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1,952 results for “actionality”
AkiraSMori/BiodProd-ProtectArea: Analyses for "Biodiversity protection and its future benefits to society are intertwined with climate change action"
<div> <h2>Abstract</h2> <a href="https://github.com/AkiraSMori/BiodProd-ProtectArea/blob/main/README.md#abstract"></a></div> <p>Biodiversity loss and climate change are incontrovertibly intertwined, yet the nuanced interplay between these global challenges is often understated in policy dialogues. Here, we illustrate that conservation through protected areas can effectively preserve primary productivity and carbon capture in forests worldwide, which directly depend on tree diversity. However, we also discover that failing to mitigate future climate change has the potential to diminish the effectiveness of terrestrial protected areas in conserving tree diversity-dependent forest productivity, especially in warmer biomes. This holds true even under the most optimized selection of protected areas designed to meet the global biodiversity target of 30% protection by 2030. Thus, climate change mitigation is critical for the success of many conservation actions aimed at achieving global targets; otherwise, existing and future efforts to conserve biodiversity and their benefits to society could be in vain. Addressing anthropogenic climate change will sustain the many biodiversity-derived ecosystem benefits to society.</p>
Fig. 1 in Insecticidal and repellent action of pogostone against Myzus persicae (Hemiptera: Aphididae)
Fig. 1. Structure of pogostone.
A Database of In-Game Player Movements (Actions and Events) in Gaelic Football
<p>In this study, data was acquired by fitting GPS sensors to Gaelic football players which are worn during game time. These wearable devices collect internal (heart rate) and external (gps positioning) data related to the movement of players. However, this form of raw data is not well suited to machine learning algorithms as it lacks the necessary semantics which can identify the type and duration of movements. The dataset presented here is created by a data engineering exercise, driven by domain experts, to transform the GPS coordinates into a series of (player) actions. The end result is a database comprising 12 variables and almost 160k actions. It’s reuse potential is targeted at machine learning researchers, sport scientists and coaches who are seeking to understanding the effort and load of players during game time. Analysis is enables across five dimensions: games, players, actions, duration and speed. In addition, the concept of an event groups together actions that belong to the same sequence and enables analysis at a different level of abstraction. </p> <p> </p>
Human Microbiome Action - Social Media Templates
<p>This comprehensive resource pack includes ready-to-use messages in PNG format and versatile templates for Twitter/X, LinkedIn, and Instagram available as PowerPoint files. Designed to streamline your communication efforts, these templates enable you to effectively share the latest advancements and insights in human microbiome research with your audience.</p>
Blue-Action NorCPM AMOC 26N reconstruction
<p>Reconstruction of the past variability of the AMOC at 26°N using the NorCPM system</p>
Ca transient properties vs action potential morphology
<p>Analysis and raw data on properties of intracellular Ca transients recorded in voltage-clamped rabbit atrial myocytes. Ca transients were elicited by pacing atrial myocytes with 2 different action potential (AP) waveforms prerecorded during Ca and AP alternans.</p>
Predictive perception of self-generated movements: Commonalities and differences in the neural processing of tool and hand actions
<p>Dataset relative to the following publication:</p> <p>Pazen, M., Uhlmann, L., van Kemenade, B.M., Steinsträter, O., Straube, B., Kircher, T. Predictive perception of self-generated movements: Commonalities and differences in the neural processing of tool and hand actions. <em>NeuroImage</em>. DOI: <a href="https://doi.org/10.1016/j.neuroimage.2019.116309">10.1016/j.neuroimage.2019.116309</a></p> <p>Details are specified in the "readme.docx" file.</p>
Fig. 1 in Synthesis of new α-amino nitriles with insecticidal action on Aedes aegypti (Diptera: Culicidae)
Fig. 1. Structures of insecticide agents and molecules studied in this work.
Figure 2 in A new record of the freshwater turtle Mauremys rivulata (Valenciennes, 1833) in the Ofkos river, Cyprus: Conservation actions required
Figure 2. Ponds where fresh water turtles were trapped.
