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Fig. 2 in The Nomenclature And Systematics Of Some Australasian Homalopsid Snakes (Squamata: Serpentes: Homalopsidae)
Fig. 2. The holotype of Myron karnsi, SMF 19569. A and B: show the overall of head plates. C: illustrates the enlarged occipital scales (O) and their relationship to the temporal (T). D: has the three pair of chin shields numbered and the 3rd pair is as wide as long.
Fig. 7 in An overlooked case for a century: taxonomy and systematics of a new Iberian species of Eumerus Meigen, 1822 (Diptera, Syrphidae)
Fig. 7. Eumerus colladoi Ricarte & Aguado-Aranda sp. nov., holotype, ♂ (CEUA-CIBIO), genitalia. A. Hypandrium, lateral view. B. Epandrium, lateral view. C. Epandrium, right side, ventral view. Abbreviations: asl = anterior surstylar lobe; cc = cercus; hl = hyaline lobes; pr = prominence; psl = posterior surstylar lobe. Scale bars: 250 μm.
Fig. 4 in An overlooked case for a century: taxonomy and systematics of a new Iberian species of Eumerus Meigen, 1822 (Diptera, Syrphidae)
Fig. 4. Measurements of Eumerus colladoi Ricarte & Aguado-Aranda sp. nov. A, C–D. Holotype, ♂ (CEUA-CIBIO). B. Paratype, ♀ (CEUA-CIBIO). Abbreviations: bl = basoflagellomere length; bw = basoflagellomere width; hh = head height; hw = head width; l = body length; tg = tegula; w = body width; wl = wing length. Scale bars: A–B = 1 mm; C–D = 500 μm.
Fig. 3 in An overlooked case for a century: taxonomy and systematics of a new Iberian species of Eumerus Meigen, 1822 (Diptera, Syrphidae)
Fig. 3. Eumerus colladoi Ricarte & Aguado-Aranda sp. nov. A. Holotype, ♂ (CEUA-CIBIO), head, general view. B. Paratype, ♀ (CEUA-CIBIO), head, general view. C. Holotype, ♂, head, lateral view. D. Paratype, ♀ (CEUA-CIBIO), head, lateral view. E. Holotype, ♂, antenna, lateral view. F. Paratype, ♀ (CEUA-CIBIO), antenna, lateral view. Abbreviation: fs = fossette. Scale bars: A–C = 500 μm; D–F = 250 μm.
Fig. 2 in An overlooked case for a century: taxonomy and systematics of a new Iberian species of Eumerus Meigen, 1822 (Diptera, Syrphidae)
Fig. 2. Eumerus colladoi Ricarte & Aguado-Aranda sp. nov. A. Holotype, ♂, dorsal view (CEUA- CIBIO). B. Holotype, ♂, lateral view. C. Paratype, ♀, dorsal view (CEUA-CIBIO). D. Paratype, ♀, lateral view view (CEUA-CIBIO). Scale bars = 1 mm.
Fig. 6 in An overlooked case for a century: taxonomy and systematics of a new Iberian species of Eumerus Meigen, 1822 (Diptera, Syrphidae)
Fig. 6. Eumerus colladoi Ricarte & Aguado-Aranda sp. nov., paratype, ♂ (CEUA-CIBIO), sternum IV. Abbreviation: vs = valves. Scale bar: 250 μm.
Fig. 8 in An overlooked case for a century: taxonomy and systematics of a new Iberian species of Eumerus Meigen, 1822 (Diptera, Syrphidae)
Fig. 8. Tree inferred using the Maximum Likelihood method. Bootstrap values> 50 are shown near nodes. Branch lengths measured in number of substitutions per site.
Fig. 5 in An overlooked case for a century: taxonomy and systematics of a new Iberian species of Eumerus Meigen, 1822 (Diptera, Syrphidae)
Fig. 5. Metalegs of species of Eumerus Meigen, 1822. A–B. Eumerus colladoi Ricarte & Aguado- Aranda sp. nov., holotype, ♂ (CEUA-CIBIO). C. Eumerus amoenus Loew, 1848, ♂ (CEUA-CIBIO). Scale bars: 500 μm.
