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13,017 results for “Positionning”
Women's team soccer positioning data, collected during 2023/2024 season. Third category of female soccer, Spain.
<p>Positioning data of 20 female football players collected during the first 5 matchdays of the regular league during the season 2023/2024. They correspond to the third Spanish female category, considered semi-professional.</p>
Positive autoregulation of Sox17 is necessary for gallbladder and extrahepatic biliary duct formation
<p>This is a processed data (Seurat object) that contain single cell RNA-seq data from mouse , E10.5, Sox17∆50/∆50 mutant and Sox17+/+ embryos enriched for EPCAM+/CXCR4+ endodermal cells. Dataset contains 2912 total cells post qc. Sox17+/+ and Sox17Δ50/Δ50 cell samples are labelled with barcodes from 3'CellPlex Kit (10X Genomics). CellPlex Barcode ID CMO307 represent Sox17+/+ and CMO309 represent Sox17Δ50/Δ50 cells (included in assay named "CMO"). Genotype labels are under metadata column "genotype" as well. Libraries were constructed according to the manufacturer’s instructions for 10x Genomics Single Cell 3′ Library kit v3. Demultiplex, qc and alignment was performed using 10X Genomics Cell Ranger software v3.0.2 and mm10 genome version index from 10X genomics(https://cf.10xgenomics.com/supp/cell-exp/refdata-gex-mm10-2020-A.tar.gz) was used. Additional quality control filtration, normalization, unsupervised clusteringwas performed using Seurat v4 R package. <br><br>The raw data will be available in Biostudies (https://www.ebi.ac.uk/biostudies/) when published under accession ID E-MTAB-14000.</p> <p> </p>
Figs 1–3 in Mating position in Peloridiidae (Hemiptera: Coleorrhyncha)
Figs 1–3. Mating Peloridiidae: 1 — Peloridium hammoniorum Breddin, 1897, dorsal view, male on the left; 2–3 — Hemiodoecus leai China, 1924: 2 — dorsal view, male on the right (note female right tegmen visible through male tegmina); black dots are ascomycete pycnidia [Helmsing, China, 1937: 487]; 3 — right lateral view, male in front. Рис. 1–3. Спаривание у Peloridiidae: 1 — Peloridium hammoniorum Breddin, 1897, вид сверху, самец слева; 2–3 — Hemiodoecus leai China, 1924: 2 — вид сверху, самец справа (череЗ его надкрыльЯ просвечивает правое надкрылье самки); чёрные точки — пикнидии аскомицетов [Helmsing, China, 1937: 487]; 3 — вид справа, самец спереди.
Supplementary material 4 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Complete maximum likelihood trees reconstructed using the COI, 28S, 18S, and concatenated 18S+28S+COI datasets
Figs 1–4 in On the systematic position of Circularva reichardti Shcherbakov et Ponomarenko, 2023
Figs 1–4. Circularva reichardti and interpretations of its morphology: 1 — Circularva reichardti Shcherbakov et Ponomarenko, 2023, drawing from the original description, left half, unclear structures not shown; 2–4 — putative tagmosis of Circularva due to hypotheses about its belonging to crustaceans, millipedes and coleopterans, respectively. Рис. 1–4. Circularva reichardti и интерпретации её строениЯ: 1 — Circularva reichardti Shcherbakov et Ponomarenko, 2023, рисунок иЗ первоописаниЯ, леваЯ половина, неЯсные структуры не покаЗаны; 2–4 — предполагаемый тагмоЗис Circularva в рамках гипотеЗ о её принадлежности к ракообраЗным, многоножкам и насекомым, соответственно.