Table 1 in America's Most Wanted Fishes: cataloging risk assessments to prioritize invasive species for management action
<p><b>Table 1.</b> List of fish species with high-risk statuses in the conterminous U.S., in the Great Lakes region, and in the state of Florida. Horizontal lines separate families and species for clarity.</p><table><tbody><tr><th>Family Name</th><th>Fish species name</th><th>Conterminous U.S.</th><th>Great Lakes</th><th>Florida</th></tr></tbody><tbody><tr><th>Atherinidae</th><td><i>Atherina boyeri</i> (Risso, 1810)</td><td>X</td><td>X</td><td></td></tr><tr><th>Atherinopsidae</th><td><i>Menidia beryllina</i> (Cope, 1867)</td><td>X</td><td></td><td></td></tr><tr><td><i>Odontesthes bonariensis</i> (Valenciennes, 1835)</td><td>X</td><td></td><td></td></tr><tr><th>Callichthyidae</th><td><i>Hoplosternum littorale</i> (Hancock, 1828)</td><td></td><td></td><td>X</td></tr><tr><th>Centrarchidae</th><td><i>Lepomis microlophus</i> (Günther, 1859)</td><td>X</td><td>X</td><td></td></tr><tr><td><i>Micropterus dolomieu</i> (Lacepède, 1802)</td><td>X</td><td></td><td></td></tr><tr><td><i>Micropterus salmoides</i> (Lacepède, 1802)</td><td>X</td><td></td><td></td></tr><tr><th>Centropomidae</th><td><i>Lates niloticus</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><th>Channidae</th><td><i>Channa argus</i> (Cantor, 1842)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Channa marulius</i> (Hamilton, 1822)</td><td></td><td></td><td>X</td></tr><tr><th>Characidae</th><td><i>Pygocentrus nattereri</i> (Kner, 1858)</td><td>X</td><td></td><td></td></tr><tr><th>Cichlidae</th><td><i>Amatitlania nigrofasciata</i> (Günther, 1867)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Astronotus ocellatus</i> (Agassiz, 1831)</td><td>X</td><td></td><td></td></tr><tr><td><i>Cichla kelberi</i> (Kullander & Ferreira, 2006)</td><td>X</td><td></td><td></td></tr><tr><td><i>Cichla ocellaris</i> (Bloch & Schneider, 1801)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Cichlasoma uropthalma</i> (Günther, 1862)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Coptodon rendalli</i> (Boulenger, 1897)</td><td>X</td><td></td><td></td></tr><tr><td><i>Coptodon zilli</i> (Gervais, 1848)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Hemichromis letourneuxi</i> (Sauvage, 1880)</td><td>X</td><td></td><td></td></tr><tr><td><i>Herichthys cyanoguttatus</i> (Baird & Girard, 1854)</td><td>X</td><td></td><td></td></tr><tr><td><i>Oreochromis aureus</i> (Steindachner, 1864)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Oreochromis mossambicus</i> (Peters, 1852)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Oreochromis niloticus</i> (Linnaeus, 1758)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Parachromis managuensis</i> (Günther, 1862)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Pelmatotilapia mariae</i> (Boulenger, 1899)</td><td>X</td><td></td><td></td></tr><tr><td><i>Sarotherodon melanotheron</i> (Rüppell, 1852)</td><td>X</td><td></td><td></td></tr><tr><td><i>Serranochromis robustus</i> (Günther, 1864)</td><td>X</td><td></td><td></td></tr><tr><th>Clariidae</th><td><i>Clarias batrachus</i> (Linnaeus, 1758)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Clarias fuscus</i> (Lacepède, 1803)</td><td>X</td><td></td><td></td></tr><tr><td><i>Clarias gariepinus</i> (Burchell, 1822)</td><td>X</td><td></td><td></td></tr><tr><th>Clupeidae</th><td><i>Alosa aestivalis</i> (Mitchell, 1814)</td><td>X</td><td></td><td></td></tr><tr><td><i>Alosa pseudoharengus</i> (Wilson, 1811)</td><td>X</td><td>X</td><td></td></tr><tr><th>Cobitidae</th><td><i>Misgurnus anguillicaudatus</i> (Cantor, 1842)</td><td>X</td><td></td><td>X</td></tr><tr><th>Cyprinidae</th><td><i>Abramis