Figure 23-32 in Systematic revision of Gonaphodiellus taxa, with description of two new genera and fourteen new species (Coleoptera: Scarabaeidae: Aphodiinae)
Figure 23-32. Gonaphodiellus manantlanicus, new species (Las Joyas, Sierra de Manantlán, Jalisco, Mexico). 23) Epipharynx. 24-25) Habitus (length ideogram and morphological details). 26-27) Aedeagus (dorsal and lateral view). Gonaphodiellus martinpierai, new species (Acajete, Veracruz, Mexico). 28) Epipharynx. 29-30) Habitus (morphological details and length ideogram). 31-32) Aedeagus (dorsal and lateral view).
Dataset for "On Closure Phase and Systematic Bias in Multilooked SAR Interferometry"
<ul> <li>Datasets of the Barstow-Bristol Trough area -- unwrapped interferograms of con-1 through con-10, and con-20 and their associated correlation, connected components.</li> <li>Jupyter notebook tutorial can be found in https://github.com/insarlab/MintPy-tutorial/tree/main/applications</li> </ul>
Supplementary data for: McFadden et al., Revisionary systematics of Octocorallia (Cnidaria: Anthozoa) guided by phylogenomics
<p class="MsoNormal">The anthozoan sub-class Octocorallia includes over 3500 nominal species of soft corals and gorgonian sea fans, many of which serve as critical foundation species in benthic marine ecosystems in shallow waters to the deep sea. Despite their familarity and ecological importance, the diversity and taxonomy of octocorals remain poorly known. All of the orders, subordinal groups and a majority of families have been recognized to be poly- or paraphyletic, but poor resolution of the deeper nodes in mitochondrial or single-locus nuclear gene trees have hindered formal revision of the higher level taxonomy of the group. We used sequence data from target-capture of 739 ultraconserved and exon loci to reconstruct a fully resolved phylogeny for 185 octocoral taxa representing 55 of 63 currently recognized families. We use this phylogeny, supplemented with a gene tree for mitochondrial <em>mtMutS</em> for an additional 107 taxa, to guide a revision of the families and orders of Octocorallia. We: (1) elevate the anthozoan sub-classes Octocorallia and Hexacorallia to the rank of Class; (2) replace the three currently recognized orders of Octocorallia (Alcyonacea, Pennatulacea, Helioporacea) with two new orders reflecting reciprocally monophyletic major clades; and (3) revise all families with the exception of the 15 recognized families of sea pens, which we accommodate within a new superfamily. The revised classification of Octocorallia thus comprises 79 families, including 18 that are newly described and three that have been reinstated or elevated in rank. In addition, two new genera are described and another three reinstated. We leave the family assignment of 46 of 411 genera as <em>incertae sedis</em> until further molecular or morphological data can be obtained to confirm their phylogenetic affinities.</p>
Characterization data for the manuscript: "Using genetic algorithms to systematically improve the synthesis conditions of Al-PMOF"
<p>This entry contains characterization data for the manuscript "Using genetic algorithms to systematically improve the synthesis conditions of Al-PMOF", which we exported from the electronic lab notebook (ELN).</p> <p>To visualize the data in this dataset: <a href="https://www.cheminfo.org/flavor/zenodo/index.html?id=6620502">open entry</a></p>
Is Open Data Strategy for Covid-19 used for other global health threats? A systematic review of the literature
