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Fig. 1 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 1. Geographic range of the western whiptail lizard, Cnemidophorus tigris sensu lato, in the continental southwestern United States and northern Mexico. Rectangle (SE Arizona and SW New Mexico) outlines the contact region (detailed in figs. 3–5) where C. t. punctilinealis interbreeds with C. t. marmoratus. Numbers designate collecting sites (appendix 2) for specimens additional to those obtained within the contact region (fig. 3; appendix 1).

Fig. 7 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 7. Habitats at collecting sites in the northern transect, Animas Valley, north of Lordsburg (table 2; figs. 3, 4; appendix 1), 22 August 1990. Top. Site 3, midpoint of the northern hybrid zone, looking E from NM Hwy 464. Bottom. Site 4, looking NW from NM Hwy 464; mesquite grassland.

Fig. 6 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 6. Habitats at collecting sites in the northern transect, Animas Valley, north of Lordsburg (table 2; figs. 3, 4; appendix 1), 22 August 1990. Top. Site 1, looking E from NM Hwy 464; riparian thornscrub. Bottom. Site 2, looking W from NM Hwy 464.

Fig. 11 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 11. Habitats near the northern transect (tables 2, 3; figs. 3, 4; appendix 1), Animas Valley, NW of Lordsburg along NM Hwy 70, 2 September 1990. Top. Grassland about halfway between sites 10 and 13, at 27.9 km (by road) NW Lordsburg, looking N. Bottom. Site 14, looking WSW.

Fig. 4 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 4. The northern hybrid zone, with collecting sites numbered (enlarged from fig. 3). Transect sites are numbers within squares (1–7), but the midpoint (50:50 point of gene exchange) is within a diamond (site 3). Associated sites are numbers in circles (table 2; appendix 1).

Fig. 9 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 9. Habitats at collecting sites in the northern transect and near an associated site, Animas Valley north of Lordsburg (tables 2, 3; figs. 3, 4; appendix 1), 22 August 1990. Top. Site 7, looking W from NM Hwy 464. Bottom. Abrupt ecotone of mesquite grassland and creosote desertscrub (in near background), 5.8 km (by road) W of site 3, looking NW. Site 8 is 0.3 km off the left side of the photo.

Figure 2. Bayesian posterior probability 50 in Population genetic structure and demographic history of the Chinese endemic Mongoloniscus sinensis (Dollfus, 1901) (Isopoda: Oniscidea)

Figure 2. Bayesian posterior probability 50% majority-rule consensus tree of the M. sinensis haplotypes. Out-group was Ligia occidentalis; the map showed mitochondrial haplotype clades of Porcellio gigliotose and Trachelipus semiproiectus. The numbers above joints are the bootstrap support values of MP value, ML value, and the posterior probabilities of the BI tree, respectively (MP/ML/BI).

Figure 1 in Population genetic structure and demographic history of the Chinese endemic Mongoloniscus sinensis (Dollfus, 1901) (Isopoda: Oniscidea)

Figure 1. Locations of sampled populations and geographical distribution of Mongoloniscus sinensis mtDNA clades. Mountain ranges are in green letters as follows: H—Heng Mountain, TH—Taihang Mountain, WT—Wutai Mountain, LL—Lvliang Mountain, TY–Taiyue Mountain, ZT—Zhongtiao Mountain.

Figure 3 in Population genetic structure and demographic history of the Chinese endemic Mongoloniscus sinensis (Dollfus, 1901) (Isopoda: Oniscidea)

Figure 3. Parsimonious network of M. sinensis haplotypes. Each circle represents a haplotype, with the area of the circle proportional to its frequency. The evolutionary clades C1 - C6 are shown in different colors, and median vector (mvl-mv3) is indicated in red.

opencc-by-4.0Dec 2021View details →

Figure 4 in Genetic diversity, population structure and demographic history of Dugesia japonica in Taihang Mountains

Figure 4. Median-joining haplotype network based on mitochondrial gene COI. The four ellipses represent four clades in Figure 3, respectively. Each circle represents a haplotype, the area of the circle is proportional to the frequency of haplotypes, and black dots represent hypothetical unobserved haplotypes. Different populations are shown in different colors.

opencc-by-4.0Dec 2021View details →

Figure 3 in Genetic diversity, population structure and demographic history of Dugesia japonica in Taihang Mountains

Figure 3. Maximum likelihood (ML) and Bayesian inference (BI) phylogentic trees based on mitochondrial gene COI. Dugesia ryukyuensis (Genbank accession no. AB618488) serves as the outgroup. The broken lines denote inconsistent branches. Bootstrap percentages (BP,>50 only) of ML analysis and posterior probabilities (PP,>0.50 only) of Bayesian inference are shown above and below the branch, respectively. HG—haplogroup.

