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Fig. 8 in A new leanchoiliid megacheiran arthropod from the lower Cambrian Emu Bay Shale, South Australia

Fig. 8. Strict consensus of 14 shortest cladograms (77 steps) based on character data in Table 1. Numbers above nodes are Bremer support; those below nodes are jackknife frequencies>50%. Cheliceramorpha corresponds to a clade with the same composition in Cotton and Braddy (2004).

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Fig. 1 in A new leanchoiliid megacheiran arthropod from the lower Cambrian Emu Bay Shale, South Australia

Fig. 1. Geology of the area near Buck Quarry, north east coast of Kangaroo Island, South Australia (modified from García−Bellido et al. 2009).

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Fig. 4 in A new leanchoiliid megacheiran arthropod from the lower Cambrian Emu Bay Shale, South Australia

Fig. 4. Leanchoiliid megacheiran arthropod Oestokerkus megacholix gen. et sp. nov. SAM P45167. A. P45167a. A1, cephalic shield and most of trunk; A2, detail of cephalic shield. B. P45167b. A2 and B light from NE. Overlap between adjacent tergites offset on left (Lol) and right (Rol) sides of body. Boundaries between cephalic shield and anterior trunk tergites delimited in B by dashed lines. Arrows mark positions of inferred dorsal transverse tendons. Abbreviations: cn1–2, cephalic endopods; cs, cephalic shield; gap, peduncle of great appendage; ol, overlap between adjacent trunk tergites; t1–t3, tergites of trunk segments 1–3; tn, trunk endopods.

Fig. 1 in Are feral goats intermediate hosts for Linguatula (Pentastomida) in Australia?

Fig. 1. Anterior end of infective nymph of Linguatula sp. removed from capsule within mesenteric lymph node of a feral goat examined in this study. Lateral view. Note capsule wall on left side of photograph. ah, anterior hook; as, annular spine; bc, buccal capsule; dap, dorsal accessory piece; ph, posterior hook. Scale bar 50 μm.

Fig. 7 in Rediscovery of Ixodes confusus in Australia with the first description of the male from Australia, a redescription of the female and the mitochondrial (mt) genomes of five species of Ixodes

Fig. 7. Maximum likelihood (ML) phylogenetic tree from entire mt genomes (15,254 bp alignment). Tip-labels indicate NCBI accession numbers. Numbers above branches show Maximum Likelihood bootstrap support whereas numbers below branches show the Bayesian Posterior Probability support. Ixodes pavlovskyi Pomerantzev, 1946, one of the species of "other Ixodes" clade (sensu Barker et al., 2021), for which an entire mitochondrial (mt) genome was available in GenBank, was set as the outgroup. The scale bar indicates 0.07 nucleotide substitutions per nucleotide site for the 15,254 nucleotide sites in our alignment of theses entire mt genomes. So, for example, there were about 1067 nucleotide substitutions along the branch that leads to I. (Ceratixodes) uriae plus I. (Sternalixodes) holocyclus plus I. (Exopalpiger) fecialis, which is marked with an asterisk (i.e. 0.07 nucleotide substitutions per nucleotide site x 15,254 nucleotide sites (bps) = 1067 nucleotide substitutions). Ticks in bold were sequenced in the present study.

Fig. 6 in Rediscovery of Ixodes confusus in Australia with the first description of the male from Australia, a redescription of the female and the mitochondrial (mt) genomes of five species of Ixodes

Fig. 6. The mitochondrial genomes of Ixodes (Sternalixodes) confusus, I. (St.) myrmecobii, I. (St.) cornuatus, I. (St.) hirsti and I. (St.) trichosuri. Protein-coding genes are shown in green, tRNAs are in yellow, rRNAs are in red whereas the two control regions are in blue. Protein-coding genes are labelled by their fourcharacter abbreviations, tRNAs are labelled by their one-letter amino acid abbreviations whereas the two control regions are labelled as CR1 and CR2. Variation in the size of mitochondrial genome is indicated in parenthesis. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 5 in Rediscovery of Ixodes confusus in Australia with the first description of the male from Australia, a redescription of the female and the mitochondrial (mt) genomes of five species of Ixodes

Fig. 5. Ixodes confusus Roberts (1960), scanning electron micrographs of female. A, Idiosoma, dorsal view; B, Idiosoma showing posterior portion of scutum and alloscutum; C, Idiosoma, ventral view; D, Spiracular plate; E, Gnathosoma, dorsal view; F, Porose areas; G, Gnathosoma, ventral view; H, Coxae. Specimens: A-H, B5510 Etty Bay, Qld. Scale-bars: A, C, 1 mm; B, E, G, H, 0.5 mm; D, F, 0.2 mm.

