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Figure 8 in Diversity of late Maastrichtian Tyrannosauridae (Dinosauria: Theropoda) from western North America

Figure 8. Comparison of the dorsal skull roof of LACM 28345 with other tyrannosaurids. AMNH 5027 modified after Osborn (1912) and CMN 8506 modified after Russell (1970).

Figure 6 in Diversity of late Maastrichtian Tyrannosauridae (Dinosauria: Theropoda) from western North America

Figure 6. Comparison of the snouts of tyrannosaurids in left lateral view showing the contact of the antorbital fossa and nasal suture among tyrannosaurids. AMNH 5027 modified after Osborn (1912), CMN 8506 modified after Russell (1970).

Figure 5 in Diversity of late Maastrichtian Tyrannosauridae (Dinosauria: Theropoda) from western North America

Figure 5. Comparison of the right dentary (reversed) of LACM 28471 with those of other tyrannosaurid juveniles.

Figure 7 in Diversity of late Maastrichtian Tyrannosauridae (Dinosauria: Theropoda) from western North America

Figure 7. Comparison of tyrannosaurid snouts in dorsal view, showing the appressed state of the nasal processes of the premaxilla in Tyrannosaurus rex. AMNH 5027 modified after Osborn (1912), CMN 8506 modified after Russell (1970).

Figure 13 in Diversity of late Maastrichtian Tyrannosauridae (Dinosauria: Theropoda) from western North America

Figure 13. Comparison of the surangular of LACM 23845 with other tyrannosaurids in left lateral view. AMNH 5027 modified after Osborn (1912) and CMN 8506 after Russell (1970).

Figure 3 in Diversity of late Maastrichtian Tyrannosauridae (Dinosauria: Theropoda) from western North America

Figure 3. Mandibular bones of LACM 28471. Right surangular in lateral (A), dorsal (B), and ventral (C) views; left (D) and right (E) dentaries in lateral view with diagrammatic cross sections of teeth. Cross sections are not to scale.

Figure 1 in Diversity of late Maastrichtian Tyrannosauridae (Dinosauria: Theropoda) from western North America

Figure 1. Facial bones of LACM 28471. Snout in dorsal view (A); frontal process of nasals in dorsal (B) and ventral (C) views; snout in left lateral (D) and right lateral (E) views, and the nasal process of the right maxilla in lateral (F) and medial (G) views.

Figure 2 in Diversity of late Maastrichtian Tyrannosauridae (Dinosauria: Theropoda) from western North America

Figure 2. Dorsal skull roof of LACM 28471. Left frontal (A) and right frontal (B) in dorsal view; joint surface of the parietal in caudal view (C); joint surface of the postorbital in lateral view (D) and cross section of this contact (E); left frontal in ventral (F) and lateral (G) views and cross section through the orbit (H); parietals in left lateral (I), rostral (J), right lateral (K), dorsal (L), and ventral (M) views; nuchal crest fragment in rostral (N), dorsal (O), and caudal (P) views.

Figure 4 in Diversity of late Maastrichtian Tyrannosauridae (Dinosauria: Theropoda) from western North America

Figure 4. Diagrammatic sketches of cross sections of the dentition of LACM 28471 in comparison with that of another juvenile Tyrannosaurus rex (CMNH 7541). Numbers indicate alveolus position from mesial to distal.

Figure 14 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 14. Internal mould of Paracyclas proavia (Goldfuss, 1840) from the Devonian, Eifel, Germany (BMNH Pal. Department L25554). Shell length = 56 mm. A, right side, anterior adductor scar arrowed; B, detail of anterior adductor scar showing ventral detachment from pallial line. aas, anterior adductor muscle scar; pl, pallial line.

Figure 13. A, B in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 13. A, B, internal moulds showing right sides of Ilionia prisca, Silurian, Gotland, Sweden. A, BMNH, Shell length (SL) = 70 mm; B, BMNH, SL = 55 mm. C, D, outside and inside of left valve of Eomiltha voorhoevi, Recent, Mozambique, ANSP 234103, SL = 70 mm.

