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382 results for “high elevation”

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zenodo36/100

Figure 1 in Living in a cold tropical mountain: do the microhabitat use and activity pattern change with elevation in the high-Andean lizard Stenocercus trachycephalus (Squamata: Tropiduridae)?

Figure 1. Study locations in the Andes eastern mountain range. (A) Guanentá, 3,750-3,950 m; (B) Las Moyas Páramo, 3,200 m; (C) La Chacua, 2,670 m.

opencc-by-nc-4.0Aug 2021View details →
zenodo36/100

Assessing the peatland hummock-hollow classification framework using high-resolution elevation models: Implications for appropriate complexity ecosystem modelling

<p>The hummock-hollow classification framework used to categorize peatland ecosystem microtopography is pervasive throughout peatland experimental designs and current peatland ecosystem modelling approaches. However, identifying what constitutes a representative hummock-hollow pair within a site and characterizing hummock-hollow variability within or between peatlands remains largely unassessed. Using structure-from-motion (SfM), high resolution digital elevation models (DEM) of hummock-hollow microtopography were used to: 1) examine how much area needs to be sampled to characterize site-level microtopographic variation; and 2) examine the potential role of microtopographic shape/structure on biogeochemical fluxes using data from 9 northern peatlands. This data set is comprised of plot DEMs, supporting data, and the script used to analyze data and produce figures presented in the manuscript submitted to Biogeosciences Discussion &quot;ASSESSING THE PEATLAND HUMMOCK-HOLLOW CLASSIFICATION FRAMEWORK USING HIGH-RESOLUTION ELEVATION MODELS: IMPLICATIONS FOR APPROPRIATE COMPLEXITY ECOSYSTEM MODELLING&quot;.</p>

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

Supporting Data - Shallow Fracture Buffers High Elevation Runoff in Northwest Greenland

<p>This dataset contains supporting data accompanying Culberg, Chu, &amp; Schroeder, &quot;Shallow Fracture Buffers High Elevation Runoff in Northwest Greenland&quot;, <em>Geophysical Research Letters</em>, 2022. It includes the following:</p> <ul> <li>Ice-penetrating radar-derived mappings of transient firn aquifers and buried refrozen ice complexes (ice blobs) beneath ice slabs in Northwest Greenland.</li> <li>Porosity estimates derived from the inversion of ice-penetrating radar reflectivity for the 20150510_01 Ultrawideband MCoRDS transect flow in Northwest Greenland as part of NASA OIB.</li> <li>An NDWI stack image showing the maximum NDWI on a per pixel basis from all Landsat images between 2000 and 2016 for the region.</li> <li>Data for a time series of NDWI within the upslope catchment of each aquifer or blob.</li> <li>Locations of moulins, supraglacial lakes, and drained supraglacial lakes from high resolution optical imagery.</li> <li>Linear features extracted from the high resolution optical imagery.</li> <li>Surface crevasse densities and surface water feature densities inferred from the extracted linear features for the northern and southern portions of the ice slab region.</li> <li>Resistive stress and fracture toughness data for each location where fractures are inferred from the high resolution optical imagery.</li> <li>Full resolution image files for WorldView imagery used in the Supporting Information Figure S6.</li> </ul>

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

High-resolution digital elevation models and orthomosaics generated from historical aerial photographs (since the 1960s) of the Bale Mountains in Ethiopia

<p>This dataset&nbsp;contains the results of photogrammetric processing (Digital Elevation&nbsp;Models, Orthomosaics and&nbsp; subset data used for volumetric calculation and visualization) named: &ldquo;DEM_1967.7z&rdquo;: inside the zipped folder &ldquo;1967_DEM.tif&rdquo; (digital elevation model produced for the year 1967), &ldquo;DEM_1984.7z&rdquo;: inside the zipped folder &ldquo;1984_DEM.tif&rdquo; exist (digital elevation model produced for the year 1984).&nbsp;In addition, under&nbsp;&ldquo;1967_Orthomosaic.7z&quot; and &quot;1984_Orthomosaic.7z&rdquo; zipped folders, there are&nbsp;orthomosaic files produced namely,&nbsp;&ldquo;1967_orthomosaic.tif&rdquo; and&nbsp;&quot;1984_orthomosaic.tif&rdquo; for the year 1967 and 1984, respectively. The DEMs and Orthomosaics&nbsp;&nbsp;subset&nbsp;from the results for sites (data example 1 and data example 2)&nbsp;reside under &quot;Data_Examples.zip&quot;. Accuracy of the&nbsp;resulted data were assessed and the extracted elevation values are under &quot;Accuracy_assessment.zip&quot;.&nbsp;&nbsp;All DEMs and Orthomosaics are in GeoTIFF format in the Adindan UTM Zone 37 N (EPSG: 20137) projected coordinate system.</p> <p>&nbsp; &nbsp;&nbsp;Potential application of the presented dataset include:</p> <p>1. watershed management</p> <p>2. analyses of historical landscape change</p> <p>3. detailed mapping and analyses of geological and archaeological features, as well as natural resources</p> <p>4. analyses of geomorphological processes</p> <p>5. socioecological patterns and dynamics</p> <p>6. modelling and planning for telecommunications&nbsp;</p> <p>7. biodiversity research.&nbsp;</p> <p>The inputs for the above resulted DEMs and Orthomosaics are found under Zenodo repository &quot;10.5281/zenodo.7271617&quot;.&nbsp;</p>

