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1,918 results for “molecular evidence”

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zenodo32/100

FIGURE 1 in Athyrium aberrans (Athyriaceae), a new species of the lady ferns from southeastern Xizang, China, based on morphological and molecular evidence

FIGURE 1. Maximum likelihood phylogeny of Athyrium based on five plastid markers (rbcL, rps4, rps4-trnS, trnL, and trnL-F). Maximum likelihood bootstrap support (MLBS) and Bayesian inference posterior probability (BIPP) are given above and below the branches, respectively. The asterisk indicates MLBS = 100, BIPP = 1.00. The new species (in red) belongs to the A. otophorum clade (Wei et al. 2018b).

opennotspecifiedFeb 2022View details →
zenodo32/100

FIGURE 5. Cymbidium purpureisepalum. A. Flowering plant. B. Tepals. C. Pollinarium, front view. D in Cymbidium purpureisepalum (Orchidaceae; Epidendroideae), a new species from China: evidence from morphological and molecular data

FIGURE 5. Cymbidium purpureisepalum. A. Flowering plant. B. Tepals. C. Pollinarium, front view. D. Column, front view. Drawn by Wenqi Hu.

opennotspecifiedMar 2022View details →
zenodo32/100

FIGURE 4. Cymbidium purpureisepalum. A. Flowering plant. B. Flower, front view. C. Flower, back view. D in Cymbidium purpureisepalum (Orchidaceae; Epidendroideae), a new species from China: evidence from morphological and molecular data

FIGURE 4. Cymbidium purpureisepalum. A. Flowering plant. B. Flower, front view. C. Flower, back view. D. Structure of the flower. E. Flower of C. serratum. F. Flowers of C. tortisepalum

opennotspecifiedMar 2022View details →
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FIGURE 2 in Cymbidium purpureisepalum (Orchidaceae; Epidendroideae), a new species from China: evidence from morphological and molecular data

FIGURE 2. Phylogenetic relationships of C. purpureisepalum based on the plastid DNA (matK) data. The three numbers near the nodes are Bayesian posterior probabilities (PP), maximum likelihood bootstrap percentages (BP ML) and maximum parimony bootstrap percentages (BP MP). "-" indicates that the node is incongruent between the topology of the Bayesian tree and the MP/ML trees.

opennotspecifiedMar 2022View details →
zenodo32/100

FIGURE 1 in Cymbidium purpureisepalum (Orchidaceae; Epidendroideae), a new species from China: evidence from morphological and molecular data

FIGURE 1. Phylogenetic relationships of C. purpureisepalum based on combined plastid and nuclear data. The three numbers near the nodes are Bayesian posterior probabilities (PP), maximum likelihood bootstrap percentages (BP) and maximum parimony bootstrap ML percentages (BP). "-" indicates that the node is incongruent between the topology of the Bayesian tree and the MP/ML trees. MP

opennotspecifiedMar 2022View details →
zenodo32/100

FIGURE 3 in Cymbidium purpureisepalum (Orchidaceae; Epidendroideae), a new species from China: evidence from morphological and molecular data

FIGURE 3. Phylogenetic relationships of C. purpureisepalum based on nuclear DNA data (nrITS). The three numbers near the nodes are Bayesian posterior probabilities (PP), maximum likelihood bootstrap percentages (BP ML) and maximum parimony bootstrap percentages (BP MP). "-" indicates that the node is incongruent between the topology of the Bayesian tree and the MP/ML trees.

opennotspecifiedMar 2022View details →
zenodo32/100

FIGURE 3. Toxicodendron oligophyllum and related species. T in Toxicodendron oligophyllum (Anacardiaceae), a new species from Fujian, China: evidence from morphological and molecular analyses

FIGURE 3. Toxicodendron oligophyllum and related species. T. oligophyllum (A. Habitat; B. Flowering branches; C. Leaf, abaxial view; D–E. Flowers; F. Infructescence; G. seed); T. sylvestre (H. Branchlets, I. Leaves); T. succedaneum (J. Branchlets, K. Leaves).

opennotspecifiedMar 2022View details →
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FIGURE 2. Toxicodendron oligophyllum S. L in Toxicodendron oligophyllum (Anacardiaceae), a new species from Fujian, China: evidence from morphological and molecular analyses

