Find research datasets worth reusing

FIGURE 45 in Diversity of cave-dwelling pseudoscorpions from Guizhou in China, with the description of twenty-four new species of the genus Tyrannochthonius (Pseudoscorpiones, Chthoniidae)

FIGURE 45. Tyrannochthonius hispidus sp. nov., holotype male: A. Carapace (dorsal view); B. Left chelicera (dorsal view), with details of teeth; C. Coxal spines on coxae II (ventral view); D. Left pedipalp (minus chela, dorsal view); E. Rallum. Scale bars: 0.20 mm (A–B, D); 0.10 mm (C, E).

FIGURE 29 in Diversity of cave-dwelling pseudoscorpions from Guizhou in China, with the description of twenty-four new species of the genus Tyrannochthonius (Pseudoscorpiones, Chthoniidae)

FIGURE 29. Tyrannochthonius brevispinus sp. nov., holotype male (A–F), paratype female (G): A. Left chela (lateral view); B. Left chela (dorsal view); C. Carapace (dorsal view); D. Left chelicera (dorsal view); E. Left pedipalp (minus chela, dorsal view); F. Male genital area (ventral view); G. Female genital area (ventral view).

FIGURE 36 in Diversity of cave-dwelling pseudoscorpions from Guizhou in China, with the description of twenty-four new species of the genus Tyrannochthonius (Pseudoscorpiones, Chthoniidae)

FIGURE 36. Tyrannochthonius duo sp. nov., holotype male: A. Left chela (lateral view), with details of teeth and with trichobothrial pattern; B. Left chela (dorsal view); C. Leg I (lateral view); D. Leg IV (lateral view). Scale bars: 0.20 mm.

FIGURE 7 in Diversity of cave-dwelling pseudoscorpions from Guizhou in China, with the description of twenty-four new species of the genus Tyrannochthonius (Pseudoscorpiones, Chthoniidae)

FIGURE 7. Shenren Cave, type locality of Tyrannochthonius altus sp. nov., A. Cave location (red arrow); B. Entrance; C. Inside the cave entrance; D–E. Areas where T. altus sp. nov. specimens were collected; F. Live male of T. altus sp. nov. in its natural environment.

FIGURE 33 in Diversity of cave-dwelling pseudoscorpions from Guizhou in China, with the description of twenty-four new species of the genus Tyrannochthonius (Pseudoscorpiones, Chthoniidae)

FIGURE 33. Tyrannochthonius duo sp. nov., A. Holotype male, habitus (dorsal view); B. Paratype female, habitus (dorsal view).

FIGURE 3 in Diversity of cave-dwelling pseudoscorpions from Guizhou in China, with the description of twenty-four new species of the genus Tyrannochthonius (Pseudoscorpiones, Chthoniidae)

FIGURE 3. Tyrannochthonius acutus sp. nov., A. Holotype male, habitus (dorsal view); B. Paratype female, habitus (dorsal view).

FIGURE 4 in Diversity of cave-dwelling pseudoscorpions from Guizhou in China, with the description of twenty-four new species of the genus Tyrannochthonius (Pseudoscorpiones, Chthoniidae)

FIGURE 4. Tyrannochthonius acutus sp. nov., holotype male (A–F), paratype female (G): A. Left chela (lateral view); B. Left chela (dorsal view); C. Carapace (dorsal view); D. Left chelicera (dorsal view); E. Left pedipalp (minus chela, dorsal view); F. Male genital area (ventral view); G. Female genital area (ventral view).

FIGURE 1 in Diversity of cave-dwelling pseudoscorpions from Guizhou in China, with the description of twenty-four new species of the genus Tyrannochthonius (Pseudoscorpiones, Chthoniidae)

