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38 results for “Original research”
Рис. 3. Фотографии Laternula elliptica, сделанные около cтанции «Прогресс», ВосточнаЯ Антарктида. L. elliptica на морском дне с медкими камнЯми или гравием, глубина 27 м (А); несколько сифональных отверстий L. elliptica над поверхностью мЯгких осадков вокруг голотурии Staurocucumis turqueti, глубина 27 м (В); раковина L. elliptica (длина около 110 мм) на снегу около майны сраЗу после иЗвлечениЯ иЗ воды (С); пустые раковины L. elliptica на морском дне, глубина 56 м (D); раковина L. elliptica (вид с дорсального краЯ) на мЯгких осадках с камнЯми, покрытыми иЗвестковыми водорослЯми, глубина 30 м (Е); пара сифональных отверстий L. elliptica на поверхности мЯгких осадков, глубина 27 м (F). Фотографии О. Савинкина (A, B, D–F) и В. Потина (С). Fig. 3. Photographs of Laternula elliptica taken near «Progress» Research Station (East Antarctica). Softshelled clam L. elliptica on sea bottom with small stowns or gravel, depth 27 m (A); several open siphons of L. elliptica above soft bottom sediments around holothurian Staurocucumis turqueti, depth 27 m (B); a shell of L. elliptica (length about 110 mm) on snow near a dive hole just after dragging out of water (C); empty shells of L. elliptica on seafloor, depth 56 m (D); a shell of Laternula elliptica (dorsal view) on soft deposits among stones, covering by Lithothamnion, depth 30 m (E); pair of siphonal opening of L. elliptica on surface of soft sediments, depth 27 m (F). Photographs are taken by O. Savinkin (A, B, D–F) and V. Potin (C). in Species of warm-water origin Laternula elliptica (King, 1832) (Mollusca: Bivalvia: Laternulidae), a widespread mollusk in recent Antarctica
Рис. 3. Фотографии Laternula elliptica, сделанные около cтанции «Прогресс», ВосточнаЯ Антарктида. L. elliptica на морском дне с медкими камнЯми или гравием, глубина 27 м (А); несколько сифональных отверстий L. elliptica над поверхностью мЯгких осадков вокруг голотурии Staurocucumis turqueti, глубина 27 м (В); раковина L. elliptica (длина около 110 мм) на снегу около майны сраЗу после иЗвлечениЯ иЗ воды (С); пустые раковины L. elliptica на морском дне, глубина 56 м (D); раковина L. elliptica (вид с дорсального краЯ) на мЯгких осадках с камнЯми, покрытыми иЗвестковыми водорослЯми, глубина 30 м (Е); пара сифональных отверстий L. elliptica на поверхности мЯгких осадков, глубина 27 м (F). Фотографии О. Савинкина (A, B, D–F) и В. Потина (С). Fig. 3. Photographs of Laternula elliptica taken near «Progress» Research Station (East Antarctica). Softshelled clam L. elliptica on sea bottom with small stowns or gravel, depth 27 m (A); several open siphons of L. elliptica above soft bottom sediments around holothurian Staurocucumis turqueti, depth 27 m (B); a shell of L. elliptica (length about 110 mm) on snow near a dive hole just after dragging out of water (C); empty shells of L. elliptica on seafloor, depth 56 m (D); a shell of Laternula elliptica (dorsal view) on soft deposits among stones, covering by Lithothamnion, depth 30 m (E); pair of siphonal opening of L. elliptica on surface of soft sediments, depth 27 m (F). Photographs are taken by O. Savinkin (A, B, D–F) and V. Potin (C).
Figure 11 in French research on fisheries in the Northwest Atlantic, from its origins to the present
Figure 11. – Results of a 10-minute dredging on the Saint-Pierre Bank Iceland scallop beds aboard the R/V Cryos in 1974 (Photo A. Forest).
Figure 10. – Plankton sampling aboard the R in French research on fisheries in the Northwest Atlantic, from its origins to the present
Figure 10. – Plankton sampling aboard the R/V Cryos in 1975 to study herring pre-recruitment on George's Bank as part of an ICNAF project (Photo A. Forest).
