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.
92
datasets available to search
ShareScore release 0.9.0
Dataset results
92 results for “Duplex”
Fig. 3. Hirsutocrinus duplex n in Hirsutocrinus duplex, a New Genus and Species of Sea Lilies (Crinoidea, Comatulida, Bathycrinidae) from the Western North Pacific
Fig. 3. Hirsutocrinus duplex n. gen. and sp., holotype. A, Isolated plates from the sides of tegmen; B, plates from anal sac; C, plates from tegmen top; D, plates from Brs 2–4; E, plates from Brs 5–8; F, typical (well developed) cover plates from pinnule; G, typical side plates from pinnule.
Fig. 5. Hirsutocrinus duplex n in Hirsutocrinus duplex, a New Genus and Species of Sea Lilies (Crinoidea, Comatulida, Bathycrinidae) from the Western North Pacific
Fig. 5. Hirsutocrinus duplex n. gen. and sp. Scheme, showing position of cover, side and tube feet plates relative to each other in an area of genital expansion of proximal pinnule (oblique view from inner lateral and oral pinnule sides).
Fig. 2. Hirsutocrinus duplex n in Hirsutocrinus duplex, a New Genus and Species of Sea Lilies (Crinoidea, Comatulida, Bathycrinidae) from the Western North Pacific
Fig. 2. Hirsutocrinus duplex n. gen. and sp., holotype. A, Radial ring with arms; B, dististele and radix with fouling; C, IBr1, view from inside; D, IBr2 with knobby process, view from inside; E, detail of knobby process articular surface; F, distal facet of Br6 (muscular synarthry); G, proximal facet of Br3 (muscular synarthry); H, Br2 with knobby process, view from inside; I, Br2 with knobby process, distal view (muscular synarthry); J, Br1 with knobby process, proximal view (asymmetrical muscular synarthry).
Fig. 4. Hirsutocrinus duplex n in Hirsutocrinus duplex, a New Genus and Species of Sea Lilies (Crinoidea, Comatulida, Bathycrinidae) from the Western North Pacific
Fig. 4. Hirsutocrinus duplex n. gen. and sp., holotype. A, Distal facet of hyposynostosial IIBr7 (ligamentary synarthry); B, IIBr4, aboral external view; C, detail of B showing numerous needle-like spines; D, synarthrial facet of columnal 38 (mesistele); E, synarthrial facet of columnal 59 (dististele); F, detail of E showing fulclar ridge axis of columnal 59.
Racemic crystal structures of A-DNA duplexes
<p>X-ray diffraction data collected for d/l-d(CCCGGG) crystals at IECB, using a microfocus rotating anode Rigaku FRX diffractometer, with Cu Kα radiation and a hybrid pixel detector (Dectris Pilatus 200K). </p> <p>PDB ID: 6GN2</p> <p>PDB Title: Racemic crystal structure of A-DNA duplex formed from d(CCCGGG) in space group R3bar </p> <p>PDB DOI: http://doi.org/10.2210/pdb6GN2/pdb</p>
Racemic crystal structures of A-DNA duplexes
<p>X-ray diffraction data collected for d/l-d(CCCGGG) crystals at IECB, using a microfocus rotating anode Rigaku FRX diffractometer, with Cu Kα radiation and a hybrid pixel detector (Dectris Pilatus 200K).</p> <p>PDB ID: 6GN3</p> <p>PDB Title: Racemic crystal structure of A-DNA duplex formed from d(CCCGGG) in space group P21/n</p> <p>PDB DOI: http://doi.org/10.2210/pdb6GN3/pdb</p>
Hieracium duplex Nägeli & Peter (BR0000011718895)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Fig. 4 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
Fig. 4. Photographs of the left side of the tails of three recaptured snakes. (a) A juvenile male with 338 mm in SVL and the profile code 1212-12222- 122121-112222-112221, recorded on 15 March 2018, (b) The snake's recapture 159 days later, with 460 mm in SVL on 21 August 2018 and more cream flecks, and (c) the snake's additional recapture a further 373 days later, with 612 mm in SVL on 29 August 2019 and no additional increase in the number of flecks. (d) A juvenile male with 415 mm in SVL and the profile code 2221-1222-123222-123232-1222322, recorded on 22 August 2018. (e) The snake's recapture 58 days later with 437 mm in SVL on 19 October 2018 with enlarged flecks, and (f) another recapture a further 268 days later, with 551 mm in SVL on 14 July 2019 and no additional change in the flecks. (g) A semi-adult female with 499 mm in SVL and the profile code 21221-12221-222222-222232-23223322, recorded on 7 July 2017. (h) The snake's recapture 527 days later with 636 mm in SVL on 16 December 2018 and more flecks, and (i) another recapture a further 404 days later, with 691 mm in SVL on 24 January 2020 and no additional change in the flecks.
2 3 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
2 3 anterior ˱ posterior anterior ˱ posterior Fig. 3. The present coding system when there is an insertion of a scale row from the posterior to the anterior within a single cream band. a) When a large scale is followed by two small scales, the large scale is counted twice and the code for this example is "232232". b) When a new row is inserted between two rows, the inserted scale is judged as an independent row and the code for this example is "2221323".
Fig. 11 in Fig. 4 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
Fig. 11. Ultrametric Bayesian phylogenetic tree of 22 species of the genus Stolephorus with evolution of the (modal) number of prepelvic scutes. Modal number of prepelvic scutes classified into three categories: six prepelvic scutes (black), five prepelvic scutes (grey), four prepelvic scutes (white). Character states at nodes estimated using likelihood optimization and a symmetric one-rate (''Mk1") model of evolution. At each node, relative probabilities of each diet category drawn using pie charts, with corresponding coding-colour. Pie charts at deepest nodes enlarged for clarity. Stolephorus specimens identified by museum registration number, specimen code or GenBank (GB) sequence accession number (see Table 1 for details). Outgroups Encrasicholina not shown. Branch lengths proportional to relative time (tree height scaled to 1). Posterior Probabilities shown at nodes when <1.
