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1,092 results for “resurrection”
Figure 1 from: Shah SA, Sultan A, Wen J, Ullah Z, Nisa SU, Ren Z, Alam MM, Iqbal J, Mumtaz AS (2021) Taxonomy of Vincetoxicum s.str. (Asclepiadoideae, Apocynaceae) from southern Asia including three new species and resurrected names. PhytoKeys 179: 35-73. https://doi.org/10.3897/phytokeys.179.62514
Figure 1 Habitats of Vincetoxicum species A–DV. arnottianumE–GV. cardiostephanumH–JV. kenourienseKV. lenifoliumLV. luridumM, NV. stocksiiO, PV. subcanescens.
FIGURE 15 in Resurrection of Salvia species (Lamiaceae) recently synonymized in Flora Mesoamericana
FIGURE 15. Salvia unicostata, inflorescence. (picture taken by J.G. González-Gallegos)
Fig. 9. — Hilsenbergia darcyana J.S in Classification of Boraginaceae subfam. Ehretioideae: Resurrection of the genus Hilsenbergia Tausch ex Meisn.
Fig. 9. — Hilsenbergia darcyana J.S. Mill.: A, flowering branch; B, whole flower with urceolate corolla; C, flower with open corolla showing androecium and gynoecium; D, lateral view of fruit with persistent calyx; E, basal view of fruit with persistent calyx; F, dorsal view of pyrene. A-C, Herb. Jard. Botanique 5404; D-E, Service Forestier: SF11930bis. Drawn by A. JOUY.
FIGURE 7 in Cryptic speciation within Asthenodipsas vertebralis (Boulenger, 1900) (Squamata: Pareatidae), the description of a new species from Peninsular Malaysia, and the resurrection of A. tropidonotus (Lidth de Jude, 1923)
FIGURE 7. Microhabiat of Asthenodipsas vertebralis at Brinchong Trail, Cameron Highlands.
FIGURE 4 in Resurrection of the genus Similisinocarum (Apiaceae) based on evidence from morphology and ITS sequences
FIGURE 4. Types of Similisinocarum normanianum. A. Holotype; B. Isotype.
FIGURE 1 in The genus Emitrombidium Lombardini, 1949 (Actinotrichida: Trombidiidae) resurrected
FIGURE 1. Emitrombidium giocondi sp. nov., holotype, adult. Habitus. Not to scale.
FIGURE 1 in New Hamacantha from Peru and resurrection of Zygherpe as subgenus (Demospongiae, Poecilosclerida, Hamacanthidae)
FIGURE 1. Schematic representation of the Peruvian coast, showing collecting localities in detail.
Figure 1 from: Grusz A, Windham M (2013) Toward a monophyletic Cheilanthes: The resurrection and recircumscription of Myriopteris (Pteridaceae). PhytoKeys 32: 49-63. https://doi.org/10.3897/phytokeys.32.6733
Figure 1 - Summary phylogeny for cheilanthoid ferns, indicating the placement of Cheilanthes micropteris (the type species for Cheilanthes) within the hemionitid clade—only distantly related to the myriopterid clade. The six major clades of cheilanthoid ferns are shown with tips roughly proportional to clade size. The most recent common ancestor (mrca) of Cheilanthes micropteris and the myriopterid clade is indicated. Modified with permission from Windham et al. (2009).
Figure 2 from: Jabbour F, Renner S (2011) Resurrection of the genus Staphisagria J. Hill, sister to all the other Delphinieae (Ranunculaceae). PhytoKeys 7: 21-26. https://doi.org/10.3897/phytokeys.7.2010
Figure 2 - Staphisagria macrosperma A young plant with the cotyledons and two palmate leaves B young inflorescence with floral buds subtended by a bract and bracteoles C side view of a flower showing the very short spur (or bulge) on the dorsal petaloid tepal D three-quarter view of a flower showing four developed staminodes: two lateral (black arrows) and two spurred (white arrows). The tips of the spurs are nested within the bulge of the dorsal tepal E three follicles F Gravity-dispersed poisonous seeds (c. 6 mm in length). Scale bars: 1 cm.
