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Figure 2 in Morphology, molecular phylogeny and biomass evaluation of Desmodesmus abundans (Scenedesmaceae-Chlorophyceae) from Brazil

Figure 2. Lipids and carbohydrate production of D. abundans LGMM0013 andT.obliquus LGMM0001 under autotrophic conditions after 22 days. Bars indicate standard deviation.

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Figure 1 in Morphology, molecular phylogeny and biomass evaluation of Desmodesmus abundans (Scenedesmaceae-Chlorophyceae) from Brazil

Figure 1. Growth comparison in autotrophic conditions between D. abundans LGMM0013 and T. obliquus LGMM0001 by dry biomass production. Bars indicate standard deviation.

opencc-by-4.0Feb 2014View details →

Fig. 3 in Molecular phylogeny of Indonesian Lymantria Tussock Moths (Lepidoptera: Erebidae) based on CO I gene sequences

Fig. 3. Neighbor-Joining tree based on K2P distance model of all substitutions of CO I gene (Bootstrap support are shown at the nodes; ID=specimens from Indonesia).

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Fig. 4. Maximum likelihood tree for 43 in Molecular phylogeny of Indonesian Lymantria Tussock Moths (Lepidoptera: Erebidae) based on CO I gene sequences

Fig. 4. Maximum likelihood tree for 43 species of Lymantria based all substitutions of CO I gene (Bootstrap support are shown at the nodes; ID=specimens from Indonesia).

opencc-by-4.0Dec 2003View details →

Figure 1 in The first molecular phylogeny of Buthidae (Scorpiones)

Figure 1: Maximum Likelihood (ML) tree of Old World and New World Buthidae inferred from a 296 bp fragment of the mitochondrial ribosome 16S region. The DNA substitution model was TVM + I + Γ; base frequencies: πA = 0.34, πT = 0.42, πC = 0.14, Rmatrix = (A-G = 11.50, A-C = 2.95, C-G ~ 0, A-T = 2.44, G-T = 1, C-T = 11.50), gamma shape parameter α = 0.67, and proportion of invariable sites = 0.28, respectively. The tree was rooted using the outgroup species Pseudochactas ovchinnikovi.

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◂Fig. 6 A molecular phylogeny of 56 systematically representative Peridiniaceae, including 42 accessions assignable to P. cinctum from various geographic regions. Maximum likelihood tree (– ln = 21,884.93), as inferred from a rRNA nucleotide alignment (1137 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (CZE Czech Republic, E East, GER Germany, HET Heterocapsaceae, N North, PPE Protoperidiniaceae, POL Poland, rbn ribotype n, S South, SWE Sweden, UKR Ukraine, W West) in Bumps on the back: An unusual morphology in phylogenetically distinct Peridinium aff. cinctum (= Peridinium tuberosum; Peridiniales, Dinophyceae)

◂Fig. 6 A molecular phylogeny of 56 systematically representative Peridiniaceae, including 42 accessions assignable to P. cinctum from various geographic regions. Maximum likelihood tree (– ln = 21,884.93), as inferred from a rRNA nucleotide alignment (1137 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (CZE Czech Republic, E East, GER Germany, HET Heterocapsaceae, N North, PPE Protoperidiniaceae, POL Poland, rbn ribotype n, S South, SWE Sweden, UKR Ukraine, W West)

Fig. 41 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Fig. 41. Molecular phylogeny of Acerentomidae inferred from concatenated COI, 18S rRNA, 28S rDNA D1–D2, and 28S rDNA D3–D6 sequences with maximum likelihood (ML). ML bootstrap values shown above the branches.

Figs. 11–15 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Figs. 11–15. Acerentuloides bernardi sp. nov. 11. Pronotum and mesonotum, right side; 12. lateral part of metanotum; 13. anterior part of prosternum; 14. anterolateral part of mesosternum; 15. anterolateral part of metasternum. Arrows indicate pores (al = tergal anterolateral, sl = tergal sublateral). Scale bars: 20 µm.

Figs. 1–10 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Figs. 1–10. Acerentuloides bernardi sp. nov. 1. Head, right side; 2. pseudoculus with seta l3; 3. cephalic seta sd5; 4. maxillary palpus; 5. labial palpus; 6. maxillary gland; 7. comb; 8. female squama genitalis; 9. foretarsus, exterior view; 10. foretarsus, interior view. Arrows indicate pores (cp = clypeal pore, fr = frontal pore). Scale bars: 20 µm.