Figure 8 in French research on fisheries in the Northwest Atlantic, from its origins to the present
Figure 8. – Study of the Gulf of St. Lawrence cod stock: results of a 30-minute trawl haul aboard the R/V Cryos in 1977 (Photo A. Forest).
Figure 9 in French research on fisheries in the Northwest Atlantic, from its origins to the present
Figure 9. – Recording of a thermal profile using an expendable bathythermograph probe temperature recorder aboard the R/V Cryos in 1985 (Photo A. Forest).
Figure 6. – The R in French research on fisheries in the Northwest Atlantic, from its origins to the present
Figure 6. – The R/V Président Théodore Tissier of the Office Scien-Scien- tifique et Technique des Pêches Maritimes carried out surveys in the North West Atlantic mainly during the 1950s (source: www.lepetit-manchot.fr).
Figure 7 in French research on fisheries in the Northwest Atlantic, from its origins to the present
Figure 7. – The Saint-Pierre and Miquelon research center and the R/V Cryos in the 1970s (Photo A. Forest).
Figure 4 in French research on fisheries in the Northwest Atlantic, from its origins to the present
Figure 4. – Map of areas claimed by Canada and France as their Economic Exclusive Zones and the Court of Arbitration decision (from Parsons, 1993).
Original reconstructions for the research in "X-ray nanotomography of individual pulp fibre bonds reveals the effect of wall thickness on contact area"
<p>The following data set contains the original cropped and straightened reconstruction stacks of all the cellulose fibre bond samples imaged for the study outlined in the article<strong> “</strong>X-ray nanotomography of individual pulp fibre bonds reveals the effect of wall thickness on contact area” by T. Sormunen, A. Ketola, A. Miettinen, J. Parkkonen and E. Retulainen. The article is currently (23.11.2018) in decision phase.</p> <p>In addition, the algorithm for reconstruction stack processing conducted in ImageJ and the MATLAB function for contact area and pixelwise correlation calculations are included.</p>
Research data for "Origins of structural and electronic transitions in disordered silicon"
<p>This is a dataset related to the publication "Origins of structural and electronic transitions in disordered silicon" (<em>Nature</em> <strong>2021</strong>, <em>589</em>, 59–64). The paper is available online here: https://doi.org/10.1038/s41586-020-03072-z.</p> <p>Three separate .tar.gz archive files are provided:</p> <ul> <li>"coordinates": structural data in (extended) XYZ format including atomic information</li> <li>"ML_DOS_data": original data for the electronic DOS analysis (Fig. 3)</li> <li>"other_potentials": tests with further ML potential models (as described in the Methods section)</li> </ul>
Original research data for the paper "Additive Manufacturing of Polymeric Gradient Index Optics via Grayscale Digital Light Processing Vat Photopolymerization Technology"
<p>[CMOS camera data]</p> <p>[conversion maps]</p> <p>[cure kinetics]</p> <p>[GRIN profiles arbitrary]</p> <p>[MonoPrinter grayscale power density]</p> <p>[MonoPrinter print files]</p> <p>[pictures of arbitrary GRINs]</p> <p>[predicted printing param matrices]</p> <p>[refractive index vs conversion]</p> <p>[working curve]</p>
Data for the original research article 'Enhanced anaerobic digestion of dairy wastewater in a granular activated carbon amended sequential batch reactor'
<p>All data that support the findings of the study 'Enhanced anaerobic digestion of dairy wastewater in a granular activated carbon amended sequential batch reactor' published in GCB Bioenergy Journal are openly available in the file.</p>
Dataset from research: Origin, characteristics, predominance and conceptual networks of eponyms in bibliometric literature
<p>Dataset in a xlsx file used by Juan-Carlos Valderrama-Zurián & collaborators in the research “Origin, characteristics, predominance and conceptual networks of eponyms in bibliometric literature”.</p>
The comparison of structured abstracts generated by the ChatGPT language model with the author's original abstracts derived from research papers
<p>The study utilized publications in the field of information science, both in Polish and English, which appeared in the journal <em>Zagadnienia Informacji Naukowej – Studia Informacyjne</em> during the 2022-2023 period. A total of 10 research papers were selected – 5 in Polish (PL1-PL5) and 5 in English (EN1-EN5).</p>
Fig. 3 in Research Reconciling fossils with phylogenies reveals the origin and macroevolutionary processes explaining the global cycad biodiversity
Fig. 3 Ages of extant genera and fossil placements. (a) Phylogenetic relationships for extant (genera are collapsed) and extinct cycads with support values (Posterior Probability indicated when> 0.3). Node support for extant genera is only indicated when <1. (b) Posterior distributions for the crown ages of the extant genera. Eo, Eocene; M, Miocene; N, Neogene; O, Oligocene; Pg, Paleogene. Ma, million years ago.
