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1,175 results for “coating”
Fig. 5 in Surface Coat Differences between and Non-Invasive Entamoeba dispar Invasive Entamoeba histolytica
Fig. 5. Confocal, and fluorescence intensity assays were carried-out using FITC-conjugated streptavidin (1: 100) for the localization of biotinylated proteins in E. dispar (A, C) and E. histolytica (B, D). Observation conditions were the same for both species, but had to be modified for E. dispar to improve image quality, since the high intensity of fluorescence produced distortion of the image. E – Graphical representation in arbitrary fluorescence units. Bar: 20 µm.
Fig. 1 in Surface Coat Differences between and Non-Invasive Entamoeba dispar Invasive Entamoeba histolytica
Fig. 1. Transmission electron photomicrographs of amoebas treated with ruthenium red and cationized ferritin. E. histolytica (A) and E. dispar (B) stained with ruthenium red. The stain on the cell surface of E. histolytica is seen as a dense solid layer. In contrast, in E. dispar the stain is observed as a slight deposit. Small groups of ferritin particles were observed in E. histolytica (C) while substantially large particles clumps were found in E. dispar (D). Bar: 0.1 µm.
Fig. 4 in Surface Coat Differences between and Non-Invasive Entamoeba dispar Invasive Entamoeba histolytica
Fig. 4. (A) Silver staining of the protein profile of E. dispar and E. histolytica, and densitometry analysis of the 60 kDa band as loading control. (B) Biotinylated patterns of membrane proteins of E. dispar and E. histolytica.
Fig. 2. A and B in Surface Coat Differences between and Non-Invasive Entamoeba dispar Invasive Entamoeba histolytica
Fig. 2. A and B. Cell coat of E. histolytica and E. dispar as observed in thin sections after treatment with Con A. The cell coat of E. histolytica (A) was observed as a thick layer of relatively homogenous electron- dense precipitate all along the cell surface. In contrast, in E. dispar, (B) the cell coat was strongly positive. Bar: 0.1 µm. C to D. Confocal and phase contrast microscopy images of amoebae after incubation with fluoresce- in-tagged Concanavalin A. As observed by confocal microscopy (C) and phase contrast (D) in E. histolytica trophozoites the displacement of surface lectin receptors formed a defined cap at the posterior pole of the cell, but such structure is not formed by E. dispar and only irregular patches were seen (E) confocal and (F) phase contrast. Bar: 20 µm.
Fig. 1 in Short communication First documented observation of differential dorsoventral coat colouration in wild boar Sus scrofa (Artyodactyla: Suidae) in Italy
Fig. 1 - The juvenile wild boar object of this note showing the differential dorsoventral colouration pattern (right) next another wild-type individual (left). Additional footage available at: https://youtu.be/gTc0BFSE9kA. / Il giovane esemplare di cinghiale oggetto di questa nota in cui è visibile il pattern cromatico a demarcazione dorsoventrale (a destra) accanto a un altro individuo con la tipica colorazione marrone uniforme (a sinistra). È anche disponibile un filmato aggiuntivo: https://youtu.be/ gTc0BFSE9kA. (Photo and video: / Foto e video: Francesco Gallozzi).
