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Fig 2. A-H in Eight New Species of Charinus Simon, 1892 (Arαchnidα: Amblypygi: Chαrinidαe) Endemic for the Brαziliαn Amαzon, with Notes on Their Conservαtionαl Stαtus
Fig 2. A-H. Mesal view of the right chelicerae of all new species here described. A. Charinus brescoviti sp. n. (female paratype, IBSP 149); B. Charinus ricardoi sp. n. (female paratype, MZSP 22036); C. Charinus bonaldoi sp. n. (female paratype, MPEG 0061); D. Charinus guto sp. n. (female paratype, MZSP 41460); E. Charinus carajas sp. n. (male paratype, MZSP 28291); F. Charinus orientalis sp. n. (female paratype, MZSP 29118); G. Charinus ferreus sp. n. (female paratype, MZSP 29106); H. Charinus bichuetteae sp. n. (male paratype, MNRJ 9173). Scale bars: 1mm. doi:10.1371/journal.pone.0148277.g002
Fig 1. A-E in Eight New Species of Charinus Simon, 1892 (Arαchnidα: Amblypygi: Chαrinidαe) Endemic for the Brαziliαn Amαzon, with Notes on Their Conservαtionαl Stαtus
Fig 1. A-E. Habitus and details of the sternum and pedipalp of Charinus brescoviti sp. n. (female, MNRJ 9186). A. Dorsal habitus; B. Sternum; C. Frontal view of left the pedipalp basitiba, distitiba and claw; D. Dorsal view of the right pedipalp; E. Ventral view of the left pedipalp. Scale bars: 1mm. doi:10.1371/journal.pone.0148277.g001
Fig. 1 in Description of a new water mite of the genus Zschokkea Koenike, 1892 (Acari, Hydrachnidia, Hydryphantidae) from Northeastern Russia
Fig. 1. Zschokkea orientalis sp. n., male: 1 — idiosoma, dorsal view; 2 — idiosoma, ventral view; 3 — medial eye; 4 — fragment of integument. Scale bars: 1–2 = 200 μm, 3–4 = 50 μm Рис. 1. Zschokkea orientalis sp. n., самец: 1 — иÃиосома, ÃорсаΛьная сторона; 2 — иÃиосома, вентраΛьная сторона; 3 — меÃиаΛьный гΛаз; 4 — фрагмент покрова. ШкаΛы: 1–2 = 200 μm, 3–4 = 50 μm
Fig. 2 in Description of a new water mite of the genus Zschokkea Koenike, 1892 (Acari, Hydrachnidia, Hydryphantidae) from Northeastern Russia
Fig. 2. Zschokkea orientalis sp. n., male: 5 — capitulum, lateral view; 6 — chelicera, lateral view; 7 — pedipalp, lateral view; 8 — tarsus of pedipalp; 9 — I–Leg–4–6; 10 — claw of leg IV. Scale bars: 5–7, 9 = 100 μm, 8, 10 = 20 μm Рис. 2. Zschokkea orientalis sp. n., 5 — капитуΛум, боковой виÃ; 6 — хеΛицера, боковой виÃ; 7 — пеÃипаΛьпа, боковой виÃ; 8 — Λапка пеÃипаΛьпы; 9 — коΛено, гоΛень и Λапка ноги IV; 10 — коготок ноги IV. ШкаΛы: 5–7, 9 = 100 μm, 8, 10 = 20 μm
Fig. 3 in Morphometric variation of the Herichthys bartoni (Bean, 1892) species group (Teleostei: Cichlidae): How many species comprise H. labridens (Pellegrin, 1903)?
Fig. 3. Phylogenetic analysis of the Herichthys bartoni species group obtained from the Bayesian analysis of an approximately 652 bp fragment of the mitochondrial cytochrome c oxidase subunit I (DNA Barcode). Numbers above nodes are the Bayesian Posterior Probabilities (BPP) for the principal clades recovered in the analysis. The haplotypes of the species included in the H. cyanoguttatus species group were collapsed to facilitate representation.
Fig. 2 in Morphometric variation of the Herichthys bartoni (Bean, 1892) species group (Teleostei: Cichlidae): How many species comprise H. labridens (Pellegrin, 1903)?
Fig. 2. Landmarks recorded in this study. 1. Anterior end of the lower maxilla 2. Anterior end of the upper maxilla 3. Length of the ascending premaxillary process 4. End of the supraoccipital bone 5. Start of the dorsal fin 6. Last spine of the dorsal fin 7. End of the dorsal fin 8. Upper boundary of the caudal fin 9. Center of the caudal fin 10. Base of the caudal fin 11. End of the anal fin 12. Last spine of the anal fin 13. Origin of the anal fin 14. Origin of the pelvic fin 15. Posterior end of the lower maxilla 16. Posterior end of the upper lip 17. Maximum point of curvature at the preoperculum 18. Upper end of the preoperculum 19. Upper end of the operculum 20. Most posterior end at the operculum 21. Origin of the pectoral fin 22. Upper extreme of the sphenotic orbit 23. Base of the sphenotic orbit 24. Left extreme of the sphenotic orbit 25. Right extreme of the sphenotic orbit.
Fig. 5 in Morphometric variation of the Herichthys bartoni (Bean, 1892) species group (Teleostei: Cichlidae): How many species comprise H. labridens (Pellegrin, 1903)?