Figs. 24–34 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Figs. 24–34. Acerentuloides bernardi sp. nov. scanning electron microscopy photographs. 24. Habitus; 25. labial palp (apical tuf with 4 setae broken; s = labial sensillum); 26. foretarsus, interior view: sensilla t1, t3 and a'; 27. modified seta P2a on mesonotum; 28. modified seta A2 on prosternum; 29. modified seta M2 on prosternum; 30. modified seta A5 on tergite I and P1a on sternite I; 31. abdominal leg on segment III (sa = subapical, am = apical medial, al = apical lateral setae; apical lateral seta is broken); 32. hind margin of sternite VI; 33. hind margin of sternite VII; 34. sternites VIII–XII. Scale bars = 300 µm (Fig. 24), 4 µm (Figs. 25 and 27–29), 10 µm (Fig. 31), and 20 µm (Figs. 26, 30, and 32–34).

Figs. 35–40 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Figs. 35–40. Acerentulus confinis (Berlese, 1908), American specimen scanning electron microscopy photographs. 35. Habitus; 36. pseudoculus and cephalic setae sd4 and l3; 37. foretarsus, exterior view: sensilla t1, t3 and a'; 38. labial palpi with apical tuf of setae and basal sensillum (s); 39. sternite VIII; 40. modified seta P4 on metanotum. Scale bars = 300 µm (Fig. 35), 20 µm (Figs. 36 and 38), and 40 µm (Figs. 37, 39, and 40).

Figs. 16–23 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Figs. 16–23. Acerentuloides bernardi sp. nov. 16. Tergite I, right side; 17. tergite VI, right part; 18. tergite VII, right part; 19. tergite VIII; 20. sternite II; 21. abdominal leg of sternite II; 22. sternite VI; 23. sternites VII–IX. Arrows indicate pores (psm = tergal posterosubmedial, psl = tergal posterosublateral, spsm = sternal posterosubmedial, spm = sternal posteromedial). Scale bars: 20 µm.

Fig. 3 in Epidemiology and molecular phylogeny of Babesia sp. in Little Penguins Eudyptula minor in Australia

Fig. 3. Agarose gel electrophoresis of amplification products obtained through nested PCR tests targeting the 18S rRNA gene of Babesia (primers Bab5.1/BabB followed by RLBF/RLBR) or the mitochondrial cytochrome b gene of Haemoproteus/Plasmodium (primers HaemNFI/HaemNR3 followed by HaemF/HaemR2). The following samples are represented: (a) captive-born little penguin chick, negative blood smear; (b) adult wild little penguin, negative blood smear; (c) Babesia-infected adult wild little penguin, as confirmed through blood smear; (d) Haemoproteus-infected adult tropical screech owl, as confirmed through blood smear; (e) Plasmodium-inoculated chicken, raised in arthropod-free environment; (f) blood parasite-free chicken, raised in arthropodfree environment.

Fig. 1 in Epidemiology and molecular phylogeny of Babesia sp. in Little Penguins Eudyptula minor in Australia

Fig. 1. Geographic distribution of sampling locations, southeast Australia. Site details are given in Table 1. The geographic distribution of little penguins (black area) is shown in the top right map (adapted from Marchant and Higgins, 1990).

Fig. 4 in Epidemiology and molecular phylogeny of Babesia sp. in Little Penguins Eudyptula minor in Australia

Fig. 4. Maximum likelihood phylogenetic tree of the 18S rRNA gene of the studied Babesia lineages. Lineages identified in this study are emphasized in red, and other avianinfecting lineages are emphasized in blue. For each lineage, the following information is provided: morphospecies (Genbank ascension number) host species. For avianinfecting lineages, the geographic location is also provided. Branch lengths are drawn proportionally to evolutionary distance (scale bar is shown). 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 Epidemiology and molecular phylogeny of Babesia sp. in Little Penguins Eudyptula minor in Australia

Fig. 2. Babesia sp. in the blood smear of a little penguin. Individual details: TAS- 124, male, adult, moulting, sampled at "Darlington Foreshore" (Maria Island, Tasmania) in 21/02/2013, Genbank ascension number KP144323, Giemsa stain.

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.