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13,017 results for “Positionning”
Synchronous generator experimental data (voltage, current and rotor position data)
<p>This database is composed of stator voltages and currents, field voltage and rotor position of a three-phase synchronous generator under resistive load. The data were acquired by means of two Tektronix MSO 2014B oscilloscopes with 4 channels each. Data were collected on 8 channels corresponding to phase voltages (Va,Vb,Vc), phase currents (Ia,Ib,Ic), field current of the generator (Ifd) and a pulse signal for angular position reference of the rotor (theta_m). For the simultaneous collection of the signals, a trip circuit was designed and implemented, the output of which was used as the triggering signal for the oscilloscopes. The synchronous generator was connected to a synchronous motor (Y-Y) and to a resistive circuit (18 units of 40W lamps) which served as loads. Voltage data were collected by means of a Keysight N2791 voltage probes; current data were collected using Tektronix A622 current tips. An PHCT203 optical key was used to collect rotor position pulse signal. The generator model is MOTROM M610-75-B-1K8-GS of 0.5 cv, 1800 rpm, 4 poles. The generator parameters obtained by means of physical bench tests were:</p> <p>Rs = 32.5 ohms (stator winding resistance)</p> <p>Rfd = 358.9 ohms (field winding resistance)</p> <p>Ld = 0.803H (direct axis stator inductance)</p> <p>Lq = 0.691H (quadrature axis stator inductance)</p> <p>Lls = 0.12H (stator winding leakage inductance)</p> <p>Lfd = 2.23H (field winding inductance)</p> <p>Vf = 64V (field voltage applied during the experiment, supplied by an regulated DC source)</p> <p> </p> <p>The database is composed by the following files of preprocessed data sampled at 10kHz in which the following variables are given, respectively, time, Va, Vb, Vc, Theta_r, Ia, Ib, Ic:</p> <p>1) data0001.txt</p> <p>2) data0002.txt</p> <p>3) data0003.txt</p> <p>4) data0001.csv</p> <p>5) data0002.csv</p> <p>6) data0003.csv</p> <p> </p> <p>Further, the database contains the following files of raw data:</p> <p>1) T0001A.txt</p> <p>2) T0001B.txt</p> <p>3) T0002A.txt</p> <p>4) T0002B.txt</p> <p>5) T0003A.txt</p> <p>6) T0003B.txt</p> <p>Each realization is contained in two files (suffixes A,B) and contain:</p> <p>Suffix A</p> <p>time</p> <p>CH1 (Va)</p> <p>CH1_peak (Va peak)</p> <p>CH2 (Vb)</p> <p>CH2_peak (Vb peak)</p> <p>CH3 (Vc)</p> <p>CH3_peak (Vc peak)</p> <p>CH4 (Theta_r)</p> <p>CH4_peak (Theta_r peak)</p> <p> </p> <p>Suffix B</p> <p>time</p> <p>CH1 (Ia)</p> <p>CH1_peak (Ia peak)</p> <p>CH2 (Ib)</p> <p>CH2_peak (Ib peak)</p> <p>CH3 (Ic)</p> <p>CH3_peak (Ic peak)</p> <p>CH4 (EMPTY)</p> <p>CH4_peak (EMPTY)</p> <p> </p> <p>When using the raw data, it is important to consider that the values were acquired in the following conditions:</p> <p>- Voltage probe scale: 100:1</p> <p>- Current probe scale: 100mV/A</p> <p>- Oscilloscope probe scale: 10x<br> <br> - Oscilloscope configuration: check header of raw files.</p> <p> </p> <p>Contact information: jose.grzybowski@uffs.edu.br</p>
Testing phantoms & SARAS' arms position - Part 1
<p>The SARAS project will allow the next generation of surgical robots to execute minimally invasive procedures with only the main surgeon, without the need of an assistant. In this video a small team of experts of the SARAS Consortium met in Verona to test progresses of Prostate’s phantom and the positioning of the SARAS arms with respect to the phantom and the Commercial Robot.</p> <p> </p>
Fig. 12 in Two new species of the Macrobiotus hufelandi complex (Tardigrada: Eutardigrada: Macrobiotidae) from Australia and India, with notes on their phylogenetic position
Fig. 12. Macrobiotus kamilae sp. nov., buccal apparatus and the oral cavity armature seen in PCM (paratypes, IZiBB). A. Dorso-ventral projection of the entire buccal apparatus. B–E. Oral cavity armature visible in dorsal (B, D) and ventral (C, E) views in a large and a small specimen, respectively. F–G. Placoid morphology visible in dorsal (F) and ventral (G) views, respectively. Empty indented arrowheads indicate the second band of teeth in the oral cavity, filled indented arrowheads indicate the third band of teeth in the oral cavity, whereas empty flat arrowheads indicate central constrictions in first macroplacoids and subterminal constriction in second macroplacoids. Scale bars in μm.
