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Fig. 2. a in Revalidation and redescription of Steindachnerina nigrotaenia and redescription of S. insculpta (Characiformes: Curimatidae)
Fig. 2. a. Steindachnerina nigrotaenia, lectotype of Curimatus nigrotaenia, BMNH 1902.2.10.30, 43.5 mm SL, Brazil, Mato Grosso, rio Coxipó, upper rio Paraguai; b. LBP 1477, 43.4 mm SL, Brazil, Mato Grosso do Sul, Coxim, rio Taquari, upper rio Paraguai.
Fig. 7 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa
Fig. 7. (a) Lectotype of Enteromius alberti (Poll, 1939) (MRAC 64723) with 74.3 mm SL. (b) Fresh specimen of E. alberti (RMCA 2018.008.P.0248 HP 3246) with 62.4 mm SL.
Fig. 4 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa
Fig. 4. Scatterplots of PC2 against PC1 of the PCA on (a) 24 log-transformed measurements (n = 69) and (b) on 15 meristics (n = 62). Specimens of group A, the filled circles (●) represent the genetically analysed specimens, the open circles (Ǫ) indicate the additional specimens. Specimens of E. alberti (Poll, 1939) (lectotype) (♦), E. alberti (paralectotypes) (◊), specimens from Tshambi (), E. cercops (Whitehead, 1960) (holotype) (▲), E. cercops (paratypes) (), E. mimus (Boulenger, 1912) (lectotype) (▼), E. mimus (paralectotypes) (▼), E. perince (R̹ppell, 1835) (syntypes) (+) and E. stigmatopygus (Boulenger, 1903) (syntypes) (×).
Fig. 6 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa
Fig. 6. Scatterplot of PC2 against PC1 of the PCA (n = 83) on 24 log-transformed measurements. For group B, the filled squares (■) represent the specimens used for the genetic analysis, the open squares (□) indicate the additional specimens of the Lake Edward system and the two specimens from Tshambi. Specimens of E. mimus (Boulenger, 1912) (lectotype) (▼) and E. mimus (paralectotypes) (▼).
Fig. 2 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa
Fig. 2. Scatterplot of PC2 against PC1 of a PCA on 24 log-transformed measurements on 71 specimens of Enteromius Cope, 1867. Specimens of the genetic groups A (●) (n = 21) and B (■) (n = 50) are indicated separately.
Fig. 5 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa
Fig. 5. Scatterplots of PC2 against PC1 of (a) the PCA (n = 105) on 24 log-transformed measurements and (b) the PCA (n = 95) on 15 meristics. Specimens of group B, the filled squares (■) represent the genetic analysed specimens, the open squares (□) indicate the additional specimens. Specimens of E. alberti (Poll, 1939) (lectotype) (♦), E. alberti (paralectotypes) (◊), specimens from Tshambi (), E. cercops (Whitehead, 1960) (holotype) (▲), E. cercops (paratypes) (), E. mimus (Boulenger, 1912) (lectotype) (▼), E. mimus (paralectotypes) (▼), E. perince (R̹ppell, 1835) (syntypes) (+) and E. stigmatopygus (Boulenger, 1903) (syntypes) (×).
Fig. 1 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa
Fig. 1. Haplotype network of 651-bp-long COI sequences (n = 137) of the specimens of Enteromius Cope, 1867 with a smooth, flexible last unbranched dorsal fin ray from the Lake Edward system. Each circle represents a haplotype, with the size of the circles indicating the number of individuals with this haplotype and the colour indicating the different parts of the basin. Each bar represents a mutation between two haplotypes.
Fig. 3 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa
Fig. 3. Scatterplots of (a) interorbital width (IOW), (b) pre-pelvic distance (PrPelD), (c) body depth (BD), (d) maximum caudal peduncle depth (MxCPD), (e) minimum caudal peduncle depth (MnCPD), (f) head width (HW), and (g) head depth (HD) in % SL against SL (in mm) on 72 specimens of Enteromius Cope, 1867. The genetic groups A (●) (n = 22) and B (■) (n = 50) are indicated separately. The dashed lines indicate the size class used for the MWU tests.