Fig. 3 in Rediscovery of Ixodes confusus in Australia with the first description of the male from Australia, a redescription of the female and the mitochondrial (mt) genomes of five species of Ixodes

Fig. 3. Holotype (male) of Ixodes confusus Roberts (1960) from Sogeri, Papua New Guinea (QM QM-G2456), horizontal scale bar 1 mm, vertical scale bar 2.7 mm.

Fig. 4 in Rediscovery of Ixodes confusus in Australia with the first description of the male from Australia, a redescription of the female and the mitochondrial (mt) genomes of five species of Ixodes

Fig. 4. Ixodes confusus Roberts (1960), scanning electron micrographs of male. A, Idiosoma, dorsal view; B, Idiosoma, ventral view; C, Anal plate; D, Spiracular plate; E, Gnathosoma, dorsal view; F, Gnathosoma, anteroventral view; G, Coxae. Specimens: A, B6697 Mt Molloy, Qld; B, C, D, F, G B5511 Etty Bay; E, B5537 Cardwell. Scale-bars: A, B, 1 mm; C, D, 0.4 mm; E, F, 0.2 mm; G, 0.5 mm.

Fig. 2 in Rediscovery of Ixodes confusus in Australia with the first description of the male from Australia, a redescription of the female and the mitochondrial (mt) genomes of five species of Ixodes

Fig. 2. Paratype (female) of Ixodes confusus Roberts (1960) from Etty Bay, Queensland Australia (ANIC 48–001875), horizontal scale bar 1 mm, vertical scale bar 3.3 mm.

Fig. 1 in Rediscovery of Ixodes confusus in Australia with the first description of the male from Australia, a redescription of the female and the mitochondrial (mt) genomes of five species of Ixodes

Fig. 1. The five known localities in Queensland (Qld) Australia of Ixodes confusus Roberts (1960), indicated by white-with-red dots. Note that there were two sites at Etty Bay: (i) near Etty Bay Caravan Park; and (ii) Etty Bay, in the vicinity of 195 Mourilyan Harbour Rd, Etty Bay. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1. 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. 1. Dermopristis pterophilus n. sp. attached to the skin adjacent to the base of left pectoral fin of juvenile green sawfish Pristis zijsron Bleeker, 1851 (photograph DLM, 2011).

Fig. 9 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 9. Similarity of Toxoplasma gondii from Little Penguins with representative strains from Archetypals I, II, and III in the B1 gene. A: shows polymorphisms at the 366 nucleotide. B: shows polymorphisms at the 504 nucleotide. Declaration of competing interest

Fig. 6 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 6. (And detail) – four parasites in a cyst within the cytoplasm of a host cell, spleen (x3810, bar = 2 μm) Image left: E - erythrocyte, Ph - phagocyte, P - protozoa; image right (detail): N - nucleus.

Fig. 5 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 5. Splenic impression smear, erythrocytes (E), splenic stromal cells (S) and numerous protozoa (arrows) (Wright's Giemsa stain, 1000x).

Fig. 4 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 4. Liver, intact and necrotic hepatocytes and numerous protozoa (arrows), free and within cysts (5 μm section, Martius Scarlet Blue stain, 400x). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 11 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 11. Liver, staining of protozoan antigen in intact and necrotic hepatocytes (x400 Toxoplasma polyclonal antibody IHC).

Fig. 4. 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. 4. Dermopristis pterophilus n. sp. various soft parts, ventral perspective. (A) Reproductive system (excluding testes). (B) Spermatophores. (C & D) Pharynx with papillae retracted vs extended. Abbreviations: dr, distal region of tubular male reproductive tract; gm, germarium; gt1–3, first through third major gut sub-trees; mf, muscle fibres; mp, male pore; o, o¨otype; p, digitiform papillae; pr, proximal region of tubular male reproductive tract; sr, seminal receptacle; sv, seminal vesicle; v, vagina; vd, vas deferens; vid, vitelline duct; vr, vitelline reservoir. Scale bars: (A) 250 μm; (B) 300 μm; (C & D) 100 μm.

Fig. 3 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 3. Liver, necrotic focus (the area of relative pallor, within which numerous organisms were identifiable) (5 μm section, Haematoxylin and Eosin stain, 100x).

Fig. 3. 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. 3. Dermopristis pterophilus n. sp. holotype, ventral perspective. Abbreviations: b, bladder; bc, buccal cavity; dr, distal region of tubular male reproductive tract; g, gut; gm, germarium; h, haptor; m, mouth; mf, muscle fibres; mp, male pore; o, o¨otype; ph, pharynx; pr, proximal region of tubular male reproductive tract; sr, seminal receptacle; t, testis; vd, vas deferens; ve, vasa efferentia; vf, vitelline follicle; vr, vitelline reservoir. Scale bar: 500 μm.