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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).
Figure 6 in Integrative taxonomy reveals cryptic Amazonian species of Pristimantis (Anura: Strabomantidae)
Figure 6. Principal component analysis (PCA) of bioacoustic characters for Pristimantis sp. 2 and P. danae. Abbreviations are: P, principal component; NP, number of pulses; NL, note length; FF, fundamental frequency.
Figure 3 in Integrative taxonomy reveals cryptic Amazonian species of Pristimantis (Anura: Strabomantidae)
Figure 3. Principal component analysis (PCA) of bioacoustic characters for Pristimantis sp. 1, P. fenestratus and P. samaipatae. Abbreviations are: P, principal component; NOT, numbers of notes; NL, note length; NR, note rate.
Figure 5 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 5. Vigtorniella spp. Haplotype network of cytochrome c oxidase subunit I (COI). Each large circle represents a sequence from an individual of Vigtorniella ardabilia that has been collected in Sweden (white) or Norway (grey). Black circles represent V. flokati, collected in the Pacific Ocean, three specimens sampled sharing the same haplotype. Letters in circles, A-G, represent haplotypes of V. ardabilia sampled in this study (Table 1). Each line represents a mutation and small empty circles are inferred haplotypes not present in the current study.
Figure 4 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 4. Vigtorniella ardabilia sp. nov., specimen from whale-fall in Sweden, light micrographs: (A) parapodia from mid-body region, (B) detail of neuropodial falcigers, (C) detail of notopodial spine. Scale bar in (A) is 100 Mm, in (B) and (C) 10 Mm.
Figure 3 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 3. Vigtorniella ardabilia sp. nov., specimen from whale-fall in Sweden. SEM micrographs of (A) head region dorsal view, (B) head region ventral view, (C) fine neuropodial falcigers from segment 2, (D) neuropodial falcigers from mid-body region, and (E) notopodial spine. Scale bars in (A) and (B) are 150 Mm, in (C) 7.5 Mm, in (D) 15 Mm and in (E) 6 Mm.
Figure 2 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 2. Vigtorniella ardabilia sp. nov., live photo of specimen from whale-fall in Sweden. The worm is 6 mm long.
Figure 6 in High molecular and phenotypic diversity in the Merodon avidus complex (Diptera, Syrphidae): cryptic speciation in a diverse insect taxon
Figure 6. Scatterplot of individual scores from the canonical variate analysis (CVA) of female specimens of: A, sympatric populations of Merodon avidus A and M. avidus B from Dubašnica Mt (ADUB, BDUB) and Greece (AGRE, BGRE) (Wilks' L = 0.003; F(48,30) = 3.64; P <0.001); B, allopatric populations of M. avidus A from FYR MACEDONIA (AMKD), Morinj (AMOR), and the Pannonian region (APAN) (Wilks' L = 0.09; F(32,48) = 3.59; P <0.0001); C, allopatric populations of M. avidus B from Durmitor Mt (BDUR), Stara Mt (BSPL), Kopaonik Mt (BKOP), and FYR MACEDONIA (BMKD) (Wilks' L = 0.36; F(32,32) = 0.66; P <0.879); D, allopatric populations of M. avidus A and M. avidus B (Wilks' L = 0.09; F(80,245) = 1.94; P <0.0001). The amount of variation explained by each canonical axis is in parentheses.
Figure 5 in High molecular and phenotypic diversity in the Merodon avidus complex (Diptera, Syrphidae): cryptic speciation in a diverse insect taxon
Figure 5. Scatterplot of individual scores from the canonical variate analysis (CVA) of all specimens (both sexes) of metapopulations: A, Merodon avidus A from Dubašnica Mt (ADUB) (Wilks' L = 0.04; F(48,72) = 3.06; P <0.000); B, M. avidus B from Dubašnica Mt (BDUB) (Wilks' L = 0.10; F(64,174) = 2.18; P <0.000); C, M. avidus B from Durmitor Mt (BDUR) (Wilks' L = 0.10; F(64,174) = 2.21; P <0.000); D, M. avidus A from FYR MACEDONIA (AMKD) (Wilks' L = 0.002; F(112,171) = 2.40; P <0.000); E, M. avidus A from Greece (AGRE) (Wilks' L = 0.009; F(64,53) = 1.93; P <0.007). The amount of variation explained by each canonical axis is in parentheses. The number of misclassified specimens/total number of analysed
Figure 3 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 3. Relationship between the number of chaetigers and total bodylength in 15 specimens of Vigtorniella ardabilia and 33 specimens of V. flokati.
Figure 6. Diagram showing Kimura 2 in Cryptic speciation at organic-rich marine habitats: a new bacteriovore annelid from whale-fall and fish farms in the North-East Atlantic
Figure 6. Diagram showing Kimura 2 Parameter (K2P)-distances between congeneric species in four chrysopetalid genera, for two nuclear genes (18S, 28S) and two mitochondrial genes (16S, cytochrome c oxidase subunit I (COI)).
Figure 1 in High molecular and phenotypic diversity in the Merodon avidus complex (Diptera, Syrphidae): cryptic speciation in a diverse insect taxon
Figure 1. Origin of the analysed populations using wing geometric morphometrics from the Balkan Peninsula: 1, Pannonian Plain (PAN, Serbia); 2, Dubašnica Mt, E 21°59′, N 44°01′ (DUB, Serbia); 3, Stara Mt, E 22°41′, N 43°20′ (SPL, Serbia); 4, Kopaonik Mt, E 20°40′, N 43°15′ (KOP, Serbia); 5, Durmitor Mt, E 19°00′, N 43°11′ (DUR, Montenegro); 6, Morinj, E 18°40′, N 43°29′30″ (MOR, Montenegro); 7, Former Yugoslav Republic of Macedonia (MKD); 8, Greece (GRE). (Numbers within region are noted sampling sites of populations).
Figure 11 in Development, phylogeny, and taxonomy of Bostrycapulus (Caenogastropoda: Calyptraeidae), an ancient cryptic radiation
Figure 11. The shells of the holotypes of the four new species. A, Bostrycapulus latebrus (FMNH 282358). B, B. odites (Natal Museum V9447/T1783). C, B. pritzkeri (Australian Museum #C400000). D, B. urraca (ANSP 412178). Scale bar = 10 mm.
Figure 4 in Development, phylogeny, and taxonomy of Bostrycapulus (Caenogastropoda: Calyptraeidae), an ancient cryptic radiation
Figure 4. Unrooted haplotype network of COI sequences from Bostrycapulus calyptraeformis. Slashes on branches show the number of differences between the haplotypes. Branches without slashes have a length of one. Size of the circles represent the number of individuals with that haplotype.
Figure 1 in Development, phylogeny, and taxonomy of Bostrycapulus (Caenogastropoda: Calyptraeidae), an ancient cryptic radiation
Figure 1. Photographs of (A) Bostrycapulus calyptraeformis from Venado Beach in Panama and (B) B. odites sp. nov. from the subtidal of Playa Orengo (the three shells on the right) and the intertidal zone of nearby San Antonio Oeste (the shell on the left), Argentina. Both plates show the variation in shell colour and spine development found in samples collected from the same site. Samples from within a site do not differ in more than three or four base pairs in COI sequences. Scale bars = 10 mm.
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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.