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2,620 results for “Molecular Phylogeny”
Figure 7 from: Ribera I, Reboleira ASPS (2019) The first stygobiont species of Coleoptera from Portugal, with a molecular phylogeny of the Siettitia group of genera (Dytiscidae, Hydroporinae, Hydroporini, Siettitiina). ZooKeys 813: 21-38. https://doi.org/10.3897/zookeys.813.29765
Figure 7 Soprador do Carvalho Cave, type locality of Iberoporuspluto sp. n.
Figure 4 from: Ribera I, Reboleira ASPS (2019) The first stygobiont species of Coleoptera from Portugal, with a molecular phylogeny of the Siettitia group of genera (Dytiscidae, Hydroporinae, Hydroporini, Siettitiina). ZooKeys 813: 21-38. https://doi.org/10.3897/zookeys.813.29765
Figure 4 Iberoporuspluto sp. n., holotype, ventral view (previous to DNA extraction).
Figure 2 from: Talamas EJ, Bon M-C, Hoelmer KA, Buffington ML (2019) Molecular phylogeny of Trissolcus wasps (Hymenoptera, Scelionidae) associated with Halyomorpha halys (Hemiptera, Pentatomidae). In: Talamas E (Eds) Advances in the Systematics of Platygastroidea II. Journal of Hymenoptera Research 73: 201-217. https://doi.org/10.3897/jhr.73.39563
Figure 2 Phylogenetic tree, Bayesian analysis.
Figure 1 from: Talamas EJ, Bon M-C, Hoelmer KA, Buffington ML (2019) Molecular phylogeny of Trissolcus wasps (Hymenoptera, Scelionidae) associated with Halyomorpha halys (Hemiptera, Pentatomidae). In: Talamas E (Eds) Advances in the Systematics of Platygastroidea II. Journal of Hymenoptera Research 73: 201-217. https://doi.org/10.3897/jhr.73.39563
Figure 1 Phylogenetic tree, RaxML analysis.
Figure 3 from: Talamas EJ, Bon M-C, Hoelmer KA, Buffington ML (2019) Molecular phylogeny of Trissolcus wasps (Hymenoptera, Scelionidae) associated with Halyomorpha halys (Hemiptera, Pentatomidae). In: Talamas E (Eds) Advances in the Systematics of Platygastroidea II. Journal of Hymenoptera Research 73: 201-217. https://doi.org/10.3897/jhr.73.39563
Figure 3 Phylogenetic tree, PAUP* analysis.
Table 1 in Molecular phylogeny of the Aplodactylidae (Perciformes: Cirrhitoidea), a group of Southern Hemisphere marine ® shes
<p>Table 1. Species of aplodactylids and outgroups from other cirrhitoid families analysed. Names of aplodactylids follow the revision by Russell (2000).</p><table><tbody><tr><th>Species</th><th>Family</th><th>Collection site</th></tr></tbody><tbody><tr><th><i>Aplodactylus arctidens</i> Richardson 1839</th><td>Aplodactylidae</td><td>Maria Island, Tasmania</td></tr><tr><td></td><td></td></tr><tr><th><i>Aplodactylus etheridgii</i> (Ogilby 1889)</th><td>Aplodactylidae</td><td>Norfolk Island</td></tr><tr><th><i>Aplodactylus lophodon</i> (GuÈnther 1859)</th><td>Aplodactylidae</td><td>Camden Head, NSW, Australia <b>†</b></td></tr><tr><th><i>Aplodactylus punctatus</i> Valenciennes 1832</th><td>Aplodactylidae</td><td>Punta de Tralca, Chile</td></tr><tr><td></td><td></td></tr><tr><th><i>Aplodactylus westralis</i> Russell 1987</th><td>Aplodactylidae</td><td>Rottnest Island, Western Australia</td></tr><tr><th><i>Chironemus marmoratus</i> GuÈnther 1860</th><td>Chironemidae</td><td>Diamond Head, NSW, Australia <b>†</b></td></tr><tr><th><i>Cheilodactylus fasciatus</i> Lacépède 1803</th><td>Cheilodactylidae</td><td>Tsitsikamma National Park, South Africa</td></tr><tr><td></td></tr><tr><th><i>Cirrhitus splendens</i> (Ogilby 1889)</th><td>Cirrhitidae</td><td>Lord Howe Island</td></tr></tbody></table><p><b>†</b> Australian Museum frozen tissue collection (<i>A. lophodon</i> I 3125202 3 NI 252; <i>C. marmoratus</i> I 3125304 8 NI 330).</p>
Figure 1 from: Basibuyuk H, Budak M, Korkmaz E (2011) A molecular phylogeny of the Cephinae (Hymenoptera, Cephidae) based on mtDNA COI gene: a test of traditional classification. ZooKeys 130: 363-378. https://doi.org/10.3897/zookeys.130.1466
Figure 1 - Percentage of nucleotide composition at each codon position.
