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.
3,505
datasets available to search
ShareScore release 0.9.0
Dataset results
3,505 results for “completive”
IO Islamic 1665. Ta'rîkh-i-'âlamârâi-'abbâsî, A Complete Copy of Iskandar Munshî's History of Shâh 'Abbâs the Great
<p>IO Islamic 1665. Ta’rîkh-i-‘âlamârâi-‘abbâsî, A Complete Copy of Iskandar Munshî’s History of Shâh ‘Abbâs the Great</p>
IO Islamic 1441. Ta'rîkh-i-'âlamârâi-'abbâsî, A Complete Copy of Iskandar Munshî's History of Shâh 'Abbâs the Great
<p>IO Islamic 1441. Ta’rîkh-i-‘âlamârâi-‘abbâsî, A Complete Copy of Iskandar Munshî’s History of Shâh ‘Abbâs the Great</p>
IO Islamic 298. Ta'rîkh-i-'âlamârâi-'abbâsî, A Complete Copy of Iskandar Munshî's History of Shâh 'Abbâs the Great
<p>IO Islamic 298. Ta’rîkh-i-‘âlamârâi-‘abbâsî, A Complete Copy of Iskandar Munshî’s History of Shâh ‘Abbâs the Great</p>
FIGURE 12. Peltogaster reticulata, nauplius V. A in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 12. Peltogaster reticulata, nauplius V. A, ventral view; B, head shield setae; C, frontolateral horn; D, hind body; E, antennula. Cf, cuticular fringes; su, suture; 1–2a, head shield setae; 5, 6, antennular setae.
FIGURE 13. Peltogaster reticulata, cypris larva. A in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 13. Peltogaster reticulata, cypris larva. A, lateral view of male larva; B, anterior lattice organ 2 (LO2); C, posterior lattice organs 3–5; D, pores of frontolateral horn gland; E, F, porefields; G, hole with porefield; H, antennules of male cyprid; I, J, attachment disc of male larva; K, the fourth antennular segment of male larva; L, M, attachment disc of female larva; N, the fourth antennular segment of female larva. As, axial sense seta; bz, breakage zone; fe, flap-like extension; fp, filamentous processes; ma, male aesthetasc; oes, open-ended seta; p, pore; pas1, postaxial sense seta 1; pas2, postaxial sense seta 2; pf, porefield; sa, subterminal aesthetasc; sk, skirt; ts, terminal setae.
FIGURE 4 in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 4. BI consensus tree of partial mt COI gene sequences of the genus Peltogaster. The HKY+G substitution model was used for the analysis. The Bayesian posterior probability and bootstrap values higher than 50% for the NJ analyses are shown near nodes (the order of their values is BI/NJ).
FIGURE 8 in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 8. Outlines of antennules (Al I–Al V), antenna (An) and mandible (Md) of the naupliar stages of Peltogaster reticulata. 1–6, antennular setae; bs, basipod seta. Scale bar 25 µm.
FIGURE 11. Peltogaster reticulata, nauplius IV. A in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 11. Peltogaster reticulata, nauplius IV. A, ventral view; B, hind body; C, furca; D, antennule. De, denticles; 5, 6, antennular setae.
FIGURE 3 in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 3. Transverse sections of the externa of Peltogaster reticulata. A, mature ovary; B, embryos; C, colleteric gland; D, colleteric gland near posterior end; E, left and right receptacles (colleteric gland does not reach the stalk); F, left receptacle near anterior end; G, receptacle duct; H, receptacle duct before outlet in the mantle cavity. Cg, colleteric gland; em, embryos; ov, ovary; m, mantle; r, receptacle; rd, receptacle duct; sh, shield; st, stalk.
FIGURE 10. Peltogaster reticulata, nauplius III. A in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 10. Peltogaster reticulata, nauplius III. A, ventral view; B, frontolateral horn; C, hind body with furca; D, antennular setae; E, antenna. Bs, basipod seta; se, subterminal seta; su, suture.
FIGURE 2 in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 2. SEM showing cuticle structure of the externa of Peltogaster reticulata. A, external cuticle (arrows show longitudinal and transverse ridges); B, internal cuticle; C, a group of two retinacula on one base; D, groups of two or four retinacula; E, a single balloon-like retinaculum; F, lamp-brush retinaculum is released out of balloon-like envelope.
