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2,366 results for “Grade”
Ciência Vitae controlled vocabulary - Type of grade
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Using Parkrun Age Grading as an Indicator of Adolescent Health
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Ancillary files for "Graded transcendental functions: an application to four-point amplitudes with one off-shell leg"
<p>We provide ancillary files to "Graded transcendental functions: an application to four-point amplitudes with one off-shell leg".</p> <p>All attached files are in Mathematica format. See also appendix C of the manuscript for details on the ancillary files. </p> <ul> <li><strong>Families.zip: </strong><br>For each integral family, we provide in a single file <em>familyname.m</em> the list of propagators, a canonical basis and the corresponding differential equations, and a regularised boundary vector at the point (x, y) = (0, 0). <br>Files contain a list of Mathematica replacement rules in the format {prop["familyname"]-> {...}, basis["familyname"]-> {...}, boundaries["familyname"]-> {....}, DE["familyname"]-> {...}}. </li> <li><strong>BoundariesDemo.zip</strong>: An executable notebook implementing the fixing of boundary constants using the method for a two-loop example.</li> <li><strong>TridentFunctions.zip</strong>: For each relevant canonical integral and kinematic crossing listed in <em>basis_labels.m</em>, we provide a map to the trident functions in the form of a sparse rational array of size 13812 × 1282 in <em>mapping_positions.m</em> and <em>mapping_values.m</em>. We also provide the UT Laurent expansions of the trident functions in terms of 42258 iterated integrals and transcendental constants in <em>sb_labels.m</em>, again as a sparse array in <em>expansion_positions.m</em> and <em>expansion_values.m</em>.</li> <li><strong>FormFactor.zip</strong>: We provide the three-loop finite remainders R(3) and E(3) of the N = 4 sYM form factor in terms of Chen iterated integrals and MPLs.</li> <li><strong>Hjet.zip</strong>: The three independent helicity coefficients for the decay of a H boson to three partons at three loops are given in terms of iterated integrals and in a manifestly real MPL representation. In particular, we provide the part of the finite remainders containing new letters, with rational coefficients evaluated at x = 3/13, y = 11/17. </li> </ul>
Data from: A new pliosaurid (Sauropterygia, Plesiosauria) from the Oxford Clay Formation (Middle Jurassic, Callovian) of England: evidence for a gracile, longirostrine grade of Early–Middle Jurassic pliosaurids
A partial skeleton from the Sigiloceras enodatum ammonite Subzone (early Callovian, Middle Jurassic) of the Oxford Clay Formation of Quest Pit, near Stewartby, Bedfordshire, UK respresents one of the basalmost Middle Jurassic pliosaurids. Marmornectes candrewi gen. et sp. nov. possesses seven autapomorphies and a longirostrine snout. Reassessment of pliosauroid relationships demonstrates that Thalassiodracon hawkinsii, Hauffiosaurus spp. and Attenborosaurus conybeari are successively more derived basal representatives of Pliosauridae. This indicates that a longirostrine snout was acquired among Early Jurassic pliosaurids (such as Hauffiosaurus), but that these early taxa had a small body size, long neck, and gracile skull and limb bones relative to the contemporaneous rhomaleosaurids, which were robust, large-bodied macropredators. The pliosaurid lineage only acquired its 'characteristic' large size, robust skull and short neck in the late Middle Jurassic after the extinction of Rhomaleosauridae.
Data from: A chorus of color: hierarchical and graded information content of rapid color change signals in chameleons
Animals rely on information-rich signals to minimize costs associated with competition. If fighting ability is linked to stable individual attributes (e.g. morphology), the signals that communicate information about such ability should be relatively static. Conversely, the temporal variability of motivation should favor dynamic threat signals that indicate an animal's likelihood of escalating a contest. Though static colors are used by many animals to signal quality or fighting ability, the function of dynamic color change as a social signal has only recently begun to be investigated. Here, we examined the information content of rapid physiological color changes displayed by adult male veiled chameleons Chamaeleo calyptratus during agonistic interactions by conducting experimental trials between live chameleons and standardized, experimentally-controlled robochameleon models. Chameleons reliably communicated motivation with dynamic color displays – individuals that brightened were 14 times more likely to approach the robochameleon than non-brightening individuals. Additionally, chameleons with shorter latencies to maximum stripe brightness had stronger bites, and those displaying brighter, yellower stripes exhibited more aggression. The parallels between dynamic color changes and the vocalizations used to mediate aggressive interactions in other taxa are numerous. The use of particular vocalizations/color changes can signal motivation levels while specific signal elements (e.g. pitch, timing, brightness) may be linked to fighting ability. Because the complexity and potential information content of color signals increases markedly when organisms can display context-specific variation in the expression of these ornaments, the study of dynamic color signals is a field ripe for the investigation of complex visual and signaling strategies.
