Skip to main content
Powered by ShareScore

Find research datasets worth reusing

Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.

222

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

222 results for “temporal change”

Learn how ShareScore rates datasets ↗
dryad32/100

Data from: Spatial and temporal aridity gradients provide poor proxies for plant-plant interactions under climate change: a large-scale experiment

1. Plant-plant interactions may critically modify the impact of climate change on plant communities. However, the magnitude and even direction of potential future interactions remains highly debated, especially for water limited ecosystems. Predictions range from increasing facilitation to increasing competition with future aridification. 2. The different methodologies used for assessing plant-plant interactions under changing environmental conditions may affect the outcome but they are not equally represented in the literature. Mechanistic experimental manipulations are rare compared to correlative approaches that infer future patterns from current observations along spatial climatic gradients. 3. Here, we utilize a unique climatic gradient in combination with a large-scale, long-term experiment to test whether predictions about plant-plant interactions yield similar results when using experimental manipulations, spatial gradients or temporal variation. We assessed shrub-annual interactions in three different sites along a natural rainfall gradient (spatial) during 9 years of varying rainfall (temporal) and 8 years of dry and wet manipulations of ambient rainfall (experimental) that closely mimicked regional climate scenarios. 4. The results were fundamentally different among all three approaches. Experimental water manipulations hardly altered shrub effects on annual plant communities for the assessed fitness parameters biomass and survival. Along the spatial gradient, shrub effects shifted from clearly negative to mildly facilitative towards drier sites, whereas temporal variation showed the opposite trend: more negative shrub effects in drier years. 5. Based on our experimental approach, we conclude that shrub-annual interaction will remain similar under climate change. In contrast, the commonly applied space-for time approach based on spatial gradients would have suggested increasing facilitative effects with climate change. We discuss potential mechanisms governing the differences among the three approaches. 6. Our study highlights the critical importance of long-term experimental manipulations for evaluating climate change impacts. Correlative approaches, e.g. along spatial or temporal gradients, may be misleading and overestimate the response of plant-plant interactions to climate change.

opencc-zeroDec 2014View details →
dryad32/100

Data from: Temporal patterns of genetic variation in a salmon population undergoing rapid change in migration timing

Though genetic diversity is necessary for population persistence in rapidly changing environments, little is known about how climate-warming influences patterns of intra-population genetic variation. For a pink salmon population experiencing increasing temperatures, we used temporal genetic data (microsatellite = 1993, 2001, 2009; allozyme = 1979, 1981, 1983) to quantify the genetic effective population size (Ne) and genetic divergence due to differences in migration timing and to estimate whether these quantities have changed over time. We predicted that temporal trends toward earlier migration timing and a corresponding loss of phenotypic variation would decrease genetic divergence based on migration timing and Ne. We observed significant genetic divergence based on migration timing and genetic heterogeneity between early- and late-migrating fish. There was also some evidence for divergent selection between early- and late-migrating fish at circadian rhythm genes, but results varied over time. Estimates of Ne from multiple methods were large (>1200) and Ne/Nc generally exceeded 0.2. Despite shifts in migration timing and loss of phenotypic variation, there was no evidence for changes in within-population genetic divergence or Ne over the course of this study. These results suggest that in instances of population stability, genetic diversity may be resistant to climate-induced changes in migration timing.

opencc-zeroDec 2012View details →
dryad32/100

Data from: Community-wide changes in inter-taxonomic temporal co-occurrence resulting from phenological shifts

Global climate change is known to affect the assembly of ecological communities by altering species' spatial distribution patterns, but little is known about how climate change may affect community assembly by changing species' temporal co-occurrence patterns, which is highly likely given the widely observed phenological shifts associated with climate change. Here we analyzed a 29-year phenological data set comprising community-level information on the timing and span of temporal occurrence in 11 seasonally occurring animal taxon groups from 329 local meteorological observatories across China. We show that widespread shifts in phenology have resulted in community-wide changes in the temporal overlap between taxa that are dominated by extensions, and that these changes are largely due to taxa's altered span of temporal occurrence rather than the degree of synchrony in phenological shifts. Importantly, our findings also suggest that climate change may have led to less phenological mismatch than generally presumed, and that the context under which to discuss the ecological consequences of phenological shifts should be expanded beyond asynchronous shifts.

