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1,751 results for “molecular phylogenetics”
FIGURE 3 in Revision of Hygrochilus (Orchidaceae: Epidendroideae: Aeridinae) and a molecular phylogenetic analysis
FIGURE 3. Bayesian inference result for plastid DNA. Numbers at nodes are Bayesian posterior probabilities and bootstrap percentages (PP, BBML, BBMP) ''-'' indicates that the node receives weak support in the ML and MP analysis.
FIGURE 6. Hygrochilus tsii. A. Habit. B. Flower. C in Revision of Hygrochilus (Orchidaceae: Epidendroideae: Aeridinae) and a molecular phylogenetic analysis
FIGURE 6. Hygrochilus tsii. A. Habit. B. Flower. C. Side view of flower (sepal and petal removed). D. Lip, lateral sepal, petal and dorsal sepal (clockwise). E. Pollinaria. F. Lateral sepal (left) and dorsal sepal (right). G. Lip and column. Illustration based on the holotype.
FIGURE 3 in Codonopsis gongshanica (Campanulaceae), a new species from NW Yunnan based on morphology and molecular phylogenetic analysis
FIGURE 3. Field photographs of Codonopsis gongshanica: A. a simple stem with sub-rosulate leaves; B. a short tubular corolla with a dark purple ring below the corolla throat; C. a carrot-shaped root; and D. field individuals.
FIGURE 1. The 50 in Codonopsis gongshanica (Campanulaceae), a new species from NW Yunnan based on morphology and molecular phylogenetic analysis
FIGURE 1. The 50% majority rule consensus tree derived from the Bayesian analysis of combining five chloroplast DNA fragments. Ranges of parsimony jackknife support (JK) above 50 are reported with bootstrap value of likelihood, and Bayesian posterior probability values (MP/ML/BI) above branches. The inferred new species is indicated by grey shadow.
FIGURE 2 in Codonopsis gongshanica (Campanulaceae), a new species from NW Yunnan based on morphology and molecular phylogenetic analysis
FIGURE 2. Illustration of Codonopsis gongshanica: a. a plant possessing a simple stem, a solitary flower, and sub-rosulate leaves, scale bar = 1 cm; b. a dissected flower with the dark purple ring below the corolla throat, scale bar = 0.5 cm; and c. a carrot-shaped root, scale bar = 2 cm.
FIGURE 2 in Vanda malipoensis, a new species of Vanda (Orchidaceae: Epidendroideae; Vandeae) from China: evidence from morphological and molecular phylogenetic analyses
FIGURE 2. Bayesian tree from the analysis of the plastid DNA matrix. Numbers above branches are Bayesian posterior probabilities and bootstrap percentages (PP, BS ML, BS MP);''-'' indicates that the node receives less than 50% support in the corresponding analysis.
FIGURE 1 in Vanda malipoensis, a new species of Vanda (Orchidaceae: Epidendroideae; Vandeae) from China: evidence from morphological and molecular phylogenetic analyses
FIGURE 1. Bayesian tree from the analysis of the nrITS matrix. Numbers above branches are Bayesian posterior probabilities and bootstrap percentages (PP, BS , BS ); ''-'' indicates that the node receives less than 50% support in the corresponding analysis.
FIGURE 4. Vanda malipoensis L.H.Zou, J.X.Huang & Z.J.Liu. A. Flowering plant. B. Flower, front view. C. Column without anther cap. D in Vanda malipoensis, a new species of Vanda (Orchidaceae: Epidendroideae; Vandeae) from China: evidence from morphological and molecular phylogenetic analyses
FIGURE 4. Vanda malipoensis L.H.Zou, J.X.Huang & Z.J.Liu. A. Flowering plant. B. Flower, front view. C. Column without anther cap. D. Longitudinal section of flower (sepal and petal removed). E. Pollinarium.
