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1,620 results for “springs”
Greenland 2022 GHOST Project: Sampling Greenland Geothermal Springs - Expedition Report Data
Data from the GHOST GRL22 Leg 1 Expedition report
Spring Goddess Ora Tallo (Birth of Venus)
Neon perspective of the Botticelli's Birth of Venus. Representation of the right side of the painting in the neon light. Source: Objaverse 1.0 / Sketchfab
Eternal Spring
Eternal Spring (1884), Auguste Rodin (1840-1917), marble, Nye Carlsberg Glyptotek (Copenhagen, Denmark). Made with Memento Beta. Source: Objaverse 1.0 / Sketchfab
Mercy Hot Springs
This building is old , but the fancy ends are new. This hot spring was occupied by native Americas, Spanish, and now Anglos off Rout 5 in Central CA. Created in RealityCapturefrom 57 images in 00h:12m:00s. Source: Objaverse 1.0 / Sketchfab
Spring Break Wreck - 04-18-18
This is a section of a 19th-century merchant vessel that wrecked on Ponte Vedra Beach on 28 March 2018. The remaining hull section is the forward port side of the vessel broken above the keel. The 48-foot section shows tool marks across many of the timbers and Roman numerals on the frames. The images for this model were acquired one day before the wreck was moved to the Guana Tolomato Matanzas National Estuarine Research Reserve. Source: Objaverse 1.0 / Sketchfab
Indian Springs Angel Headstone
This is a headstone dating to 1827 located in the Angel Springs Cemetery near Tallahassee, FL. The angel figure, aside from the inscription, indicates that this is an infant's headstone. Source: Objaverse 1.0 / Sketchfab
Corn Springs Miners Cabin
Corn Springs Miners Cabin Corn Springs Cabin is located near Desert Center California. Corn Springs Mining District was established in 1897. Miners came to the area and used the water for processing their gold ore, in the late 19th century. The most notable resident of the spring was Gus Lederer. The self-proclaimed "Mayor of Corn Springs", was Gus Lederer. He lived at the spring until 1932, when he died from a black widow spider bite. There is a Bureau of Land Management (BLM) campground nearby and Chemehuevi, Desert Cahuilla and Yuma bands carved elaborate petroglyphs in the nearby rocks. In 1998, the springs were added to the United States National Register of Historic Places. This 3D model was created in Pix4D merging double grid and orbits. Mavic Pro 2. Information was found: https://en.wikipedia.org/wiki/Corn_Springs Source: Objaverse 1.0 / Sketchfab
The Spring
The Spring public space installation statue sculpture, white marble Artist: Zdeněk Preclík, 1984 @ public street, Prague, Czechia • https://goo.gl/maps/SsJsnScq5u2kdBRh6 Aug 30 2021 Photogrammetry scan 130x24 MPix Created in RealityCapture by Capturing Reality Source: Objaverse 1.0 / Sketchfab
Data from: Signatures of autumn deluges revealed during spring drought in a semi-arid grassland
<p>Increases in extremely large precipitation events (deluges) and shifts in seasonal patterns of water availability with climate change will both have important consequences for ecosystem function, particularly in water-limited regions. While previous work in the semi-arid shortgrass steppe of northeastern Colorado has demonstrated this ecosystem's strong sensitivity to growing season deluges, our understanding of ecosystem responses to deluges during the dormant season is limited. Here, we imposed experimental 100 mm deluges (~ 30% of mean annual precipitation) in either September or October in a native C<sub>4</sub>-dominated shortgrass steppe ecosystem to evaluate the impact of this post-growing season shift in water availability during the autumn and the following growing season. Soil moisture for both deluge treatments remained elevated compared with ambient levels through April as spring precipitation was atypically low. Despite overall low levels of productivity with spring drought, these deluges from the previous autumn increased aboveground net primary production (ANPP), primarily due to increases with C<sub>4</sub> grasses. C<sub>3</sub> ANPP was also enhanced, largely due to an increase in the annual C<sub>3 </sub>grass,<em> Vulpia octoflora</em>, in the October deluge treatment. While spring precipitation has historically been the primary determinant of ecosystem function in this ecosystem, this combination of two climate extremes – an extremely wet autumn followed by a naturally occurring spring drought – revealed the potential for meaningful carryover effects from autumn precipitation. With climate change increasing the likelihood of extremes during all seasons, experiments that create novel climatic conditions can provide new insight into the dynamics of ecosystem functioning in the future.</p>
Determinants of spring migration departure dates in a New World sparrow: weather variables reign supreme