opencc-zeroDec 2015View details →
zenodo32/100

Fig. 2. Climogram showing average month temperature and rainfall from June 1996 in Aquatic Coleoptera In The Subtropical-Pampasic Ecotone (Argentina, Buenos Aires): Species Composition And Temporal Changes

Fig. 2. Climogram showing average month temperature and rainfall from June 1996 to July 1998 (Data from Estación Meteorológica La Plata, Facultad de Ciencias Astronómicas y Geofísicas, Universidad Nacional de La Plata).

opennotspecifiedDec 2000View details →
zenodo32/100

Reproducible network changes occur in a mouse model of temporal lobe epilepsy but do not correlate with disease severity

<p><strong>Dataset for the publication: 'Reproducible network changes occur in a mouse model of temporal lobe epilepsy but do not correlate with disease severity '</strong><br><strong>Rigoni et al. 2023, Neurobiology of Disease, doi: <a title="Persistent link using digital object identifier" href="https://doi.org/10.1016/j.nbd.2023.106382" target="_blank" rel="noreferrer noopener"><span>https://doi.org/10.1016/j.nbd.2023.106382</span></a></strong></p> <p><strong>Dataset description</strong></p> <p><em>Data\data2publish\sub- </em>: 50 epochs of raw epicranial EEG data (31 x 8001 x 50, channels x time x n_epochs,<em> </em>Fs=4k Hz). The epochs are available for 29 mice, on different sessions (ses-d0, ses-d28, ses-d29) depending on the animal&nbsp;</p> <p><em>Data\data2publish\EA_info.xlsx</em>: number of epileptiform activities automatically detected for each animal at d28 and d29</p> <p><em>Data\data2publish\derivatives\eeg_preprocessing: </em>results of the script A_EEG_preprocessing.m, for each animal and session</p> <p><em>Data\data2publish\derivatives\elec_layout: </em>different layouts used to plot results. Mouse_layout_modif is the one used in Fig 4</p> <p><em>Data\data2publish\derivatives\network_metrics</em>_<em>wpli: </em>results of network analyses (script C_network_analyses.m)</p> <p><em>Data\data2publish\derivatives\wpli</em>: connectivity matrices (30 x 30) obtained with the script B_connectivity_wpli.m for each animal, in each session, for each frequency band wit</p> <p><strong>Code for analyses available here:&nbsp;</strong> <a href="https://github.com/IsottaR/ir_mice_project_Zenodo">https://github.com/IsottaR/ir_mice_project_Zenodo&nbsp;</a></p> <p>Abbreviations:</p> <p>EEG= electroencephalography</p>

opencc-by-4.0Dec 2023View details →
zenodo32/100

Supplementary Movie 1 from: A genetically encoded biosensor to monitor dynamic changes of c-di-GMP with high temporal resolution

<p>This record contains<strong> Supplementary Movie 1</strong> from:</p> <p><strong>A genetically encoded biosensor to monitor dynamic changes of c-di-GMP with high temporal resolution</strong></p> <p>Andreas Kaczmarczyk, Simon van Vliet, Roman Peter Jakob, Raphael Dias Teixeira, Inga Scheidat, Alberto Reinders, Alexander Klotz, Timm Maier, Urs Jenal</p> <p>Biozentrum, University of Basel, 4056 Basel, Switzerland</p> <p>Correspondence to: urs.jenal[at]unibas.ch, andreas.kaczmarczyk[at]unibas.ch</p> <p>&nbsp;</p>

opencc-by-4.0Apr 2024View details →
zenodo32/100

ALCC: Temporally consistent annual land cover maps over China from 1985 to 2022 based on an ensemble change detection method