brama</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Alburnus alburnus</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Barbus barbus</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Carassius auratus</i> (Linnaeus, 1758)</td><td></td><td></td><td>X</td></tr><tr><td><i>Carassius gibelio</i> (Bloch, 1782)</td><td>X</td><td></td><td></td></tr><tr><td><i>Ctenopharyngodon idella</i> (Valenciennes, 1844)</td><td>X</td><td>X</td><td>X</td></tr><tr><td><i>Culter alburnus</i> (Basilewsky, 1855)</td><td>X</td><td></td><td></td></tr><tr><td><i>Cyprinella lutrensis</i> (Baird & Girard, 1853)</td><td>X</td><td></td><td></td></tr><tr><td><i>Cyprinus carpio</i> (Linnaeus, 1758)</td><td>X</td><td>X</td><td>X</td></tr><tr><td><i>Gobio gobio</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Hypophthalmichthys molitrix</i> (Valenciennes, 1844)</td><td>X</td><td></td><td></td></tr><tr><td><i>Hypophthalmichthys nobilis</i> (Richardson, 1845)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Leuciscus idus</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Mylopharyngodon piceus</i> (Richardson, 1846)</td><td>X</td><td></td><td></td></tr><tr><td><i>Opsariichthys uncirostris</i> (Temminck & Schlegel, 1846)</td><td>X</td><td></td><td></td></tr><tr><td><i>Pimephales promelas</i> (Rafinsque, 1820)</td><td></td><td></td><td>X</td></tr><tr><td><i>Phoxinus phoxinus</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Protochondrostoma genei</i> (Bonaparte, 1839)</td><td>X</td><td></td><td></td></tr><tr><td><i>Pseudorasbora parva</i> (Temminck & Schlegel, 1846)</td><td>X</td><td></td><td></td></tr><tr><td><i>Rhodeus amarus</i> (Bloch, 1782)</td><td>X</td><td></td><td></td></tr><tr><td><i>Rutilus aula</i> (Bonparte,1841)</td><td>X</td><td></td><td></td></tr><tr><td><i>Rutilus rutilus</i> (Linnaeus, 1758)</td><td>X</td><td>X</td><td></td></tr><tr><td><i>Scardinius erythrophthalmus</i> (Linnaeus, 1758)</td><td>X</td><td>X</td><td></td></tr><tr><td><i>Tinca tinca</i> (Linnaeus, 1758)</td><td>X</td><td>X</td><td></td></tr><tr><th>Esocidae</th><td><i>Esox lucius</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Esox masquinongy</i> (Mitchill, 1824)</td><td>X</td><td></td><td></td></tr><tr><th>Gasterosteidae</th><td><i>Gasterosteus aculeatus</i> (Linnaeus, 1758)</td><td>X</td><td>X</td><td></td></tr><tr><th>Gobiidae</th><td><i>Neogobius melanostomus</i> (Pallas, 1814)</td><td>X</td><td>X</td><td></td></tr><tr><td><i>Ponticola platyrostris</i> (Pallas, 1814)</td><td>X</td><td></td><td></td></tr><tr><td><i>Proterorhinus semilunaris</i> (Heckel, 1837)</td><td>X</td><td></td><td></td></tr><tr><th>Heteropneustidae</th><td><i>Heteropneustes fossilis</i> (Bloch, 1794)</td><td>X</td><td></td><td></td></tr><tr><th>Ictaluridae</th><td><i>Ictalurus furcatus</i> (Valenciennes, 1840)</td><td>X</td><td></td><td></td></tr><tr><td><i>Pylodictis olivaris</i> (Rafinesque, 1818)</td><td>X</td><td></td><td></td></tr><tr><th>Loricariidae</th><td><i>Hypostomus plecostomus</i> (Linnaeus, 1758)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Pterygoplichthys anisitsi</i> (Eigenmann & Kennedy, 1903)</td><td></td><td></td><td>X</td></tr><tr><td><i>Pterygoplichthys disjunctivus</i> (Weber, 1991)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Pterygoplichthys multiradiatus</i> (Hancock, 1828)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Pterygoplichthys pardalis</i> (Castelnau, 1855)</td><td>X</td><td></td><td></td></tr><tr><th>Moronidae</th><td><i>Morone americana</i> (Gmelin, 1789)</td><td>X</td><td>X</td><td></td></tr><tr><th>Notopteridae</th><td><i>Chitala ornata</i> (Gray, 1831)</td><td>X</td><td></td><td></td></tr><tr><th>Odontobutidae</th><td><i>Perccottus