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1,918 results for “molecular evidence”
Fig. 5. Maximum Likelihood tree, produced with Cytochrome oxidase subunit I in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.
Fig. 5. Maximum Likelihood tree, produced with Cytochrome oxidase subunit I (COI) sequences of Dipturus argentinensis, D. lamillai, Zearaja brevicaudata, Z. chilensis, Z. nasuta and Amblyraja doellojuradoi as outgoup. Barcode Index Number assigned by Barcode of Life Datasystem (A) and the results of species delimitation analyses using bPTP (B) and ABGD (C) algorithms are shown as vertical bars on the right. Dipturus lamillai sequences are marked in bold.
Fig. 6. Maximum Likelihood tree produced with NADH dehydrogenase subunit 2 in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.
Fig. 6. Maximum Likelihood tree produced with NADH dehydrogenase subunit 2 (NADH2) sequences of Dipturus argentinensis, D. lamillai, Zearaja brevicaudata, Z. chilensis, Z. nasuta and D. olseni as outgroup. Dipturus lamillai sequences are marked in bold and sequences corresponding to the description of the species (Concha et al. 2019) are indicated with *.
Fig. 4 in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.
Fig. 4. External components of the clasper of a mature male of Zearaja brevicaudata (RM 186, 783 mm TL). Cl: cleft, Dl: distal lobe, P: pocket, Pr: pseudorhiphidion, Rh: rhiphidion, Sh: shield, Sl: slit, Sp: Spike, Sr: spur, Tb: terminal bridge. Scale bar = 30 mm.
Fig. 1 in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.
Fig. 1. Principal component analysis based on morphological data expressed as percentage of total length. a) PC1 vs PC2 b) PC2 vs PC3. PC1: first principal component, PC2: second principal component, PC3: third principal component. ▲, ellipse with whole line: Zearaja brevicaudata; ■, holotype of Raia brevicaudata; ●, ellipse with dotted line: Z. chilensis; ◊, ellipse with dashed line: Dipturus lamillai.
Fig. 3 in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.
Fig. 3. Female specimen of Zearaja brevicaudata (RM 317, 427 mm TL) showing the same coloration pattern as female paratype of Dipturus lamillai (cf. Concha et al., 2019, fig. 7B). Scale bar = 50 mm.
Fig. 2 in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.
Fig. 2. Dorsal spinulation pattern of an adult female of Zearaja brevicaudata (RM 170, 943 mm TL). White arrows point the dorsal thorns. Scale bar = 50 mm.
Fig. 3. Maximum likelihood tree constructed from 38 nuclear rDNA ITS1 and ITS2 sequences from Apiaceae genus Daucus and relatives using a in Molecular phylogeny of Daucus (Apiaceae): Evidence from nuclear ribosomal DNA ITS sequences
Fig. 3. Maximum likelihood tree constructed from 38 nuclear rDNA ITS1 and ITS2 sequences from Apiaceae genus Daucus and relatives using a transition/transversion rate ratio of 1.6. Branch lengths are proportional to the number of expected nucleotide substitutions per site.
Fig. 2 in Molecular phylogeny of Daucus (Apiaceae): Evidence from nuclear ribosomal DNA ITS sequences
Fig. 2. Neighbor-joining tree inferred form the analysis of 39 nuclear rDNA ITS1 and ITS2 sequences from Apiaceae genus Daucus and its relatives using a transition/transversion rate ratio of 1.6. Branch lengths are proportional to distance estimated from the two parameter method of Kimura. Numbers at nodes indicate bootstrap values for 100 replicate analyses. On this tree, bootstrap values <20% are not indicated.
Fig. 1 in Molecular phylogeny of Daucus (Apiaceae): Evidence from nuclear ribosomal DNA ITS sequences
Fig. 1. Strict consensus of 11 parsimony trees derived from equally-weighted parsimony analysis of combined nuclear DNA ITS1 and ITS2 sequences from Daucus and its relatives using all unambiguously-aligned positions (CIs with and without uninformative characters= 0.6613 and 0.5817; RI=0.8387). From the left to the right, names of taxa, sections, and clades are given. Numbers above the nodes indicate the number of times a monophyletic group occurred in 100 bootstrap replicates; AutoDecay values are given below.
Figure 2. a in Evidence of Ehrlichia chaffeensis in Argentina through molecular detection in marsh deer (Blastocerus dichotomus)
Figure 2. a_Summary of the E. chaffeensis molecular amplification of the 16SrRNA and the VLPT genes in marsh deer and tick samples at different time points. b_ Alignment of a fragment of the 16SrRNA nucleotide sequences from reference Anaplasma and Ehrlichia strains and those amplified from deer (C2, C7, D11 and C12) and a tick (tick1_C7) in the present study. The red line marks the hypervariable V1 region.