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

High-resolution digital elevation models and orthomosaics generated from historical aerial photographs (since the 1960s) of the Bale Mountains in Ethiopia

<p>This dataset&nbsp;contains the inputs used for Structure from Motion Multiview Stereo photogrammetry&nbsp;processing for the year 1967 and 1984 i.e Unprocessed scanned historical aerial Photographs, camera position coordinates, flight index and Ground Control Points.&nbsp;All the scanned historical aerial photographs&nbsp;data are in TIFF format except four photographs in JPEG format under a zipped folder (&quot;1967_Scanned_HAPs_Part1.7z and&nbsp;1967_Scanned_HAPs_Part2.7z&quot; for the 1967 Historical Aerial Photographs&nbsp;and &quot;1984_Scanned_HAPs_Part1.7z&nbsp;and&nbsp;1984_Scanned_HAPs_Part2.7z&quot; for the 1984&nbsp; Historical Aerial Photographs). The &quot;Flight_Index.Zip&quot; contains shapefiles of the camera position and polygon of consecutive aerial photograph index; &quot;GCP.Zip&quot; contains text file of the GCPs used for the 1967 and 1984; and&nbsp;&quot;Camera_Position.Zip&quot; contains the file of the camera position (Label, Easting, Northing and Altitude) of each historical aerial photographs.&nbsp;</p> <p>The results of the above dataset could be accessible on Zenodo repository &quot;10.5281/zenodo.7269999&quot;.</p> <p>Anyone can reuse the presented dataset to produce&nbsp;DEMs and Orthomosaics; and use for the following&nbsp;application&nbsp; areas:</p> <p>1. watershed management</p> <p>2. analyses of historical landscape change</p> <p>3. detailed mapping and analyses of geological and archaeological features, as well as natural resources</p> <p>4. analyses of geomorphological processes</p> <p>5. socioecological patterns and dynamics</p> <p>6. modelling and planning for telecommunications&nbsp;</p> <p>7. biodiversity research.&nbsp;</p> <p>&nbsp;</p>

opencc-by-4.0Oct 2022View details →
dryad36/100

Experimental warming increases the vulnerability of high-elevation plant populations to a specialist herbivore

<ol> <li>Ongoing climate change may impact alpine plant populations via both direct effects of increased temperature and climate-driven changes in interactions between plants and other organisms, such as insect herbivores. Rates of herbivory in high-elevation environments are predicted to increase with warmer temperatures, which may also lead to changes in morphological and physiological traits that influence plant resistance. Yet, we currently know little about how temperature-mediated changes in traits will impact alpine plant vulnerability to herbivores, as well as the extent to which populations from high-elevation environments might need to rapidly adapt to increasing herbivore pressure with rising temperatures.</li> <li>We assessed the effect of experimental warming on the relative vulnerability of populations of the alpine plant <em>Arabis</em> <em>alpina</em> from different elevations to a specialist herbivore. Herbivore performance was measured on plants from nine populations grown in climate chambers at two temperatures, representing low (warm) and high (cold) elevations. We also measured changes in putative drivers of performance: plant phenological, chemical and defence traits. Assuming populations would be adapted to local climates and levels of herbivory, we predicted that low-elevation populations would be more resistant to herbivores under warmer temperatures than high-elevation populations.</li> <li>We found reduced performance of a specialist herbivore on <em>A</em>. <em>alpina</em> grown under warm rather than cold conditions, though this effect varied with elevation. Larvae grew faster on high-elevation populations than low-elevation populations when grown under warm temperatures, whereas similar growth rates were observed for plants grown under colder temperatures, consistent with plant adaptation to the lower existing herbivore pressure in cold, high-elevation environments. Regression analyses suggested that polar metabolite variation explained more variance in larval performance than changes in defensive glucosinolates or morphological traits.</li> <li>Our results suggest that although physiological responses to warming may increase the resistance of cold-adapted plants to herbivory, populations from different elevations may differ in their interactions with herbivores under climate warming. Without genetic adaptation, existing physiological responses of high-elevation populations to warmer temperatures may leave these populations vulnerable to the increases in herbivore pressure predicted under climate change.</li> </ol>