FIGURE 9. Peltogaster reticulata, nauplius II. A in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 9. Peltogaster reticulata, nauplius II. A, ventral view; B, dorsal view; C, flotation collar; D, head shield setae; E, the third head shield seta with subterminal pore; F, head shield pore; G, attachment ridge; H, frontolateral horn; I, labrum; J, hind body; K, furca; L, antennules and antennae. Bs, basipod seta; cf, cuticular fringes; fc, flotation collar; po, pore on shield head (D) and on attachment disc (G); se, subterminal seta; su, suture; 1, 2, 2a, anterior head shield setae; 1–5, antennular setae.
FIGURE 6 in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 6. Body outlines (ventral view) of male and female larvae of Peltogaster reticulata. A, NI–NV, naupliar stages; B, cypris stages; C, head shield of nauplius III (dorsal view with setation); D, carapace of cyprid (lateral view with lattice organs). 1–5, head shield setae (C), lattice organs (D); p, pore; pf, porefield. Scale bar 100 µm.
FIGURE 5 in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 5. Size-frequency distribution of male (black bars) and female (grey bars) cyprids of Peltogaster reticulata.
FIGURE 7. Peltogaster reticulata, nauplius I. A in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 7. Peltogaster reticulata, nauplius I. A, ventral view; B, dorsal view; C, details of B; D, frontolateral horn; E, appendages. Al, antennule; an, antenna; fh, frontolateral horn; fr, furcal rami; md, mandible; po, pore; se, subterminal seta; su, suture; 2, 2a, head shield setae.
The data of complete chloroplast genome sequence of Sorbus amabilis (Rosaceae) in China
<p>This dataset includes the complete chloroplast genome of <em>Sorbus amabilis </em> in China.</p>
Complete tag loss in capture-recapture studies affects abundance estimates: an elephant seal case study
<p>1. In capture-recapture studies, recycled individuals occur when individuals lose all of their tags and are recaptured as though they were new individuals. Typically, the effect of these recycled individuals is assumed negligible.</p> <p>2. Through a simulation-based study of double tagging experiments, we examined the effect of recycled individuals on parameter estimates in the Jolly-Seber model with tag loss (Cowen & Schwarz, 2006). We validated the simulation framework using long-term census data of elephant seals.</p> <p>3. Including recycled individuals did not affect estimates of capture, survival, and tag-retention probabilities. However, with low tag-retention rates, high capture rates, and high survival rates, recycled individuals produced over estimates of population size. For the elephant seal case study, we found population size estimates to be between 8 and 53% larger when recycled individuals were ignored.</p> <p>4. Ignoring the effects of recycled individuals can cause large biases in population size estimates. These results are particularly noticeable in longer studies.</p>
Supplementary material 7 from: Wiemers M, Chazot N, Wheat CW, Schweiger O, Wahlberg N (2020) A complete time-calibrated multi-gene phylogeny of the European butterflies. ZooKeys 938: 97-124. https://doi.org/10.3897/zookeys.938.50878
Figure S5. Time-calibrated tree of European butterflies Section IV: Nymphalidae Part II: Subfamilies Libytheinae, Danainae & Satyrinae
Supplementary material 4 from: Wiemers M, Chazot N, Wheat CW, Schweiger O, Wahlberg N (2020) A complete time-calibrated multi-gene phylogeny of the European butterflies. ZooKeys 938: 97-124. https://doi.org/10.3897/zookeys.938.50878
Figure S2. Time-calibrated tree of European butterflies Section I: Papilionidae, Hesperiidae & Pieridae
Supplementary material 6 from: Wiemers M, Chazot N, Wheat CW, Schweiger O, Wahlberg N (2020) A complete time-calibrated multi-gene phylogeny of the European butterflies. ZooKeys 938: 97-124. https://doi.org/10.3897/zookeys.938.50878
Figure S4. Time-calibrated tree of European butterflies Section III: Nymphalidae Part I: Subfamilies Limenitidinae, Heliconiinae, Apaturinae & Nymphalinae
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.