Monthly pCO2, gas transfer velocity and CO2 efflux rate in global streams and rivers (the GRADES river networks)
<p>The datasets contain monthly partial pressure of dissolved CO<sub>2</sub> (<em>p</em>CO<sub>2</sub>, µatm), gas transfer velocity (<em>k</em>, m d<sup>-1</sup>), and CO<sub>2</sub> efflux rate (g C m<sup>-2</sup> d<sup>-1</sup>) estimates for global streams and rivers in both comma separated values (csv) and GeoTIFF formats. These datasets served as the base for monthly CO<sub>2</sub> emission estimates for global streams and rivers and can be used to support regional terrestrial carbon balances. Original vector-version of products is based on the Global Reach–level A priori Discharge Estimates for SWOT or GRADES river networks, which have ~ 3 million individual reaches of global streams and rivers. The GeoTIFF version has a spatial resolution of approximately 0.0083º (1 km). The datasets also contain direct CO<sub>2</sub> measurements compiled from the literature (Supplementary Data 1).</p>
The dataset of early mortality in patient with surgically treated recurrent lower grade glioma
<p>The dataset is the record of recurrent lower grade glioma (LGG), with hematological and oncological markers. Meanwhile, an online calculator has been generated to predict early mortality in patient with surgically treated recurrent LGG, the R studio code used has also been uploaded.</p>
TMD GRADE assessment tables
<p>sheet 1 for pain; sheet 2 for physical functioning; sheet 3 for adverse events</p>
FIGURE 24. FUM-N 17242 in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 24. FUM-N 17242: A, photograph, B, drawing. A fore- or hind wing. Both to scale, 5 mm. Diagonal bands in the lower left and upper right are plant material.
FIGURE 22. MGUH 34113, a in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 22. MGUH 34113, a forewing: A, photograph of the part; B, photograph of the counterpart; C, drawing from both A and B. Note infuscation very light on the part as preserved, darker on the counterpart (see text). All to scale, 5 mm.
FIGURE 19. 14M-3801 in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 19. 14M-3801: A; drawing of forewing; B, drawing of the hind wing; C, photograph, complete. All to scale, 5 mm.
FIGURE 20. A in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 20. A, "Furagrion morsi" MOA 769 redrawn from part and counterpart photographs (Zessin 2011 Figs. 6 and 7); B–D, F. morsi (red) superimposed on F. jutlandicus wings: B, MHM 1742; C, D, FUM-N 11616. All to scale, 5 mm.
FIGURE 16. FUM-N 11696 in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 16. FUM-N 11696: A, drawing of bottom wing in 17C; B, drawing to top wing in 17C; C, photograph. All to scale, 5 mm.
FIGURE 15. 14M-2765 in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 15. 14M-2765: A, photograph; B, drawing as preserved; C, the fore- or hind wing graphically unfolded. All to scale, 5 mm.
FIGURE 23. A, Furagrion ansorgei MOA 770 redrawn from a in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 23. A, Furagrion ansorgei MOA 770 redrawn from a higher resolution copy of Zessin's (2011) figure 3 photograph provided by J. Ansorge; shape compared with that of the proposed neotype (blue) B, forewing; C, hind wing. A to scale, 5 mm; B, C wings to no scales, the sizes of proposed neotype wings are adjusted to match arculus to apex and anterior wing margin of MOA 770 to compare shape.
FIGURE 12 in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 12. Wings of MM-4785A: A, top wing in Fig. 9 (red), a forewing; B, wing below (blue), a hind wing. Both to scale, 5 mm.
FIGURE 8 in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 8. Wings of MM-10750, colour-coded forewings (FW) and hind wings (HW) to match colours in Fig. 7. All to scale, 5 mm.
FIGURE 10 in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 10. Principle component analysis of Furagrion wings. F. jutlandicus forewings in red, hindwings in blue, those unknown as fore- or hind wings in green, and the F. ansorgei wing is in purple. A, based on ratios only; B, based on both measured distances and ratios. See Table 4 for input data.
FIGURE 2. FUM-N 13856 in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 2. FUM-N 13856, with which Petrulevičius et al. (2008) defined Furagrion (as ERK-KL-T1): A, photograph; B, drawing. Both to scale, 5 mm. A forewing. Ax1, Ax2 = antenodal cross veins 1 and 2; arc = arculus; b = brace vein; CuA = anterior branch of the cubitus; IR1, IR2 = intercalar vein 1 and 2; MA, MP = the anterior and posterior branches of the media; nod = nodus; pt = pterostigma; Q = quadrangle; RA = radius anterior; RP1, RP2, RP3-4 = branches of the radius posterior; sn = subnodus; * = origin of RP2.
FIGURE 1. MGUH 1819 in The damselfly genus Furagrion Petrulevičius et al. (Odonata, Zygoptera) from the early Eocene Fur Formation of Denmark and the dysagrionoid grade
FIGURE 1. MGUH 1819, Henriksen's type specimen of Phenacolestes jutlandica: A, photograph; B, drawing; C–E, labelled wings. A, B to scale, C–E to scale, both scales 5 mm.
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.