glenii</i> (Dybowski, 1877)</td><td>X</td><td></td><td></td></tr><tr><th>Osmeridae</th><td><i>Hypomesus nipponensis</i> (McAllister, 1963)</td><td>X</td><td></td><td></td></tr><tr><td><i>Osmerus eperlanus</i> (Linnaeus, 1758)</td><td>X</td><td>X</td><td></td></tr><tr><td><i>Osmerus mordax</i> (Mitchill, 1814)</td><td>X</td><td></td><td></td></tr><tr><th>Osphronemidae</th><td><i>Trichogaster lalius</i> (Hamilton, 1822)</td><td>X</td><td></td><td></td></tr><tr><td><i>Trichopodus trichopterus</i> (Pallas, 1770)</td><td>X</td><td></td><td></td></tr><tr><th>Percidae</th><td><i>Gymnocephalus cernua</i> (Linnaeus, 1758)</td><td>X</td><td>X</td><td></td></tr><tr><td><i>Perca flavescens</i> (Mitchill, 1814)</td><td>X</td><td></td><td></td></tr><tr><td><i>Perca fluviatilis</i> (Linnaeus, 1758)</td><td>X</td><td>X</td><td></td></tr><tr><td><i>Sander lucioperca</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Sander vitreus</i> (Mitchill, 1818)</td><td>X</td><td></td><td></td></tr><tr><th>Petromyzontidae</th><td><i>Petromyzon marinus</i> (Linnaeus, 1758)</td><td></td><td>X</td><td></td></tr><tr><th>Poeciliidae</th><td><i>Belonesox belizanus</i> (Kner, 1860)</td><td>X</td><td></td><td></td></tr><tr><td><i>Gambusia affinis</i> (Baird & Girard, 1853)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Gambusia holbrooki</i> (Girard, 1859)</td><td>X</td><td></td><td></td></tr><tr><td><i>Poecilia latipinna</i> (Lesueur, 1821)</td><td>X</td><td></td><td></td></tr><tr><td><i>Poecilia reticulata</i> (Peters, 1859)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Poecilia sphenops</i> (Valciennes, 1846)</td><td>X</td><td></td><td>X</td></tr><tr><td><i>Xiphophorus helleri</i> (Heckel, 1848)</td><td>X</td><td></td><td></td></tr><tr><td><i>Xiphophorus variatus</i> (Meek, 1904)</td><td>X</td><td></td><td></td></tr><tr><th>Polypteridae</th><td><i>Polypterus delhezi</i> (Boulenger, 1899)</td><td></td><td></td><td>X</td></tr><tr><th>Pomacentridae</th><td><i>Neopomacentrus cyanomos</i> (Bleeker, 1856)</td><td>X</td><td></td><td></td></tr><tr><th>Potamotrygonidae</th><td><i>Potamotrygon falkneri</i> (Castex & Maciel, 1963)</td><td>X</td><td></td><td></td></tr><tr><td><i>Potamotrygon motoro</i> (Müller & Henle, 1841)</td><td>X</td><td></td><td></td></tr><tr><td><i>Potamotrygon schuhmacheri</i> (Castex, 1964)</td><td>X</td><td></td><td></td></tr><tr><th>Salmonidae</th><td><i>Coregonus albula</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Coregonus lavaretus</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Coregonus maraena</i> (Bloch, 1779)</td><td>X</td><td></td><td></td></tr><tr><td><i>Coregonus peled</i> (Gmelin, 1789)</td><td>X</td><td></td><td></td></tr><tr><td><i>Hucho hucho</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><td><i>Oncorhynchus kisutch</i> (Walbaum, 1792)</td><td></td><td>X</td><td></td></tr><tr><td><i>Oncorhynchus mykiss</i> (Walbaum, 1792)</td><td></td><td>X</td><td></td></tr><tr><td><i>Oncorhynchus tshawytscha</i> (Walbaum, 1792)</td><td></td><td>X</td><td></td></tr><tr><td><i>Salmo trutta</i> (Linnaeus, 1758)</td><td></td><td>X</td><td></td></tr><tr><th>Scorpaenidae</th><td><i>Pterois miles</i> (Bennett, 1828)</td><td>X</td><td></td><td></td></tr><tr><td><i>Pterois volitans</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr><tr><th>Siluridae</th><td><i>Silurus glanis</i> (Linnaeus, 1758)</td><td>X</td><td></td><td></td></tr></tbody></table>
Data from: Heterogeneous zonal impacts of climate change on a wide hyperendemic area of human and animal fascioliasis assessed within a One Health action for prevention and control
Open the record for dataset details and reuse information.
