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1,918 results for “molecular evidence”
Linked collectors and determiners for: Huchimingia, a new genus segregated from Millettia (Leguminosae, Millettieae) based on morphological and molecular evidence.
Natural history specimen data linked to collectors and determiners held within, "Huchimingia, a new genus segregated from Millettia (Leguminosae, Millettieae) based on morphological and molecular evidence". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/9cb10461-a420-4771-8a40-afec4ced8332">https://bionomia.net/dataset/9cb10461-a420-4771-8a40-afec4ced8332</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/9cb10461-a420-4771-8a40-afec4ced8332">https://gbif.org/dataset/9cb10461-a420-4771-8a40-afec4ced8332</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Morphological and molecular evidence support the taxonomic separation of the medically important Neotropical spiders Phoneutria depilata (Strand, 1909) and P. boliviensis (F. O. Pickard-Cambridge, 1897) (Araneae, Ctenidae).
Natural history specimen data linked to collectors and determiners held within, "Morphological and molecular evidence support the taxonomic separation of the medically important Neotropical spiders Phoneutria depilata (Strand, 1909) and P. boliviensis (F. O. Pickard-Cambridge, 1897) (Araneae, Ctenidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/0a8bdd92-7bf8-44fb-8e8e-5c300df51a20">https://bionomia.net/dataset/0a8bdd92-7bf8-44fb-8e8e-5c300df51a20</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/0a8bdd92-7bf8-44fb-8e8e-5c300df51a20">https://gbif.org/dataset/0a8bdd92-7bf8-44fb-8e8e-5c300df51a20</a>. Formatted as a Frictionless Data package.
FIG. 3 in A new species of Verbascum L. (Scrophulariaceae) from the Gilan province (Iran), based on morphological and molecular evidences
FIG. 3. — Distance based trees on morphological (left) and genetic (right) characters used to differentiate species of Verbascum parsana Sotoodeh, Attar & Civeyrel, sp. nov., V. punalense Boiss. & Buhse and V. shahsavarensis Sotoodeh, Attar & Civeyrel.
FIG. 1 in A new species of Verbascum L. (Scrophulariaceae) from the Gilan province (Iran), based on morphological and molecular evidences
FIG. 1. — Verbascum parsana Sotoodeh, Attar & Civeyrel, sp. nov.: A, herbarium specimen; B, C, a part of inflorescence and fruits, bract and no bracteole; D, co- rolla and androecium; E, arrows show two anterior anthers. Photographs from the type specimen by A. Sotoodeh. Scale bars: 1 cm.
FIG. 2 in A new species of Verbascum L. (Scrophulariaceae) from the Gilan province (Iran), based on morphological and molecular evidences
FIG. 2. — Distribution of Verbascum parsana Sotoodeh, Attar & Civeyrel, sp. nov. (ê) The magnified view on the right is from Google map (maps.google.com).
Fig. 4 in Molecular Evidence For Direct Development In The Rhacophorid Frog, Philautus Acutus (Rhacophoridae, Anura) From Borneo
Fig. 4. Consensus dendrogram of neighbour joining bootstrapping analysis illustrating distances of 12S and 16S rDNA sequences. The four Philautus acutus specimens are conspecific.
Fig. 2 in Molecular Evidence For Direct Development In The Rhacophorid Frog, Philautus Acutus (Rhacophoridae, Anura) From Borneo
Fig. 2. Colouration in life of Philautus acutus, from Gunung Mulu,Sarawak, Malaysia (Borneo). Daytime colouration of specimen somewhat stressed during photography.
Fig. 3 in Molecular Evidence For Direct Development In The Rhacophorid Frog, Philautus Acutus (Rhacophoridae, Anura) From Borneo
Fig. 3. Eggs with froglets assigned to Philautus acutus, from Gunung Mulu, Sarawak, Malaysia (Borneo): a, close-up of two eggs, containing froglets; b, close-up of a single egg. Note the bright iris colouration of the froglet and the opaque yellow outer jelly capsule of the eggs; c, dorsal view of froglet in the vitelline layer, after compact outer jelly capsule was removed. Note X-shaped pattern on dorsum and reduced tail with blood vessels. d, ventral view of froglet in vitelline layer, with compact outer jelly capsule removed. Note gut filled with yolk visible through skin and scattered iridophores.
Figure 5. A in Geometric morphometric and molecular evidence suggest a new fruit fly species in Bactrocera (Zeugodacus) tau complex (Diptera: Tephritidae)
Figure 5. A Bayesian phylogenetic tree (COI sequence, 580 bp) generated with the generalized time reversible model. Labels at branch ends are species and group names. Numbers at nodes represent the posterior possibilities that supported by sequences.
Figure 3 in Geometric morphometric and molecular evidence suggest a new fruit fly species in Bactrocera (Zeugodacus) tau complex (Diptera: Tephritidae)
Figure 3. Discrimination of wing shape in four groups projected by CVs. Each polygon defines the outermost individuals in each group. A. Male. B. Female.
Figure 4 in Geometric morphometric and molecular evidence suggest a new fruit fly species in Bactrocera (Zeugodacus) tau complex (Diptera: Tephritidae)
Figure 4. Gr.I and Gr.II discrimination by aculeus outlines. A distribution of samples on the best CV–x axis, in which the y axis shows the number of individuals in each interval. An inset displays a superimposition of aculeus shapes.
