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3,484 results for “Plastics”
Figure 8 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 8. Morphometrics of eryopiform skulls, depicting crucial skull proportions relative to size. Arrows in (a) highlight ontogeny in O. labyrinthicus and S. haeuseri.
Figure 6 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 6. Cranial morphology in eryopid temnospondyls, exemplified by reconstructed skull dorsal views. (a) Actinodon frossardi (after Werneburg, 1997), (b) Osteophorus roemeri (after Meyer, 1860), (c) Glaukerpeton avinoffi (after Werneburg and Berman, 2012), (d) Onchiodon labyrinthicus (after Boy, 1990), (e) Onchiodon thuringiensis (after Werneburg, 2008), (f) Clamorosaurus nocturnus (after Gubin, 1983, and photographs courteously provided by Ralf Werneburg), (g) Eryops sp. from the Moran Formation (MCZ 1914), (h) Eryops anatinus (AMNH 4310), (i) Eryops megacephalus (MCZ 1129). Darker shading figures depressions on the dorsal side of the skull roof.
Figure 7 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 7. Morphospace occupation of eryopiform skulls, showing differences in ontogenetic change and morphometric variance between Onchiodon labyrinthicus and Sclerocephalus spp. and adult skulls of other eryopids. (a) PC1–PC2 axes, (b) areas occupied by immature Onchiodon and Sclerocephalus compared, (c) close-up of (a) with focus on variation in O. labyrinthicus, and (d) PC1 plotted against size.
Figure 2 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 2. Larger juveniles of Onchiodon labyrinthicus Geinitz. (a) LFUG 13570, (b) LFUG 13501, (c) MMG SaP 356, (d) LFUG 13391, (e) LFUG 13398, (f) LFUG 13609, (g) LFUG 13047. Darker shading figures depressions on the dorsal side of the skull roof. Scale equals 10 mm.
Figure 4 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 4. Reconstruction of skulls in dorsal view Onchiodon labyrinthicus Geinitz. (a) MMG SaP 237, (b) LFUG 13343, (c) LFUG 13405, (d) MMG SaP 356, (e) LFUG 13391, (f) LFUG 13570, (g) LFUG 13501, (h) LFUG 13292. Darker shading figures depressions on dorsal side of skull roof. Scale equals 10 mm.
Figure 5 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 5. Palate of Onchiodon labyrinthicus Geinitz, in ventral view. (a) LFUG 13394, (b) LFUG 13514. Darker grey is the inner side of the skull roof. Scale equals 10 mm.
Figure 3 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 3. Ontogeny of the dermal ornament in Onchiodon labyrinthicus Geinitz. (a) LFUG 13343, (b) MMG SaP 390, (c) MMG SaP 356, (d) MMG SaP 361, (e) LFUG 13395, (f) LFUG 13391, (g) LFUG 13570, (h) LFUG 13292.
Datasets and code for Rapljenović et al. 2024: Adsorption of trace metals onto different plastics during long-term exposure in an estuarine environment: influence of time, stratified water column, and specific surface area
<p>This repository contains datasets and R code to reproduce results from Rapljenović et al. 2024: Adsorption of trace metals onto different plastics during long-term exposure in an estuarine environment: influence of time, stratified water column, and specific surface area.</p>
Fig. 1 in Ingestion of plastics in the European bass (DIcentrarchus labrax Linnaeus, 1758): first known observation in the city of Plovdiv, Bulgaria
Fig. 1. Different plastic products found in the gut of European bass, purchased from the city of Plovdiv (photograph: Velichka Pachedzhieva).