Fig. 9 in Revalidation and taxonomic revision of Teloneria Aczél (Diptera, Neriidae), with description of two new species
Fig. 9. Distribution of species of Teloneria Aczél, 1954. Conventions: Teloneria apicata (Edwards, 1919) comb. nov. (●); Teloneria bimaculata (Edwards, 1919) comb. nov. (●); Teloneria juceliae Sepúlveda & Souza sp. nov. (●); Teloneria ladyae Sepúlveda & Souza sp. nov. (●).
Fig. 8 in Revalidation and taxonomic revision of Teloneria Aczél (Diptera, Neriidae), with description of two new species
Fig. 8. Thorax in dorsal view and wing. A. Loxozus cornutus (Walker, 1853). B. Telostylus philippinensis Cresson, 1926. C. Derocephalus angusticollis Cresson, 1926. D. Chaetonerius claricoxa Enderlein, 1922. E. Chaetonerius latifemur Enderlein, 1922. F. Eoneria blanchardi Aczél, 1951. G. Teloneria apicata (Edwards, 1919) comb. nov. H. Teloneria bimaculata (Edwards, 1919) comb. nov. I. Telostylus marshalli Sepúlvesa & de Carvalho, 2019 (NHMUK 1179). J. Teloneria apicata comb. nov. (UCDC 1821). K. Teloneria bimaculata comb. nov. (ZMHB).
Fig. 7 in Revalidation and taxonomic revision of Teloneria Aczél (Diptera, Neriidae), with description of two new species
Fig. 7. Inner margin of antenna and head in lateral view. A. Nerius czernyi Aczél, 1961. B. Antillonerius cinereus (R̂der, 1885). C. Eoneria blanchardi Aczél, 1951. D. Cerantichir enderleini Hennig, 1937. E. Glyphidops bullatus (Enderlein, 1922). F. Glyphidops durus (Cresson, 1926). G. Indonesicesa annulipes (Doleschall, 1857). H. Chaetonerius claricoxa Enderlein, 1922. I. Telostylus philippinensis Cresson, 1926. J. Teloneria apicata (Edwards, 1919) comb. nov. K. Teloneria bimaculata (Edwards, 1919) comb. nov. L. Telostylus marshalli Sepúlveda & de Carvalho, 2019 (NHMUK 1179). M. Chaetonerius claricoxa (TAUI 895). N. Teloneria apicata comb. nov. (UCDC 1821). O. Teloneria bimaculata comb. nov. (ZMHB). Abbreviations: i proc ped = inner process of pedicel; u fc = upper face.
Fig. 5 in Revalidation and taxonomic revision of Teloneria Aczél (Diptera, Neriidae), with description of two new species
Fig. 5. Teloneria ladyae Sepúlveda & Souza sp. nov., holotype (NHMUK 1898). A. Head, lateral view. B. Thorax, lateral view. C. Habitus, lateral view. D. Habitus, dorsal view.
Fig. 3 in Revalidation and taxonomic revision of Teloneria Aczél (Diptera, Neriidae), with description of two new species
Fig. 3. Type material, habitus, lateral view. A. Telostylus apicatus Edwards, 1919, lectotype, ♀. B. Telostylinus apicalis Enderlein, 1922, lectotype, ♂. C. Telostylus bimaculatus Edwards, 1919, holotype, ♀. D. Telostylinus ornatipennis Enderlein, 1922, lectotype, ♀.
Fig. 2. Male genitalia. A in Revalidation and taxonomic revision of Teloneria Aczél (Diptera, Neriidae), with description of two new species
Fig. 2. Male genitalia. A. Teloneria apicata (Edwards, 1919) comb. nov. B. Teloneria bimaculata (Edwards, 1919) comb. nov. C. Teloneria juceliae Sepúlveda & Souza sp. nov. D. Teloneria ladyae Sepúlveda & Souza sp. nov.
