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Text-fig. 50. Scanning electron microscope (SEM, a, b) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c–f) images of "Foveolate seed sp. 2"; Catefica locality, Portugal. a, b) Lateral (a) and apical (b) views of seed showing the coarsely foveolate surface; note the truncate apex and the slightly depressed hilar-micropylar region; c) Longitudinal section (volume rendering cut between orthoslices xz0740 and xz0840) through the middle of seed showing the truncate apex with slightly depressed hilar-micropylar region and basal rounded chalazal region; note thick outer integument (oi) composed of an exotesta of thickwalled palisade-like cells and a thin inner integument (ii); d, e, f) Transverse (d, orthoslice xy0800) and longitudinal sections (e, orthoslice xz1100, f, orthoslice yz0800) through seed hilar-micropylar region, showing the exotesta comprised of the thick-walled palisade-like cells of the outer integument (oi), small, thin-walled meso- endotestal cells of the outer integument (arrows) and thin inner integument (ii). Specimen, Catefica 153-S172332 (a–f). Scale bars = 300 Μm (a–f). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 50. Scanning electron microscope (SEM, a, b) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c–f) images of "Foveolate seed sp. 2"; Catefica locality, Portugal. a, b) Lateral (a) and apical (b) views of seed showing the coarsely foveolate surface; note the truncate apex and the slightly depressed hilar-micropylar region; c) Longitudinal section (volume rendering cut between orthoslices xz0740 and xz0840) through the middle of seed showing the truncate apex with slightly depressed hilar-micropylar region and basal rounded chalazal region; note thick outer integument (oi) composed of an exotesta of thickwalled palisade-like cells and a thin inner integument (ii); d, e, f) Transverse (d, orthoslice xy0800) and longitudinal sections (e, orthoslice xz1100, f, orthoslice yz0800) through seed hilar-micropylar region, showing the exotesta comprised of the thick-walled palisade-like cells of the outer integument (oi), small, thin-walled meso- endotestal cells of the outer integument (arrows) and thin inner integument (ii). Specimen, Catefica 153-S172332 (a–f). Scale bars = 300 Μm (a–f).
Text-fig. 48. Scanning electron microscope (SEM, a, b, d–i) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c) images of "One-seeded fruit sp. 2" (a–c), "Unassigned, unnamed fruits" (d–f), Pazliopsis sp. (g, h) and "Follicular fruit with exotestal seeds" (i); Catefica locality, Portugal. a) Lateral view of fruit showing remains of tepals (te) and a single stamen (st); b) Detail of fruit surface showing short, scale-like, peltate trichomes (arrows); c) Transverse section (orthoslice xy0475) of fruit containing a single seed showing tepals (te) and fruit surface with peltate trichomes (arrow); note partial preservation of internal nutritive tissue; d) Fruit in lateral view showing the almost smooth epidermis with scattered openings; e) Detail of fruit surface from (d) showing the scattered openings in the epidermis interpreted as burst secretory cells (arrows); f) Dorsi-ventral view of tiny fruit with an irregular surface; g) Lateral view of exotestal seed assigned to cf. Pazliopsis sp.; h) Detail of fruit surface of seed in (g) showing faint facets of outer palisade layer with fine jigsaw-puzzle outlines of the anticlinal walls; i) Lateral view of fragmentary follicular fruit showing two exposed exotestal seeds. Specimens, Catefica 153-S174314 (a–c), Catefica 50-S170420 (d, e), Catefica 152-S174300 (f), Catefica 49-S172319 (g, h), Catefica MM158-P0272 (i). Scale bars = 300 Μm (a, c, d, f, g, i), 100 Μm (e), 50 Μm (b, h). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 48. Scanning electron microscope (SEM, a, b, d–i) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c) images of "One-seeded fruit sp. 2" (a–c), "Unassigned, unnamed fruits" (d–f), Pazliopsis sp. (g, h) and "Follicular fruit with exotestal seeds" (i); Catefica locality, Portugal. a) Lateral view of fruit showing remains of tepals (te) and a single stamen (st); b) Detail of fruit surface showing short, scale-like, peltate trichomes (arrows); c) Transverse section (orthoslice xy0475) of fruit containing a single seed showing tepals (te) and fruit surface with peltate trichomes (arrow); note partial preservation of internal nutritive tissue; d) Fruit in lateral view showing the almost smooth epidermis with scattered openings; e) Detail of fruit surface from (d) showing the scattered openings in the epidermis interpreted as burst secretory cells (arrows); f) Dorsi-ventral view of tiny fruit with an irregular surface; g) Lateral view of exotestal seed assigned to cf. Pazliopsis sp.; h) Detail of fruit surface of seed in (g) showing faint facets of outer palisade layer with fine jigsaw-puzzle outlines of the anticlinal walls; i) Lateral view of fragmentary follicular fruit showing two exposed exotestal seeds. Specimens, Catefica 153-S174314 (a–c), Catefica 50-S170420 (d, e), Catefica 152-S174300 (f), Catefica 49-S172319 (g, h), Catefica MM158-P0272 (i). Scale bars = 300 Μm (a, c, d, f, g, i), 100 Μm (e), 50 Μm (b, h).
