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Fig. 9 in Forbidden islands. The absence of endemics among the insular non-volant terrestrial mammalian fauna of the Red Sea

Fig. 9 - � dead house mouse, Mus musculus L., 1758, photographed on the island of Dahret, in the Dalhak archipelago, in 2010 (photo by Giuseppe De Marchi).

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Fig. 16 in Forbidden islands. The absence of endemics among the insular non-volant terrestrial mammalian fauna of the Red Sea

Fig. 16 - The type of the misterious Arabian gazelle, Gazella arabica (Lichtenstein, 1827), includes this skull and a skin, both designated with catalogue number ZMB_MAM_2115 (Museum für Naturkunde, Berlin). The German explorers Hemprich and Ehrenberg seemingly collected the specimen in the Farasan islands in 1825. However, recent genetic evidence suggests that while the skin comes from a Farasan gazelle, the skull is that of an Israeli or Syrian mountain gazelle. Probably, there was a mistake in the past in assigning skull and skin to the same individual. This combination of specimens from different sources originated the type now preserved in Berlin. Recently, Bärmann et al. (2014) proposed to consider only the skin of ZMB_M�M_2115 as the lectotype of Antilope arabica Lichtenstein, 1827 (courtesy of Museum für Naturkunde Leibniz Institut for Research on Evolution and Biodiversity at the Humboldt University, Berlin).

Fig. 2 in New localities of four Bulgarian endemic Hydrobiidae species (Mollusca: Gastropoda: Risooidea)

Fig. 2. Belgrandiella angelovi from the new locality: 1 – shell, front view, 2 – shell, side view, 3 - penis.

Fig. 1 in New localities of four Bulgarian endemic Hydrobiidae species (Mollusca: Gastropoda: Risooidea)

Fig. 1. Shells of the stygobite snails of the Temnata Dupka cave (Lakatnik): 1 – the newly recorded Belgrandiella pussila, 2 – Belgrandiella hessei, 3 – Bythiospeum bureschi. The shells are displayed in respective proportions.

Fig. 4 in New localities of four Bulgarian endemic Hydrobiidae species (Mollusca: Gastropoda: Risooidea)

Fig. 4. Grossuana thracica from the spring at the Tri Voditsi fish farms near village of Hadzievo: 1 – shell, 2 – soft body (the snout, eye, tentacle and mantle pigmentation are visible) with penis (up on right), 3 – penis, 4 – the louvered distal part of the penis, penis tip was showed with an arrow (light microscope photography).

Fig. 3 in New localities of four Bulgarian endemic Hydrobiidae species (Mollusca: Gastropoda: Risooidea)

Fig. 3. Bythiospeum copiosus from Glava Panega spring, front (left) and back (right) side view of the shell.

Fig. 4 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 4. Rank-abundance curves for bird species at each of the four elevation sites in the Sierra Madre del Sur in southern Mexico. Bird species code: Aphelocoma sumichrasti (Asu), Catharus aurantiirostris (Cau), Cyanocitta coronata (Cco), Icterus pustulatus (Ipu), Junco phaeonotus (Jph), Melanerpes formicivorus (Mfo), Myadestes occidentalis (Moc), Myioborus miniatus (Mmi), Peucaea acuminata (Pac), Setophaga nigrescens (Sni), Tyrannus verticalis (Tve).

Fig. 5 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 5. Differences in the abundance and composition of bird species per sampling point along an elevational gradient in the Sierra Madre del Sur in southern Mexico ordered by a non-metric multidimensional scaling based on the Bray-Curtis similarity index. Ellipses indicate 95% significance.

Fig. 2 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 2. Bird species richness (q0) and diversity (q1 and q2) along an elevational gradient in the Sierra Madre del Sur in southern Mexico.

Fig. 1 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 1. Geographic location of the (a) state of Guerrero in southern Mexico and (b) sampling sites (white triangles) within the Sierra Madre del Sur (red polygon). The nearest human settlements to each study site are shown as green stars.