Figure 1 from: Jabbour F, Renner S (2011) Resurrection of the genus Staphisagria J. Hill, sister to all the other Delphinieae (Ranunculaceae). PhytoKeys 7: 21-26. https://doi.org/10.3897/phytokeys.7.2010
Figure 1 - Schematic representation of the phylogenetic relationships in the Delphinieae A as suggested by studies anterior to the findings of Jabbour and Renner (unpublished data) and B as found with combined nuclear (ITS) and plastid (trnL intron and adjacentrnL-trnF intergenic spacer) DNA sequences (2088 aligned nucleotides) from 191 accessions representing 185 species of Delphinieae (Jabbour and Renner, unpublished data). In this study, taxon sampling covered all genera and subgenera of the tribe. Numbers above branches indicate Maximum Likelihood bootstrap supports.
Figure 4 from: Cognato A (2010) Resurrection of Dryotomicus Wood and description of two new species from the Amazon River Basin (Coleoptera, Curculionidae, Scolytinae, Phloeotribini). ZooKeys 56: 49-64. https://doi.org/10.3897/zookeys.56.518
Figure 4 - Dryotomicus oenophilis sp. n. male genitalia, A Dorsal B Lateral. Spiculum gastrale not shown.
Figure 1 from: Cognato A (2010) Resurrection of Dryotomicus Wood and description of two new species from the Amazon River Basin (Coleoptera, Curculionidae, Scolytinae, Phloeotribini). ZooKeys 56: 49-64. https://doi.org/10.3897/zookeys.56.518
Figure 1 - Phylogeny of Phloeotribini species, 1 of 180 most parsimonious trees (tree length=35, RC=0.6429). Numbers above branches are Bremer support and numbers below are bootstrap values (< 50 not shown). Nodes with zero Bremer support were unresolved in a strict consensus of the 180 mpts. Vertical lines represent unambiguous character state changes inferred using accelerated transformations. Numbers above vertical lines are the characters and numbers below are the character state changes.
Figure 1 from: Kanzaki N, Ragsdale E, Giblin-Davis R (2014) Revision of the paraphyletic genus Koerneria Meyl, 1960 and resurrection of two other genera of Diplogastridae (Nematoda). ZooKeys 442: 17-30. https://doi.org/10.3897/zookeys.442.7459
Figure 1 - Paraphyly of Koerneria sensu lato. Tree is simplified from Kanzaki et al. (2014b), which was inferred from nearly full-length small subunit ribosomal DNA sequences. A subsequent study that included several more species of Koerneria sensu lato likewise showed the well-supported exclusion (99% bootstrap support in likelihood analysis, 100% posterior probability in Bayesian analysis) of a clade of Koerneria luziae + Koerneria ruehmi from all other Diplogastridae, including a monophyletic clade of what is designated herein as Allodiplogaster (Atighi et al. 2013). Asterisks indicate nodes with very strong support as inferred in the former study (>95% bootstrap support, 100% posterior probability).
Figure 2 from: Kanzaki N, Ragsdale E, Giblin-Davis R (2014) Revision of the paraphyletic genus Koerneria Meyl, 1960 and resurrection of two other genera of Diplogastridae (Nematoda). ZooKeys 442: 17-30. https://doi.org/10.3897/zookeys.442.7459
Figure 2 - Schematic drawings of the generic characters of Koerneria and Allodiplogaster. From left to right: stenostomatous form, eurystomatous form, female tail, and male tail characters. From top to bottom: Koerneria, aquatic Allodiplogaster ("striata" species group) and two types of terrestrial Allodiplogaster ("henrichae" species group). For the stenostomatous form of Allodiplogaster sudhausi (not shown), see Fürst von Lieven (2008). Squared bracket indicates cheilostom, which as undivided separates Koerneria from Allodiplogaster. Further diagnosing Koerneria is the arrangement of male genital papillae v5-v7. Unique to the striata group of Allodiplogaster relative to the henrichae group and to Koerneria are a long tail in both sexes, setiform genital papillae, and in many cases setiform labial papillae. Genital papillae and phasmids are labeled following the terminology in Sudhaus and Fürst von Lieven (2003). The phasmids are not clearly described in species of the striata group.
