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Fig. 7 in On the phylogenetic position of the palaeopteran Syntonopteroidea (Insecta: Ephemeroptera), with a new species from the Upper Carboniferous of England

Fig. 7 Bojophlebia prokopi Kukalová-Peck, 1985, holotype (No. 1/ 1985, National Museum Prague, Czech Republic); photograph of counterpart. Scale bar 50 mm

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Fig. 1 in On the phylogenetic position of the palaeopteran Syntonopteroidea (Insecta: Ephemeroptera), with a new species from the Upper Carboniferous of England

Fig. 1 Anglolithoneura magnifica gen. et sp. n., holotype; composite line drawing of hind wing. Scale bar 10 mm. For abbreviations of wing veins, see the "Material and methods" section

Fig. 7 in Phylogenetic position of the Amazonian nurse frog Allobates gasconi (Morales 2002) revealed by topotypical data

Fig. 7 Coloration in life of A, B, C topotypic adult males and D females of Allobates gasconi. Note the densely pigmented throat and vocal sac of actively calling males. Photographs by B, C A.P. Lima and A, D W. E. Magnusson

Fig. 9 in Phylogenetic position of the Amazonian nurse frog Allobates gasconi (Morales 2002) revealed by topotypical data

Fig. 9 Advertisement call of Allobates gasconi from its type locality. A Oscillogram showing the continuous emission of 10 calls with distinct note arrangements (2–4 notes per call). Spectrograms and

Fig. 11 in Phylogenetic position of the Amazonian nurse frog Allobates gasconi (Morales 2002) revealed by topotypical data

Fig. 11 Detailed views of the oral disc of tadpoles of Allobates gasconi, Gosner stage 36, from Jainú West. A Mouth dyed with blue dye and B mouth without dye. Photographs by A. S. Ferreira

Fig. 5 in Molecular phylogeny and comparative morphology reveal the species validity and systematic position of Lepidodesma (Bivalvia: Unionidae)

Fig. 5 Fossil-calibrated phylogeny based on the three-gene dataset. Node bars denote the mean ages of 95% highest posterior density (HPD). Fossil calibrations are marked by star signs. Mya, million years ago

Fig. 2 A in Phylogenetic position of the Amazonian nurse frog Allobates gasconi (Morales 2002) revealed by topotypical data

Fig. 2 A Phylogeny of Allobates showing the relationships of the main large clades inferred through maximum likelihood based on five mitochondrial genes (12S, 16S, COI, Cytb, ND1) and 6,251 bp. B A detailed view of the A. caeruleodactylus and A. trilineatus clades. Dark gray vertical bars denote species delimitation from the Bayes-

Fig. 5 A in Phylogenetic position of the Amazonian nurse frog Allobates gasconi (Morales 2002) revealed by topotypical data

Fig. 5 A Ventral surface of the right foot of a preserved topotypic adult male (MPEG 44622) and B right foot of topotypic adult female (MPEG 44620) of Allobates gasconi. Photographs by A. S. Ferreira

Fig. 4 in Molecular phylogeny and comparative morphology reveal the species validity and systematic position of Lepidodesma (Bivalvia: Unionidae)

Fig. 4 Phylogenetic trees inferred from Bayesian Inference (BI) and Maximum Likelihood (ML) analyses. Left is the BI and ML tree based on the AA dataset. Right is the BI tree based on the NT dataset; taxon names correspond to the left tree. Numbers close to the nodes for the left tree indicate bootstrap support (BS)/posterior probabilities (PP), and those for the right tree indicate PP. Hidden node numbers and asterisks (*) denote PP> 0.9 and BS> 75%. Different colored clades represent four subfamilies in Unionidae. Pentagrams symbolize sequences from this study. Dotted lines in the right tree indicate inconsistent clades compared to the left tree. The figure depicts the topology of Unionidae, while the complete topology is presented in Supplementary Fig. S5

Fig. 2 in Molecular phylogeny and comparative morphology reveal the species validity and systematic position of Lepidodesma (Bivalvia: Unionidae)

