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478 results for “High temperature”

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edi40/100

PIE LTER year 2012, 5 minute and 15 minute measurements of specific conductance, water temperature in a small headwater stream draining a highly suburban catchment (72% residential), Saw Mill Brook, Burlington, MA.

Year 2012, continuous measurements, every 5 minutes for the first deployment and 15 minutes until the end of the year, were made of conductivity, water temperature in a small headwater stream, Saw Mill Brook, Burlington, MA, draining a highly suburban catchment (72% residential). in the Ipswich River watershed.

openCC (other)Jun 2018View details →
edi40/100

PIE LTER year 2013, 15 minute measurements of specific conductance, water temperature in a small headwater stream draining a highly suburban catchment (72% residential), Saw Mill Brook, Burlington, MA.

Year 2013, continuous measurements, every 15 minutes were made of conductivity, water temperature in a small headwater stream, Saw Mill Brook, Burlington, MA, draining a highly suburban catchment (72% residential) in the Ipswich River watershed.

openCC (other)Jun 2018View details →
edi40/100

PIE LTER year 2014, 15 minute measurements of specific conductance, water temperature in a small headwater stream draining a highly suburban catchment (72% residential), Saw Mill Brook, Burlington, MA.

Year 2014, continuous measurements, every 15 minutes were made of conductivity, water temperature in a small headwater stream, Saw Mill Brook, Burlington, MA, draining a highly suburban catchment (72% residential) in the Ipswich River watershed.

openCC (other)Jun 2018View details →
edi40/100

PIE LTER year 2015, 15 minute measurements of specific conductance, water temperature in a small headwater stream draining a highly suburban catchment (72% residential), Saw Mill Brook, Burlington, MA.

Year 2015, continuous measurements, every 15 minutes were made of conductivity, water temperature in a small headwater stream, Saw Mill Brook, Burlington, MA, draining a highly suburban catchment (72% residential) in the Ipswich River watershed.

openCC (other)Jun 2018View details →
zenodo36/100

A 3D resistivity model of the Acoculco high temperature geothermal system, Mexico

<p>The dataset is the final three-dimensional resistivity model of the high temperature geothermal field Acoculco, in Mexico.</p> <p>The model is described in deliverable 5.2 of the GEMex Project, funded by the European Union&rsquo;s Horizon 2020 research and innovation programme under grant agreement No. 727550, and by the Mexican Energy Sustainability Fund<br> CONACYT-SENER, Project 2015-04-268074.</p>

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

In-situ high temperature FTIR, Raman data and breakdown temperature for phlogopite

<p>This dataset contains all new data corresponding to figures in&nbsp;the manuscript, including in situ high temperature FTIR,&nbsp;Raman data, and breakdown temperature from previous studies and this study.</p>

opencc-by-4.0Jul 2020View details →
dryad36/100

Data from: Temperature amplifies the effect of high CO2 on the photosynthesis, respiration and calcification of the coralline algae Phymatolithon lusitanicum

The combination of ocean acidification (OA) and global warming is expected to have a significant effect on the diversity and functioning of marine ecosystems, particularly on calcifying algae such as rhodoliths (maërl) that form extensive beds worldwide, from polar to tropical regions. In addition, the increasing frequency of extreme events, such as heatwaves, threaten coastal ecosystems and may affect their capacity to fix blue carbon. The few studies where the simultaneous effects of both temperature and CO2 were investigated have revealed contradictory results. To assess the effect that high temperature spells can have on the maërl beds under OA, we tested the short-time effects of temperature and CO2 on the net photosynthesis, respiration and calcification of the recently described species Phymatolithon lusitanicum, the most common maërl species of southern Portugal. Photosynthesis, calcification and respiration increased with temperature, and the differences among treatments were enhanced under high CO2. We found that in the short term, the metabolic rates of Phymatolithon lusitanicum will increase with CO2 and temperature as will the coupling between calcification and photosynthesis. However, under high CO2, this coupling will favor photosynthesis over calcification, which, in the long term, can have a negative effect on the blue carbon fixing capacity of the maërl beds from southern Portugal.

opencc-zeroJul 2020View details →
zenodo36/100

An ultrasound probe array for a high-pressure, high-temperature solid medium deformation apparatus: CAD drawings

