Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
3,761
datasets available to search
ShareScore release 0.9.0
Dataset results
3,761 results for “phylogenetic relationship”
FIGURE 1 in Phylogenetic relationships among the Iranian Triticum diploid gene pool as inferred from the loci Acc1 and Pgk1
FIGURE 1. Geographic distribution of the 3 haplotypes seen among the wild gene pool of diploid Triticum in Iran.
FIGURE 5 in Phylogenetic relationships among the Iranian Triticum diploid gene pool as inferred from the loci Acc1 and Pgk1
FIGURE 5. Phylogenetic relationships based on Pgk1 sequences among three Iranian haplotypes (1, 2 and 3) of wild diploid Triticum and related genera. This tree topology was obtained in both MP and BI analyses. Branch lengths are proportional to the mean number of substitutions per site as measured by the scale bar. Bayesian posterior probabilities and bootstrap values over 50% are shown above and below the branches, respectively. Sequences obtained from the NCBI are marked with the sequence accession numbers. Secale cereale and Hordeum vulgare sequences were defined as outgroups.
FIGURE 1 in Phylogenetic relationships of Ibervillea and Tumamoca (Coniandreae, Cucurbitaceae), two genera of the dry lands of North America
FIGURE 1. Habit, flowers and / or fruits of: A) Ibervillea macdougalii, B–D) Ibervillea fusiformis, E) Ibervillea lindheimeri, F) Ibervillea tenuisecta, G) Ibervillea millspaughii, H) Ibervillea sonorae, I) Ibervillea maxima.
FIGURE 4 in Phylogenetic relationships among the Iranian Triticum diploid gene pool as inferred from the loci Acc1 and Pgk1
FIGURE 4. Phylogenetic relationships based on Acc1 sequences among three Iranian haplotypes (1, 2 and 3) of wild diploid Triticum and related genera. This tree topology was obtained in both MP and BI analyses. Branch lengths are proportional to the mean number of substitutions per site as measured by the scale bar. Bayesian posterior probabilities and bootstrap values over 50% are shown above and below the branches, respectively. Sequences obtained from the NCBI are marked with the sequence accession numbers. Secale cereale and Hordeum vulgare sequences were defined as outgroups.
FIGURE 3 in Phylogenetic relationships of Petunia patagonica (Solanaceae) revealed by molecular and biogeographical evidence
FIGURE 3. Representatives of Petunia scheideana (A), Petunia patagonica (B), Fabiana sp. (C), and Nierembergia linariifolia Graham (1821: 378) (D). Photographs by J.R. Stehmann (A, D) and A.A. Cocucci (B, C).
FIGURE 2. A in Phylogenetic relationships of Petunia patagonica (Solanaceae) revealed by molecular and biogeographical evidence
FIGURE 2. A. Bayesian tree of tribe Petunieae based on concatenated plastid intergenic spacers (trnS-trnG and trnL-trnF) and internal transcribed spacers of nuclear ribosomal DNA (ITS). Posterior probabilities values are shown above branches. Petunia highland clade: P. mantiqueirensis, P. bonjardinensis, P. reitzii, P. scheideana, P. saxicola, P. guarapuavensis, P. altiplana, and P. interior. Petunia lowland clade: P. integrigolia subsp. integrifolia, P. integrifolia subsp. depauperata, P. riograndensis, P. littoralis, P. bajeensis, P. inflata, P. axillaris subsp. axillaris, P. axillaris subsp. parodii, P. axillaris subsp. subandina, P. secreta, and P. occidentalis. Circles on nodes represent the most likely ancestral areas obtained with S-DIVA analyses. B. Ancestral area reconstructions for selected nodes (in rows) based on Bayesian binary Markov chain Monte Carlo (BBM). Pie graphs show probabilities of alternative ancestral range, low probability ancestral areas were merged and indicated in black (* Others). Each column shows the results for the different root distribution assumption.
