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91,407 results for “Effectiveness”
X-ray and ion irradiation effects on azurite, malachite and alizarin pictorial samples
<p>XPS was used to analyze X-ray effects on pellets of azurite, malachite and alizarin pure pigments and on azurite and alizarin tempera paint mock-ups, where the pigments were mixed with egg yolk. X-ray radiation damage was assessed by comparing successive high-resolution spectra acquired on the same spot. The spectra of the pure pigments show low radiation sensitivity and reactivity under the selected X-ray irradiation conditions, although some differences among them were detected. Whereas alizarin does not experience surface chemical changes during the prolonged irradiation experiment, a slow progressive chemical reduction of azurite and malachite (copper-based pigments), together with the formation of cuprite, is observed. On the other side, tempera paint mock-ups are sensitive to X-rays and alterations of the egg yolk binding medium are displayed in a shorter time scale than the induced chemical modifications of the pure pigments. Besides, XPS allows to determine that the azurite pigment and the binder interact chemically. Azurite is partially reduced in the tempera paint from the beginning of the irradiation experiment and the subsequent X-ray exposure induces further reduction</p>
Data related to "Effective Publication Strategies in Clinical Research"
<p>Data and supplementary material in support of "Deutz, D.B., Vlachos, E., Drongstrup, D., Dorch, B.F., Wien, C. (2019). Effective Publication Strategies in Clinical Research, PLOS ONE".</p> <p>Content:</p> <p>A README file with details regarding the purpose of the data collection, the setting and methodology and descriptions of the rest of the files, the Python script used to extract publication data from the Scopus API, the interview invitation email, the interview guidelines, the information regarding the interviews, supporting information on raw publication data, two tables as presented at the publication, and the coordinates of a plot.</p>
example stimuli of "Behavioral effects of rhythm, carrier frequency and temporal cueing on the perception of sound sequences"
<p>Exemplary subset of stimuli accompanying the manuscript "Behavioral effects of rhythm, carrier frequency and temporal cueing on the perception of sound sequences"</p>
Dataset for the article "Cost-effective Potential for Accurate Polarizable Embedding Calculations in Protein Environments"
<p>This dataset contains additional material related to the article: "Cost-effective Potential for Accurate Polarizable Embedding Calculations in Protein Environments". Final version of the article is available at <a href="https://doi.org/10.1021/acs.jctc.9b00616">https://doi.org/10.1021/acs.jctc.9b00616</a> (paywall). A preprint is freely available at <a href="https://doi.org/10.26434/chemrxiv.8126912">https://doi.org/10.26434/chemrxiv.8126912</a>. See <em>readme.md</em> for further description.</p>
Figure 1 in Effect of thiamethoxam (organophosphate) on the flies and beetle visitation and cadaveric decomposition process
Figure 1 Decomposition phases in the carcasses of control group and the contaminated group with Thiamethoxam: A fresh, B bloated, C decay, D postdecay, E skeletal.
Figure 4 in Effect of thiamethoxam (organophosphate) on the flies and beetle visitation and cadaveric decomposition process
Figure 4 Nonmetric Multidimensional Scaling (nMDS) obtained from data on the presence and absence of species in each stage of decomposition, for the contaminated and control groups.
Figure 2 in Spatial distribution and effects of land use and cover on cutaneous leishmaniasis vectors in the municipality of Paracambi, Rio de Janeiro, Brazil
Figure 2 Monthly mean relative abundance of medically relevant sand fly species. Please note the scale difference in the Y axis. Paracambi, RJ, Brazil, 1992-1994.
Fig. 2 in Protocol for collecting Mutillidae (Hymenoptera, Aculeata) in ecological studies: species-area effects on Mutillidae communities
Fig. 2. Rarefaction of Mutillidae species in each fragment (A) and general (B) sampled in Cerrado fragments from January to December 2012.
Fig. 5 in Effect of Bacillus sphaericus Neide on Anopheles (Diptera: Culicidae) and associated insect fauna in fish ponds in the Amazon
Fig. 5. Regression analysis of diversity and richness data compared to application of Bacillus sphaericus.
Fig. 3 in Effect of Bacillus sphaericus Neide on Anopheles (Diptera: Culicidae) and associated insect fauna in fish ponds in the Amazon
Fig. 3. Abundance over time of aquatic insects and values LNMH at C3 and C4, Manaus, Amazonas, Brazil.
