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1,840 results for “Representative”
Replication package for: Looming Large or Seeming Small? Attitudes Towards Losses in a Representative Sample
<p>This package contains data and replication files to reproduce the results from "Looming Large or Seeming Small? Attitudes Towards Losses in a Representative Sample" by Chapman, Snowberg, Wang, and Camerer, to be published in the Review of Economic Studies. This includes 6 original survey datasets (3 general population studies, two student studies, and an expert survey), matlab code to reproduce DOSE parameter estimates, and STATA code to produce the exhibits in the paper.<br><br></p>
FIGURES 27–32 in Achnanthidium petuniabuktianum sp. nov. (Achnanthidiaceae, Bacillariophyta), a new representative of the A. pyrenaicum group from Spitsbergen (Svalbard Archipelago, High Arctic)
FIGURES 27–32. Achnanthidium petuniabuktianum sp. nov. Light and scanning electron micrographs. All pictures taken from the type population (BR-4177). 27–28. SEM external views of an entire rapheless valve. 29. SEM internal view of an entire rapheless valve. 30. SEM detail of an external rapheless valve. 31. SEM detail of an internal rapheless valve. 32. SEM view showing a frustule in girdle view. Scale bars always 10 μm, except Figs 30–31 where scale bar is 1 μm.
FIGURES 2–26 in Achnanthidium petuniabuktianum sp. nov. (Achnanthidiaceae, Bacillariophyta), a new representative of the A. pyrenaicum group from Spitsbergen (Svalbard Archipelago, High Arctic)
FIGURES 2–26. Achnanthidium petuniabuktianum sp. nov. Light and scanning electron micrographs. All pictures taken from the type population (BR-4177). 1. LM view of a frustule in girdle view. 3–11. LM views of raphe valves. 12–19. LM views of rapheless valves. 20–22. SEM external views of an entire raphe valve. 23. SEM detail of the distal raphe ending of a raphe valve. 24. SEM detail of the internal raphe valve. 25–26. SEM internal views of an entire raphe valve. Scale bars always 10 μm, except Figs 23–24 where scale bar is 1 μm and Fig. 25 where scale bar is 5 μm.
FIGURE 6. A–F in A new species of Inocybe representing the Nothocybe lineage
FIGURE 6. A–F: Inocybe cutifracta (K(M)203101). A. Basidiomata; B. Basidiospores; C. Basidium; D. Cheilocystidia; E. Pileipellis. F. Stipitipellis. Scale bars: A = 10 mm; B–F = 10 μm. Photos by K.P. Deepna Latha.
FIGURE 3. A–C in A new species of Inocybe representing the Nothocybe lineage
FIGURE 3. A–C: SEM images of basidiospores of I. distincta (CAL 1310, holotype). Scale bars: A = 5 μm; B–C = 1 μm. Photos by K.P. Deepna Latha.
FIGURE 4. A combined nrLSU and RPB2 in A new species of Inocybe representing the Nothocybe lineage
FIGURE 4. A combined nrLSU and RPB2-sequence based phylogram generated from ML analysis showing the placement of Inocybe distincta within the Nothocybe clade. Except the Mallocybella clade, which was proposed as the genus Tubariomyces by Alvarado et al. (2010), all other clade nomenclature follows Matheny et al. (2009). Values at nodes indicate bootstrap support. BS values ≥50% are shown.
FIGURE 5. A–E in A new species of Inocybe representing the Nothocybe lineage
FIGURE 5. A–E: Inocybe cutifracta (K(M)203103, holotype). A. Basidiomata; B. Basidiospores; C. Cheilocystidia; D. Pileipellis. E. Stipitipellis. Scale bars: A = 10 mm; B–E = 10 μm. Photos by K.P. Deepna Latha
FIGURE 1. A–G in A new species of Inocybe representing the Nothocybe lineage
FIGURE 1. A–G: Inocybe distincta (CAL 1310, holotype). A. Basidiomata; B. Basidiospores; C. Basidium; D. Cheilocystidia; E. Pileipellis; F. Stipitipellis; G. Caulocystidia. Scale bars: A=10 mm; B–D, G=10 μm; E–F=100 μm. Photos by K.P. Deepna Latha.
