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1,918 results for “molecular evidence”
FIGURE 2 in Recognition of a new species of Hedysarum (Fabaceae, Hedysareae) from China based on morphological and molecular evidence
FIGURE 2. Bayesian tree based on combined plastid psbA-trnH, trnC-petN, petN-psbM sequences. The Bayesian posterior probabilities are below the branches, and the maximum parsimony (left) and maximum likelihood (right) bootstrap supports are above the branches.
FIGURE 1 in Recognition of a new species of Hedysarum (Fabaceae, Hedysareae) from China based on morphological and molecular evidence
FIGURE 1. Bayesian tree based on combined nuclear ETS and ITS sequences. The Bayesian posterior probabilities are below the branches, and the maximum parsimony (left) and maximum likelihood (right) bootstrap supports are above the branches. A dash indicates a branch that is not found in the maximum likelihood tree.
FIGURE 3. Liparis meihuashanensis S. M. Fan. A in Liparis meihuashanensis, a new orchid species from Fujian, China: Evidence from morphological and molecular analyses
FIGURE 3. Liparis meihuashanensis S. M. Fan. A. Flowering plant (green flower). B. Pseudobulbs. C. Flower (purple flower), front view. D. Lip (green flower). E. Column.F. Anther cap and pollinarium. G. Fruit.
FIGURE 2. Liparis meihuashanensis S. M. Fan. A. Flowering plant. B. Flower, side view. C in Liparis meihuashanensis, a new orchid species from Fujian, China: Evidence from morphological and molecular analyses
FIGURE 2. Liparis meihuashanensis S. M. Fan. A. Flowering plant. B. Flower, side view. C. Dorsal sepal, petal, lateral sepal, and lip. D. Column and anther cap. E. Pollinarium. F. Fruit.
FIGURE 1 in Liparis meihuashanensis, a new orchid species from Fujian, China: Evidence from morphological and molecular analyses
FIGURE 1. Phylogenetic placement of L. meihuashanensis in the Bayesian analysis of the combined nrITS and plastid matK. Support percentages and posterior probabilities displayed on the branches are PP BI /BP MP. The scale bar denotes the estimated number of substitutions in Bayesian analysis.
FIGURE 3 in Ceriporia albomellea (Phanerochaetaceae, Basidiomycota), a new species from tropical China based on morphological and molecular evidences
FIGURE 3. Strict consensus tree illustrating the phylogeny of Ceriporia albomellea and its related species generated by maximum parsimony based on ITS+nLSU sequences. Branches are labeled with parsimony bootstrap proportions (before slanting line) high than 50% and bayesian posterior probabilities (after slanting line) more than 0.95.
FIGURE 2 in Ceriporia albomellea (Phanerochaetaceae, Basidiomycota), a new species from tropical China based on morphological and molecular evidences
FIGURE 2. Microscopic structures of Ceriporia albomellea (Dai 15205). a Basidiospores. b Basidia and basidioles. c Cystidia. d Rhombic crystals. e Hyphae from trama. f Hyphae from subiculum.
FIGURE 2 in A common Bistorta was misidentified as a novel species in Fagopyrum (Polygonaceae): the confirmation of the taxonomic identify of F. hailuogouense by morphological and molecular evidences
FIGURE 2. Morphology of Bistorta pergracilis. A. habit; B. rhizome; C. sessile and clasping cauline leaves, and terminal and axillary spicate inflorescences; D. axillary infructescence with achenes exceeding from persistent perianth. A, D photographed by Bo Li, and B, C provided by Xing-xing Zhu.
FIGURE 1 in A common Bistorta was misidentified as a novel species in Fagopyrum (Polygonaceae): the confirmation of the taxonomic identify of F. hailuogouense by morphological and molecular evidences
FIGURE 1. Morphology of Fagopyrum hailuogouense. A. line-drawing illustration (from Zhang 2013); B. leaves and inflorescences (from Zheng 2012).
FIGURE 3. The Bayesian 50 in A common Bistorta was misidentified as a novel species in Fagopyrum (Polygonaceae): the confirmation of the taxonomic identify of F. hailuogouense by morphological and molecular evidences
FIGURE 3. The Bayesian 50% majority-rule consensus tree of subfamily Polygonoideae based on combined matK+rbcL+trnL-F dataset. Support values displayed on the branches are Bayesian posterior probabilities / ML bootstrap percentages. A dash "−" indicates support values of less than 0.90 in BI or 50% in ML, respectively, while bold lines indicate PP = 1.00 and ML-BP = 100, simultaneously. Tribes recognized by Schuster et al. (2015) are distinguished by different colors, and Fagopyrum hailuogouense was marked in red bold font.