<p><span>Numerous factors influence the timing of spring migration in birds, yet the relative importance of intrinsic and extrinsic variables on migration initiation remains unclear. To test for interactions among weather, migration distance, parasitism, and physiology in determining spring departure date, we used the Dark-eyed Junco (<em>Junco</em> <em>hyemalis</em>) as a model migratory species known to harbor diverse and common haemosporidian parasites. Prior to spring migration departure from their wintering grounds in Indiana, USA, we quantified the intrinsic variables of fat, body condition (i.e., mass~tarsus residuals), physiological stress (i.e., ratio of heterophils to lymphocytes), cellular immunity (i.e., leukocyte composition and total count), migration distance (i.e., distance to the breeding grounds) using stable isotopes of hydrogen from feathers, and haemosporidian parasite intensity. We then attached nanotags to determine the timing of spring migration departure date using the Motus Wildlife Tracking System. We used additive Cox proportional hazard mixed models to test how risk of spring migratory departure was predicted by the combined intrinsic measures, along with meteorological predictors on the evening of departure (i.e., average wind speed and direction, relative humidity, and temperature). Model comparisons found that the best predictor of spring departure date was average nightly wind direction and a principal component combining relative humidity and temperature. Juncos were more likely to depart for spring migration on nights with largely southwestern winds and on warmer and drier evenings (relative to cooler and more humid evenings). Our results indicate that weather conditions at take-off are more critical to departure decisions than the measured physiological and parasitism variables.</span></p>
Data from: LHFPL5 is a key element to the gating spring of cochlear hair cells: comparison of mechanotransduction channel activation in presence or absence of LHFPL5
<p>During auditory transduction, sound-evoked vibrations of the hair cell stereociliary bundles open mechanotransducer (MET) ion channels via tip links extending from one stereocilium to its neighbor. How tension in the tip link is delivered to the channel is not fully understood. The MET channel comprises a pore-forming subunit, transmembrane channel-like protein (TMC1 or TMC2), aided by several accessory proteins, including LHFPL5 (lipoma HMGIC fusion partner-like 5). We investigated the role of LHFPL5 in transduction by comparing MET channel activation in outer hair cells of <em>Lhfpl5-/- </em>knockout mice with those in <em>Lhfpl5+/-</em> heterozygotes. The 10-90 percent working range of transduction in <em>Tmc1+/+; Lhfpl5+/-</em> was 52 nm, from which the single-channel gating force, Z was evaluated as 0.34 pN. However, in <em>Tmc1+/+; Lhfpl5‑/- </em>mice,<em> </em>the<em> </em>working range increased to 123 nm and Z more than halved to 0.13 pN, indicating reduced sensitivity. Tip link tension is thought to activate the channel via a gating spring, whose stiffness is inferred from the stiffness change on tip link destruction. The gating stiffness was ~40 percent of the total bundle stiffness in wild-type but was virtually abolished in <em>Lhfpl5-/-,</em> implicating LHFPL5 as a principal component of the gating spring. The mutation <em>Tmc1 </em>p.D569N reduced the LHFPL5 immunolabeling in the stereocilia and like <em>Lhfpl5-/-</em> doubled the MET working range but other deafness mutations had no effect on the dynamic range. We conclude that tip-link tension is transmitted to the channel primarily via LHFPL5; residual activation without LHFPL5 may occur by direct interaction between PCDH15 and TMC1.</p>
Spring tropical cyclones modulate near-surface isotopic compositions of atmospheric water vapour at Kathmandu, Nepal
<p>All these data have been published in a ACP paper. If you use these data in any conditions, please cite the following publicaiton: Adhikari, N., Gao, J., Zhao, A., Xu, T., Chen, M., Niu, X., and Yao, T.: Spring tropical cyclones modulate near-surface isotopic compositions of atmospheric water vapour at Kathmandu, Nepal, EGUsphere, https://doi.org/10.5194/egusphere-2023-2186, 2023.</p>
Dataset for "Overwinter and spring thaw nitrous oxide fluxes in a northern Prairie cropland are limited but a significant proportion of annual emissions"
<p>This dataset contains the data used in the publication "Overwinter and spring thaw nitrous oxide fluxes in a northern Prairie cropland are limited but a significant proportion of annual emissions" in Global Biogeochemical Cycles. This study presented micrometeorological N2O fluxes measured using the flux-gradient method over 4 years in Saskatchewan, Canada, to evaluate the magnitude of freeze-thaw N2O emissions and investigate its driving factors. The files contain the daily average N2O emissions and supporting environmental data.</p>
tRIBS benchmark: Basin-scale simulation, Big Spring, AZ, USA.
