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Fig. 9 in Contributions to the herpetofauna of the Angolan Okavango-Cuando-Zambezi River drainages. Part 2: Lizards (Sauria), chelonians, and crocodiles

Fig. 9. Adult female Afroedura wulfhaackei (PEM R22490) from 1 km west of Candumbo on road to Boas Águas. Photo by Luke Verburgt.

Map 1 in Contributions to the herpetofauna of the Angolan Okavango-Cuando-Zambezi River drainages. Part 2: Lizards (Sauria), chelonians, and crocodiles

Map 1. Distribution of Acanthocercus cf. cyanocephalus in Angola. Historical records are indicated by white dots while all new records are indicated by black dots. Axis values are in degrees (°). Purple polygon – Okavango River basin, blue polygon – Cuando River basin, brown polygon – Zambezi River basin.

Fig. 5 in Contributions to the herpetofauna of the Angolan Okavango-Cuando-Zambezi River drainages. Part 2: Lizards (Sauria), chelonians, and crocodiles

Fig. 5. Adult male Agama schacki (PEM R23367) from near source of the Cubango River. Photo by Werner Conradie.

Fig. 2 in Contributions to the herpetofauna of the Angolan Okavango-Cuando-Zambezi River drainages. Part 2: Lizards (Sauria), chelonians, and crocodiles

Fig. 2. Adult male Acanthocercus cf. cyanocephalus (PEM R27387) from Luvu River camp. Photo by Chad Keates.

Fig. 1 in Contributions to the herpetofauna of the Angolan Okavango-Cuando-Zambezi River drainages. Part 2: Lizards (Sauria), chelonians, and crocodiles

Fig. 1. Adult female Acanthocercus cf. cyanocephalus (PEM R23560) from Quembo River source. Photo by Werner Conradie.

Fig. 1 in Equal contributions of feline immunodeficiency virus and coinfections to morbidity in African lions

Fig. 1. FIV infection is common in lions of Kruger National Park. Within the sample population, 72.8% (142/195) of lions were infected with FIV. Prevalence of FIV infection was similar between males and females (75.6% versus 70.2%; n = 74 and 121, respectively), but increased with host age (a). For ease of visualization, age has been broken up by life stage into cubs (0–2yrs), subadults (2.1–4yrs), young adults (4.1–6yrs), prime adults (6.1–8yrs), and seniors (>8yrs) based on previous age classifications (Schaller, 1976). Regional prevalence of FIV was highest in the central region and lowest in the north (b). The map to the right shows locations where lion prides were sampled.

Fig. 4 in Equal contributions of feline immunodeficiency virus and coinfections to morbidity in African lions

Fig. 4. FIV has strong direct and indirect effects on overall health. The final path model (a) shows only statistically significant relationships between manifest variables (rectangles) and latent variables (circles) for FIV infection, immune response (IMM), coinfections with hemoparasites (Hemoparasites), co-infections with gastrointestinal parasites (Helminths), and morbidity (Morbidity). Note that the parameter βx,z between each variable of interest represents the path coefficient obtained from least squares regression examining the relationship between one latent variable and the next (for example, FIV to IMM). Blue arrows represent positive relationships, whereas red arrows denote negative relationships. Final sample size was 106 lions.

Fig. 3 in Equal contributions of feline immunodeficiency virus and coinfections to morbidity in African lions

Fig. 3. FIV significantly increases the prevalence of select gastrointestinal and hemoparasitic coinfections, as well as overall parasite richness for both groups. Graph (a) shows the prevalence of coinfecting parasites isolated in lions from this study. Sample size for the parasite groups included is as follows: n = 114 for gastrointestinal parasites; n = 190 for hemoparasites; and n = 195 for viral parasites. Coinfections are broken down by FIV status (positive versus negative). The two additional graphs illustrate the relationship between FIV status and gastrointestinal parasite richness (b) and hemoparasite richness (c).

Fig. 2 in Equal contributions of feline immunodeficiency virus and coinfections to morbidity in African lions

Fig. 2. FIV has broad effects on lion health and is associated with progressive immune impairment. Box (2a) above provides a complete list of the health metrics measured for the purposes of this study. Arrows to the right of each variable summarize the directionality of statistically significant changes with FIV infection. Descriptive statistics and reference values can be found in Table 2. Complete model output can be found in supplementary tables S1–S4. For ease of visualization, each parameter has been broken into categories of clinical relevance. To the right, age-related changes in lymphocyte profiles are shown for total lymphocyte counts in FIV-positive versus FIV-negative lions (b); as well as specific lymphocyte subsets in FIV-positive lions (c). Due to small sample size for lymphocyte subsets, subadults, and cubs have been included together under the 'juvenile' category.

Fig. 8 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 8. Morphological features distinguishing the distal portion of the humerus of Rangifer tarandus (A) and Cervus elaphus (B), in anterior (A1, B1), distal (A2,B2), and posterior (A3,B3) views (modified from Breda 2005).

Fig. 7 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 7. Morphological features distinguishing the proximal portion of the humerus of Rangifer tarandus (A) and Cervus elaphus (B) (modified from Pales and García 1981).

Fig. 6 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 6. Scatterplots of different combinations of scapular measurements and indices for Rangifer tarandus and Cervus elaphus from Kiputz IX (southern Pyrenees, Spain), Late Pleistocene. Abbreviations: GLP, greatest anteroposterior length of the glenoid process; LG, greatest anteroposterior length of the glenoid cavity; SLC, minimum diameter of the scapular neck.

