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Fig. 7 in Pentastomids of wild snakes in the Australian tropics

Fig. 7. Waddycephalus spp. body lengths versus the first principal components (PC1) of a principal components analysis of hook dimensions (anterior AD, anterior BC, posterior AD, posterior BC). Contour lines show quantile contours in 5% intervals from a nonparametric density analysis. Different genetic species groupings are denoted by different symbols (triangle = Waddycephalus sp. 2; circles = Waddycephalus sp. 3; crosses = Waddycephalus sp. 5; body size data was not attained for Waddycephalus sp. 1 or 4).

Fig. 5 in Pentastomids of wild snakes in the Australian tropics

Fig. 5. Comparison of posterior hook morphology of Raillietiella orientalis from the Northern Territory of Australia versus Asia. Raw barb length (AB) versus overall length (BC) of posterior hooks of R. orientalis measured in the current study (circles) and in Ali et al., 1982 (triangles). Gray symbols denote female pentastomes and open symbols denote male pentastomes.

Fig. 2 in Pentastomids of wild snakes in the Australian tropics

Fig. 2. Waddycephalus spp. in the lungs of road-killed snakes collected in the Northern Territory of Australia. (a) One female Waddycephalus sp. (short arrow) and three lesions surrounding Waddycephalus attachment sites (long arrows) in the dissected lung of a green tree snake, Dendrelaphis punctulatus; (b) Three (one is partially obscured) female Waddycephalus sp. (arrows), in the dissected lung of D. punctulatus. Note also multiple visible attachment sites (lines); (c) Two large female and several small male Waddycephalus sp. filling the trachea of the same D. punctulatus depicted in (b); (d) One Waddycephalus sp. deeply embedded in the lung tissue of an ethanol-preserved slaty-grey snake, Stegonotus cucullatus. All scale rules are in centimetres; all photo credits to Crystal Kelehear.

Fig. 4 in Pentastomids of wild snakes in the Australian tropics

Fig. 4. Posterior hook morphology of Raillietiella orientalis, collected from snakes in the Northern Territory of Australia. Barb length (AB) versus overall length (BC) of pentastomids measured from four snake species: Northern death adder (Acanthophis praelongus; black diamonds), lesser black whip snake (Demansia vestigiata; grey circles), keelback (Tropidonophis mairii; grey triangles), and water python (Liasis fuscus; dark grey squares). (a) Raw hook measurements uncorrected for pentastome body size, note potential species clusters; (b) Hook measurements corrected for pentastome body size (residual scores from a linear regression of hook measurements against pentastome body size), note that clusters now disappear.

Fig. 1 in Pentastomids of wild snakes in the Australian tropics

Fig. 1. Raillietiella orientalis in road-killed lesser black whip snakes, Demansia vestigiata, collected in the Northern Territory of Australia. (a) Dissected trachea containing a single long R. orientalis; (b) Severe occlusion of the lung by 68 R. orientalis; (c) R. orientalis crawling out of the mouth of a snake. All scale rules are in centimetres; all photo credits to Crystal Kelehear.

Fig. 5 in Phylogeographic Structure within the Fiddler Crabs and (Brachyura, Ocypodidae) along the Tropical West Atlantic.

Fig. 5. Mismatch distribution for one Caribbean and nine Brazilian populations of Uca maracoani with 606 basepairs (A) and one Brazilian and one Caribbean population with 825 basepairs (B).

Fig. 2 in Phylogeographic Structure within the Fiddler Crabs and (Brachyura, Ocypodidae) along the Tropical West Atlantic.

Fig. 2. Haplotype network of Leptuca thayeri constructed with Popart, with a connection limit of 95%, derived from Cox1 mtDNA with 609 basepairs (A) and 826 basepairs (B). Black dots represent missing haplotypes (one-step edges); numbered 'H' indicate most common haplotypes.

Fig. 1 in Phylogeographic Structure within the Fiddler Crabs and (Brachyura, Ocypodidae) along the Tropical West Atlantic.

Fig. 1. Sample sites of Leptuca thayeri (black dots) and Uca maracoani (grey dots) populations from throughout the West Atlantic: Luperón & Sánchez from the Dominican Republic; Priory (St. Ann) from Jamaica; Marudá (Pará), Acuípe (Bahia), Bertioga (São Paulo) from Brazil. Grey squares correspond to localities sampled by Wieman et al. (2014), with sequences of U. maracoani in GenBank.

Fig. 4 in Phylogeographic Structure within the Fiddler Crabs and (Brachyura, Ocypodidae) along the Tropical West Atlantic.

Fig. 4. Mismatch distribution for two Caribbean and three Brazilian populations of Leptuca thayeri with 609 basepairs (A) and three Brazilian populations with 826 basepairs (B).

Fig. 3 in Phylogeographic Structure within the Fiddler Crabs and (Brachyura, Ocypodidae) along the Tropical West Atlantic.

Fig. 3. Haplotype network of Uca maracoani constructed with Popart, with a connection limit of 95%, derived from Cox1 mtDNA with 606 base pairs (A) and 825 base pairs (B). Black dots represent missing haplotypes (one-step edges), numbered 'H' indicate most common haplotypes.