FIGURE 3. Bulbophyllum yongtaiense. A. Habitat and habit. B. Flowering plant. C. Flower, front view. D. Dorsal sepal. E. Lateral sepal. F. Petal. G in Bulbophyllum yongtaiense (Orchidaceae, Epidendroideae, Dendrobiinae), a new species from Fujian, China: Evidence from morphological and molecular analyses
FIGURE 3. Bulbophyllum yongtaiense. A. Habitat and habit. B. Flowering plant. C. Flower, front view. D. Dorsal sepal. E. Lateral sepal. F. Petal. G. Lip and column, side view. H. Lip, front view. I. Lip, side view. J. Anther cap. K. Pollinarium.
FIGURE 1 in Bulbophyllum yongtaiense (Orchidaceae, Epidendroideae, Dendrobiinae), a new species from Fujian, China: Evidence from morphological and molecular analyses
FIGURE 1. Phylogenetic tree obtained by maximum-likelihood analysis of the combination of nrITS and plastid regions. Numbers near the nodes are bootstrap percentages and Bayesian posterior probabilities (BS ML, BS MP, PP). Analyses of the parts of new species based on separate nrITS (A) and plastid cpDNA (B) data are shown in the top left corner. A dash (–) indicates a node is inconsistent between the topology of the MP/ML trees and the Bayesian tree; *node is 100 bootstrap percentage or 1.00 posterior probability.
FIGURE 2. Bulbophyllum yongtaiense. A. Plant. B. Dorsal sepal. C. Petal. D in Bulbophyllum yongtaiense (Orchidaceae, Epidendroideae, Dendrobiinae), a new species from Fujian, China: Evidence from morphological and molecular analyses
FIGURE 2. Bulbophyllum yongtaiense. A. Plant. B. Dorsal sepal. C. Petal. D. Lateral sepal, lip, column, side view. E. Lip. F. Anther cap and pollinarium. (Drawn by Bi-Dan Lai).
FIGURE 3. Liparis vivipara H.X.Huang, Z.J.Liu & M.H.Li. A. Flowering plant. B. Flower, front view. C. Flower, side view. D in Liparis vivipara (Orchidaceae: Malaxideae), a new species from China: evidence from morphological and molecular analyses
FIGURE 3. Liparis vivipara H.X.Huang, Z.J.Liu & M.H.Li. A. Flowering plant. B. Flower, front view. C. Flower, side view. D. Dorsal sepal, petal, lateral sepal, and lip. Drawn by Li-Jun Chen.
FIGURE 1 in Liparis vivipara (Orchidaceae: Malaxideae), a new species from China: evidence from morphological and molecular analyses
FIGURE 1. Phylogenetic tree obtained by maximum-likelihood analysis of the combined matrix. Numbers near the nodes are bootstrap percentages and Bayesian posterior probabilities (BP ML, BP MP, PP). Separate nrITS (A) and plastid matK (B) results are shown in the top left corner. A dash (–) indicates a node is inconsistent between the topology of the MP/ML trees and the Bayesian tree; *node is 100 BP and 1.00 PP.
FIGURE 2. Liparis vivipara H.X.Huang, Z.J.Liu & M.H.Li in Liparis vivipara (Orchidaceae: Malaxideae), a new species from China: evidence from morphological and molecular analyses
FIGURE 2. Liparis vivipara H.X.Huang, Z.J.Liu & M.H.Li (A–D) and L. odorata (E). A. Flowering plant. B. Flower, front view. C. Flower, side view. D. Bulbil. Photographs by Wen-Hui Rao.
FIGURE 4. Rhododendron microcarpum. A, B, Habitat. C in A new species of Rhododendron (Ericaceae) from Jiangxi of China based on morphological and molecular evidences
FIGURE 4. Rhododendron microcarpum. A, B, Habitat. C, Flowers and leaveas. D, Axillary flower. E, Stamens and filaments. F, Leaveas and small fruits.
FIGURE 3 in A new species of Rhododendron (Ericaceae) from Jiangxi of China based on morphological and molecular evidences
FIGURE 3. Rhododendron microcarpum (from the holotype, drawn by Ling Wang from KUN). A, Flowering branches with leaves. B, Flower. C, Scales and unopened flower. D, Flower branch and pistil. E, Calyx. F, Stamen. G, Corolla.
FIGURE 5 in A new species of Rhododendron (Ericaceae) from Jiangxi of China based on morphological and molecular evidences
FIGURE 5. Comparison of leaves and friuts between Rhododendron microcarpum and R. ovatum. A-1, Leaves of R. ovatum; A-2, Leaves of R. microcarpum. B-1, Fruits of R. microcarpum; B-2: Fruits of R. ovatum.
FIGURE 2 in A new species of Rhododendron (Ericaceae) from Jiangxi of China based on morphological and molecular evidences
FIGURE 2. Neighbor-joining tree based on the ITS sequences with the P-distance model. Bootstrap values (>50%) of the clade are shown above the branches.
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.