Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
72
datasets available to search
ShareScore release 0.9.0
Dataset results
72 results for “spore morphology”
Fig. 1 in Spore Dimorphism in Nosema pyrausta (Microsporidia, Nosematidae): from Morphological Evidence to Molecular Genetic Verification
Fig. 1. DAPI fluorescence (A, С) and Nomarski contrast (B, D) of monokaryotic (A, B) and diplokaryotic (C, D) spores of microsporidia detected in Ostrinia nubilalis larvae. Arrows and double arrows indicate single nuclei and diplokarya, respectively. Scale bar = 4 µm.
Fig. 6. Spore morphology. A. S. kurzii megaspores from W.M in Selaginella subvaginata (Selaginellaceae), a new spikemoss from China
Fig. 6. Spore morphology. A. S. kurzii megaspores from W.M. Chu et al. 15682 (PE), B. S. kurzii microspores from W.M. Chu et al. 15682 (PE), C. S. repanda megaspores from K.H. Shing 06679 (PE01563529), D. S. repanda microspores from Y.M. Shui 139035 (PE00452047), E. S. subvaginata megaspores from Nanshuibeidiao Team 4374 (PE), F. S. repanda microspores from Nanshuibeidiao Team 4374 (PE), G. S. vaginata megaspores from X.C. Zhang. 0777 (PE00452208), H. S. vaginata microspores (30/30 μm) from X.C. Zhang 2250 (PE00452230). Scale bars = 200 μm (A and G), 100 μm (C and E), 30 μm (proximal in B, D, H, and distal in F), and 20 μm (distal in B, and proximal in F).
Text-fig. 5. Tumidopteris astra sp. nov., holotype GIN 4851/343h, morphology of sori. a, b: line tracing of the sorus; c: an isolated spore preserved on the sporangium. Scale 500 Μm (a, b), 20 Μm (c). in A New Species Of The Genus Tumidopteris Naugolnykh From The Permian Of The Pechora Cis-Urals, Russia
Text-fig. 5. Tumidopteris astra sp. nov., holotype GIN 4851/343h, morphology of sori. a, b: line tracing of the sorus; c: an isolated spore preserved on the sporangium. Scale 500 Μm (a, b), 20 Μm (c).
FIGURE. Coprolites preserved in an early Permian fern mesophyll. A, Gross morphology of a fragmentary fern frond, specimen PB23532. B, Basal part of a penultimate pinna showing sphenopteroid vegetative pinnules. C, Polished surface showing two sporangia with typical annulus structures (white arrowheads). D, SEM image showing an in situ trilete spore. E, The fertile pinnule which contains numerous coprolites along a transverse wound area. F, Enlargement showing coprolites filled with brown to black contents. G, SEM image of the same part in E. H, SEM image showing locally preserved epidermal cells and nearby coprolites. in Discovery of coprolites in an Early Permian fern mesophyll
FIGURE. Coprolites preserved in an early Permian fern mesophyll. A, Gross morphology of a fragmentary fern frond, specimen PB23532. B, Basal part of a penultimate pinna showing sphenopteroid vegetative pinnules. C, Polished surface showing two sporangia with typical annulus structures (white arrowheads). D, SEM image showing an in situ trilete spore. E, The fertile pinnule which contains numerous coprolites along a transverse wound area. F, Enlargement showing coprolites filled with brown to black contents. G, SEM image of the same part in E. H, SEM image showing locally preserved epidermal cells and nearby coprolites.
Supplementary material 3 from: Ordynets A, Scherf D, Pansegrau F, Denecke J, Lysenko L, Larsson K-H, Langer E (2018) Short-spored Subulicystidium (Trechisporales, Basidiomycota): high morphological diversity and only partly clear species boundaries. MycoKeys 35: 41-99. https://doi.org/10.3897/mycokeys.35.25678
Basidiospore size ranges of 67 Subulicystidium specimens which were sequenced or represent important historical collections : Explanation note: For the parameters of basidiospore length (L), width (W) and length to width ratio (Q), the following values are presented: minimal value, 5% data quantile, mean, 95% data quantile and maximum. Minimum and maximum do not consider outliers which were found for some specimens in raw data (see Materials and methods for details of excluding outliers).
Supplementary material 2 from: Ordynets A, Scherf D, Pansegrau F, Denecke J, Lysenko L, Larsson K-H, Langer E (2018) Short-spored Subulicystidium (Trechisporales, Basidiomycota): high morphological diversity and only partly clear species boundaries. MycoKeys 35: 41-99. https://doi.org/10.3897/mycokeys.35.25678
Measurements of 2840 basidiospores from 67 Subulicystidium specimens which were sequenced or represent important historical collections : Explanation note: Each row contains data on length (L_sp), width (W_sp) and length to width ratio (Q_sp) of a single basidiospore and information on specimen and species from which the basidiospore was measured is provided in separate columns. Dataset does not contain outliers which were found for some specimens in raw data (see Materials and methods for details of excluding outliers). In the case of S. brachysporum, the capital "B" following epithet means morphological species concept following Boidin and Gilles (1988), while "T" means the species as described by Talbot (1958).