Dataset for "Dissociable Roles of the mPFC-to-VTA pathway in the control od Impulsive action and Risk-Related Decision-Making in Roman High- and Low-Avoidance Rats"
<p>This dataset corresponds to the study "Dissociable Roles of the mPFC-to-VTA Pathway in the Control of Impulsive Action and Risk-Related Decision-Making in Roman High- and Low-Avoidance Rats". In this study, we used Positron Emission Tomography with [18F]-Fluorodeoxyglucose to evaluate brain metabolic activity in Roman High- (RHA) and Low-avoidance (RLA) rats, which exhibit innate differences in impulsivity. Notably, we used a viral-based intersectional chemogenetic strategy to isolate the role of the mPFC-to-VTA pathway in controlling impulsive behaviors. We selectively activated the mPFC-to-VTA pathway in RHA rats and inhibited it in RLA rats, assessing the effects on impulsive action and RDM in the rat gambling task. Our results showed that RHA rats displayed higher impulsive action, less optimal decision-making, and lower cortical activity than RLA rats at baseline. Chemogenetic activation of the mPFC-to-VTA pathway reduced impulsive action in RHA rats, whereas chemogenetic inhibition had the opposite effect in RLA rats. However, these manipulations did not affect RDM. Our findings suggest a dissociable role of the mPFC-to-VTA pathway in impulsive action and RDM, highlighting its potential as a target for investigating impulsivity-related disorders.</p> <p><strong>Contributions for usage of this data in publications:</strong></p> <p>If you publish any work using these data, please cite this repository and the associated publication.</p>
Thalamic input to motor cortex facilitates goal-directed action initiation
<p>Data set for: Takahashi N, Moberg S, Zolnik TA, Catanese J, Sachdev RNS, Larkum ME, Jaeger D (2021) Thalamic input to motor cortex facilitates goal-directed action initiation. <em>Current Biology</em> (DOI: <a href="https://doi.org/10.1016/j.cub.2021.06.089">https://doi.org/10.1016/j.cub.2021.06.089</a>) </p> <p>The file named "Takahashi_Data&Code.zip" is a zipped version of a folder "Takahashi_Data&Code", which contains the data analyzed in the study along with the Matlab code used to generate the published figures. To access the data and the code, first unzip the file. Then add the folder with subfolders to the Matlab path. Before running the code (e.g., "PlotData_Fig1.m"), load the related Matlab data file (e.g., "Data_Pharmacology_Fig1.mat") in Workspace. Each code plots the results used in the corresponding figure.</p>
A selective role for receptor activity-modifying protein in sub-chronic action of the amylin selective receptor agonist NN1213 compared to salmon calcitonin on body weight and food intake in male mice
<p>Raw data prism files for the manuscript "A selective role for receptor activity-modifying protein in sub-chronic action of the amylin selective receptor agonist NN1213 compared to salmon calcitonin on body weight and food intake in male mice"</p>
Cyclist Actions: Motion History Images and Trajectories
<p>The dataset consists of over 1.1 million samples of labeled cyclists actions. Every sample consists of two motion history images (MHI), consisting of motion over the past second, from two different cameras, the past trajectory of the cyclist of the last second (50 past positions), and a label of the currently performed action.</p> <p>The samples were extracted from 1,639 video sequences of cyclists moving across an urban intersection at the University of Applied sciences in Aschaffenburg: <a href="https://www.th-ab.de/ueber-uns/organisation/labor/kooperative-automatisierte-verkehrssysteme/ausstattung/">https://www.th-ab.de/ueber-uns/organisation/labor/kooperative-automatisierte-verkehrssysteme/ausstattung/</a></p> <p>The uploaded files consist of a numpy file with MHI, trajectories and labels, and a json file containing 5-fold cross validation/test split.</p> <p>Every MHI has a size 192x192x2. The two channels contain the separate motion contours of the bike and the cyclist.</p> <p>The manually created labels are:</p> <ul> <li>straight: cyclists is moving and not turning</li> <li>tr/tl: cyclist is turning left/right</li> <li>move: cyclist is moving with nearly constant velocity and not turning</li> <li>start: cyclist was standing and starts moving</li> <li>starting_movement: first movement of cyclist before starting</li> <li>stop: cyclist was moving/starting and slows down to a halt</li> <li>wait: cyclist is standing</li> <li>hand_signal_left/right: cyclist indicates a turn by hand signal</li> <li>shoulder_check_left/right: cyclist looks over left/right shoulder</li> <li>out_of_saddle: cyclist is standing</li> </ul> <p>The numpy file consists of python dictionaries with scenes