Fig. 10 in Fig. 4 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
Fig. 10. Morphometric comparisons between Stolephorus dubiosus (open triangles) and S. taurus sp. nov. (closed circles). (a) for pectoral-fin length (P1L; as % of standard length; SL); (b) for pelvicfin length (P2L; as % of SL); (c) for second dorsal-fin ray length (2DRL; as % of SL); (d) for third dorsal-fin ray length (3DRL; as % of SL); (e) for second anal-fin ray length (2ARL; as % of SL); (f) for third anal-fin ray length (as % of SL); (g) for interorbital width (as % of head length; HL) to SL.
Fig. 8 in Fig. 4 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
Fig. 8. Lateral (a), dorsal (b), and ventral (c) views of the holotype of Stolephorus taurus sp. nov., OCF-P 10434, 52.2 mm SL, estuary of Hooghly River, West Bengal, India.
Fig. 9 in Fig. 4 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
Fig. 9. Stained scale removed from right side of midbody (just below dorsal fin) of paratype of Stolephorus taurus. KAUM–I. 157581, 53.2 mm SL, estuary of Hooghly River, West Bengal, India (left-right inverted). Grooves on scales forming a few separations.
Fig. 5 in Fig. 4 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
Fig. 5. Left side of left hyoid arch of Stolephorus dubiosus (THNHM-F021239, 63.6 mm SL, cleared and stained). hypo lo, lower hypohyal; hypo up, upper hypohyal; chy, ceratohyal; gha, groove for hyoidean artery; eph, epihyal; inh, interhyal (broken); br, branchiostegal rays (seventh branchiostegal ray detached).
Fig. 7 in Fig. 4 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
Fig. 7. Distributional records of Stolephorus dubiosus (circles) and S. taurus sp. nov. (triangles). Closed symbols, based on specimens examined in this study; open symbols, based on literature records or molecular evidence.
Fig. 2 in Fig. 4 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
Fig. 2. (a) Lateral and (b) dorsal views of dorsal-fin origin of Stolephorus dubiosus, NSMT-P 127425, 55.7 mm SL, Songkhla Lake, Thailand (stained with Alizarine Red). Arrows indicate predorsal scute.
Fig. 4 in Fig. 4 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
Fig. 4. Stained scale removed from right side of midbody (just below dorsal fin) of Stolephorus dubiosus. NSMT-P 127425, 49.9 mm SL, Songkhla Lake, Thailand (left-right inverted). Grooves on posterior part forming numerous separations.
Fig. 1 in Fig. 4 in Verification of Natural Marking for Individual Identification Using a Duplex Marking Approach in Ijima's Sea Snakes, (Reptilia: Elapidae).
Fig. 1. Stolephorus dubiosus: (a) Lateral view of holotype (BMNH 1969.4.22.1826, 70.0 mm SL, Thailand); (b) lateral view in fresh condition; (c) dorsal and (d) ventral views in preserved condition of non-type specimen (THMHM-F021237, 66.0 mm SL, Samut Sakhon Province, Thailand).
Research data supporting "Duplex-Specific Nuclease-Amplified Detection of MicroRNA Using 2 Compact Quantum Dot−DNA Conjugates"
<p>Raw research data supporting the publication:</p> <p>Wang, Y. et al., 2018, ACS Applied Materials & Interfaces, "Duplex-Specific Nuclease-Amplified Detection of MicroRNA Using 2 Compact Quantum Dot−DNA Conjugates", DOI: 10.1021/acsami.8b07250.</p>
Data from: Effect of pH regulation by microbes on corrosion behaviour of duplex stainless steel 2205 in acidic artificial seawater environment
Sulphate reducing bacteria (SRB) can regulate environmental pH because of their metabolism. Since local acidification results in pitting corrosion, the potential capacity of pH regulation by SRB would have important consequences for electrochemical aspects of the bio-corrosion process. This study focussed on identifying the effect of pH on the corrosion of duplex stainless steel (DSS) 2205 in a nutrient rich artificial seawater medium containing SRB species, Desulfovibrio vulgaris. DSS samples were exposed to the medium for 13 days at 37 0C at pH ranging from 4.0 to 7.4. The open circuit potential value (OCP), sulphide level, pH and number of bacteria in the medium were recorded daily. Electrochemical impedance spectroscopy (EIS) and potential dynamic polarization were used to study the properties of the films and corrosion behaviour of the material. Inductively coupled plasma mass spectrometry (ICPMS) was used to measure the concentration of cations Cr, Fe, Ni, Mo, Mn in the experimental solution after 13 days. Scanning electron microscopy (SEM) and Energy Dispersive X-Ray Spectroscopy (EDX) were used for surface analysis. The results showed the pH changed from acidic values set at the beginning of the experiment to approximately pH 7.5 after 5 days due to bacterial metabolism. After 13 days, the highest iron concentration was in the solution that was initially at pH 4 accompanied by pitting on the stainless steel. Sulphide was present on all specimens but with more sulphide corrosion products at pH 4. The results of this study suggest that the corrosion process for the first few days exposure at low pH was driven by pH in solution rather than by bacteria. The increasing pH during the course of the experiment slowed down the corrosion process of materials originally at low pH. The nature and mechanism of SRB attack on duplex stainless steel at different acidic environments are discussed.
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.