Figure 1 in Geometric morphometric and molecular evidence suggest a new fruit fly species in Bactrocera (Zeugodacus) tau complex (Diptera: Tephritidae)
Figure 1. Criteria of sample classification. A. A medial vitta of Gr.I, characterized by a plain yellow band with posterior expansion. B. A medial vitta pattern of Gr.II, characterized by a yellow band inserted with a black strip in presutural region, and posteriorly constricted. Scale bar = 1 mm.
Figure 2 in Geometric morphometric and molecular evidence suggest a new fruit fly species in Bactrocera (Zeugodacus) tau complex (Diptera: Tephritidae)
Figure 2. Landmark design for wing and aculeus GM analyses. A. Type 1 landmarks on wing venation labeled with downward arrows and numbers indicating locations in geometric analysis. B. A trilobed aculeus. C. A yellow line representing the alignment of pseudolandmarks along an outline of aculeus tip, from one lateral apex to another lateral. Scale bars: A = 1 mm; B = 50 μm.
Figure 5 in Two new species from the Hygrobates nigromaculatus-complex (Acariformes, Hydrachnidia, Hygrobatidae), based on morphological and molecular evidence
Figure 5 Genital field: A-B –Hygrobates lacrima sp. nov., paratypes (A, ♂; B, ♀), Trebaljevo, Montenegro; C-F –Hygrobates limnocrenicus sp. nov. (C-D, F, ♀; E, ♂); C, holotype, Mareza, Montenegro; D, paratype, Struga, North Macedonia; E-F, Vitoja, Montenegro; G-HH –. setosus Besseling, 1942, ♂, G, Farver Au, Germany; H, redrawn from Besseling (1964).
Figure 9 in Two new species from the Hygrobates nigromaculatus-complex (Acariformes, Hydrachnidia, Hygrobatidae), based on morphological and molecular evidence
Figure 9 Sampling sites: A-B – River Tara near Trebaljevo; C – River Tara near Mateševo; D – the "Kraljičino Oko" (the Queen's Eye) spring near Podgorica; E – River Crni Drim near Struga; F – the Vitoja spring located on the north-eastern shore of Lake Skadar flooded in the winter and spring months.
Figure 3 in Two new species from the Hygrobates nigromaculatus-complex (Acariformes, Hydrachnidia, Hygrobatidae), based on morphological and molecular evidence
Figure 3 Hygrobates lacrima sp. nov., holotype ♀, Mateševo, Montenegro: A – idiosoma, ventral view; B – palp, lateral view; C – palp, medial view; D – chelicera; E – I-L-5 and -6; F – IV-L-5 and -6. Scale bars = 100 µm.
Figure 8 in Two new species from the Hygrobates nigromaculatus-complex (Acariformes, Hydrachnidia, Hygrobatidae), based on morphological and molecular evidence
Figure 8 Distribution of H. lacrima sp. nov. (green square) andH. limnocrenicus sp. nov. (purple circle). Sampling site numbers: 1, River Tara near Mateševo; 2, River Tara near Trebaljevo; 3, Mareza
Figure 7 in Two new species from the Hygrobates nigromaculatus-complex (Acariformes, Hydrachnidia, Hygrobatidae), based on morphological and molecular evidence
Figure 7 Hygrobates limnocrenicus sp. nov. (A-C, male; D, female), Vitoja, Montenegro: A – coxal and genital field; B – IV-L-5 and -6; C – palp, lateral view (P-1 lacking); D – palp, lateral view. Scale bars = 100 µm.
Figure 2 in Morphological and molecular evidence for phylogeny and classification of South American pitvipers, genera Bothrops, Bothriopsis, and Bothrocophias (Serpentes: Viperidae)
Figure 2. Bayesian Markov Chain Monte Carlo (MCMC) 50% majority-rule consensus phylogram, including taxa with morphological data only (analysis 8). The phylogram is derived from an analysis of 2343 bp mitochondrial and 85 gap-weighted or majority-coded morphological characters. The posterior probabilities are shown above nodes; bootstrap values from parsimony analysis of the same data set are shown below nodes (analysis 7). The parsimony analysis shows minor topological differences from the Bayesian analysis; refer to Figure S3 for the parsimony cladogram. Grey circles indicate posterior probabilities of 95 or greater, and bootstrap values of 70 or greater. Dashes indicate support values of less than 50. Letters correspond to the major lineages: A, Bothrocophias clade; B, Bothrops alternatus clade; C, Bothrops neuwiedi + Bothrops jararaca clade; D, Bothriopsis clade; E, Bothrops atrox clade.
Figure 1 in Morphological and molecular evidence for phylogeny and classification of South American pitvipers, genera Bothrops, Bothriopsis, and Bothrocophias (Serpentes: Viperidae)
Figure 1. Bayesian Markov Chain Monte Carlo (MCMC) 50% majority-rule consensus phylogram, excluding taxa with morphological data only (analysis 11). The phylogram is derived from an analysis of 2343 bp of mitochondrial DNA and 85 gap-weighted or majority-coded morphological characters. The posterior probabilities are shown above nodes; bootstrap values from parsimony analysis of the same data set are shown below nodes (analysis 10). The parsimony analysis shows minor topological differences from Bayesian analysis; refer to Figure S1 for parsimony cladogram. Grey circles indicate posterior probabilities of 95 or greater and bootstrap values of 70 or greater. Letters correspond to major lineages: A, Bothrocophias clade; B, Bothrops alternatus clade; C, Bothrops neuwiedi + Bothrops jararaca clade; D, Bothriopsis clade; E, Bothrops atrox clade.
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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.