Figure 3 from: Larraín J, Carter B, Shaw B, Hentschel J, Strozier LS, Furuki T, Heinrichs J, Crandall-Stotler B, Engel J, von Konrat M (2015) The resurrection of Neohattoria Kamim. (Jubulaceae, Marchantiophyta): a six decade systematic conflict resolved through a molecular perspective. PhytoKeys 50: 101-122. https://doi.org/10.3897/phytokeys.50.4940
Figure 3 - Neohattoria herzogii. A Habit, dorsal view B Habit, ventral view with distal lobules detached C Regenerant shoot originating from a detached lobule D Lobule E Underleaf F–K Leaves. All from Furuki 22673 (F). Scale bar: 350 µm (A, B), 200 µm (C), 180 µm (D), 300 µm (E), 150 µm (F–K).
Figure 1 from: Larraín J, Carter B, Shaw B, Hentschel J, Strozier LS, Furuki T, Heinrichs J, Crandall-Stotler B, Engel J, von Konrat M (2015) The resurrection of Neohattoria Kamim. (Jubulaceae, Marchantiophyta): a six decade systematic conflict resolved through a molecular perspective. PhytoKeys 50: 101-122. https://doi.org/10.3897/phytokeys.50.4940
Figure 1 - Maximum likelihood (ML) tree showing the systematic position of Neohattoria relative to the Jubulaceae, Frullaniaceae and Lejeuneaceae. Wide black branches indicate ML bootstrap support > 90 % and PP > 0.95.
Figure 2 from: Larraín J, Carter B, Shaw B, Hentschel J, Strozier LS, Furuki T, Heinrichs J, Crandall-Stotler B, Engel J, von Konrat M (2015) The resurrection of Neohattoria Kamim. (Jubulaceae, Marchantiophyta): a six decade systematic conflict resolved through a molecular perspective. PhytoKeys 50: 101-122. https://doi.org/10.3897/phytokeys.50.4940
Figure 2 - Maximum likelihood (ML) tree showing the systematic position of Neohattoria herzogii within the Jubulaceae. Only 1/2 of the length of the branch between the Frullaniaceae and the Lejeuneaceae/Jubulaceae clade is depicted. Wide black branches indicate ML bootstrap support > 90 % and PP > 0.95.
Figure 4 from: Werding B, Hiller A (2015) Description of a new species of Petrolisthes in the Indo-West Pacific with a redefinition of P. hastatus Stimpson, 1858 and resurrection of P. inermis (Heller, 1862) (Crustacea, Anomura, Porcellanidae). ZooKeys 516: 95-108. https://doi.org/10.3897/zookeys.516.9923
Figure 4 - Petrolisthes elegantissimus sp. n., paratype male RMNH.CRUS.D.56408, NW Guinea, Indonesia. A Dorsal view of left ocular peduncle and basal segments of left antennal peduncle B Dorsal view of basal segment of left antennular peduncle C External view of sixth abdominal segment with telson D Lateral view of first to third left walking legs. Scale bar - 1 mm (A–C), 2 mm (D).
Figure 2 from: Werding B, Hiller A (2015) Description of a new species of Petrolisthes in the Indo-West Pacific with a redefinition of P. hastatus Stimpson, 1858 and resurrection of P. inermis (Heller, 1862) (Crustacea, Anomura, Porcellanidae). ZooKeys 516: 95-108. https://doi.org/10.3897/zookeys.516.9923
Figure 2 - Petrolisthes inermis (Heller, 1862). Dorsal (A) and ventral (B) views of female RMNH.CRUS.D.56417, Ambon, Indonesia. Scale bar - 5 mm.
Figure 3 from: Werding B, Hiller A (2015) Description of a new species of Petrolisthes in the Indo-West Pacific with a redefinition of P. hastatus Stimpson, 1858 and resurrection of P. inermis (Heller, 1862) (Crustacea, Anomura, Porcellanidae). ZooKeys 516: 95-108. https://doi.org/10.3897/zookeys.516.9923
Figure 3 - Petrolisthes elegantissimus sp. n. Dorsal (A) and ventral (B) views of paratype male RMNH.CRUS.D.56375, NW Guinea, Indonesia. Scale bar - 4 mm.
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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.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.