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Fig. 5 in Long Term (1985-2018) Changes Of The Habitat Suitability Of European Souslik Assessed By Maxent Modelling Based On Landsat Satellite Imagery - A Case Study From A Mountain Landscape Of Central Bulgaria

Fig. 5. Changes in the habitat suitability in the study area (white – not suitable, black – high suitability) of European souslik assessed by maxent modelling based on data from 2006–2018 (B) and extrapolated for the period 1985–2005 (A). The results are presented in

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Fig. 3 in Long Term (1985-2018) Changes Of The Habitat Suitability Of European Souslik Assessed By Maxent Modelling Based On Landsat Satellite Imagery - A Case Study From A Mountain Landscape Of Central Bulgaria

Fig. 3. Negative and positive anomalies (white and black bars) of the Mean Annual Temperature time series for the period of 1985–2018 (data from the meteorological station Sofia)

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Fig. 2 in Long Term (1985-2018) Changes Of The Habitat Suitability Of European Souslik Assessed By Maxent Modelling Based On Landsat Satellite Imagery - A Case Study From A Mountain Landscape Of Central Bulgaria

Fig. 2. Changes in the number of grazing livestock in the southern central Bulgarian planning region for the period 2001–2018

Figures 18–20 in A new species of Vaejovis from the Mule Mountains above Bisbee, Arizona (Scorpiones: Vaejovidae)

Figures 18–20: Vaejovis miscionei sp. n. Figure 18. Paratype female, specimen RA2076, giving birth. Figure 19. Paratype female, specimen RA2075 with newborns. Visible is the lining up of the early instars in the classic position on the female's dorsum (Ayrey, 2012). Figure 20. Paratype female, specimen RA2075 with juveniles after the first ecdysis.

Figure 6 in A new species of Vaejovis from the Mule Mountains above Bisbee, Arizona (Scorpiones: Vaejovidae)

Figure 6. Vaejovis miscionei sp. n., paratype male, carapace and tergites I–IV (6a–b) and sternopectinal area (6c–d). Figures 6a and 6c under white light and figures 6b and 6d under UV light.

Figures 1–4 in A new species of Vaejovis from the Mule Mountains above Bisbee, Arizona (Scorpiones: Vaejovidae)

Figures 1–4: Vaejovis miscionei sp. n. Figure 1. Holotype female in natural habitat. Figure 2. Paratype male in natural habitat. Figure 3. Holotype female, dorsal and ventral views. Scale bar: 5mm.

Figures 7–12 in A new species of Vaejovis from the Mule Mountains above Bisbee, Arizona (Scorpiones: Vaejovidae)

Figures 7–12: Vaejovis miscionei sp. n., paratypes female (7, 10–12) and male (8–9). Figures 7–8. Telson in ventral (7a, 8a), lateral (7b, 8b), and dorsal (7c, 8b) views. Figure 9. Telson dorsal showing absence of visible dorsal gland, white (9a) and UV (9b) lights. Figure 10. Right chelicera in dorsal (10b) and ventral (10a) views. Figure 11. Right chelal movable (11a) and fixed (11b) fingers, showing dentition (see arrows). Figure 12. Tarsomere II of right leg III.

Figures 16–17 in A new species of Vaejovis from the Mule Mountains above Bisbee, Arizona (Scorpiones: Vaejovidae)

Figures 16–17: Vaejovis miscionei sp. n., type locality, habitat (16) and microhabitat in cracks and crevices of rocks (17).

Figure 5 in A new species of Vaejovis from the Mule Mountains above Bisbee, Arizona (Scorpiones: Vaejovidae)

Figure 5. Vaejovis miscionei sp. n., holotype female, carapace and tergites I–IV (5a–b) and sternopectinal area (5c–d). Figures 5a and 5c under white light and figures 5b and 5d under UV light.

Figure 15 in A new species of Vaejovis from the Mule Mountains above Bisbee, Arizona (Scorpiones: Vaejovidae)

Figure 15. Vaejovis miscionei sp. n., Paratype male, right hemispermatophore in ventral (15a), internal (15b), and dorsal (15c) views. Scale bar = 1mm.

Figures 13–14 in A new species of Vaejovis from the Mule Mountains above Bisbee, Arizona (Scorpiones: Vaejovidae)

Figures 13–14: Vaejovis miscionei sp. n., metasoma and telson in lateral (13a, 14a), dorsal (13b), 14b) and ventral (13c, 14c) views. Figure 13. Holotype female. Figure 14. Paratype male.

Figure 5 in A new species of the genus Tylototriton (Amphibia: Urodela: Salamandridae) from the Eastern Dalou Mountains in Guizhou, China

Figure 5. Tylototriton daloushanensis Zhou, Xiao & Luo, sp. nov. in preserved status. A–B. Male holotype, GZNU20180806001, dorsal and ventral views. C–D. Female paratype, GZNU20180607001, dorsal and ventral views. E. Female paratype, GZNU20180607001, dorsal view of head. F. Female paratype, GZNU20180607001, view of oral cavity (yellow arrows represent vomerine teeth). Scale bars: A–D = 5.0 mm; E–F = 4.0 mm.

