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.
275
datasets available to search
ShareScore release 0.9.0
Dataset results
275 results for “Form 1”
Figure 1 in Seven new species of Night Frogs (Anura, Nyctibatrachidae) from the Western Ghats Biodiversity Hotspot of India, with remarkably high diversity of diminutive forms
Figure 1 Morphometric differentiation of species using the discriminant function analyses. (A) Projection on factor plane first and second explaining 79.1% of the variations among seven miniature-sized species. (B) Projection on factor plane first and second explaining 83.9% of the variations among five medium-sized species. (C) Projection on factor plane first and second explaining 86.3% of the variations among six large-sized species.
FIGURE 1 in A new species of habitat – forming Suberites (Porifera, Demospongiae, Suberitida) in the Benguela upwelling region (South Africa)
FIGURE 1. Locator map of study the area, with trawl stations (points) conducted during 2010/11 used to display the typical distribution of sampling.
FIGURE 1. A–D in A new Neotibicen cicada subspecies (Hemiptera: Cicadidae) from the southeastern USA forms hybrid zones with a widespread relative despite a divergent male calling song
FIGURE 1. A–D, Neotibicen similaris apalachicola, n. subsp., dorsal view, ventral view, pygofer ventral view, pygofer lateral view (holotype specimen 08.US.FL.TRA.03). E–H, N. similaris similaris, dorsal view, ventral view, pygofer ventral view, pygofer lateral view (specimen 08.US.GA.HAH.01). Scale bars = 12.5 mm.
FIGURE 1. Psychotria stolonifera. A, forming a in Additions to the rubiaceous flora of Papua New Guinea: Psychotria stolonifera and P. ternatifolia, two remarkable species from the Muller limestone
FIGURE 1. Psychotria stolonifera. A, forming a dense groundcover on limestone karst, stems 15–20 cm tall (Takeuchi et al. 24618A); B, blue scale bar with white lines marked in 1 cm increments.
FIGURE 1. Habitat and field form photographs. A–B in Obliquicauda longipens sp. nov. and Obliquicauda xianninga sp. nov.: two new species of foliicolous algae from China
FIGURE 1. Habitat and field form photographs. A–B: The studied leaf of Ficus pumila Linnaeus. C–E: Scanning electron microscopy photographs of the biofilm on the leaf. Scale bars: 20 μm.
Supplementary material 1 from: Marino de Remes Lenicov AM, Faltlhauser AC, Foieri A, Salinas NA, Hernández MC, Sosa AJ (2024) New morphological and biological contributions to adults and immature forms of Pissonotus paraguayensis (Fulgoromorpha, Delphacidae) in wetlands of Argentina. ZooKeys 1188: 227-250. https://doi.org/10.3897/zookeys.1188.113350
Graphical figures of Kaplan-Meier curves of Pissonotus paraguayensis males and female survival probability on different test plants
Fig. 1 in Increase in isoflavonoid content in Glycine max cells transformed by the constitutively active Ca independent form of the AtCPK1 gene
Fig. 1. The branch of phenylpropanoid pathway leading to flavonoids. PAL, phenylalanine ammonia-lyase; C4H, cinnamate 4-hydroxylase; CHS, chalkone synthase; CHR, chalkone reductase; CHI, chalkone isomerase; FN3H, flavanone 3-hydroxylase; IFS, isoflavone synthase; HID, 2-hydroxyisoflavanone dehydratase, IDT1, isoflavone dimethylallyltransferase 1; IDT2, isoflavone dimethylallyltransferase 2; C4DT, coumestrol 4-dimethylallyltransferase.
1. A natural fusion between a flavodiiron protein, rubredoxin and NADH:rubredoxin oxidoreductase is responsible for the H2O-forming oxidase activity in Trichomonas vaginalis
<p>Homology models fit to a 6.8Å cryo-EM map of <em>T. vaginalis</em> FDPF3.</p>
FIGURE 1. A in Anemone pindariensis (Ranunculaceae), most recently described from the western Himalaya in India, is a teratological form of A. rivularis
FIGURE 1. A metamorphosed flower (A: top view; B: lateral view) in Anemone rivularis from Gyirong county in southern Xizang, China. Photographed by You-Pai Zeng.
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM.
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).
FIGURE 1 in Description of a new species of Hamamelistes forming galls on Fothergilla spp (Hamamelidaceae) and the generic limits of Hormaphidini (Sternorrhyncha Aphididae: Hormaphidinae)
FIGURE 1. Galls of Hamamelistes blackmani sp. n. on Fothergilla. A. Fothergilla gardenii plant with multiple galls (fawnbrown, oblong, displacing seed pods) (Carteret Co., North Carolina USA). B - C, galls on F. milleri, Baldwin Co., Alabama USA. B. Cut gall showing aphids in the interior. C. Close-up of gall interior, with fundatrix (large oval), adult alate, and nymphs of several instars. Photo credits: Ron Miller (A, B); Lyle Buss (C).
FIGURES 1‒5 in Taxonomy of 'Euconnus complex'. Part XXIV. Intermediate forms between Psomophus, Eupentarius and Euconnus s. str. in the East Palaearctic fauna unify problematic subgenera (Coleoptera, Staphylinidae, Scydmaeninae)
FIGURES 1‒5. Euconnus chinensis Franz, holotype male. Dorsal habitus (1); aedeagus in ventral (2, 4) and lateral (3, 5) views.