FIGURE 6 in Salamandridae) using molecular and morphological data. Revalidation of the taxon Pleurodeles nebulosus (Guichenot, 1850)
FIGURE 6. Ventral aspect of the skull of A. adult P. p o i re t i, BMNH 1920.1. 20.1383 (Bône) and B. adult P. nebulosus, BMNH 130 a (Algiers).
FIGURE 1 in Salamandridae) using molecular and morphological data. Revalidation of the taxon Pleurodeles nebulosus (Guichenot, 1850)
FIGURE 1. Map of North Africa showing localities of Pleurodeles used in the present study. See Table 1 and Fig. 5 for further details. The dashed line delimits the approximate distribution range of P. poireti. We refer to it in the text as the Edough Peninsula.
FIGURE 3 in Salamandridae) using molecular and morphological data. Revalidation of the taxon Pleurodeles nebulosus (Guichenot, 1850)
FIGURE 3. Photograph showing nine specimens of P. p i o i re t i (above) and four P. nebulosus (below). A 23 centimetres scale bar is shown on the lefthand side of the picture; black rectangles and intermediate white spaces all represent 1 cm. Numbers above the specimens refer to: 1. BMNH 1920.1. 20.1327. 2, largest specimen of P. p oireti included in the present study. Female from Bône (Annaba); 2. BMNH 1946.9. 6.77, male of P. poireti from Mount Edough; 3. BMNH 1946.9. 6.78, male of P. p o i re t i from Mount Edough; 4. BMNH 1946.9. 6.79, male of P. poireti from Mount Edough; 5. BMNH 1946.9. 6.80, male of P. p o i re t i from Mount Edough; 6. BMNH 1946.9. 6.81, male of P. p o i re t i from Mount Edough; 7. BMNH 1946.9. 6.79, male of P. poireti from Mount Edough; 8. MNHNP 4744, female, paralectotype of P. p o i re t i from Bône (Annaba); 9. MNHNP 4744 A, male, lectotype of P. p o i ret i from Bône (Annaba); 10. BMNH 1.1.3.1. a, largest specimen of P nebulosus recorded to date. Male from N. Africa; 11. BMNH 88.4. 9.3, female of P. nebulosus from Algiers; 12. BMNH 88.4. 4, male of P. nebulosus from Algiers; 13. MNHNP 1442, female, lectotype of P. nebulosus from Algiers.
Figure 7 in Revalidation of Leucetta floridana (Haeckel, 1872) (Porifera, Calcarea): a widespread species in the tropical western Atlantic
Figure 7. Box-and-whisker plot (maximum and minimum size; upper and lower quartiles and median) of spicule size of Leucetta spp. A, triactine I length; B, triactine I width; C, triactine II length; D, triactine II width; E, tetractine I length; F, tetractine I width; G, tetractine II length; H, tetractine II width. Leucetta floridana (Caribbean), Z Leucetta floridana (Brazil), Leucetta sp., Leucetta microraphis.
Figure 5 in Revalidation of Leucetta floridana (Haeckel, 1872) (Porifera, Calcarea): a widespread species in the tropical western Atlantic
Figure 5. Leucetta floridana from the Caribbean (UFRJPOR 5360). A, L. floridana in situ (photo: S. Zea). B, transversal section of the cortex and choanosome; C, transversal section of the choanosome and atrium; D, triactine I; E, triactine II and the small triactines I; F, tetractine I; G, detail of the apical actine of tetractines I protruding into the atrium; H, tetractine II and several triactines I and tetractines I. Scale bars: A = 1 cm; B–H = 100 Mm.
Figure 1 in Revalidation of Leucetta floridana (Haeckel, 1872) (Porifera, Calcarea): a widespread species in the tropical western Atlantic
Figure 1. Sampling sites. Caribbean: 1 – Bocas del Toro (BDT), 2 – San Andrés Island (SAN), 3 – Urabá (URA); Brazil: 4 – Ceará (CEA), 5 – Rio Grande do Norte (RGN), 6 – Rocas Atoll (RAT), 7 – Fernando de Noronha Archipelago (FNO), 8 – Abrolhos Archipelago (ABR); Pacific: 9 – Australia (GBR), 10 – New Caledonia (NCA).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.