FIGURE 1 in Phylogenetic relationships of Petunia patagonica (Solanaceae) revealed by molecular and biogeographical evidence
FIGURE 1. Geographic distribution of P. patagonica relative to those of Fabiana and Petunia genera in South America showing its congruence with Fabiana distribution.
FIGURE 2 in Two new species of Euphorbia subg. Chamaesyce (Euphorbiaceae) from Baja California Sur, Mexico and their phylogenetic relationships
FIGURE 2. Phylogenetic reconstruction using the majority rule consensus from Bayesian analyses of the nuclear region ITS. Numbers above the branches are Bayesian posterior probabilities (PP). The new species are marked in bold. "Exvarieties" of Euphorbia polycarpa are marked with an asterisk.
FIGURE 1 in Two new species of Euphorbia subg. Chamaesyce (Euphorbiaceae) from Baja California Sur, Mexico and their phylogenetic relationships
FIGURE 1. Phylogenetic reconstruction using the majority rule consensus from Bayesian analyses of the chloroplast region psbA-trnH. Numbers above the branches are Bayesian posterior probabilities (PP). The new species are marked in bold. "Exvarieties" of Euphorbia polycarpa are marked with an asterisk.
FIGURE 5. Euphorbia vizcainensis Maya Lastra & V.W. Steinm. A in Two new species of Euphorbia subg. Chamaesyce (Euphorbiaceae) from Baja California Sur, Mexico and their phylogenetic relationships
FIGURE 5. Euphorbia vizcainensis Maya Lastra & V.W. Steinm. A. Capsule; B. seed (1. basal, 2. ventral and 3. dorsal view); C. involucral lobes detail; D. mature cyathium; E. detail of stipule trichomes; F. internode detail; G. immature cyathium; H. prostrate habit; I. detail of a flowering branch. Based on C.A.Maya-L. 437 (IEB).
FIGURE 3 in Two new species of Euphorbia subg. Chamaesyce (Euphorbiaceae) from Baja California Sur, Mexico and their phylogenetic relationships
FIGURE 3. Distribution map of the new species of Euphorbia in Baja California Sur (Mexico). A. Detail of Cerralvo Island.
FIGURE 4. Euphorbia cerralvensis Maya Lastra & V.W. Steinm. A in Two new species of Euphorbia subg. Chamaesyce (Euphorbiaceae) from Baja California Sur, Mexico and their phylogenetic relationships
FIGURE 4. Euphorbia cerralvensis Maya Lastra & V.W. Steinm. A. Detail of involucral lobes; B. seed (basal view) C. seed (1. ventral and 2. dorsal view); D. mature cyathium; E. immature cyathium; F. capsule; G. habit; H. detail of a flowering branch. Based on J. León de la Luz 9584 (HCIB).
FIGURE 1. Phylogenetic relationships among 33 in Ochrolechia kerguelensis sp. nov. from the Southern Hemisphere and O. antarctica reinstated from the synonymy of O. parella
FIGURE 1. Phylogenetic relationships among 33 samples of Ochrolechia (with three Marfloraea species used as outgroup taxa) based on a data set of mtSSU sequences that resulted from a Bayesian analysis using MrBayes. Posterior probabilities are shown above internal branches. Internal branches considered strongly supported are represented by thicker lines. The newly sequenced specimens are in bold. Collecting numbers of the authors or the GenBank accession numbers following the species names act as specimen and sequence identifiers. Species of interest, discussed in the paper, are highlighted in colour. The length of the branch represented by dashed lines was reduced by 50% for editing reason.
FIGURE 1. Phylogenetic relationship between Metarhizium synnematis GZUHXCHL12 in Delimitation of a novel member of genus Metarhizium (Clavicipitaceae) by phylogenetic and network analysis
FIGURE 1. Phylogenetic relationship between Metarhizium synnematis GZUHXCHL12 and its allies based on ITS-5.8S rDNA sequence data. Bootstrap values (1,000 replicates) are indicated above the nodes.
