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.
403
datasets available to search
ShareScore release 0.9.0
Dataset results
403 results for “morphological characteristics”
FIG. 2 in Analyses of morphological and molecular characteristics of Telotylenchinae from Iran point at the validity of the genera Bitylenchus and Sauertylenchus
FIG. 2. Photomicrographs of Bitylenchus parvus. Females (A–N). A: Pharynx; B–D: Head and stylet; E: Terminal bulb; F & G: Lateral field; H: Vulva; I: Spermatheca; J: Entire body; K–N: Tail. (Scale bars: A = 20 μm; J: = 100 μm; B–I & K–N = 10 μm); [ph = phasmid; s = spermatheca].
FIG. 5 in Analyses of morphological and molecular characteristics of Telotylenchinae from Iran point at the validity of the genera Bitylenchus and Sauertylenchus
FIG. 5. Photomicrographs of Tylenchorhynchus clarus. Females (A-–I). A: Pharynx; B &C: Head and stylet; D: Lateral field; E: Vulva and spermatheca; F: Entire body; G-–I: Tail. (Scale bars: A = 20 μm; F-–G = 100 μm; B-–E & H-–J = 10 μm); [a = anus].
FIG. 6 in Analyses of morphological and molecular characteristics of Telotylenchinae from Iran point at the validity of the genera Bitylenchus and Sauertylenchus
FIG. 6. Photomicrographs of Tylenchorhynchus microconus. Females (A–M). A: Pharynx; B–D: Head and stylet; E: Terminal bulb; F: Lateral field; G: Vulva; H: Spermatheca; I: Entire body; J–M: Tail. (Scale bars: A = 20 μm; I = 100 μm; B–H & J–M = 10 μm); [a = anus; ph = phasmid; s = spermatheca].
FIG 1 in Analyses of morphological and molecular characteristics of Telotylenchinae from Iran point at the validity of the genera Bitylenchus and Sauertylenchus
FIG 1. Photomicrographs of Bitylenchus dubius. Females (A–C, E–I & K–M) and males (D, J & N). A: Pharynx; B–D: Head and stylet. E: Terminal bulb; F: Lateral field; G: Vulva and fasciculi; H: Spermatheca; I & J: Entire body; K–N: Tail. (Scale bars: A = 20 μm; I–J =100 μm; B–H, K–N = 10 μm); [a = anus; ph = phasmid; s = spermatheca].
Global catalog of alluvial fans and other fan-shaped features on Mars, with morphology characteristics
<p>Alluvial fans on Mars record evidence of depositional environments that represent the final era of potential habitability on the Martian surface. Alluvial fan deposits can often look similar to deltaic or fluvial systems in visible remote sensing images but are firmed in depositional and climatic environments that are distinct from those that lead to other radial depositional features. In order to better constrain the regional and global depositional environments and further inform the analysis of the sedimentary history of Mars, this study expands the global catalog of alluvial fans on Mars by adding newly identified features and characterizing all new and previously identified features based on morphologic parameters. Based on how closely they fit the morphologic definition of alluvial fans, as established by terrestrial sedimentology, each feature is classified as either an alluvial fan or another depositional feature.</p> <p>The .csv files made available here contain the full global database of features investigated in the referenced paper (Mondro et al., 2022). Five different .csv files are included, divided according to feature classification category based on the morphological parameters described in Mondro, et al. 2022. The five classification categories are: alluvial fan, possible alluvial fan, non-alluvial radial feature (NARF), small feature, and non-fan.</p> <p>For each individual depositional feature, the database contains the lat/long location of the fan apex, a reference to the first publication to identify it, the results of the characterization parameters, and the final morphologic classifications. The characterization parameters are planform shape, radius (meters), average radial slope (degrees), adjusted average radial slope (degrees), and radial profile shape. When a parameter is listed as NA, the morphologic categorization for that class of feature did not include that specific parameter.</p> <p>See referenced paper for more detail on methodology and discussion of results:</p> <p><a href="https://www.sciencedirect.com/science/article/pii/S0019103522003311?via%3Dihub" rel="noopener">Mondro, C.A., J.E. Moersch, C.M. Fedo. An updated global survey of alluvial fans on Mars: Distinguishing alluvia fans from other fan-shaped features through morphologic characterization. <em>Icarus</em>, 398C. doi: 10.1016/j.icarus.2022.115238.</a></p> <p>Please reference the above paper when using this dataset.</p>
FIGURE 1. Characteristic pool zone for Lepidostoma abruptum Banks 1931 in Larval morphology, life cycle and nutritional values of Lepidostoma abruptum Banks 1931 (Trichoptera: Lepidostomatidae) from Lower-Hill Evergreen Forests of Southern Thailand
FIGURE 1. Characteristic pool zone for Lepidostoma abruptum Banks 1931at the study site in Tai Rom Yen National Park, Thailand.