Text-fig. 43. Synchrotron radiation X-ray tomographic microscopy SRXTM images of "Tricarpellate flower sp. 2"; Catefica locality, Portugal. a) Lateral view of floral structure (volume rendering) showing the apical projection of the carpels and the semiinferior organization; b) Apical view of floral structure (volume rendering) showing the triangular shape of the hypanthial rim, the tricarpellate ovary with a single apical style; note that one locule is fully developed while the other two are collapsed; note also slits of unknown nature in the corners of the triangular hypanthial rim (arrows); c) Transverse section (orthoslice xy0712) close to the floral apex showing the locule of the one fully developed carpel with ovules borne along ventral placentae; note amorphous substance (asterisk) associated with the developing ovules that fills part of the locule space; d) Longitudinal section (orthoslice xz0858) through the locule of the one fully developed carpel showing the semi-inferior organization and ovules arranged along the full length of the carpel; note amorphous substance (asterisk) associated with the developing ovules that fills part of the locule space; e) Tangential longitudinal section (orthoslice yz1019) through the one fully developed locule, showing the densely packed ovules and the amorphous substance (asterisk) with which they are associated. Specimen, Catefica 50-S174901 (a–e). Scale bars = 300 Μm (a–e). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 43. Synchrotron radiation X-ray tomographic microscopy SRXTM images of "Tricarpellate flower sp. 2"; Catefica locality, Portugal. a) Lateral view of floral structure (volume rendering) showing the apical projection of the carpels and the semiinferior organization; b) Apical view of floral structure (volume rendering) showing the triangular shape of the hypanthial rim, the tricarpellate ovary with a single apical style; note that one locule is fully developed while the other two are collapsed; note also slits of unknown nature in the corners of the triangular hypanthial rim (arrows); c) Transverse section (orthoslice xy0712) close to the floral apex showing the locule of the one fully developed carpel with ovules borne along ventral placentae; note amorphous substance (asterisk) associated with the developing ovules that fills part of the locule space; d) Longitudinal section (orthoslice xz0858) through the locule of the one fully developed carpel showing the semi-inferior organization and ovules arranged along the full length of the carpel; note amorphous substance (asterisk) associated with the developing ovules that fills part of the locule space; e) Tangential longitudinal section (orthoslice yz1019) through the one fully developed locule, showing the densely packed ovules and the amorphous substance (asterisk) with which they are associated. Specimen, Catefica 50-S174901 (a–e). Scale bars = 300 Μm (a–e).
