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275 results for “Form 1”
Figure 1. A in The limpet form in gastropods: evolution, distribution, and implications for the comparative study of history
Figure 1. A, external and internal views of Haliotis varia (Linnaeus, 1758) (Haliotidae), Kinabohutan, north-east Sulawesi, Indonesia; Vermeij collection. B, external and internal views of Cranopsis Dall, 1914 (Fissurellidae), off Iceberg Point, Lopez Island, Washington State, USA; Vermeij collection. C, external and internal views of Patelloidea saccharina (Linnaeus, 1758) (Lottiidae), Ngerdis Cove, Arakabesan, Palau; Vermeij collection. Note the strong radial ribs that extend beyond the shell margin. D, external and internal views of Concholepas concholepas (Lamarck, 1801) (Muricidae: Ralpaninaek), Montemar, Chile; Vermeij collection. E, external and internal views of Theodoxus vespertinus (Sowerby, 1849) (Neritidae), near the mouth of Wainiha River, Kauai, Hawaii; Vermeij collection. Note the internal septum and the wing-like sides of the limpet-like shell. F, external and internal views of Crepidula lessonii (Broderip, 1834) (Calyptraeidae), Playa Venado, Pacific coast of Panama; Vermeij collection. Note the internal septum, and the external sculpture of imbricated lamellae. G, external and internal views of Siphonaria gigas (Sowerby, 1825) (Siphonariidae), Playa de Panam� a, Pacific coast of Costa Riica; Vermeij collection. Note the convergence with Patelloida saccharina. H, external view of Delminiella soklici Kochansky-Devide & Sli� skovi� c, 1972, Vu� cipolje near Tomislavgrad, Bosnia and Herzegovina, late early Miocene. Holotype, stored in the National Museum of Bosnia and Herzegovina, Sarajevo (MG3631). Figured from Harzhauser et al. (2016), fig. 3A). Photograph provided by T. A. Neubauer. I, Valenciennius reussi (Neumayr in Neumayr & Paul, 1875), Tirol (=Konigsgnad), Romania, late Miocene (Pannonian). Specimen stored in the Natural History Museum Vienna (NHMW 1900/0009/0005). Photograph provided by T. A. Neubauer.
FIGURE 1 in A review of growth form and plant duration (life cycle) in Kalanchoe (Crassulaceae subfam. Kalanchooideae) in an evolutionary and classificatory framework
FIGURE 1. Kalanchoes are variously annual or perennial succulents that survive the dry season and droughts predominantly through accumulating water in their leaves. The small-shrubby Kalanchoe pumila is shown here. Photograph: Gideon F. Smith.
Figure 1 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 1. Species of the genus Petrarca (Thecostraca: Ascothoracida) endoparasitic in Turbinaria corals in Taiwan. A, globular galls (circled) formed by Petrarca on the surface of Turbinaria coral (modified after Kolbasov et al., 2021). B, gall formed by Petrarca on the coral surface. C, underneath the gall chipped off from coral shows two individuals of Petrarca goana (indicated by
Health Economic Analysis of Islet Cell Transplantation for the Stabilization of the Severe Forms of Type 1 Diabetes
ClinicalTrials.gov study NCT02854696. IPD Sharing: NO. Countries: 2. Publications: 5.
