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Figure 10. A in Taxonomy, biogeography and evolution of Euproctus (Amphibia: Salamandridae), with the resurrection of the genus Calotriton and the description of a new endemic species from the Iberian Peninsula
Figure 10. A, female Calotriton arnoldi sp. nov. from population A2 with uniform chocolate coloration. B, male specimen of C. arnoldi from population A2 showing several yellowish blotches on the sides of the tail and body. C, close up of same female as in A. D, female C. arnoldi from population B2 showing the typical uniform chocolate coloration of this population. E, larvae of C. arnoldi from population B1. F, same female as in A in ventral view. G–H, juvenile of C. arnoldi from population A2 with several yellowish blotches on the sides of the tail and body (note the absence of the vertebral line that is typical of C. asper). I–J, details of the female cloaca of the same specimen as in A. K–L, detail of the female cloaca of a living specimen of C. asper from Berga, Spain (K) and Ordesa, Spain (L).
Figure 2 in Taxonomy, biogeography and evolution of Euproctus (Amphibia: Salamandridae), with the resurrection of the genus Calotriton and the description of a new endemic species from the Iberian Peninsula
Figure 2. Maximum likelihood (ML) tree for some representatives of the Salamandridae (log likelihood −6882.66489, GTR + I + G model of sequence evolution) inferred from the combined dataset, which included cytb, 12S and 16S mtDNA sequences. Bootstrap support and Bayesian posterior probabilities for particular nodes are shown in the boxes with the figures indicating the percentage support for different analyses. Upper left, bootstrap support derived by ML (GTR + I + G). Upper right, posterior probability values from the Bayesian analysis (GTR + I + G). Lower left, maximum parsimony (MP) bootstrap support derived by MP (ts = 1; tv = 1). Lower right, bootstrap support derived by MP (ts = 1; tv = 4 and cytb 3rd codon ts = 0). When the difference between the four support values was <5%, only the average value is shown. The '<' symbol is used to show that the bootstrap/posterior probability value for that node is lower than 50% and the '–' symbol indicates that a particular node is never recovered when using this method. Estimated ages are given for some bifurcations, which are marked by filled circles. Numbers in square brackets refer to localities shown in Fig. 1 and listed in Table 1.
Figure 1 in Taxonomy, biogeography and evolution of Euproctus (Amphibia: Salamandridae), with the resurrection of the genus Calotriton and the description of a new endemic species from the Iberian Peninsula
Figure 1. Map showing the distribution range of the Thyrrenian brook newts and the Western brook newts (shadowed areas). Numbers refer to the following localities: 1, El Montseny. 2, Irati. 3, Vidrà. 4, Xixarella. 5, Vall d'en Bac. 6, Collada de Tosses. 7, Font de l'Ús. 8, Berga. 9, Ordesa. 10, Monrepos. 11, Susqueda. 12, Vilanova de Meià, 13 Corsica. 14, Sardinia. Additional data are given in Table 1.
Figure 8 in Taxonomy, biogeography and evolution of Euproctus (Amphibia: Salamandridae), with the resurrection of the genus Calotriton and the description of a new endemic species from the Iberian Peninsula
Figure 8. Plot of first and second canonical variables for female Western brook newts. Filled squares indicate specimens from the El Montseny massif and filled circles the remaining specimens analysed.
Figure 5 in Taxonomy, biogeography and evolution of Euproctus (Amphibia: Salamandridae), with the resurrection of the genus Calotriton and the description of a new endemic species from the Iberian Peninsula
Figure 5. Scatter plot of principal component scores for the first three principal axes of the principal component analysis of male Western brook newts. Filled squares indicate specimens from the El Montseny massif and open circles the remaining specimens analysed.
Figure 9. A in Taxonomy, biogeography and evolution of Euproctus (Amphibia: Salamandridae), with the resurrection of the genus Calotriton and the description of a new endemic species from the Iberian Peninsula
Figure 9. A, detail of a hind leg of a male Euproctus platycephalus showing the spur (s) that characterizes the Tyrrhenian brook newts. B, detail of hind leg of a male E. montanus showing the spur (s). C, detail of a male cloaca of E. platycephalus; the spur on the right hind leg is also visible. D, detail of a male cloaca of E. montanus showing the pseudopenis (pp) and the spur. E, detail of a female cloaca of E. platycephalus. F, detail of a female cloaca of E. montanus.
