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Figure 7 in Diversity in Australia's tropical savannas: An integrative taxonomic revision of agamid lizards from the genera Amphibolurus and Lophognathus (Lacertilia: Agamidae)

Figure 7. Variation in white pigmentation on tympanums of Lophognathus sp. nov., L. gilberti and L. gilberti centralis. Orientation of the tympanums is provided under images. Museum registration numbers for the individual lizards photographed are also provided.

Figure 5 in Diversity in Australia's tropical savannas: An integrative taxonomic revision of agamid lizards from the genera Amphibolurus and Lophognathus (Lacertilia: Agamidae)

Figure 5. Primary type specimens: a,Amphibolurus centralis (MCZ 35207); b, Gowidon longirostris (BMNH 1946.8.28.73); c, Lophognathus gilbert (BMNH1946.8.28.69); d, Tropicagama temporalis (BMNH 1946.8.28.72).

Figure 3 in Diversity in Australia's tropical savannas: An integrative taxonomic revision of agamid lizards from the genera Amphibolurus and Lophognathus (Lacertilia: Agamidae)

Figure 3. Results from the integrative taxonomic approach to species delimitation. Genera are designated by a multicoloured horizontal bars at the top of the figure, and species within genera are designated by a number in black above a coloured vertical segment. Segment colours and species numbers correspond to those in fig.1.

Figure 1 in Diversity in Australia's tropical savannas: An integrative taxonomic revision of agamid lizards from the genera Amphibolurus and Lophognathus (Lacertilia: Agamidae)

Figure 1. MtDNA phylogenetic tree for the genera Lophognathus, Amphibolurus and Chlamydosaurus reproduced from Melville et al. (2011). Tree presented is a Bayesian 50% majority-rule consensus tree based on ~1200 bp mitochondrial DNA (ND2). Bayesian posterior probabilities and ML boostraps are provided on branches. Sample identification numbers are either Genbank accession numbers for previously published sequences or museum IDs (shown in brackets) for samples sequenced previously. Vertical bars indicate species following the taxonomic revision.

FIGURE 14. A-G in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia

FIGURE 14. A-G. Amamriabatis heni nov gen. nov. sp. A. anterior tooth KEB 1-218, A1. Occlusal view, A2. Basal view, A3. Lingual view, B. antero-lateral tooth KEB 1-219 (Holotype), B1. Occlusal view, B2. Lingual view, B3. Basal view, C. juvenile tooth KEB 1-220, occlusal view, D. antero-lateral tooth KEB 1-221, D1. Occlusal view, D2. Basal view, D3. Labial view, E. lateral tooth KEB 1-222, E1. Occlusal view, E2. Lingual view, E3. Basal view, F. antero-lateral tooth KEB 1-223, F1. Occlusal view, F2. Basal view, F3. Labial view, G. lateral tooth KEB 1-224, G1. Occlusal view, G2. Basal view, G3. Lingual view; H. Archaeomanta sp. KEB 1-225, H1. Lateral view, H2. Labial view.

FIGURE 12. A-C in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia

FIGURE 12. A-C. Mecotrygon asperodentulus nov. gen nov. sp. A. anterior tooth KEB 1-188, A1. occlusal view, A2. Profile, A3. Basal view; B. lateral tooth KEB 1-189, B1. occlusal view, B2. labial view, B3. Profile; C. lateral tooth KEB 1-190, HOLOTYPE, C1. Occlusal view, C2. Lingual view, C3. Basal view, C4. Profile; D-M. Himantura souarfortuna nov. sp. D.?posterior tooth KEB 1-191, D1. Occlusal view, D2. Profile, D3. Basal view; E. antero-lateral tooth KEB 1- 192, occlusal view; F. anterior tooth KEB 1-193, F1. Occlusal view, F2. Labial view; G. antero-lateral tooth KEB 1-194, G1. Occlusal view, G2. Profile; H. anterior tooth KEB 1-195, occlusal view; I. lateral tooth KEB 1-196, occlusal view; J. A. anterior tooth KEB 1-197, occlusal view; K. lateral tooth KEB 1-198, K1. Occlusal view, K2. Basal view; L. A. anterior tooth KEB 1-199, occlusal view; M. lateral tooth KEB 1-200, occlusal view. N-O. Dasyatoid indet. N. antero-lateral tooth KEB 1-201, N1. Occlusal view, N2. Basal view; O. A. antero-lateral tooth KEB 1-202, occlusal view; P-Q. Arechia sp. P. lateral tooth KEB 1-203, occlusal view; Q. A. anterior tooth KEB 1-204, Q1. Occlusal view, Q2. Lingual view.

FIGURE 10. A-D in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia

FIGURE 10. A-D: Propristis cf. schweinfurti. A. Rostral denticle KEB 1-172, A1. Profile, A2. dorsal view; B. Rostral denticle KEB 1-173, Profile; C. Rostral denticle KEB 1-174, C1. Profile, C2. Dorsal view, C3. basal view; D. Rostral denticle KEB 1-175, D1. profile. D2. dorsal view; E: Pristis sp. Rostral denticle, KEB 1-165, dorsal view; F-G. Rhynchobatus cf. vincenti. F. anterior tooth KEB 1-176, F1. Occlusal view, F2. Basal view; G. anterior tooth KEB 1-177, occlusal view; H-I.?Torpedo sp. H. lateral tooth KEB 1-178, occlusal view, I. lateral tooth KEB 1-179, occlusal view.