Figure 6 in A new species of the genus Tylototriton (Amphibia: Urodela: Salamandridae) from the Eastern Dalou Mountains in Guizhou, China

Figure 6. Habitat and eggs of Tylototriton daloushanensis Zhou, Xiao & Luo, sp. nov. at the type locality. A. Microhabitats. B. Individual found in the type locality. C. Eggs laid by GZNU20180607001 on 7 June 2018. D. Individual GZNU20180608001 collected on 8 June 2018 in Kuankuoshui National Nature Reserve.

Figure 4 in A new species of the genus Tylototriton (Amphibia: Urodela: Salamandridae) from the Eastern Dalou Mountains in Guizhou, China

Figure 4. Tylototriton daloushanensis Zhou, Xiao & Luo, sp. nov. in life. A–C. Male holotype, GZNU20180806001, dorsal, ventral, and dorsolateral views. D–F. Female paratype, GZNU20180607001, dorsal, ventral, and dorsolateral views. H–I. Male holotype, GZNU20180806001, ventral view of the hand, foot, and cloaca. J–L. Female paratype, GZNU20180607001, ventral view of the hand, foot, and cloaca (yellow arrow). All photos were taken at around 9:00 am.

Figure 2 in A new species of the genus Tylototriton (Amphibia: Urodela: Salamandridae) from the Eastern Dalou Mountains in Guizhou, China

Figure 2. Bayesian inference (BI) tree based on 16S+ND2 gene sequences. Bayesian posterior probabilities (BPP) from BI analyses/ ultrafast bootstrap supports (UFB) from ML analyses were noted beside nodes. The scale bar represents 0.04 nucleotide substitutions per site. The numbers at the tip of branches correspond to the ID numbers in Table 1.

Figure 1 in A new species of the genus Tylototriton (Amphibia: Urodela: Salamandridae) from the Eastern Dalou Mountains in Guizhou, China

Figure 1. Sampling localities of the Tylototriton daloushanensis Zhou, Xiao & Luo, sp. nov., T. maolanensis, and T. kweichowensis in Guizhou, China. A. Huoqiuba Nature Reserve, Suiyang County. B. Kuankuoshui National Nature Reserve, Suiyang County. C. Maolan National Nature Reserve, Libo County. D. Nayong County.

Fig. 3 in Occurrence of a Skin Parasite Argulus coregoni (Branchiura: Argulidae) on Salmonids in Mountain Streams, Central Japan, with Discussion on Its Longitudinal Distribution and Host Utilization in Rivers

Fig. 3. Mountain streams where the salmonids infected with Argulus coregoni were caught in Gifu Prefecture, central Japan. A, Main stream of the upper Maze River (locality 1 in Fig. 2); B, tributary of the Hida River (locality 2); C, tributary of the Tsukechi River (locality 3); D, tributary of the Yoshida River (locality 4); E, main stream of the Itoshiro River (locality 5); F, tributary of the Itoshiro River (locality 5); G, tributary of the Sho River (locality 6); H, main stream of the Gamada River (locality 7).

Fig. 2 in Occurrence of a Skin Parasite Argulus coregoni (Branchiura: Argulidae) on Salmonids in Mountain Streams, Central Japan, with Discussion on Its Longitudinal Distribution and Host Utilization in Rivers

Fig. 2. Map showing the collection localities of salmonids infect- ed with Argulus coregoni (closed circles 1–7) in rivers of Gifu Prefecture, central Japan. The collection localities of ayu, Plecoglossus altivelis altivelis, infected with A. coregoni, are also shown (open triangles 8–11). 1, Upper reaches of the Maze River; 2, tributary of the Hida River; 3, tributary of the Tsukechi River; 4, tributary of the Yoshida River; 5, the Itoshiro River; 6, tributary of the Sho River; 7, the Gamada River; 8, middle reaches of the Maze River; 9, middle reaches of the Shira River; 10. middle reaches of the Nagara River; 11, lower reaches of the Nagara River.

Fig. 1 in Occurrence of a Skin Parasite Argulus coregoni (Branchiura: Argulidae) on Salmonids in Mountain Streams, Central Japan, with Discussion on Its Longitudinal Distribution and Host Utilization in Rivers

Fig. 1. Argulus coregoni, male, NSMT-Cr 30777, from a white-spotted char, Salvelinus leucomaenis, from the Gamada River, Gifu Prefecture, ethanol-preserved specimen, A, Dorsal view; B, ventral view; C, two females infecting a white-spotted char (180 mm FL) near the left pectoral fin (from the Maze River); D, one female infecting a red-spotted masu salmon, Oncorhynchus masou ishikawae (103 mm FL), near the base of the dorsal fin (from a tributary of the Hida River); E, one female (left) and one male (right) infecting a masu salmon, O. m. masou (257 mm FL), near the left pectoral fin (from the Itoshiro River); F, one female infecting a hybrid between white-spotted char and masu salmon (165 mm FL) near the dorsal fin (from the Itoshiro River). Arrowheads indicate individuals of A. coregoni. See Fig. 2 for the locations of the rivers. Scale bars: A, B, 2 mm; C–F, 20 mm.

Fig. 4 in Occurrence of a Skin Parasite Argulus coregoni (Branchiura: Argulidae) on Salmonids in Mountain Streams, Central Japan, with Discussion on Its Longitudinal Distribution and Host Utilization in Rivers

Fig. 4. Distribution of 31 specimens of Argulus coregoni (closed circles) on the host's body surface. A total of 32 specimens of A. coregoni were collected, but the attachment site for one individual was not recorded.