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319 results for “Mode 2”
Series data for the 22PN nonlinear memory effect in the l=2, m=0 mode.
<p>Dataset associated with the preprint arXiv:2407.19017, “Waveform models for the gravitational-wave memory effect: Extreme mass-ratio limit and final memory offset” by Arwa Elhashash and David A. Nichols. It contains the 22 post-Newtonian-order series data for the l=2, m=0 spin-weighted spherical harmonic mode of the gravitational-wave memory signal from an extreme-mass ratio inspiral with nonspinning black holes.</p>
Fig. 2 in Covariation In Shapes Between The Sternum And Pelvis In Aquatic Birds With Different Locomotor Modes
Fig. 2. Phylogenetic relationships among the studied birds based on Jetz et al. (2012), with their locomotor modes marked as: FP for foot-propelled divers, WP for wing-propelled divers, and SSW for surface swimmers.
Fig. 2 in Variation In Reproductive Modes Of Allium Oleraceum, A. Scorodoprasum And A. Vineale In Field Collection
Fig. 2. Correlations between mean mass of an aerial bulbil and flower number per plant in four Allium scorodoprasum accessions (No. 315, 437, 447 and 604). Ellipses show a 95 % confidence area
Fig 2 in Determination of limited histotrophy as the reproductive mode in Mustelus schmitti Springer, 1939 (Chondrichthyes: Triakidae): analysis of intrauterine growth of embryos
Fig 2. Mean yolk mass and standard deviation as a function of the ordinal day of the year considering the two consecutive years (2006 and 2007) for Mustelus schmitti embryos. Using the same y axis values the continuous line represents the logistic curve adjusted for presence/absence of yolk sac, the probability of an embryo having external yolk sac is given by Yt=1/(1+e(-13.749 + 0.072*t)) for 2006 and Yt=1/(1+e(-10.472 + 0.054*t)) for 2007.
Figure 2 in Morphological and Morphometrical Features in Dunaliella salina (Chlamydomonadales, Dunaliellaceae) During the Two-phase Cultivation Mode
Figure 2. Changes of D. salina morphometrical parameters: cell height and width (A, B), dividing and non-dividing cells volume (C, D) and percentage of cells with different volume (E, F) in "green" and "red" cultivation phase
Fig. 2 in Diversification rates in Tardigrada indicate a decreasing tempo of lineage splitting regardless of reproductive mode
Fig. 2 Bayesian phylogenetic reconstructions for three distinct evolutionary lineages of Tardigrada with respective lineage-through-time plots. The trees were calculated based on the reduced datasets with singular sequence representing a given species/entity delimited in this study with multiple DNA taxonomy approaches (see the "Mate-
Fig. 2 in Genome size of chrysophytes varies with cell size and nutritional mode
Fig. 2 Genome size [pg] of investigated chrysophytes. Different colors represent the different nutritional modes present. Heterotrophic chrysophytes (dark red) tend to have smaller genome sizes, compared to phototrophic chrysophytes (light green), while mixotrophic chrysophytes (blue) show intermediate genome sizes. *Dinobryon sociale var. americana cf. div. schauinslandii; HF = Heterotrophic flagellate
BRAIN Journal-Motor Imagery signal Classification for BCI System Using Empirical Mode Décomposition and Bandpower Feature Extraction-Figure 4. The EMD decomposition results for subject 2 when he imagines left hand movement
<p>Fig. 4 shows the EMD decomposition result of one-trial (left hand movement imagination) for subject 2 in the channels C3 and C4 respectively (the pre-filtered EEG signal used for this illustration is not corrupted by blinking artifact.). Each channel is decomposed into ten IMFs and one residue</p>
BRAIN Journal-Motor Imagery signal Classification for BCI System Using Empirical Mode Décomposition and Bandpower Feature Extraction-Figure 4b. The EMD decomposition results for subject 2 when he imagines left hand movement
<p>d et al., 2011). Fig. 4 shows the EMD decomposition result of one-trial (left hand movement imagination) for subject 2 in the channels C3 and C4 respectively (the pre-filtered EEG signal used for this illustration is not corrupted by blinking artifact.). Each channel is decomposed into ten IMFs and one residue.</p>
BRAIN Journal-Motor Imagery signal Classification for BCI System Using Empirical Mode Décomposition and Bandpower Feature Extraction-Figure 2. Timing of one trial of the experiment with continuous feedback (Guger et al, 2001)
<p>At the beginning of each trial (t = 0 s), a fixation cross appeared on the black screen. After two seconds a warning stimulus was given in the form of a beep. From 3 to 4.25s, an arrow (cue stimulus), pointing to the left or right, was shown on the screen. The subject was instructed to imagine a left or right hand movement until the end of the trial, depending on the direction of the arrow. The EEG was sampled and classified on line throughout the session. Between 4.25 and 8s, the classification result was used to give a continuously updated feedback stimulus in the form of a horizontal bar that appeared in the center of the screen. The paradigm is illustrated in fig (2).</p>
Fig. 2 in Mode of life and hydrostatic stability of orthoconic ectocochleate cephalopods: Hydrodynamic analyses of restoring moments from 3D printed, neutrally buoyant models
Fig. 2. Shell and septum thickness measured from three specimens of Baculites compressus (WSU-1400, WSU-1401, and WSU-1405). Exponential curves were fit to these points to define thickness for the full 3D model as a function of whorl height.