of the form:</p> <pre><code class="language-python">{SCENE_NAME: 'mhi_hk1/2': [...], # list of zip compressed, python pickled mhi from cameras 1 and 2 'x/y/z_tracked': [...], # tracked cyclists positions in x/y/z directions, 'x/y/z_smoothed': [...], # smoothed (by rts smoother) cyclists positions in x/y/z directions, 'orientation': [...], # orientation of the cyclists estimated by kalman filters 'ts': [...], # utc timestamps in micro seconds LABEL_NAME: [...], # labels of different actions (0 or 1)}</code></pre> <p>The zipped/pickled mhi can be decompressed using:</p> <pre><code class="language-python">import numpy as np import pickle import zlib d = np.load('mhi_dataset_0,1,2,3,4,6,9,13,18,26,33,41,49.npy', allow_pickle=True, encoding='latin1').item() for scene_name in d: for i in range(len(d[scene_name]['mhi_hk1']) - 50): # ommit 50 first frames as they have no mhi mhi1 = pickle.loads(zlib.decompress(d[scene_name]['mhi_hk1'][49 + i].encode('latin1')), encoding='latin1') mhi2 = pickle.loads(zlib.decompress(d[scene_name]['mhi_hk2'][49 + i].encode('latin1')), encoding='latin1')</code></pre> <p> </p> <p>This work results from the project DeCoInt 2, supported by the German Research Foundation (DFG) within the priority program SPP 1835: "Kooperativ interagierende Automobile", grant numbers DO 1186/1-2, FU 1005/1-2, and SI 674/11-2. Additionally, the work is supported by "Zentrum Digitalisierung Bayern".</p> <p>Due to privacy laws in germany, we are not permitted to publish raw image data.</p>
Supplemental material to 'A variational rigid-block modelling approach to nonlinear elastic and kinematic analysis of failure mechanisms in historic masonry structures subjected to lateral actions'
<p>This repository contains the data necessary to reproduce the content of the article:</p> <blockquote> <p>A variational rigid-block modelling approach to nonlinear elastic and kinematic analysis of failure mechanisms in historic masonry structures subjected to lateral actions (2021). Earthquake Engineering & Structural Dynamics, 1–23. <a href="https://onlinelibrary.wiley.com/doi/full/10.1002/eqe.3512">https://doi.org/10.1002/eqe.3512</a></p> </blockquote> <p>The file <strong>01_Dataset.zip</strong> contains the dataset. The companion document <strong>00_Dataset_description.pdf </strong>describes the content of the dataset, guiding the analyst to its use in order to (i) reproduce the article's results and (ii) compare the article's results to new results brought by the analyst, e.g. by comparison with other numerical models.</p> <p>Version history</p> <p>v2: updated references in 00_dataset description.pdf </p>
Open Science for Action (OS4A): A working model for libraries
<p>A diagram outlining a conceptual model for how libraries can contribute to and advance open science in principle and practice. </p>
Breakfast Dataset with I3D features for Action Segmentation Using MuCon
<p>Breakfast Dataset with I3D features for Action Segmentation Using MuCon</p> <p> </p> <p>Visit: https://github.com/yassersouri/MuCon</p>
Mu-rhythm modulation associated with the observation and execution of a goal-directed action in healthy toddlers estimated using two different baseline conditions
<p>The database includes mu-rhythm ERD/ERS values elicited by the observation and execution of a goal-directed action in healthy toddlers (N=19). ERD/ERS values has been computed using to different baseline conditions: 1) observation of a black and white static image (BL1) and 2) short period of stillness (BL2).</p> <p>The first sheet of the database refers to action execution (AE) data, whereas the second sheet refers to action observation (AO) data. The database table in each sheet includes for each subject single trial ERD/ERS values (table rows) registered in 7 different scalp sites (table columns) for both BL1 and BL2.</p> <p>The database was used for the statistical analysis of the following paper: Piazza, C.; Visintin, E.; Reni, G.; Montirosso, R. The Effect of Baseline on Toddler Event-Related Mu-Rhythm Modulation. <em>Brain Sci.</em> <strong>2021</strong>, <em>11</em>, 1159. https://doi.org/10.3390/brainsci11091159 (<a href="https://www.mdpi.com/2076-3425/11/9/1159/htm">https://www.mdpi.com/2076-3425/11/9/1159/htm</a>)</p> <p>All the details about data acquisition and preprocessing are reported in the above mentioned publication.</p>
Action Prediction Error: a value-free dopaminergic teaching signal that drives stable learning - Behavioral dataset
<p>Behavioral data to reproduce figures of this paper: https://doi.org/10.1101/2022.09.12.507572</p> <p>See Github repository: https://github.com/HernandoMV/APE_paper</p>
ScienceDex guides
Understand access before you commit
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.