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1,140 results for “TOPS”
Data for manuscript "Long-term variation in the quasi-five-day wave in the top layer of Venus clouds"
<p>The dataset contain the derived cloud motions from Akatsuki LIR level3c and the corrected LIR level3c brightness temperature. The data of each figure used for drawing are also contained.</p>
Figure 3: Number of branches for each generation, in the asymmetric (TOP) and symmetric (BOTTOM) generation. Notice that the Y-axis is logarithmic.-THE RESPIRATORY IMPEDANCE IN AN ASYMMETRIC MODEL OF THE LUNG STRUCTURE
<p>Figure 3 shows the number of branches that are in one generation, for the symmetric and asymmetric<br> lung structure. Notice the diferent slope which characterizes the space-filling distribution.</p>
Figure 3: Number of branches for each generation, in the asymmetric (TOP) and symmetric (BOTTOM) generation. Notice that the Y-axis is logarithmic.
<p>Figure 3 shows the num-<br> ber of branches that are in one generation, for the symmetric and asymmetric<br> lung structure. Notice the di®erent slope which characterizes the space-¯lling<br> distribution.</p>
Figure 2. HMM with weights and necessary conditions on top of edges-Neuroevolution Mechanism for Hidden Markov Model
<p>Based on the HMM structure in Figure 2, we can perform the following steps:<br> 1. Make the number of nodes of inputs in the input layer of the NN as the number of states<br> (visible states not the observations). Each input node represents one state.<br> 2. Number of nodes in the output layer in the NN is equal to the number of states and<br> observations (visible and invisible states), where each node corresponds to one state (visible<br> or invisible).<br> 3. We construct a hidden layer in NN with n number of nodes, where n is the same number of<br> nodes in the input layer.<br> 4. We make a connection from every input to every hidden layer node with a very negligible<br> weight.<br> 5. Connect every hidden node in the hidden layer to every node in the output layer.<br> 6. Assign weights from the hidden layer to output layer in a way that as every node in the<br> hidden layer corresponding to input state. The weight on top of the link between the hidden<br> node to the output node is the probability value between the states in the HMM.<br> In our proposed structure, we injected a hidden layer to have a multilayer perceptron which<br> is more efficient than single layer perceptron.<br> To make this process clear, Figure 3 shows the neural networks for the HMM presented in<br> Figure 2.</p>
Рис. 1–6. Новые виΑы огневок с острова Борнео: 1, 3, 4 — Cirrhochrista milada Korb, sp. n., гоΛотип самец (1 — виΑ сверху; 3 — генитаΛии, эΑеагус уΑаΛен; 4 — эΑеагус); 2, 5, 6 — Paracymoriza platon Korb, sp. n., гоΛотип самец (2 — виΑ сверху; 5 — генитаΛии, эΑеагус уΑаΛен; 6 — эΑеагус) Fig. 1–6. New species of pyralid moths of the Borneo island: 1, 3, 4 — Cirrhochrista milada Korb, sp. n., male holotype (1 — top view; 3 — genitals, aedegus removed; 4 — aedeagus); 2, 5, 6 — Paracymoriza platon Korb, sp. n., male holotype (2 — top view; 5 — genitalia, aedeagus removed; 6 — aedeagus) in Contribution To The Knowledge Of Pyraloid Moths (Lepidoptera, Pyraloidea) Of The Borneo Island With The Descriptions Of Two New Species
Рис. 1–6. Новые виΑы огневок с острова Борнео: 1, 3, 4 — Cirrhochrista milada Korb, sp. n., гоΛотип самец (1 — виΑ сверху; 3 — генитаΛии, эΑеагус уΑаΛен; 4 — эΑеагус); 2, 5, 6 — Paracymoriza platon Korb, sp. n., гоΛотип самец (2 — виΑ сверху; 5 — генитаΛии, эΑеагус уΑаΛен; 6 — эΑеагус) Fig. 1–6. New species of pyralid moths of the Borneo island: 1, 3, 4 — Cirrhochrista milada Korb, sp. n., male holotype (1 — top view; 3 — genitals, aedegus removed; 4 — aedeagus); 2, 5, 6 — Paracymoriza platon Korb, sp. n., male holotype (2 — top view; 5 — genitalia, aedeagus removed; 6 — aedeagus)
