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.
1,084
datasets available to search
ShareScore release 0.9.0
Dataset results
1,084 results for “substrate”
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Seeing speech: The cerebral substrate of tickertape synesthesia
<p>We report the first functional MRI study of a tickertape synesthete. These synesthetes were described by Galton as "persons [who] see mentally in print every word that is uttered and they read them off usually as from a long imaginary strip of paper".</p> <p>Our synesthete and 35 other non-synesthetes controls were presented different auditory stimuli. We performed univariate and multivariate analysis, as dynamic causal modelling for the synesthete.</p>
Raw data for standardization of phenolic substrate for serum phenoloxidase from the grub of Oryctes rhinoceros
<p>The raw data consists of absorption maxima and time course of phenoloxidase activity of serum tested with each phenolic substrate.</p>
FIGURE 8 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 8. Dorsal views of hypopygia. A–D Larva living in Nostoc. B, C adapted from Willis W. Wirth (1957). D adapted from Ashe & Murray (1980). E, F adapted from Sasa M. & Kikuchi M. (1995). Bars: 50 µm.
FIGURE 7 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 7. Left two drawings: a tunnel made by Cricotopus nostocicola in a spherical colony of the cyanobacteria Nostoc parmelioides from Brock (1960). Right picture: Nostoc colony with larva found at Ashiu, Japan.
FIGURE 6. 3D in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 6. 3D computer tomography scan images of Nostoc colony with larva. The white dashed line encloses the larva.
FIGURE 1. A in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 1. A map of the collection sites (S1–S3) of Nostoc colonies symbiotic with chironomids. Information on the sites is listed in Table 1.
FIGURE 5 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 5. Cricotopus cataractaenostocicola sp. nov., larva and pupa. Larva (A–G), A and A': general appearance, B: dorsal view of head capsule, C: frontal view of head, D: larval left antenna, E: top of the head, F: anterior parapods, G: posterior parapods. Pupa, H, H' and H": general appearance. H' is a combination of three pictures, two dotted lines are borders. I: tergite IV from the side, J: tergite VII from the side, K: face. Photos C–F, H' and K were obtained by an electronic microscope. Abbreviations (larva). Ap: anterior parapods; As: anal seta; Pp: posterior parapods; Ta: anal tubules. Abbreviations (pupa). Al: anal lobe.
FIGURE 2 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 2. Landscapes of the habitats of the Nostoc colonies symbiotic with chironomids. Information on the sites is listed in Table 1.
FIGURE 4 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 4. Cricotopus cataractaenostocicola sp. nov. Adult male (A–G'), A: general appearance, B: antenna, C: thorax, D: hypopygium, E: eye, F: thorax and head, G, G', and G": right wing. Adult female (H–L), H and H': general appearance, I: head, J and J': genitalia, K: antenna. Abbreviations (adult). Al: alula; An: anal vein; Ap: anal point; Ce: cercus; Clw: craw, Cp: cibarial pump; Dc: dorsocentrals; Gc: gonocoxite; Gs: gonostylus; Hl: halter; Ivo: inferior volsella; La: labrum; Pm: palpal segments; Po: Postnotum; Sct: scutelium; Scu: scutum; Sq: squama.
FIGURE 3 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 3. Phylogeny based on the COI dataset. Information on the sequences used for this analysis is shown in Table 2.
Metabolite-induced in vivo fabrication of substrate-free organic bioelectronics
<p>Dataset accompanying paper: Metabolite-induced in vivo fabrication of substrate-free organic bioelectronics. </p> <p>Corresponding author: M. Berggren</p>
FIGURE. Dothiorella viticola on dead branch of Morus sp. (MFLU 19-0621). a, b. Conidiomata on host substrate. c. Vertical section through conidioma. d. Ostiole. e. Peridium of conidioma. f–j. Conidia attached to conidiogenous cells. k–m. Conidia. n. Germinating conidium. o, p. Colony on PDA (o upper, p lower). Scale bars: a = 1 mm, b = 100 μm, c = 50 μm, d = 20 μm, e–n = 10 μm. in Two new species of Botryosphaeriaceae (Botryosphaeriales) and new host/ geographical records
FIGURE. Dothiorella viticola on dead branch of Morus sp. (MFLU 19-0621). a, b. Conidiomata on host substrate. c. Vertical section through conidioma. d. Ostiole. e. Peridium of conidioma. f–j. Conidia attached to conidiogenous cells. k–m. Conidia. n. Germinating conidium. o, p. Colony on PDA (o upper, p lower). Scale bars: a = 1 mm, b = 100 μm, c = 50 μm, d = 20 μm, e–n = 10 μm.
