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FIGURE 5 in Hypselobarbus bicolor, a new species of large barb (Teleostei: Cyprinidae) from the Western Ghats of India

FIGURE 5. Maximum liklihood tree based on concatanated Cytb and COI partial gene sequences. Sequence in red is for the holotype of Hypselobarbus bicolor and sequences in blue are from wrongly identified specimens in NCBI database, which can be attributed to H. bicolor (see Appendix for sequence details). River names are provided in parenthasis. Garra mullya is used as an outgroup. Values along the nodes are bootstrap values for 1000 iterations.

FIGURE 2 in Description of a new species of Euptychia Hübner, 1818 (Lepidoptera: Nymphalidae: Satyrinae) from the western Andes

FIGURE 2. Genitalia of E. favonius: A) male genitalia, in lateral view; B) aedeagus, in lateral view; C) juxta, in posterior view; D) female genitalia, in posterior view; E) lamella antevaginalis, in ventral view; F) ductus bursae and corpus bursae, in dorsal view; G) signa (SN- 15 - 131; SN- 15 - 126) Scale bar = 1 mm.

FIGURE 5. a in Two new species of the genus Xenotoca Hubbs and Turner, 1939 (Teleostei, Goodeidae) from central-western Mexico

FIGURE 5. a) Xenotoca doadrioi, Holotype male CPUM- 9589 and female from San Sebastian b) Xenotoca lyonsi, Holotype male CPUM- 9590 and female from Tamazula c) Xenotoca eiseni, male and female from Compostela population picture by Wolfgang Gessl www. pisces. at

FIGURE 2. Landmarks used for obtain the linear measurements, 1 in Two new species of the genus Xenotoca Hubbs and Turner, 1939 (Teleostei, Goodeidae) from central-western Mexico

FIGURE 2. Landmarks used for obtain the linear measurements, 1 to 9 standard length (SL); 1 to 5 head length (HL); 4 to 17 head high (HH); 1 to 2 preorbital length (PrOL); 3 to 5 postorbital length (POL); 2 to 3 eye diameter (ED); 8 to 11 body least depth (BLD); 13 to 14 pelvic-anal fin distance (PAD); 14 to 6 pelvic-dorsal fin distance (PDD); 14 to 15 pelvic-pectoral fin distance (PPD); 6 to 13 dorsal-anal fin distance (DAD); 6 to 12 dorsal fin origin to anal fin posterior extent distance (DOAE); 7 to 13 dorsal fin posterior extent to anal fin origin distance (DEAO); 7 to 9 end of dorsal fin-hypural plate distance (EDHP); 9 to 12 end of the anal fin-hypural plate distance (EAHP); 6 to 7 dorsal fin base length (DFL); 12 to 13 anal fin base length (AFL); 15 to 16 pectoral fin base length (PFL); 10 to 12 caudal peduncle length (CPL).

FIGURE 4 in New molecular phylogeny of Lucinidae: increased taxon base with focus on tropical Western Atlantic species (Mollusca: Bivalvia)

FIGURE 4. Single gene tree for Lucinidae based on cyt b sequences, using Bayesian inference as implemented by MrBayes. Support values are posterior probabilities (PP); branches with PP <50 % were collapsed. Western Atlantic species in red. See Table 1 for sample details. Monitilorinae and Lucininae expanded in Fig. 5.

FIGURE 1 in New molecular phylogeny of Lucinidae: increased taxon base with focus on tropical Western Atlantic species (Mollusca: Bivalvia)

FIGURE 1. Combined gene tree for Lucinidae based on sequences from three genes (18 S rRNA, 28 S rRNA and cyt b), using Bayesian inference as implemented by MrBayes. Support values are posterior probabilities (PP). Codakiinae and Lucininae expanded in Figs 2 and 3. See Table 1 for sample details. Western Atlantic species in red. Scale is number of substitutions per site. Locality codes used on trees. ABD—Abu Dhabi; ANG—Angola; BD—Bermuda; BOC—Bocas, Panama; BR—Broome, Australia; CAL—California; CB – Chesterfield Bank; COSRIC West Costa Rica; CR—Croatia; DMP—Dampier, Australia; DEV—Devon, UK; FK—Florida Keys; FR—France; GD—Guadeloupe; HK—Hong Kong; JPN – Japan; KK—Kungkraben Bay, Thailand; LH—Lord Howe Island; LI – Lizard Island, Australia; MAD—Madagascar; MADANG—Madang, Papua New Guinea; MAUR – Mauritius; MB—Moreton Bay, Australia; MEX—West Mexico; NC—New Caledonia; NIG—Nigeria; OK— Okinawa; PAN – Panglao, Philippines; PNG – Papua New Guinea; ROD—Rodrigues; RUK—Ryukyus, Japan; SAF—Safaga, Red Sea; SGP—Singapore; SOL—Solomon Sea; SYD—Sydney, Australia; TCB—Tin Can Bay, Australia; TIM—East Timor; TJ—Tjärnö, Sweden; TUN—Djerba, Tunisia; VAN—Vanuatu; VEN—Venezuela; UK—England.

Fig. 8 in A new vertebrate for Europe: the discovery of a range-restricted relict viper in the western Italian Alps

Fig. 8. Currently known extent of occurrence of Vipera walser sp. nov. (in blue) and V. berus (in red) in north western Italy

Fig. 3 in A new vertebrate for Europe: the discovery of a range-restricted relict viper in the western Italian Alps

Fig. 3. Results of the non-metric multidimensional scaling (nMDS, Bray – Curtis with similarity index), for the females (left) and males (right) conducted separately. The following variables were considered: subcaudals, crown scales, apicals, perioculars, parietals and loreals (only on the right side because V. walser show a much higher degree of asymmetry on loreal scales count, compared to V. berus). The analysis was carried out on V. walser and three groups of V. berus having the same number of samples, in order to evaluate intraspecific variability. V. walser are in red. The graphs show V. walser to be well differentiated in respect to the three groups of V. berus, which are mostly overlapping.