Figure 4. X in Taxonomy, biogeography and evolution of Euproctus (Amphibia: Salamandridae), with the resurrection of the genus Calotriton and the description of a new endemic species from the Iberian Peninsula
Figure 4. X-ray images of several species of newts and pictures of two clear-stained specimens showing a close-up of the caudosacral and caudal vertebrae. Numbers from 1 to 4 correspond to the first caudosacral vertebrae. A, Calotriton arnoldi sp. nov. female from El Montseny (MZB2004-0188). B, C. arnoldi male from El Montseny (MZB 82–8789). C, C. arnoldi male from El Montseny (MZB2004-0187). D, C. arnoldi male from El Montseny (MZB 82-8784). E, C. arnoldi female from El Montseny (MZB2004-0189). F, C. asper male from Baños de Benasque, Huesca, Spain (BMNH, 1970.2448). G, C. asper male from Torrent de Castelmouly, near Bagnères de Bigorre, France (BMNH, 1928.11.18-22). H, C. asper male from Pla de l'Estany, northern slope of the Maladeta, Spain (BMNH, 1928.11.22.13-14). I, C. asper female from Lac d'Oncet, French Pyrenees (BMNH, 1920.1.20.20). J, Euproctus montanus male (BMNH 82.11.15.50-55). K, E. platycephalus male (BMNH, 1947.1.4.4.x6). L, Neurergus kaisseri male (paratype – BMNH, 1952.4.2.85). M, Triturus marmoratus male (BMNH 86.6.29.52-56). N, T. cristatus male (BMNH, 1950.1.4.81-82). O, T. karelinii male (BMNH 96.3.28.18-19). P, ventral view of the caudosacral and caudal vertebrae of a clear-stained male of C. asper from Berga (locality 8 in Fig. 1). Q, dorsal view of the same C. asper specimen as in P. R, ventral view of male from Bergo. S, dorsal view of C. arnoldi from population B1 (locality 1 in Fig. 1).
Fig. 8 in Resurrection of Pareas yunnanensis (Vogt, 1922) with description of a new species of Pareas from Yunnan Province, China (Squamata, Pareidae)
Fig. 8. Map showing the type locality of Pareas yunnanensis (Vogt, 1922) (black star), the type locality of P. geminatus Ding, Chen, Suwannapoom, Nguyen, Poyarkov & Vogel, 2020 (black square), the type locality of P. xuelinensis Liu & Rao, 2021 (black circle), the type locality of P. nigriceps Guo & Deng, 2009 (black diamond), and the type locality of P. tigerinus sp. nov. (black triangle).
Fig. 1 in Resurrection of Pareas yunnanensis (Vogt, 1922) with description of a new species of Pareas from Yunnan Province, China (Squamata, Pareidae)
Fig. 1. Bayesian phylogeny tree of Pareas Wagler, 1830 inferred from cyt b sequences. Node numbers before slashes indicate BPP (values below 0.90 are not shown) and numbers after slashes indicate UFB (values below 90 are not shown).
Fig. 2 in Resurrection of Pareas yunnanensis (Vogt, 1922) with description of a new species of Pareas from Yunnan Province, China (Squamata, Pareidae)
Fig. 2. Pareas yunnanensis (Vogt, 1922), syntypes in preservative. A–D. ZMB 27660. A. Dorsal view. B. Ventral view. C–D. Close up views of the head. E–H. ZMB 65431. E. Dorsal view. F. Ventral view. G–H. Close up views of the head. Photos by G. Vogel.
Fig. 6 in Resurrection of Pareas yunnanensis (Vogt, 1922) with description of a new species of Pareas from Yunnan Province, China (Squamata, Pareidae)
Fig. 6. Pareas tigerinus sp. nov. in preservative, head. A–C. Holotype, ♀ (KIZ 20210705). A. Dorsal view. B. Lateral view. C. Ventral view. D–F. Paratype, ♂ (KIZ 20210703). D. Dorsal view. E. Lateral view. F. Ventral view. Photos by S. Liu.
Fig. 5 in Resurrection of Pareas yunnanensis (Vogt, 1922) with description of a new species of Pareas from Yunnan Province, China (Squamata, Pareidae)
Fig. 5. Pareas tigerinus sp. nov., type specimens in preservative. A. Dorsal views. B. Ventral views. Photos by S. Liu.
