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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.

Fig. 4 in Haemoprotozoa: Making biological sense of molecular phylogenies

Fig. 4. Phenotypic characters mapped against broad molecular phylogenies of trypanosomatid haemoflagellates. Molecular phylogenetic relationships are indicated on the left as a consensus (macro-evolutionary) tree derived from multiple studies cited within the text.

Fig. 5. Maximum likelihood tree for 10 in Molecular phylogeny of Indonesian Zeuzera (Lepidoptera: Cossidae) wood borer moths based on CO I gene sequence

Fig. 5. Maximum likelihood tree for 10 species of Zeuzera based on all substitution of CO I gene (Bootstrap support are shown ath the nodes).

Fig. 3 in Molecular phylogeny of Indonesian Zeuzera (Lepidoptera: Cossidae) wood borer moths based on CO I gene sequence

Fig. 3. Scatter plots of pairwise seqeunce divergence based on K2P model versus Transition/Transversion (Ts/Tv).

Fig. 4. A 50 in Molecular phylogeny of Indonesian Zeuzera (Lepidoptera: Cossidae) wood borer moths based on CO I gene sequence

Fig. 4. A 50% majority-rule consensus tree based on all substitutions of CO I gene (Bootstrap support are shown only for the nodes which have value>50%.

Fig. 1 in Molecular phylogeny of Indonesian Zeuzera (Lepidoptera: Cossidae) wood borer moths based on CO I gene sequence

Fig. 1. Cladogram of Zeuzera (Schoorl, 1990) (all the numbers showed in each branch are apomorphies charactes that are listed in Table 1).

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Fig. 3. Maximum likelihood tree constructed from 38 nuclear rDNA ITS1 and ITS2 sequences from Apiaceae genus Daucus and relatives using a in Molecular phylogeny of Daucus (Apiaceae): Evidence from nuclear ribosomal DNA ITS sequences

Fig. 3. Maximum likelihood tree constructed from 38 nuclear rDNA ITS1 and ITS2 sequences from Apiaceae genus Daucus and relatives using a transition/transversion rate ratio of 1.6. Branch lengths are proportional to the number of expected nucleotide substitutions per site.

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Fig. 2 in Molecular phylogeny of Daucus (Apiaceae): Evidence from nuclear ribosomal DNA ITS sequences

Fig. 2. Neighbor-joining tree inferred form the analysis of 39 nuclear rDNA ITS1 and ITS2 sequences from Apiaceae genus Daucus and its relatives using a transition/transversion rate ratio of 1.6. Branch lengths are proportional to distance estimated from the two parameter method of Kimura. Numbers at nodes indicate bootstrap values for 100 replicate analyses. On this tree, bootstrap values <20% are not indicated.