Fig. 1 in Evidence of Ehrlichia chaffeensis in Argentina through molecular detection in marsh deer (Blastocerus dichotomus)
Fig. 1. Map of the two marsh deer populations (Paraná River Delta and Ibera Wetlands) located along the alluvial plain of the Paraná River (Argentina).
Fig. 4 in A new distribution record of Chrysosplenium grayanum Maxim. (Saxifragaceae) in Korea: Evidence from morphological and molecular data
Fig. 4. Phylogenetic relationships resulting from the maximum parsimony analysis of nrITS sequences from eight Chrysosplenium taxa and two outgroup taxa (C. flagelliferaum in ser. Flagellifera and C. japonicum in ser. Alternifolia). Numbers above the branches indicate bootstrap values (≧80) for maximum parsimony (left) and neighbor-joining (right) analysis.
Fig. 2 in A new distribution record of Chrysosplenium grayanum Maxim. (Saxifragaceae) in Korea: Evidence from morphological and molecular data
Fig. 2. Photos of Chrysosplenium grayanum Maxim. A. Plant habit during flowering; B. Leaves; C. Inflorescence with bracteal leaves; D. Close-up of sepals and stamens.
Fig. 3 in A new distribution record of Chrysosplenium grayanum Maxim. (Saxifragaceae) in Korea: Evidence from morphological and molecular data
Fig. 3. Scanning electron micrograph of seed of Chysosplenium grayanum Maxim. A. Seed; B. Close-up of seed surface, showing smooth surface with cylindrical papillose with roundish head at the tip.
Fig. 1 in A new distribution record of Chrysosplenium grayanum Maxim. (Saxifragaceae) in Korea: Evidence from morphological and molecular data
Fig. 1. Illustrations of Chrysosplenium grayanum Maxim. A. Flowering plant; B. Inflorescence; C. Sepals and stamens; D. Capsule with persistent sepals; E. Leaf arrangement. Illustrations of Chrysosplenium grayanum were drawn by Park Chan-Ae.
Figure 1 in Morphological and molecular evidence of the occurrence of Artibeus amplus (Chiroptera: Phyllostomidae) in Brazil
Figure 1. Collecting localities of Artibeus amplus in South America. The letters are the initials of the countries. Red squares are previous records compiled by Ramoni-Perazzi et al. (2012), white circle is a record cited by Redondo et al. (2008), and white stars are the two new records in the state of Roraima, Brazil. Image Landsat/Copernicus – 12/13/2015. Google Earth – Data SIO, NOAA, U.S. Navy, NGA, GEBCO.
Figure 2 in Morphological and molecular evidence of the occurrence of Artibeus amplus (Chiroptera: Phyllostomidae) in Brazil
Figure 2. (A) Male Artibeus amplus (CJ 1176) from Roraima state, Brazil; (B) wingtip of the same specimen of Artibeus amplus; (B) the wingtip of Artibeus planirostris (CJ 989). Photo by Felipe Zenha.
Fig. 2 in New systematic position of Itatingamyia Albuquerque (Diptera, Muscidae) based on molecular evidence, and description of the female of I. couriae
Fig. 2. Molecular phylogenetic hypothesis using Bayesian inference of the combined mitochondrial (COI) and nuclear (AATS, CAD, and EF1-a) protein-coding genes for 68 species of Muscidae highlighting the position of Itatingamyia within the Cyrtoneurininae.Subfamily-level classification follows Haseyama et al. (2015). Numbers are Bayesian posterior probabilities values.
Fig. 2 in Molecular Phylogenetics Evidence for a Novel Lineage of Amoebae Within Discosea (Amoebozoa: Lobosa)
Fig. 2. Maximum-Likelihood SSU tree of subphylum Lobosa, with emphasis on major representatives of the class Discosea. The monophyletic resolution of Flabellinia and Longamoebia was obtained after omitting unstable taxa Stygamoeba and Vermistella (see Fig. 1). Members of the class Tubulinea were used as outgroup. Bootstrap values (BV) for ML/NJ/MP were presented at nodes; filled circles – 100% BV with all methods; * – node supported but BV <40%. For acc. nos. – see Fig. 1.
Fig. 1 in Molecular Phylogenetics Evidence for a Novel Lineage of Amoebae Within Discosea (Amoebozoa: Lobosa)
Fig. 1. Maximum-Likelihood tree based on SSU rDNA of major representatives of the subphylum Lobosa and the class Discosea, following the classification of Smirnov et al. (2011). Members of the class Tubulinea were used as outgroup. Subclasses and orders were indicated, and for Dermamoebida families also. Bootstrap values (BV) for ML/NJ/MP were presented at nodes; filled circles – 100% BV with all methods; * – node supported but BV <40%.
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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.