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3,630 results for “Forming”
Données d'enquête sur les formes de partenariat et de réciprocité entre chercheurs et acteurs
<p>Ce jeu de données présente les résultats d’une enquête de l'Apes (Acteurs pour une économie solidaire, Hauts-de-France) et du Service commun de la documentation de l'université de Lille. Cette enquête par questionnaire a été menée du 14 novembre 2017 au 12 janvier 2018 auprès du réseau d’acteurs de l’Apes. 75 réponses ont été recueillies.</p> <p>Les résultats montrent que ces acteurs ont un accès restreint aux productions scientifiques issues de leurs collaborations avec des chercheurs, ce qui leur pose des difficultés dans un nombre significatif de cas. Cependant, à travers les réponses des acteurs des pistes d’amélioration se dessinent par l’entremise d’une redéfinition plus large des relations entre acteurs et chercheurs.</p> <p>La structuration du jeu de données est explicitée dans le fichier Readme. Un poster a été réalisé à partir des réponses à cette enquête. Il est disponible dans Zenodo à l’adresse suivante : <a href="https://dx.doi.org/10.5281/zenodo.1174362">https://dx.doi.org/10.5281/zenodo.1174362</a> </p> <p> </p> <p>English description</p> <p>This dataset presents the results of a survey of the Apes (Acteurs pour une économie solidaire, Hauts-de-France, a network of organizations of social and solidarity economy in Northern France) and of the University library of Lille. This survey based on a questionnaire was led from the 14<sup>th</sup> of November 2017 to the 12<sup>th</sup> of January 2018 among the organizations of the Apes network. 75 answers were collected.</p> <p>Results indicate that these organizations have a limited-access to research products coming from research in which they were engaged. This causes difficulties to quite many of them. However, from the answers of these organizations some ways of improving the situation may be drawn, by changing in a broader way the relationship between these organizations and the researchers they are working with.</p> <p>The dataset organization is explained in the Readme file. A poster was designed from these survey results and is available in Zenodo at this URL: <a href="https://dx.doi.org/10.5281/zenodo.1174362">https://dx.doi.org/10.5281/zenodo.1174362</a></p>
Using the Genetic Algorithm for the Optimization of Dynamic School Bus Routing Problem-Figure 7. Application main form which includes route, bus stops and GA parameters
<p>For this study, the school bus routes within the Ankara Province were used as case studies. The school bus routes were recorded by using the Android application and instantaneous GPS monitoring method. The home address of each student was taken as a stopping point. At the end of each route, the distances between the beginning and end points were recorded. After transferring the obtained route data into the database, the ill-adapted points were eliminated. By means of the developed application, the existing school bus routes are dynamically optimized using GA. It was developed both as a mobile and desktop application. Using Android- based mobile software, the information regarding GPS locations of bus stops and school buses is transferred to the server on a real-time basis. Using the desktop software, where GAs are run, these coordinates are shown on a Google map, and the most suitable route is produced and sent to the school bus via server. This method provides the opportunity to dynamically reflect certain factors such as a different initial point for the school bus, some students being absent from the school on a particular day, and eventual changes on the existing roads on the route production process.</p>
Diffraction images of a crystal of the complex formed by fragments of the integrin beta4 and the bullous pemphigoid antigen 1 (BP230, BPAG1e). PDB entry 6GVL.
<p>Data were collected on a single crystal at the beamline i03 of the Diamond synchrotron facility (Didcot, UK) using radiation of 0.97625 Å wavelength and a PILATUS3 6M detector. The dataset consists of 2400 images (0.15 degree oscillation per image).</p>
Diffraction images of a crystal of the complex formed by fragments of the integrin beta4 and the bullous pemphigoid antigen 1 (BP230, BPAG1e). Integrin high affinity point mutant. PDB entry 6GVK.
<p>Data were collected on a single crystal at the beamline XALOC of the ALBA-CELLS synchrotron facility (Cerdanyola del Vallés, Barcelona, Spain) using radiation of 0.97915 Å wavelength and a PILATUS 6M detector. The complete dataset is build up of three sub-sets measured at three different positions of a single crystal. Each sub-set consists of 1800 images (0.2 degree oscillation per image).</p>
Distribution of invalid children due to forms of diseases in Russian regions
<p>It is a dataset, which shows distribution of invalid children due to forms of diseases in Russian regions. Data is focused on children under 18 years old.</p>
Plate VII: Figures. 58-60. Anatya guttata, male anal appendages, left lateral view. (58) "normalis" form; (59) "guttata" form (both Base Camp); (60) intermediate specimen (Venezuela, Tachira, La Fria). Figures 61-64. Erythrodiplax amazonica, male ultimate instar exuviae (61), Exuviae, dorsal view; (62) left antenna; (63) labium with right palp, dorsal view; (64) anal pyramid, dorsal view. in Dragonflies (Odonata) From The Sierras Of Tapirapeco And Unturan, In The Extreme South Of Venezuela
Plate VII: Figures. 58-60. Anatya guttata, male anal appendages, left lateral view. (58) "normalis" form; (59) "guttata" form (both Base Camp); (60) intermediate specimen (Venezuela, Tachira, La Fria). Figures 61-64. Erythrodiplax amazonica, male ultimate instar exuviae (61), Exuviae, dorsal view; (62) left antenna; (63) labium with right palp, dorsal view; (64) anal pyramid, dorsal view.