High-speed video observation of needles formed during the leader stage in a positive cloud-to-ground flash
<p>The data supports the manuscript entitled “<span>High-speed video observation</span><span> of needles formed during </span><span><span>the </span></span><span><span><span>leader</span></span></span><span><span><span> </span></span></span><span><span><span>stage</span></span></span><span> in a positive cloud-to-ground flash</span>”. The high-speed video data files of the positive cloud-to-ground lightning of *.cihx and *.avi can be opened by Photron Camera Control software (Photron Fastcam Viewer) that can be download from this link: https://photron.com/photron-support/</p> <p>In addition, MATLAB can open the *.mat file (electric field change data), and Microsoft Excel can open the *.xlsx file (Guangdong-Hong Kong-Macao Lightning Location data.</p> <p>The data can be used freely for scientific purposes with the appropriate citation.</p>
Supporting Data for "Radiation-circulation destabilization of ITCZ position in an idealized GCM: Response to hemispherically asymmetric forcing"
<p>Code and netcdf files of processed Isca simulations to reproduce the figures of the submitted manuscript of Timothy M. Merlis, Chiung-Yin Chang, Pablo Zurita-Gotor, and Isaac M. Held (2024): "Radiation-circulation destabilization of ITCZ position in an idealized GCM: Response to hemispherically asymmetric forcing".</p>
FIGURE. Bayesian tree based on nuclear (ITS) sequence data showing phylogenetic position of Hedysarum sunhangii sp. nov. in Subsect. Crinifera. Bayesian posterior probability (PP) / maximum parsimony (MP) are given on each branch, respectively; maximum likelihood (ML) is below branches. in Hedysarum sunhangii (Fabaceae, Hedysareae), a new species from Pamir-Alay (Babatag Ridge - Uzbekistan)
FIGURE. Bayesian tree based on nuclear (ITS) sequence data showing phylogenetic position of Hedysarum sunhangii sp. nov. in Subsect. Crinifera. Bayesian posterior probability (PP) / maximum parsimony (MP) are given on each branch, respectively; maximum likelihood (ML) is below branches.
FIGURE. Bayesian tree based on combined plastid (matK, trnL-trnF) sequence data showing phylogenetic position of Hedysarum sunhangii sp. nov. in Subsect. Crinifera. Bayesian posterior probability (PP) / maximum parsimony (MP) are given on each branch, respectively; maximum likelihood (ML) is below branches in Hedysarum sunhangii (Fabaceae, Hedysareae), a new species from Pamir-Alay (Babatag Ridge - Uzbekistan)
FIGURE. Bayesian tree based on combined plastid (matK, trnL-trnF) sequence data showing phylogenetic position of Hedysarum sunhangii sp. nov. in Subsect. Crinifera. Bayesian posterior probability (PP) / maximum parsimony (MP) are given on each branch, respectively; maximum likelihood (ML) is below branches
Testing the Acoustic Localisation Positioning System-algorithm: Data sets
<p>The data is from 3 separate experimental setups: Tracking a device of constant speed using the Audio1 (single processor) software (B.1); and tracking a faster device using the al-Qt (multi processor) software (B.2) The experiments were also recorded on video. (see Video folder). For the experiments in B.1 a visualisation of the data has been made with the help of a MATLAB script which also included. The dimensions of the room and loudspeaker spacings were identical for both set-ups, namely 3 x 2 meters, with the loudspeakers at the corners of the rectangle. the loudspeakers were situated on the floor, approximately level with the tracked devices.</p> <p>Setup C collects debug log examples of experiments with very short capture cycles with 2 mics and 2 loudspeakers running ALPS al-Qt.</p> <p>The source code for Audio is available from: <a href="https://github.com/spatmus/alps/tree/master/Audio1">https://github.com/spatmus/alps/tree/master/Audio1</a><br> The source code for al-Qt is available from: <a href="https://github.com/spatmus/alps/tree/master/al-Qt">https://github.com/spatmus/alps/tree/master/al-Qt</a><br> A binary of al-Qt for macOS 11, can be found in the assets folder of the release <a href="https://github.com/spatmus/alps/releases">https://github.com/spatmus/alps/releases</a></p>
Subspecies and Distribution. P. g. gymnocercus Fischer, 1814 — subtropical grasslands of NE Argentina, SE Brazil, Paraguay, and Uruguay. Pg. antiquus Ameghino, 1889 — Pampas grasslands, monte scrublands, and open woodlands of C Argentina. P. g. lordi Massoia, 1982 — Chaco-montane tropical forest ecotone in NW Argentina (Salta & Jujuy Provinces). The subspecific status of the Pampas Fox from Entre Rios Province in Argentina remains unclear, and there are no data regarding the taxonomic position of Bolivian foxes. in Canidae
Subspecies and Distribution. P. g. gymnocercus Fischer, 1814 — subtropical grasslands of NE Argentina, SE Brazil, Paraguay, and Uruguay. Pg. antiquus Ameghino, 1889 — Pampas grasslands, monte scrublands, and open woodlands of C Argentina. P. g. lordi Massoia, 1982 — Chaco-montane tropical forest ecotone in NW Argentina (Salta & Jujuy Provinces). The subspecific status of the Pampas Fox from Entre Rios Province in Argentina remains unclear, and there are no data regarding the taxonomic position of Bolivian foxes.