<p><span><span>We develope <span><span>&nbsp;</span>a consistent annual land cover&nbsp;product for China (ALCC)&nbsp; from 1985 to 2022. First, change areas for each year was detected baesd on an ensemble change detection method combing CCDC, BFASTm, and Chow Test. Then, stable training samples were derived from both CLCD and CLUDs. The Random Forest classifier was locally trained and used to classify change areas year by year. Finally, ALCC was generated by updating land cover classification results for change areas and remaining class label the same as the base map forthe unchanged areas. ALCC achieved a mean overall accuracy of 81.11&plusmn;0.67% nationwide and exceeded 72.00% across seven geographical regions.</span></span></span></p>

opencc-by-4.0Aug 2024View details →
dryad32/100

Temporal changes in the potential geographic distribution of Histiotus velatus (Chiroptera, Vespertilionidae), the "decade effect"

<p>Also investigate how the potential distribution of this species changes with the addition of new records over the decades (decade effect). Assuming that (1: hypothesis of the effect of the decade) the addition of new occurrence records over time increases the potential size of the species distribution; and (2: Wallacean distance hypothesis) over the years, the new points added are increasingly distant from the research centers. Considering the geographic knowledge gap of <i>Histiotu velatus</i>, our objective is to report a new record of this species and estimate its potential distribution in South America through ENMs. For this, we compiled records of occurrence of species, selected from 1900 to 2015. We used 19 bioclimatic variables available in the WorldCLim database to estimate the potential distribution of the species and we used three modeling algorithms: Maximum Entropy (MXT) Random Forest (RDF) and Support Vector Machine (SVM). We selected the main bat research centers in Brazil, using the Lattes platform for the Wallacean distance hypothesis, using the Euclidean distance calculation. To test the hypothesis of the decade effect, we used beta regression analysis, taking conservative and non-conservative approaches. The results showed that the predicted area expanded and retracted over the decades, with an improvement in the accuracy of the models with the addition of new data. Most of the records are located in the southeastern region of Brazil, but the algorithms predicted areas in countries where there were no records. Only the conservatism approach has had a positive relationship over the decades. The distance from new points does not increase over the years of research centers.</p>

opencc-zeroOct 2022View details →
zenodo32/100

Pollination-related plant traits under environmental changes: seasonal and daily mismatches produce temporal constraints

Open the record for dataset details and reuse information.

opencc-by-4.0Apr 2024View details →
zenodo32/100

Data from: Attributing drivers to spatio-temporal changes in tree density across a suburbanizing landscape since 1944

<p><strong>Paper Abstract:</strong></p> <p>Urban expansion, especially suburbanization, represents a major social, economic and environmental shift that has escalated since the mid-1900s in North America. Suburban development leads to corresponding changes in the treed environment of urban-rural fringes. It is important to understand where, when and why trees change in response to development over many decades, but this is difficult since long-term data are scarce. We used 70+ years (1944&ndash;2017) of leaf-off aerial photographs, often representing the only long-term landscape record, to quantify and map spatio-temporal changes in tree density through the entirety of the agricultural-suburban transitional period. Photo-interpretation of individual tree locations, along with recording observable drivers of change, was completed across six different modern landscapes in Mississauga, Ontario, Canada. Results indicate that tree density often recovers, or even increases, post-development. There are differences between landscapes, but most tree density gains are associated with forest expansion and tree planting, while most losses are associated with building and road construction. The influence of these drivers, along with the temporal trajectory of tree density changes, are shaped by a landscape&rsquo;s socioecological legacy and the length, scope and intensity of development (as decided by decision makers). Processes include initial tree losses followed by recovery from tree planting, and forest succession in abandoned fields after land purchase and nearby development. We assert that the spatio-temporal changes in tree density and related drivers quantified here can be generalized to gain knowledge on how tree density and distribution across agricultural landscapes will change under different development scenarios.</p> <p>&nbsp;</p> <p><strong>Data details:</strong></p> <p>See paper: <a href="https://www.sciencedirect.com/science/article/pii/S0169204619301914?via%3Dihub">Attributing drivers to spatio-temporal changes in tree density across a suburbanizing landscape since 1944 - ScienceDirect</a></p> <p>See code on GitHub:&nbsp;<a href="https://github.com/ZZMitch/SuburbanizingTreeDensity_1944to2017">ZZMitch/SuburbanizingTreeDensity_1944to2017: Code from "Attributing drivers to spatio-temporal changes in tree density across a suburbanizing landscape since 1944" (L&amp;UP, 2019) (github.com)</a></p> <p>- Note: High resolution imagery is not included in this repository.&nbsp;</p> <p>&nbsp;</p> <p><strong>If you use these data, please reference:&nbsp;</strong></p> <p>Bonney, M.T., He, Y., 2019. Attributing drivers to spatio-temporal changes in tree density across a suburbanizing landscape since 1944. Landscape and Urban Planning 192, https://doi.org/10.1016/j.landurbplan.2019.103652.&nbsp;</p>

