Find research datasets worth reusing

FIG. 5 in Cryptic but ubiquitous: Claviradulomyceae fam. nov. with five novel species of the lenticel fungus Claviradulomyces from Brazil

FIG. 5. — Claviradulomyces tabebuiae sp. nov. (VIC 42848, holotype): A, Tabebuia roseo-alba (Ridl.) Sandwith stem with abnormal lenticels colonized by C. tabebuiae sp. nov.; B, pycnidium with rostrate-vermiform ostiole neck; C, group of conidia. Scale bars: B, 30 µm; C, 10 µm.

FIG. 4 in Cryptic but ubiquitous: Claviradulomyceae fam. nov. with five novel species of the lenticel fungus Claviradulomyces from Brazil

FIG. 4. — Claviradulomyces schini sp. nov. (VIC 42845, holotype): A. Schinus terebinthifolia Raddi. Individual branch with dieback symptom and abnormal lenticels colonized by C. schini; B, close-up of hypertrophyed lenticels; C, conidiophores with immature conidia still attached; D, conidia; E, pycnidium with sinuose and rostrate-vermiform ostiole neck. Scale bars: B, C, 10 µm; E, 30 µm.

FIG. 3. — Claviradulomyces machaeriae D.M.Macedo & R.W in Cryptic but ubiquitous: Claviradulomyceae fam. nov. with five novel species of the lenticel fungus Claviradulomyces from Brazil

FIG. 3. — Claviradulomyces machaeriae D.M.Macedo & R.W.Barreto, sp. nov.: A, branch of Machaerium sp. showing abnormal lenticels colonized by C. machaeriae sp. nov. (VIC 42840); B, C, pycnidia on lenticels. D, E, pycnidia; F, group of immature conidia attached to the conidiogenous cells; G, conidium. Scale bars: B-E 20 µm; F, G, 10 µm.

FIG. 2. — Claviradulomyces casearia L.L.Duarte, D.M.Macedo & R.W in Cryptic but ubiquitous: Claviradulomyceae fam. nov. with five novel species of the lenticel fungus Claviradulomyces from Brazil

FIG. 2. — Claviradulomyces casearia L.L.Duarte, D.M.Macedo & R.W.Barreto sp. nov. (VIC 42849, holotype): A, B, Casearia ulmifolia Vahl ex. Vent. branches with abnormal lenticels colonized by C. casearia; C, pycnidium with rostrate ostiole neck; D, conidiophores with attached imature conidia. Scale bars: C, 20 µm; D, 10 µm.

FIG. 1 in Cryptic but ubiquitous: Claviradulomyceae fam. nov. with five novel species of the lenticel fungus Claviradulomyces from Brazil

FIG. 1. — Phylogenetic tree of the Claviradulomyces isolates inferred by Bayesian analysis of nuclear LSU and rpb2 sequences. Bayesian posterior probabilities are given at the nodes and the accession numbers are presented together with the species names. The newly proposed family Claviradulomyceae is indicated. The tree is rooted with Pleopsidium chlorophanum (Wahlenb.) Zopf and Acarospora laqueata Stizenb. ex Flagey.

FIGURE 8 in Deciphering "cryptic" nature of European rock-dwelling Pyramidula snails (Gastropoda: Stylommatophora)

FIGURE 8 Linear regressions of selected shell parameters in relation to climatic variables inferred from the population locations. Regression lines, 95% confidence intervals, Adj R2 values and P-values are shown.

FIGURE 6 in Deciphering "cryptic" nature of European rock-dwelling Pyramidula snails (Gastropoda: Stylommatophora)

FIGURE 6 Upper face shell microsculpture on the last whorl in four Pyramidula species; a) P. jaenensis (from left to right): Jijona, Spain (P368), Città di San Marino (P207), P368; b) P. rupestris: Xàtiva, Spain (P374), Encio, Spain (P366), P374; c) P. saxatilis: Villeret, Switzerland (P208), Hochschwab, Austria (P189), P189; d) P. pusilla: Pavlov, Czech Republic (P211), Tatranská Kotlina, Slovakia (P213), P211. Scale bar: 0.1 mm.

FIGURE 7 in Deciphering "cryptic" nature of European rock-dwelling Pyramidula snails (Gastropoda: Stylommatophora)

FIGURE 7 Type specimens of the four studied species: a) Pyramidula jaenensis, lectotype (design. nov.), collection of S. Clessin, no. SMNS-ZI0142153, State Museum of Natural History Stuttgart, Germany. b) P. rupestris, lectotype, Draparnaud colection xxvi 97a, Natural History Museum, Vienna, Austria. c) P. saxatilis lectotype (design. nov.), collection of J. D. W. Hartmann, M562.1, Natural History Museum St. Gallen, Switzerland. d) P. pusilla, neotype, no. 210.996.MO.1, Natural History Museum, Dijon, France.