Fig. 4 in Resurrection of Pareas yunnanensis (Vogt, 1922) with description of a new species of Pareas from Yunnan Province, China (Squamata, Pareidae)
Fig. 4. Pareas yunnanensis (Vogt, 1922), specimens from its type locality in life. A–C. ♀, KIZ 2022033. D–F. ♀, KIZ 2022034. G–I. ♀, KIZ 2022035. Photos by S. Liu.
Fig. 3 in Resurrection of Pareas yunnanensis (Vogt, 1922) with description of a new species of Pareas from Yunnan Province, China (Squamata, Pareidae)
Fig. 3. Pareas yunnanensis (Vogt, 1922), specimens from its type locality in preservative. A. Dorsal views. B. Ventral views. Photos by S. Liu.
Figure 19 in The resurrection of Cerasommatidiidae, an enigmatic group of coccinelloid beetles (Coleoptera: Coccinelloidea) based on molecular and morphological evidence
Figure 19. Habitats where type specimens of Cerasommatidiidae spp. were collected. A, track near the point where Yamuy constratus sp. nov. female paratype was collected. B, flight intercept trap in El Yunque National Forest where Y. constratus sp. nov. female paratype was collected. C, road-side habitat near Ifotaka, the type locality of MahaƲelo madagasus sp. nov. D, campsite at Forêt de Mahavelo, near the point where M. madagasus sp. nov. type series was collected.
Figure 20 in The resurrection of Cerasommatidiidae, an enigmatic group of coccinelloid beetles (Coleoptera: Coccinelloidea) based on molecular and morphological evidence
Figure 20. Geographical distribution of Cerasommatidiidae spp. A, distribution of species in eastern Caribbean region. B, distribution of species in southeastern Brazil. C, distribution of species in Madagascar.
Figure 18 in The resurrection of Cerasommatidiidae, an enigmatic group of coccinelloid beetles (Coleoptera: Coccinelloidea) based on molecular and morphological evidence
Figure 18. Morphology of MahaƲelo madagasus sp. nov. A, antenna. B, head, dorso-frontal (arrow: antennal grooves). C, left half of pronotum (arrow: indentation on postero-lateral corner of pronotum). D, prosternum (arrow: median carina). E, pterothorax and first abdominal ventrite (white arrow: epipleural groove; black arrows: meso- and metatrochanters). F, left elytron, dorsal. G, left half of abdomen, ventral (arrow: anterior bordering carina).
Figure 16 in The resurrection of Cerasommatidiidae, an enigmatic group of coccinelloid beetles (Coleoptera: Coccinelloidea) based on molecular and morphological evidence
Figure 16. Morphology of Yamuy marginatus sp. nov. A, head, dorsal. B, pronotum. C, prosternum (arrow: narrowed prosternal process). D, meso- and metaventrite (arrow: short postcoxal longitudinal carinae). E, protarsus, ventral. F, abdomen, ventral (arrow: short postcoxal longitudinal carinae).
Figure 14 in The resurrection of Cerasommatidiidae, an enigmatic group of coccinelloid beetles (Coleoptera: Coccinelloidea) based on molecular and morphological evidence
Figure 14. Terminalia of Yamuy gen. nov. A–C, Yamuy constratus sp. nov.: A, abdominal segment VIII and male genital segment, ventral. B, aedeagus, ventral. C, female genitalia. D–F, Yamuy marginatus sp. nov.: D, male genital segment, ventral. E, aedeagus, ventral. F, female genitalia.
Figure 7 in The resurrection of Cerasommatidiidae, an enigmatic group of coccinelloid beetles (Coleoptera: Coccinelloidea) based on molecular and morphological evidence
Figure 7. Morphology of Karumbe gen. nov. A–E, G, J–K, M, Karumbe pakaluki sp. nov. F, I, L, Karumbe geiseri sp. nov. H, Karumbe brethesi sp. nov. A, head without mouthparts, ventral. B, labrum, dorsal. C, maxilla, ventral. D, labium, ventral. E, mandible, ventral. F, prothorax, ventral, G, metanotum. H, hindwing. I, meso- and metaventrite. J, details of metaventrite showing metendosternite. K, hindleg, ventral. L, metatarsus. M, abdomen, ventral.
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