Ci-contre: Instantanés sur la biologie de quelques Cigales thaïlandaises 1, Cryptotympana aquila (Walker, 1850), mâle en train de s'alimenter (objectif de 100 mm, en cage). – 2, Cryptotympana mandarina Distant, 1891, femelle achevant sa métamorphose (objectif de 135 mm, in natura, 0 h 45). – 3, Meimuna durga (Distant, 1881); mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura, 14 h 15). – 4, Meimuna durga (Distant, 1881), mâle et femelle accouplés (objectif de 135 mm, in natura, 13 h 45). – 5, Pomponia linearis (Walker, 1850), mâle au repos (objectif de 135 mm, in natura, le matin, vers 11 heures). – 6 et 7, Tanna ventriroseus n. sp., mâle cymbalisant (6); mâle s'alimentant (7); (objectif de 100 mm, en cage). – 8, Terpnosia nonusaprilis n. sp., mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura). – 9, Terpnosia nonpareil s n. sp., mâle et femelle accouplés (objectif de 300 mm, in natura, 11 h 55). – 10, Meimuna tavoyana (Distant, 1888), mâle; vue des 3/4 ventraux mettant en évidence la forme et l'écartement de ses opercules (objectif de 100 mm, en cage). – 11, Gaeana cheni Chou & Yao, 1985, mâle achevant de se métamorphoser (objectif de 135 mm, in natura, la nuit, 3 h 17). – 12, Gaeana cheni Chou & Yao, 1985, couple venant de chuter à terre (objectif de 135 mm, 14 h 35). – 13, Ambragaeana ambra Chou & Yao, 1985, mâle dans la phase finale de sa métamorphose, achevant de pigmenter sa livrée (objectif de 135 mm, in natura, au milieu d'une matinée ensoleillée). (Photographies Michel Boulard). in Éthologie sonore et statut acoustique de quelques Cigales thaïlandaises, incluant la description de deux espèces nouvelles (Hemiptera : Auchenorhyncha*, Cicadoidea, Cicadidae)
Ci-contre: Instantanés sur la biologie de quelques Cigales thaïlandaises 1, Cryptotympana aquila (Walker, 1850), mâle en train de s'alimenter (objectif de 100 mm, en cage). – 2, Cryptotympana mandarina Distant, 1891, femelle achevant sa métamorphose (objectif de 135 mm, in natura, 0 h 45). – 3, Meimuna durga (Distant, 1881); mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura, 14 h 15). – 4, Meimuna durga (Distant, 1881), mâle et femelle accouplés (objectif de 135 mm, in natura, 13 h 45). – 5, Pomponia linearis (Walker, 1850), mâle au repos (objectif de 135 mm, in natura, le matin, vers 11 heures). – 6 et 7, Tanna ventriroseus n. sp., mâle cymbalisant (6); mâle s'alimentant (7); (objectif de 100 mm, en cage). – 8, Terpnosia nonusaprilis n. sp., mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura). – 9, Terpnosia nonpareil s n. sp., mâle et femelle accouplés (objectif de 300 mm, in natura, 11 h 55). – 10, Meimuna tavoyana (Distant, 1888), mâle; vue des 3/4 ventraux mettant en évidence la forme et l'écartement de ses opercules (objectif de 100 mm, en cage). – 11, Gaeana cheni Chou & Yao, 1985, mâle achevant de se métamorphoser (objectif de 135 mm, in natura, la nuit, 3 h 17). – 12, Gaeana cheni Chou & Yao, 1985, couple venant de chuter à terre (objectif de 135 mm, 14 h 35). – 13, Ambragaeana ambra Chou & Yao, 1985, mâle dans la phase finale de sa métamorphose, achevant de pigmenter sa livrée (objectif de 135 mm, in natura, au milieu d'une matinée ensoleillée). (Photographies Michel Boulard).
Figure 1 from: Haelewaters D, De Kesel A (2020) Checklist of thallus-forming Laboulbeniomycetes from Belgium and the Netherlands, including Hesperomyces halyziae and Laboulbenia quarantenae spp. nov. MycoKeys 71: 23-86. https://doi.org/10.3897/mycokeys.71.53421
Figure 1 Maximum clade creditability tree of Hesperomyces isolates reconstructed from an ITS dataset, with H. coleomegillae as outgroup. The topology is the result of Bayesian inference performed with BEAST. For each node, ML BS (≥ 65) and Bayesian pp (≥ 0.7) are presented above/below the branch leading to that node. Hesperomyces virescens sensu lato is highlighted with light gray shading, isolates are color-coded by host; H. virescens sensu stricto and H. halyziae sp. nov. are highlighted with dark gray shading.