<p>This repository hosts the setup for executing a basin-scale simulation of the Big Spring watershed that drains into Sycamore Creek in northern Arizona, USA, using the TIN-Based Real-Time Integrated Basin Simulator (<a href="https://tribshms.readthedocs.io/en/latest/">tRIBS</a>). </p> <p>This repository consists of : </p> <p>(1) A data subdirectory, which contains all the necessary data to run the basin-scale simulation of Big Spring, using tRIBS. </p> <p>2) A doc subdirectory, which contains a jupyter notebook for analyzing and visualizing this specific benchmark case, alongside additional documentation. </p> <p>(3) A src subdirectory that is currently empty but intended to contain source code for the tRIBS executable, which can be obtained <a href="https://github.com/tribshms/tRIBS">here</a>. </p> <p>(4) A bin subdirectory, that is currently empty but intended to store the tRIBS executable, with instructions to build the model <a href="https://tribshms.readthedocs.io/en/latest/man/Model_Execution.html#compilation-instructions">here</a>. </p> <p>(5) A results directory, which contains reference model output for results comparison.</p> <p>Instructions for running this benchmark are available in the README.html file within the repository, which can be opened with your web browser, and can also be found in the latest tRIBS <a href="https://tribshms.readthedocs.io/en/latest/man/Model_Execution.html#run-instructions">documentation</a>. </p> <p>Data from this model were obtained from a number of public sources: </p> <p>Soil properties were obtained from ISRIC (https://www.isric.org), with tRIBS input parameters derived from the ROSETTA pedotransfer functions (<a href="https://github.com/usda-ars-ussl/rosetta-soil">https://github.com/usda-ars-ussl/rosetta-soil</a>). Precipitation and vegetation parameters related to tree height and vegetation fraction were provided by Salt River Project. Meteorological forcing was obtained from NLDAS-2 (<a href="https://ldas.gsfc.nasa.gov/nldas/v2/forcing">https://ldas.gsfc.nasa.gov/nldas/v2/forcing</a>),with rainfall data provided from Salt River Project rain gauges.</p> <p><strong>NOTE:</strong> If you encounter a situation where, after downloading and extracting the <code>big_spring.gz</code> file, the extracted file has no extension, please follow these steps:</p> <ol> <li> <p><strong>Rename the File</strong>: Manually rename the extracted file to <code>big_spring.zip</code>.</p> </li> <li> <p><strong>Extract Again</strong>: After renaming, unzip the <code>big_spring.zip</code> file to access the full folder with all the necessary files.</p> </li> </ol> <p>This issue may occur if the file extraction process doesn't automatically add the <code>.zip</code> extension. By renaming the file and unzipping it again, you should be able to access the complete set of files without any issues.</p>
Fig. 2 in A new genus and species of spring snails (Caenogastropoda, Tateidae) from the ultramafic South of New Caledonia
Fig. 2. Philippe Bouchet collecting Viriiella touaouroua gen. et sp. nov.