<p>CAD drawings of cooled load plate and base plate for integrating pizoelectric needle sensors. Electrical schema of heating system. Dimensional pdf drawings of sigma 1 piston for integration of pizoelectric needle sensors. Matalb code for basic 1D source localization, synchronization of triggered AE data with mechanical data and plotting of AE rate.</p>

opencc-by-4.0Feb 2020View details →
dryad36/100

High temperatures drive offspring mortality in a cooperatively breeding bird

<p><span>An improved understanding of life history responses to current environmental variability is required to predict species-specific responses to anthopogenic climate change. Previous research has suggested that cooperation in social groups may buffer individuals against some of the negative effects of unpredictable climates. We use a 15-year dataset on a cooperative-breeding arid-zone bird, the southern pied babbler <i>Turdoides bicolor</i>, to test i) whether environmental conditions and group size correlate with survival of young during three development stages (egg, nestling, fledgling), and ii) whether group size mitigates the impacts of adverse environmental conditions on reproductive success. Exposure to high mean daily maximum temperatures (mean T<sub>max</sub>) during early development was associated with reduced survival probabilities of young in all three development stages. No young survived when mean T<sub>max </sub>&gt; 38°C across all group sizes. Low reproductive success at high temperatures has broad implications for recruitment and population persistence in avian communities given the rapid pace of advancing climate change.<b> </b>That impacts of high temperatures were not moderated by group size, a somewhat unexpected result given prevailing theories around the influence of environmental uncertainty on the evolution of cooperation, suggests that cooperative breeding strategies are unlikely to be advantageous in the face of rapid anthropogenic climate change. </span><span>An improved understanding of life history responses to current environmental variability is required to predict species-specific responses to anthopogenic climate change. Previous research has suggested that cooperation in social groups may buffer individuals against some of the negative effects of unpredictable climates. We use a 15-year dataset on a cooperative-breeding arid-zone bird, the southern pied babbler <i>Turdoides bicolor</i>, to test i) whether environmental conditions and group size correlate with survival of young during three development stages (egg, nestling, fledgling), and ii) whether group size mitigates the impacts of adverse environmental conditions on reproductive success. Exposure to high mean daily maximum temperatures (mean T<sub>max</sub>) during early development was associated with reduced survival probabilities of young in all three development stages. No young survived when mean T<sub>max </sub>&gt; 38°C across all group sizes. Low reproductive success at high temperatures has broad implications for recruitment and population persistence in avian communities given the rapid pace of advancing climate change.<b> </b>That impacts of high temperatures were not moderated by group size, a somewhat unexpected result given prevailing theories around the influence of environmental uncertainty on the evolution of cooperation, suggests that cooperative breeding strategies are unlikely to be advantageous in the face of rapid anthropogenic climate change. </span></p>

opencc-zeroAug 2020View details →
dryad36/100

Data from: Differing thermal sensitivities in a host-parasitoid interaction: high, fluctuating developmental temperatures produce dead wasps and giant caterpillars

<p>1. Insect parasitoids, and the arthropod hosts they consume during development, are important ecological players in almost all environments across the globe. As ectothermic organisms, both parasitoid and host are strongly impacted by environmental temperature. If thermal tolerances differ between host insect and parasitoid, then the outcome of their interaction will be determined by the ambient temperature. As mean temperatures continue to rise and extreme temperatures become more frequent, we must determine the effect of high temperature stress on host-parasitoid systems to predict how they will fare in the face of climate change.</p> <p class="MsoNoSpacingCxSpMiddle">2. The majority of studies conducted on host-parasitoid systems focus on either performance under constant temperature, or a fixed metric of thermal tolerance (CT<sub>max</sub>) for individual organisms. However, performance at constant temperatures is not predictive of performance under ecologically relevant, fluctuating temperatures, and measurements of thermal thresholds provide little information regarding the effects of temperature throughout development. We address this by testing the effects of increasing mean temperature in both constant and fluctuating (±10°C) environments throughout development on the performance of the parasitoid wasp <i>Cotesia congregata</i> and its lepidopteran larval host, <i>Manduca sexta.</i></p> <p class="MsoNoSpacingCxSpLast">3. The growth of <i>M. sexta</i> was influenced by mean temperature, diurnal fluctuations, and parasitization status. Caterpillar growth rate increased with increasing mean temperature, but decreased in response to diurnal fluctuations and parasitization by <i>C. congregata </i>wasps.</p> <p>4. Wasp survival decreased with increasing mean temperature, and diurnal fluctuations decreased wasp survival, especially at higher mean temperatures. Diurnal fluctuations at our highest mean temperature treatment (30°C±10°C) resulted in complete wasp mortality, and parasitized hosts displayed abnormal physiology, wherein they failed to exhibit wasp emergence, did not enter the prepupal stage, continued to feed, and grew up to two-fold larger than a normal, unparasitized caterpillar.</p> <p>5. Our results indicate hosts and parasitoids in this system have different thermal tolerances during development; the parasitoid wasp suffered complete mortality at a temperature regime that is mildly stressful for the unparasitized caterpillar host species. Our findings suggest <i>C. congregata </i>will suffer more severely under increasing temperatures than <i>M. sexta</i>, with cascading trophic and ecological effects.</p>