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Fig. 2 in Review of the (Branchiopoda: Spinicaudata: Limnadiidae) of Tropical Asia, with the Description of a New Species.

Fig. 2. Eulimnadia cryptus sp. nov. A, Hermaphrodite habitus; B, Male habitus; C, Hermaphrodite head; D, Male head; E, Hermaphrodite telson. Scale bars: A–E = 0.5 mm).

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Fig. 1 in Review of the (Branchiopoda: Spinicaudata: Limnadiidae) of Tropical Asia, with the Description of a New Species.

Fig. 1. Eulimnadia cryptus sp. nov. A–C, Resting eggs overall structure and variation; D, Single egg polygon. Scale bars: A = 0.2 mm; B and C = 0.05 mm; D = 0.02 mm.

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Fig. 3 in Persistent low avian malaria in a tropical species despite high community prevalence

Fig. 3. Maximum likelihood phylogenetic inference of (A) Haemoproteus and (B) Plasmodium from the Australasian region. Sequences were included if they were at least 479 nucleotides in length and were found to be unique from a pairwise distance analysis (see methods). Bootstrap support values are shown if greater than 50. Dots indicate the 14 lineages that were detected in this study and their colour denotes the bird species they occurred within [Purple = PCFW (M. c. coronatus), Red = RBFW (M. melanocephalus), Yellow = BSR (P. cerviniventris), Grey = WGH (L. unicolor)]. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

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Fig. 2 in Persistent low avian malaria in a tropical species despite high community prevalence

Fig. 2. (A) Malarial parasite prevalence across years in four bird species, buff-sided robin (BSR, n = 66), purple-crowned fairy-wren (PCFW, n = 731), red-backed fairy-wren (RBFW, n = 78), white-gaped honeyeater (WGH, n = 25). Fisher's exact P-values test for annual differences in infection within each bird species. (B) Longitudinal sampling of infected PCFW adults (individuals presented were sampled more than twice and were identified as infected with Haemoproteus or Plasmodium). Dotted lines indicate uncertainty in years when no sample was available. Each individual was infected with a single lineage. (C) Percentage of individual PCFW infected within each age category. (D) Local phylogenetic relationship between parasite lineages, colours refer to host species as for (A). Maximum likelihood tree was inferred using GTR + G + I with 1000 bootstrap replicates; novel lineages are indicated by *. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

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Fig. 1 in Persistent low avian malaria in a tropical species despite high community prevalence

Fig. 1. Map of Australia and the Kimberly region. Sampling was conducted at the Australian Wildlife Conservancy's Mornington Wildlife Sanctuary (17̊31′S, 126̊6'E). Star indicates the location of the field site where samples were collected.

Fig. 14. Kelleriella quadridens n. gen. n in Copepods of the family Kelleriidae (Crustacea, Copepoda, Cyclopoida) from tropical waters of the Asia-Pacific

Fig. 14. Kelleriella quadridens n. gen. n. sp., female. A, maxillule; B, maxilla; C, maxilliped; D, leg 1; E, leg 2; F, leg 4; G, exopod of leg 5. Scale bars: A-C, 0.02 mm; D-G, 0.05 mm.

Fig. 12. Kelleria robusta n in Copepods of the family Kelleriidae (Crustacea, Copepoda, Cyclopoida) from tropical waters of the Asia-Pacific

Fig. 12. Kelleria robusta n. sp., female. A, maxilliped; B, leg 1; C, leg 2; D, endopod of leg 3; E, leg 4; F, exopod of leg 5; G, genital aperture. Scale bars: A, F, G, 0.05 mm; B-E, 0.1 mm.

Fig. 10. Kelleria phuketensis n in Copepods of the family Kelleriidae (Crustacea, Copepoda, Cyclopoida) from tropical waters of the Asia-Pacific

Fig. 10. Kelleria phuketensis n. sp., female. A, maxillule; B, maxilliped; C, leg 1; D, leg 2; E, endopod of leg 3; F, leg 4; G, exopod of leg 5; H, right genital aperture, dorsal. Scale bars: 0.02 mm.

Fig. 8. Kelleria latipes n in Copepods of the family Kelleriidae (Crustacea, Copepoda, Cyclopoida) from tropical waters of the Asia-Pacific

Fig. 8. Kelleria latipes n. sp., female. A, maxilliped; B, leg 1; C, leg 2; D, endopod of leg 3; E, leg 4; F, exopod of leg 5; G, right genital aperture, dorsal. Scale bars: 0.02 mm.

Fig. 9. Kelleria phuketensis n in Copepods of the family Kelleriidae (Crustacea, Copepoda, Cyclopoida) from tropical waters of the Asia-Pacific

Fig. 9. Kelleria phuketensis n. sp., female. A, habitus, dorsal; B, urosome, dorsal; C, anal somite and caudal rami, dorsal; D, rostrum; E, antennule; F, antenna; G, labrum; H, mandible; I, maxilla. Scale bars: A, 0.2 mm; B, 0.1 mm; C, D, H, I, 0.02 mm; E-G, 0.05 mm.