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Fig. 3 in The prevalence of Leucocytozoon spp. in nestlings of three wild raptor species including implications on haematological and blood chemistry values

Fig. 3. Results of linear discriminant analysis (LDA) comparing 15 selected blood parameters between uninfected and infected raptor nestlings. a) Distribution of the LDA according to uninfected and infected nestlings. b) Correlation plot of the first axis of the 15 selected variables.

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Fig. 2 in The prevalence of Leucocytozoon spp. in nestlings of three wild raptor species including implications on haematological and blood chemistry values

Fig. 2. Proportion of infected individuals of common buzzard (Buteo buteo), red kite (Milvus milvus) and northern goshawk (Accipiter gentilis) nestlings (n = 528) in relation to the proportion of the nestling period, determined by age and the species-specific average nestling duration. Calculated nestling periods were grouped into steps of ten percent (0.2–0.9). Each step represents the proportion of all individuals examined within this period. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 3 in Copepod consumption by amphibians and fish with implications for transmission of Dracunculus species

Fig. 3. Average copepods ingested by tadpole species during the feeding trial. Bars represent average copepods ingested, error bars represent standard error, and dotted line shows average copepod loss in control trials. The lack of significant differences (p <0.05) determined by Tukey post-hoc contrasts are indicated by 'a'.

Fig. 2 in Copepod consumption by amphibians and fish with implications for transmission of Dracunculus species

Fig. 2. Average copepods ingested by fish species during the feeding trial. Bars represent average copepods ingested, error bars represent standard error, and dotted line shows average copepod loss in control trials. Significant differences (p <0.05) determined by Tukey post-hoc contrasts are indicated by 'a' and 'b'.

Fig. 1 in Copepod consumption by amphibians and fish with implications for transmission of Dracunculus species

Fig. 1. Average copepods ingested by animal type during the feeding trial. Bars represent average copepods ingested, error bars represent standard error, and dotted line shows average copepod loss in control trials. Significant differences (p <0.05) determined by Tukey post-hoc contrasts are indicated by 'a', 'b', and 'c'.

Fig. 5. A in Whale lice (Isocyamus deltobranchium & Isocyamus delphinii; Cyamidae) prevalence in odontocetes off the German and Dutch coasts - morphological and molecular characterization and health implications

Fig. 5. A: Ulcerative lesion with whale lice in harbour porpoise (Phocoena phocoena); B: rake marks with whale lice on pilot whale (Globicephala melas).

Fig. 4 in Whale lice (Isocyamus deltobranchium & Isocyamus delphinii; Cyamidae) prevalence in odontocetes off the German and Dutch coasts - morphological and molecular characterization and health implications

Fig. 4. Maximum likelihood phylogeny tree produced with MEGA (version X), sequences in red box from this study. Bootstrap values (n = 1000 replicates) above 50% are shown above the branches.

Fig. 3 in Whale lice (Isocyamus deltobranchium & Isocyamus delphinii; Cyamidae) prevalence in odontocetes off the German and Dutch coasts - morphological and molecular characterization and health implications

Fig. 3. (A) Isocyamus deltobranchium and (B) Isocyamus delphinii showing the characteristic accessory gills (asterisk).

Fig. 2. A in Whale lice (Isocyamus deltobranchium & Isocyamus delphinii; Cyamidae) prevalence in odontocetes off the German and Dutch coasts - morphological and molecular characterization and health implications

Fig. 2. A: Isocyamus deltobranchium adult male ventral view showing genitalia and accessory gills; B: Isocyamus deltobranchium adult female dorsal view; C: Isocyamus deltobranchium adult female ventral view showing genitalia and broodpouch; D: adult female ventral view with juveniles in brood pouch, all sampled from a stranded harbour porpoise (Phocoena phocoena) on the Dutch coast.

Fig. 6 in Whale lice (Isocyamus deltobranchium & Isocyamus delphinii; Cyamidae) prevalence in odontocetes off the German and Dutch coasts - morphological and molecular characterization and health implications

Fig. 6. Intralesional whale lice (arrow) in lesion with mild hyperplasia of the adjacent epidermis and granulation tissue in the superficial dermis (scale bar 2 mm).

Fig. 1 in Helminth's assemblage of Trachemys dorbigni (Testudines: Emydidae) in southern Brazil: implications of anthropogenic environments and host's genders

Fig. 1. Overall layout of the collection environments in the study of helminth assemblage of Trachemys dorbigni in southern Brazil: A, detail of the Centro Agropecuário da Palma (UFPel), rural area of CapÃo do LeÃo, State of Rio Grande do Sul, Brazil; B, detail of the urban Área of Pelotas, Rio Grande do Sul, Brazil. Source: extracted and modified the site Google® Earth (©2014 Google – Images ©2014 Digital Globe).

Fig. 13 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids

Fig. 13. The tibia of multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 (IVPP V19030) from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. A. Right tibia in anterior (A1) and posterior (A2) views, proximal end in lateral (A3) and proximal (A4) views. B. Femur-tibia articulation in posterior (B1) and anterior (B2) views.