Poly(benzodifurandione) Coated Silk Yarn for Thermoelectric Textiles
<p>Each file reports the raw data used for the corresponding figure indicated in the file name. </p> <p>For more details about the methods and instrument, please refer to Section 4 "Experimental Section".</p>
A dataset on "Coating of self-sensing AFM cantilevers with boron-doped nanocrystalline diamond films at low temperatures"
<p>The data set to paper: </p> <p>Coating of self-sensing AFM cantilevers with boron-doped nanocrystalline diamond at low temperatures</p> <p>Štěpán Potocký1*, Jaroslav Kuliče1k, Egor Ukraintsev1, Ondřej Novotný2, Alexander Kromka3, and Bohuslav Rezek1</p> <p>1 Faculty of Electrical Engineering, Czech Technical University in Prague, Technická 2, 16627 Prague, Czech Republic<br>2 NenoVision s.r.o., Purkyňova 649, 61200 Brno, Czech Republic <br>3 Institute of Physics, Czech Academy of Sciences, Prague 6, Czech Republic<br>*corresponding author: potocky@fel.cvut.cz</p> <p>Data manager: Kristýna Dostálová: dostalovak@fzu.cz</p> <p>Date of data collection: 1. 10. 2023 - 31. 3. 2024</p> <p>All the data showed in the pictures are provided in X-Y format with described sample. Always, the respective figure to which the data belong is provided in high resolution. <br>The data are in the following formats: <br>Figure 1: pdf<br>Figure 2: pdf<br>Figure 3: pdf, csv<br>Figure 4: pdf, csv, gwy<br>Figure 5: pdf, gwy<br>Figure S1: pdf<br>Figure S2: pdf</p> <p>The comma separated values file (csv) always contain the description of the columns in the first row. Gwy correspond to free Gwyddion SPM data analysis software (gwyddion.net). In case of composed image the name of the file corresponds to the corresponding figure.</p> <p>Data acquistion and processing is provided in the Experimental part in the publication: DOI:10.1002/pssa.202400553.</p>
Microstructure and mechanical performance of cold spray Cr coatings
<p>This dataset includes the data associated with the publication titled "Microstructure and mechanical performance of cold spray Cr coatings", published in Journal of Nuclear Materials (https://doi.org/10.1016/j.jnucmat.2024.155492). The zip folder contains the following items:</p> <ol> <li>Data for producing the grain size distribution plots.</li> <li>Microhardness data for the reported values.</li> <li>Nanohardness data.</li> <li>SEM images that were analysed to produce the porosity distribution plot.</li> <li>SEM images that were used to quantify the interfacial roughness and thickness variation of the two coatings.</li> <li>XRD data for measuring residual stresses in the coatings.</li> <li>In-situ DIC data to quantify the crack density and average strain in the coatings after in-situ tensile testing.</li> <li>A jupyter lab notebook to analyse and produce the plots that were presented in the publication.</li> </ol>
Microstructure and mechanical performance of cold spray Cr coatings
<p>This dataset includes the data associated with the publication titled "Microstructure and mechanical performance of cold spray Cr coatings", published in Journal of Nuclear Materials (https://doi.org/10.1016/j.jnucmat.2024.155492). The zip folder contains the following items:</p> <ol> <li>Data for producing the grain size distribution plots.</li> <li>Microhardness data for the reported values.</li> <li>Nanohardness data.</li> <li>SEM images that were analysed to produce the porosity distribution plot.</li> <li>SEM images that were used to quantify the interfacial roughness and thickness variation of the two coatings.</li> <li>XRD data for measuring residual stresses in the coatings.</li> <li>In-situ DIC data to quantify the crack density and average strain in the coatings after in-situ tensile testing.</li> <li>A jupyter lab notebook to analyse and produce the plots that were presented in the publication.</li> </ol>
In situ polyaniline coating of Prussian blue as cathode material for sodium-ion battery
<p>Prussian blue has great potential for using as a sodium cathode material owing to its high working potential and cube frame structure. Herein, this work reports a two-step method to synthesize Prussian blue with ascorbic acid (AA) as the ball-milling additive, which improves electrochemical rate performance of Prussian blue during the traditional co-precipitation method. The obtained Prussian blue sample exhibited a superior specific capability (113.3 mAh g<sup>-1</sup> even at 20 C, 1 C=170 mA g<sup>-1</sup>) and a specific capacity retention of 84.8% after 100 cycles at 1 C rate. In order to enhance the cycling performance of the Prussian blue, an in situ polyaniline (PANI) coating strategy was employed in which aniline was added into the electrolyte and polymerized under electrochemical conditions. The coated anode exhibited a high specific capacity retention of 62.7% after 500 cycles, which is significantly higher than that of the non-coated sample which only remains 40.1% after 500 cycles. This development has shown a great potential as a low-cost, high-performance and environmental-friendly technology for large-scale industrial application of PB.</p>
Figure 3. Grania crassiducta Coates, 1990 in The diverse Grania fauna (Clitellata: Enchytraeidae) of the Esperance area, Western Australia, with descriptions of two new species
Figure 3. Grania crassiducta Coates, 1990. (A) Ventral chaeta of segment XIII; (B) cephalic region, dorsal view (note, in particular, the globular inclusions of the head organ just above the anterior end of the dorsal blood vessel); (C) cephalic region of a different specimen in laterosagittal view, showing the position of the head organ inside the peristomium; (D) coelomocytes; (E) sperm funnel; (F) lateral view of the penial apparatus, showing the terminal tract of stylet inside the aglandular sac.