Fig. 10 in A new vertebrate for Europe: the discovery of a range-restricted relict viper in the western Italian Alps

Fig. 10. Current and projected (2035; CMIP 5 [IPPC Fifth Assessment]) mean annual rainfall and mean minimum temperatures (° C) for the months May – October within the current range of Vipera walser sp. nov.

Fig. 9 in A new vertebrate for Europe: the discovery of a range-restricted relict viper in the western Italian Alps

Fig. 9. Habitat of Vipera walser sp. nov. Valle Strona at about 1650 m (upper left), Valle Strona at about 1800 m (upper right), Valle Mastallone at 2070 m (bottom left) and Valle della Vecchia at 1830 m (bottom right)

Fig. 7 in A new vertebrate for Europe: the discovery of a range-restricted relict viper in the western Italian Alps

Fig. 7. Variation in head scalation in adult female (upper four photographs) and adult male (lower four photographs) of Vipera walser sp. nov.

Fig. 4 in A new vertebrate for Europe: the discovery of a range-restricted relict viper in the western Italian Alps

Fig. 4. Discriminant analysis, based on the six meristic variables, correctly classifies 94 % of females (left) and 88 % of males. The strongest discriminatory variables are crown scales and parietals. Blue = V. berus; red = V. walser

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Fig. 1 in A new Pararistolochia Hutch. & Dalziel (Aristolochiaceae) from the Beanka Tsingy (western Madagascar)

Fig. 1. – Detailed map of western Madagascar showing the distribution of Pararistolochia enricoi Luino, L. Gaut. & Callm. (stars) in Beanka, plotted on a map of forest cover in 2000 (grey) following Harper et al. (2007).

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Fig. 2 in A new Pararistolochia Hutch. & Dalziel (Aristolochiaceae) from the Beanka Tsingy (western Madagascar)

Fig. 2. – Pararistolochia enricoi Luino, L. Gaut. & Callm. A. Young shoot; B. Variable forms of the leaves; C. Inflorescence; D. Flowers detail; E. Longitudinal section of the flower showing gynostemium, utricule, and throat. [Photos: A-B, E: I. Luino; C-D: L. Gautier]

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Fig. 3 in A new Pararistolochia Hutch. & Dalziel (Aristolochiaceae) from the Beanka Tsingy (western Madagascar)

Fig. 3. – Pararistolochia enricoi Luino, L. Gaut. & Callm. A. Corky stem and leaves; B. Flower; C. Gynostemium; D. Young fruit; E. Transversal section of fruit; F. Seeds. [A-B, F: Gautier et al. 5886, G; C: Luino 116, G; D-E: Luino 248, G] [Drawings: A, C, F: S. Da-Giau; B, D-E: G. Loza]

February 2017 Western Turkey Earthquake Swarm Sentinel-1 TOPS Differential Interferogram (20170131-20170212)

In february 2017 a series of earthquakes affected the Biga Peninsula in Western Turkey. Over 350 buildings sustained extensive damage. The seismic events occurred at the intersection of the Kestanbol Fault and the Edremit Fault Zone. The Sentinel-1 TOPS co-seismic interferogram was generated with the ESA SNAP toolbox (http://step.esa.int/). S1A data were downloaded from the Sentinel-1 Scientific Data Hub: S1A_20170131-S1A_20170212 from ASCENDING orbit 131.

Figure 2b. from: A new record of Potamanthellus caenoides Ulmer 1939 (Ephemeroptera: Neoephemereidae) from the southern Western Ghats of India - Biodiversity Data Journal 3: e5021 (08 May 2015) https://doi.org/10.3897/BDJ.3.e5021

Figure 2b. - Potamanthelluscaenoides Ulmer 1939.Figure 2a.ForelegFigure 2b.Dorsal forefemora with transverse row of setae Dorsal forefemora with transverse row of setae

Figure 2a. from: A new record of Potamanthellus caenoides Ulmer 1939 (Ephemeroptera: Neoephemereidae) from the southern Western Ghats of India - Biodiversity Data Journal 3: e5021 (08 May 2015) https://doi.org/10.3897/BDJ.3.e5021

Figure 2a. - Potamanthelluscaenoides Ulmer 1939.Figure 2a.ForelegFigure 2b.Dorsal forefemora with transverse row of setae Foreleg

Figures 50, 51. from New species and records of ortholasmatine harvestmen from Mexico, Honduras, and the western United States (Opiliones, Nemastomatidae, Ortholasmatinae) - ZooKeys 52: 9-45 (30 July 2010) https://doi.org/10.3897/zookeys.52.471

Figures 50, 51. - Photographs of bodies, dorsal views. 50 female Trilasma chipinquensis sp. n. 51 male Trilasma hidalgo sp. n.

Figures 2, 3. from New species and records of ortholasmatine harvestmen from Mexico, Honduras, and the western United States (Opiliones, Nemastomatidae, Ortholasmatinae) - ZooKeys 52: 9-45 (30 July 2010) https://doi.org/10.3897/zookeys.52.471

Figures 2, 3. - Scanning electron micrographs of Ortholasma colossus sp. n., dorsal views. 2 male 3 female.