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1,416 results for “Evidence Base”

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zenodo28/100

Figure 4. Reproductive system. A – D in Dina serbica, a new species of leeches (Annelida: Hirudinea: Erpobdellidae) from Serbia, based on morphological and molecular evidence

Figure 4. Reproductive system. A – D. minuoculata Grosser, Moritz & Pešić, 2007, paratype, a first order stream in the Tara river canyon, Montenegro. B – Dina serbica sp. nov., paratype, spring along the road to Kamena Gora, Serbia. Abbreviations: a = genital atrium, b = vas deferens, c = ovarian sacks, d = testisacs.

opencc-by-4.0Feb 2022View details →
zenodo28/100

Figure 4 in Sperchon milisai nov. sp., an overlooked new species of water mites (Acari, Hydrachnidia, Sperchontidae) from Montenegro and Croatia, based on morphological and DNA barcode evidence

Figure 4. Sperchon milisai sp. nov. (A, C-D, holotype ♂; B, E-F, paratype ♀), Rikavac, Montenegro: A – idiosoma, dorsal view; B – idiosoma, dorsal view, partially; C – chelicera; D – gnathosoma in dorsal view; D – genital field and left coxae; F – excretory pore area. Scale bars = 100 µm.

opencc-by-4.0Feb 2022View details →
zenodo28/100

FIGURE 4 in Porpomyces submucidus (Hydnodontaceae, Basidiomycota), a new species from tropical China based on morphological and molecular evidence

FIGURE 4. Porpomyces submucidus (holotype). A basidiocarp.

opennotspecifiedOct 2015View details →
zenodo28/100

FIGURE 2. A in Fulvifomes parviungulatus (Hymenochaetales, Basidiomycota), a new species from China based on morphological and molecular evidence

FIGURE 2. A fresh basidiocarp of Fulvifomes parviungulatus (Holotype). Scale bar = 1 cm.

opennotspecifiedMar 2024View details →
zenodo28/100

FIGURE8 in Taxonomic evaluation of Miscanthus nudipes (Poaceae) based on morphological and molecular evidence

FIGURE8. Temperature and precipitation data of habitats of 15 populations of Miscanthus nudipes.

opennotspecifiedApr 2015View details →
zenodo28/100

FIGURE 6 in A revision of the genus Leontodon (Asteraceae) in the Azores based on morphological and molecular evidence

FIGURE 6. Holotype of Leontodon × friasi (= L. saxatilis × L. hochstetteri) (AZB).

opennotspecifiedMay 2015View details →
zenodo28/100

FIGURE 2 in Daedaleopsis hainanensis sp. nov. (Polyporaceae, Basidiomycota) from tropical China based on morphological and molecular evidence

FIGURE 2. Basidiocarps of Daedaleopsis hainanensis (holotype, scale bar = 2 cm).

opennotspecifiedSep 2016View details →
zenodo28/100

FIGURE 4 in Recognition of a new species of Hedysarum (Fabaceae, Hedysareae) from China based on morphological and molecular evidence

FIGURE 4. Living plant of Hedysarum cuonanum. A, in the habitat; B, upper part of the plant.

opennotspecifiedFeb 2017View details →
zenodo28/100

FIGURE 3 in Recognition of a new species of Hedysarum (Fabaceae, Hedysareae) from China based on morphological and molecular evidence

FIGURE 3. Holotype of Hedysarum cuonanum.

opennotspecifiedFeb 2017View details →
zenodo28/100

FIGURE 6 in Senecio kumaonensis (Asteraceae, Senecioneae) is a Synotis based on evidence from karyology and nuclear ITS/ETS sequence data

FIGURE 6. Distribution of Synotis penninervis (= Senecio kumaonensis) (●).

opennotspecifiedJan 2017View details →
zenodo28/100

FIGURE 1. A in Ceriporia albomellea (Phanerochaetaceae, Basidiomycota), a new species from tropical China based on morphological and molecular evidences

FIGURE 1. A fresh basidiome of Ceriporia albomellea (Dai 15223). Scale bar = 3 cm.

opennotspecifiedMar 2017View details →
zenodo28/100

FIGURE 1 in Croton aemulus and C. graomogolensis (Euphorbiaceae): Two new species from Minas Gerais, Brazil, based on distinct lines of evidence and their relation to C. muscicapa and C. longibracteatus

FIGURE 1. Map showing known distribution of the four species.

opennotspecifiedAug 2018View details →
zenodo28/100

TABLE 2 in Two new diploid species of Isoetes (Isoetaceae: Lycopodiopsida) from Southeastern China based on morphological and molecular evidence