Figure 1 in Three new species of gall-forming psyllids (Hemiptera: Psylloidea) from Papua New Guinea, with new records and notes on related species
Figure 1. Adult Trioza incrustata Percy, sp. nov. (A) Forewing and hindwing (inset); (B, C) head and antenna; (D) clypeus; (E) proboscis; (F) thorax dorsum; (G) hind leg; (H) male terminalia; (I) paramere (inner surface); (J) distal aedeagus segment; (K) female terminalia; (L) ovipositor.
Figure 4 from: Logoyda L (2021) Novel HPLC-UV method for simultaneous determination of valsartan and atenolol in fixed dosage form; Study of green profile assessment. Pharmacia 68(1): 43-51. https://doi.org/10.3897/pharmacia.68.e53631
Figure 4 Chromatogram obtained using Shimadzu Nexera XR UPLC system and mobile phase 20% acetonitrile, 80% of 0.16% ammonium acetate and 0.2% of 1.5 M tetramethylammonium hydroxide (V/V), column Discovery C18 (4.6 mm i.d. × 150 mm, 5 μm) at 2 wavelengths 225 nm and 237 nm (first figure), with 3-D UV contour diagram extracted analytes UV spectra and peak purity (second figure).
Figure 6 from: Logoyda L (2021) Novel HPLC-UV method for simultaneous determination of valsartan and atenolol in fixed dosage form; Study of green profile assessment. Pharmacia 68(1): 43-51. https://doi.org/10.3897/pharmacia.68.e53631
Figure 6 Chromatogram obtained using final established, optimized and validated chromatographic method at wavelength 237 nm.
Supplementary material 1 from: Logoyda L (2021) Novel HPLC-UV method for simultaneous determination of valsartan and atenolol in fixed dosage form; Study of green profile assessment. Pharmacia 68(1): 43-51. https://doi.org/10.3897/pharmacia.68.e53631
Supplementary data
Figure 3 from: Logoyda L (2021) Novel HPLC-UV method for simultaneous determination of valsartan and atenolol in fixed dosage form; Study of green profile assessment. Pharmacia 68(1): 43-51. https://doi.org/10.3897/pharmacia.68.e53631
Figure 3 Elution profiles obtained for test samples prepared of Valsartan + Atenolol tablets (80 + 100) mg using mobile phases: a) 20% acetonitrile and 80% of 0.16% ammonium acetate (V/V); b) 20% acetonitrile, 80% of 0.16% ammonium acetate and 0.2 % of 1.5 M tetramethylammonium hydroxide (V/V). Chromatographic conditions: Shimadzu Nexera XR UPLC system, C18 chromatographic column Discovery C18 (4.6 mm i.d. × 150 mm, 5 μm), flow rate 1.0 mL/min, column temperature 30 °C.
Figure 5 from: Logoyda L (2021) Novel HPLC-UV method for simultaneous determination of valsartan and atenolol in fixed dosage form; Study of green profile assessment. Pharmacia 68(1): 43-51. https://doi.org/10.3897/pharmacia.68.e53631
Figure 5 Chromatogram obtained using final established, optimized and validated chromatographic method at wavelength 225 nm.
Figure 7 from: Piponski M, Balkanov T, Logoyda L (2021) Development and validation of a fast and simple HPLC method for the simultaneous determination of bisoprolol and enalapril in dosage form. Pharmacia 68(1): 69-77. https://doi.org/10.3897/pharmacia.68.e50919
Figure 7 Linearity illustrating chromatograms obtained using final established, optimized and validated chromatographic method, with 55% methanol. First peak is bisoprolol and second enalapril Dionex Ultimate 3000 UHPLC system.
Figure 6 from: Piponski M, Balkanov T, Logoyda L (2021) Development and validation of a fast and simple HPLC method for the simultaneous determination of bisoprolol and enalapril in dosage form. Pharmacia 68(1): 69-77. https://doi.org/10.3897/pharmacia.68.e50919
Figure 6 Chromatograms chracteristics obtained using final established optimized validated chromatographic method (upper run), compared with more reteaining with 10% less methanol (lower run), with their system suitabilitiy parameters,worked on Dionex Ultimate 3000 UHPLC system.