Text-fig. 11. Scanning electron microscope (SEM) images of isolated "Stamen fragment with Clavatipollenites-type pollen sp. 2"; Catefica locality, Portugal. a) Fragment of tetrasporangiate stamen with pollen in situ; b) Detail from stamen fragment showing distal and proximal surfaces of in situ pollen grains; c) Pollen grain in distal view showing short colpus with irregular margin and aperture membrane covered by irregular verrucae; d) Detail of pollen wall showing tiny spherical orbicules; e) Detail of pollen wall showing the semitectate-reticulate tectum and long, scattered columellae supporting the narrow muri with finely verrucate supratectal ornamentation. Specimen, Catefica 50-S170389 (a–e). Scale bars = 600 Μm (a), 20 Μm (b), 6 Μm (c), 3 Μm (d), 1.5 Μm (e). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 11. Scanning electron microscope (SEM) images of isolated "Stamen fragment with Clavatipollenites-type pollen sp. 2"; Catefica locality, Portugal. a) Fragment of tetrasporangiate stamen with pollen in situ; b) Detail from stamen fragment showing distal and proximal surfaces of in situ pollen grains; c) Pollen grain in distal view showing short colpus with irregular margin and aperture membrane covered by irregular verrucae; d) Detail of pollen wall showing tiny spherical orbicules; e) Detail of pollen wall showing the semitectate-reticulate tectum and long, scattered columellae supporting the narrow muri with finely verrucate supratectal ornamentation. Specimen, Catefica 50-S170389 (a–e). Scale bars = 600 Μm (a), 20 Μm (b), 6 Μm (c), 3 Μm (d), 1.5 Μm (e).
Text-fig. 2. Scanning electron microscope (SEM, a, c–f) and synchrotron radiation X-ray tomographic microscopy (SRXTM, b, g) images of the flower of Mugideiriflora portugallica (a, b) and fruits, seeds and pollen of Canrightia resinifera (c–g); Catefica locality, Portugal. a) Oblique, apical view of flower showing multiparted organization with numerous laminar tepals, stamens that are rhomboidal and flattened in transverse section and carpels that are borne on the short conical apex of the receptacle; b) Transverse section (orthoslice xy0800) through basal part of flower showing the elongate bases of the laminar tepals and the flattened rhomboidal bases of the stamens; c) Fruit in lateral view showing irregular surface resulting from the abundant resin bodies in the fruit and hypanthium wall, scars from stamens on the rim of the hypanthium (arrowheads) and the lobed apical stigmatic region (st); d) Broken fruit with one or two seeds missing but showing three pendant, orthotropous seeds with pointed micropylar regions (mi) and a finely pitted crystalliferous endotesta; note the remains of the apical vascular bundles (vb); e) Single seed isolated from a fruit showing two distinct bundles (vb) still attached apically to the chalazal region of the seed, the pointed micropyle (mi) and the finely pitted surface of the crystalliferous endotesta; f) Monocolpate pollen from stigmatic region of fruit showing the long colpus and coarse reticulum; g) Transverse section (orthoslice xy0705) through a fruit showing four seeds all with radially elongated endothelium cells formed from the inner epidermis of the tegmen (asterisks). Specimens, Catefica 150-S174254 (a, b), Catefica 49-S170377 (c), Catefica 49-S170372 (d), Catefica 50-S170401 (e), Catefica 50-S170404 (f), Catefica 50-S174906 (g). Scale bars = 300 Μm (a–e, g), 6 Μm (f). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 2. Scanning electron microscope (SEM, a, c–f) and synchrotron radiation X-ray tomographic microscopy (SRXTM, b, g) images of the flower of Mugideiriflora portugallica (a, b) and fruits, seeds and pollen of Canrightia resinifera (c–g); Catefica locality, Portugal. a) Oblique, apical view of flower showing multiparted organization with numerous laminar tepals, stamens that are rhomboidal and flattened in transverse section and carpels that are borne on the short conical apex of the receptacle; b) Transverse section (orthoslice xy0800) through basal part of flower showing the elongate bases of the laminar tepals and the flattened rhomboidal bases of the stamens; c) Fruit in lateral view showing irregular surface resulting from the abundant resin bodies in the fruit and hypanthium wall, scars from stamens on the rim of the hypanthium (arrowheads) and the lobed apical stigmatic region (st); d) Broken fruit with one or two seeds missing but showing three pendant, orthotropous seeds with pointed micropylar regions (mi) and a finely pitted crystalliferous endotesta; note the remains of the apical vascular bundles (vb); e) Single seed isolated from a fruit showing two distinct bundles (vb) still attached apically to the chalazal region of the seed, the pointed micropyle (mi) and the finely pitted surface of the crystalliferous endotesta; f) Monocolpate pollen from stigmatic region of fruit showing the long colpus and coarse reticulum; g) Transverse section (orthoslice xy0705) through a fruit showing four seeds all with radially elongated endothelium cells formed from the inner epidermis of the tegmen (asterisks). Specimens, Catefica 150-S174254 (a, b), Catefica 49-S170377 (c), Catefica 49-S170372 (d), Catefica 50-S170401 (e), Catefica 50-S170404 (f), Catefica 50-S174906 (g). Scale bars = 300 Μm (a–e, g), 6 Μm (f).