FIGURE 2. A–E in A new species of Inocybe representing the Nothocybe lineage
FIGURE 2. A–E: Inocybe distincta (CAL 1310, holotype). A. Basidiomata; B. Basidiospores; C. Basidia; D. Cheilocystidia; E. Caulocystidia. Scale bars: A=10 mm; B–E=10 μm. Drawings by K.P. Deepna Latha.
FIGURE 44. Daviesia flava. A. Flowering branchlet. B. Inflorescence with calyces representing flowers. C. Pod. A–C in A monograph of Daviesia (Mirbelieae, Faboideae, Fabaceae)
FIGURE 44. Daviesia flava. A. Flowering branchlet. B. Inflorescence with calyces representing flowers. C. Pod. A–C from Wrigley & Telford NQ1490. Drawn by B-J. Osborne.
FIGURE 1. Diagnostic characters among the taxa studied. A−C in ×Polascontria (Cactaceae), a nothogenus that represents the gene flow between Escontria and Polaskia
FIGURE 1. Diagnostic characters among the taxa studied. A−C: fruits, D−F: flowers, G−I: areoles on the stems, J−L: ribs of stems (Escontria chiotilla in the first column, natural hybrids in the second one, P. chichipe in the third column). A. Fruits of E. chiotilla (triangular, largest and papiraceous bracts - white arrow). B. Fruits of hybrids [papiraceous, short and broad, but not triangular bracts (white arrow), and spines (yellow arrow)]. Hybrids form normal fruits with seeds (in the left). Some fruits are abortive and smaller in the same individual hybrid (in the right). C. Fruits of P. chichipe (spines - yellow arrow). D. Flowers of E. chiotilla (yellowish and with triangular and large papiraceous bracts forming tubular to funnel shape with not revolute tepals). E. Flowers of the hybrid (shorter bracts than those of E. chiotilla, tepals are scarce, creamy and not revolute, but are more extended than in E. chiotilla). F. Flowers of P.chichipe (with spines but not bracts and tepals revolute and yellowish-green coloured). G. The stem of natural hybrids is similar in color, branch number and areole shape to those of E. chiotilla (H) and P. chichipe (I). J. Each stem branch in E. chiotilla has seven ribs as those of hybrid individuals (K), whereas P. chichipe can have up to nine ribs (L).
FIGURE 5. A in ×Polascontria (Cactaceae), a nothogenus that represents the gene flow between Escontria and Polaskia
FIGURE 5. A. UPGMA dendrogram based on Jaccard´s similarity coefficient based on molecular markers: three major clusters are generated (E. chiotilla, P. chichipe and hybrids). B. UPGMA dendrogram obtained from DNA markers of hybrids based on Jaccard´s similarity coefficient: two main groups are formed (artificial hybrids, and natural hybrids).
FIGURE 4 in ×Polascontria (Cactaceae), a nothogenus that represents the gene flow between Escontria and Polaskia
FIGURE 4. PCoA scatter plots based on molecular markers: A. Distribution of Escontria chiotilla, Polaskia chichipe and the four natural hybrids. B. Analysis including the natural hybrids and the hybrid 1 progeny. E = E. chiotilla, P = P. chichipe, H = Hybrids.
FIGURE 6 in ×Polascontria (Cactaceae), a nothogenus that represents the gene flow between Escontria and Polaskia
FIGURE 6. Illustration of ×Polascontria huajuapensis. A. Plant habit. B. Branch. C. Branch in cross section. D. Areole. E. Bracts with areoles on fruits. F. Floral dissection. G. Flower (apical view). H. Bud flower with bracts. I. Fruit [drawing (from herbarium specimens: Cruz-González 1 (MEXU), vouchers 1025386, 1025387 1040183 (MEXU), and photographs by the authors)].