Рис. 2. Распредение биомассы Mytilus trossulus septentrionalis на литорали дальневоcточных морей России. Здесь и далее на гистограммах по оси абцисс после географических пунктов в скобках укаЗана выборка (число иЗученных проб), по оси ординат – максимальные ЗначениЯ биомассы вида. Под Значением биомассы 0.1 г/м² подраЗумеваютсЯ качественные пробы. СокраЩениЯ (бмп) и (топ) оЗначают соответственно беринговоморское и тихоокеанское побережьЯ Восточной Камчатки. Побережье Зал. Петра Великого от устьЯ р. Туманной к северу до м. Поворотного условно отноcитсЯ к южному Приморью; побережье к северу от м. Поворотного (пос. Преображение, б. СоколовскаЯ) до б. Ольга, включительно, условно относитсЯ к среднему Приморью; побережье к северу от б. Ольга до м. Белкина и материковое побережье Татарского пролива относим к северному Приморью. Fig. 2. The distribution of biomass of Mytilus trossulus septentrionalis in the intertidal zone of the Far Eastern seas of Russia. Here and throughout on histograms, on the abcissa is the number of studied samples (numbers in parentheses following the names geographic localities), on the ordinate is the maximum biomass of species. The number 0.1 g wet wt m-2 means the qualitative samples. Abbreviations (bmp) and (top) mean the Bering Sea coast and the Pacific coast of eastern Kamchatka. The coast of Peter the Great Bay from the mouth of the Tumannaya River to Cape Povorotny is conditionally referred to as southern Primorye; the area north of Cape Povorotny (Preobrazhenie Settlement, Sokolovskaya Bay) to Olga Bay inclusive is conditionally referred to as middle Primorye; north of Olga Bay to Cape Belkin and the mainland coast of the Tatar Strait to as northern Primorye. in Bivalve mollusks of the intertidal zone of the Far Eastern seas of Russia
Рис. 2. Распредение биомассы Mytilus trossulus septentrionalis на литорали дальневоcточных морей России. Здесь и далее на гистограммах по оси абцисс после географических пунктов в скобках укаЗана выборка (число иЗученных проб), по оси ординат – максимальные ЗначениЯ биомассы вида. Под Значением биомассы 0.1 г/м² подраЗумеваютсЯ качественные пробы. СокраЩениЯ (бмп) и (топ) оЗначают соответственно беринговоморское и тихоокеанское побережьЯ Восточной Камчатки. Побережье Зал. Петра Великого от устьЯ р. Туманной к северу до м. Поворотного условно отноcитсЯ к южному Приморью; побережье к северу от м. Поворотного (пос. Преображение, б. СоколовскаЯ) до б. Ольга, включительно, условно относитсЯ к среднему Приморью; побережье к северу от б. Ольга до м. Белкина и материковое побережье Татарского пролива относим к северному Приморью. Fig. 2. The distribution of biomass of Mytilus trossulus septentrionalis in the intertidal zone of the Far Eastern seas of Russia. Here and throughout on histograms, on the abcissa is the number of studied samples (numbers in parentheses following the names geographic localities), on the ordinate is the maximum biomass of species. The number 0.1 g wet wt m-2 means the qualitative samples. Abbreviations (bmp) and (top) mean the Bering Sea coast and the Pacific coast of eastern Kamchatka. The coast of Peter the Great Bay from the mouth of the Tumannaya River to Cape Povorotny is conditionally referred to as southern Primorye; the area north of Cape Povorotny (Preobrazhenie Settlement, Sokolovskaya Bay) to Olga Bay inclusive is conditionally referred to as middle Primorye; north of Olga Bay to Cape Belkin and the mainland coast of the Tatar Strait to as northern Primorye.
Supplementary data accompanying Hess et al. (2025) 'The I/Ca paleo-oxygenation proxy in planktonic foraminifera: A multispecies core-top calibration' published in Geochimica et Cosmochimica Acta
<p>This data accompanies Hess et al. (2025) 'The I/Ca paleo-oxygenation proxy in planktonic foraminifera: A multispecies core-top calibrations' published in Geochimica et Cosmochimica Acta.</p> <p>Data columns and explanation:</p> <table> <tbody> <tr> <td>reference</td> <td>reference for the I/Ca and Mg/Ca data</td> </tr> <tr> <td>site</td> <td>site name</td> </tr> <tr> <td>sample_depth_cm</td> <td>sample depth (cm below sediment surface)</td> </tr> <tr> <td>basin</td> <td>ocean basin</td> </tr> <tr> <td>site_depth_km</td> <td>site water depth (km)</td> </tr> <tr> <td>species</td> <td>foraminifera species</td> </tr> <tr> <td>calcification_depth</td> <td>foraminifera calcification depth</td> </tr> <tr> <td>size_fraction</td> <td>foraminifera size fraction</td> </tr> <tr> <td>cleaning_oxidative_reductive</td> <td>cleaning applied to sample before trace element analysis (O = oxidative, O+R = oxidative and reductive)</td> </tr> <tr> <td>local_O2_variability</td> <td>indication of whether the site experiences local O2 variability, rows with "yes" are excluded from Figure 4</td> </tr> <tr> <td>MgCa</td> <td>Mg/Ca (mmol/mol)</td> </tr> <tr> <td>MgCa_corr</td> <td>Mg/Ca corrected for effect of reductive cleaning, as necessary (mmol/mol)</td> </tr> <tr> <td>T_anand</td> <td>calcification temperature calculated from Mg/Ca using Anand et al. (2003) multispecies