Text-fig. 2. Zamites pateri J.KVAČEK sp. nov.; Pecínov locality, holotype, No. NM-F 5185. a: Abaxial cuticle showing costal and intercostal zones, SEM micro-photograph, scale bar 100 µm. b: Abaxial cuticle, detail of syndetocheilic stoma, SEM microphotograph, scale bar 10 µm. c: Abaxial cuticle showing transversely oriented stomata, SEM micro-photograph, scale bar 50 µm. d: Abaxial cuticle, detail of syndetocheilic stoma showing ledges of guard cells, SEM micro-photograph, scale bar 10 µm. e: Abaxial cuticle showing costal ordinary cells seen from inside, SEM micro-photograph, scale bar 50 µm. f: External side of abaxial cuticle showing stoma sunken in a stomatal pit surrounded by papillae, SEM micro-photograph, scale bar 10 µm. g: External side of abaxial cuticle showing papillae, SEM micro-photograph, scale bar 100 µm. h: External side of abaxial cuticle showing detail of fused papillae, SEM micro-photograph, scale bar 10 µm. in New Species Of Zamites From The Cenomanian Of The Bohemian Cretaceous Basin
Text-fig. 2. Zamites pateri J.KVAČEK sp. nov.; Pecínov locality, holotype, No. NM-F 5185. a: Abaxial cuticle showing costal and intercostal zones, SEM micro-photograph, scale bar 100 µm. b: Abaxial cuticle, detail of syndetocheilic stoma, SEM microphotograph, scale bar 10 µm. c: Abaxial cuticle showing transversely oriented stomata, SEM micro-photograph, scale bar 50 µm. d: Abaxial cuticle, detail of syndetocheilic stoma showing ledges of guard cells, SEM micro-photograph, scale bar 10 µm. e: Abaxial cuticle showing costal ordinary cells seen from inside, SEM micro-photograph, scale bar 50 µm. f: External side of abaxial cuticle showing stoma sunken in a stomatal pit surrounded by papillae, SEM micro-photograph, scale bar 10 µm. g: External side of abaxial cuticle showing papillae, SEM micro-photograph, scale bar 100 µm. h: External side of abaxial cuticle showing detail of fused papillae, SEM micro-photograph, scale bar 10 µm.
Fig. 2. 50 in Revision of the Nearctic species of the Lasioglossum (Dialictus) gemmatum species complex (Hymenoptera: Halictidae)
Fig. 2. 50% majority-rule consensus tree of species of Lasioglossum Curtis, 1833 with enlarged tegulae and representatives of other major lineages, based on 654-bp COI sequences and 15 morphological characters. MCMC tree search was performed in MrBayes ver. 3.2.7 using a GTR+I+Γ4 model for the molecular data, gamma-distributed rate variation for the morphological data, partitioning by data type, two simultaneous runs with 8 chains each, temperature of 0.0375, 20 000 000 generations, and L. sordidum (Smith, 1853) set as the outgroup (other settings program defaults). Node labels are posterior probabilities. Taxa names are followed by their BOLD accession numbers. Bold branches on the tree are species with enlarged tegulae.
Fig. 2. 50 in Two new chasmophytic species of Silene (Caryophyllaceae, sect. Siphonomorpha) from Iran
Fig. 2. 50% majority-rule consensus tree obtained from the Bayesian inference analysis of the cpDNA rps16 sequences in selected species of Silene L. Posterior probabilities (PP) ≥ 0.70 are shown above the branches and Maximum likelihood bootstrap (MLB) values ≥ 70% below. Accessions newly sequenced are indicated by a star. Accessions of S. ruprechtii Schischk. (MN460318 and MN460319) are misidentified by Bahmani et al. (2020).