FIGURE 9. A-F in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia

FIGURE 9. A-F: Propristis cf. schweinfurti, A. Anterior oral tooth KEB 1-166, A1. Lingual view, A2. Occlusal view, A3. profile; B. Antero-lateral oral tooth KEB 1-167, B1. Occlusal view, B2. Lingual view, B3. Labial view; C. Anterior oral tooth KEB 1-168, C1. Lingual view, C2. Basal view, C3. Profile; D. lateral tooth KEB 1-169, D1. Lingual view, D2. Occlusal view, D3. Basal view, D4. Magnificence of crown-root boundary of D3; E.?male lateral tooth KEB 1-170, E1. Occlusal tooth, E2. Basal view; F.?male anterior tooth KEB 1-171, F1. Lingual view, F2. Occlusal view; G-L: Pristis sp. G. porterior tooth KEB 1-158, G1. Occlusal view, G2. Basal view; H. anterior tooth KEB 1-159, occlusal view; I. lateral tooth KEB 1-160, I1 occlusal view, I2., lingual view. J lateral tooth KEB 1-161, occlusal view; K. anterior tooth KEB 1-162, occlusal view; L. lateral tooth of?juvenile KEB 1-163, L1. Occlusal view, L2. Basal view; M. lateral tooth of juvenile KEB 1-164, M1. Occlusal view, M2. Profile.

FIGURE 1 in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia

FIGURE 1. Paleotemperatures (ice-free deep-ocean T°/ tropical sea surface T°) and Thermic events during the "doubthouse" conditions of Eocene period (from Cramwinckel et al., 2018 modified with events dating from Hollis et al., 2019). Stratigraphically and geographical locations of the main deposits with Elasmobranch associations along the southwestern Tethys. Abbreviations: DAK: Dakhla (Adnet et al., 2010), GEN: Genam (Zouhri et al., 2017, in press); AZ: Aznag (Tabuce et al., 2005) PM: Phosphate ores (see Noubhani and Cappetta, 1997), Morocco; GAF: Gafsa basin (see Arambourg, 1952); KEBAR: Kébar (this work and Adnet et al., 2019); MBK: Mabrouk (see Sweydan et al., 2019), Tunisia; EG: ElGedida (see Strougo et al., 2007); KM: KM11 (see Adnet et al., 2011) MT: Minqar Tabaghbagh (see Zalmout et al., 2012); BQ: Birquet Qarun QS: Quar et Sa; GE: Genahamm Fm.; MI: Midawara FM. from Wadi al Hitan, see Underwood et al., 2011), Egypt; QD: Qa Faydat al Dahikya, Jordania, see Mustafat and Zalmout, 2002).

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Fig 2. Three dwarf spinner dolphins, Stenella l in Cetacean Diversity And Habitat Preferences In Tropical Waters Of East Kalimantan, Indonesia

Fig 2. Three dwarf spinner dolphins, Stenella l. roseiventris with obscure, lateral color pattern, photographed in the Berau Archipelago, October 2003. Photo: Budiono.

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Fig 3 in Cetacean Diversity And Habitat Preferences In Tropical Waters Of East Kalimantan, Indonesia

Fig 3. Two Gray's (pantropical) spinner dolphins, Stenella longirostris with distinctive tripartite color pattern, photographed in the Berau Archipelago, October 2003. Photo: Budiono.

Fig. 9. A in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 9. A species delimitation of Bornean Myrsidea studied inferred from a partial sequence of the mitochondrial COI gene. Validation methods shown on Bayesian tree of hypothetical species. Colors represent unique partitions and correspond to operational taxonomic units (OTU) by various methods of species delimitation: morphological, Automatic Barcode Gap Discovery (ABGD), Generalized Mixed Yule Coalescent analyses (GMYC), and Poisson Tree Process analyses (PTP) respectively.

Fig. 10 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 10. Tanglegram of phylogenies of Bornean avian host (left) and associated Myrsidea lice (right) studied. Colored circles above nodes indicate cospeciation events recovered from Jane (they correspond to 83% of the solutions with p-value of 0.001). Arrow indicates a host switching event recovered by Jane. Red lines indicate significant host-parasite links estimated by the ParaFitLink1 test.

Fig. 7 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 7. Habitus. Myrsidea ramoni sp.n. A-B, holotype female (A), paratype male (B). Myrsidea victoriae sp.n. C-D, holotype female (C), paratype male (D).

Fig. 6 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 6. Habitus. Myrsidea carmenae sp.n. A-B, holotype female (A), paratype male (B). Myrsidea franciscae sp.n. C-D, holotype female (C), paratype male (D).

Fig. 8 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 8. Bayesian phylogeny of Bornean Myrsidea studied based on analysis of the mitochondrial cytochrome c oxidase subunit I (COI) and elongation factor-1α (EF- 1α) genes. Outgroup taxon was removed from this figure for readability. Hosts belong to family Pycnonotydae are indicated on the right.

Fig. 4 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 4. Myrsidea ramoni sp.n. A, dorso-ventral view of female thorax and abdomen; B, head shape; C, dorsal view of male abdomen; D, male metasternal plate and sternites I–II; E, male genital sac sclerite.

Fig. 3 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 3. Myrsidea franciscae sp.n. A, dorso-ventral view of female thorax and abdomen; B, head shape; C, male metasternal plate and sternites I–II; D, male genital sac sclerite.

Fig. 2 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 2. Myrsidea carmenae sp.n. A, dorso-ventral view of female thorax and abdomen; B, head shape; C, male metasternal plate and sternites I–II; D, male genital sac sclerites.

Fig. 5 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 5. Myrsidea victoriae sp.n. A–D, dorso-ventral view of female thorax and abdomen (A), head shape (B), male metasternal plate and sternites I–II (C), male genital sac sclerite (D); Myrsidea macronoi E, male genital sac sclerite.