equation</td> </tr> <tr> <td>T_Hollstein_multispec</td> <td>calcification temperature calculated from Mg/Ca using Hollstein et al. (2017) multispecies equation</td> </tr> <tr> <td>T_Hollstein_spec</td> <td>calcification temperature calculated from Mg/Ca using species-specific Hollstein et al. (2017) equations</td> </tr> <tr> <td>T_Cleroux</td> <td>calcification temperature calculated from Mg/Ca using species-specific Cléroux et al. (2008) equations</td> </tr> <tr> <td>depth_anand</td> <td>calcification depth from water column temperature data (Moffett et al., 2020) and T_anand</td> </tr> <tr> <td>depth_Hollstein_multispec</td> <td>calcification depth from water column temperature data (Moffett et al., 2020) and T_Hollstein_multispec</td> </tr> <tr> <td>depth_Hollstein_spec</td> <td>calcification depth from water column temperature data (Moffett et al., 2020) and T_Hollstein_spec</td> </tr> <tr> <td>depth_Cleroux</td> <td>calcification depth from water column temperature data (Moffett et al., 2020) and T_Cleroux</td> </tr> <tr> <td>ICa</td> <td>I/Ca (µmol/mol)</td> </tr> <tr> <td>ICa_corr</td> <td>I/Ca corrected for effect of reductive cleaning, as necessary (µmol/mol)</td> </tr> <tr> <td>O2av_0-500m</td> <td>average oxygen concentration in the top 500 m of the water column at this site, calculated from Moffett et al. (2020) CTD data</td> </tr> <tr> <td>O2min_0-500m</td> <td>minimum oxygen concentration in the top 500 m of the water column at this site, calculated from Moffett et al. (2020) CTD data</td> </tr> <tr> <td>O2min_alldepths</td> <td>minimum oxygen concentration at any depth in the water column at this site, calculated from Moffett et al. (2020) CTD data</td> </tr> <tr> <td>O2av_0-100m</td> <td>average oxygen concentration in the top 100 m of the water column at this site, calculated from Moffett et al. (2020) CTD data</td> </tr> <tr> <td>O2min_0-100m</td> <td>minimum oxygen concentration in the top 100 m of the water column at this site, calculated from Moffett et al. (2020) CTD data</td> </tr> </tbody> </table>
Dataset: Top Wealth Group Holding Limited (TWG) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Dataset: TOP Financial Group Limited (TOP) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Dataset: Top KingWin Ltd (TCJH) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
◂Fig. 4 Gynoecium of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A–R light microscopy; TS in horizontal orientation). A Secantial section. B, C TS %note cellular organisation). D Secantial section. E, F TS %note cellular organisation). G Secantial section of young gynoecium showing cellular organisation. H–J TS %note lacking cellular organisation, localisation in K–M). K–M LS at different levels from outside to inside of the same specimen %note strongly stained peripheral tissue; asterisks indicate tissue illustrated in H–J). N TS %note dehiscence lines of the prospective endocarp). O, P TS showing transmission tissue and dorsal bundles at top of style. Q vascularisation at base of gynoecium %note strongly stained peripheral tissue). R Vascularisation at base of flower %LS, longisection; TS, transverse section; db, dorsal bundle; dl, dehiscent line; ep, epidermis; lb, lateral bundle; tt, transmission tissue; ut, peripheral tissue; vb, ventral bundle; vs, ventral slit) in Observations on flower and fruit anatomy in dioecious species of Cordia (Cordiaceae, Boraginales) with evolutionary interpretations
◂Fig. 4 Gynoecium of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A–R light microscopy; TS in horizontal orientation). A Secantial section. B, C TS %note cellular organisation). D Secantial section. E, F TS %note cellular organisation). G Secantial section of young gynoecium showing cellular organisation. H–J TS %note lacking cellular organisation, localisation in K–M). K–M LS at different levels from outside to inside of the same specimen %note strongly stained peripheral tissue; asterisks indicate tissue illustrated in H–J). N TS %note dehiscence lines of the prospective endocarp). O, P TS showing transmission tissue and dorsal bundles at top of style. Q vascularisation at base of gynoecium %note strongly stained peripheral tissue). R Vascularisation at base of flower %LS, longisection; TS, transverse section; db, dorsal bundle; dl, dehiscent line; ep, epidermis; lb, lateral bundle; tt, transmission tissue; ut, peripheral tissue; vb, ventral bundle; vs, ventral slit)