Figure 37 from: Faille A, Bourdeau C, Fresneda J (2012) Molecular phylogeny of the Trechus brucki group, with description of two new species from the Pyreneo-Cantabrian area (France, Spain) (Coleoptera, Carabidae, Trechinae). ZooKeys 217: 11-51. https://doi.org/10.3897/zookeys.217.3136
Figure 37 - Sinkhole area of the Plateau of Esturou (Hautes–Pyrénées, France).
Figure 36 from: Faille A, Bourdeau C, Fresneda J (2012) Molecular phylogeny of the Trechus brucki group, with description of two new species from the Pyreneo-Cantabrian area (France, Spain) (Coleoptera, Carabidae, Trechinae). ZooKeys 217: 11-51. https://doi.org/10.3897/zookeys.217.3136
Figure 36 - The MSS of Lizarraga pass (Navarra, Spain).
Figure 33 from: Faille A, Bourdeau C, Fresneda J (2012) Molecular phylogeny of the Trechus brucki group, with description of two new species from the Pyreneo-Cantabrian area (France, Spain) (Coleoptera, Carabidae, Trechinae). ZooKeys 217: 11-51. https://doi.org/10.3897/zookeys.217.3136
Figure 33 - Lectotype and paralectotype of Trechus brucki.
Figures 6-7 from: Faille A, Bourdeau C, Fresneda J (2012) Molecular phylogeny of the Trechus brucki group, with description of two new species from the Pyreneo-Cantabrian area (France, Spain) (Coleoptera, Carabidae, Trechinae). ZooKeys 217: 11-51. https://doi.org/10.3897/zookeys.217.3136
Figures 6-7 - Habitus of 6 Trechus bruckoides sp. n. (Montagnon) and 7 Trechus brucki (Jaout).
Figure 1 from: Faille A, Bourdeau C, Fresneda J (2012) Molecular phylogeny of the Trechus brucki group, with description of two new species from the Pyreneo-Cantabrian area (France, Spain) (Coleoptera, Carabidae, Trechinae). ZooKeys 217: 11-51. https://doi.org/10.3897/zookeys.217.3136
Figure 1 - Habitus of Trechus bouilloni sp. n. (Lizarraga pass).
Data from: A complete molecular phylogeny of Claravis confirms its paraphyly within small New World ground-doves (Aves: Peristerinae) and implies multiple plumage state transitions
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FIGURE 8 in Morphological Redescriptions and Molecular Phylogeny of Three Stentor Species (Ciliophora: Heterotrichea: Stentoridae) from Korea
FIGURE 8. Photomicrographs of S. tartari after protargol impregnation (A–C). A. Ventral view of voucher specimen; showing nuclear apparatus and symbiotic algae; B. Indicating buccal and ventral somatic ciliature; C. Showing ventral somatic ciliature, macronuclear nodules and micronuclei; Arrowheads in (A) point to symbiotic green algae after protargol impregnation; Arrowheads in (B) point to rows of somatic cilia; AM, adoral membranelles; AZM, adoral zone of membranelles; MA, macronucleus; MI, micronuclei; PK, peristomial kineties; PM, paroral membrane; SK, somatic kineties. Scale bars: A=50 μm, C=10 μm.
FIGURE 9 in Morphological Redescriptions and Molecular Phylogeny of Three Stentor Species (Ciliophora: Heterotrichea: Stentoridae) from Korea
FIGURE 9. SSU rRNA gene phylogeny inferred from the MAFFT alignment (60 taxa and 1,603 nucleotide sites). Results from maximum likelihood (ML) analyses are mapped onto the Bayesian inference (BI) tree. The scale bar indicates two substitutions per 100 nucleotide positions. Sequences newly obtained during this study are indicated by red font and arrowheads.