Supplementary material 1 from: Ordynets A, Scherf D, Pansegrau F, Denecke J, Lysenko L, Larsson K-H, Langer E (2018) Short-spored Subulicystidium (Trechisporales, Basidiomycota): high morphological diversity and only partly clear species boundaries. MycoKeys 35: 41-99. https://doi.org/10.3897/mycokeys.35.25678
Detailed data on 144 specimens of Subulicystidium used in the study : Explanation note: Specimens for which coordinates were available on herbarium labels or from field notes contain "gps" in the column "COORD_source". Specimens for which coordinates were estimated from the map web sources (see Materials and Methods) are marked with the word "map".
Supplementary material 4 from: Ordynets A, Scherf D, Pansegrau F, Denecke J, Lysenko L, Larsson K-H, Langer E (2018) Short-spored Subulicystidium (Trechisporales, Basidiomycota): high morphological diversity and only partly clear species boundaries. MycoKeys 35: 41-99. https://doi.org/10.3897/mycokeys.35.25678
Basidiospore size ranges of Subulicystidium species included in the study : Explanation note: Calculations are based on a set of 67 specimens which were sequenced or represent important historical collections. For the parameters of basidiospore length (L), width (W) and length to width ratio (Q), the following values are presented: minimal value, 5% data quantile, mean, 95% data quantile and maximum. Minimum and maximum do not consider outliers which were found for some specimens in raw data (see Materials and methods for details of excluding outliers). Calculations were provided separately for the type specimens (of S. meridense and S. nikau), as well as for the collection as S. boidinii LY 11247 which was used to propose "Subulicystidium allantosporum ad interim" (Boidin and Gilles 1988). In S. brachysporum, the capital "B" following epithet means morphological species concept following Boidin and Gilles (1988), while "T" means the species as described by Talbot (1958).
FIGURE 32. A–E in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 32. A–E. Spore morphology of Selaginella biformis (A–C. Megaspores, D–E. Microspores). F–I. S. davidii (F–G. Megaspores, H–I. Microspores). J–L. S. gebaueriana (J–L. Megaspore).—A, D, G, H. Proximal surfaces.—C, E, F, I, K. Distal surfaces.—J. Lateral surface.—B, L. Portions of proximal surface enlarged to show infrastructural detail. Scale bars = 100 µm (A, C, F, G, J & K), 50 µm (B), 20 µm (D, E, H & I), 10 µm (L).
FIGURE 33. A–F in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 33. A–F. Spore morphology of Selaginella gebaueriana (A–D. Megaspores, E–G. Microspores). G–L. S. moellendorffii (G–J. Megaspores, K–L. Microspores).—A, E, G. Proximal surfaces.—C, I. Distal surfaces.—H. Lateral surface.—F, K, L. Tetrads.—B, D, J. Portions of surfaces enlarged to show infrastructural detail (B, J. Proximal surfaces; D. Distal surface). Scale bars = 100 µm (A, C, G, H & I), 50 µm (B, J); 20 µm (E, F, K & L), 10 µm (D).
FIGURE 29. A–E in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 29. A–E. Spore morphology of Selaginella commutata (A–C. Megaspores, D–E. Microspores). F–L. S. frondosa (F–J. Megaspores, K–L. Microspores).—A, D, F, H, K. Proximal surfaces.—C, E, G, I. Distal surface.—L. Tetrad.—B, J. Portions of proximal surface enlarged to show infrastructural detail. Scale bars = 100 µm (A, C, F, G, H & I), 50 µm (B, J); 20 µm (D, E, K, L).
FIGURE 30. A–F in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 30. A–F. Spore morphology of Selaginella rolandi-principis (A–D. Megaspores, E–F. Microspores). G–L. S. superba (G–I. Megaspores, J–L. Microspores).—A, E, G, J. Proximal surfaces.—C, H, K. Distal surfaces.—I. Lateral surface.—F, L. Tetrads.—B, D. Portions of surfaces enlarged to show infrastructural detail (B. Proximal surface, D. Distal surface). Scale bars = 100 µm (A, C, G, H & I), 20 µm (E, F, J, K & L), 10 µm (B, D).