Electron microscopy images and morphometric data of SARS-CoV-2 variants in ultrathin plastic sections - Dataset 06 (SARS-CoV-2 Omicron B.1.1.529; BA.2)
<p>Dataset 06 comprises 164 transmission electron microscopy images of extracellular SARS-CoV-2 (isolate Omicron B.1.1.529; BA.2) particles in ultrathin plastic sections (45 nm) through Vero cell cultures. The images were recorded with dimensions of 4112 x 3008 pixels at a pixel size of 0.1641 nm and stored in 16-bit TIF format. It is recommended that an image viewer capable of reading 16-bit images, such as IrfanView, be used to visualize the images. The image files have been size calibrated and can be opened with the correct size calibration using ImageJ or Fiji with the Bioformats importer. A PDF document is provided with the image files, which describes the methods used for the generation of the images. Additionally, an XLSX file is included, offering morphometric particle measurements and the calculated statistical values for their distribution. The dataset was produced as dataset 06 for a comparative morphometric analysis of evolving SARS-CoV-2 variants. Further datasets used for the analysis are available in this repository (see dataset description document).</p>
Electron microscopy images and morphometric data of SARS-CoV-2 variants in ultrathin plastic sections - Dataset 04 (SARS-CoV-2 Beta B.1.351)
<p>Dataset 04 comprises 132 transmission electron microscopy images of extracellular SARS-CoV-2 (isolate Beta B.1.351) particles in ultrathin plastic sections (45 nm) through Vero cell cultures. The images were recorded with dimensions of 4112 x 3008 pixels at a pixel size of 0.1641 nm and stored in 16-bit TIF format. It is recommended that an image viewer capable of reading 16-bit images, such as IrfanView, be used to visualize the images. The image files have been size calibrated and can be opened with the correct size calibration using ImageJ or Fiji with the Bioformats importer. A PDF document is provided with the image files, which describes the methods used for the generation of the images. Additionally, an XLSX file is included, offering morphometric particle measurements and the calculated statistical values for their distribution. The dataset was produced as dataset 04 for a comparative morphometric analysis of evolving SARS-CoV-2 variants. Further datasets used for the analysis are available in this repository (see dataset description document).</p>
Electron microscopy images and morphometric data of SARS-CoV-2 variants in ultrathin plastic sections - Dataset 02 (SARS-CoV-2 Italy-INMI1)
<p>Dataset 02 comprises 154 transmission electron microscopy images of extracellular SARS-CoV-2 (isolate Italy-INMI1) particles in ultrathin plastic sections (45 nm) through Vero cell cultures. The images were recorded with dimensions of 4112 x 3008 pixels at a pixel size of 0.1641 nm and stored in 16-bit TIF format. It is recommended that an image viewer capable of reading 16-bit images, such as IrfanView, be used to visualize the images. The image files have been size calibrated and can be opened with the correct size calibration using ImageJ or Fiji with the Bioformats importer. A PDF document is provided with the image files, which describes the methods used for the generation of the images. Additionally, an XLSX file is included, offering morphometric particle measurements and the calculated statistical values for their distribution. The dataset was produced as dataset 02 for a comparative morphometric analysis of evolving SARS-CoV-2 variants. Further datasets used for the analysis are available in this repository (see dataset description document).</p>
Functional plasticity in vertebrate scavenger assemblages in the presence of introduced carnivores
<p>Data for manuscript focusing on the consumption of varying amounts of carrion by coastal scavengers in Queensland, Australia. </p>
database of Chemicals associated with Plastic Packaging (CPPdb), updated Oct 9, 2018
<p>CPPdb: database of Chemicals associated with Plastic Packaging. Includes chemicals associated with plastic packaging both in terms of use during manufacturing as well as presence in the final plastic packaging articles.</p> <p>CPPdb_ListA: chemicals LIKELY associated with plastic packaging</p> <p>CPPdb_ListB: chemicals POSSIBLY associated with plastic packaging</p>
Main dataset 'Environmental specificity in Drosophila-bacteria symbiosis affects host developmental plasticity'
<p>Main dataset from the manuscript 'Environmental specificity in <em>Drosophila</em>-bacteria symbiosis affects host developmental plasticity' (2019)</p>