FIGURE 3 in Vanda malipoensis, a new species of Vanda (Orchidaceae: Epidendroideae; Vandeae) from China: evidence from morphological and molecular phylogenetic analyses
FIGURE 3. Bayesian tree from the analysis of the combined matrix. Numbers above branches are Bayesian posterior probabilities and bootstrap percentages (PP, BS ML, BS MP); ''-'' indicates that the node receives less than 50% support in the corresponding analysis.
FIGURE 5. Vanda malipoensis L.H.Zou, J.X.Huang & Z.J.Liu. A. Flowering plant. B. Flower, front view. C. Flower, side view. D in Vanda malipoensis, a new species of Vanda (Orchidaceae: Epidendroideae; Vandeae) from China: evidence from morphological and molecular phylogenetic analyses
FIGURE 5. Vanda malipoensis L.H.Zou, J.X.Huang & Z.J.Liu. A. Flowering plant. B. Flower, front view. C. Flower, side view. D. Dorsal sepal, petal, lateral sepal and lip. E. Pollinarium. Drawn by Xue-Yong Ma from the holotype, Liu 6644 (NOCC).
FIGURE 2 in Molecular phylogenetics and morphology support two new genera (Memoremea and Nihon) of Boraginaceae s.s.
FIGURE 2. Bayesian majority rule consensus tree based on nuclear (ITS) sequences. Numbers below nodes are Bayesian posterior probabilities, some indicated by solid arrows. Major clades are indicated. SEM photographs of species of Omphalodes are shown in their respectives clades, some indicated by lined arrows. Scale bar represents the number of substitutions per site and is positioned at the end of the figure.
FIGURE 1 in Molecular phylogenetics and morphology support two new genera (Memoremea and Nihon) of Boraginaceae s.s.
FIGURE 1. Bayesian majority rule consensus tree based on plastid (trnL–trnF) sequences. Numbers below nodes are Bayesian posterior probabilities, some indicated by solid arrows. Major clades are indicated. SEM photographs of species of Omphalodes are shown in their respectives clades, some indicated by lined arrows. Scale bar represents the number of substitutions per site and is positioned at the end of the figure.
Figure 3 in A new deep-sea benthopelagic chaetognath of the genus Bathyspadella (Chaetognatha) with ecological and molecular phylogenetic remarks
Figure 3. Molecular phylogenetic trees of chaetognaths based on (A) nuclear 18S rRNA and (B) mitochondrial 16S rRNA. Scale is units of expected substitution per site. Support values on each clade are Bayesian posterior probabilities. Accession numbers: Aidanosagitta crassa, D14363; Eukrohnia hamata (E. bathypelagica), DQ351886; Eukrohnia fowleri, DQ351889; Eukrohnia hamata, DQ351887, AB617779; Flaccisagitta enflata, DQ351877, AP011547; Krohnitta pacifica, DQ351879, DQ351891; Mesosagitta decipiens, DQ351881, AP011545; Parasagitta megalophthalma, DQ351878; Parasagitta setose, DQ351900; Parasagitta elegans, Z19551; Paraspadella gotoi, D14362, AY619710; Pseudosagitta lyra, DQ351880; DQ351892; Zonosagitta nagae, AP011545; Pterosagitta draco, DQ351885; Sagitta bipunctata, DQ351894, DQ351890; Serratosagitta tasmanica, DQ351893; Spadella cephaloptera, DQ351884, AY545549; Spadella ledoyeri, DQ351883, DQ351899; Xenokrohnia sorbei, DQ351888; Heterokrohnia davidi, AB617780, AB617781; Heterokrohnia longidentata, AB617782, AB617783; Bathyspadella oxydentata, AB617784, AB617785.