Fig. 9 in Two new species of the Macrobiotus hufelandi complex (Tardigrada: Eutardigrada: Macrobiotidae) from Australia and India, with notes on their phylogenetic position
Fig. 9. Macrobiotus kamilae sp. nov., cuticular structures on legs (paratypes, IZiBB). A–B. External granulation on legs III and I seen in PCM (A) and SEM (B), respectively. C–D. A cuticular bulge (pulvinus), granulation and a cuticular fold on the internal surface of leg III seen in PCM (C) and SEM (D). E–F. Granulation on leg IV seen in PCM (E) and SEM (F). Filled indented arrowheads indicate the cuticular bulge, filled flat arrowheads indicate patch of granulation and empty indented arrowheads indicate the cuticular fold under the claws. Scale bars in μm.
Fig. 8 in Two new species of the Macrobiotus hufelandi complex (Tardigrada: Eutardigrada: Macrobiotidae) from Australia and India, with notes on their phylogenetic position
Fig. 8. Macrobiotus kamilae sp. nov., habitus. A. Dorso-ventral projection (holotype, Hoyer's medium, PCM, IZiBB IN.030.08). B–C. Cuticular pores on the dorsal part of the body seen in PCM (B: holotype) and in SEM (C: paratype, IZiBB). Scale bars in μm.
Fig. 5 in Two new species of the Macrobiotus hufelandi complex (Tardigrada: Eutardigrada: Macrobiotidae) from Australia and India, with notes on their phylogenetic position
Fig. 5. Macrobiotus noongaris sp. nov., mouth opening and the oral cavity armature seen in SEM (paratype, IZiBB). A. Mouth opening with peribuccal sensory lobes and ten peribuccal lamellae. B–C. The oral cavity armature of a single paratype seen in SEM from different angles, in dorsal (B) and ventral (C) views, respectively. Empty flat arrowheads indicate the first band of teeth in the oral cavity, empty indented arrowheads indicate the second band of teeth in the oral cavity, filled indented arrowheads indicate the third band of teeth in the oral cavity. Scale bars in μm.
Fig. 2 in Two new species of the Macrobiotus hufelandi complex (Tardigrada: Eutardigrada: Macrobiotidae) from Australia and India, with notes on their phylogenetic position
Fig. 2. Macrobiotus noongaris sp. nov., cuticular structures on legs (paratypes, IZiBB). A–B. External granulation on legs II and III seen in PCM (A) and SEM (B), respectively. C–D. A cuticular bulge (pulvinus) and a faint cuticular fold, covered by granulation, on the internal surface of legs I and III seen in PCM (C) and SEM (D), respectively. E–F. Granulation on leg IV seen in PCM (E) and SEM (F). Filled indented arrowheads indicate the cuticular bulge and empty indented arrowheads indicate the faint cuticular fold under the claws. Scale bars in μm.
Fig. 13 in Two new species of the Macrobiotus hufelandi complex (Tardigrada: Eutardigrada: Macrobiotidae) from Australia and India, with notes on their phylogenetic position
Fig. 13. Macrobiotus kamilae sp. nov., mouth opening and the oral cavity armature seen in SEM (paratype, IZiBB). A. Mouth opening with peribuccal sensory lobes and ten peribuccal lamellae. B–C. The oral cavity armature of a single paratype seen in SEM from different angles, in dorsal (B) and ventral (C) views, respectively. Empty flat arrowheads indicate the first band of teeth in the oral cavity, empty indented arrowheads indicate the second band of teeth in the oral cavity and filled indented arrowheads indicate the third band of teeth in the oral cavity. Scale bars in μm.
Fig. 11 in Two new species of the Macrobiotus hufelandi complex (Tardigrada: Eutardigrada: Macrobiotidae) from Australia and India, with notes on their phylogenetic position
Fig. 11. Macrobiotus kamilae sp. nov., claws. A–B. Claws III and IV seen in PCM, with smooth and dentate lunules, respectively (holotype, IZiBB IN.030.08). C–D. Claws III and IV seen in SEM, with smooth and dentate lunules, respectively (paratype, IZiBB). Filled indented arrowheads indicate double muscle attachments under the claws whereas empty indented arrowhead indicates the horseshoe structure connecting the anterior and the posterior claw. Scale bars in μm.