FIGURE 2 in ×Polascontria (Cactaceae), a nothogenus that represents the gene flow between Escontria and Polaskia
FIGURE 2. Pollen micromorphology of Polaskia chichipe, Escontria chiotilla and hybrids. A, D, G and J: E. chiotilla; B, E, H and K: hybrids; C, F, I and L: P. chichipe. A. Seeds of E. chiotilla (oval, black-brown and rugose seeds with smaller cells toward hilum forming a spanded border as those of hybrids). B‒C. Seeds of P. chichipe (oval, black-brown, but ruminate, with interstices cratered, the cells close hilum are smaller and form a spanded border around it). D. Cuticle of seeds in E. chiotilla [striate as in hybrids (E, top), although some hybrids produce some seeds with irregular striations on seed coat, specially forming cuticles thickness extended and hardly visible between cells walls, mainly on lateral regions (E, bottom)]. F. Cuticle in P. chichipe (striate). Pollen grains in E. chiotilla (G), hybrids (H, upper) and P. chichipe (I) (spheroidal, radiosymetric and tricolpate). The exine in all taxa is tectate, perforate and spinulose (J−L). The aperture membrane is granular (K). The hybrids produce several non-viable pollen grains that are empty and collapsed (H, in the bottom). Scales are: A, B and C=500 μm; D, E (in the top) and F=100 μm, E (in the bottom) =10 μm; G, H (in the top and in the bottom) and I= 10 μm; J, K and L= 1μm.
FIGURE 3. A in ×Polascontria (Cactaceae), a nothogenus that represents the gene flow between Escontria and Polaskia
FIGURE 3. A. PCA referred to Escontria chiotilla, Polaskia chichipe and natural hybrid. Variance accumulate on the first two axes = 68.86% (axis 1= 56.84%, axis 2 = 12.02%). E = E. chiotilla, P = P. chichipe, H = natural hybrids. B. UPGMA dendrogram based on Jaccard´s similarity coefficient. Asimilarity coefficient for the first two main clusters (E. chiotilla and P. chichipe/hybrid) is -0.51.
PLATE 8, Basidiocarps representing sect. Sicci ser. Haematocephali a in Biodiversity and phylogeny of Marasmius (Agaricales, Basidiomycota) from Madagascar
PLATE 8, Basidiocarps representing sect. Sicci ser. Haematocephali a) Marasmius haematocephalus (JES 202) b) Marasmius ferruginoides (JES 209) c) Marasmius hinnuleus (JES 217). Scale bar = 10 mm. Photography by D.S. Newman.
PLATE 6. Basidiocarps representing sect. Sicci ser. Atrorubentes a in Biodiversity and phylogeny of Marasmius (Agaricales, Basidiomycota) from Madagascar
PLATE 6. Basidiocarps representing sect. Sicci ser. Atrorubentes a) Marasmius corrugatiformis (JES 164) b) Marasmius katangensis (JES 227). Scale bar = 10 mm. Photography by D.S. Newman.
PLATE 4. Basidiocarps representing sect. Marasmius subsect. Sicciformes. a in Biodiversity and phylogeny of Marasmius (Agaricales, Basidiomycota) from Madagascar
PLATE 4. Basidiocarps representing sect. Marasmius subsect. Sicciformes. a) Marasmius madagascariensis (JES 225); sect. Globulares b) Marasmius bekolacongoli (Lockwood 2131638), photo generously donated by Taylor Lockwood. Scale bar = 10 mm (a); 20 mm (b). Photography by D.S. Newman.
PLATE 2. Basidiocarps representing sect. Marasmius subsect. Sicciformes a in Biodiversity and phylogeny of Marasmius (Agaricales, Basidiomycota) from Madagascar
PLATE 2. Basidiocarps representing sect. Marasmius subsect. Sicciformes a) Marasmius conicopapillatus (JES 180) b) Marasmius aff. curreyi (JES 135) c) Marasmius rubrobrunneus (JES 183). Scale bar = 5 mm (a); = 10 mm (b, c). Photography by D.S. Newman.
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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.