Fig. 10 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids

Fig. 10. Fragmentary pterygoid and middle ear cavity of multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. A. IVPP V19025, middle ear with part of the promontorium in ventral view; photograph (A1), explanatory drawing (A2). B. IVPP V19029, possible bony shell of the inflated vestibule in lateral (B1) and inside (B2) views. The anterior end of each element is toward upside.

Fig. 3 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids

Fig. 3. Multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 (IVPP V19025) from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. Partial right rostrum with I2–3 in lateral (A) and ventral (B) views. A2, B2, explanatory drawings; A3, B3 details of A1, B1.

Fig. 2 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids

Fig. 2. Multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 from the late Paleocene Gashato Formation at Shabarakh Usu, Mongolia. A. Holotype (AMNH 21736), the upper left M2 in occlusal, lingual and buccal views (A1–A3). B. Paratype (AMNH 21713), anterior part of a left m2 in occlusal view. C. Paratype (AMNH 21715), anterior parts of a left m1 in occlusal view. D. AMNH 21719.001, broken?M2 in occlusal ( D1) and lateral (D2) views. E. AMNH 21719.002, anterior parts of a left m1 in occlusal view.

Fig. 7 in Middle Miocene conoidean gastropods from western Ukraine (Paratethys): Integrative taxonomy, palaeoclimatogical and palaeobiogeographical implications

Fig. 7. SEM images of protoconch features of conoidean gastropods from early Serravallian of western Ukraine, Varovtsi (A, C–F) and Horodok (B). A. Bela? robusta sp. nov., MGGC-24519/8. B. Pyrgocythara turrispiralata sp. nov., MGGC-24515/11. C. Raphitoma cf. R. ringicula (Boettger, 1902), MGGC-24522/5. D. Andonia sp. aff. A. transsylvanica (Hoernes and Auinger, 1890), MGGC 24523/2. E. Teretia cf. T. turritelloides Bellardi, 1847), MGGC-24524/5. F. Haedropleura sp. aff. H. septangularis (Montagu, 1803), MGGC-24520/6. Views: A1, B1, C–F, lateral; A2, B2, apical. Scale bars 0.1 mm.

Fig. 6 in Middle Miocene conoidean gastropods from western Ukraine (Paratethys): Integrative taxonomy, palaeoclimatogical and palaeobiogeographical implications

Fig. 6. Photomicrographs of holotype shell of new conoidean gastropods from early Serravallian of western Ukraine, Varovtsi (A, B) and Horodok (C). A. Bela varovtsiana sp. nov., MGGC-24516. B. Bela? robusta sp. nov., MGGC-24518. C. Pyrgocythara turrispiralata sp. nov., MGGC-24514. Views: A1−C1, apertural; A2−C2, dorsal; A3−C3, lateral. Scale bars 1 mm.

Fig. 4 in Middle Miocene conoidean gastropods from western Ukraine (Paratethys): Integrative taxonomy, palaeoclimatogical and palaeobiogeographical implications

Fig. 4. SEM images of protoconch features of new conoidean gastropods from early Serravallian of western Ukraine, Varovtsi (A–C, F) and Velyka Levada (E). A. Mangelia angulicosta sp. nov., MGGC 24506/6. B. Mangelia larga sp. nov., MGGC-24508/1. C. Mangelia larga sp. nov., MGGC-24508/7. D. Mangelia pseudorugulosa sp. nov., MGGC-24510/9. E. Mangelia odovychenae sp. nov., MGGC-24512/1. F. Bela varovtsiana sp. nov., MGGC-24517/5. Views: A1, B, D1−F1, lateral; A2, C, D2−F2, apical. Scale bars 0.1 mm.

Fig. 3 in Middle Miocene conoidean gastropods from western Ukraine (Paratethys): Integrative taxonomy, palaeoclimatogical and palaeobiogeographical implications

Fig. 3. Photomicrographs of holotype shells of new conoidean gastropods from early Serravallian of western Ukraine, Varovtsi (A–C) and Velyka Levada (D). A. Mangelia angulicosta sp. nov., MGGC-24505. B. Mangelia larga sp. nov., MGGC-24507. C. Mangelia pseudorugulosa sp. nov., MGGC-24509. D. Mangelia odovychenae sp. nov., MGGC-24511. Views: A1−D1, apertural; A2−D2, dorsal; A3−D3, lateral. Scale bars 1 mm.

Fig. 2 in Middle Miocene conoidean gastropods from western Ukraine (Paratethys): Integrative taxonomy, palaeoclimatogical and palaeobiogeographical implications

Fig. 2. Comparison of 10 assessed variables between allied taxa: sample mean, horizontal line; 95% confidence intervals (CI), shaded boxes; ranges, open boxes (specimen measurements in SOM 2). The mean sample is a point estimate of the population mean (μ), and the corresponding CI is a range of plausible values for μ. If two parameters have non-overlapping CI, they are considered to be significantly different. The 95% confidence interval is based on the standard error for the estimate of the mean and the t distribution. For extremely small samples (n <5; SOM 2) only ranges are reported (see Beninger et al. 2012). Abbreviations: M., Mangelia; B., Bela; P., Pyrgocythara; H., Haedropleura.