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7,920 results for “implications”
Data set for "Implications of lidar depolarized signal for deformed raindrops remote sensing"
<p>This is the dataset used in the paper "Implications of lidar depolarized signal for deformed raindrops remote sensing"</p>
Inverted S-wave velocity model for "Anomalous radial anisotropy and its implications for upper mantle dynamics beneath South China from multimode surface wave tomography"
<p># Instructions for the South China velocity model dataset from multi-mode surface-wave inversion.</p> <p> </p> <p>1. The detailas can be found at the paper: Tang Q, Sun W, Yoshizawa K, et al. Anomalous radial anisotropy and its implications for upper mantle dynamics beneath South China from multimode surface wave tomography. Journal of Geophysical Research: Solid Earth, 2022, 127(8): e2021JB023485.</p> <p> </p> <p>2. The relative SV-wave and SH-wave velocity models at different depths (from 0 to 300 km) are stored in the "data" foder. Each file follows the name convention: shear_{SV/SH}.{depth}.dat representing SV or SH velocity at a given depth.</p> <p> </p> <p>3. In each velocity file, each line have three columns: longitude (deg) latitude (deg) relative_velocity (%)</p> <p> </p> <p>4. The reference velocity can be found in the two files "SV_velocity" and "SH_velocity", depth and velocity.</p> <p> </p> <p>5. The relative velocity is calculated from (absolute-reference)/reference*100%. Thus one can have the absolute velocity via absolute = relative * (1+relative/100).</p>
Data from: Newly discovered morphology of the Silurian sea spider Haliestes and its implications
<p>The three-dimensionally preserved Haliestes dasos from the Silurian (Wenlock) Lagerstätte is the most complete fossil sea spider and the oldest unambiguous pycnogonid known from the fossil record. The discovery of two new specimens to add to the holotype reveals new features including proximal annulations of the appendages and segmentation of the trunk end, critical details for comparison with pycnogonids from the Devonian (Emsian) Hunsrück Slate and for the interpretation of the evolutionary significance of Palaeozoic genera. There is some evidence of sexual dimorphism. H. dasos was nektobenthic and its morphology indicates an unusual mode of feeding compared to living pycnogonids. The new morphological features of H. dasos are closely similar to those in Palaeoisopus problematicus from the Hunsrück Slate and it clearly belongs, together with that species, in stem Pycnogonida and not the crown group.</p>
Stability of Biogenic Amino Acids in Concentrated Sulfuric Acid: Implications for the Habitability of Venus' Clouds
<p><strong>DESCRIPTION OF THE DATASET: </strong><br> <br> <strong>Supplementary Datasets for the paper published in Astrobiology, Venus 2 Special Collection:</strong><br> </p> <p><em>Supplementary Dataset S1:</em> The original 1D <sup>1</sup>H and <sup>13</sup>C NMR data collected in 81% w/w and 98% w/w concentrated sulfuric acid at all three time intervals for all 20 amino acids. Supplementary Dataset S1 also contains original 1D <sup>1</sup>H and <sup>13</sup>C NMR data for modified amino acids such as <em>S</em>-sulfocysteine, <em>O</em>-sulfoserine, oxidized cysteine, oxidized methionine as well as original 1D <sup>1</sup>H and <sup>13</sup>C NMR data for tests with formic acid and FeO.<br> </p> <p><em>Supplementary Dataset S2:</em> The original 2D <sup>1</sup>H-<sup>13</sup>C HMQC NMR data for all 20 amino acids collected in 98% w/w concentrated sulfuric acid.</p> <p> </p>
FIGURE 3. ZMB 2796 in On the importance of types and the perils of "en passant" taxonomy: a brief history of the typification of Coluber naja Linnaeus, 1758 (Serpentes: Elapidae) and its implications, with the designation of a lectotype
FIGURE 3. ZMB 2796, here designated as lectotype of Coluber naja Linnaeus, 1758, also the holotype of Naja brasiliensis Laurenti, 1768. (A) Hood mark with additional small ocelli, as shown in Seba (1735, Pl. 89, fig. 4), indicated by arrows. (B) Underside of animal, arrows indicate multiple dark crossbands characteristic of Sri Lankan Naja naja. (C) Side view of head, arrow indicates the single cuneate scale. (D) Table 89, fig. 4 in Seba (1735), referenced by Linnaeus (1758) in his description of Coluber naja and Laurenti (1768) in his description of Naja brasiliensis.
FIGURE 2. ZMB 2795 in On the importance of types and the perils of "en passant" taxonomy: a brief history of the typification of Coluber naja Linnaeus, 1758 (Serpentes: Elapidae) and its implications, with the designation of a lectotype
FIGURE 2. ZMB 2795, syntype of Coluber naja Linnaeus, 1758, showing the (A) characteristic hood mark of Naja naja, and (B) the underside with multiple dark crossbands characteristic of Sri Lankan Naja naja indicated by white arrows. (C) Plate 85 from Seba (1735); note the great similarity between the illustration and specimen ZMB 2795.