Text-fig. 10.—A possible hunting set of Hell Creek theropods, drawn to scale. A, Tyrannosaurus rex. B, Albertosaurus lancensis. C, the Jordan theropod. D, Saurornithoides mongoliensis. S. mongoliensis is not present in the Hell Creek, but is used to represent those saurornithoidids and dromaeosaurids present and represented by isolated teeth. A fifth form, Paronychodon lacustris, also represented only by isolated teeth has not been included but was probably intermediate between the saurornithoidids and the Jordan theropod. in A new Theropod Dinosaur from the Upper Cretaceous of Central Montana
Text-fig. 10.—A possible hunting set of Hell Creek theropods, drawn to scale. A, Tyrannosaurus rex. B, Albertosaurus lancensis. C, the Jordan theropod. D, Saurornithoides mongoliensis. S. mongoliensis is not present in the Hell Creek, but is used to represent those saurornithoidids and dromaeosaurids present and represented by isolated teeth. A fifth form, Paronychodon lacustris, also represented only by isolated teeth has not been included but was probably intermediate between the saurornithoidids and the Jordan theropod.
ATXN1 N-terminal region explains the binding differences of wild-type and expanded forms
<p>Additional file 12 of the publication "<strong>ATXN1 N-terminal region explains the binding differences of wild-type and expanded forms</strong>". Each PDB file describes the docking of wt/expanded ATXN1 with an interactor.</p>
Observations and Simulations of Tin Plasmas Formed by CO2 Laser Pulses
<p>This is the experimental and simulation data associated with an article submitted to Physics of Plasmas. It contains two folders and one data file. </p> <p>Folder #1: dual probe csv files</p> <p>This folder contains the data from a complete experimental run with two probes in the chamber.</p> <p>Each csv file has 4 columns of data from Row 22.</p> <ol> <li>Column 1 contains the time data.</li> <li>Column 2 contains the laser pulse data</li> <li>Column 3 contains the planar probe data</li> <li>Column 4 contains the wire probe data</li> </ol> <p>Please note that the planar probe is positioned only at 100 mm, 80 mm, 60 mm, 40 mm and 20 mm from the target, while the wire probe is positioned at a greater range of distances from the target.</p> <p>Please see the data naming convention below which explains how to determine the distance of each probe from the target for each data file.</p> <p>Folder #2: planar probe csv files</p> <p>This folder contains the data from a complete experimental run with the planar probe inside the chamber.</p> <p>Each csv file has 3 columns of data from Row 22.</p> <ol> <li>Column 1 contains the time data.</li> <li>Column 2 contains the laser pulse data</li> <li>Column 3 contains the planar probe data</li> </ol> <p>Please note that the planar probe is positioned a range of distances from the target.</p> <p>Please see the data naming convention below which explains how to determine the distance of the probe from the target for each data file.</p> <p>File: complete_541ns.plt</p> <p>This is a text file which contains the simulation data for a range of parameters which were outputted from the 541 ns simulation at different edit times. All units are cgs.</p> <p>Data Naming Convention</p> <p>As each data sample was taken, it was important to name the saved correlated files in line with a strict convention, which would later enable the analysis of concomitant data sets and the proper association of probe-response with laser voltage and probe distances. Periods were avoided within the naming convention to avoid subsequent potential software conflicts.</p> <p>The naming convention selected contained reference to the following (see Figure 1).</p> <ul> <li>The base position of the probe: from 100 mm to 20 mm in steps of 20 mm. (In the dual probe csv files, the planar probe is held at this base position)</li> <li>The bias on the probe: ±15 V.</li> <li>The laser driving voltage: 22.5 kV, 25.0 kV, 27.5 kV.</li> <li>The actuator offset. In Figure 1, posn120 indicates that the probe has been moved 12 mm towards the target, closer than its starting position 020 mm i.e. it is 8 mm from the target. (The wire probe moves with this offset in the dual probe csv files. The planar probe moves with this offset in the planar probe csv files.)</li> <li>The sequence number of the shot within the group.</li> </ul> <p>e.g. : 020mm_pos15_27-5kV_posn120_003.csv</p> <p>Questions for clarification may be directed to Frank McQuillan at +353 87 7109085, or frank@frankmcquillan.com.</p> <p> </p>
Figure 3 in Interpopulation differences in shell forms of the pearl oyster, Pinctada imbricata radiata (Bivalvia: Pterioida), in the northern Persian Gulf inferred from principal component analysis and elliptic Fourier analysis
Figure 3. The first and second principal components scores of P. imbricata radiata from Hendourabi () and Lavan (▲) islands generated by PCA.
