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Fig. 7 in Fig. 14 in An Integrative Description of Two New Species (Tardigrada: Eutardigrada: Macrobiotidae) with Updated Genus Phylogeny.

Fig. 7. Platynereis shihmenensis sp. nov.; holotype (NMNS 8390-4): A, whole animal; B, anterior body; C, close-up of Area IV, right side; C, closeup of Area VI. Scale bars: A = 2.0 mm; B = 1.0 mm; C–D = 0.1 mm.

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Fig. 3 in Fig. 13 in An Integrative Description of Two New Species (Tardigrada: Eutardigrada: Macrobiotidae) with Updated Genus Phylogeny.

Fig. 3. Relationship between the monthly total size of wounds (overall bark-stripping intensity) and the product of sambar abundance and necessity index. Pearson's correlation coefficient was 0.925 (p <0.001).

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Fig. 4 in Fig. 13 in An Integrative Description of Two New Species (Tardigrada: Eutardigrada: Macrobiotidae) with Updated Genus Phylogeny.

Fig. 4. Predicted probability of bark-stripping by sambar for seven tree species along the diameter at breast height (DBH) at Tataka, Yushan National Park in Taiwan. Month was set to September and slope was set to zero. Range of the DBH for each species was based on the observed values.

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Fig. 2 in Fig. 13 in An Integrative Description of Two New Species (Tardigrada: Eutardigrada: Macrobiotidae) with Updated Genus Phylogeny.

Fig. 2. Averages of indexes of (a) the bark-stripping frequency (b) bark-stripping intensity and necessity index (average size per wound) and (c) sambar abundance from November 2018 to January 2021 at Tataka, Yushan National Park in Taiwan.

Fig. 8 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.

Fig. 8. Cladogram of East Asian Bruggmanniella based on the Neighbor-joining method based on the DNA COI region. Support values at the nodes are Neighbor-joining (left)/ Maximum-likelihood (media)/ Bayesian inference (right). "–" indicates support values less than 50% in ML and NJ, and 0.5 in BI inference.

Fig. 7 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.

Fig. 7. Bruggmanniella cinnamomi (A) Male head (ventral view). (B) Male 5th tarsomere. (C) Female 5th tarsomere. (D) Male wing. Scale bars: A = 0.03 mm; B–C = 0.1 mm; D = 1 mm.

Fig. 5 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.

Fig. 5. Male genitalia of Taiwanese Cinnamomum–associated Bruggmanniella. (A) Bruggmanniella turoguei sp. nov., (B) B. shianguei sp. nov., and (C) B. sanlianensis sp. nov. Scale bar = 0.1 mm.

Fig. 6 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.

Fig. 6. Taiwanese Cinnamomum–associated Bruggmanniella. Bruggmanniella turoguei sp. nov. (A, D), B. shianguei sp. nov. (B, E), B. sanlianensis sp. nov. (C, F). Scale bars: pupal head (A–C) = 0.5 mm and for larval sternal spatula (D–F) = 0.1 mm. Larval lateral papillae shown in dotted blue circles.

Fig. 3 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.

Fig. 3. Bruggmanniella shianguei sp. nov. (A) Male head (ventral view) (B) Male antenna (8–12 segment). (C) Female antenna (8–12 segment). (D) Male 1st tarsomere. (E) Male 5th tarsomere. (F) Female 5th tarsomere. (G) Male wing. (H) Female wing. Scale bars: A–C = 0.03 mm; D–F = 0.1 mm; G–H = 1 mm.

Fig. 2 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.

Fig. 2. Bruggmanniella turoguei sp. nov. (A) Male head (ventral view) (B) Male antenna (7–12 segment). (C) Female antenna (7–12 segment). (D) Male 1st tarsomere. (E) Male 5th tarsomere. (F) Female 5th tarsomere. (G) Male wing. (H) Female wing. Scale bars: A–C = 0.03 mm; D–F = 0.1 mm; G–H = 1 mm.

Fig. 1 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.

Fig. 1. Plant galls induced by Taiwanese Bruggmanniella species on Cinnamomum species. (A) Stem galls on C. insularimontanum. (B) Stem galls on C. subavenium. (C) Stem galls on C. osmophloeum. (D) Leaf galls on C. osmophloeum.

Fig. 4 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.

Fig. 4. Bruggmanniella sanlianensis sp. nov. (A) Male head (ventral view) (B) Male antenna (8–12 segment). (C) Female antenna (8–12 segment). (D) Male 1st tarsomere. (E) Male 5th tarsomere. (F) Female 5th tarsomere. (G) Male wing. (H) Female wing. Scale bars: A–C = 0.03 mm; D–F = 0.1 mm; G–H = 1 mm.

Fig. 8 in Haemoprotozoa: Making biological sense of molecular phylogenies

Fig. 8. Phenotypic characters mapped against broad molecular phylogenies of haemosporidian parasites. Molecular phylogenetic relationships are indicated on the left as a consensus (macro-evolutionary) tree derived from multiple studies cited within the text.

Fig. 7 in Haemoprotozoa: Making biological sense of molecular phylogenies

Fig. 7. Phenotypic characters mapped against broad molecular phylogenies of haemogregarine parasites. Molecular phylogenetic relationships are indicated on the left as a consensus (macro-evolutionary) tree derived from multiple studies cited within the text.

Fig. 6 in Haemoprotozoa: Making biological sense of molecular phylogenies

Fig. 6. Phenotypic characters mapped against broad molecular phylogenies of haemococcidian parasites (blood-borne genera shown in red). Molecular phylogenetic relationships are indicated on the left as a consensus (macro-evolutionary) tree derived from multiple studies cited within the text. (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 Haemoprotozoa: Making biological sense of molecular phylogenies

Fig. 5. Developmental cycles and hosts for apicomplexan blood parasites (DH = definitive host; IH = intermediate host; PH = paratenic host; bm = blood meal; bmi = injected during blood meal; ve = vector eaten).

Fig. 3 in Haemoprotozoa: Making biological sense of molecular phylogenies

Fig. 3. Developmental stages formed by kinetoplastid flagellates (blood-borne genera shown in red). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Fig. 2 in Haemoprotozoa: Making biological sense of molecular phylogenies

Fig. 2. Geological time periods with milestones in the development of life on Earth, together with historical extent of fossil records for particular assemblages.

Fig. 10 in Haemoprotozoa: Making biological sense of molecular phylogenies

Fig. 10. Probable evolutionary origins of haemoprotozoan parasites (solid lines = strong inferential support; dotted lines = presumptive).

Fig. 9 in Haemoprotozoa: Making biological sense of molecular phylogenies

Fig. 9. Phenotypic characters mapped against broad molecular phylogenies of piroplasm blood parasites. Molecular phylogenetic relationships are indicated on the left as a consensus (macro-evolutionary) tree derived from multiple studies cited within the text.