Fig. 2 in Research Reconciling fossils with phylogenies reveals the origin and macroevolutionary processes explaining the global cycad biodiversity
Fig. 2 Bayesian total-evidence dated phylogeny of Cycadales. This chronogram is the resulting consensus tree from the MrBayes analyses performed with the fossilized-birth-death model and an uncorrelated relaxed molecular clock. The tree includes 321 extant species and 60 extinct species with median divergence times along with 95% Highest Posterior Density (blue bars) for each node. C, Carboniferous; J, Jurassic; K, Cretaceous; N, Neogene; P, Permian; Pg, Paleogene; T, Triassic.
Fig. 4 in Research Reconciling fossils with phylogenies reveals the origin and macroevolutionary processes explaining the global cycad biodiversity
Fig. 4 Historical biogeography of cycads. Estimates of ancestral areas were performed with a time-stratified model in Dispersal–Extinction–Cladogenesis (DEC) with fossils included (a) and with fossils excluded (b). The extant genera have been collapsed to focus on deep-time biogeography (for details within each genus, see Supporting Information Fig. S6 when fossils are included and Fig. S7 when fossils are excluded). The bottom-right corner legend indicates colored areas used in this study corresponding to colored squares for each node, representing inferred ancestral area(s) with the DEC model, and colored circles for fossil species representing known distributions (except for extant genera with one or two species only). The red-highlighted shades show the cycad expansion into Gondwana during the Jurassic and Cretaceous. The bottom-left corner map represents the global paleogeography in the Jurassic (180 million years ago (Ma)). Paleomap used with permission © 2020 Colorado Plateau Geosystems Inc. Arrows indicate fossil species illustrated. Pictures from Mario Coiro. C, Carboniferous; N, Neogene; Perm, Permian; Pg, Paleogene.
Fig. 1 in Research Reconciling fossils with phylogenies reveals the origin and macroevolutionary processes explaining the global cycad biodiversity
Fig. 1 Global distribution of Cycadales. (a) Species richness of the 10 extant cycad genera across continents. (b) IUCN threat categories for 337 extant cycad species (redrawn from IUCN, 2022). (c) Map showing the extant distribution of cycad diversity (red areas) and sampled fossil localities (purple dots), indicating broader geographic distribution in the past.
Fig. 6 in Research Reconciling fossils with phylogenies reveals the origin and macroevolutionary processes explaining the global cycad biodiversity
Fig. 6 Reconstruction of the latitudinal span of cycads during geological times. This estimate has been obtained using the method of Silvestro et al. (2018b) as implemented in Zhang et al. (2022). Gray polygon represents the reconstructed span, black dots represent the paleolatitude and age of fossil tips, while black triangles show the latitude of extant species. C, Carboniferous; J, Jurassic; K, Cretaceous; N, Neogene; P, Permian; Pg, Paleogene; Tr, Triassic.
Fig. 5 in Research Reconciling fossils with phylogenies reveals the origin and macroevolutionary processes explaining the global cycad biodiversity
Fig. 5 Biogeographic processes explaining the global distribution pattern of cycads. The number of dispersal events into a region and out of a region as well as the number of local extinctions (extirpations) are compared between analyses including fossils (a, b) and analyses excluding fossils (c, d). Area names: WP, West Palearctic; EP, East Palearctic; WN, West Nearctic; EN, East Nearctic; CA, Central America; WI, Caribbean Islands; SA, South America; AF, Africa; IN, India; WA, Southeast Asia; AU, Australasia; GR, Greenland; AN, Antarctica.
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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.