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Fig. 10 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 10. Liver, several foci of brown staining indicate Toxoplasma antigen within a necrotic focus (x100, Toxoplasma polyclonal antibody IHC). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 2. Dermopristis pterophilus n in A new microbothriid monogenean Dermopristis pterophilus n. sp. from the skin of the Critically Endangered green sawfish Pristis zijsron Bleeker, 1851 (Batoidea: Pristidae) in Western Australia

Fig. 2. Dermopristis pterophilus n. sp. holotype, ventral perspective. Abbreviations: dr, distal region of tubular male reproductive tract; gm, germarium; h, haptor; mf, muscle fibres; mp, male pore; ph, pharynx; pr, proximal region of tubular male reproductive tract; t, testis; vd, vas deferens; vf, vitelline follicles; vr, vitelline reservoir. Scale bar: 500 μm.

Fig. 6 in A new microbothriid monogenean Dermopristis pterophilus n. sp. from the skin of the Critically Endangered green sawfish Pristis zijsron Bleeker, 1851 (Batoidea: Pristidae) in Western Australia

Fig. 6. (A) Mean abundance with 95% CI's of Dermopristis pterophilus n. sp. recorded on or adjacent to one of six attachment sites on Pristis zijsron. (B) Green sawfish Pristis zijsron gross morphology with combined total number of D. pterophilus n. sp. infections and the percentage of hosts infected with at least one worm per attachment site, from 16 fish examined. *No infections were found on the head (anterior to host gills, including the rostrum).

Fig. 5. Dermopristis pterophilus n in A new microbothriid monogenean Dermopristis pterophilus n. sp. from the skin of the Critically Endangered green sawfish Pristis zijsron Bleeker, 1851 (Batoidea: Pristidae) in Western Australia

Fig. 5. Dermopristis pterophilus n. sp. detail of dendritic gut, ventral perspective. (A) Extensiveness and pattern of gut diverticula with position of the major gut subtrees extending from each side of the main lateral gut arms. (B) Fine details of minor gut diverticula dorsal to the coiled vas deferens. Abbreviations: g, gut; gt1–6, first through sixth major gut sub-trees; o, o¨otype; sr, seminal receptacle; u, uterus; v, vagina; vd, vas deferens. Scale bars: (A) 500 μm; (B) 100 μm.

Fig. 2 in Genetic characterisation of Echinocephalus spp. (Nematoda: Gnathostomatidae) from marine hosts in Australia

Fig. 2. Genetic relationship based on Bayesian Inference analysis of the small subunit nuclear ribosomal DNA (SSU) sequences of Echinocephalus spp. collected form sea snake, stingray and octopus in Australia determined in this study (bold). Nodal support is given as a posterior probability for BI analysis followed by bootstrap values for NJ analysis on this tree. Gnathostoma lamothei (Bertoni-Ruiz et al., 2011) was used as the outgroup, however the GenBank entry for this parasite is with its old name, Gnathostoma neoprocyonis Z96947. The scale bar indicates the number of inferred substitutions per nucleotide site.

Fig. 1. A in Genetic characterisation of Echinocephalus spp. (Nematoda: Gnathostomatidae) from marine hosts in Australia

Fig. 1. A, Anterior end of Echinocephalus larva from Octopus djinda (formerly Octopus O. aff. tetricus), showing six rows of hooks on the cephalic inflation; B, Apical view of the spiniform papillae on the larva from O. djinda, showing a posterior row of three papillae; C, Apical view of the spiniform papillae on the larva from Codakia paytenorum, showing posterior row of three papillae joined by irregular areas of sclerotization. Scale bars: Fig. 1A and 40 μm; Fig. 1B and C, 10 μm.

Fig. 4 in New records of Hepatozoon and Oswaldofilaria from saltwater crocodiles (Crocodylus porosus) in Australia

Fig. 4. Relationship of a new species of Oswaldofilaria (bold) from the blood of the saltwater crocodile with representative taxa represented in the GenBank database, established based on a phylogenetic analysis of sequence data from part of the mitochondrial cytochrome c oxidase subunit 1 gene (cox1; 681 bp) employing the neighbour-joining distance method. Branch supports are represented by neighbour-joining bootstrap percentages. Members of the genus Spirocerca were used as outgroups.

Fig. 3 in New records of Hepatozoon and Oswaldofilaria from saltwater crocodiles (Crocodylus porosus) in Australia

Fig. 3. Microfilaria of a species of Oswaldofilaria in a blood smear from a saltwater crocodile (Crocodylus porosus). Stained with Wright's Giemsa; examined at 100-times magnification; scale bar = 5 μm.

Fig. 1. A in New records of Hepatozoon and Oswaldofilaria from saltwater crocodiles (Crocodylus porosus) in Australia

Fig. 1. A stage of Hepatozoon identified in erythrocytes in blood smears from a saltwater crocodile (Crocodylus porosus). Stained with Wright's Giemsa; examined at 100× magnification; scale bar = 5 μm.