Рис. 2. Черношапочные сурки и их местообитания на хребте КоΑар: A — виΑ на ЦентраΛьный КоΑар и ΑоΛину р. СреΑний Сакукан; B — местообитание сурков поΑ переваΛом; C — местообитание сурков по берегам р. Того; D — местообитание сурков на вершине гребня, каΑр с фотоΛовушки; E — сурки; F — черношапочный сурок обΛизывает пΛасты каменного угΛя, каΑр из виΑеосъемки Fig. 2. Black-capped marmots and their habitats on the Kodar Ridge: A — view of the Central Kodar and the valley of the Middle Sakukan River; B — habitat of marmots under the mountain pass; C — habitat of marmots along the banks of the Togo River; D — marmot habitat at the top of the mountain ridge, camera trap frame; E — marmots; F — the black-capped marmot licks coal, freeze frame from video in On the ecology of the Doppelmayer`s Black-capped marmot (Marmota camtschatica doppelmayeri Birula, 1922): Kodar Mountain Ridge, Transbaikalia, Russia
Рис. 2. Черношапочные сурки и их местообитания на хребте КоΑар: A — виΑ на ЦентраΛьный КоΑар и ΑоΛину р. СреΑний Сакукан; B — местообитание сурков поΑ переваΛом; C — местообитание сурков по берегам р. Того; D — местообитание сурков на вершине гребня, каΑр с фотоΛовушки; E — сурки; F — черношапочный сурок обΛизывает пΛасты каменного угΛя, каΑр из виΑеосъемки Fig. 2. Black-capped marmots and their habitats on the Kodar Ridge: A — view of the Central Kodar and the valley of the Middle Sakukan River; B — habitat of marmots under the mountain pass; C — habitat of marmots along the banks of the Togo River; D — marmot habitat at the top of the mountain ridge, camera trap frame; E — marmots; F — the black-capped marmot licks coal, freeze frame from video
Figure 3. (Top): Illustration of the therapy selection main menu. This enables the user to select one of three options for the therapy. Stimuli sequence selectors; (Bottom): (a) Short distance – complete visual field; (b) Short distance – macular; (c) Middle-long distance.-Design of a Novel Servo-motorized Laser Device for Visual Pathways Diseases Therapy
<p>distance therapies for the prescribed time suggested by the ophthalmologist.<br> Note that the complete visual field therapy stimulates different parts in the entire visual field<br> whereas macular therapy stimulate only a small part of the visual field, only the first 10° of vision<br> range. In contrast, middle-long distance therapies are not developed inside the device; instead the<br> patient must sit watching a wall, where the stimuli will be presented. Figure 3 (Bottom) shows the<br> sequence selectors for the three different cases. The therapist will choose a desired number of<br> sequences according to the results of the examination to each patient; hence it is completely patient<br> dependent.<br> Once the therapist finishes the particular design of the stimuli sequence, the software<br> automatically displays a window where he can save the customized patient-specific details for future<br> use as a text file.</p>
Datenanhang zu Ergebnisse der ZKI Top Concerns-Umfrage des ZKI-Arbeitskreises Strategie und Organisation für das Jahr 2017/18
<p>Der Arbeitskreis Strategie und Organisation des ZKI-Vereins führt eine jährliche Umfrage zu den wichtigsten Themen und Schwerpunkten der Mitgliedseinrichtungen durch. Im Jahr 2016 wurde die Umfrage auf eine elektronische Umfrage im Web mittels Lime-Survey umgestellt. Basierend auf dieser ersten Ergebnismenge konnte im Herbst 2017 eine erweiterte Umfrage durchgeführt werden, die auch einen Vergleich zum Vorjahr und die Relevanzverschiebungen bei den Top-Themen berücksichtigt. Der Artikel stellt die Kernergebnisse dar und wird durch die aufbereiteten Rohdaten im Excel-Format ergänzt.</p>
Soil scans for parcels in Netherlands (Pietje tops voor huisClass 3)
<p>Parcel soil scan with electric conductivity measurement</p>
Asti Top Percentages By Post Code
<p>JSON data related to top preferences on children food habits and physical activities (per postcode)</p>
Milan Top Percentages by School
<p>JSON data related to top preferences on children food habits and physical activities (per school)</p>
Asti Top Percentage By School
<p>JSON data related to top preferences on children food habits and physical activities (per school)</p>
Milan Top Percentages by Area
<p>JSON data related to top preferences on children food habits and physical activities (per Area)</p>
Milan Top Percentages by Postcode
<p>JSON data related to top preferences on children food habits and physical activities (per postcode)</p>
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.