Supplementary material 4 from: Ortiz-Rodriguez AE, Escobar-Castellanos MA, Pérez-Farrera MA (2016) Phylogenetic analyses and morphological characteristics support the description of a second species of Tridimeris (Annonaceae). PhytoKeys 74: 79-96. https://doi.org/10.3897/phytokeys.74.10371
Figure S4. The 50% majority-rule consensus tree from the Bayesian analysis of trnLF spacer : Explanation note: Numbers on branches of the major clades indicate Bayesian posterior probabilities (PP), maximum likelihood (MLBS) and parsimony (MPBS) bootstrap values in that order.
Supplementary material 1 from: Ortiz-Rodriguez AE, Escobar-Castellanos MA, Pérez-Farrera MA (2016) Phylogenetic analyses and morphological characteristics support the description of a second species of Tridimeris (Annonaceae). PhytoKeys 74: 79-96. https://doi.org/10.3897/phytokeys.74.10371
Figure S1. The 50% majority-rule consensus tree from the Bayesian analysis of rbcL coding region : Explanation note: Numbers on branches of the major clades indicate Bayesian posterior probabilities (PP), maximum likelihood (MLBS) and parsimony (MPBS) bootstrap values in that order.
Supplementary material 2 from: Ortiz-Rodriguez AE, Escobar-Castellanos MA, Pérez-Farrera MA (2016) Phylogenetic analyses and morphological characteristics support the description of a second species of Tridimeris (Annonaceae). PhytoKeys 74: 79-96. https://doi.org/10.3897/phytokeys.74.10371
Figure S2. The 50% majority-rule consensus tree from the Bayesian analysis of matK coding region : Explanation note: Numbers on branches of the major clades indicate Bayesian posterior probabilities (PP), maximum likelihood (MLBS) and parsimony (MPBS) bootstrap values in that order.
Supplementary material 3 from: Ortiz-Rodriguez AE, Escobar-Castellanos MA, Pérez-Farrera MA (2016) Phylogenetic analyses and morphological characteristics support the description of a second species of Tridimeris (Annonaceae). PhytoKeys 74: 79-96. https://doi.org/10.3897/phytokeys.74.10371
Figure S3. The 50% majority-rule consensus tree from the Bayesian analysis of ycf1 coding region : Explanation note: Numbers on branches of the major clades indicate Bayesian posterior probabilities (PP), maximum likelihood (MLBS) and parsimony (MPBS) bootstrap values in that order.
FIGURE 4 in Identification of Neoceratitis asiatica (Becker) (Diptera: Tephritidae) based on morphological characteristics and DNA barcode
FIGURE 4. Neighbour-joining (NJ) (a) and maximum likehood (ML) (b) phylogenetic trees developed from COI barcodes analysis. The number at each branch point is the percentage supported by bootstrap.
FIGURE 1 in Identification of Neoceratitis asiatica (Becker) (Diptera: Tephritidae) based on morphological characteristics and DNA barcode
FIGURE 1. Neoceratitis asiatica and its damage symptoms. (a) Mating of male and female in the field; (b) Damage of N. asiatica resulting in reduced quality of wolfberry; (c) one larva in one fruit and (d) pupae.
