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2,208 results for “coupling”
Heterometallic palladium–iron metal–organic framework as a highly active catalyst for cross-coupling reactions
<p>Relevant data for the publication with DOI: <a title="Link to landing page via DOI" href="https://doi.org/10.1039/D2SC05192C">10.1039/D2SC05192C</a></p>
input files for CROCO-WRF-OASIS3-MCT coupled model with a nest in CROCO
<p><span>This tar file contains all the input files needed to run the coupled model CROCO-WRF with OASIS3-MCT coupler with one 2-way nested domain in CROCO. This example configuration is based on the BENGUELA region at low resolution (this is the example of regional configuration of the CROCO model: see CROCO documentationa nd tutorials for more details</span>)</p>
input files for CROCO-WW3-WRF-OASIS3-MCT coupled model
<div>This tar file contains all the input files needed to run the coupled model CROCO-WW3-WRF with OASIS3-MCT coupler over an example configuration of the BENGUELA region at low resolution (this is the example of regional configuration of the CROCO model: see CROCO documentation and tutorials for more details)</div>
A pharmacological chaperone stabilizer rescues the expression of the vast majority of pathogenic variants in a G protein-coupled receptor
Open the record for dataset details and reuse information.
On the Understandability of Coupling-Related Practices in Infrastructure-as-Code Based Deployments
Open the record for dataset details and reuse information.
Dataset for publication "Resolving the Orbital Character of Low-energy Excitations in Mott Insulator with Intermediate Spin-orbit Coupling"
<p>Dataset providing the sourcedata of the main figures in the publication "Resolving the Orbital Character of Low-energy Excitations in Mott Insulator with Intermediate Spin-orbit Coupling"</p>
Model data for: Upper-lower layer coupling of recurrent circulation patterns in the Gulf of Mexico
<p>Post processed model output data for "Upper-lower layer coupling of recurrent circulation patterns in the Gulf of Mexico" submitted to Journal of Physical Oceanography. There are two datasets, one for the upper layer (H1) and one for the lower layer (H2). Each one contains the demeaned, detrended, and filtered (Lanczos low-pass) daily fields of layer thickness anomaly to which the authors computed the Hilbert EOFs.</p> <p>File list:</p> <p>H1_GoM_day_ssk15_st30dl.mat - this file contains the layer thickness anomaly fields for the upper layer (<250m)</p> <p>H2_GoM_day_ssk15_st30dl.mat - this file contains the layer thickness anomaly fields for the lower layer (>1000m)</p> <p>Scripts for plotting and processing the data into the model domain are available at:</p> <p>https://github.com/erickolvera/Olvera_et_al_21</p>
The role of spin-lattice coupling for ultrafast changes of the magnetic order in rare earth metals
<p>Dataset presented in the publication in Applied Physics Letters 119, "The role of spin-lattice coupling for ultrafast changes of the magnetic order in rare earth metals" (2021). Files are in .txt format. Raw data of time- and spin-resolved spectra measured on Gadolinium and Terbium surface states at different pump-probe delays are provided. In the data file, E_B = E- E_F represents the binding energy of the surface state of Tb and Gd. Spin polarization is normalized.</p> <p>Spin, energy, and time-resolved photoemission data of the Tb and Gd surface state for Tb and Gd (0001)<br> films of 10 nm prepared on W(110) in ultrahigh vacuum by molecular beam epitaxy. Measurements in normal emission with an angular resolution of \pm 2.5 degree.</p> <p>Fig.1 Raw data of spin-resolved spectra (majority and minority spin channel) measured on Gadolinium and Terbium surface states at different pump probe delays (ps) and simulated spectra according to the fit described in the paper.</p> <p>Fig. 2 Dynamics of the spin polarization of Terbium and Gadolinium extracted at fixed binding energy as a function of pump-probe delay and from EDCs at various delay.</p> <p>Fig.3 Raw data for the false color plot: Counts as a function of pump-probe delay and binding energy.<br> The Figure is composed of individually measured EDCs as a function of delay as measured.</p> <p>Fig. 4 Surface state binding energy and electron temperature of Gd and Tb as a function of pump probe delay. Binding energy and electron temperature for Tb have been extracted fitting the raw data of Fig. 3.<br> Data for Gd are as published in B. Andres et al. Phys. Rev. Lett. 115, 207404 (2015).</p>
Innate preference hierarchies coupled with adult experience, rather than larval imprinting or transgenerational acclimation, determine host plant use in Pieris rapae
The evolution of host range drives diversification in phytophagous insects, and understanding the female oviposition choices is pivotal for understanding host specialization. One controversial mechanism for female host choice is Hopkins' host selection principle, where females are predicted to increase their preference for the host species they were feeding upon as larvae. A recent hypothesis posits that such larval imprinting is especially adaptive in combination with anticipatory transgenerational acclimation, so that females both allocate and adapt their offspring to their future host. We study the butterfly <i>Pieris rapae</i>, for which previous evidence suggests that females prefer to oviposit on host individuals of similar nitrogen content as the plant they were feeding upon as larvae, and where the offspring show higher performance on the mother's host type. We test the hypothesis that larval experience and anticipatory transgenerational effects influence female host plant acceptance (no-choice) and preference (choice) of two host plant species (<i>Barbarea vulgaris</i> and <i>Berteroa incana</i>) of varying nitrogen content. We then test the offspring performance on these hosts. We found no evidence of larval imprinting affecting female decision-making during oviposition, but that an adult female experience of egg laying in no-choice trials on the less-preferred host <i>Be. incana</i> slightly increased the <i>P. rapae</i> propensity to oviposit on <i>Be. incana</i> in subsequent choice trials. We found no transgenerational effects on female host acceptance or preference, but negative transgenerational effects on larval performance, because the offspring of <i>P. rapae</i> females that had developed on<i> Be. incana</i> as larvae grew slower on both hosts, and especially on <i>Be. incana</i>. Our results suggest that among host-species preferences are guided by hard-wired preference hierarchies linked to species-specific host traits and less affected by larval experience or transgenerational effects, which may be more important for females evaluating different host individuals of the same species.