Fig. 3 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 3. Osteological measurements of the scapula (A, B) and the humerus (C, D) (modified from Weinstock 2000a). All drawings are based on Rangifer tarandus.

Fig. 4 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 4. Morphological features distinguishing the scapulae of the cervid mammals Rangifer tarandus, BGG KI-IX.2D.39.618 (A) and Cervus elaphus, BGG KI-IX.2C.28.142 (B), from Kiputz IX (southern Pyrenees, Spain), Late Pleistocene, in lateral (A 1, B 1) and distal (A 2, B 2) views; α, the angle formed by the glenoid cavity and the supraglenoid tubercle.

Fig. 9 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 9. Scatterplot of the greatest breadth of the trochlea (BT) vs. the depth of the distal epiphysis (Dd) of the humerus of Rangifer tarandus and Cervus elaphus from Kiputz IX and other European sites.

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Figs 90-94 in Contribution to the knowledge of Afrotropical Rutelinae VI (Coleoptera, Scarabaeidae, Rutelinae)

Figs 90-94 Adoretus (Lepadoretus) amoenus from Loma Mt., E. Konbaia (Sierra Leone) habitus (9 mm): (90) dorsal view; (91) lateral view; (92) aedeagus of Holotype: lateral view (93) parameres, dorsal view; (94) distribution map.

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Figs 9-16 in Contribution to the knowledge of Afrotropical Rutelinae VI (Coleoptera, Scarabaeidae, Rutelinae)

Figs 9-16. Anomala nigrosulcata from Kisangani (R. D. Congo) habitus (15mm): (9) dorsal view; (10) lateral view; (11) habitus female dorsal view (16mm); (12) lateral view; (13) aedeagus, lateral view (14) parameres, dorsal view; (15) parameres, ventral view; (16) distribution map.

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Fig. 9 in Taxonomic implications of the residual colour patterns of ampullinid gastropods and their contribution to the discrimination from naticids

Fig. 9. Species of the genus Pachycrommium Woodring, 1928, under UV light. A. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30476 (Faullummel coll.), Chaussy, Val d'Oise, France, Lutetian, in ventral view. B. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30874 (Faullummel coll.), Fontenay−en−Vexin, Eure, France, Lutetian, in ventral (B1) and dorsal (B2) views. C. Pachycrommium acuminatum, MNHN A25003 (Faullummel coll.), Chaussy, in dorsal view. D. Pachycrommium acuminatum (Lamarck, 1804), MNHN A25004 (Faullummel coll.), VilliersSaint−Frédéric, Yvelines, France, Lutetian, in apical view. E. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30479 (Faullummel coll.), Chaussy, in ventral view. F. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30875 (Faullummel coll.), Fontenay−en−Vexin, in ventral (F1) and dorsal (F2) views. G. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30872 (Faullummel coll.), Fontenay−en−Vexin, in ventral (G1) and dorsal (G2) views. H. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30873 (Faullummel coll.), Fontenay−en−Vexin, in ventral (H1) and dorsal (H2) views. I. Pachycrommium eburnoides (Grateloup, 1847), MNHN A30405 (Faullummel coll.), Saint−Paul−lès−Dax, Landes, France, Burdigalian, in ventral (I1) and apical (I2) views. J. Pachycrommium eburnoides (Grateloup, 1847), MNHN A30411 (Cossman coll.), Dax, Landes, France, Early Miocene, in detailed view of the first whorls (J1) and apical (J2) view. K. Pachycrommium eburnoides (Grateloup, 1847), MNHN A30410 (Cossmann coll.), Dax, in ventral (K1), dorsal (K2), and apical (K3) views. Scale bars for all 10 mm, except 5 mm (I3, J2), 2 mm (J1). Photographs by C. Lemzaouda and P. Loubry (MNHN).

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Fig. 8 in Taxonomic implications of the residual colour patterns of ampullinid gastropods and their contribution to the discrimination from naticids

Fig. 8. Species of the genus Pachycrommium Woodring, 1928, under UV light. A. Pachycrommium suessoniensis (d'Orbigny, 1850), MNHN A30881 (Pacaud coll.), Celles−sur−Aisne, Aisne, France, Ypresian (Cuisian), in ventral (A1) and apical (A2) views. B. Pachycrommium suessoniensis (d'Orbigny, 1850), MNHN A30882 (Pacaud coll.), Celles−sur−Aisne, in apical (B1) and dorsal (B2) views. C. Pachycrommium productum (Deshayes, 1864), MNHN A30945 (Pacaud coll.), Chaussy, Val d'Oise, France, Lutetian, in dorsal view. D. Pachycrommium sp., MNHN A30482 (Pacaud coll.), Monampteuil, Aisne, France, Ypresian (Cuisian), in ventral (D1) and dorsal (D2) views. E. Pachycrommium scalariformis (Deshayes, 1825), MNHN A30401 (Ledon leg.), Fontenay−en−Vexin, Lutetian, in apical view. F. Pachycrommium scalariformis (Deshayes, 1825), MNHN A30402 (Ledon leg.), Fontenay−en−Vexin, view of a shell fragment. Scale bars 10 mm. Photographs by C. Lemzaouda and P. Loubry (MNHN).