Figure 1 in A new deep-sea benthopelagic chaetognath of the genus Bathyspadella (Chaetognatha) with ecological and molecular phylogenetic remarks
Figure 1. Bathyspadella oxydentata sp. nov.: (A) Dorsal view; (B) dorsal view of head; (C) eye structure (arrow and arrowhead show boundary of eye structure; asterisk indicates the lens of the eye.); (D) seminal receptacle; (E) seminal vesicle; (F) spermatic duct. VG, ventral ganglion; SR, seminal receptacle; SD, spermatic duct; AG, apical grand cell complex; GC, gland canals.
FIGURE 7 in Two newly recorded invasive alien ascidians (Chordata, Tunicata, Ascidiacea) based on morphological and molecular phylogenetic analysis in Korea*
FIGURE 7. Phylogenetic relationship of some ascidians including three invasive alien species inferred from mt–COI dataset. Species, sampling locations in Korea and Genbank accession numbers were given and numbers on branches were Bayesian posterior probabilities (if ≥ 0.80). The tree was rooted with Branchiostoma floridae. The scale bar represents the number of expected changes per site.
FIGURE 6 in Two newly recorded invasive alien ascidians (Chordata, Tunicata, Ascidiacea) based on morphological and molecular phylogenetic analysis in Korea*
FIGURE 6. Phylogenetic relationship of some ascidians including four invasive alien species inferred from nuclear 18S rDNA dataset. Species, sampling locations in Korea and Genbank accession numbers were given and numbers on branches were Bayesian posterior probabilities (if ≥ 0.80). The tree was rooted with Branchiostoma floridae. The scale bar represents the number of expected changes per site.
FIGURE 3 in Two newly recorded invasive alien ascidians (Chordata, Tunicata, Ascidiacea) based on morphological and molecular phylogenetic analysis in Korea*
FIGURE 3. Different invasive ascidians attached to same rope at different dates at Tongyeong yacht marina: A, B, S. plicata (Oct. 2010); C, D, A. aspersa (June 2011). The red arrow indicates that an individual of S. plicata was surrounded by several individuals of A. aspersa.
FIGURE 5 in Two newly recorded invasive alien ascidians (Chordata, Tunicata, Ascidiacea) based on morphological and molecular phylogenetic analysis in Korea*
FIGURE 5. Molgula manhattensis: A, C, Individuals densely aggregated on a rope; B, Individuals on a fish trap; D, Right side; E, Left side; F, Sagittal section of branchial sac; G, Oral and Atrial siphon; H, Tentacles; I, Dorsal tubercle; J, Six folds of branchial sac; K, Stigmata; L, Individuals attached to fish trap. 1—oral siphon, 2—atrial siphon, 3—tentacles, 4—dorsal tubercle, 5—folds of branchial sac, 6—stigmata, 7—intestine, 8—gonads, 9—renal sac, 10—tunic, 11—endostyle. Scale bars: A–B. 50 mm; C–F, L. 5 mm; G–K. 1 mm.
FIGURE 2 in Two newly recorded invasive alien ascidians (Chordata, Tunicata, Ascidiacea) based on morphological and molecular phylogenetic analysis in Korea*
FIGURE 2. Five invasive alien ascidians at four collection sites in Korea: A, C. lepadiformis attached to dock wall at 4.7 m depth in Busan port; B, A. aspersa attached to ropes at Tongyeong yacht marina; C, C. intestinalis attached on thick cloth at Gampo harbor; D, M. manhattensis attached on floating buoy at Mokpo yacht marina; E, S. plicata attached to rope at Tongyeong yacht marina. Scale bars: A–E. 10 cm.
FIGURE 2 in Phylogenetics of the tribe Phalacropsyllini (Siphonaptera: Ctenophthalmidae: Neopsyllinae) based on molecular and morphological evidence
FIGURE 2. Some of the morphological characters used in the cladistic analysis. a) Number of teeth in genal comb; b) metacoxa with spiniforms; c) sternum VIII expanded; d) distal arm of IX sternum with membranous flap; e) fixed process bifurcated; f) five pairs of lateral plantar bristles on fifth tarsal segment of hind legs.
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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)
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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.