Fig. 6 in Two new species of the Macrobiotus hufelandi complex (Tardigrada: Eutardigrada: Macrobiotidae) from Australia and India, with notes on their phylogenetic position
Fig. 6. Macrobiotus noongaris sp. nov. A–E. Egg, seen in PCM (IZiBB). A. Midsection under 400 × magnification. B. Surface under 400× magnification. C–D. Midsection under 1000 × magnification. E. Surface and terminal discs under 1000× magnification. F. Testis seen in PCM, with visible spermatozoa in male freshly mounted in Hoyer's medium (paratype, IZiBB). Scale bars in μm.
Fig. 4 in Two new species of the Macrobiotus hufelandi complex (Tardigrada: Eutardigrada: Macrobiotidae) from Australia and India, with notes on their phylogenetic position
Fig. 4. Macrobiotus noongaris sp. nov., buccal apparatus and the oral cavity armature seen in PCM (paratypes, IZiBB). A. Dorso-ventral projection of the entire buccal apparatus. B–C. Oral cavity armature visible in dorsal (B) and ventral (C) views, respectively. D–E. Placoid morphology visible in dorsal (D) and ventral (E) views, respectively. Empty indented arrowheads indicate the second band of teeth in the oral cavity, filled indented arrowheads indicate the third band of teeth in the oral cavity, empty flat arrowheads indicate central constrictions in first macroplacoids and subterminal constriction in second macroplacoids. Scale bars in μm.
Fig. 3 in Two new species of the Macrobiotus hufelandi complex (Tardigrada: Eutardigrada: Macrobiotidae) from Australia and India, with notes on their phylogenetic position
Fig. 3. Macrobiotus noongaris sp. nov., claws (paratypes, IZiBB). A–B. Claws II and IV seen in PCM, with smooth and dentate lunules, respectively. C–D. Claws I and IV seen in SEM, with smooth and dentate lunules, respectively. Filled indented arrowheads indicate double muscle attachments under the claws. Scale bars in μm.
Fig. 8. Mastigograptus aff. tenuiramosus. A in The ultrastructure, development, and systematic position of the graptolite genus Mastigograptus
Fig. 8. Mastigograptus aff. tenuiramosus. A. Thecal base of Fig. 6B. Scale bar 50 µm. B, C. Fractured thecal bases, and occluded autotheca (arrowed) (ZPAL G.30/17). Scale bars: B, 100 µm, C, 50 µm. D. Thecal base on main stem, with occluded autotheca (arrowed), a needle preparation from ZPAL G.30/18. Scale bar 20 µm. E. Stem, looking obliquely proximally, with two thecal bases (ZPALG.30/15). Scale bar 200 µm. F, G, H. Successively more distal cross−sections of thecal bases. Scale bars 10 µm, 50 µm, 100 µm. I. Thecal base with occluded autotheca (ZPALG.30/17). Scale bar 50 µm. J. Diaphragm of stolonal triad in thecal base, looking proximally (ZPALG.30/15). Scale bar 10 µm. K. Stolotheca looking proximally with adjacent thecal base displaying astolothecaltriad,seeH(ZPALG.30/11).Scalebar200µm. L.Crassal,fusellarandcorticaltissuesinthecalbase(ZPALG.30/17).Scalebar5µm. M."E.T. head" of thecal base, with central occluded autotheca (ZPAL G.30/4). Scale bar 50 µm.
Fig. 4. Mastigograptus aff. tenuiramosus. A in The ultrastructure, development, and systematic position of the graptolite genus Mastigograptus
Fig. 4. Mastigograptus aff. tenuiramosus. A. Fractured wall of stolotheca. The head of a fusellus is arrowed (ZPALG.30/9). Scale bar 10 µm B, C. External ornament on stolothecae (ZPAL G.30/10). Scale bars 100 µm, 50 µm. D. Sectional view of stolonal triad on main stem, looking distally (ZPAL G.30/11). Scale bar 50 µm. E. Stolonal triad on main stem, looking proximally; diaphragm at base of occluded autotheca (arrowed) (ZPALG.30/12). Scale bar 50 µm. F. Base of diaphragm on main stem, looking distally, and showing two pores (ZPALG.30/13). Scale bar 10 µm. G. Portion of stem with monopodial branch to right. a, occluded first thecal base on branch, with short stolotheca. b, borings on main stem (ZPAL G.30/14). Scale bar 500 µm.
