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951 results for “places”

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zenodo36/100

Gazetteer and map of place names in Eustorgio y Clorilene (1629)

<p>Output data for the project &quot;Beyond the canon: the Byzantine genre in the Spanish baroque literature&quot;.</p> <p>The dataset&nbsp;contains a gazetteer of places (CSV)&nbsp;and a&nbsp;self-contained HTML file with a map of the places&nbsp;(frequencies and proximity) of the novel&nbsp;<em>Eustorgio y Clorilene</em> (1629).</p> <p>The dataset&nbsp;has been&nbsp;produced during a research visit at the Universit&eacute; de Gen&egrave;ve funded by the Swiss National Science Foundation (SNSF).</p>

opencc-by-4.0Jun 2019View details →
zenodo36/100

D-PLACE dataset derived from NASA TERRA/MODIS 'Net Primary Productivity'

<p>Cite the source of the dataset as:</p> <blockquote> <p>NASA. Net Primary Productivity (1 month - TERRA/MODIS)</p> </blockquote>

opencc-by-nc-4.0Nov 2023View details →
zenodo36/100

Data related to Mapping user-related comfort conditions to identify urban planning issues for improved quality of places in cities: The case of Ljubljana, Slovenia

<p>The data consists of parameters including air temperature, noise levels, humidity, and air quality (PM 2.5), measured using a portable ICT device while cycling through the city of Ljubljana between August 1 and August 30, 2022. The data is available as raw CSV files, with each measurement session stored in a separate file. An additional QGIS Project file (qgz) is included, along with maps (in jpg format in ppt) that visually represent the results presented in the article.</p>

opencc-by-4.0Sep 2024View details →
zenodo36/100

MAGOS Glove Two Fingers EggPlant Pick and Place

<div> <div>Welcome to the Two_fingers_EggPlant_PickAndPlace dataset, a unique data collection showcasing human pick-and-place actions using a Magos Glove for the delicate object (in this case a vegetable - Eggplant). This dataset is designed to facilitate research in robotics and machine learning, particularly in human-robot interaction and manipulation, and to show how human manipulation knowledge can be transferred to intelligent gripper solutions.</div> </div>

opencc-by-4.0Nov 2024View details →
zenodo36/100

Spatially Gridded Vehicle Count Analysis for Connaught Place, New Delhi

<p>Our Gridded Vehicle Count Analysis for Connaught Place, New Delhi, is a detailed geospatial analysis focusing on vehicular emissions in a highly trafficked urban area. Here's an overview:</p> <h3>Objective</h3> <p>The analysis aims to quantify vehicle density in Connaught Place, a major commercial and tourist hub, by generating a spatially gridded vehicle count dataset. By doing this, the project provides insights into traffic patterns and potential emission hotspots, supporting air quality forecasts and urban planning.</p> <h3>Data Collection</h3> <ol> <li><strong>Satellite Imagery</strong>: You collected high-resolution WorldView satellite imagery, zoomed specifically over Connaught Place to ensure the detail needed for vehicle detection.</li> <li><strong>Image Preprocessing</strong>: Using PyQGIS, you loaded the satellite imagery, created a 0.09-degree buffer around Connaught Place, and generated a grid layer with 150m x 150m cells to spatially segment the area for analysis.</li> <li><strong>Geotagged .tiff Files</strong>: The images were exported as geotagged .tiff files, preserving spatial information for each grid cell, facilitating precise location-based analysis.</li> </ol> <h3>Detection and Analysis</h3> <ol> <li><strong>Object Detection Models</strong>: You employed YOLOv8 through YOLOv10 and other state-of-the-art deep learning models to detect various vehicle types, such as cars, buses, and trucks. This approach helped accurately identify vehicle counts in real time.</li> <li><strong>Class-wise Detection</strong>: Specific object classes were defined, allowing for detailed counts by vehicle type, which is crucial for emission factor calculations.</li> <li><strong>Result Export</strong>: The detected vehicle counts and corresponding latitude/longitude data were stored in netCDF files, enabling the creation of gridded emission inventories.</li> </ol> <h3>Outcomes and Applications</h3> <p>The gridded dataset enables real-time monitoring of vehicular density and emissions over time. This data:</p> <ul> <li>Enhances air quality models by integrating localized emission sources.</li> <li>Assists policymakers in targeting emission reduction initiatives.</li> <li>Provides a foundational layer for studies on urban traffic flow and its environmental impacts in high-density zones like Connaught Place.</li> </ul> <p>In summary, this analysis provides a scientifically robust and spatially precise view of vehicular density, supporting both atmospheric studies and practical urban management decisions.</p>

opencc-by-4.0Nov 2024View details →
dryad36/100

First explorations: ontogeny of central-place-foraging directions in two tropical seabirds