FIGURE 36. A–F in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 36. A–F. Spore morphology of Selaginella chuweimingii (A–D. Megaspores, E–F. Microspores). G–L. S. heterostachys (G–I. Megaspores, J–L. Microspores).—F, G, J, K. Proximal surfaces.—B, H, L. Distal surfaces.—A. Lateral surface.—E. Tetrad.—C, D, I. Portions of surfaces enlarged to show infrastructural detail (C. Proximal surface, D, Laesurae; I. Distal surface). Scale bars = 100 µm (A, B, G & H), 20 µm (E, F, J, K & L), 10 µm (C, D, I).
FIGURE 26. A–F in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 26. A–F. Spore morphology of Selaginella tricholada (A–D. Megaspores, E–F. Microspores). G–L. S. uncinata (G–J. Megaspores, K–L. Microspores).—A, F, G, K. Proximal surfaces.—C, E, I, L. Distal surfaces.—B, D, H, J. Portions of surfaces enlarged to show infrastructural detail (B, H. Proximal surfaces; D, J. Distal surfaces). Scale bars = 100 µm (A, C, G & I), 50 µm (H), 20 µm (E, F, K & L), 10 µm (B, D, J).
FIGURE 23. A–D in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 23. A–D. Spore morphology of Selaginella picta f. viridis (A–C. Megaspores, D. Microspore). E–H. S. picta f. picta (E–G. Megaspores, H. Microspore). I–L. S. delicatula (I–J. Megaspores, K–L. Microspores).—A, D, E, H, I, K. Proximal surfaces.—L. Distal surface.—B, C, F, G, J. Portions of proximal surface enlarged to show infrastructural detail. Scale bars = 100 µm (A, E, I); 50 µm (B, F), 20 µm (D, H, K & L), 10 µm (C, G, J).
FIGURE 27. A–F in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 27. A–F. Spore morphology of Selaginella willdenowii (A–D. Megaspores, E–G. Microspores). G–L. S. siamensis (G–J. Megaspores, K–L. Microspores).—D, E, G, K. Proximal surfaces.—C, F, L. Distal surfaces.—A, I. Lateral surfaces.—B, H, J. Portions of proximal surface enlarged to show infrastructural detail. Scale bars = 100 µm (A, C, D, G & I), 50 µm (B, H), 20 µm (E, F, K & L), 10 µm (J).
FIGURE 22. A–F in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 22. A–F. Spore morphology of Selaginella bisulcata (A–D. Megaspores, E–F. Microspores). G–L. S. pennata (G–J. Megaspores, K–L. Microspores).—A, F, G, K. Proximal surfaces.—C, E, J, L. Distal surfaces.—B, D, H, I. Portions of surfaces enlarged to show infrastructural detail (B, H, I. Proximal surfaces; D. Distal surface). Scale bars = 100 µm (A, C, G & J); 50 µm (B, H), 20 µm (E, F, K & L), 10 µm (D, I).
FIGURE 24. A–E in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 24. A–E. Spore morphology of Selaginella hainanensis (A–C. Megaspores, D–E. Microspores). F–L. S. helferi (F–J. Megaspores, K–L. Microspores).—A, D, F, K. Proximal surfaces.—B, E, I, L. Distal surfaces.—C, G, H, J. Portions of surfaces enlarged to show infrastructural detail (G, H. Proximal surfaces; C, J. Distal surfaces). Scale bars = 100 µm (A, B, F & I), 50 µm (G), 20 µm (D, E, K & L), 10 µm (C, H, J).
FIGURE 28. A–F in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 28. A–F. Spore morphology of Selaginella mairei (A–D. Megaspores, E–F. Microspores). G–L. S. decipiens (G–J. Megaspores. K–L. Microspores).—A, E, G, J, K. Proximal surfaces.—C, F, I, L. Distal surfaces.—B, D, H. Portions of surface enlarged to show infrastructural detail (B, H. Proximal surfaces; D. Distal surface). Scale bars = 100 µm (A, C, G, I & J), 50 µm (B, H), 20µm (E, F, K & L), 10µm (D).
FIGURE 18. A–F in Spore morphology of Selaginella (Selaginellaceae) from China and its systematic significance
FIGURE 18. A–F. Spore morphology of Selaginella effusa var. dulongjiangensis (A–D. Megaspores, E–F. Microspores). G–L. S. hengduanshanicola (G–I. Megaspores, J–L. Microspores).—A, E, G, J, K, L. Proximal surfaces.—B, F, I. Distal surfaces.—C, D, H. Portions of surfaces enlarged to show infrastructural detail (H. Proximal surface; C, D. Distal surfaces). Scale bars = 100 µm (A, B, G & I), 50 µm (C, H), 20 µm (E, F, J, K & L), 10 µm (D).
ScienceDex guides
Understand access before you commit
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.