Fig.3. Mastigograptus aff. tenuiramosus. A in The ultrastructure, development, and systematic position of the graptolite genus Mastigograptus
Fig.3. Mastigograptus aff. tenuiramosus. A.Stipewiththickcortexandfracturedthecalbase.(ZPALG.30/4).Scalebar100µm. B.Occludedthecalbaseon proximal portion of stem (ZPALG.30/3). Scale bar 10 µm. C. Proximal portion of stem, with occluded sicula and first thecal base. (ZPALG.30/2). Scale bar 200 µm. D. Portion of stem with monopodial branch (ZPALG.30/5). Scale bar 2 µm. E. Fractured stolotheca; distal to left (ZPALG.30/6). Scale bar 50 µm. F. Fractured stem with thick cortex and borings (ZPALG.30/7). Scale bar 50 µm. G. Amphorate stolothecae, and broken thecal bases (ZPALG.30/4) Scale bar 1 mm. H. Amphorate stolotheca, looking proximally. (ZPAL G.30/8). Scale bar 100 µm. I. Stereopair view of thecal base (ZPAL G.30/4). Scale bar 100 µm.
Fig. 2. Mastigograptus aff. tenuiramosus. A in The ultrastructure, development, and systematic position of the graptolite genus Mastigograptus
Fig. 2. Mastigograptus aff. tenuiramosus. A. Fusellar fabric of holdfast (ZPAL G.30/2). Scale bar 1 µm. B. Fusellar and cortical fabrics in the laminae of holdfast (ZPAL G.30/3). Scale bar 20 µm. C. Sheet fabric of laminae of holdfast (ZPAL G.30/1). Scale bar 1 µm. D. Laminae of holdfast. Bundled parallel cortical fibrils and sheet fabric with vesicles (ZPALG.30/1). Scale bar 1 µm. E. Two siculae on holdfast. The left hand one is occluded (ZPALG.30/1). Scale bar 100 µm. F. Occluded sicula (arrowed) (ZPAL G.30/3). Scale bar 100 µm. G, H. Broken thecal base on proximal portion of stem (ZPAL G.30/2). Scale bars: G, 50 µm; H, 100 µm.
Fig. 2 in New systematic position of Itatingamyia Albuquerque (Diptera, Muscidae) based on molecular evidence, and description of the female of I. couriae
Fig. 2. Molecular phylogenetic hypothesis using Bayesian inference of the combined mitochondrial (COI) and nuclear (AATS, CAD, and EF1-a) protein-coding genes for 68 species of Muscidae highlighting the position of Itatingamyia within the Cyrtoneurininae.Subfamily-level classification follows Haseyama et al. (2015). Numbers are Bayesian posterior probabilities values.
Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group. in Distribution of extracellular enzyme-producing bacteria in the digestive tracts of 4 brackish water fish species
Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group.
Text-fig. 1. Bohemian Massif with position of the Prague Basin (in black) and distribution of Ordovician rocks in the Prague Basin, with geographic position of main localities of the siliceous nodules. in Porambonites Havliceki Sp. Nov., A New Brachiopod From The Šárka Formation (Darriwilian) From Bohemia And Its Contribution To Early History Of The Porambonitidae
Text-fig. 1. Bohemian Massif with position of the Prague Basin (in black) and distribution of Ordovician rocks in the Prague Basin, with geographic position of main localities of the siliceous nodules.
Text-fig. 6. Platanaceae 1–3. Platanites raynoldsii (NEWBERRY) comb. nov. 1. Holotype of Platanus raynoldsii NEWBERRY (1868, 1898), Banks of the Yellowstone River, Montana, USNM 7000. 2. Holotype of Platanites canadensis MCIVER et BASINGER (1993), here treated as synonym of P. raynoldsii, showing clearly the position of the lateral leaflets, US 3-66, Ravenscrag Formation, Saskatchewan, Canada. 3. Specimen from Yellowstone Bridge, Miles City, Montana. UF19021-39390. 4. Detail from fig. 2. Scale bars 5 cm. in Revisions To Roland Brown'S North American Paleocene Flora
Text-fig. 6. Platanaceae 1–3. Platanites raynoldsii (NEWBERRY) comb. nov. 1. Holotype of Platanus raynoldsii NEWBERRY (1868, 1898), Banks of the Yellowstone River, Montana, USNM 7000. 2. Holotype of Platanites canadensis MCIVER et BASINGER (1993), here treated as synonym of P. raynoldsii, showing clearly the position of the lateral leaflets, US 3-66, Ravenscrag Formation, Saskatchewan, Canada. 3. Specimen from Yellowstone Bridge, Miles City, Montana. UF19021-39390. 4. Detail from fig. 2. Scale bars 5 cm.
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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.