FIGURE 7 in Morphological Redescriptions and Molecular Phylogeny of Three Stentor Species (Ciliophora: Heterotrichea: Stentoridae) from Korea
FIGURE 7. Photomicrographs of S. tartari from life (A–F). A. Ventral view of a representative cell showing body shape, position of contractile vacuole, macronuclear nodules; B, C, D. Indicating buccal and somatic ciliature with cortical granulation; E. Showing specimens attached to debris; F. Squeezed specimen, showing macronuclear nodules and micronuclei; G. Ventral view of a typical specimen, showing contractile vacuole with collecting canal; Arrowheads in (C) point to colorless cortical granules; Arrowheads and double arrowhead in (D) indicating mitochondria (?) and somatic cilia, respectively; Arrowhead in (E inset) points to holdfast organelle; Arrowheads in (F) point to symbiotic green algae; Arrowheads in (G) indicating collecting canal; AZM, adoral zone of membranelles; CG, cortical granules; CV, contractile vacuole; MA, macronucleus; MI, micronuclei; PK, peristomial kineties, SC, somatic cilia; SK, somatic kineties. Scale bars: A=100 μm, F=10 μm, G=75 μm.
FIGURE 6 in Morphological Redescriptions and Molecular Phylogeny of Three Stentor Species (Ciliophora: Heterotrichea: Stentoridae) from Korea
FIGURE 6. Line diagrams of S. tartari from life (A–D) and after protargol impregnation (E, F). A. Ventral view of a representative specimen; B. Cortical granulation; C. Somatic cilia; D. Body shapes of freely motile and extended cells; E, F. Ventral and dorsal views of infraciliature; Arrowhead in (E) point to basal bodies of somatic cilia. AM, adoral membranelles; AZM, adoral zone of membranelles; CG, cortical granules; CV, contractile vacuole; MA, macronucleus; MI, micronuclei; PK, peristomial kinety; PM, paroral membrane; SC, somatic cilia; SK, somatic kinety. Scale bars: A= 100 μm, C=10 μm, E, F=50 μm.
FIGURE 5 in Morphological Redescriptions and Molecular Phylogeny of Three Stentor Species (Ciliophora: Heterotrichea: Stentoridae) from Korea
FIGURE 5. Photomicrographs of S. muelleri after protargol impregnation (A–D). A, B. Ventral views of representative specimens, showing ciliature and nuclear apparatus; C. Showing paroral membrane; D. Basal bodies of somatic cilia; Arrowheads in (D) point to basal bodies of somatic cilia; AM, adoral membranelles; AZM, adoral zone of membranelles; MA, macronuclear nodules; MI, micronuclei; PM, paroral membrane; PK, peristomial kineties; SK, somatic kineties. Scale bars: A=50 μm, B=10 μm.
FIGURE 3 in Morphological Redescriptions and Molecular Phylogeny of Three Stentor Species (Ciliophora: Heterotrichea: Stentoridae) from Korea
FIGURE 3. Line diagrams of S. muelleri from life (A–C) and after protargol impregnation (D, E). A. A representative specimen; B. Showing cortical granulation; C. Somatic cilia; D, E. Ventral and dorsal views of the voucher specimens, showing the somatic ciliature and the nuclear apparatus; Arrowhead in (D) point to basal bodies of somatic cilia; AM, adoral membranelles; AZM, adoral zone of membranelles; CG, cortical granules; MA, macronuclear nodules; MI, micronuclei; PK, peristomial kinety; PM, paroral membrane; SC, somatic cilia; SK, somatic kinety. Scale bars: A=100 µm, C=10 µm, D, E=50 µm.
FIGURE 2 in Morphological Redescriptions and Molecular Phylogeny of Three Stentor Species (Ciliophora: Heterotrichea: Stentoridae) from Korea
FIGURE 2. Photomicrographs of S. coeruleus from life (A–G) and after protargol impregnation (H–J). A. Showing specimens in extended form, arrowheads indicate macronuclear nodules; B. Ventral view of a representative specimen, arrowheads indicating the oral cavity; C. Indicating buccal ciliature; D. Cortical granulation and somatic cilia; E. Position of contractile vacuole, arrowheads indicating lipid droplets; F. Posterior end of an typical extended specimen, arrows indicating somatic cilia and arrowheads indicating holdfast; G. Section showing macronuclear nodules; H. Ventral views of representative specimens, showing ciliature and nuclear apparatus; arrowheads indicating oral cavity; I. Indicating buccal ciliature, arrowheads indicating oral cavity; J. Basal bodies of somatic cilia; AM, adoral membranelles; CV, contractile vacuole; CG, cortical granules; OC, oral cavity; MA, macronuclear nodules; PK, peristomial kineties, SC, somatic cilia, SK, somatic kineties. Scale bars: A=200 μm, B=100 μm, E=50 μm, G–J=50 μm.
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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.