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164 results for “mode 1”
HYCOM mode 1 steric SSH M2 amplitude and phase
<p>This data set contains data from a forward global HYCOM simulation (22.1) with realistic tide and atmospheric forcing as discussed in <a href="https://doi.org/10.1016/j.ocemod.2020.101656">https://doi.org/10.1016/j.ocemod.2020.101656</a> (On the interplay between horizontal resolution and wave drag and their effect on tidal baroclinic mode waves in realistic global ocean simulations, 2020, MC Buijsman, GR Stephenson, JK Ansong, BK Arbic, JAM Green, ... Ocean Modelling 152, 101656). <strong>Please cite this article when using these data. </strong></p> <p>This is a 4-km simulation with 41 layers. All data is on the native tripole grid. Data is stored as netcdf4 classic. The 2D data sets are 7055 x 9000 (lat x lon).</p> <p>The data set contains</p> <ol> <li>the M2 mode 1 complex amplitude (RE+i*IM) of steric SSH computed for a two-week time series; the phase is relative to GMT 01-Sep-2016 01:00:00; the mode-1 amplitude is computed from the mode-1 surface pressure value (see <a href="https://doi.org/10.1016/j.ocemod.2020.101656">https://doi.org/10.1016/j.ocemod.2020.101656</a>). </li> <li>Mode-1 eigenspeed</li> <li>Positive seafloor depth, and latitude and longitude coordinates</li> </ol> <p>To convert eigenspeed to wavelength, phase speed and group speed, see <a href="https://doi.org/10.1016/j.ocemod.2020.101656">https://doi.org/10.1016/j.ocemod.2020.101656</a></p> <p><a href="https://sites.google.com/site/maartenbuijsman/">https://sites.google.com/site/maartenbuijsman/</a></p>
Fig. 1 in Covariation In Shapes Between The Sternum And Pelvis In Aquatic Birds With Different Locomotor Modes
Fig. 1. The sternum and pelvis in Common guillemot (Uria aalge) (wing-propelled diver) and Imperial cormorant (Phalacrocorax atriceps) (foot-propelled diver).
Fig 1 in Determination of limited histotrophy as the reproductive mode in Mustelus schmitti Springer, 1939 (Chondrichthyes: Triakidae): analysis of intrauterine growth of embryos
Fig 1. Mean embryo total length 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. Dashed line represents the linear model adjusted to the individual data, continuous line is for the Gompertz model and the pointed line represents the Von Bertalanffy growth curve.
Figure 1 in Morphological and Morphometrical Features in Dunaliella salina (Chlamydomonadales, Dunaliellaceae) During the Two-phase Cultivation Mode
Figure 1. Dunaliella salina cell density and dividing cells percentage dynamics in "green" (A) and "red" (B) cultivation phase.
Fig. 1 in Genome size of chrysophytes varies with cell size and nutritional mode
Fig. 1 Cell volumes [μm 3] of different chrysophytes. Different colors represent the different nutritional modes present. Phototrophic chrysophytes (light green) do have highest cell volumes compared to
BRAIN Journal-Motor Imagery signal Classification for BCI System Using Empirical Mode Décomposition and Bandpower Feature Extraction-Figure 1. General architecture of an online (BCI)
<p>One major challenge of our BCI system is to describe the signals EEG by a few relevant values called features i.e. step 3 in Fig (1). The success of the mental imagery classification depends on the choice of features used to characterize the raw EEG signals. These features can then be used in step 4 in order to classify the user’s mental state. Several approaches for feature extraction have been proposed in literature. </p>
Text-fig. 5. Free living colonies, showing a mode of preservation which does not allow for precise determination but clearly exhibiting features characteristic for Smittipora and/or Cupuladria and/or Reusirella. (note the clear intrazooecial buds). Specimen deposited in NM Prague under number T 3319. A – imprint, B – counterpart to fig A. C – Specimen deposited in SNM under number Z 37724. Optic photography. Scale bar 1 mm. in The Priabonian Bryozoan-Decapod Association From The Borové Formation (The Ďurkovec Quarry, Ne Slovakia) And Its Palaeoecological Implications
Text-fig. 5. Free living colonies, showing a mode of preservation which does not allow for precise determination but clearly exhibiting features characteristic for Smittipora and/or Cupuladria and/or Reusirella. (note the clear intrazooecial buds). Specimen deposited in NM Prague under number T 3319. A – imprint, B – counterpart to fig A. C – Specimen deposited in SNM under number Z 37724. Optic photography. Scale bar 1 mm.