A widespread hypothesis for the ontogeny of behaviour and decision-making is the early-exploration-later-canalization hypothesis. It postulates that juveniles are more exploratory and adults more consistent in their behavior. In addition, it is often assumed that naïve juveniles could overcome the costs of individual experience building by copying more the decisions of others than adults (early-conformism-later-self-defining hypothesis). Here we compare the central-place-foraging movements of adults and post-fledging juveniles in their first flights around the colony before dispersal and migration, in two sympatric species of tropical seabirds: red-footed boobies and great frigatebirds. Using GPS records of individual movements, we analyzed the foraging directions of seabirds from the colony across successive trips. Juveniles of both species showed significant within-individual consistency in foraging direction but at lower levels than adults. Juveniles leaving the colony within the same time-window showed significant but low between-individual resemblance in foraging direction, at levels similar to adults. In both species, homing efficiency was lower in juveniles than in adults. Juvenile foraging directions were initially influenced by wind conditions, particularly in low-wing-loading frigatebirds. Wind conditions progressively lost influence on juvenile foraging directions during their first weeks of flights. In contrast within-individual consistency, between-individual resemblance and homing efficiency did not show signs of progression in juveniles. Our results support the early-exploration-later-canalization hypothesis but not the early-conformism-later-self-defining hypothesis. Relaxed constraints on self-feeding efficiency could favour high variability in post-fledging tropical seabirds. Our simple approach could be applied to further test these hypotheses by comparing strategies across a wide range of central-place foragers.

opencc-zeroMar 2020View details →
zenodo36/100

FIGURE 8 in Phylogenetic relationships of Paralamellobates: immature characters of P. misella (Berlese) place the genus in Punctoribatidae (Acari, Oribatida)

FIGURE 8: Bayesian tree of brachypyline mites using 18S sequences; Paralamellobates misella (Berlese) is indicated by dot.

opencc-by-nd-4.0May 2016View details →
zenodo36/100

FIGURE 5 in Phylogenetic relationships of Paralamellobates: immature characters of P. misella (Berlese) place the genus in Punctoribatidae (Acari, Oribatida)

FIGURE 5: Paralamellobates misella (Berlese), tritonymph, dorsal aspect, legs not illustrated. Scale bar = 50.

opencc-by-nd-4.0May 2016View details →
zenodo36/100

FIGURE 3 in Phylogenetic relationships of Paralamellobates: immature characters of P. misella (Berlese) place the genus in Punctoribatidae (Acari, Oribatida)

FIGURE 3: Paralamellobates misella (Berlese). Differential interference contrast microscope images of adults: A – gnathosoma ventral view, with arrow to axillary saccule; B – prodorsum (4 layers combined), with arrow to bothridium; C – detail of prodorsum, with arrow to rostrum; D – lateral region of coxisternum with arrow to lateral ridges; E – posterior region showing single pair of anal setae and overlapping lobes of posterior notogastral tectum (indicated by arrow). Scale bars: A-D = 20.

opencc-by-nd-4.0May 2016View details →
zenodo36/100

FIGURE 4 in Phylogenetic relationships of Paralamellobates: immature characters of P. misella (Berlese) place the genus in Punctoribatidae (Acari, Oribatida)

FIGURE 4: Paralamellobates misella (Berlese), larva, dorsal aspect, legs not illustrated. Scale bar = 50.

opencc-by-nd-4.0May 2016View details →
zenodo36/100

FIGURE 2 in Phylogenetic relationships of Paralamellobates: immature characters of P. misella (Berlese) place the genus in Punctoribatidae (Acari, Oribatida)

FIGURE 2: Paralamellobates misella (Berlese), adult female, legs I-IV, all antiaxial aspect: A – leg I, trochanter not illustrated; B – leg II,

opencc-by-nd-4.0May 2016View details →
zenodo36/100

FIGURE 1 in Phylogenetic relationships of Paralamellobates: immature characters of P. misella (Berlese) place the genus in Punctoribatidae (Acari, Oribatida)

FIGURE 1: Paralamellobates misella (Berlese), adult female, dorsal aspect, legs not illustrated, except for proximal segments of leg I. Scale bar = 50.

opencc-by-nd-4.0May 2016View details →
zenodo36/100

FIGURE 6 in Phylogenetic relationships of Paralamellobates: immature characters of P. misella (Berlese) place the genus in Punctoribatidae (Acari, Oribatida)