FIGURE 2. Toxicodendron oligophyllum S. L. Tang, Liang Ma & S. P. Chen. A. Flowering branch; B. Infructescence; C. Flower, front view; D. Flower, side view.

opennotspecifiedMar 2022View details →
zenodo32/100

FIGURE 1 in Toxicodendron oligophyllum (Anacardiaceae), a new species from Fujian, China: evidence from morphological and molecular analyses

FIGURE 1. The resulting phylogram (Bayesian inference) from the combined plastid and nrITS data for Toxicodendron. Separate nrITS (A) and plastid trnL-F (B) results are shown in the top left corner. Numbers near branch are Bayesian posterior probabilities/ML bootstrap percentages/maximum parsimony bootstrap percentages (PP, BS ML, BS MP). A dash (–) represents BS<50% or PP<0.50.

opennotspecifiedMar 2022View details →
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FIGURE 3. Vincetoxicum junzifengense B.J in Vincetoxicum junzifengense (Apocynaceae), a new species from Fujian, China: Evidence from morphological and molecular analyses

FIGURE 3. Vincetoxicum junzifengense B.J.Ye & S.P.Chen. A. Habit. B. Front view of corolla. C. Lateral view of corolla. D. Corona. E. Pollinia. F. Follicles.

opennotspecifiedMar 2022View details →
zenodo32/100

FIGURE 1 in Vincetoxicum junzifengense (Apocynaceae), a new species from Fujian, China: Evidence from morphological and molecular analyses

FIGURE 1. Phylogenetic tree obtained by maximum-likelihood analysis of the combined matrix. The numbers near the nodes are bootstrap percentages and Bayesian posterior probabilities (BP ML, PP, BP MP). Only bootstrap percentages>50% are shown. Separate combined nrITS (A) and plastid (B) results are shown in the top right corner. A dash (-) indicates that 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.

opennotspecifiedMar 2022View details →
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FIGURE 2. Vincetoxicum junzifengense B.J in Vincetoxicum junzifengense (Apocynaceae), a new species from Fujian, China: Evidence from morphological and molecular analyses

FIGURE 2. Vincetoxicum junzifengense B.J.Ye & S.P.Chen. A. Habit. B. Back of leaf. C. Root. D. Front view of corolla. E. Back view of corolla. F. Corona. G. Gynostegium. H. Follicles. I. Pollinarium.

opennotspecifiedMar 2022View details →
dryad32/100

Revised taxonomy of the Arctotis Annual Clade (Arctotideae, Asteraceae) from Southern Africa: integration of molecular phylogenetic and morphological evidence

<p>Previous phylogenetic analysis of ITS nrDNA sequence data for Arctotidinae species resolved a highly supported clade containing all but one of the showy annual <i>Arctotis </i>species (informally designated the '<i>Arctotis</i> Annual Clade')<i>.</i> In the present study, phylogenetic relationships in the <i>Arctotis </i>Annual<i> </i>Clade were investigated by Bayesian inference and maximum parsimony analyses of cpDNA (<i>trnT-trnL-trnF</i> and <i>trnH-psbA</i>) and nrDNA (ITS) sequence data. The cpDNA and nrDNA phylogenies were notably incongruent. <i>Arctotis venusta </i>and a putative unnamed species<i> </i>('sp. B') were highly supported as monophyletic by both datasets. The monophyly of <i>A. leiocarpa </i>was strongly supported by the ITS dataset, whereas the remaining accessions formed a poorly resolved complex (the '<i>A. fastuosa </i>complex'). Within the <i>A. fastuosa </i>complex, <i>A. hirsuta </i>was monophyletic with high support in the ITS phylogeny. A statistical parsimony-derived cpDNA haplotype network resolved five broad groups of haplotypes and showed no consistent geographical structure, but species-specific haplotype lineages<i> </i>for<i> A. venusta </i>and sp. B were resolved. <i>Arctotis fastuosa </i>accessions were distributed among four haplotype groups. Incongruence between the datasets and poor resolution within the <i>A. fastuosa </i>complex may reflect reticulate evolution, ancestral polymorphism, and incomplete lineage sorting, in tandem with the low information content of the datasets. The greatest phenotypic diversification in the clade is in cypsela morphology. Comparison of cypsela morphology with the phylogenies suggests a general trend for reduction in the sizes of the cypsela, abaxial wings, and pappus scales, and loss of pubescence during diversification. A revised taxonomy, integrating currently available evidence, accompanied by full descriptive accounts and a key to the taxa are presented. Eight species are recognized, including the nomenclatural novelties <span><b><i><span>Arctotis chrysantha</span></i></b></span> (sp. nov.) and <span><b><i><span>Arctotis namibiensis</span></i></b></span><i> </i>(sp. nov.). The names <i>Arctotis karasmontana</i>, <i>Venidium fugax</i>, and <i>Venidium macrocephalum</i> are lectotypified.</p>