Fig. 2. Maximum Likelihood species tree from the concatenated 50 in Ultraconserved elements-based phylogenomic systematics of the snake superfamily Elapoidea, with the description of a new Afro-Asian family
Fig. 2. Maximum Likelihood species tree from the concatenated 50 % complete dataset consisting of 4561 loci. Values on the branch indicate Shimodaira Hasegawalike approximate likelihood ratio test and ultrafast bootstrap. Abbreviations as in Fig. 1.
Abb. 2 in Schwarzgefleckter Ameisenbläuling Phengaris (Maculinea) arion (Linnaeus, 1758) (Lepidoptera: Lycaenidae) - Wiederfund im Kanton Zürich nach über 50 Jahren
Abb. 2. Fundort von Phengaris (Maculinea) arion (Linnaeus, 1758) auf einer Extensivweide unterhalb des Schnebelhorns (Fischenthal, ZH) auf 1150 m ü. M. (Foto J. Schlegel)
Fig. 2. Map showing all the 50 in Atlas of European millipedes 2: Order Julida (Class Diplopoda)
Fig. 2. Map showing all the 50 km squares which provided records included in this volume.
Figure 2. - Bayesian (GTR+Γ+I and HKY+Γ models) and maximum likelihood 50% majority-rule consensus tree. Numbers in the nodes represent posterior probabilities (GTR+Γ+I and HKY+Γ, respectively), and bootstrap value for maximum likelihood and parsimony analyses, respectively. c1–Bragança, Pará; c2–Santa Maria do Pará, Pará; c3–National Forest of Amapá, Amapá; c4–Belém, Pará; i1–Solimões River, near Manaus, Amazonas; i2–Xingu River, Altamira, Pará; i3 and i4–Itacoatiara, Amazonas. MYBP–million years before present.
Figure 2. - Bayesian (GTR+Γ+I and HKY+Γ models) and maximum likelihood 50% majority-rule consensus tree. Numbers in the nodes represent posterior probabilities (GTR+Γ+I and HKY+Γ, respectively), and bootstrap value for maximum likelihood and parsimony analyses, respectively. c1–Bragança, Pará; c2–Santa Maria do Pará, Pará; c3–National Forest of Amapá, Amapá; c4–Belém, Pará; i1–Solimões River, near Manaus, Amazonas; i2–Xingu River, Altamira, Pará; i3 and i4–Itacoatiara, Amazonas. MYBP–million years before present.
Data for high-clay content submarine slope failure flume experiments. Experiment 50% clay, static 2, part 3.
<p>These video and photographic data support the following manuscripts:</p><p>Silver, M.M.W., Dugan, B., 2020, The influence of clay content on submarine slope failure: insights from laboratory experiments and numerical models, Geological Society of London, Special Publications, 500, 301-309, <a href="https://doi.org/10.1144/SP500-2019-186">https://doi.org/10.1144/SP500-2019-186</a>. </p><p>Silver, M.M.W., Dugan, B., 2023, Cohesion, permeability, and slope failure dynamics: implications for failure morphology and tsunamigenesis from benchtop flume experiments, Marine Geology, 462, <a href="https://doi.org/10.1016/j.margeo.2023.107079">https://doi.org/10.1016/j.margeo.2023.107079</a>.</p><p>Log sheets are included for each experiment file.</p>
Data for high-clay content submarine slope failure flume experiments. Experiment 50% clay, static 2, part 2.