FIGURE 6: Paralamellobates misella (Berlese): A – Egg and larva photographed live among fungal hyphae in growth medium, surrounded by faecal pellets of adults; B – deutonymph photographed live, showing length of interlamellar seta, usually broken in preserved specimens; C – tritonymph, dorsal showing absence of sclerotization; D,E, Differential interference contrast microscope images of immatures: D – tritonymph, ventral, showing absence of sclerotization; E – larva, part of prodorsum, showing tubercle nature of cerotegument (arrow). Scale bars: A, B = 100, C, D =20, E = 30.

opencc-by-nd-4.0May 2016View details →
zenodo36/100

D-PLACE/dplace-data: D-PLACE – the Database of Places, Language, Culture and Environment

<p>The data repository for the D-PLACE Project (Database of Places, Language, Culture and Environment)</p>

opencc-by-nc-4.0Oct 2018View details →
zenodo36/100

Wikidata Dump Swedish places

<p>RDF dump of wikidata produced with <a href="//wdumps.toolforge.org/">wdumper</a>.</p><p>Swedish places with coordinates<br><a href="//wdumps.toolforge.org/dump/3241">View on wdumper</a></p><p><b>entity count<b>: 9813372, <b>statement count</b>: 91203322, <b>triple count</b>: 100921154</b></b></p>

opencc-zeroMay 2023View details →
zenodo36/100

Place name data for "Skeid – uncovering a fleeting meeting site"

<p>The data contains the spatial distribution of 320&nbsp;skeid (<em>skei&eth;</em> n.) -names that are&nbsp;closer than two kilometres from a medieval church site, or one or more of the following place names: <em>hov/hof, ting</em>, or<em> leik/lek</em>. Through an examination of the landscape, archaeological finds and place names, 37 sites are highlighted as most likely to have hosted a skeid-type assembly. From these four case studies are discussed more in detail in the paper &quot;Skeid &ndash; uncovering a fleeting meeting site&quot;</p>

opencc-by-4.0Oct 2021View details →
zenodo36/100

An Extensive Dataset of Geometric Objects Placed in a Watertank for Electrical Impedance Tomography

<p>Open-access experimental Electrical Impedance Tomography (EIT) data set.<br> The measurements were generated using the ScioSpec EIT device from which 16 electrodes were connected to a phantom tank filled with saline. Four 3D-printed cylindrical objects of different sizes were placed in this tank area-wide. Adjacent and opposite injection patterns have been used to measure large datasets with more than 125000 samples.</p> <p>The tutorial can be found here: https://github.com/JacobTh98/sciospeceit/blob/main/tutorial.ipynb</p> <p>Contact: jacob.thoenes@uni-rostock.de</p>

opencc-by-4.0Jul 2023View details →
zenodo36/100

Data to D3.3 - Institutional arrangements of water supply, distribution and uses within and across case studies -identifying the barriers and drivers in place

<p>The transition towards a water circular economy (WCE) in the sense of water reuse may generate new water loops with additional challenges to water governance such as new and different types or qualities of water, new associated risks, new responsibilities,and new sets of actors involved. These challenges demand for clear-defined responsibilities, well-engaging of the various stakeholders, strong cooperation, and coordination among actors to prevent risks. Institutional arrangements, build the formal, and informal, design schemes to ensure adequate procedures and standards to better catalyse such transition. This deliverable analyses the institutional arrangements associated to the water management on the demosites, to assess their preparedness for the implementation of the new water loops as those foreseen with use of Project &Ocirc; new technologies. Using the Institutional Analysis and Development Framework, the analysis showed that the more water uses and users a new water loop involves the more critical the institutional arrangements become. Nevertheless, the institutional arrangements of the demosites do not always configure severe barriers. This is the case of Omis (Croatia) where the water reuse loop is located inside a textile company, and Eilat (Israel) where the water reuse loop is located inside amariculture centre. On the contrary, on Almendralejo (Spain) and Lecce (Italy), there are different players involved in the management ofthe water loop,andinstitutional arrangements appear more critical. Among the different institutional design principles, the clearly defined boundaries of responsibilities among stakeholders, the congruence between appropriation and provision rules and local conditions, raise more concerns on the case studies and call for the attention of future research on water circular economy. Fairly share of cost, benefits, and risks, dedicated graduated sanctions, conflict prevention and resolution mechanisms also deserve particular attention given the limited awareness of stakeholders of their features and influence for a successful implementation of demosites. Trust building, stakeholder empowerment and investment on transparency mechanisms related to water monitoring and sharing of communities and environmental benefits and costs of water reuse may be powerful approaches to implement water circular economy.</p>

opencc-by-4.0Mar 2022View details →
zenodo36/100

Data to Deliverable 3.2 - Policy design for the transition to circular economy: Barriers and drivers in place

<p>Data to assessment of the policy and planning contexts in Almendralejo (Spain), Lecce (Italy), Omis (Croatia) and Eilat (Israel)</p>

opencc-by-4.0Jul 2023View details →
zenodo36/100

Matériel supplémentaire pour "Quelle place pour les abeilles sauvages et leurs services dans les cultures fruitières de plaine du Rhône (VS)?"

