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Fig. 6 in Contemporary integrative taxonomy for sexually deprived protists: A case study of Trachelomonas (Euglenaceae) from western Ukraine
Fig. 6. Loricae showing different shape and ornamentation (SEM; all at the same scale). A, Lorica of Trachelomonas sp.GeoM*524; B, Lorica of Trachelomonas sp. GeoM 526; C, Lorica of Trachelomonas hispida var. irregularis GeoM 529; D, Protologue of Trachelomonas hispida var. irregularis.
Fig. 2 in Biogeography and integrative taxonomy of Epipterygium (Mniaceae, Bryophyta)
Fig. 2. Single best ML tree for 109 Epipterygium specimens inferred from the partitioned ITS + chloroplast DNA matrix plus coded indels. Regular bootstrap and ultrafast bootstrap values are shown on the branches, posterior probabilities above the bootstrap values. Black arrows indicate the E. tozeri specimen from Scotland that was nested within the Macaronesian clade and one specimen from Madeira that grouped in the Mediterranean-Continental clade.
Fig. 4 in Contemporary integrative taxonomy for sexually deprived protists: A case study of Trachelomonas (Euglenaceae) from western Ukraine
Fig. 4. Different ontogenetic stages and empty loricae of selected Trachelomonas strains (LM; all at the same scale). M–P, Young immature cell, mature naked cell, mature loricate cell and empty lorica of Trachelomonas teres var. minor GeoM 527; Q–T, Young immature cell, mature naked cell, mature loricate cell and empty lorica of Trachelomonas hispida var. irregularis GeoM 529; U–X, Young immature cell, mature naked cell, mature loricate cell and empty lorica of Trachelomonas teres var. granulata GeoM 540.
Fig. 2 in Contemporary integrative taxonomy for sexually deprived protists: A case study of Trachelomonas (Euglenaceae) from western Ukraine
Fig. 2. Box plot display of cell width of investigated mature naked cells and mature loricate cells of Trachelomonas strains. Statistically significant clusters are indicated with letters a or b and green or red colour, corresponding to the phylogenetic tree (see Fig. 7).
Fig. 1 in Contemporary integrative taxonomy for sexually deprived protists: A case study of Trachelomonas (Euglenaceae) from western Ukraine
Fig. 1. Box plot display of cell length of investigated mature naked cells and mature loricate cells of Trachelomonas strains. Statistically significant clusters are indicated with letters a or b and green or red colour, corresponding to the phylogenetic tree (see Fig. 7).
Fig. 5 in Contemporary integrative taxonomy for sexually deprived protists: A case study of Trachelomonas (Euglenaceae) from western Ukraine
Fig. 5. LM, epitype, SEM and protologue images of mature Trachelomonas cells from selected strains. A–F, Mature loricate cells (A & B), epitype images (C & D), SEM image (E) and protologue (F) of Trachelomonas hispida var. volicensis GeoM 520; G–L, Mature loricate cells (G & H), epitype images (I & J), SEM image (K) and protologue (L) of Trachelomonas teres var. minor GeoM 527; M–R, Mature loricate cells (M & N), epitype images (O & P), SEM image (Q) and protologue (R) of Trachelomonas teres var. granulata GeoM 540.
Fig. 3 in Contemporary integrative taxonomy for sexually deprived protists: A case study of Trachelomonas (Euglenaceae) from western Ukraine
Fig. 3. Different ontogenetic stages and empty loricae of selected Trachelomonas strains (LM; all at the same scale). A–D, Young immature cell, mature naked cell, mature loricate cell and empty lorica of Trachelomonas hispida var. volicensis GeoM 520; E–H, Young immature cell, mature naked cell, mature loricate cell and empty lorica of Trachelomonas sp. GeoM*524; I–L, Young immature cell, mature naked cell, mature loricate cell and empty lorica of Trachelomonas sp. GeoM 526.
Fig. 1. A in Biogeography and integrative taxonomy of Epipterygium (Mniaceae, Bryophyta)
Fig. 1. A, Results of the principal component analysis (PCA) for Epipterygium tozeri specimens. Colors represent the six different populations of E. tozeri s.l. Individual specimens are shown by small points, big points represent group means, and 95% confidence ellipses were drawn around group means; B, The correlation of each measured trait to the PCA is displayed by vectors. Coloration and arrow length represent contribution to total variance.
Fig. 8 in Biogeography and integrative taxonomy of Epipterygium (Mniaceae, Bryophyta)
Fig. 8. Epipterygium yunnanense sp. nov. A, Habitus; B, Perichaetial leaf; C, Perichaetial leaf apex; D, Marginal cells of dorsal leaf.