<p><b>TABLE 2.</b> Summary of complete chloroplast genomes for <i>Isoetes changleensis</i> and I. yuhangensis.</p><table><tbody><tr><th>Genome features</th><th>I. changleensis</th><th><i>I. yuhangensis</i></th></tr></tbody><tbody><tr><th>Genome size (bp)</th><td>145,494</td><td>145,501</td></tr><tr><th>GC content (%)</th><td>38</td><td>38</td></tr><tr><th>LSC size (bp)</th><td>91,859</td><td>91,839</td></tr><tr><th>SSC size (bp)</th><td>27,221</td><td>27,225</td></tr><tr><th>IR size (bp)</th><td>26,414</td><td>26,414</td></tr><tr><th>Number of genes</th><td>125</td><td>125</td></tr><tr><th>Protein coding genes</th><td>81</td><td>81</td></tr><tr><th>tRNA genes</th><td>36</td><td>36</td></tr><tr><th>rRNA genes</th><td>8</td><td>8</td></tr></tbody></table>

opennotspecifiedMar 2024View details →
zenodo28/100

FIGURE 5 in A generic revision and new combinations in the Hyptidinae (Lamiaceae), based on molecular and morphological evidence

FIGURE 5. Phylogenetic relationships of genera of Hyptidinae

opennotspecifiedJun 2012View details →
dryad28/100

Data from: Genomic evidence that resource-based trade-offs limit host-range expansion in a seed beetle

Trade-offs have often been invoked to explain the evolution of ecological specialization. Phytophagous insects have been especially well studied, but there has been little evidence that resource-based trade-offs contribute to the evolution of host specialization in this group. Here, we combine experimental evolution and partial genome resequencing of replicate seed beetle selection lines to test the trade-off hypothesis and measure the repeatability of evolution. Bayesian estimates of selection coefficients suggest that rapid adaptation to a poor host (lentil) was mediated by standing genetic variation at multiple genetic loci and involved many of the same variants in replicate lines. Sublines that were then switched back to the ancestral host (mung bean) showed a more gradual and variable (less repeatable) loss of adaptation to lentil. We were able to obtain estimates of variance effective population sizes from genome-wide differences in allele frequencies within and between lines. These estimates were relatively large, which suggests that the contribution of genetic drift to the loss of adaptation following reversion was small. Instead, we find that some alleles that were favored on lentil were selected against during reversion on mung bean, consistent with the genetic trade-off hypothesis.

opencc-zeroDec 2015View details →
zenodo28/100

Evidence-based dentistry and research methodology knowledge among orthodontic postgraduate residents in four universities

<p>Dataset for all analyses</p>

opencc-by-4.0Jan 2021View details →
zenodo28/100

Figure 1 in May a hybridogenetic complex regenerate the nuclear genome of both sexes of a missing ancestor? First evidence on the occurrence of a nuclear non-hybrid Squalius alburnoides (Cyprinidae) female based on DNA sequencing

Figure 1. Minimum spanning network among cytb haplotypes. The majority of the haplotypes (represented by circles) are exclusive of Squalius alburnoides (in grey) and of S. pyrenaicus (in white) individuals, except for the central one which is a haplotype shared between one S. alburnoides and two S. pyrenaicus individuals. NH indicates the haplotype of the non-hybrid female. The number of mutations between haplotypes is represented by small black dots.

opencc-by-4.0Oct 2006View details →
zenodo28/100

Figure 6 in Two new species from the Hygrobates nigromaculatus-complex (Acariformes, Hydrachnidia, Hygrobatidae), based on morphological and molecular evidence

Figure 6 Hygrobates limnocrenicus sp. nov., holotype ♀, Mareza, Montenegro: A – coxal and genital field; B – palp, lateral view; C – palp, medial view; D – I-L-5 and -6; E – IV-L-5 and -6. Scale bars = 100 µm.

opencc-by-4.0Oct 2020View details →
zenodo28/100

Figure 4 in Two new species from the Hygrobates nigromaculatus-complex (Acariformes, Hydrachnidia, Hygrobatidae), based on morphological and molecular evidence

Figure 4 Hygrobates lacrima sp. nov., ♂. Montenegro, Trebaljevo: A – idiosoma, ventral view; B – palp, medial view; C – IV-L-5 and -6. Scale bars = 100 µm.

opencc-by-4.0Oct 2020View details →
zenodo28/100

Figure 1 in Two new species from the Hygrobates nigromaculatus-complex (Acariformes, Hydrachnidia, Hygrobatidae), based on morphological and molecular evidence

Figure 1 Phylogenetic tree (BI/FastTree) used for species-delimitation analysis. Values near branches show Bayesian posterior probability/Shimodaira-Hasegawa local supports; only values&gt; 0.9/70 are shown.

opencc-by-4.0Oct 2020View details →

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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