Text-fig. 4. Reteporella sp., deposited in NM Prague under number T 3318. A – Large colony suggesting very short transport. Scale bar 10 mm. Optic photography. B – the detail of branch showing the mode of preservation (no original skeleton preserved). Scale bar 1 mm. SEM photography (BSE detector). in The Priabonian Bryozoan-Decapod Association From The Borové Formation (The Ďurkovec Quarry, Ne Slovakia) And Its Palaeoecological Implications
Text-fig. 4. Reteporella sp., deposited in NM Prague under number T 3318. A – Large colony suggesting very short transport. Scale bar 10 mm. Optic photography. B – the detail of branch showing the mode of preservation (no original skeleton preserved). Scale bar 1 mm. SEM photography (BSE detector).
Fig. 1 in Evidence for cryptic diversity in the Neotropical water snake, Helicops angulatus (Linnaeus, 1758) (Dipsadidae, Hydropsini), with comments on its ecology, facultative reproductive mode, and conservation
Fig. 1. The distribution of Helicops angulatus in the Neotropics. Locality data is from the VertNet and GBIF databases, as well as the literature. Diamonds (green oviparous, yellow viviparous): specimens reported in Appendix B of Braz et al. (2016); red stars represent localities where Helicops was sampled for DNA; small black markers: localities from Helicops angulatus map in Nogueira et al. (2019). As currently defined Helicops angulatus occurs in Freshwater Ecoregions: 301 North Andean Pacific Slopes, Rio Atrato; 302 Magdalena, Sinu; 304 South America Caribbean Drainages, Trinidad; 307 Orinoco Llanos; 308 Orinoco Guiana Shield; 311 Guianas; 313 Western Amazon Piedmont; 317 Ucayali, Urubamba Piedmont; 318 Mamore, Madre de Dios Piedmont; 319 Guapore, Itenez; 320 Tapajos, Juruena; 321 Madeira Brazilian Shield; 323 Amazonas Estuary and Coastal Drainages; 324 Tocantins, Araguaia; 325 Parnaiba; and 328 Northeastern Mata Atlantica.
Fig. 1 in Mode of life and hydrostatic stability of orthoconic ectocochleate cephalopods: Hydrodynamic analyses of restoring moments from 3D printed, neutrally buoyant models
Fig. 1. Three-dimensional reconstruction of a fragmentary baculite Baculites compressus Say, 1820 (WSU-1400) from the late Campanian Pierre Shale of Meade County, South Dakota. A. Model of a fragmentary specimen generated by photogrammetry with the software (3DF Zephyr). B. Broken septum isolated from the photogrammetry model. C. Suture pattern. D. Complete septum created by reconstructing the higher-order frilling with the suture pattern as a template.
Fig. 1. A in Revision of the flexible crinoid genus Ammonicrinus and a new hypothesis on its life mode
Fig. 1. A. Reconstruction of the Ammonicrinus life time position (modified after Piotrowski 1977: 208, fig. 2). B. Ammonicrinus plate diagram (not to scale).
Fig. 10. The lecanocrinid species Ammonicrinus sulcatus from locality 1 in Revision of the flexible crinoid genus Ammonicrinus and a new hypothesis on its life mode
Fig. 10. The lecanocrinid species Ammonicrinus sulcatus from locality 1 (A–G, I–Q) and 2 (H) (see Appendix 1). A–D. Facet views of GIK−2104–2107, showing nodular tubercles and spine−tubercles on exterior flanks of the columnals of the mesistele. E. Facet view (E1) and view of the exterior flank of a specimen (E2) (GIK−2108), showing tubercles and spine−tubercles on exterior flank of the columnal of the mesistele. F. Facet view of a specimen (GIK−2109), showing tubercles and spine−tubercles on exterior flank of the columnal of the mesistele. G. Facet view of a strongly sculptured columnal (GIK−2110) of the distal−most mesistele, showing connection to the dististele. H. Facet view of a columnal of the distal−most mesistele (GIK−2111), showing long LCEE and connection to the dististele. I. Facet view of a columnal of the distal−most mesistele (GIK−2112), showing relatively long LCEE and connection to the dististele. J. Interior view of a distal−most, barrel−like columnal of the mesistele (GIK−2113) with LCEE. K. Interior view of a distal−most, barrel−like columnal of the mesistele (GIK−2114), with partly preserved LCEE. L. Facet view of a juvenile distal columnal of the mesistele (GIK−2115) with nodular tubercles on exterior flank and on LCEE. M–N. Juvenile columnals of the proximal mesistele in facet views, showing well developed nodes on exterior flanks. M. GIK−2116. N. GIK−2117. O. Facet view of a juvenile distal columnal of the mesistele (GIK−2118) with nodular tubercles on exterior flank and on LCEE. P. Lateral view (P1) and view of the exterior flank (P2) of the partly preserved mesistele (GIK−2119); the specimen shows nodular tubercles, spine−tubercles and a few partly preserved spines (arrow). Q. Facet view (Q1) and lateral view (Q2) of a cracked, coiled mesistele (GIK−2120), showing several tuberculated and concave ossicles of the cup (arrows). Scale bars 10 mm.