FIGURE 2 in Morphological and phylogenetic relationships of the threatened geophyte Wurmbea novae-zelandiae (Colchicaceae) from New Zealand, with notes on typification
FIGURE 2. Maximum likelihood phylogeny of the concatenated plastid regions (ndhF and trnL-F). Bootstrap values are shown above branches.
FIGURE 1. Wurmbea novae-zelandiae. a in Morphological and phylogenetic relationships of the threatened geophyte Wurmbea novae-zelandiae (Colchicaceae) from New Zealand, with notes on typification
FIGURE 1. Wurmbea novae-zelandiae. a, damp seepage (centre) where W. novae-zelandiae occurs (Spider Lakes, Canterbury); b, flowering plant; c, ovoid corm with fine roots at base; d, flower nestled in crown of two basal leaves; e, flower with two locules and styles; f, flower with three locules and styles; g, leaf-like petal; h, petals showing position of nectaries 1/3 from base; i, capsules with one locule and two valves (left), two locules and four valves (centre), and three locules and six valves (right); j, small round seeds with a reticulate surface.
FIGURE 3. Phylogenetic relationships among 27 in Taxonomy and phylogeny of the genus Steinera (Arctomiales, Arctomiaceae) in the subantarctic islands of Crozet and Kerguelen
FIGURE 3. Phylogenetic relationships among 27 Steinera samples (with Gregorella humida as outgroup) based on a dataset of nuLSU, mtSSU, RPB1 and nuITS sequences that resulted from a Bayesian analysis using MrBayes. Posterior probabilities ≥ 0.95 are shown above internal branches, and Maximum Likelihood bootstrap values ≥ 70 obtained from a Garli analysis are shown below internal branches. Internal branches, considered strongly supported by both analyses, are represented by thicker lines. All Steinera samples are newly sequenced. Lineages representing new species of Steinera are highlighted.
FIGURE 479 in The morphology and molecular phylogenetics of some marine diatom taxa within the Fragilariaceae, including twenty undescribed species and their relationship to Nanofrustulum, Opephora and Pseudostaurosira
FIGURE 479. Scatter plot on the first two principal component axis of morphometric data for taxa within Serratifera. 80% variations of each species are encircled by an ellipse.
FIGURES 465–471 in The morphology and molecular phylogenetics of some marine diatom taxa within the Fragilariaceae, including twenty undescribed species and their relationship to Nanofrustulum, Opephora and Pseudostaurosira
FIGURES 465–471. Scanning electron micrographs of Stauroforma rinceana (culture SZCZCH1603). Figs 465–466. External views, showing clavate valve with striae consisting of several slit-like areolae extending from valve face to mantle continuously, and short striae (indicated by arrows) near foot pole APFs. Fig. 467. A smaller external view, showing elliptical valve with short striae (indicated by white arrows) near foot APFs and branched volae (indicated by black arrow) projecting from apical side of areolae. Fig. 468. Internal view, showing the absence of rimoportulae. Fig. 469. Close up of a valve, showing head APFs composed by radiate pores from the end of sternum to mantle. Fig. 470. Close up of a valve, showing hyaline area near the apex and foot apical pore field with five observed vertical rows of pores located on valve mantle. Fig. 471. Plain copulae.
FIGURES 459–464 in The morphology and molecular phylogenetics of some marine diatom taxa within the Fragilariaceae, including twenty undescribed species and their relationship to Nanofrustulum, Opephora and Pseudostaurosira
FIGURES 459–464. Scanning electron micrographs of Serratifera sp. 2 (clone SZCZP526). Figs 459–461. External views, showing narrowly-linear sternum and each stria composed of a single transapically-elongate areola (sometimes two) on both valve face and mantle. Fig. 462. Internal view, showing the absence of rimoportulae. Fig. 463. Girdle view, showing spatulate marginal spines associated with swelling base (indicated by arrowhead). Fig. 464. Girdle view, showing plain and open copulae, and fringed structure (indicated by arrowhead) observed at the margin of copula.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.