Fig. 5. Canonical variance analysis derived from the geometric morphometric analysis of the species included in the Herichthys bartoni species group. A) canonical variate 1 and 2 for the head, B) canonical variate 2 and 3 for the head, C) canonical variate 1 and 2 for the body, D) canonical variate 2 and 3 for the body. Symbology: Blue: H. bartoni, Red: H. cf. labridens, Green: H. labridens, Violet: H. molango, Black: H. pame, Gray: H. pantostictus, Brown: H. steindachneri.
Fig. 1 in Morphometric variation of the Herichthys bartoni (Bean, 1892) species group (Teleostei: Cichlidae): How many species comprise H. labridens (Pellegrin, 1903)?
Fig. 1. Geographic distribution of the species included in the Herichthys bartoni group. Note: The species H. pratinus was not included in this work.
Fig. 4 in Morphometric variation of the Herichthys bartoni (Bean, 1892) species group (Teleostei: Cichlidae): How many species comprise H. labridens (Pellegrin, 1903)?
Fig. 4. Canonical variance analysis derived from the discriminant function analysis of the species included in the Herichthys bartoni species group. A) Meristic data B) Morphometric data adjusted by the method of Mossimann C) Morphometric data adjusted as proportions. Symbology: Blue: H. bartoni, Red: H. cf. labridens, Green: H. labridens, Violet: H. molango, Black: H. pame, Gray: H. pantostictus, Brown: H. steindachneri.
Fig. 8 in Psammoecus simonis Grouvelle 1892
Fig. 8. Underwater photographs of Dongsha Atoll octocorals: (A) Litophyton sp. colonies densely occupy reef space, (B) colony of Sarcophyton ehrenbergi overgrowing Acropora sp., (C) colonies of Sinularia penghuensis surrounding colony of the stony coral Symphyllia agaricia and (D) colony of S. ehrenbergi inhibiting growth of Acropora sp.
Fig. 6 in Psammoecus simonis Grouvelle 1892
Fig. 6. Underwater photographs of Dongsha Atoll octocorals: (A) Sarcophyton ehrenbergi, (B) Lobophytum hsiehi, (C) Litophyton sp., (D) Sinularia ceramensis, (E) S. brassica, (F) S. flexibilis. © 2018 Academia Sinica, Taiwan
Fig. 5 in Psammoecus simonis Grouvelle 1892
Fig. 5. Underwater photographs of Dongsha Atoll octocorals: (A) Sarcophyton cinereum, (B) S. nanwanensis, (C) S. trocheliophorum, (D) S. trocheliophorum, (E) Lobophytum crassum and (F) L. pauciflorum. © 2018 Academia Sinica, Taiwan
Fig. 3 in Psammoecus simonis Grouvelle 1892
Fig. 3. Underwater photographs of Dongsha Atoll octocorals: (A) Sinularia lochmodes, (B) S. abrupta, (C) S. acuta, (D) S. penghuensis, (E) S. erecta and (F) Lobophytum rigidum. © 2018 Academia Sinica, Taiwan
Fig. 4 in Psammoecus simonis Grouvelle 1892
Fig. 4. Maximum likelihood tree based on concatenated mtMutS and igr1 + COI sequences (1552 bp) for the soft coral genera Lobophytum and Sarcophyton. Circled letters indicate clades: M, "mixed" clade; C, "Crassocaule" clade; S, "Sarcophyton" clade; L, "Lobophytum" clade (see McFadden et al. 2006). Numbers above nodes: ML bootstrap values; below nodes: Bayesian posterior probabilities. Boldface taxon labels: reference sequences from other studies; *specimen from Penghu Archipelago (Benayahu et al. 2012). Co: ZMTAU accession number.
Fig. 7 in Psammoecus simonis Grouvelle 1892
Fig. 7. Underwater photographs of Dongsha Atoll octocorals: (A) Sinularia tumulosa, (B) S. acuta, (C) S. maxima, (D) S. wanannensis, (E) Cladiella australis and (F) Cladiella sp. © 2018 Academia Sinica, Taiwan
Fig. 3 in Psammoecus simonis Grouvelle 1892
Fig. 3. (A) Swimming depths of EEL-B with all daily data superimposed. The vertical migrations were separated into 4 phases by sunset, sunrise, end point of ascending and start point of descending for the analyses of this study. (B) Frequency of EEL-B depth records separated into daytime (gray) and nighttime (black) periods.
Fig. 6 in Psammoecus simonis Grouvelle 1892
Fig. 6. Relationship between moon altitude and swimming depth of EEL-B during nighttime periods with the moon in the sky.
Fig. 8 in Psammoecus simonis Grouvelle 1892
Fig. 8. Maximum swimming depths (A) and minimum experienced temperatures (B) of EEL-B each day for the 31 days.
Fig. 10 in Psammoecus simonis Grouvelle 1892
Fig. 10. Relationship between the sun altitude and the swimming depth for all records during the descending and ascending periods.
Fig. 4 in Psammoecus simonis Grouvelle 1892
Fig. 4. Length frequency distribution of the anguillid leptocephali collected in the two sampling areas during the March 2010 survey in the northern Sulawesi Island region. © 2018 Academia Sinica, Taiwan
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