Fig. 3 in Expanded morphological definition and molecular phylogenetic position of the Tam Dao mountain stream keelback Opisthotropis tamdaoensis (Squamata: Natricidae) from Vietnam
Fig. 3. Drawings showing the head scalation in Opisthotropis tamdaoensis. (A) Male holotype after Ziegler et al. (2008), with the additional scale below the eye earmarked. (B) Female IEBR A.1016.33. (C) Male ZFMK 100000) compared to O. lateralis (D: Male IEBR 3645). Supralabials are numbered to show the differences between the new series of O. tamdaoensis (B, C) and O. lateralis (D). Drawings: T. Ziegler
Fig. 1 in Expanded morphological definition and molecular phylogenetic position of the Tam Dao mountain stream keelback Opisthotropis tamdaoensis (Squamata: Natricidae) from Vietnam
Fig. 1. Head portraits of the new series of Opisthotropis tamdaoensis in preserved state, showing the head scalation and the insertion of the black lateral stripe in the midst of the dark dorsal colouration. (A) Female IEBR A.2016.33. (B) Male ZFMK 100000. (C) Female IEBR A.2016.32. (D) Female MHNG 2767.60. Photos: T. Ziegler
Data for "Association of lightning occurrence with precipitation cloud column structure at a fixed position"
<p>Here are the data for the paper titled "Association of lightning occurrence with precipitation cloud column structure at a fixed position" and submitted to Atmospheric Research. The abstract is as follow.</p> <p> </p> <p>In this study, a C-band frequency-modulated continuous-wave (C-FMCW) radar, with its feature of vertical detection, was combined with lightning discharge recordings within a 3 km range to investigate the dependence of lightning occurrence on the structure of precipitation cloud columns (PCCs) from the perspective of a fixed position. The results show that, relative to PCCs without lightning, PCCs with lightning exhibit greater maximum reflectivity, maximum upward radial velocity, maximum velocity spectrum width, cloud top height, and vertically integrated liquid in terms of their average values, and wider-range distributions of these parameters. Using the Light Gradient Boosting Machine algorithm, a lightning diagnosis program that integrates multiple C-FMCW radar parameters was developed. Its hit rate of lightning occurrence is 93.5% and it has a threat score of 0.421. The maximum velocity spectrum width above the melting layer was found to be the most effective in distinguishing PCCs with or without lightning. It was suggested that the hydrometeor properties at a specific location, specifically the size diversity and content of ice-phase particles, should be the key elements determining the occurrence of lightning discharge in PCCs; meanwhile, the convection characteristics in the PCCs may be not the most critical.</p>
Seed size and capitulum position drive germination and dormancy responses to projected warming for the threatened dune endemic Cirsium pitcheri (Asteraceae)
<p>Among coastal plant species at risk from rapid environmental changes is the North American Great Lakes dune endemic Cirsium pitcheri. Despite being listed as federally threatened, little is known about how C. pitcheri seed attributes influence germination and dormancy-break patterns in the context of climate change. Following a previous work where we found differences in the number and weight of C. pitcheri seeds among capitulum positions and study sites, here we examine the effects of seed attributes (capitulum position, seed weight and site of origin) on the proportion and timing of C. pitcheri seed germination under temperature treatments that simulate projected warming in the Great Lakes (20/10°C, 25/10°C and 30/10°C day/night). Our results demonstrate that C. pitcheri produces diverse cohorts of seeds with seed attributes that significantly influence the timing and probability of germination over a three-year soil seed bank. C. pitcheri seed germination proportions were highest at 20°C and decreased successively at 25°C and 30°C. Seeds from terminal capitula had higher germination proportions and took longer to germinate than those from secondary capitula. The effect of seed weight on germination probability also depended on site of origin and capitulum position, with all effects varying in size and significance over time. Our results highlight the considerable differences in germination patterns exhibited by seeds from different capitulum positions and sites of origin and provide insight into the dormancy-break patterns that C. pitcheri might experience under the predicted temperature rise in the Great Lakes region of North America.</p>
FIGURE 2 in A new phosphatized ophiuroid from the lower Triassic of Nevada and its position in the evolutionary history of the Ophiuroidea (Echinodermata)
FIGURE 2: Early Triassic paleogeographic reconstruction of the western US. The Lost Cabin Springs Locality is denoted with a green star and the various shades depict the depositional environment during the Early Triassic (modified from Hoffmann et al., 2013).