Figure 5 from: Piponski M, Balkanov T, Logoyda L (2021) Development and validation of a fast and simple HPLC method for the simultaneous determination of bisoprolol and enalapril in dosage form. Pharmacia 68(1): 69-77. https://doi.org/10.3897/pharmacia.68.e50919
Figure 5 Chromatogram obtained using Shimadzu Nexera XR UPLC system and mobile phase 50% metanol and 40% of 0.07% (V/V) perchloric acid, column Zorbax Rx C8 (4.6 mm i.d. × 250 mm, 5 μm), with 3-D UV contour diagram extracted ,analytes UV spectra and peak purity. First peak at about 6.1min is bisoprolol and peak at about 7.1min is enalapril.
Figure 3 from: Piponski M, Balkanov T, Logoyda L (2021) Development and validation of a fast and simple HPLC method for the simultaneous determination of bisoprolol and enalapril in dosage form. Pharmacia 68(1): 69-77. https://doi.org/10.3897/pharmacia.68.e50919
Figure 3 Elution profiles obtained for test samples prepared of bisoprolol+ enalapril tablets (10 + 10) mg using three different mobile phases: a) 55% metanol and 45% of 0.07% (V/V) perchloric acid; b) 40% metanol and 10% acetonitrile and 50% of 0.07% (V/V) perchloric acid; and c) 50% metanol and 50% of 0.07% (V/V) perchloric acid. First peak is bisoprolol and second enalapril. Chromatographic conditions: Shimadzu Nexera XR UPLC system, C-8 column Zorbax Rx (4.6 mm i.d. X 250 mm, 5 μm), flow rate 1.0 mL/min, column temperature 42 °C, injection volume 10 μL.
Figure 4 from: Piponski M, Balkanov T, Logoyda L (2021) Development and validation of a fast and simple HPLC method for the simultaneous determination of bisoprolol and enalapril in dosage form. Pharmacia 68(1): 69-77. https://doi.org/10.3897/pharmacia.68.e50919
Figure 4 Chromatogram obtained using Shimadzu Nexera XR UPLC system and mobile phase 55% metanol and 45% of 0.07% (V/V) perchloric acid, column Zorbax Rx C8 (4.6 mm i.d. × 250 mm, 5 μm), with 3-D UV contour diagram extracted, analytes UV spectra and peak purity. First peak at about 4.7min is bisoprolol and peak at about 5.2min is enalapril.
Figure 8 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 8 Photographs of Talonostrea salpinx sp. nov. beds and reefs from Al-Bakri et al. 1985A–C reefs and beds in Khor Al-Subiyah D oyster field at Al-Memlahah, south-eastern end of Kuwait Bay.
Figure 7 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 7 Anatomy of Talonostrea salpinx sp. nov. A gross view after removal of upper (right) valve B gross view including route of alimentary canal after removal of ctenidia, gonad and digestive diverticula C mantle edge D rectum and anus E excised labial palp F portion of ctenidium showing fine structures. Abbreviation: am, adductor muscle; an, anus; cp, ciliated pad; ct, ctenidium; ct/m, ctenidium mantle edge junction; hg, hind gut; hg loop, hind gut loop behind stomach; imf, inner mantle fold; ljct, longitudinal junction; lp, labial palp; me, mantle edge; mg, mid gut; mmf, middle mantle fold; mt, mantle; oe,oesophagus; og, oral groove; pc, pericardium; r, rectum; rods, ctenidial filaments; s, stomach; ss, style sac; tjct, transverse junction; vm, visceral mass.
Figure 6 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 6 Talonostrea salpinx sp. nov. shells from Umm Al-Namil A, B external and internal views of a shell with marginal fluted spines, Paratypes NMW.Z.2021.009.006/ C, D Paratypes, NMW.Z.2021.009.006/2–3, shells of differing colours and lacking marginal fluted spines E clump of shells some with fluted spines associated with the tubeworm Spirobranchus kraussi (Baird, 1864) and the barnacle Amphibalanus amphitrite (Darwin, 1854). F, rock encrusted with irregular shaped shells mostly lacking fluted spines.
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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)
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.