FIGURE 1 in On the importance of types and the perils of "en passant" taxonomy: a brief history of the typification of Coluber naja Linnaeus, 1758 (Serpentes: Elapidae) and its implications, with the designation of a lectotype
FIGURE 1. Comparison between the throat patterns of an (A) an Indian and (B) a Sri Lankan specimen of Naja naja, showing overlap in the number of dark ventral bands. Indian specimen from Rathnapuri, Karnataka, Sri Lankan specimen from Kokuvil East, Jaffna, Sri Lanka. Photos by W. Wüster (A) and Aravinth Sukumar (B)
FIGURE 4. Specimen BMNH 1946.1.18.50 in On the importance of types and the perils of "en passant" taxonomy: a brief history of the typification of Coluber naja Linnaeus, 1758 (Serpentes: Elapidae) and its implications, with the designation of a lectotype
FIGURE 4. Specimen BMNH 1946.1.18.50, from Polonnaruwa, Sri Lanka. Holotype of Naia naia colour variety polyocellata Deraniyagala, 1939. (A) Top of the head and hood with hood mark. White arrows indicate the additional ocelli underlying the description of Deraniyagala's colour variety polyocellata. The blue patch is part of a nitrile glove holding down a flap of skin that is part of the hood. (B) Ventral view. White arrows indicate the four clearly defined ventral bands of the specimen. (C) Side view of the head; white arrow indicates the cuneate scale between the 4th and 5th infralabial, which is absent on the contralateral side of the head.
Supplemental information data from: "Alkali Trace Elements Observed by MarSCoDe LIBS at Zhurong Landing Area on Mars: Quantitative Analysis and Its Geological Implications"
<p>This dataset includes the normalized peak areas of MarSCoDe scietific targets used in Table 3 of the corresponding article. The specific peaks are listed below.</p> <p>Data Set S1: Li 670.97 nm, Fe 260.04 nm, Al 309.37 nm, Ca 318.03 nm, Mg 518.15 nm, K 766.70 nm, and Na 818.55/819.70 nm.</p> <p>Data Set S2: Sr 421.67 nm, Fe 260.04 nm, Al 309.37 nm, Ca 318.03 nm, Mg 518.15 nm, K 766.70 nm, and Na 818.55/819.70 nm.</p> <p>Data Set S3: S 564 nm, Fe 260.04 nm, Al 309.37 nm, Ca 612.39 nm, Mg 448.24 nm, K 766.70 nm, and Na 589.16/589.76 nm.</p>
FIGURE 6 in Mitochondrial genomes of three Mylabris (Pseudabris) species (Coleoptera: Meloidae, Mylabrini) and their phylogenetic implications
FIGURE 6. Secondary structure of the tRNAs of M. longiventris mitochondrial genome. The base differences among three Mylabris (Pseudabris) species are marked in green.
FIGURE 8 in Mitochondrial genomes of three Mylabris (Pseudabris) species (Coleoptera: Meloidae, Mylabrini) and their phylogenetic implications
FIGURE 8. Phylogenetic trees of Meloidae inferred using maximum likelihood and Bayesian inference methods based on the nucleotide sequences of the 13 PCGs + 2 rRNAs. The posterior probabilities (pp) and ultra-fast bootstrap values (uBV) are indicated by dot colors on branches.
FIGURE 4 in Mitochondrial genomes of three Mylabris (Pseudabris) species (Coleoptera: Meloidae, Mylabrini) and their phylogenetic implications
FIGURE 4. Nucleotide diversity (Pi) and non-synonymous (Ka) to synonymous (Ks) substitution rate ratios of 13 PCGs of M. hingstoni, M. longiventris, and M. przewalskyi.
FIGURE 3 in Mitochondrial genomes of three Mylabris (Pseudabris) species (Coleoptera: Meloidae, Mylabrini) and their phylogenetic implications
FIGURE 3. Relative synonymous codon usage in the protein-coding genes of the mitochondrial genomes of M. hingstoni, M. longiventris, and M. przewalskyi.
FIGURE 1 in Mitochondrial genomes of three Mylabris (Pseudabris) species (Coleoptera: Meloidae, Mylabrini) and their phylogenetic implications
FIGURE 1. Mitochondrial genome maps of M. hingstoni, M. longiventris, and M. przewalskyi. The arrows indicated the orientation of gene transcription. The tRNAs are denoted by the color blocks and are labelled according to the IUPACIUB single-letter amino acid codes (L1: CUN; L2: UUR; S1: AGN; S2: UCN). The GC content was plotted using a black sliding window, as the deviation from the average GC content of the entire sequence. GC-skew was plotted as the deviation from the average GC-skew of the entire sequence. The inner cycle indicated the location of the genes in the mt genome.
Prevalence, Phenotypes, Predictors and Prognostic Implication of Obstructive Sleep Apnea in Pulmonary Hypertension
ClinicalTrials.gov study NCT05595200. IPD Sharing: UNDECIDED. Countries: 1. Publications: 4.
Clinical Implication of the Tunable Crack Sensor
ClinicalTrials.gov study NCT03805815. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.
Implication of Long Non-coding RNA HOTTIP Haplotype on Liver Cancer Metastasis
ClinicalTrials.gov study NCT06544005. IPD Sharing: UNDECIDED. Countries: 1. Publications: 12.
Potential Role of CD9 and Implication of Motility Process in Pathogenesis of TEL/ALM1-positive ALL Relapses (LAL TEL/ALM1 and CD9).
ClinicalTrials.gov study NCT01282593. IPD Sharing: Not stated. Countries: 1. Publications: 6.
COVID-19 - Implications on Surgeons' Burnout and Career Satisfaction
ClinicalTrials.gov study NCT04433286. IPD Sharing: NO. Countries: 1. Publications: 1.
Physical Activity in Youth: Implications for Reversing Risk Factors for Type 2 Diabetes
ClinicalTrials.gov study NCT00739180. IPD Sharing: Not stated. Countries: 1. Publications: 3.
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.