Figure S1 in Genetic analysis and ecological niche modeling delimit species boundary of the Przewalski's scorpion (Scorpiones: Buthidae) in arid Asian inland

Figure S1. Bayesian consensus tree of the Mesobuthus caucasicus complex reconstructed from mitochondrial DNA sequences.

Figure 9 in Genetic analysis and ecological niche modeling delimit species boundary of the Przewalski's scorpion (Scorpiones: Buthidae) in arid Asian inland

Figure 9. Phylogeny the Mesobuthus caucasicus complex reconstructed using mitochondrial DNA sequences. The Przewalski's scorpion (M. przewalskii) is deeply diverged from other species and the Chinese scorpion (M. martensii) belongs to the species complex. Node supports are shown by bootstrapping probabilities from 1000 replicates and Bayesian posterior probabilities.

Figures 1–8 in Genetic analysis and ecological niche modeling delimit species boundary of the Przewalski's scorpion (Scorpiones: Buthidae) in arid Asian inland

Figures 1–8. Mesobuthus przewalskii stat. nov., from Qiemo, Xinjiang. 1. Male, dorsal view. 2. Male, ventral view. 3. Female, dorsal view. 4. Female, ventral view. 5. Male, dentition of pedipalp chela movable finger. 6. Male, dentition of pedipalp chela fixed finger. 7. Male, ventral aspect of genital operculum and pectines. 8. Female, ventral aspect of genital operculum and pectines. Scale bars: 1–4 = 5.0 mm; 5–8 = 2.0 mm.

Figure 11 in Genetic analysis and ecological niche modeling delimit species boundary of the Przewalski's scorpion (Scorpiones: Buthidae) in arid Asian inland

Figure 11. Ecological niche models of Mesobuthus scorpions. Potential distribution areas for the Przewalski's scorpion M. przewalsii (purple) is shown together with the Chinese scorpion M. martensii (green) and other species of the M. caucasicus complex (yellow). The entire Tarim Basin and adjacent Gobi region are suitable for survival of M. przewalskii. No area to the west of the Tianshan Mountains and the Pamir Plateau is suitable for M. przewalskii, and similarly no area to the east of the Tianshan Mountains and the Pamir Plateau is suitable for other species of the M. caucasicus complex. There are overlaps in predicted suitable distribution areas between M. przewalskii and M. martensii along the northeast edge of the Qinghai-Tibet Plateau. The suitable areas in the Junggar Basin and to the north of the Tianshan Mountains are likely due to over prediction of the model, because M. przewalskii does not occur in these regions. Ecological niche model for M. martensii was adopted from Shi et al. 2007.

Figure 10 in Genetic analysis and ecological niche modeling delimit species boundary of the Przewalski's scorpion (Scorpiones: Buthidae) in arid Asian inland

Figure 10. Phylogenetic network for the Mesobuthus caucasicus species complex. Although the interrelationships between species is poorly resolved, no reticulations have occurred in the most recent common ancestors for each species. The Przewalski's scorpion M. przewalskii is clearly diverged from other member of the species complex and warrants a species rank. The divergence of the Chinese scorpion M. martensii is comparable to the divergences among the members of the species complex.

Figure 1 in Cryptic genetic diversity and host specificity of Bothriocephalus acheilognathi Yamaguti, 1934 (Eucestoda: Bothriocephalidea)

Figure 1. Sample localities of Bothriocephalus acheilognathi studied in China. The code number is corresponding to the locality in Table 1.

Figiure 3 in Cryptic genetic diversity and host specificity of Bothriocephalus acheilognathi Yamaguti, 1934 (Eucestoda: Bothriocephalidea)

Figiure 3. Phylogenetic relationships of Bothriocephalus based on the ribosoml internal transcribed spacer sequences (ITS1+ITS2) using maximum likelihood (ML) method. Numbers near branch node are the bootstrap support value for ML, maximum parsimoy (MP), and posterior probability for Bayesian inference (BI).

opencc-by-4.0Jun 2018View details →

Fig. 2 in Genetic diversity among white-nest swiftlets of the genus Aerodramus (Aves: Apodidae: Collocaliini) of house-farms in Malaysia

Fig. 2. Schematic diagram of the mitochondrial cyt-b region sequenced in the previous and present studies. Dark bands on the grey strip indicate the location of the five clade-specific sites.