Figure 1. Grania bykane Coates, 1990 in The diverse Grania fauna (Clitellata: Enchytraeidae) of the Esperance area, Western Australia, with descriptions of two new species
Figure 1. Grania bykane Coates, 1990. (A) Cephalic region, dorsolateral view showing the head organ; (B) clitellum (lateral view); (C) coelomocytes; (D) ventral chaeta of segment XIV; (E) late spermatid bundle, showing the spiral structure of the nuclei; (F) sperm funnel; (G) penial bulb with stylet; the arrowhead points to the proximal constriction of the stylet.
Fig. 2 in Diet of the smooth-coated otter Lutrogale perspicillata (Geoffroy, 1826) at natural and modified sites in Singapore
Fig. 2. Linear fit of vertebrae length and total length of cichlids caught in Serangoon Reservoir (SR).
Fig. 3 in Diet of the smooth-coated otter Lutrogale perspicillata (Geoffroy, 1826) at natural and modified sites in Singapore
Fig. 3. Frequency distribution of the size classes of fish vertebrae represented in spraints in Serangoon Reservoir (SR) and Sungei Buloh Wetland Reserve (SBWR).
Fig. 4 in Spatial genetic structure in the vulnerable smooth-coated otter (Lutrogale perspicillata, Mustelidae): towards an adaptive conservation management of the species
Fig. 4. Multidimensional Scaling (MDS) plot (stress: 0.0045) performed using average pairwise TN93 (Tamura & Nei, 1993) distances among investigated Lutrogale perspicillata groups created according to the country of origin of samples (modern + museum DNA and GenBank entries).
Fig. 3. A in Spatial genetic structure in the vulnerable smooth-coated otter (Lutrogale perspicillata, Mustelidae): towards an adaptive conservation management of the species
Fig. 3. A, Lutrogale perspicillata network computed using haplotypes (h) from the 305 bp-long sequence alignment (modern + museum DNA and GenBank entries). A scale to infer the number of sequences for each pie (i.e., haplotype) was provided together with a length bar to compute the number of mutational changes. The colour of each country and the number of each haplotype are indicated. See Table S1 for more details. B, Mismatch Distributions (MD) of the mtDNA pairwise differences (dotted: observed; line: expected) calculated for South East Asia haplogroup (Fig. 3A). Estimates of FS and R2 statistics (with related P values), r (raggedness index) and the outcome of SSD and SSD* test under a model (H0) of sudden demographic and spatial population expansion, respectively, are provided.
Fig. 2 in Spatial genetic structure in the vulnerable smooth-coated otter (Lutrogale perspicillata, Mustelidae): towards an adaptive conservation management of the species
Fig. 2. Photos of MNHN-ZM-MO-2001-350, L. p. perspicillata holotype resident in the mammal collection of the National Museum of Natural History of Paris, France. A, right side, lateral view (bar length = 20 cm); B, left forelimb, lateral view; C, basement, in French "Lutra perspicillata = Lutra leptonix Horsf., loutre de Java par m Diard, mai 1821, la tête est au lab d'anatomie", which can be translated into and interpreted as: "Lutra perspicillata = Lutra leptonix (Horsfield, 1824), Java otter from M. Diard, May 1821, skull is in the lab of anatomy" (see also Material and Methods). Photos courtesy and copyright: © MNHN - RECOLNAT - Laura Flamme - 2014.