opencc-zeroDec 2020View details →
dryad36/100

Data from: Two-year bee, or not two-year bee? How voltinism is affected by temperature and season length in a high-elevation solitary bee

Organisms must often make developmental decisions without complete information about future conditions. This uncertainty—for example, about the duration of conditions favorable for growth—can favor bet-hedging strategies. Here, we investigated the causes of life-cycle variation in Osmia iridis, a bee exhibiting a possible bet-hedging strategy with co-occurring one- and two-year life cycles. One-year bees reach adulthood quickly but die if they fail to complete pupation before winter; two-year bees adopt a low-risk, low-reward strategy of postponing pupation until the second summer. We reared larval bees in incubators in various experimental conditions and found that warmer—but not longer—summers, and early birth dates, increased the frequency of one-year life cycles. Using in situ temperature measurements and developmental trajectories of laboratory- and field-reared bees, we estimated degree-days required to reach adulthood in a single year. Local long-term (1950–2015) climate records reveal that this heat requirement is met in only ~7% of summers, suggesting that the observed distribution of life cycles is adaptive. Warming summers will likely decrease average generation times in these populations. Nevertheless, survival of bees attempting one-year life cycles—particularly those developing from late-laid eggs—will be &lt;100%; consequently, we expect the life-cycle polymorphism to persist.

opencc-zeroDec 2017View details →
zenodo36/100

High-resolution air temperature observations near the surface using fiber-optic distributed temperature sensing

<p>Time-lapse animation of air temperature observations near the surface, highlighting wave-like motion in opposite direction of the mean wind.&nbsp;</p> <p>&nbsp;</p>

opencc-by-sa-4.0Dec 2013View details →
zenodo36/100

Synthesis of Ti3AuC2, Ti3Au2C2 and Ti3IrC2 by noble-metal substitution reaction in Ti3SiC2 for high-temperature-stable ohmic contacts to SiC

<p>Repository data for paper "Synthesis of Ti<sub>3</sub>AuC<sub>2</sub>, Ti<sub>3</sub>Au<sub>2</sub>C<sub>2</sub> and Ti<sub>3</sub>IrC<sub>2</sub> by noble-metal substitution reaction in Ti<sub>3</sub>SiC<sub>2</sub> for high-temperature-stable ohmic contacts to SiC".</p> <p>Detailed information:</p> <p>Data from calculations include relaxed structures, electronic band-structure (selected compounds), electronic density of states and crystal overlap Hamilton population (selected compounds). In addition, spin-orbit coupling used for selected compounds. Data fro each compound are found in separate zip files. Scripts used to extract data are found in tools.zip.</p> <p>EDX-mapping:<br> Fig1d.xlsx</p> <p>XRD data:<br> Fig1h.xlsx, Fig2g.xlsx, FigS3.xlsx, FigS7a.xlsx</p> <p>I/V-measurements:<br> Fig4c.xlsx, FigS7b.xlsx, FigS13.xlsx</p> <p>Electrical resistance:<br> FigS5.xlsx, FigS14.xlsx</p>

opencc-by-4.0Mar 2017View details →
zenodo36/100

Dataset for: Hug et al. Unexpected behavioural adaptation of yellow fever mosquitoes in response to high temperatures

<p>Dataset for the manuscript: Hug et al. Unexpected behavioural adaptation of yellow fever mosquitoes in response to high temperatures</p>

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

Thermodynamic parameters and elasticity data of phase D at high pressures and temperatures

<p>This dataset contains all the original data for figures in the article "Thermoelasticity of phase D and implications for low-velocity anomalies and local discontinuities at the uppermost lower mantle" submitted to American Mineralogist.</p>

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

Data from: Neuronal function and dopamine signaling evolve at high temperature in Drosophila

