian Plain (PAN, Serbia); 2, Dubašnica Mt, E 21°59′, N 44°01′ (DUB, Serbia); 3, Stara Mt, E 22°41′, N 43°20′ (SPL, Serbia); 4, Kopaonik Mt, E 20°40′, N 43°15′ (KOP, Serbia); 5, Durmitor Mt, E 19°00′, N 43°11′ (DUR, Montenegro); 6, Morinj, E 18°40′, N 43°29′30″ (MOR, Montenegro); 7, Former Yugoslav Republic of Macedonia (MKD); 8, Greece (GRE). (Numbers within region are noted sampling sites of populations).

Figure 18 in First record of the taxon Echinopsyllus (Copepoda, Harpacticoida, Ancorabolidae) from the deep sea of Campos Basin, Brazil, with the description of three new species and their contribution to phylogenetic analysis

Figure 18. The proposed phylogeny of Echinopsyllus based on morphological characters listed in the text.

Figure 17 in First record of the taxon Echinopsyllus (Copepoda, Harpacticoida, Ancorabolidae) from the deep sea of Campos Basin, Brazil, with the description of three new species and their contribution to phylogenetic analysis

Figure 17. Cephalothorax with dorsal (D I, D II, and D III) and lateral (L I, L II, and L III) processes. A, C, E. normani (after Conroy-Dalton, 2003a); B, E. nogueirae sp. nov.

Figure 14 in First record of the taxon Echinopsyllus (Copepoda, Harpacticoida, Ancorabolidae) from the deep sea of Campos Basin, Brazil, with the description of three new species and their contribution to phylogenetic analysis

Figure 14. Echinopsyllus grohmannae sp. nov., female. A, A1; B, A2 (distal minute seta on the allobasis arrowed). Scale bar = 50 Mm.

Figure 13 in First record of the taxon Echinopsyllus (Copepoda, Harpacticoida, Ancorabolidae) from the deep sea of Campos Basin, Brazil, with the description of three new species and their contribution to phylogenetic analysis

Figure 13. Echinopsyllus grohmannae sp. nov., female. A, FR, lateral view; B, B′, md; C, mx. Scale bar = 50 Mm.

Figure 10 in First record of the taxon Echinopsyllus (Copepoda, Harpacticoida, Ancorabolidae) from the deep sea of Campos Basin, Brazil, with the description of three new species and their contribution to phylogenetic analysis

Figure 10. Echinopsyllus nogueirae sp. nov., female. A, telson and FR, dorsal view; B, P1. Scale bar = 50 Mm.