Interseismic coupling along the Mexican subduction seen by InSAR and GNSS
<p>Data associated with 'Interseismic coupling along the Mexican subduction seen by InSAR and GNSS' submitted in EPSL.</p>
Pyramidal Cell-Interneuron Coupling with Positive Correlation
<p>The firing-rate maps of the pyramidal cells and interneurons had a pronounced spatial-overlap with the positive correlation in the rectangular-shaped track at higher firing rates.</p>
Data Associated with Manuscript Titled "Development of a graphical resilience framework to understand a coupled human-natural system in a remote arid highland of Baja California Sur"
<p>This is a dataset in support of analyses of water chemistry and social networks described and interpreted in the associated manuscript titled "Development of a graphical resilience framework to understand a coupled human-natural system in a remote arid highland of Baja California Sur"</p>
The pocketome of G-protein-coupled receptors reveals previously untargeted allosteric sites
<p>Supplementary Data 1: list of all analysed structures together with the docking files</p> <p>Supplementary Data 2: grid files, template and README for visualising the class-specific density maps by using Pymol</p>
Figure 5 in Harpacticoida (Copepoda) from the pelagic zone of the Sea of Okhotsk: diversity, spatiotemporal distribution, and role in benthopelagic coupling
Figure 5. Composition (% from abundance) of harpacticoids life forms in pelagic zone in different months (A), on different depths and shores of Prostor Bay (B).
Figure 2 in Harpacticoida (Copepoda) from the pelagic zone of the Sea of Okhotsk: diversity, spatiotemporal distribution, and role in benthopelagic coupling
Figure 2. Average intermonthly dynamics of weather conditions in the Prostor Bay 2013–2015 (sea surface temperature (SST) and storminess).
Figure 1. A in Harpacticoida (Copepoda) from the pelagic zone of the Sea of Okhotsk: diversity, spatiotemporal distribution, and role in benthopelagic coupling
Figure 1. A. Map of Russian Far East with position of the Iturup Island; B. Map of Iturup Island with location of the Prostor Bay; C. four sampling transects in south-west part of the Prostor Bay. Black points – zooplankton sampling stations; white points – station of catching salmon fry.
Figure 4 in Harpacticoida (Copepoda) from the pelagic zone of the Sea of Okhotsk: diversity, spatiotemporal distribution, and role in benthopelagic coupling
Figure 4. Variations of harpacticoids species richness (A) and diversity (B) in pelagic zone at different depths and near different shores of Prostor Bay.
Figure 7 in Harpacticoida (Copepoda) from the pelagic zone of the Sea of Okhotsk: diversity, spatiotemporal distribution, and role in benthopelagic coupling
Figure 7. Composition (% of abundance) of diatoms from different life forms in harpacticoids diet in pelagic zone.
Figure 6 in Harpacticoida (Copepoda) from the pelagic zone of the Sea of Okhotsk: diversity, spatiotemporal distribution, and role in benthopelagic coupling
Figure 6. Harpacticoids dominance structure (% of abundance) in pelagic zone near southern (A) and western (B) shores of Prostor Bay.
Figure 3 in Harpacticoida (Copepoda) from the pelagic zone of the Sea of Okhotsk: diversity, spatiotemporal distribution, and role in benthopelagic coupling
Figure 3. The abundance of adults harpacticoids and copepodites in pelagic zone in different months (A) and on different depths (B).
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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.