FIGURE 5 in A new phosphatized ophiuroid from the lower Triassic of Nevada and its position in the evolutionary history of the Ophiuroidea (Echinodermata)
FIGURE 5: Dissociated disc plates of the ophiuroid Ophiosuperstes praeparvus gen. et sp. nov., from the Virgin Limestone Member of the Moenkopi Formation, Spathian, lower Triassic, Lost Cabin Springs locality, southern Nevada. A: paratype (OPH188), oral plate in abradial view. B: paratype (OPH189), radial shield in external view, with outline of missing proximal tip reconstructed using a dashed grey line. C: paratype (OPH190) adradial genital plate in dorsal view. Abbreviations: AMF: abradial muscle fossa; do: dorsal; LG: longitudinal groove; pr: proximal. All scale bars equal 0.2 mm.
FIGURE 4 in A new phosphatized ophiuroid from the lower Triassic of Nevada and its position in the evolutionary history of the Ophiuroidea (Echinodermata)
FIGURE 4: Dissociated arm plates of the ophiuroid Ophiosuperstes praeparvus gen. et sp. nov., from the Virgin Limestone Member of the Moenkopi Formation, Spathian, lower Triassic, Lost Cabin Springs locality, southern Nevada. A–B: holotype (OPH177), proximal lateral arm plate in external view (A) and with detail of spine articulations (B). C–D: paratype (OPH178), median lateral arm plate in external view (C) and with detail of spine articulations (D). E: paratype (OPH179), median lateral arm plate in internal view. F: paratype (OPH181), distal lateral arm plate in external view. G: paratype (OPH180), median lateral arm plate in internal view. H: paratype (OPH182), proximal ventral arm plate in external view. I: paratype (OPH183), median to distal ventral arm plate in external view. J: paratype (OPH184), proximal vertebra in distal view. K: paratype (OPH185), proximal vertebra in ventral view. L: paratype (OPH186), median vertebra in lateral view. M: paratype (OPH187), median vertebra in dorso-distal view. Abbreviations: AS: articular structure; di: distal; DL: dorsal lobe; do: dorsal; MO: muscle opening; NO: nerve opening; pr: proximal; PB: podial basin; SA: spine articulations; TO: tentacle opening; VAR: vertebral articular ridge; VF: ventral furrow; VL: ventral lobe; ZC: zygocondyle; ZS: zygosphene. All scale bars equal 0.2 mm.
FIGURE 6 in A new phosphatized ophiuroid from the lower Triassic of Nevada and its position in the evolutionary history of the Ophiuroidea (Echinodermata)
FIGURE 6: Arm fragment of Praeaplocoma hessi Broglio Loriga & Berti Cavicchi, 1972, (MHI 1307/nnn) from the Werfen Formation, Lower Triassic, of Weisshorn, Italy. A: arm fragments in ventral view. B: detail of part marked by white rectangle in A. Abbreviations: AS: arm spine; di: distal; LAP: lateral arm plate; MO: muscle opening; NO: nerve opening; SA: spine articulation; TO: tentacle opening; TS: tentacle scale; VAP: ventral arm plate. All scale bars equal 0.2 mm. Arrow in A indicates direction of view shown in B; refer to tentacle scales (TS) for better correspondence between A and B.
FIGURE 1 in A new phosphatized ophiuroid from the lower Triassic of Nevada and its position in the evolutionary history of the Ophiuroidea (Echinodermata)
FIGURE 1: Locality map of the Virgin Limestone Member at the Lost Cabin Springs Locality, Southern Nevada, Western United States (36°4′57.18′N, 115°39′12.05′W is near the base of the section). (modified from Maxwell, 2020).
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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.