Fig. 1 in Spatial genetic structure in the vulnerable smooth-coated otter (Lutrogale perspicillata, Mustelidae): towards an adaptive conservation management of the species
Fig. 1. Lutrogale perspicillata distribution (in yellow; see insets for Iraq and Pakistan) including sampling localities of modern (white circles) and museum (green squares) individuals. As far as the latter are concerned, we reported only sites for which samples were successfully investigated (see Table S1 for the entire sample size of this study; symbol "?" stands for unknown locality). The white stars indicate, in Iraq, the locality (TaqTaq, Kurdistan) where the sample of Omer et al. (2012) was collected, in Cambodia/Thailand and Malaysia, the country/ies of origin of EF472348 and KY117557 GenBank sequence, respectively. In Iraq, Pakistan, and supposedly Java, Indonesia, the green squares indicate localities (when known) of L. p. maxwelli, L. p. sindica, and L. p. perspicillata museum holotypes, respectively. Finally, Naga Hills at the border between Myanmar and India as well as Bahoo-Kalat River Basin between Iran and Pakistan are indicated (see text for more details). The species' geographic range was adapted from IUCN (International Union for Conservation of Nature) 2015. Lutrogale perspicillata. The IUCN Red List of Threatened Species 2019-3 was modified using CorelDraw!12 (2003). Digital images (insets) were obtained from Google Earth 7.1.5.1557 (2015 Google Inc.) and Google Earth map data (Data SIO, NOAA, U.S. Navy, NGA, GEBCO - Image Landsat). Please note that thick dotted lines mark out new borders for L. p. sindica and L. p. perspicillata subspecies as established in this study (see text for more details).
Text-fig. 54. Scanning electron microscope (SEM; a–e, g, h) and synchrotron x-ray microscopy (SRXTM; f, i) images of unnamed angiosperm fruits and seeds; Torres Vedras locality, Portugal. a) Follicle sp. 1, narrow elongate follicle with sessile and decurrent stigma; b) Follicle sp. 2, broad, dehisced follicle with elongate and transverse fibers lining the locule; c) Angiosperm seed sp. 1 with thin, smooth seed coat; d) Angiosperm seed sp. 2 with verrucate seed coat; e) Angiosperm seed sp. 3 with exotestal and foveolate seed coat; f) Angiosperm seed sp. 4 with smooth seed coat; g, h) Angiosperm seed sp. 5 with raised epidermal cells forming a reticulate pattern; i) Wedge-shaped angiosperm fruit with remains of floral parts near apex. Specimens, TV43-S136726 (a), TV44-S148144 (b), TV43-S170074 (c), TV43-S136747 (d), TV43-S170073 (e), TV38-S174615 (f), TV44-S148003 (g), TV44-S148004 (h), TV43-S174685 (i). Scale bars 300 Μm (a–i). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 54. Scanning electron microscope (SEM; a–e, g, h) and synchrotron x-ray microscopy (SRXTM; f, i) images of unnamed angiosperm fruits and seeds; Torres Vedras locality, Portugal. a) Follicle sp. 1, narrow elongate follicle with sessile and decurrent stigma; b) Follicle sp. 2, broad, dehisced follicle with elongate and transverse fibers lining the locule; c) Angiosperm seed sp. 1 with thin, smooth seed coat; d) Angiosperm seed sp. 2 with verrucate seed coat; e) Angiosperm seed sp. 3 with exotestal and foveolate seed coat; f) Angiosperm seed sp. 4 with smooth seed coat; g, h) Angiosperm seed sp. 5 with raised epidermal cells forming a reticulate pattern; i) Wedge-shaped angiosperm fruit with remains of floral parts near apex. Specimens, TV43-S136726 (a), TV44-S148144 (b), TV43-S170074 (c), TV43-S136747 (d), TV43-S170073 (e), TV38-S174615 (f), TV44-S148003 (g), TV44-S148004 (h), TV43-S174685 (i). Scale bars 300 Μm (a–i).
Text-fig. 7. p4 of U. deningeri from Šandalja I compared with other bear species. a: Šandalja I (specimen H; 1 – occlusal, 2 – lingual view), b: U. etruscus, Casa Frata (private collection), c: U. etruscus, Olivola (IGF 4605), d: U. deningeri, C 718 cave (NM-Rv 20003), e: U. t. mediterraneus, Azykh cave (ZIN 32549) (all in occlussal view). Specimens coated by ammonium chloride; d reversed. in Šandalja I (Croatia) And
Text-fig. 7. p4 of U. deningeri from Šandalja I compared with other bear species. a: Šandalja I (specimen H; 1 – occlusal, 2 – lingual view), b: U. etruscus, Casa Frata (private collection), c: U. etruscus, Olivola (IGF 4605), d: U. deningeri, C 718 cave (NM-Rv 20003), e: U. t. mediterraneus, Azykh cave (ZIN 32549) (all in occlussal view). Specimens coated by ammonium chloride; d reversed.
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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.