Fig. 3 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 3. Endemic bird species richness (q0) along an elevational gradient in the Sierra Madre del Sur in southern Mexico.

Fig. 6 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 6. Faunal congruence curves for endemic bird species along an elevational gradient in the Sierra Madre del Sur in southern Mexico.

Fig 11. A-F in Eight New Species of Charinus Simon, 1892 (Arαchnidα: Amblypygi: Chαrinidαe) Endemic for the Brαziliαn Amαzon, with Notes on Their Conservαtionαl Stαtus

Fig 11. A-F. Habitus and details of the sternum and pedipalp of Charinus bichuetteae sp. n. (male holotype, MNRJ 09204). A. Dorsal habitus; B. Young live specimen in the soil in Altamira. C. Sternum; D. Frontal view of the right pedipalp basitiba, distitiba and claw; E. Dorsal view of the right pedipalp; F. Ventral view of the right pedipalp. Scale bars: 1mm. Photo B by Denis Pedroso.

Fig 12 in Eight New Species of Charinus Simon, 1892 (Arαchnidα: Amblypygi: Chαrinidαe) Endemic for the Brαziliαn Amαzon, with Notes on Their Conservαtionαl Stαtus

Fig 12. Distributional map of the new species. Green: ombrophilous forest. Yellow: white-sand forest (Amazonian Caatinga).

Fig 10. A-F in Eight New Species of Charinus Simon, 1892 (Arαchnidα: Amblypygi: Chαrinidαe) Endemic for the Brαziliαn Amαzon, with Notes on Their Conservαtionαl Stαtus

Fig 10. A-F. Habitus and details of the sternum and pedipalp of Charinus ferreus sp. n. (female holotype, MZSP 29104). A. Dorsal habitus; B. Live specimen in the soil of a cave in Carajás. C. Sternum; D. Frontal view of the right pedipalp basitiba, distitiba and claw; E. Dorsal view of the right pedipalp; F. Ventral view of the right pedipalp. Scale bars: 1mm. Photo B by Denis Pedroso.

Fig 7. 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 7. A-E. Habitus and details of the sternum and pedipalp of Charinus guto sp. n. (female holotype, MZSP 48146) A. Dorsal habitus; B. Sternum; C. Frontal view of the left pedipalp basitiba, distitiba and claw; D. Dorsal view of the right pedipalp; E. Ventral view of the right pedipalp. Scale bars: 1mm.

Fig 9. 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 9. A-E. Habitus and details of the sternum and pedipalp of Charinus orientalis sp. n. (female paratype, MZSP 29118). A. Dorsal habitus; B. Sternum; C. Frontal view of the right pedipalp basitiba, distitiba and claw; D. Dorsal view of the right pedipalp; E. Ventral view of the right pedipalp. Scale bars: 1mm.

Fig 8. A-F in Eight New Species of Charinus Simon, 1892 (Arαchnidα: Amblypygi: Chαrinidαe) Endemic for the Brαziliαn Amαzon, with Notes on Their Conservαtionαl Stαtus

Fig 8. A-F. Habitus and details of the sternum and pedipalp of Charinus carajas sp. n. (male, MZSP 29126). A. Dorsal habitus; B. Live specimen in an iron cave in Carajás. C. Sternum; D. Frontal view of the right pedipalp basitiba, distitiba and claw; E. Dorsal view of the right pedipalp; F. Ventral view of the right pedipalp. Scale bars: 1mm. Photo B by Denis Pedroso

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Fig. 1 in Wangsania, a new genus of Apiaceae endemic to Korea

Fig. 1. Strict consensus of three minimal length 790-step trees derived from equally weighted maximum parsimony analysis of combined nuclear rDNA ITS and 5.8S sequences (CI's with and without uninformative characters = 0.560 and 0.462, respectively; RI = 0.477). Numbers above nodes indicate the number of times a monophyletic group occurred in 100 bootstrap replicates.