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FIGURE 13 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 13. Land filling for civil construction projects in the type-locality of Hypsolebias gongobira and H. longignatus.
FIGURE 9 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 9. Bayesian inference based on the mitochondrial gene cox1 used for lineage delimitation of the Hypsolebias antenori species-group. Vertical bars represent the number of lineages delimited by ABGD (7), sGMYC (6), mGMYC (11), and b-PTP (10). Numbers adjacent to nodes represent posterior probabilities; values <0.50% are not shown.
FIGURE 12 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 12. Environmental impact of the duplication of the CE-40 highway in the type-locality of Hypsolebias gongobira and H. longignatus.
FIGURE 11. Hypsolebias longignatus, UFRN 5846, male 35.8 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 11. Hypsolebias longignatus, UFRN 5846, male 35.8 mm SL: Brazil, Ceará, Aquiraz, rio Pacoti basin.
FIGURE 5. Hypsolebias bonita new species, MZUSP 129608 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 5. Hypsolebias bonita new species, MZUSP 129608, male, paratype, 38.6 mm SL: Brazil, Rio Grande do Norte, Baraúna, Furna Feia National Park.
FIGURE 4 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 4. Type-locality of Hypsolebias gongobira new species, Brazil, Ceará, Aquiraz, rio Pacoti basin.
FIGURE 15 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 15. Locality of H. antenori, Brazil, Ceará, Russas, seasonal pool in the floodplain of the rio Jaguaribe basin.
FIGURE 3. Hypsolebias gongobira new species, MZUSP 129607 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 3. Hypsolebias gongobira new species, MZUSP 129607, female, paratype, 35 mm SL: Brazil, Ceará, Aquiraz, rio Pacoti basin.
FIGURE 1 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 1. Map of northeastern Brazil showing the distribution of the Hypsolebias antenori species-group. Stars represent type localities, and circles indicate sampled localities. Hypsolebias bonita new species in pink, H. antenori in red, H. gongobira new species in orange (syntopic with H. longignatus), H. martinsi in yellow, H. coamazonicus in green, H. faouri in light blue, H. igneus in dark blue, and H. nudiorbitatus in purple. Dark blue lines represent hydrographic basins of the Caatinga ecoregions, Maranhão-Piauí (MAPE), Mid-Northeastern Caatinga (MNCE), Northeastern Atlantic Forest (NAFE) São Francisco (SFRE).
FIGURE 8 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 8. Caudal fin of living males: Hypsolebias gongobira new species (A), H. antenori (B) e H. bonita new species (C).
FIGURE 7 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 7. Type-locality of Hypsolebias bonita new species, Brazil, Rio Grande do Norte, Baraúna, seasonal pool in the Furna Feia National Park.
Figure 2. Coalescent species trees with 13 in DNA barcoding and coalescent-based delimitation of endosymbiotic clevelandellid ciliates (Ciliophora: Clevelandellida): a shift to molecular taxonomy in the inventory of ciliate diversity in panesthiine cockroaches
Figure 2. Coalescent species trees with 13 (A) and 14 (B) assumed species based on 18S rRNA gene, ITS1-5.8S-ITS2 region and 28S rRNA gene sequences. Posterior probabilities of clades are provided along internal branches and posterior probabilities for the presence of individual species are provided behind the terminal branches. Scale bars denote the fraction of substitutions per site.
Fig. 2 in Molecular Phylogenetic Analysis and Species Delimitation in the Pine Needle-feeding Aphid Genus Essigella (Hemiptera, Sternorrhyncha, Aphididae)
Fig. 2. Phylogenetic tree (ML and BI) of Essigella species using concatenate ATP6, COI, EF-1α and Gnd. Pinus species of the subgenus Strobus appear either in orange or in red, those of the subgenus Pinus either in green or in blue. Color nuances represent infragroup within each subgenus. Nonidentified Pinus and other Pinaceae are in black.Values indicate ML bootstrap % values followed by Bayesian posterior probabilities % values.
Fig. 1 in Molecular Phylogenetic Analysis and Species Delimitation in the Pine Needle-feeding Aphid Genus Essigella (Hemiptera, Sternorrhyncha, Aphididae)
Fig. 1. Essigella hoerneri on Pinus monophylla (left) and Essigella sp. on Pinus ponderosa (right) (pictures from C. Favret).
Fig. 2 in Molecular and morphological delimitation of Australian Triops species (Crustacea: Branchiopoda: Notostraca)-large diversity and little morphological differentiation
Fig. 2 Morphology of the head (a) and posterior margin of the carapace (b) and position of landmarks for morphometrics as well as position of telsonic spines on the dorsal surface of the telson (c). Landmark (LM) 1: anterior right corner of telson; LM 2: tip of largest right lateral spine; LM 3: intersection between telson and furca (right); LM 4: most posterior extension of the right telson lobe; LM 5: center of telson notch; LM 6: most posterior extension of the left telson lobe; LM 7: intersection between telson and furca (left); LM 8: tip of largest left lateral spine;
Fig. 4 in Molecular and morphological delimitation of Australian Triops species (Crustacea: Branchiopoda: Notostraca)-large diversity and little morphological differentiation
Fig. 4 Bayesian inference majority rule tree based on EF1α. Triops main and sublineages derived from COI are highlighted. All available EF1α sequences were included. Colors represent the individual's location (see Fig. 1). Numbers of terminals correspond to Australian Museum (AM) registration numbers (see also Supplement Table S1). For each node,
Fig. 1 in Molecular and morphological delimitation of Australian Triops species (Crustacea: Branchiopoda: Notostraca)-large diversity and little morphological differentiation
Fig. 1 Map showing all collection localities. The larger map depicts the main drainage systems (red lines) and the catchments basins of individual rivers (black lines). Geographically closely associated localities were grouped together, and the color-coding corresponds to Figs. 3 and 4. The numbers correspond to the locality numbers in Table 1 and Supplement Table S2. Scale bars correspond to 200 km each
Fig. 3 Chronogram showing the relationships and divergence times for 80 bears, estimated from a concatenated mitochondrial dataset comprising all 13 protein coding and 2 in Examining the sensitivity of molecular species delimitations to the choice of mitochondrial marker
Fig. 3 Chronogram showing the relationships and divergence times for 80 bears, estimated from a concatenated mitochondrial dataset comprising all 13 protein coding and 2 ribosomal RNA genes. Groups delimited as species by the GMYC analysis are shown as triangles. The horizontal axis shows the timescale, measured in millions of years.
Fig. 2 Chronogram showing the relationships and divergence times for 357 cetaceans, estimated from a concatenated mitochondrial dataset comprising all 13 protein coding and 2 in Examining the sensitivity of molecular species delimitations to the choice of mitochondrial marker
Fig. 2 Chronogram showing the relationships and divergence times for 357 cetaceans, estimated from a concatenated mitochondrial dataset comprising all 13 protein coding and 2 ribosomal RNA genes. Groups delimited as species by the GMYC analysis are shown as triangles. The horizontal axis shows the timescale, measured in millions of years.
Fig. 1 in Examining the sensitivity of molecular species delimitations to the choice of mitochondrial marker
Fig. 1 Number of markers analysed in a survey of 109 studies using GMYC published between January 2013 and December 2014. Columns indicate the total number of studies in the sample using the relevant number of markers. The lower dark grey portion of each column refers to the number of studies using only mitochondrial markers, while the upper light grey portion refers to all other studies
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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