Fig. 2 Morphological characteristics. a Double broken infraorbital ridge IOR. b in Molecular identification and morphological characteristics of native and invasive Asian brush-clawed crabs (Crustacea: Brachyura) from Japanese and German coasts: Hemigrapsus penicillatus (De Haan, 1835) versus Hemigrapsus takanoi Asakura & Watanabe 2005
Fig. 2 Morphological characteristics. a Double broken infraorbital ridge IOR. b Symmetrically arranged spots on the dorsal face. c Male pleon fold down, first pleopods facing distal/ lateral (setae of the head around a scoop-like nose appears as dark area at the end of the pleopod). d Soft hair near the movable finger of a female chela (HtY2)
Fig. 6 a–g in Polyphyly of the grass tribe Hainardieae (Poaceae: Pooideae): identification of its different lineages based on molecular phylogenetics, including morphological and cytogenetic characteristics
Fig. 6 a–g Mitotic metaphase chromosomes. of a Deschampsia cespitosa (2n = 26). b Festuca gigantea 2n = 42. c Hainardia cylindrica 2n = 26. d Phleum phleoides (2n =14+ 2B). e Vulpia bromoides (2n = 14). f Koeleria cristata (2n = 56). g Colpodium versicolor (2n = 4)
Fig. 4 a–h in Polyphyly of the grass tribe Hainardieae (Poaceae: Pooideae): identification of its different lineages based on molecular phylogenetics, including morphological and cytogenetic characteristics
Fig. 4 a–h Spikelet details. Palea of a Hainardia cylindrica and b Parapholis incurva with glabrous keels (nerves). c, d florets of Narduroides salzmannii with glabrous callus of the lemmas and long rachilla internodes. e, f Agropyropsis lolium with glabrous callus of the lemma (e) and ciliolate keels of the palea (f). g, h Scribneria bolanderi with lemma awned from a sinus of the lemma tip (g) and hairy callus (h). The margin of the lemma is marked at one side in a, b, and f with arrows. Material used: a fruits from Göttingen Botanical Garden in 2006, no. 1850 (HAL); b Röser 2517 (HAL); c Hernández s.n. (C); d Rivas-Martínez s.n. (BASBG); e, f Cosson s.n. (JE); g, h Wilken 16163 and Painter (RSA 695253)
FIGURE 3 in A new corticioid fungus, Alloexidiopsis sinensis (Auriculariales, Basidiomycota), in China, evidenced by morphological characteristics and phylogenetic analyses
FIGURE 3. Basidiomata of Alloexidiopsis sinensis (A, B) CLZhao 7343 (holotype); (C, D) CLZhao 6775; (E, F) CLZhao 16935. Bars: A, C, E= 1 cm; B, D, F= 1 mm.
FIGURE 5 in A new corticioid fungus, Alloexidiopsis sinensis (Auriculariales, Basidiomycota), in China, evidenced by morphological characteristics and phylogenetic analyses
FIGURE 5. Sections of hymenium of Alloexidiopsis sinensis (holotype, CLZhao 7343). Scale bars: A, C, E = 20 μm; B, D, F = 10 μm, 10 × 100 Oil.
FIGURE 1 in A new corticioid fungus, Alloexidiopsis sinensis (Auriculariales, Basidiomycota), in China, evidenced by morphological characteristics and phylogenetic analyses
FIGURE 1. Maximum Parsimony strict consensus tree illustrating the Alloexidiopsis and related genera based on the combined ITS+nLSU sequences. Branches are labeled with Maximum Likelihood bootstrap values equal to or above 70%, Maximum Parsimony bootstrap values equal to or above 50% and Bayesian posterior probabilities equal to or above 0.95. The new species are in bold.
FIGURE 4 in A new corticioid fungus, Alloexidiopsis sinensis (Auriculariales, Basidiomycota), in China, evidenced by morphological characteristics and phylogenetic analyses
FIGURE 4. Microscopic structures of Alloexidiopsis sinensis (holotype, CLZhao 7343). (A) Basidiospores; (B) Basidia; (C) Basidioles; (D) Cystidia; (E) Hyphidia; (F) Part of the vertical section of hymenium. Bars: A–F = 10 μm.
FIGURE 2 in A new corticioid fungus, Alloexidiopsis sinensis (Auriculariales, Basidiomycota), in China, evidenced by morphological characteristics and phylogenetic analyses
FIGURE 2. Maximum Parsimony strict consensus tree illustrating the phylogeny of the new species Alloexidiopsis sinensis and related species in the genus Alloexidiopsis based on ITS sequences. Branches are labeled with Maximum Likelihood bootstrap values equal to or above 70%, Maximum Parsimony bootstrap values equal to or above 50% and Bayesian posterior probabilities equal to or above 0.95.
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.