Fig. 8 in A new genus and species of spring snails (Caenogastropoda, Tateidae) from the ultramafic South of New Caledonia
Fig. 8. Penes of three males of Viriiella touaouroua gen. et sp. nov.
Fig. 4 in A new genus and species of spring snails (Caenogastropoda, Tateidae) from the ultramafic South of New Caledonia
Fig. 4. SEM micrographs of paratypes of Viriiella touaouroua gen. et sp. nov. (MNHN-IM-2000-39461).
Table 2 in A new genus and species of spring snails (Caenogastropoda, Tateidae) from the ultramafic South of New Caledonia
<p><b>Table 2.</b> Measurements of 22 shells. Measurements in mm. Abbreviations: AH = aperture height; AW =aperture width; BWW= body whorl width; cv = coefficient of variation; max = maximum; min = minimum; sd = standard deviation; SH = shell height; SW =shell width; W= number of whorls.</p><table><tbody><tr><th></th><th>SH</th><th>SW</th><th>AH</th><th>AW</th><th>BWW</th><th>SH/SW</th><th>W</th></tr></tbody><tbody><tr><th>holotype</th><td>1.18</td><td>0.61</td><td>0.49</td><td>0.34</td><td>0.42</td><td>1.94</td><td>3.88</td></tr><tr><th>min</th><td>1.05</td><td>0.55</td><td>0.44</td><td>0.32</td><td>0.47</td><td>1.79</td><td>3.50</td></tr><tr><th>max</th><td>1.28</td><td>0.68</td><td>0.53</td><td>0.38</td><td>0.56</td><td>2.01</td><td>4.00</td></tr><tr><th>mean</th><td>1.18</td><td>0.62</td><td>0.49</td><td>0.35</td><td>0.62</td><td>1.90</td><td>3.78</td></tr><tr><th>sd</th><td>0.07</td><td>0.04</td><td>0.03</td><td>0.02</td><td>0.04</td><td>0.05</td><td>0.15</td></tr><tr><th>cv</th><td>5.69</td><td>6.10</td><td>5.83</td><td>4.67</td><td>6.10</td><td>2.63</td><td>3.96</td></tr></tbody></table>
Dataset for: Phosphorus mobilization from intact soil monoliths flooded under simulated summer versus spring snowmelt with intermittent freeze-thaw conditions
<p>Enhanced phosphorus (P) release from flooded, anaerobic soils have been extensively studied under summer temperatures, but not under cold temperatures with intermittent freeze-thaw events. We investigated the temperature and freeze/ thaw effects during flooding on the release of P to floodwater from soil monoliths (15-cm depth) collected from eight agricultural fields in Manitoba. Soil monoliths were flooded with reverse osmosis water and incubated for 56 d under simulated summer flooding (SSF, 22±1 ℃), or snowmelt flooding with intermittent freeze thaw (IFT, 4±1 ℃ with intermittent freezing) in triplicates. Redox potential (Eh), pore water and floodwater dissolved reactive P (DRP) concentrations, pH and concentrations of Ca, Mg, Fe and Mn were determined weekly. In seven soils, Eh decreased rapidly with days after flooding (DAF) under SSF to values < 200 mV, but not under IFT. Pore water and floodwater DRP concentrations significantly increased with DAF in all soils under SSF, and in seven soils under IFT. While DRP concentrations were consistently greater under SSF than IFT in four soils, other soils had similar concentrations at certain DAFs. Significant relationships between ion concentrations and redox status , that fitted both IFT and SSF data in most soils, suggests that similar redox-driven mechanisms are responsible for the P release; however, less P is released under IFT than SSF, since soils were not severely reduced under IFT. Substantial P release in a few soils under IFT, appeared to be unrelated to redox status, suggesting other P release mechanisms that are not redox driven.</p>
Data for Impact of Salinity Origin on Microbial Communities in Saline Springs Within the Illinois Basin, U.S.
<p>Original data for Impact of Salinity Origin on Microbial Communities in Saline Springs Within the Illinois Basin, U.S.</p>
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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.
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.