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1,918 results for “molecular evidence”
FIGURE 10 in A revision of the genus Isotomurus (Collembola: Isotomidae) in northern Iran using molecular evidence
FIGURE 10. Isotomurus punctiferus: (a) Ant III organ (scale: 10μm); (b) mucro (scale: 10μm).
FIGURE 7 in A revision of the genus Isotomurus (Collembola: Isotomidae) in northern Iran using molecular evidence
FIGURE 7. Isotomurus palustris: body color pattern
FIGURE 2 in A revision of the genus Isotomurus (Collembola: Isotomidae) in northern Iran using molecular evidence
FIGURE 2. Isotomurus potapovi sp. nov.: Color pattern
FIGURE 6 in A revision of the genus Isotomurus (Collembola: Isotomidae) in northern Iran using molecular evidence
FIGURE 6. Isotomurus afghanicus: body color pattern
FIGURE 9 in A revision of the genus Isotomurus (Collembola: Isotomidae) in northern Iran using molecular evidence
FIGURE 9. Isotomurus punctiferus: body color pattern
FIGURE 4 in A revision of the genus Isotomurus (Collembola: Isotomidae) in northern Iran using molecular evidence
FIGURE 4. Isotomurus katule sp. nov.: Body color
FIGURE 8 in A revision of the genus Isotomurus (Collembola: Isotomidae) in northern Iran using molecular evidence
FIGURE 8. Isotomurus maculatus: body color pattern
Figure 17 in The resurrection of Cerasommatidiidae, an enigmatic group of coccinelloid beetles (Coleoptera: Coccinelloidea) based on molecular and morphological evidence
Figure 17. Morphology of MahaƲelo madagasus sp. nov. A, habitus dorsal. B, habitus frontal. C, habitus lateral. Scale bars: 1 mm. D, head with mouthparts removed, ventral. E, maxilla, ventral. F, mandible, ventral. G, meso- and metathorax, ventral. H, aedeagus, ventral. I, male genital segment, ventral. J, female genitalia, ventral. K, details of spermatheca.
Figure 2 in The resurrection of Cerasommatidiidae, an enigmatic group of coccinelloid beetles (Coleoptera: Coccinelloidea) based on molecular and morphological evidence
Figure 2. Results of the phylogenetic analyses of the combined, morphological and molecular dataset under Bayesian inference. Statistical support for branches show posterior probabilities. Branch lengths are kept and shown in the same proportion all along the tree. Apomorphies tracked in WINCLADA are shown upon each branch. DNA helix graphic after taxon name indicates taxa for which molecular data were available; asterisk '*' indicates interspecific chimeras (combined data from two different species of the same genus).
FIG. 1 in The Macaronesian liverwort Riccia boumanii Dirkse, Losada & M.Stech (Marchantiophyta: Ricciaceae) confirmed new to Asia by morphological and molecular evidence
FIG. 1. — Phylogeny of Riccia L. illustrating position of Riccia boumanii Dirkse, Losada & M.Stech, inferred from combined dataset (rbcL, trnL-F and ITS2) and topology displayed as majority rule consensus tree of trees recovered in stationary phase of Bayesian search. ML bootstrap values BS ≥ 65 and Bayesian posterior probabilities values PP ≥ 0.90 are shown at left and at right, respectively.
Supplementary material 1 from: Li X, Ni J-B, Xia N-H (2023) The identity of Sasa oblongula C.H.Hu (Poaceae, Bambusoideae, Arundinarieae): evidence from morphology and molecular data. PhytoKeys 226: 17-32. https://doi.org/10.3897/phytokeys.226.101221
SNP matrix
Integrating fossil flowers into the angiosperm phylogeny using molecular and morphological evidence
<p><span>F</span><span>ossils are essential to infer past evolutionary processes. The assignment of fossils to extant clades has traditionally relied on morphological similarity and on apomorphies shared with extant taxa. The use of explicit phylogenetic analyses to establish fossil affinities has so far remained limited. In this study, we built a comprehensive framework to investigate the phylogenetic placement of 24 exceptionally preserved fossil flowers. For this, we assembled a new species-level dataset of 30 floral traits for 1,201 extant species that were sampled to capture the stem and crown nodes of all angiosperm families. We explored multiple analytical approaches to integrate the fossils into the phylogeny, including different phylogenetic estimation methods, topological-constrained analyses, and combining molecular and morphological data of extant and fossil species. Our results were widely consistent across approaches and showed minor differences in the support of fossils at different phylogenetic positions. The placement of some fossils agrees with previously suggested relationships, but for others, a new placement is indicated. We also identified fossils that are well supported within particular extant families, whereas others showed high phylogenetic uncertainty. Finally, we present recommendations for future analyses combining molecular and morphological evidence, regarding the selection of fossils and appropriate methodologies, and provide some perspectives on how to integrate fossils into the investigation of divergence times and the temporal evolution of morphological traits.</span></p>
FIGUERE 1 in Thyrocarpus fujianensis (Boraginaceae; Cynoglosseae), a new species from China: evidence from morphological and molecular analyses
FIGUERE 1. Fruit difference of T. fujianensis (A), T. sampsonii (B), and T. glochidiatus (C).
Data from: Molecular evidence that the genes for dioecism and monoecism in Spinacia oleracea L. are located at different loci in a chromosomal region
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Data from: Transgenes in Mexican maize: molecular evidence and methodological considerations for GMO detection in landrace populations
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Data from: Population genetics of jaguars (Panthera onca) in the Brazilian Pantanal: molecular evidence for demographic connectivity on a regional scale
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Data from: Molecular evidence for the paraphyly of Scolecophidia and its evolutionary implications
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Data from: Molecular evidence for the monophyly of flatfishes (Carangimorpharia: Pleuronectiformes)
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Data from: Molecular evidence for the compilospecies model of reticulate evolution in Armeria (Plumbaginaceae)
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Data from: Unraveling the evolutionary radiation of the families of the Zingiberales using morphological and molecular evidence
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ScienceDex guides
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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.