Figure 5 in Interpopulation differences in shell forms of the pearl oyster, Pinctada imbricata radiata (Bivalvia: Pterioida), in the northern Persian Gulf inferred from principal component analysis and elliptic Fourier analysis
Figure 5. Shape variation of EFA analysis in P. imbricata radiata from Lavan and Hendourabi islands.
Figure 4 in Interpopulation differences in shell forms of the pearl oyster, Pinctada imbricata radiata (Bivalvia: Pterioida), in the northern Persian Gulf inferred from principal component analysis and elliptic Fourier analysis
Figure 4. The first and second principal components scores of P. imbricata radiata from Hendourabi () and Lavan (▲) islands calculated by PCA performed on the normalized EFDs.
Figure 4 in Diurnal vertical distribution of zooplankton in a newly formed reservoir (Tahtalı Reservoir, Kocaeli): the role of abiotic factors and chlorophyll a
Figure 4. The vertical distribution of A) K. cochlearis, B) P. vulgaris, C) P. sulcata, D) total Rotifera, E) B. longirostris, F) total Cladocera, G) copepod nauplii, and H) total Copepoda, denoted by the time of sampling.
Text-fig. 5. Size comparison of lion p4 and m1 from Za Hájovnou Cave with close relative forms from European sites (black: Panthera fossilis, grey: Panthera cf. fossilis or Panthera fossilis – spelaea; f = female, old c. = old collection). Data source: Wojtusiak 1953, Thenius 1972, Schütt and Hemmer 1978, Argant 1988, 1991, García 2003, Baryshnikov and Tsoukala 2010). in Panthera Fossilis (Reichenau, 1906) (Felidae, Carnivora) From Za Hájovnou Cave (Moravia, The Czech Republic): A Fossil Record From 1987-2007
Text-fig. 5. Size comparison of lion p4 and m1 from Za Hájovnou Cave with close relative forms from European sites (black: Panthera fossilis, grey: Panthera cf. fossilis or Panthera fossilis – spelaea; f = female, old c. = old collection). Data source: Wojtusiak 1953, Thenius 1972, Schütt and Hemmer 1978, Argant 1988, 1991, García 2003, Baryshnikov and Tsoukala 2010).
Figure 1. Pseudomops septentrionalis. A-F. Color variation. A-C. Light form. D-F. Melanic form. G in First records of Pseudomops septentrionalis Hebard, 1917 (Blattodea: Blattellidae) in Nuevo León, Mexico
Figure 1. Pseudomops septentrionalis. A-F. Color variation. A-C. Light form. D-F. Melanic form. G. Abdomen in dorsal view, showing tufts of piliform bristles in T-3 and T-4. H-J. Specimens in their natural habitat. / A-F. Variación de color. A-C. Forma clara. D-F. Forma melánica. G. Abdomen en vista dorsal, mostrando mechones de cerdas piliformes en T-3 y T-4. H-J. Espécimenes en su hábitat natural.
Figure 2 in A new form of Melitaea phoebe (Goeze, 1779) (Lepidoptera) from the Mediterranean region (Turkey)
Figure 2. Habitus and male genitalia of Melitaea phoebe, new form. a, b: Habitus; c, d: male genitalia.
Figure 3 in A new form of Melitaea phoebe (Goeze, 1779) (Lepidoptera) from the Mediterranean region (Turkey)
Figure 3. Habitus and male genitalia of Melitaea punica telona (=M. ornata). a, b: Habitus; c, d: male genitalia.
Fig. 2 in A new species of Lycodon (Serpentes: Colubridae) from the Deccan Plateau of India, with notes on the range of Lycodon travancoricus (Beddome, 1870) and a revised key to peninsular Indian forms
Fig. 2. Lycodon deccanensis sp. nov. in preservative: (a–b) entire and head closeup (inset) of Paratype ZSI 13271; (c) entire view of SACON/VR-93. Photos by K. Deuti and S.R.Ganesh.
Fig. 1 in A new species of Lycodon (Serpentes: Colubridae) from the Deccan Plateau of India, with notes on the range of Lycodon travancoricus (Beddome, 1870) and a revised key to peninsular Indian forms
Fig. 1. Lycodon deccanensis sp. nov. in life: (a) entire, dorsolateral view; (b–d) head profiles of a live uncollected specimen from Devarayana Durga; (e–f) live uncollected adult and juvenile from Melagiri, showing ontogenic color shift. Photos by K.G. Punith, M.V. Shreeram, and S.R.Ganesh.
Fig. 4 in A new species of Lycodon (Serpentes: Colubridae) from the Deccan Plateau of India, with notes on the range of Lycodon travancoricus (Beddome, 1870) and a revised key to peninsular Indian forms
Fig. 4. Extralimital records re-identified as (a–b) Lycodon anamallensis (BNHS 1602a and b) and (c–e) Lycodon cf. aulicus (BNHS 1603 and 1604). Photos by A. Omkar.
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.