Fig. 2 Anatomical features of Lepidodesma aligera with left valve removed and Lepidodesma languilati with right valve removed. a L. aligera; b L. languilati. c–h close-up of apertures and gills: c–e Lepidodesma aligera; f–h, Lepidodesma languilati. Abbreviations: aam, anterior adductor muscle; pam, posterior adductor muscle; exa, excurrent aperture; ia, incurrent aperture; f, foot; ig, inner gill; og, outer gill; lp, labial palps; m, mantle; p ia, papillae in incurrent aperture; pg exa, pigmentation of excurrent aperture

Fig. 1 in Molecular phylogeny and comparative morphology reveal the species validity and systematic position of Lepidodesma (Bivalvia: Unionidae)

Fig. 1 Shell images of Lepidodesma aligera and Lepidodesma languilati. a (1–4): Lepidodesma aligera; b (1–4): Lepidodesma languilati

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Fig. 4 in Turtle and tortoise mitogenomes under contrasting positive selection pressure

Fig. 4 Graphical representation denoting the distribution of PSS in Testudinoidean lineages across the OXPHOS system. All the 12 mitochondrial PCGs encoding the OXPHOS system were projected onto homologous protein structures and are represented in different colours. Grey structures represent the entire OXPHOS complex and no solved crystallized structures were available for the ATP8 gene. The NAD3 gene (lemon green) represents sites under positive selection across all Testudinoidean lineages as detected by random sites analysis. The rest of the genes, NAD1 (hot pink), NAD2 (yellow),

Fig. 3 A Dorsal and B in Phylogenetic position of the Amazonian nurse frog Allobates gasconi (Morales 2002) revealed by topotypical data

Fig. 3 A Dorsal and B ventral views of the sub-adult male holotype (INPA-H 3082) of Allobates gasconi from Jainú West, Juruá River, Amazonas, Brazil. Photographs by A. S. Ferreira

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Fig. 2 in Turtle and tortoise mitogenomes under contrasting positive selection pressure

Fig. 2 Gene-wise estimates of dN/dS for the concatenated data set of 12 PCGs using M8a-M8 nested random site models. The y-axis denotes BEB posterior mean estimate of dN/dS for each site, with

Fig. 6 in Whole mitogenomes of Turkish white-toothed shrews, genus Crocidura (Eulipotyphla: Soricidae), with new insights into the phylogenetic positions of Crocidura leucodon and the Crocidura suaveolens group

Fig. 6 Median-joining haplotype network of C. leucodon based on CYTB sequences. Bold indicates Turkish samples in the current study

Fig. 4 in Whole mitogenomes of Turkish white-toothed shrews, genus Crocidura (Eulipotyphla: Soricidae), with new insights into the phylogenetic positions of Crocidura leucodon and the Crocidura suaveolens group

Fig. 4 Median-joining haplotype network of the C. suaveolens group based on CYTB sequences. Bold indicates Turkish samples in the current study

Fig. 2 in Whole mitogenomes of Turkish white-toothed shrews, genus Crocidura (Eulipotyphla: Soricidae), with new insights into the phylogenetic positions of Crocidura leucodon and the Crocidura suaveolens group

Fig. 2 Phylogenetic tree reconstructed using Bayesian analysis of Turkish white-toothed shrews based on mitogenomes minus the D-loop region and the GTR+ G + I model

Fig. 1 in Whole mitogenomes of Turkish white-toothed shrews, genus Crocidura (Eulipotyphla: Soricidae), with new insights into the phylogenetic positions of Crocidura leucodon and the Crocidura suaveolens group

Fig. 1 Graphical maps showing the mitogenomes of three Crocidura species from Turkey: A C. gueldenstaedtii; B C. mimula; C C. leucodon

Fig. 3 in Whole mitogenomes of Turkish white-toothed shrews, genus Crocidura (Eulipotyphla: Soricidae), with new insights into the phylogenetic positions of Crocidura leucodon and the Crocidura suaveolens group

Fig. 3 Phylogenetic tree reconstructed using Bayesian analysis of C. suaveolens group and C. leucodon based CYTB sequences and the HKY+ G + I model. Asterisk indicates Turkish samples in the current study