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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.
FIG. 1 in Species Delimitation in Herpetology
FIG. 1. Flow chart of a proposal for sensible nomenclatural practice in species delimitation studies. Stage 1 and Stage 2 refer to the two primary steps of the species delimitation process.
Figure 3 in DNA-based species delimitation separates highly divergent populations within morphologically coherent clades of poorly dispersing beetles
Figure 3. Ultrametric tree for Lyponiini. Branches marked by solid lines originate from continental Asia; those by dashed lines from Taiwan, Okinawa, and Japan. The grey dots/squares designate putative species identified using the general mixed Yule-coalescent model and the barcoding threshold, respectively. Terminals without designation were recovered as independent species-level entities.
Figure 2 in DNA-based species delimitation separates highly divergent populations within morphologically coherent clades of poorly dispersing beetles
Figure 2. Phylogenetic hypothesis on Lyponiini inferred from the maximum likelihood (ML) analysis. Numbers at the branches indicate maximum parsimony and ML bootstrap values, and Bayesian posterior probabilities (left to right).
Figure 7 in DNA-based species delimitation separates highly divergent populations within morphologically coherent clades of poorly dispersing beetles
Figure 7. The number of DNA diagnostic characters as a function of time since the split from the closest relative. The black-rimmed dots designate splits supported also by morphological characters, simple dots designate splits within morphologically defined clades.
Figure 1 in DNA-based species delimitation separates highly divergent populations within morphologically coherent clades of poorly dispersing beetles
Figure 1. Sampling sites of Lyponiini in (A) Continental East Asia, Taiwan and Okinawa and (B) Honshu and Shikoku.
Figure 6 in DNA-based species delimitation separates highly divergent populations within morphologically coherent clades of poorly dispersing beetles
Figure 6. Density plots of genetic distances of Lyponiini for (A) intra- and interspecific diversity of Lyponiini (B) intraspecific diversity for species as listed.
Figure 5 in DNA-based species delimitation separates highly divergent populations within morphologically coherent clades of poorly dispersing beetles
Figure 5. Relationships between Kimura-two-parameter genetic and geographical distances of Lyponiini. A–E, interspecific and intraspecific species pairs for five clades; F, intraspecific pairs of Ponyalis quadricollis. The parameters and P-values are listed in Table 1.
Figure 4. A in DNA-based species delimitation separates highly divergent populations within morphologically coherent clades of poorly dispersing beetles
Figure 4. A, intraspecific relationships between maximum genetic and geographical distances of Lyponiini for the Chinese species pairs (blue) and Japanese species pairs (red). B, intraspecific maximum genetic divergence and geographical distances in Lyponiini (red) and Agabini (blue). The data on Agabini diving beetles are from Bergsten et al. (2012).
Fig. 38 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 38. Isotype of Xerochrysum neoanglicum (L.M. Copeland 3468, J.J. Bruhl & I.R. Telford, NE 80118).
Fig. 17 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 17. Lectotype of Xerochrysum banksii (G-DC G00328465). Image: © Conservatoire et Jardin botaniques de la Ville de Genève.
Fig. 12. STRUCTURE bar plots for Xerochrysum bicolor, X in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 12. STRUCTURE bar plots for Xerochrysum bicolor, X. halmaturorum, and X. sp. Lofty Ranges major clustering modes K = 3. Bar plots show each individual as a horizontal bar divided into segments on the basis of the proportion of ancestry suggested for 1–10 subpopulations across all of the 10 runs; n = 51. Fine black lines delineate sampling locations.
Fig. 14 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 14. STRUCTURE bar plots for Xerochrysum boreale and genetically similar putative species, major and minor clustering modes K = 6. Bar plots show each individual as a horizontal bar divided into segments on the basis of the proportion of ancestry suggested for 1–10 subpopulations across all of the 10 runs; n = 63. Fine black lines delineate sampling locations.
Fig. 9 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 9. Xerochrysum sp. North Kennedy and genetically similar entities principal coordinate analysis of 1342 single-nucleotide polymorphism loci. Each dot represents an individual sample, coloured by population. (a) Axes 1 and 2; (b) Axes 1 and 3.
Fig. 11 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 11. STRUCTURE bar plots for the putative species Xerochrysum sp. Barrington Tops (white, pale yellow and yellow phyllary colours), X. sp. Glencoe, X. sp. New England, and X. sp. Point Lookout, major clustering modes K = 5. Bar plots show each individual as a horizontal bar divided into segments on the basis of the proportion of ancestry suggested for 1–10 subpopulations across all of the 10 runs; n = 52. Fine black lines delineate sampling locations.
Fig. 15 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 15. STRUCTURE bar plots, for species of Xerochrysum associated with X. sp. Blackfellows Gap (marked with an asterisk, *), for major clustering modes K = 4–5. Bar plots show each individual as a horizontal bar divided into segments on the basis of the proportion of ancestry suggested for four or five ancestral populations across all runs at K = 4 and 9 of the 10 runs at K = 5; n = 114. Fine black lines delineate sampling locations, numbered as in Supplementary Table S14. Of the two samples collected from Namadgi National Park (Location 9), morphological characters indicated that one is clearly X. subundulatum, and the other is X. sp. Blackfellows Gap (N.T.Burbidge 6926).
Fig. 10 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 10. STRUCTURE bar plots for 'Bracteatum' samples of Xerochrysum, major clustering modes K = 6. Bar plots show each individual as a horizontal bar divided into segments on the basis of the proportion of ancestry suggested for 1–16 subpopulations across 8 of the 16 runs; n = 246. Fine black lines delineate sampling locations.
Fig. 26 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 26. Isotype of Xerochrysum frutescens (I.R.Telford 12874, J.J.Bruhl & L.M.Copeland NE 85983).
Fig. 13 in There's gold in them thar hills! Morphology and molecules delimit species in Xerochrysum (Asteraceae; Gnaphalieae) and reveal many new taxa
Fig. 13. STRUCTURE bar plots for 'Boreale' sam-ples of Xerochrysum, major and minor clustering modes K = 6. Bar plots show each individual as a horizontal bar divided into segments on the basis of the proportion of ancestry suggested for 1–10 subpopulations across all of the 10 runs; n = 148. Fine black lines delineate sampling locations.
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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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