FIGURES 1–9. Homalinotus depressus, last instar larva. 1 in First description of the larva and pupa of the coconut palm borer Homalinotus depressus (Linnaeus, 1758) (Coleoptera: Curculionidae: Molytinae) and a discussion about the terminology for immature forms
FIGURES 1–9. Homalinotus depressus, last instar larva. 1—mature larva (lateral view), 2—head capsule (frontal view), 3— antenna (lateral view), 4—antenna (frontal view), 5—clypeus and labrum, 6—epipharynx, 7—mandible (dorsal view), 8— maxillo-labial complex (ventral view), 9—spiracle. Legends [seta (ae) —s.]: AlA—alar area; als—anterolateral s.; amsanteromedian s.; Ant—antenna; CL—clipeus; cls—clypeal s.; des—dorsal epicranial s.; EPl— epipleuron; eps—epipleural s.; ES— epicranial suture; EuSt—eusternum; fs—frontal s.; FS—frontal suture; LbP—labial palp; les—lateral epicranial s.; Lmlabrum; LmR—labral rods; lms—labral s.; mds—mandibular s.; msp—median spines; MxP—maxillary palp; PdA—pedal area; pdas—pedal s.; pds—postdorsal s.; pes—posterior epicranial s.; Pl—pleurum; pms—postmental s.; PrMt—prementum; PrmS— premental sclerite; prns—pronotal s.;ps—pleural s.; Sp—spiracle; prs—prodorsal s.; ss—spiracular s.; ves—ventral epicranial s.
FIGURE 1 in Contributions to the study of gomphocerine grasshoppers calling songs (Orthoptera: Acrididae: Gomphocerinae) with notes on taxonomic status and distribution of some forms from Kyrgyzstan
FIGURE 1. Map of localities in Kyrgyzstan, where the specimens for signal recordings were collected. 1―Turkestan Mtn. Range, environs of Katran Village, the Layli Mazar River 2–3 km upstream from the source of the Lyaylyak River; 2―Northern shore of the Tortkul' Reservoir ca. 12 km West of Batken; 3― the West Tien Shan Mts., Chatkal Mtn. Range, Sary Chelek Nature Reserve, environs of Arkyt Village; 4― the Central Tien Shan Mts., the Kekemeren River Basin, the Western Karakol River ca. 10 km from the mouth (10 km East-North-East from Suusamyr Village); 5― the Central Tien Shan Mts., the Kekemeren River Gorge 8–9 km downstream from Kozhomkul Village; 6― the Central Tien Shan Mts., the Dzhumgal River Valley East of Chaek; 7―Southern shore of the Issyk-Kul' (Ysyk Köl) Lake, the mouth of the Tossor River (17 km East of Kaji Say); 8―Eastern shore of the Issyk-Kul' (Ysyk Köl) Lake, 20 km West from Mikhailovka Village.
Supplementary material 1 from: Zach P, Panigaj Ľ, Honěk A, Nedvěd O, Kulfan J, Martinková Z, Selyemová D, Viglášová S, Roy H (2014) The invasion history, distribution and colour pattern forms of the harlequin ladybird beetle Harmonia axyridis (Pall.) (Coleoptera, Coccinellidae) in Slovakia, Central Europe. ZooKeys 412: 89-102. https://doi.org/10.3897/zookeys.412.6587
Records of Harmonia axyridis in Slovakia: Explanation note: There are records from 2008 to 2012; years 2008 and 2009 marked in bold. The localities (sites of collection) are arranged in alphabetical order. Indicated are the numeric code of the mapping square (see Fig. 1), year of the first record and name of observer. Data on absence of the species are indicated by subsequent records of the species in the same squares or near squares from which it had not previously been recorded (e.g. 2008 – no record, 2009 – first record).
Figure 1 in 'Endless forms most beautiful': taxonomic revision of the planarian Geoplana vaginuloides (Darwin, 1844) and discovery of numerous congeners (Platyhelminthes: Tricladida)
Figure 1. Distribution map of the species of Geoplana addressed in this paper. Abbreviations for the Brazilian States are as follows: PR, Paraná; RJ, Rio de Janeiro; RS, Rio Grande do Sul; SC, Santa Catarina; SP, São Paulo.
FIGURES 1–8 in A new species of Schaefferia Absolon (Collembola: Hypogastruridae) from Chukotka, Russia, with remarks on the related forms
FIGURES 1–8. Schaefferia bermani sp. nov. (1–2, 5–8), S. czernovi (3) and S. cf. quinqueoculata (4): 1, dorsal chaetotaxy; 2, labial palp; 2a, labial papilla E, lateral view; 3, labial palp; 4, ibid; 5, maxillary head; 6–7, dens and mucro, different views; 8, unguis. Scales: Figs 1—0.1 mm, 2–8—0.01 mm.
FIGURE 1 in Redescription and phylogenetic placement of Cirrhilabrus sanguineus Cornic (Teleostei: Labridae), with first documentation of the female form
FIGURE 1. Cirrhilabrus sanguineus, freshly preserved male neotype, BPBM 24779, 66.5 mm SL, from Flic en Flac, off the western coast of Mauritius (top). Photo by J.E. Randall. Current neotype in preservation (below). Note broken rays in the dorsal, caudal, and anal fins. Photo by B.W. Frable.
FIGURE 1. Hybrid form Bythotrephes brevimanus x B in Morphological assessment of the North Eurasian interspecific hybrid forms of the genus Bythotrephes Leydig, 1860 (Crustacea: Cladocera: Cercopagididae)
FIGURE 1. Hybrid form Bythotrephes brevimanus x B. cederströmii, females (Rybinskoe Reservoir, Central European Russia). A, general lateral view. B, dorsal seta on proximal part of antennal basipodite. C, setae of distal end of first endopodital segment of tl I. D, E, the same of second endopodital segment of tl I. F, distal part of protopodites of tl II and tl III, outer view. G, apical setae of caudal process. H–R, caudal process and postabdominal and caudal claws. S, caudal process with highly sclerotized parts.
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.