Fig. 2 in New records of Hepatozoon and Oswaldofilaria from saltwater crocodiles (Crocodylus porosus) in Australia

Fig. 2. Relationship of a new species of Hepatozoon (bold) identified in erythrocytes from the blood of the saltwater crocodile with representative taxa represented in the GenBank database, established based on a phylogenetic analysis of sequence data from part of the small subunit of nuclear ribosomal RNA gene (SSU; 889 bp) employing the neighbour-joining distance method. Branch supports are represented by neighbour-joining bootstrap percentages. Species of Dactylosoma were used as outgroups.

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Fig. 3 in The first finding of Dictyocaulus cervi and Dictyocaulus skrjabini (Nematoda) in feral fallow deer (Dama dama) in Australia

Fig. 3. Maximum likelihood phylogenetic trees of cox1 (A), 18S rRNA (B), and ITS2 (C) Dictyocaulus sequences. Sequences from this study are indicated in bold. Square brackets indicate GenBank accessions. Coloured boxes indicate putative Dictyocaulus species groups.

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Fig. 2. A in The first finding of Dictyocaulus cervi and Dictyocaulus skrjabini (Nematoda) in feral fallow deer (Dama dama) in Australia

Fig. 2. A. Posterior end of a male specimen of Dictyocaulus cervi collected from a fallow deer from Bega (NSW), ventral view. B. Posterior end of a male specimen of Dictyocaulus skjrabini collected from a fallow deer from Bega (NSW), lateral view. Scale bar: 50 μm.

FIGURE 6 in New genus of primitive wombat (Vombatidae, Marsupialia) from Miocene deposits in the Riversleigh World Heritage Area (Queensland, Australia)

FIGURE 6. Lingual view of lower molars to show presence of enamel tracts (indicated by asterisks). 1, Nimbavombatus boodjamullensis. 2, Rhizophascolonus crowcrofti. 3, Warendja encorensis.

FIGURE 3 in New genus of primitive wombat (Vombatidae, Marsupialia) from Miocene deposits in the Riversleigh World Heritage Area (Queensland, Australia)

FIGURE 3. Left maxillary fragment of Nimbavombatus boodjamullensis from Boid Site East (QM F23774). Left panel (photographs) of 1, occlusal (ventral) view of tooth row and 2, buccal (lateral) view. Scale bar represents 10 mm. Right panel (line drawings) of 3, occlusal (ventral) view and 4, buccal (lateral) view. Grey shading represents enamel.

FIGURE 5 in New genus of primitive wombat (Vombatidae, Marsupialia) from Miocene deposits in the Riversleigh World Heritage Area (Queensland, Australia)

FIGURE 5. Isolated molars of Nimbavombatus boodjamullensis from Creaser's Ramparts. 1, Right M1 (QM F30339). 2, Left M1 (QM F51404). 3, Left Mx (probably M2 or M3) (QM F23773). From left to right views are: buccal, lingual, anterior, posterior, stereo of occlusal surface and line drawing of occlusal surface. Scale bar for photographs represents 10 mm. Grey shading on line drawings represents enamel. L indicates lingual side, B indicates buccal side.

FIGURE 2 in New genus of primitive wombat (Vombatidae, Marsupialia) from Miocene deposits in the Riversleigh World Heritage Area (Queensland, Australia)

FIGURE 2. An animation of type specimen QM F23774, reduced for web viewing, based on CT data. The specimen was scanned at the Natural History Museum, London using a Metris X-Tek HMX ST 225 system. Volumes were constructed using CT PRO (Metris X-Tek, UK) and visualised using VG Studio Max 2.0 (Volume Graphics, Heidelberg, Germany).

FIGURE 4 in New genus of primitive wombat (Vombatidae, Marsupialia) from Miocene deposits in the Riversleigh World Heritage Area (Queensland, Australia)

FIGURE 4. Left maxillary fragment of Nimbavombatus boodjamullensis from Creaser's Ramparts Site (QM F23725). Photographs of 1, occlusal (ventral) view, 2, buccal (lateral) view and 3, lingual (medial) view. Scale bar represents 10 mm. 4, Line drawing of occlusal (ventral) view. Grey shading represents enamel. Asterisk marks presence of distinctive wear facet on trailing edge enamel (see text for details).

FIGURE 8 in New genus of primitive wombat (Vombatidae, Marsupialia) from Miocene deposits in the Riversleigh World Heritage Area (Queensland, Australia)

FIGURE 8. Jaw movement during the power stroke in Nimbavombatus boodjamullensis. 1, Evidence of jaw movement on the surface of the cheek teeth. 2, Movement of the lower jaw during Phase I (left) and Phase II (right) of the power stroke.

FIGURE 7. 1, Strict consensus tree for parsimony analysis including Marada arcanum. 2 in New genus of primitive wombat (Vombatidae, Marsupialia) from Miocene deposits in the Riversleigh World Heritage Area (Queensland, Australia)

FIGURE 7. 1, Strict consensus tree for parsimony analysis including Marada arcanum. 2, Bootstrap support for single most parsimonious tree from analysis excluding Marada arcanum (see text for details). Vombatidae indicated in purple.