FIGURE 3 in Deciphering "cryptic" nature of European rock-dwelling Pyramidula snails (Gastropoda: Stylommatophora)

FIGURE 3 Variation in shell shape among genetically analyzed populations of four studied Pyramidula species; P. jaenensis: a) Jijona, Spain (P368); b) Venta del Moro, Spain (P376); c) Cazorla, Spain (P357); d) Gaeta, Italy (P210); e) Città di San Marino (P207); P. rupestris: a) Xàtiva, Spain (P374); b) Meyreuil, France (P373); c) Ollioules, France (P354); d) Encío, Spain (P366); e) Mura, Spain (P375); P. saxatilis: a) Nods, Switzerland (P229); b) Selva di Val Gardena, Italy (P249); c) Lunz am See, Austria (P231); d) Kamnik, Slovenia (P232); e) Hochschwab, Austria (P189); P. pusilla: a) Štramberk, Czech Republic; b) Johnsbach, Austria (P196); c) Liptovské Revúce, Slovakia (P369); d) Tatranská Kotlina, Slovakia (P213); e) Spital am Pyhrn, Austria (P193).

FIGURE 4 in Deciphering "cryptic" nature of European rock-dwelling Pyramidula snails (Gastropoda: Stylommatophora)

FIGURE 4 Position of measured shells along the first two axes of the Canonical Variance Analysis based on the fifteen measured shell parameters and their ratios (supplementary table S2). Numbers of measured shells / populations for each species: P. jaenensis: 29 / 7, P. saxatilis: 50 / 11, P. rupestris: 28 / 9, P. pusilla: 55 / 12. Convex polygons were added to the diagram to highlight the distinction between the four species. Type specimens of the respective species were also used in the analysis (see fig. 7 for details), and are shown in grey color. Variation in selected basic shell parameters among the four species (PP, P. pusilla; PS, P. saxatilis; PR, P. rupestris; PJ, P. jaenensis) is visualized using notched box-and-whisker plots on the right.

FIGURE 2 in Deciphering "cryptic" nature of European rock-dwelling Pyramidula snails (Gastropoda: Stylommatophora)

FIGURE 2 Maximum likelihood (ML) phylogenetic reconstruction based on mitochondrial DNA (COI) and nuclear DNA (concatenated ITS 1 and ITS 2). Support values of> 70% are shown next to the corresponding nodes as follows: NJ, upper left, bold font; MP, upper right, italic font; ML, lower left, normal font, and posterior probabilities of> 95% for BI, lower right, bold italic font. Specimens for which only mtDNA data exist are highlighted in grey color. Specimen placed in a different clade in Downloaded from Brill.com 06/24/2024 12:52:31AM mtDNA and nDNA is marked byviaasterisk Open. Access Symbols. This usedisforaneach openspecies access article correspond to distributed those in fig under. 1. the terms of the CC-BY 4.0 license. https://creativecommons.org/licenses/by/4.0/

FIGURE 1 A in Deciphering "cryptic" nature of European rock-dwelling Pyramidula snails (Gastropoda: Stylommatophora)

FIGURE 1 A. Approximate distribution of the four study species based on genetically verified data in the present study and integrative analysis of Razkin et al. (2017). B. Geographic location of all genetically analyzed Pyramidula populations. Detailed information about the localities are shown in supplementary table S1.

Fig. 1 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 1. Sampling sites and haplotypes found in and around the Carpathian Basin. Sam- ples collected in this study are marked with circles and haplotype codes, and previously

Fig. 5 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 5. Original drawings by O. Gy. Dely: male (A, B) and female (C, D) Ichthyosaura alpestris alpestris head shape from dorsal (A, C) and lateral (B, D) view

Fig. 4 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 4. Holotype of Triturus (=Ichthyosaura) alpestris bakonyiensis (Dely, 1964) (HNHM- HER-61.27.1.) from dorsal (A), lateral (B) and ventral (C) view

Fig. 8 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 8. Original drawings by O. Gy. Dely: female (A–D) and male (E–H) Ichthyosaura alpestris bakonyiensis skull from dorsal (A, E), ventral (B, F), lateral (C, G) and posterior (D, H) view

Fig. 7 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 7. Original drawings by O. Gy. Dely: female (A–D) and male (E–H) Ichthyosaura alpestris alpestris skull from dorsal (A, E), ventral (B, F), lateral (C, G) and posterior (D, H) view

Fig. 3 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 3. Median-joining network of the combined mtDNA haplotypes found in and around the Carpathian Basin (drawn with PopArt 1.7). Inset: distribution of Ichthyosaura alpestris in this region. On the network, circles with haplotype names mark haplotypes found in this

Fig. 6 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 6. Original drawings by O. Gy. Dely: male (A, B) and female (C, D) Ichthyosaura alpestris bakonyiensis head shape from dorsal (A, C) and lateral (B, D) view