<p>Dataset result of the literature review run between march and may 2022 on PubMed, Cinahl, Scopus and Google Scholar about open data and growing trend in scientific research about infection risk comparing Covid-19, Anti Microbial Resistance (AMR), and Health Assistance Correlated Infections (HAIs).</p>
Systematic analysis of disease-linked rare germline variants reveals new classes of cancer predisposing genes
<ul> <li>GEMs_Liver-HCC: 312 cancer patient-specific genome-scale metabolic models (GEMs) for Liver-HCC reconstructed using the RNA-seq data from PCAWG-TCGA Liver-HCC samples and generic human GEM 'Recon 2M.2'</li> <li>GEMs_Lung-SCC: 493 cancer patient-specific GEMs for Lung-SCC reconstructed using the RNA-Seq data from PCAWG-TCGA Lung-SCC samples and generic human GEM 'Recon 2M.2'</li> </ul> <p>All the patient-specific GEMs were generated using a previously developed method (i.e., tINIT algorithm with a rank-based weight function), which is available at <a href="https://bitbucket.org/kaistmbel/recon-manager">https://bitbucket.org/kaistmbel/recon-manager</a>.</p>
Data on the detection of clinically significant prostate cancer by magnetic resonance imaging (MRI)-guided targeted and systematic biopsy
<p>This is a dataset from the original publication “Reasons for missing clinically significant prostate cancer by targeted magnetic resonance imaging/ultrasound fusion-guided biopsy”. From 01/2014 to 04/2019 a sample collective of 785 patients with 3T multiparametric magnetic resonance imaging (mp-MRI) of the prostate and subsequent combined systematic biopsy (SB) and magnetic resonance imaging/ultrasound (US) fusion-guided biopsy (TB) was retrospectively analyzed. Prostate carcinoma (PCa) detection by TB and/or additional SB was analyzed.</p>
Fig. 30 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 30 (continued on next page). Distribution of the lutko species group fritillaries in combination with the distribution of known and suspected species of host plants from the genus Phlomoides Blume. = Melitaea lutko Evans, 1932; = M. timandra timandra Coutsis & Oorschot, 2014; = M. timandra binaludica subsp. nov.; = M. shahvarica sp. nov.; = M. mimetica mimetica Higgins, 1940; = M. mimetica delerei Heidemann, 1954;? = unconfirmed findings of M. timandra; = M. timandra with an unclear subspecies status; = Phlomoides regeliana (Aitch. & Hemsl.) Adylov, Kamelin & Makhm.; = Phlomoides boissieriana (Regel) Adylov, Kamelin & Makhm.; = Phlomoides laciniata (L.) Kamelin & Makhm.; = Phlomoides labiosiformis (Popov) Adylov, Kamelin & Makhm.; = Phlomoides loasifolia (Benth.) Kamelin & Makhm.; = Phlomoides molucelloides (Bunge) Salmaki; = Phlomoides acaulis (Beck ex Rech.f.) Salmaki; = Phlomoides labiosa (Bunge) Adylov, Kamelin & Makhm. A. Pakistan, Chitral, Chaghbini CGNP, alt. 2700–3000 m. B. Pakistan, Khyber Pakhtunkhwa, Drosh. C. Pakistan, Khyber Pakhtunkhwa, Keon Nullah. D. Pakistan, Khyber Pakhtunkhwa, Malakand. E. Pakistan, Khyber Pakhtunkhwa, Birmoglasht. F. Turkmenistan, Badkhyz, Kepeli, alt. 700 m. G. Turkmenistan, Badkhyz, Kyzyl-Jar, alt. 700 m. H. Turkmenistan, Kushka, alt. 700 m. I. Turkmenistan, Murgab river, Sary-Yazy, alt. 300 m. J. Turkmenistan, 30 km E of BairamAli, Zahmet, alt. 240 m. K. Turkmenistan, Bairam-Ali, alt. 230 m. L. Turkmenistan, Kara-Kum desert, 30 km W of Mary, alt. 200 m.M. Turkmenistan, Dushak, alt. 250 m.N. Turkmenistan, Chaacha, alt. 400 m. O. Turkmenistan, Bakharden, alt. 200 m. P. Iran, Khorossan Razavi, Kuh-e-Binalud Mts, Qadamgah area, Gerina, alt. 2000 m. Q. Iran, Khorasan Razavi, Kuh-e-Binalud Mts, 15 km SW of Zoshk, alt. 2300– 2500 m. R. Iran, S Khorosan, 75 km N of Birjant, Sedeh, alt. 1500 m. S. Iran, S Khorosan, 35 km N of Birjant, alt. 1500 