<p>These video and photographic data support the following manuscripts:</p><p>Silver, M.M.W., Dugan, B., 2020, The influence of clay content on submarine slope failure: insights from laboratory experiments and numerical models, Geological Society of London, Special Publications, 500, 301-309, <a href="https://doi.org/10.1144/SP500-2019-186">https://doi.org/10.1144/SP500-2019-186</a>. </p><p>Silver, M.M.W., Dugan, B., 2023, Cohesion, permeability, and slope failure dynamics: implications for failure morphology and tsunamigenesis from benchtop flume experiments, Marine Geology, 462, <a href="https://doi.org/10.1016/j.margeo.2023.107079">https://doi.org/10.1016/j.margeo.2023.107079</a>.</p><p>Log sheets are included for each experiment file.</p>
Data for high-clay content submarine slope failure flume experiments. Experiment 50% clay, static 3, part 2.
<p>These video and photographic data support the following manuscripts:</p><p>Silver, M.M.W., Dugan, B., 2020, The influence of clay content on submarine slope failure: insights from laboratory experiments and numerical models, Geological Society of London, Special Publications, 500, 301-309, <a href="https://doi.org/10.1144/SP500-2019-186">https://doi.org/10.1144/SP500-2019-186</a>. </p><p>Silver, M.M.W., Dugan, B., 2023, Cohesion, permeability, and slope failure dynamics: implications for failure morphology and tsunamigenesis from benchtop flume experiments, Marine Geology, 462, <a href="https://doi.org/10.1016/j.margeo.2023.107079">https://doi.org/10.1016/j.margeo.2023.107079</a>.</p><p>Log sheets are included for each experiment file.</p>
Data for high-clay content submarine slope failure flume experiments. Experiment 50% clay, static 2, part 1.
<p>These video and photographic data support the following manuscripts:</p><p>Silver, M.M.W., Dugan, B., 2020, The influence of clay content on submarine slope failure: insights from laboratory experiments and numerical models, Geological Society of London, Special Publications, 500, 301-309, <a href="https://doi.org/10.1144/SP500-2019-186">https://doi.org/10.1144/SP500-2019-186</a>. </p><p>Silver, M.M.W., Dugan, B., 2023, Cohesion, permeability, and slope failure dynamics: implications for failure morphology and tsunamigenesis from benchtop flume experiments, Marine Geology, 462, <a href="https://doi.org/10.1016/j.margeo.2023.107079">https://doi.org/10.1016/j.margeo.2023.107079</a>.</p><p>Log sheets are included for each experiment file.</p>
A Study of mRNA-1083 (SARS-CoV-2 and Influenza) Vaccine in Healthy Adult Participants, ≥50 Years of Age
ClinicalTrials.gov study NCT06097273. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Figures 50-57. Panthea male genitalia 50. P in Revision of the New World Panthea Hübner (Lepidoptera, Noctuidae) with descriptions of 5 new species and 2 new subspecies
Figures 50-57. Panthea male genitalia 50. P. virginarius, Josephine Co. OR., USA; 51. P. virginarius Wyoming variant, Lincoln Co., WY., USA; 52. P. acronyctoides nigra, Albany Co., WY, USA; 53. P. a. acronyctoides, Steuben, ME, USA; 54. P. furcilla furcilla, Norfolk Co., MA., USA; 55. P. furcilla australis, Whitfield Co., GA. USA; 56. Panthea f. furcilla - f. australis intermediate specimens, showing variation in size of basal cornuti; a. P.G. Co., MD; b, c. Owsley Co., KY; d. Elko Co., PA. 57. P. greyi. Coconino Co., AZ, USA.
FIGURE 2. Smoothed species accumulation curves for Paraguayan ants, generated over 50 in A catalogue of the ants of Paraguay (Hymenoptera: Formicidae)
FIGURE 2. Smoothed species accumulation curves for Paraguayan ants, generated over 50 sampling iterations on 3,912 randomized species records.
FIGURE 2. Maximum parsimony phylogenetic hypothesis. Heuristic search with 50 in Description of a new annual rivulid killifish genus from Venezuela
FIGURE 2. Maximum parsimony phylogenetic hypothesis. Heuristic search with 50 random additions and TBR branch swapping resulted in a single most parsimonious topology of 6206 steps. Numbers above nodes are bootstrap values based on 2000 pseudoreplicates (25 random additions each); only values over 50 are reported. Numbers below branches are Bremer support indices which are equivalent to unreversed synapomorphies.
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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
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International Brain Laboratory public data
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OpenNeuro
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