FIGURE 9 in Taxonomy of calcareous sponges (Porifera, Calcarea) sampled on artificial substrates of a recreational marina in the Tropical Northeastern Brazilian coast
FIGURE 9. Spicules of Sycon avus sp. nov. (holotype, UFBA 4526-POR). A—Diactine; B—Triactine of the cones; C—Tubar triactine; D—Subatrial tetractine; E—Subatrial triactine; F—Atrial tetractine; G—Atrial triactine.
FIGURE 8 in Taxonomy of calcareous sponges (Porifera, Calcarea) sampled on artificial substrates of a recreational marina in the Tropical Northeastern Brazilian coast
FIGURE 8. Sycon avus sp. nov. (holotype, UFBA 4526-POR). A—Preserved specimen with preoscular membrane (arrowhead) and fringe of trichoxeas (arrow); B—Detail of the fringe with a basal ring of spicules (arrowhead); C—Transversal section showing the syconoid aquiferous system; D—Distal cones with diactines and triactines (arrowheads in detail); E— Choanocyte chambers with reproductive elements (*) and tubar skeleton formed by triactines (arrowheads); F—Atrial cavity with the apical actines of tetractines (arrowhead).
FIGURE 6 in Taxonomy of calcareous sponges (Porifera, Calcarea) sampled on artificial substrates of a recreational marina in the Tropical Northeastern Brazilian coast
FIGURE 6. Sycon bellum sp. nov. (holotype, UFBA 4527-POR). A—Preserved specimen with oscular membrane (arrowheads); B—Oscular membrane; C—Transversal section showing the syconoid aquiferous system (arrowhead highlighting the tufts of diactines); D—Detail of a distal cone with diactines and triactines (arrowhead); E—Triactine (arrowhead) of the tubar skeleton; F—Transversal section of the atrial skeleton and apical actines (in detail). at – atrium; dc – distal cone.
FIGURE 7 in Taxonomy of calcareous sponges (Porifera, Calcarea) sampled on artificial substrates of a recreational marina in the Tropical Northeastern Brazilian coast
FIGURE 7. Sycon bellum sp. nov. (holotype, UFBA 4527-POR). A—Diactine; B—Triactines of the distal cones; C—Tubar triactines; D—Subatrial triactine; E—Atrial triactine. F—Atrial tetractine.
FIGURE 4 in Taxonomy of calcareous sponges (Porifera, Calcarea) sampled on artificial substrates of a recreational marina in the Tropical Northeastern Brazilian coast
FIGURE 4. Paraleucilla incomposita (UFBA 4532-POR, except for B, C, and D—UFBA 4533-POR). A—Preserved specimen and oscular fringe (in detail); B—Cross section showing the layer with subcortical lacunae (*) and free of choanocyte chambers (black line). Embryos (arrow) can be observed; C—Longitudinal section with a general view of the skeletal organisation from the cortical (cx) to the atrial (at) regions; D—Detail of the outer region (OR) and inner region below that; E—Cross section showing a choanosomal canal (cc) with apical actines of tetractines close to the atrium (at); F—Cross section of the atrium (at) with apical actines of tetractines protruding into it.
FIGURE 5 in Taxonomy of calcareous sponges (Porifera, Calcarea) sampled on artificial substrates of a recreational marina in the Tropical Northeastern Brazilian coast
FIGURE 5. Paraleucilla incomposita (A–I: UFBA 4532-POR. J, K: UFBA 4246-POR holotype). A—Diactine; B—Cortical triactine; C—Cortical tetractine; D, D'—Subatrial tetractines I; E—Subatrial triactine; F—Subatrial tetractines II; G—Thin subatrial tetractine; H, H'—Atrial tetractines; I—Pentactine; J—Pentactine of the holotype; K—Tetractine of the holotype with displaced apical actine.
FIGURE 3 in Taxonomy of calcareous sponges (Porifera, Calcarea) sampled on artificial substrates of a recreational marina in the Tropical Northeastern Brazilian coast
FIGURE 3. Leucandra serrata (UFBA 4525-POR). A—Diactine; B—Jagged microdiactine; C—Cortical triactine; D— Choanosomal triactine; E—Tetractine of the canals; F—Atrial tetractine.
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.