FIGURE 1. Distribution map of the type localities of troglomorphic Tyrannochthonius species in Guizhou (China). Each color represents an administrative area (green: Guizhou Province; red: Luodian County; yellow: Pingtang County; blue: Dushan County). 1. Shenren Cave (T. altus sp. nov.); 2. Xianren Cave (T. gracilis sp. nov.); 3. Daniu Cave (T. parcidentatus sp. nov.); 4. Guanjiadadong Cave (T. quattuor sp. nov.); 5. Yanshan Cave (T. yanshanensis sp. nov.); 6–7. Guanyin Cave & Anjialin Cave (T. multidentatus sp. nov.); 8. Babaowan Cave (T. babaowanensis sp. nov.); 9. Liangfeng Cave (T. duo sp. nov.); 10. Da Cave (T. umidus sp. nov.); 11. Yutang Cave (T. harveyi); 12. Houzi Cave (T. oblongus sp. nov.); 13. Qilin Cave (T. hispidus sp. nov. & T. qilinensis sp. nov.); 14. Gazuida Cave (T. acutus sp. nov.); 15. Jingua Cave (T. brevispinus sp. nov.); 16. Zimu Cave (T. latus sp. nov.); 17. Feng Cave (T. nanxingensis sp. nov.); 18. Liujiadadong Cave (T. infirmus sp. nov.); 19. Daxiao Cave (T. maculosus sp. nov.); 20. Hei Cave (T. arificus sp. nov.); 21. Jiangjia Cave (T. zhai); 22. Zharou Cave (T. pinguis sp. nov.); 23. Yanggong Cave (T. planus sp. nov.); 24. Yanjia Cave (T. breviculus sp. nov.); 25–28. Da Cave, Qixia Cave, Weier Cave & Xiaohui Cave (T. multicavus sp. nov.); 29–30. Gaoluo Cave & Cangjun Cave (T. pictus sp. nov.).

FIGURE 2 in Diversity of cave-dwelling pseudoscorpions from Guizhou in China, with the description of twenty-four new species of the genus Tyrannochthonius (Pseudoscorpiones, Chthoniidae)

FIGURE 2. Gazuida Cave, type locality of Tyrannochthonius acutus sp. nov., A. Entrance; B. Inside the cave entrance; C. Area where T. acutus sp. nov. specimens were collected (red arrow); D. Live male of T. acutus sp. nov. in its natural environment; E. Live female of T. acutus sp. nov. in its natural environment.

FIG. 4 in Species richness, functional diversity and assemblage structure of insectivorous bats along an elevational gradient in tropical West Africa

FIG. 4. Mean pairwise distances (MPD) of multivariate traits (A and B), forearm length (C and D), greatest skull length (E and F), narrowest breadth of skull (G and H), ear length (I and J) and tail length (K and L) of insectivorous bat assemblages along the Mount Nimba elevational gradient. Observed MPD for each elevation is represented by the blue dots. A blue line of best fit is shown for significant relationships between observed MPD and elevation. The red dots indicate the expected MPD as calculated by 999 randomized community shuffles for figures on the left, and trait shuffles for figures on the right. A red line of best fit is shown for significant relationships between expected MPD and elevation. Instances where observed MPD differs significantly from the expected MPD are indicated by black rings

FIG. 2 in Species richness, functional diversity and assemblage structure of insectivorous bats along an elevational gradient in tropical West Africa

FIG. 2. Quadratic linear regression of species richness of assemblages versus elevation (P = 0.008; species richness = 34.32 - 7.893*elevation + 0.4881*elevation2)

FIG. 5 in Species richness, functional diversity and assemblage structure of insectivorous bats along an elevational gradient in tropical West Africa

FIG. 5. Mean nearest taxon distances (MNTD) of multivariate traits (A and B), forearm length (C and D), greatest skull length (E and F), narrowest breadth of skull (G and H), ear length (I and J) and tail length (K and L) of insectivorous bats along the Mount Nimba elevational gradient. Observed MNTD for each elevation is represented by the green dots. A green line of best fit is shown for significant relationships between observed MNTD and elevation. The red dots indicate the expected MNTD as calculated by 999 randomized community shuffles for figures on the left, and trait shuffles for figures on the right. A red line of best fit is shown for significant relationships between expected MNTD and elevation. Instances where observed MNTD differs significantly from the expected MNTD are indicated by black rings

FIG. 3 in Species richness, functional diversity and assemblage structure of insectivorous bats along an elevational gradient in tropical West Africa

FIG. 3. Dendrogram of bat functional groups present on Mount Nimba. Eight functional groups were identified, each represented by a different colour. See Supplementary Table S1 for full species names