<p><strong>Abstract:</strong></p> <p>Le d&eacute;ficit de la pollinisation d&ucirc; au recul des insectes a d&rsquo;&eacute;normes cons&eacute;quences &eacute;cologiques et &eacute;conomiques. Il contribue &agrave; fragiliser les &eacute;cosyst&egrave;mes et avec eux notre s&eacute;curit&eacute; alimentaire. La pollinisation est un service &eacute;cosyst&eacute;mique majoritairement rendu par les abeilles domestiques et sauvages, dont le r&ocirc;le est central dans les cultures fruiti&egrave;res. Le but de cette &eacute;tude &eacute;tait de sonder la pr&eacute;sence des abeilles sauvages dans les cultures fruiti&egrave;res de la plaine du Rh&ocirc;ne et de la mettre en perspective avec l&rsquo;occupation de deux autres types de milieux, les vignes et les zones naturelles. L&rsquo;installation de 80 nichoirs pourvus de cavit&eacute;s de trois dimensions diff&eacute;rentes a permis de suivre le taux d&rsquo;occupation par les abeilles au fil du temps, dans chacun des trois contextes. Tous sites confondus, les trous de diam&egrave;tre de 6&nbsp;mm ont &eacute;t&eacute; les plus utilis&eacute;s par les abeilles sauvages, probablement parce qu&rsquo;ils correspondaient aux exigences du plus grand nombre d&rsquo;esp&egrave;ces potentielles. Peu occup&eacute;s en d&eacute;but de saison, les trous de diam&egrave;tre de 3&nbsp;mm ont vu leur fr&eacute;quentation par les abeilles sauvages augmenter d&egrave;s la mi-mai. Dans les cultures fruiti&egrave;res, ce sont les trous de diam&egrave;tre de 9&nbsp;mm qui ont &eacute;t&eacute; les plus occup&eacute;s et cela &agrave; un taux surpassant celui relev&eacute; dans les autres milieux. Cette dominance s&rsquo;explique par la pr&eacute;sence de l&rsquo;abeille ma&ccedil;onne (<em>Osmia cornuta</em>) en pleine p&eacute;riode de floraison des arbres (mars-avril). Les cultures fruiti&egrave;res constituent des milieux dans lesquels certaines abeilles sauvages cavicoles trouvent donc des ressources en pollen et nectar, bien que limit&eacute;es temporellement, ainsi que quelques habitats pour la nidification. En ceci, elles se d&eacute;marquent nettement des vignes, dont l&rsquo;offre r&eacute;duite en ressources alimentaires et en cavit&eacute;s naturelles constitue un obstacle &agrave; la pr&eacute;sence des abeilles sauvages cavicoles, du moins au printemps. De plus, la pr&eacute;sence de prairies proches des cultures fruiti&egrave;res influence positivement le taux de nidification des abeilles sauvages nichant dans des cavit&eacute;s de 3&nbsp;mm. Ceci tend &agrave; montrer que l&rsquo;augmentation de la diversit&eacute; structurelle au sein m&ecirc;me des cultures pourrait renforcer les &eacute;cosyst&egrave;mes et donc les rendre plus r&eacute;silients. Cette &eacute;tude met en lumi&egrave;re la n&eacute;cessit&eacute; de mieux comprendre le r&ocirc;le et les exigences des insectes sauvages pollinisateurs dans les cultures fruiti&egrave;res, sous l&rsquo;angle de leur service &eacute;cosyst&eacute;mique.</p> <p>&nbsp;</p> <p><strong>Annexe</strong></p> <p>Annexe1:&nbsp;Type et positionnement g&eacute;ographique des 80 nichoirs analys&eacute;s<br> Annexe2:&nbsp;Analyses statistiques<br> Annexe3:&nbsp;Occupation en fonction du diam&egrave;tre des trous et des habitats<br> Annexe4:&nbsp;Occupation dans les habitats (cultures fruiti&egrave;res, vignes, sites naturels) en fonction du diam&egrave;tre des trous<br> Annexe5:&nbsp;Occupation dans les cultures fruiti&egrave;res en fonction du milieu environnant<br> &nbsp;</p>

opencc-by-4.0Sep 2023View details →

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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Your academic CV and NIH biosketch

Make your CV in your school's format and your NIH biosketch from it, then download both as Word files.