Fig. 1 in Functional anatomy and mode of life of the latest Jurassic crinoid Saccocoma
Fig. 1. Restoration of Saccocoma tenella (Goldfuss, 1831). Some arms or their distal parts omitted for clarity (drawing by Jerzy Dzik based on a model constructed by the author).
Fig. 1 in Aspects of life mode among Ordovician asteroids: Implications of new specimens from Baltica
Fig. 1. Geographic and stratigraphic settings of the new fossils. A. Regional geography; specimens of Estoniaster maennili gen. et sp. nov. found near Vasalemma, Estonia; those of Urasterellidae found near Volkhov, Russia. B. Local geography in the region of Vasalemma, Estonia, discovery site for the described specimens of Estoniaster maennili. C. Local geography in the region of Volkhov, Russia, discovery site for the described specimens of Urasterellidae. D. Ordovician correlation chart, data from Webby et al. (2004). Asterisks mark positions of new fossils.
Figure 1 in Life history dynamics and biogeography of a nudibranch with contrasting developmental modes: A hypothesis for the evolution of larval types
Figure 1. Map of the lower Gulf of Maine with the distribution of Dendronotus frondosus and Dendronotus sp. from subtidal and intertidal habitats near the coasts of Maine (ME) and New Hampshire (NH), USA and New Brunswick (NB) and Nova Scotia (NS), Canada. See Table I to reference site numbers and Cartesian coordinates. Sites for seasonal monitoring of hydroid and nudibranch abundance include York (2), West Quoddy Head (12) and Eastport (13), Maine.
Figs. 1–4 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
Figs. 1–4. SEM micrographs of mature oocytes of Kelita toroi. 1. Entire oocyte, lateral view, anterior end toward left; apparent longitudinal ridge along top an artifact presumably created by criticalpoint drying. 2. Closeup of micropylar process outlined by rectangle in fig. 1. 3. Entire oocyte, dorsal view. 4. Closeup of micropylar process outlined by rectangle in fig. 3.
Figure 1. A in The relationship between skull morphology, biting performance and foraging mode in Kalahari lacertid lizards
Figure 1. A, phylogenetic relationships among major lizard clades showing the evolution of foraging mode across squamates. The cladogram is based on Estes, de Queiroz & Gauthier (1988). B, phylogenetic relationships among the taxa included in this study. Sit-and-wait foraging (black bars) is presumed to be the basal condition for both Meroles and Pedioplanis. See text for details. The cladogram is based on Arnold (1991).
Figure 1 in Postcranial element shape and function: assessing locomotor mode in extant and extinct mustelid carnivorans
Figure 1. Landmark placement on four postcranial elements (Martes pennanti as representative species). A, humeral distal extremity. B, ulnar proximal extremity. C, femoral proximal extremity. D, complete tibia, cranial aspect.
FIGURE 1 in Oviparity, viviparity or plasticity in reproductive mode of the olm Proteus anguinus: an epic misunderstanding caused by prey regurgitation?
FIGURE 1 Image of an olm (Proteus anguinus) regurgitating a fire salamander (Salamandra salamandra) larva. A) Image of an olm (22.5 cm of total length), moments before B) it started to regurgitate a salamander larva (3.1 cm of total length). C) shows a close-up of the salamander head and the larva fully regurgitated, with D) showing details of the still alive salamander larva.
Figure 1. Iporangaia pustulosa male touching the metatarsal gland IV in Mode of use of sexually dimorphic glands in a Neotropical harvestman (Arachnida: Opiliones) with paternal care
Figure 1. Iporangaia pustulosa male touching the metatarsal gland IV on a leaf (seta).
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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.