Figure 1 in Effects of forest conversion on tce assemblages' structure of aquatic insects in subtropical regions
Figure 1. Location of tce micro-basin and sampled streams in forested area (F1, F2, and F3) and converted area (C1, C2, and C3) at Parque Estadual do Turvo and adjacent areas, in soutcern Brazil.
Figure 3 in Effects of forest conversion on tce assemblages' structure of aquatic insects in subtropical regions
Figure 3. Ordination diagram of NMDS of Epcemeroptera, Plecoptera, and Triccoptera assemblages at streams in forested area (F) and converted area (C). Numbers 1-3 refer to tce stream; R refers to rocky bottom substrate, and L refers to leaf litter substrate.
Fig. 2 in Effect of Bacillus sphaericus Neide on Anopheles (Diptera: Culicidae) and associated insect fauna in fish ponds in the Amazon
Fig. 2. Abundance over time of aquatic insects and values LNMH at C1 and C2, Manaus, Amazonas, Brazil.
Figure 3 in Organic farming and moderate tillage change the dominance and spatial structure of soil Collembola communities but have little effects on bulk abundance and species richness
Figure 3. Abundance, number of species and Berger-Parker index in samples in different management types and fields. Colors show fields. Boxplots show data distribution (n = 81 per field), horizontal lines represent the medians.
Figure 1 in No effect of liming on the Eastern Red-backed Salamander after 5 years
Figure 1. Comparison of the regressions of weight as a function of snout vent length of Eastern Red-backed Salamanders captured in control (open circles, dashed line) or limed (black circles, solid line) blocks in August 2016 in the Portneuf Wildlife Sanctuary, located approximately 100 km northwest of Québec City (Quebec, Canada).
Fig. 3 in Effects of the Secondary Metabolite Producing Pseudomonas fluorescens CHA0 on Soil Protozoa and Bacteria
Fig. 3. Colony forming curves of culturable bacteria in soil microcosms harvested after 1, 7, and 14 days on non-selective agar media. For each harvest event the same plates were counted repeatedly. Statistical significant differences between the treatments at the last counting event of each harvest are indicated by different letters.
Fig. 4 in Effects of the Secondary Metabolite Producing Pseudomonas fluorescens CHA0 on Soil Protozoa and Bacteria
Fig. 4. Abundance of culturable protozoa in the four different soil microcosms. The protozoa were counted by MPN as fast-growing protozoa after 1 week of incubation and as total protozoa after 3 weeks of incubation by inspecting the same plates twice. Significant differences of treatments within each sampling time and incubation time are shown as different small letters above the bars. After one day protozoa was only counted in the control microcosm. Significant differences between the abundance of protozoa in the control microcosm are shown as capital letters. bd: below detection limit of 157 protozoa g–1 dw. nd: not determined.
Fig. 2 in Effects of the Secondary Metabolite Producing Pseudomonas fluorescens CHA0 on Soil Protozoa and Bacteria
Fig. 2. Fate of inoculated P. fluorescence CHA0/gfp1 and P. fluorescens CHA0/pME3424 during incubation in soil microcosms determined as CFU on selective agar media (see Materials and Methods for selective agents). The individual data points for each replicate are shown along with the linear regression line for each strain.
Fig. 1 in Effects of the Secondary Metabolite Producing Pseudomonas fluorescens CHA0 on Soil Protozoa and Bacteria
Fig. 1. Soil respiration measured as accumulated CO 2 during the incubation of microcosms consisting of soil, shredded barley straw and either of three bacterial inoculants: E. aerogenes, P. fluorescens CHA0/gfp1, P. fluorescens CHA0/pME3424. Control treatment did not receive any bacteria.
Fig. 9. T. thermophila cells immunostained with monoclonal anti-cdc14A in Effects of Roscovitine on Schedule of Divisional Morphogenesis, Basal Bodies Proliferation and Cell Divisions in Tetrahymena thermophila
Fig. 9. T. thermophila cells immunostained with monoclonal anti-cdc14A antibody. Cs and nCS – apical couplets of basal bodies for proter and opisthe, respectively; Ma – macronucleus. Other explanations as in Figs 1 and 8. Bar: 10 µm, bar in D for B–D.
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.