Fig. 2 in Revision of the flexible crinoid genus Ammonicrinus and a new hypothesis on its life mode
Fig. 2. The first figures of Ammonicrinus from Springer (1926) and Krause (1927). A. Ammonicrinus wanneri Springer, 1926 (from Springer 1926: pl. 6: 4a, b). A1, view of the extetrnal flanks of the coiled mesistele; A2, coiled mesistele in lateral view. B. Ammonicrinus leunisseni sp. nov. (= "A. wanneri" in Springer 1926: pl. 6: 5, 5b). B1, view of the extetrnal flanks of the coiled mesistele; B2, coiled mesistele in lateral view. C. Photograph of the holotype of Ammonicrinus wanneri Springer, 1926, USNM−S2115; lateral view of coiled mesistele; connection between mesi− and dististele, dististele and attachment missing (see fracture surface at distal mesistele). D. Photograph of USNM−S2115, the Springer (1926) original of "Ammonicrinus wanneri" (= A. leunisseni sp. nov. herein); lateral view of coiled mesistele; connection between mesi− and dististele, dististele and attachment missing (see fracture surface at distal mesistele). E. Ammonicrinus doliiformis Wolburg, 1938a (for 1937) (= "A. wanneri" in Krause 1927: pl. 8: 4, 2). E1, view of the extetrnal flanks of the coiled mesistele; E2, coiled mesistele in lateral view. A–D from the Middle Devonian, Eifel Limestone; Prüm, Eifel, Germany (Springer 1926: 25); E from the Middle Devonian of Sötenich, Eifel (Krause 1927: 456). A, B, E not to scale; C, D scale bars 10 mm.
Fig. 2 in Functional anatomy and mode of life of the latest Jurassic crinoid Saccocoma
Fig. 2. Arrangement and articulation of proximal brachials in Saccocoma tenella. Asterisks denote non−muscular (cryptosynarthrial) articulations. Not to scale.
Fig. 2 in Aspects of life mode among Ordovician asteroids: Implications of new specimens from Baltica
Fig. 2. Palastericid asteroid Estoniaster maennili gen. et sp. nov. from Keila (Upper Ordovician) of northern Estonia. A. PIN 4125/766; A1, entire specimen, dorsal view; large transverse paired ossicles are ambulacrals in life orientation (i.e., vaulted); left arrow identifies position of A2; lower right arrow indicates the madreporite; A2, four superomarginals above, medial two with apparent spine remnants (arrow); paxilliform ossicles below SMs are intermarginals; A3, ambulacral series located top center of A1, left arrow points to transverse canal with the radial canal beyond, base of arrow rests in podial basin of next−distal ambulacrum; gracile cross−furrow articular structures (upper right arrow); A4, slightly disrupted ambulacrals; contact between subsequent ambulacrals is sinuous, with transverse interambulacral articular structures (arrow); A5, madreporite (upper right) with two superomarginals (lower left) and paxillae (lower right); A6, paxillae, arrow points to basal flange that separates papulary? re−entrants; to the left of the arrow is a paxilla with pustules for accessory spinelets; madreporite partially illustrated below; A7, upper surface, distal right, arrow points to right branch of ambulacrals of buccal slit. B. PIN 4125/767; B1, ambulacrals (above) and adambulacrals (below), the latter pushed against the ambulacrals and offset from the paired life position; left arrow points to nose of adambulacral and adambulacral−ambulacral facet; a skeletal gap is lateral to the nose. Re−entrants of two left ambulacrals suggest podial pores, these re−entrants lacking from ambulacrals at right; right arrow points to a superomarginal; B2, two partially exposed inferomarginals, dorsal view (arrow points to left IM); two ambulacrals below; B3, ventral view; upper arrow is an inferomarginal, lower arrow at a nose of an adambulacral; C. PIN 4125/768; C1, dorsal view, ambulacrals (above), those to left suggest podial pores, putative pores absent to right; superomarginals (left arrow), intermarginals (right arrow) with inferomarginals barely visible at lower edge, scattered paxillae above superomarginals; C2, ventral view, inferomarginals along lower margin, adambulacrals above these with nose directed toward axial furrow. Scale bars: A1, 3 mm; all others, 1 mm.
Figure 2 in The relationship between skull morphology, biting performance and foraging mode in Kalahari lacertid lizards
Figure 2. Three-dimensional plot of mean canonical scores of each lacertid species. Hl = Heliobolus lugubris (WF); Ms = Meroles suborbitalis (SW); Pl = Pedioplanis lineoocellata (SW); Pn = Pedioplanis namaquensis (WF).
Figure 2 in Postcranial element shape and function: assessing locomotor mode in extant and extinct mustelid carnivorans
Figure 2. Canonical variates axes for CVA analyses on locomotor mode of extant and fossil mustelids. Symbol types represent locomotor modes and different colour symbols represent genera within locomotor modes. A, humerus. B, ulna. C, femur. D, tibia.
Figure 2. Iporangaia pustulosa male rubbing the right metatarsus IV in Mode of use of sexually dimorphic glands in a Neotropical harvestman (Arachnida: Opiliones) with paternal care
Figure 2. Iporangaia pustulosa male rubbing the right metatarsus IV against the substrate (seta).
Figure 2 in Variation in elasmoid fish scale patterns is informative with regard to taxon and swimming mode
Figure 2. Landmark definitions.
Atmospheric river variability over the last millennium driven by annular modes: Part 1 (AR tags for LME Members #2–7)
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Atmospheric river variability over the last millennium driven by annular modes: Part 2 (AR tags for LME Members #8–13)
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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.