Fig. 3 in Biogeography and integrative taxonomy of Epipterygium (Mniaceae, Bryophyta)
Fig. 3. Ancestral area distributions of Epipterygium inferred with DIVALIKE in BioGeoBEARS. Species names color-coded according to geographic origin of the specimens. Numbers above branches indicate best divergence time estimate according to a relaxed clock dating, blue bar indicates 95% highest posterior density. Rectangles below the branches indicate most likely ancestral states at nodes. The corner positions represent geographical ranges immediately after a dispersal or speciation even. Asterisks mark nodes with a posterior probability>0.95. The vertical bars indicate the estimated entities from the bGMYC, mPTP and our taxonomic hypothesis H1.
FIG. 4. — Avicenia kocyani n in A new Silurian Avicenia (Tabulata): taxonomy, growth pattern, and colony integration
FIG. 4. — Avicenia kocyani n. sp., paratypes: A, B, specimen (ZPAL T. 26 AVI-2) from Jastrzębia Góra; probably latest Llandovery- Wenlockian; C, D, specimen (ZPAL T. 26 AVI-4) from Kołobrzeg; probably latest Llandovery-Wenlockian; A, C, longitudinal sections; B, D, transverse sections. Scale bars: 500 μm.
FIG. 3 in A new Silurian Avicenia (Tabulata): taxonomy, growth pattern, and colony integration
FIG. 3. — Longitudinal section of Avicenia kocyani n. sp. (holotype; ZPAL T. 26 AVI-1) from the erratic boulder of Międzyzdroje, probably latest Llandovery-Wenlockian: high density zones in corallites (dashed line) do not correspond to high density zones in diaphragm distribution in coenenchymal tubes (continuous line). Scale bar: 500 μm.
FIG. 2 in A new Silurian Avicenia (Tabulata): taxonomy, growth pattern, and colony integration
FIG. 2. — Transverse section of Avicenia kocyani n. sp. (holotype; ZPAL T. 26 AVI-1) from the erratic boulder of Międzyzdroje, probably latest Llandovery-Wenlockian: A, B, general view (notice the dimetrism of corallites and differences in coenenchymal tissue distribution); C, a detail showing the connecting pore, polarized light. Scale bars: 500 μm.
Figure 5 in Integrative taxonomy reveals cryptic Amazonian species of Pristimantis (Anura: Strabomantidae)
Figure 5. Oscillograms and audiospectrograms of the advertisement call of Pristimantis sp. 2 (A) and P. danae (B).
Figure 8 in Integrative taxonomy reveals cryptic Amazonian species of Pristimantis (Anura: Strabomantidae)
Figure 8. Map of part of South America depicting the approximate distribution of Pristimantis danae, P. koehleri, P. fenestratus, P. reichlei, and P. samaipatae.
Figure 2 in Integrative taxonomy reveals cryptic Amazonian species of Pristimantis (Anura: Strabomantidae)
Figure 2. Oscillograms and audiospectrograms of the advertisement call of Pristimantis sp. 1 (A), P. fenestratus (B) and P. samaipatae (C).
Figure 1 in Integrative taxonomy reveals cryptic Amazonian species of Pristimantis (Anura: Strabomantidae)
Figure 1. Principal component analysis (PCA) of morphometric characters of adult females and adult males of Pristimantis sp. 1, P. fenestratus and P. samaipatae. Abbreviations are: P, principal component; SVL, snout–vent length; HL, head length; HW, head width.
Figure 9. A in Integrative taxonomy reveals cryptic Amazonian species of Pristimantis (Anura: Strabomantidae)
Figure 9. A, adult male of Pristimantis reichlei from Chalalán, Departamento La Paz, Bolivia (MNK-A 7178); B, adult male of P. danae from Huairuro, Departamento La Paz, Bolivia (one from the series MNCN 43054–64, 43067–8).
Figure 4 in Integrative taxonomy reveals cryptic Amazonian species of Pristimantis (Anura: Strabomantidae)
Figure 4. Majority rule consensus trees based on maximum parsimony (MP) and Bayesian (MB) phylogenetic analyses of partial 16S rDNA (c. 590 bp) of several Pristimantis selected for this study. The outgroup is composed of members of the genus Oreobates. Single values on the MP tree (left) correspond to MP boostrap values. When the MP topology coincides with neighbour-joining (NJ) topology (not illustrated) two values are shown (the second representing NJ boostrap values). Values in the MB tree are Bayesian posterior probabilities.
Figure 7. A in Integrative taxonomy reveals cryptic Amazonian species of Pristimantis (Anura: Strabomantidae)
Figure 7. A, adult male of Pristimantis koehleri from Km 6 of Angostura–Samaipata road, Departamento Santa Cruz, Bolivia (one from the type series MNK-A 6626–7, MNCN 42990–1); B, adult female of Pristimantis fenestratus from Chalalán, Departamento La Paz, Bolivia (one from the series MNCN 43239–44).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.