Figure 12 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 12. Posterior apertures of Fimbria fimbriata (Lizard Island, Queensland) showing double row of papillae, and short length of mantle fusion ventral to inhalant aperture. Abbreviations: ex, exhalant aperture; in, inhalant aperture; pg, pedal gape; vf, ventral fusion.

Figure 11 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 11. Posterior apertures of a range of lucinid species. All SEMs of critical point dried specimens. A, Anodontia omissa (Iredale, 1930), Moreton Bay Queensland; B, Phacoides pectinatus (Gmelin, 1792), Brazil; C, Bathyaustriella thionipta (Glover et al., 2004), Kermadec Ridge, New Zealand; D, Ctena bella (Conrad, 1837), Lizard Island, Queensland; E, Pillucina vietnamica Zorina, 1978, Port Douglas, Queensland; F, Wallucina assimilis (Angas, 1867), Jervis Bay, New South Wales; G, Lucina adansoni d'Orbigny, 1839, Cape Verde Islands. H, Cardiolucina pisiformis (Thiele, 1930), Shark Bay, Western Australia; I, Myrtea spinifera (Montagu, 1803), Oban Scotland. Images adjusted to similar scale. Abbreviations: ex, exhalant aperture; in, inhalant aperture; p, papillae; vf, ventral mantle fusion.

Figure 9 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 9. SEM section of ctenidial filament of Lucinisca nassula (Conrad, 1846) showing bacteriocytes and granule cells. Scale bar = 10 µm. Abbreviations b, bacteriocyte with rod-shaped bacteria. gr, granule cell and granules.

Figure 8 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 8. TEM section through part of ctenidial filament of Anodontia ovum (Reeve, 1850), Lizard Island, Queensland, showing central blood space flanked by bacteriocytes and intercalary cells. Scale bar = 5 µm. Abbreviations: b, bacteria; ba, bacteriocyte; bs, blood space; eic, distal extension of intercalary cell; ic, intercalary cell; ly, lysosome; m, microvilli; n, nucleus.

Figure 7 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 7. Composite tree of lucinid relationships derived from Bretsky (1976: figs 3–9) and including living taxa only.

Figure 10 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 10. Mantle gills in lucinids. A, Codakia tigerina; B, Lucina pensylvanica; C, Phacoides pectinatus; D, Anodontia philippiana. Scale bars = 1 mm.

Figure 6 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 6. Tree summarizing Chavan's (1969) ideas of relationships in Lucinidae derived from his subfamilial classification of genera. Recent taxa only included.

Figure 1 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 1. Diversity of form within Lucinidae. A, Plicolucina flabellata Glover, Taylor & Slack-Smith, 2003, Shell length (SL) = 22 mm; B, Lamellolucina trisulcata Taylor & Glover, 2002, SL = 10 mm; C, Codakia tigerina (Linnaeus, 1758), SL = 70 mm; D, Anodontia philippiana (Reeve, 1850), SL = 66 mm; E, Miltha childrenae (Gray 1825), SL = 82 mm; F, Eomiltha voorhoevi, SL = 80 mm; G, Austriella corrugata (Deshayes, 1843), SL = 60 mm; H, Ctena bella (Conrad, 1837), SL = 25 mm; I, Rasta lamyi (Abrard, 1942), SL = 30 mm; J, Pompholigina gibba (Gray, 1825), SL = 27 mm; K, Myrtea spinifera (Montagu, 1803), SL = 26 mm.

Figure 5 in Lucinidae (Bivalvia) - the most diverse group of chemosymbiotic molluscs

Figure 5. Tree of lucinid relationships derived from final figure (tableau chronologique de l'evolution des lucines) by Chavan, 1937−1938), including living taxa only.