MANOVA dataset 'Environmental specificity in Drosophila-bacteria symbiosis affects host developmental plasticity'
<p>MANOVA dataset from the manuscript 'Environmental specificity in <em>Drosophila</em>-bacteria symbiosis affects host developmental plasticity' (2019)</p>
Raw data for "Benchmarking the in vitro toxicity and chemical composition of plastic consumer products"
<p>These files are associated with the publication "Benchmarking the in vitro toxicity and chemical composition of plastic consumer products" published in Environmental Science & Technology at <a href="https://doi.org/10.1021/acs.est.9b02293">https://doi.org/10.1021/acs.est.9b02293</a>.</p> <p>Raw data files for the non-target chemical analysis performed on consumer plastics using GC-QTOF-MS (Agilent .D format).</p> <p>FTIR spectra of the plastic products (pdf format).</p>
Dataset of Paper "Material selection and prediction of solar irradiance in plastic devices for application of solar water disinfection (SODIS) to inactivate viruses, bacteria and protozoa"
<p>Datasets of Paper “Predictive evaluation of solar irradiance in solar disinfection water plastic containers”.</p> <p>Data of the transmission spectra of the polymers: PMMA, PET, PC and PP.</p> <p>Data of the extinction coefficient spectra of the polymers: PMMA, PP, PC and PET.</p> <p>Data of the spectral incident radiation as a function of the thickness for PMMA, PET, PC and PP containers.</p> <p>Data of the spectral incident radiation required for inactivation of <em>MS2</em> virus, <em>E. coli</em> bacteria and <em>C. parvum</em> protozoa in a PMMA, PET, PC and PP containers.</p>
Text-fig. 3. Schematic geological section of the Kristina Mine near Hrádek/N. (state in 1963–1964) – height/length ratio 3:1. Explanations: vertical hatching – lignite seam, seamlet; dotted – coarse-grained sand, pea-gravel; short lines – sandy clay; white – clay; black lines – clay ironstone concretions; black dots – individual fossiliferous horizons designated as (A) plastic clay from the upper part of the main xylitic seam (about 5 m under t of the seam, (B) clay and "Blätterkohle" from the uppermost part of the first seamlet (split off the Main Coal Seam), (C) slightly sandy brown clay under the uppermost part of the Main Coal Seam, (D) base of the sandy clay with large concretions of the clay ironstone above the Main Coal Seam, (E) sandy clay (incl. clay ironstone) supplying most of leaf material with cuticles (F) 1–2 cm thin silty lenticles or thin beds of the sandy clay with xylites and Eomastixia within peagravels and coarse-grained sands, (G) coarse-grained sands with clayish silts with Fagus, Ocotea, Pterocarya, Tectocarya, (H) brown sandy clay underlying the uppermost seamlet, (I) lignite clay, base of the uppermost seamlet (J) Glyptostrobus – "Blätterkohle", base of the uppermost seamlet (according to Holý 1975, modified). in A Review Of The Early Miocene Mastixioid Flora Of The Kristina Mine At Hrádek Nad Nisou In North Bohemia (The Czech Republic)
Text-fig. 3. Schematic geological section of the Kristina Mine near Hrádek/N. (state in 1963–1964) – height/length ratio 3:1. Explanations: vertical hatching – lignite seam, seamlet; dotted – coarse-grained sand, pea-gravel; short lines – sandy clay; white – clay; black lines – clay ironstone concretions; black dots – individual fossiliferous horizons designated as (A) plastic clay from the upper part of the main xylitic seam (about 5 m under t of the seam, (B) clay and "Blätterkohle" from the uppermost part of the first seamlet (split off the Main Coal Seam), (C) slightly sandy brown clay under the uppermost part of the Main Coal Seam, (D) base of the sandy clay with large concretions of the clay ironstone above the Main Coal Seam, (E) sandy clay (incl. clay ironstone) supplying most of leaf material with cuticles (F) 1–2 cm thin silty lenticles or thin beds of the sandy clay with xylites and Eomastixia within peagravels and coarse-grained sands, (G) coarse-grained sands with clayish silts with Fagus, Ocotea, Pterocarya, Tectocarya, (H) brown sandy clay underlying the uppermost seamlet, (I) lignite clay, base of the uppermost seamlet (J) Glyptostrobus – "Blätterkohle", base of the uppermost seamlet (according to Holý 1975, modified).
Figure 2. A-D in Observation of Megachile saulcyi (Guérin-Méneville, 1844) (Hymenoptera: Megachilidae) using plastic for nest construction in Chile
Figure 2. A-D. Megachile saulcyi cutting the plastic bag. / Megachile saulcyi cortando la bolsa de plástico.
ScienceDex guides
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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.