opencc-zeroMar 2023View details →
dryad36/100

Short-term effects of wildfire on high elevation stream-riparian food webs

<p>Understanding how wildfires affect food web structure and function remains an important challenge, especially at high elevations that historically have burned infrequently. In particular, fires may alter the magnitude of reciprocal cross-ecosystem subsidies, leading to indirect effects on aquatic and terrestrial consumers. We quantified characteristics of high-elevation (2500 to 3000 m) stream-riparian food webs at 10 locations in the southern Rocky Mountains less than one year following high-intensity, stand-replacing wildfires. Using a paired 'burned-unburned' stream survey design, we assessed benthic periphyton, aquatic macroinvertebrate community structure, trout population characteristics, trout stomach contents, inputs and emergence of insects to and from streams, and abundance of predatory riparian spiders that consume aquatic insects. Benthic macroinvertebrate density, flux of emerging aquatic insects, and riparian spider abundances were lower at burned sites. Fluxes of insect inputs entering the stream did not differ with burn status, despite the loss of riparian vegetation due to fire. Trout were somewhat less abundant, but larger on average at burned sites and did not differ in body condition. These results suggest mortality of smaller trout from fire disturbance and/or recolonization of burned sites by larger individuals. Trout showed subtle changes in diet composition with burn status, but no change in biomass or number of prey consumed. In general, burned sites showed greater variation in community characteristics than unburned sites, which may reflect differences in the timing and magnitude of post-fire flooding, erosion, and scouring of the stream bed. Taken together, our results suggest that short-term effects of fire disturbance strongly altered some food web responses, but others appeared relatively resilient, which is notable given the high severity of the wildfires in the study area.</p>

opencc-zeroMay 2023View details →
zenodo36/100

Model output data to "Land surface modeling in the Himalayas: on the importance of evaporative fluxes for the water balance of a high elevation catchment"

<p>We provide i) gridded initial conditions (.tif), ii) modeled gridded monthly outputs (.tif), and iii) modeled hourly outputs at the station locations (.txt) for the hydrological year 2019. Information about the variables and units can be found in the figures (.png) associated to each dataset. Details about the datasets can be found in the original publication by Buri and others (2023).</p><p>&nbsp;</p><p>Buri, P., Fatichi, S., Shaw, T. E., Miles, E. S., McCarthy, M. J., Fyffe, C. L., ... &amp; Pellicciotti, F. (2023). Land Surface Modeling in the Himalayas: On the Importance of Evaporative Fluxes for the Water Balance of a High‐Elevation Catchment. <i>Water Resources Research</i>, <i>59</i>(10), e2022WR033841. DOI: <a href="https://doi.org/10.1029/2022WR033841"><strong>10.1029/2022WR033841</strong></a></p>

opencc-by-4.0Oct 2023View details →
ClinicalTrials.gov36/100

Phase 2a Study of HU6 in Subjects With Elevated Liver Fat and High BMI Volunteers

ClinicalTrials.gov study NCT04874233. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov36/100

A Study of LY3473329 in Adult Participants With Elevated Lipoprotein(a) at High Risk for Cardiovascular Events

ClinicalTrials.gov study NCT05563246. IPD Sharing: YES. Countries: 8. Publications: 3.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov36/100

Evaluate SLN360 in Participants With Elevated Lipoprotein(a) at High Risk of Atherosclerotic Cardiovascular Disease Events

ClinicalTrials.gov study NCT05537571. IPD Sharing: Not stated. Countries: 7. Publications: 4.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov36/100

Study of Efficacy and Safety of Inclisiran in Asian Participants With Atherosclerotic Cardiovascular Disease (ASCVD) or ASCVD High Risk and Elevated Low Density Lipoprotein Cholesterol (LDL-C)

ClinicalTrials.gov study NCT04765657. IPD Sharing: YES. Countries: 4. Publications: 1.

controlledIPD-YESFeb 2026View details →
dryad36/100

Climate controls plant life form patterns on a high-elevation oceanic island

Open the record for dataset details and reuse information.

publicJun 2021View details →
dryad36/100

Anna's hummingbird (Calypte anna) physiological response to novel thermal and hypoxic conditions at high elevations

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publicMay 2022View details →
dryad36/100

High elevation increases the risk of Y chromosome loss in Alpine skink populations with sex reversal

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publicSep 2020View details →
dryad36/100

Exotic herbivores dominate Australian high‐elevation grasslands

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publicFeb 2022View details →
dryad36/100

Compensatory recruitment unlikely in high elevation amphibian populations challenged with disease

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publicOct 2022View details →
dryad36/100

Data from: The effect of community-wide phytochemical diversity on herbivory reverses from low to high elevation

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publicMar 2021View details →
dryad36/100

Short-term effects of wildfire on high elevation stream-riparian food webs

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publicMay 2023View details →
dryad36/100

Data from: Getting chased up the mountain- high elevation may limit performance and fitness characters in a montane insect

Open the record for dataset details and reuse information.

publicJan 2019View details →

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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