m. T. Afghanistan, Bamian, Band-e-Amir, Dzhudoi-Kvak Gorge, alt. 3200 m. U. Afghanistan, Bamian, Band-e-Amir, Hazarajat, alt. 3000–3200 m. V. Afghanistan, Bamian, Koh-iBaba Mts, Joshanak, alt. 2800 m. W. Afghanistan, Heart, Qala-i-Naw, Kashka pass. X. Iran, Semnan, Shahvar Mt., alt. 2200–2500 m. Y. Turkmenistan, Kara-Kala, Monjukly Ridge, 300–700 m. Z. Iran, Golestan, E Maraveh Tappeh, N Ghazan Ghayeh, Palizan Mts. A". Pakistan, Balochistan, Quetta, Urak, alt. 2500 m. B". Pakistan, Balochistan, Ziarat, alt. 2500 m. C". Pakistan, Balochistan, Khojak, alt. 1700 m. D". Pakistan, Balochistan, Zaghum, alt. 1600 m; E". Pakistan, Punjab, Gawar, alt. 500 m. F". Pakistan, Balochistan, Sheik Wazil, alt. 1600 m. G". Afghanistan, Bamian, Hushkak, alt. 2700–2800 m. H". Afghanistan, Bamian, Punjub Distr., 10 km NE of Varas, alt. 2400 m. I". Afghanistan, Ghor, 17 km E of Changcharan, 15 km S of Bandi-Ali, Gazak Mts, alt. 2400 m. J". Afghanistan, Ghor, Bayan Range, 15 km S of Changcharan, Kindival valley, alt. 2700 m. K". Afghanistan, Bamiyan, Kohi-Baba Mts, Panjao, alt. 3000 m. Afghanistan, Bamiyan, Koh-i-Baba Mts, Shah-tu-Kotal, alt. 4000 m. L". Afghanistan, Kapisa, Pandshir valley, alt. 2200–2800 m. M". Afghanistan, Kabul. N". Iran, Tehran, Elburz Ridge, Demavend Mt., Ask, alt. 1800 m. O". Iran, Semnan, Foulad Mohaleh, alt. 2200 m. P". Pakistan, Punjab, Murree.
Fig. 29 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 29.Differences in the structure of valva and aedeagus of the lutko species group.A. Melitaea shahvarica sp. nov. B, D, H. M. timandra binaludica subsp. nov. C–E. M. mimetica Higgins, 1940. F. M. lutko Evans, 1932. G. M. timandra timandra Coutsis &van Oorschot, 2014. A. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mts, alt. 2200–2400 m. B. Iran, Rezavi Khorassan Prov., Kuh-e-Binalud Mts, Dorrud v. vicinity, alt. 2430 m. C. Afghanistan, Bamian Prov., Punjub Distr., 10 km NE of Varas v., alt. 2400 m. D. Afghanistan, Band-i-Amir, Hazarajat. E. Pakistan, Balochistan, Quetta, Urak, alt. 2400– 2700 m. F. Pakistan, Chitral, Gol National Park, alt. 2700 m. G. Turkmenistan, Sary-Yazy, alt. 700 m. H. Iran, Rezavi Khorassan Prov., Kuh-e-Binalud Mts, Dorrud v. vicinity, alt. 2430 m.
Fig. 28 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 28.Eggs and caterpillars of Melitaea shahvarica sp. nov. in nature and in the laboratory.A–B. Freshly laid eggs under a leaf of a host plant, May 2018, Iran, Shahvar Mt., alt. 2200 m. C–D. IV–V instar caterpillars on the leaves of the host plant Phlomoides molucelloides (Bunge) Salmaki, July 2019, Iran, Shahvar Mt., alt. 2500 m. E. I instar caterpillars in the laboratory, Moscow, May 2018. F. VI instar caterpillars during diapause, Moscow, October 2018.
Fig. 18. Male genitalia and harpe. A–C in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 18. Male genitalia and harpe. A–C. Melitaea shahvarica sp. nov. D–E. M. lutko Evans, 1932. F–I. M. mimetica Higgins, 1940. A–C. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mts, alt. 2200–2400 m. D–E. Pakistan, Chitral, Chaghbini, CGNP [Chitral Gol National Park], alt. 2700 m. F–G. Afghanistan, Bamian Prov., Punjub Distr., 10 km. NE Varas v., alt. 2400 m. H–I. Afghanistan, Bamian Prov., Panjub Distr., 10 km. NE Varas vil., alt. 2400 m.
Fig. 8 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 8. Distribution of Melitaea mimetica Higgins, 1940. For a description of the symbols with letters, see Fig. 30. = M. mimetica mimetica Higgins, 1940; = M. mimetica delerei Heidemann, 1954.
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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.