FIG. 1 in Species richness, functional diversity and assemblage structure of insectivorous bats along an elevational gradient in tropical West Africa

FIG. 1. Study sites in Liberia and Guinea (Google Earth, 2015) and their assignment to the eight elevation belts. Key for site colours: red: <500 m; green: 500–600 m; yellow: 601–800 m; blue: 801–900 m; purple: 901–1100 m; black: 1101–1200 m; orange: 1201– 1400 m; white: 1401–1600 m

Figure 5 in Mitochondrial DNA and other lines of evidence clarify species diversity in the Peromyscus truei species group (Cricetidae: Neotominae)

Figure 5: Geographic ranges of members of the Peromyscus truei species group showing taxonomic changes proposed in this work: (A) P. gratus (pink) and P. truei (green); (B) P. nasutus (green) and P. difficilis (pink); (C) P. laceianus (green) and P. pectoralis (pink); (D) P. attwateri (green) and P. ochraventer (pink). Lighter colors represent possible unrecognized taxa: we suggest recognizing the species P. amplus, P. collinus, and P. felipensis because their high mitochondrial divergence and its consistency with multiple lines of evidence previously reported; however, the specific status of the highly divergent P. cf. martirensis and P. cf. zapotecae should be tested with additional data. Maps modified from the IUCN.

Figure 4 in Mitochondrial DNA and other lines of evidence clarify species diversity in the Peromyscus truei species group (Cricetidae: Neotominae)

Figure 4: Haplotype networks based on the mitochondrial cyt b of sister species in the Peromyscus truei species group: (A) P. gratus (pink) + P. truei (green); (B) P. nasutus (green) + P. difficilis (pink); and (C) P. laceianus (green) + P. pectoralis (pink). In each case, lighter colors represent possible unrecognized taxa based on their high genetic divergence (see Figure 5 and discussion). The grey outlines show the 18 clades with intraspecific genetic

Figure 3 in Mitochondrial DNA and other lines of evidence clarify species diversity in the Peromyscus truei species group (Cricetidae: Neotominae)

Figure 3: Heat map showing genetic distances (K80) as % between the 18 clades with intraspecific genetic distances ≤1.5 in the Peromyscus truei species group. Genetic distances>4% are shown above the gray line, and values>5% above the black line. Clade labels on the x- and y-axes match those from Figure 2.

Figure 1 in Mitochondrial DNA and other lines of evidence clarify species diversity in the Peromyscus truei species group (Cricetidae: Neotominae)

Figure 1: Map of Mexico and the United States showing the localities of Peromyscus truei species group samples analyzed in this work.

Figure 2 in Mitochondrial DNA and other lines of evidence clarify species diversity in the Peromyscus truei species group (Cricetidae: Neotominae)

Figure 2: Phylogenetic relationships of members in the Peromyscus truei species group based on the mitochondrial cyt b. At the left the majority-rule consensus tree obtained from Bayesian analysis, and at the right the maximum-likelihood tree. Support values are shown as posterior probabilities and ultrafast bootstrap, respectively; values <0.8/94 are not shown. Green bars indicate the 18 clades with intraspecific genetic distances ≤1.5, and the asterisk show short sequences obtained from skin-clips. Tip labels show the catalog number of each analyzed specimen.

IG. 6. Ordination diagram of PCA of the Patagonian bat assemblage for craniodental variables using A) data set not size-corrected; and B) data set size-corrected. Polygons include specimens from each species: H. macrotus (▲), H. magellanicus (), H. montanus (▲), L. varius (■), M. chiloensis (●), and T. brasiliensis (£). Vectors show the strengh of correlation of each variable with the plane of PC1 and PC2. See text for abbreviations in Ecomorphological diversity in the Patagonian assemblage of bats from Argentina

IG. 6. Ordination diagram of PCA of the Patagonian bat assemblage for craniodental variables using A) data set not size-corrected; and B) data set size-corrected. Polygons include specimens from each species: H. macrotus (▲), H. magellanicus (), H. montanus (▲), L. varius (■), M. chiloensis (●), and T. brasiliensis (£). Vectors show the strengh of correlation of each variable with the plane of PC1 and PC2. See text for abbreviations