<p>Neuronal activity is temperature sensitive and affects behavioral traits important for individual fitness, such as locomotion and courtship. Yet, we do not know enough about the evolutionary response of neuronal phenotypes in new temperature environments. Here, we use long-term experimental evolution of <em>Drosophila simulans</em> populations exposed to novel temperature regimes. Here, we demonstrate a direct relationship between thermal selective pressure and the evolution of neuronally expressed molecular and behavioral phenotypes. Several essential neuronal genes evolve lower expression at high temperatures and higher expression at low temperatures, with dopaminergic neurons standing out by displaying the most consistent expression change across independent replicates. We functionally validate the link between evolved gene expression and behavioral changes by pharmacological intervention in the experimentally evolved <em>D. simulans</em> populations as well as by genetically triggered expression changes of key genes in <em>D. melanogaster</em>. As natural temperature clines confirm our results for <em>Drosophila</em> and <em>Anopheles</em>populations, we conclude that neuronal dopamine evolution is a key factor for temperature adaptation.</p>

opencc-zeroMar 2024View details →
zenodo36/100

Data for the research article "High-Temperature Deformation of Enstatite-Olivine Aggregates" published in JGR Solid Earth

<p>The data available in this repository is the original data presented in the research article: Bystricky, M., Lawlis, J., Mackwell, S., &amp; Heidelbach, F. (2024). High-temperature deformation of enstatite-olivine aggregates, Journal of Geophysical Research: Solid Earth, 129, e2023JB027699. https://doi.org/10.1029/2023JB027699.</p> <p>Version v1: data at time of original submission (2023)</p> <p>Version v2: data at time of publication (2024)</p>

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

Data and code for the paper titled "Impact of the Tibetan Plateau on Global High-frequency Temperature Variability"

<p>This is the data and code for the paper titled "<span>Impact of the Tibetan Plateau on </span><span><span>G</span><span>lobal High-frequency Temperature Variability</span></span>", which was submitted to <em>Journal of Climate</em>.</p>

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

EEAR-Clim: A high density observational dataset of daily precipitation and air temperature for the Extended European Alpine Region

<p>Data, metadata and code for paper published in Earth System Science Data:</p> <p>A high density observational dataset of daily precipitation and air temperature for the Extended Alpine Region</p> <p>&nbsp;</p> <p><strong>Code&nbsp;</strong>(working copy all written in R statistical software): scripts.zip</p> <ul> <li>to read and process data in from different sources</li> <li>to perform intra and inter-stations quality control</li> <li>to perform break detection and homogenization</li> <li>to read results of quality control and homogenization</li> </ul> <p><strong>Data</strong>:</p> <ul> <li>Daily time series of air temperature (mean, minimum and maximum) and precipitation as .zip files, grouped by data provider.</li> <li>Information on column content is provided in separate files "data_readme.txt"</li> <li>about 10000 stations from Italy, France, Switzerland, Austria, Germany, Slovenia, Croatia, Bosnia-Herzegovina, Czech Republic, Slovakia and Hungary</li> <li>Meta data (code, name, longitude, latitude, elevation, measurements availability for each variable, starting date, ending date) in "metadata.zip", including a file for each data provider</li> <li>If you&nbsp;<strong>use the data you agree to adhere to the respective data provider's terms</strong> as listed in "License.pdf"</li> <li>The license terms especially (and additionally to any other terms of the single data providers) include:&nbsp;<strong>Attribution</strong>&nbsp;&mdash; You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use. [from&nbsp;<a href="https://creativecommons.org/licenses/by/4.0/">CC BY 4.0</a>]&nbsp;</li> </ul> <p>&nbsp;</p> <p><strong>Version history:</strong></p> <p>v1.0: initial upload</p> <p>v2.0: update of data policies; addition of France and Croatia time series</p>

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

Data for high-temperature assignment paper

<p>Data used in the paper reporting on the assignment of ICCG-S165A:</p> <p>Data used in figure 1 (folder Figure 1):&nbsp;<br>17: TROSY @ 30&ordm;C, 117: TROSY @ 50&ordm;C, 18: HSQC @ 30&ordm;C, 118: HSQC @ 50&ordm;C, 14: HMQC @ 30&ordm;C, 114: HMQC @ 50&ordm;C</p> <p>Data used for ICCG-S165A assignment (folder Assignment_ICCG_S165A):&nbsp;<br>25: HNCO, &nbsp;35: HNCACB</p> <p>Data used for Mutant2 assignment (folder Mutant2):<br>9: hNcaNNH, 15:HNCO, 17: HNCACO, 19: HNCACB, 21: HncaNNH</p>

opencc-by-4.0May 2024View 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