opencc-zeroApr 2022View details →
zenodo32/100

Supplementary material 1 from: Briñoccoli YF, Bogan S, Arcila D, Rosso JJ, Mabragaña E, Delpiani SM, de Astarloa JMD, Cardoso YP (2022) Molecular and morphological evidence revalidates Acrobrycon tarijae (Characiformes, Characidae) and shows hidden diversity. ZooKeys 1091: 99-117. https://doi.org/10.3897/zookeys.1091.73446

Molecular and taxonomic evidence unmask hidden species diversity in the genus Acrobrycon (Characiformes, Characidae). Fig. S1–S3.

opencc-zeroMay 2022View details →
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FIGURE 1 in Cymbidium ×shangrilaense (Orchidaceae; Epidendroideae), a new natural hybrid from China: evidence from morphology and molecular analyses

FIGURE 1. Phylogenetic relationships of C. ×shangrilaense based on the combined plastid DNA. Galeandra devoniana and Eulophia graminea were used as outgroups. The three numbers near the nodes are Bayesian posterior probabilities (PP), maximum likelihood bootstrap percentages (BP ML), and maximum parsimony bootstrap percentages (BP MP), respectively. "*" indicates that the node has BP=100 or PP=1.00. "-" indicates that the node is incongruent between the topology of the Bayesian and MP/ML trees.

opennotspecifiedSep 2022View details →
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FIGURE 4 in Cymbidium ×shangrilaense (Orchidaceae; Epidendroideae), a new natural hybrid from China: evidence from morphology and molecular analyses

FIGURE 4. Cymbidium ×shangrilaense S.Ke, Q.H.Zhang &amp; S.R.Lan. A. Flowering plant. B. Flower, front view. C. Lip and column, side view. D. inflorescence. E. Structure of the flower. F. Lip, upper view. G. C. tracyanum flower. H. C. gaoligongense flower.

opennotspecifiedSep 2022View details →
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FIGURE 3 in Cymbidium ×shangrilaense (Orchidaceae; Epidendroideae), a new natural hybrid from China: evidence from morphology and molecular analyses

FIGURE 3. Cymbidium ×shangrilaense S.Ke, Q.H.Zhang &amp; S.R.Lan. A. Flowering plant. B. Lateral sepal. C. Petal. D. Dorsal sepal. E. Lip. F. Pollinarium. G. Lip and column. H. Whole flower.

opennotspecifiedSep 2022View details →
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FIGURE 3 in Combination of Chloranthus flavus into C. nervosus based on morphological and molecular evidence

FIGURE 3. Inflorescence and floral diversity of Chloranthus nervosus from different places. A Xilin, Guangxi, China; B, E Debao, Guangxi, China; C Xishuangbanna, Yunnan, China; D Lingyun, Guangxi, China. Photographs taken by Yong-Bin Lu (A–D) and Ying Qin (E).

opennotspecifiedSep 2022View details →
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FIGURE 1 in Combination of Chloranthus flavus into C. nervosus based on morphological and molecular evidence

FIGURE 1. The best maximum likelihood phylogenetic trees based on the ITS (A) and concatenated plastid data (B). ML bootstrap support values and Bayesian posterior probability are indicated along nodes. The newly sequenced samples are mapped with the collection locations and the type locality of C. flavus is highlighted in bold. The serial numbers beginning with a capital "C" are given after the species names to distinguish each of individuals, and I-XIII represent different populations.

opennotspecifiedSep 2022View details →
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FIGURE 2 in Combination of Chloranthus flavus into C. nervosus based on morphological and molecular evidence

FIGURE 2. Chloranthus flavus (A–F), Chloranthus nervosus (G–L). A, G Plants in cultivation; B,H Infructescences; C, I Stems; D, J Scale-like leaves; E, K Stamen connectives; F, L Fruits. Photographs taken by Yong-Bin Lu.

opennotspecifiedSep 2022View details →

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record