opencc-by-4.0Jul 2024View details →
dryad32/100

Data for spatial and temporal refugia for an insect population declining due to climate change

<p>Insect declines have been reported worldwide, although the particular causes of the declines may be complex and are poorly understood. Meadow spittlebugs were one of the most abundant insects in the coastal prairie along the California coast 40 years ago but have largely disappeared. Evidence links this decline to changing climatic conditions, which have reduced survival of eggs and neonates. We identified several refugia where meadow spittlebug populations have persisted amidst unfavorable conditions. Protection from desiccating winds was the common attribute of these refugia. Following a wet year, adult meadow spittlebugs were able to disperse from one refuge that we studied to recolonize coastal prairie habitats, although populations declined over the next two drier years. Because of their previous high abundance, loss of meadow spittlebugs is likely to affect the functioning of this widespread habitat, including energy transfer, their host plants, and their predators. In addition, meadow spittlebugs are unusual in having been the subject of extensive physiological and long-term ecological data, so they can serve as a bellwether species, indicating the effects of climate change.</p>

opencc-zeroJul 2021View details →
zenodo32/100

Figure 2 in Temporal changes in burrow structure of the thalassinidean ghost shrimps Trypaea australiensis and Biffarius arenosus

Figure 2. Diagram showing the significant cast dimensions that were measured (representation only, not to scale). The dimensions are as follows: (A) burrow opening; (B) distance between openings; (C) U/Y depth; (D) maximum depth; (E) diameter of turning chamber; (F) diameter of tunnel; (G) peripheral chamber; (H) maximum width.

opennotspecifiedAug 2008View details →
zenodo32/100

Figure 3 in Temporal changes in burrow structure of the thalassinidean ghost shrimps Trypaea australiensis and Biffarius arenosus

Figure 3. Casts of juvenile (A) and adult (B) Trypaea australiensis burrows, and casts of adult (C) and juvenile (D) Biffarius arenosus burrows.

opennotspecifiedAug 2008View details →
zenodo32/100

Figure 1 in Temporal changes in burrow structure of the thalassinidean ghost shrimps Trypaea australiensis and Biffarius arenosus

Figure 1. Map of Western Port, Victoria, showing its relative position in south-eastern Australia and the study site, Warneet.

opennotspecifiedAug 2008View details →
zenodo32/100

Figure 5 in Temporal changes in burrow structure of the thalassinidean ghost shrimps Trypaea australiensis and Biffarius arenosus

Figure 5. Dendrogram showing how casts of Trypaea australiensis burrows cluster together based on overall morphological similarities (W denotes casts made in winter, P are casts made in spring, S are casts made in summer and A are casts made in autumn). The horizontal dashed line shows 85% similarity with two main groups of casts, each containing a representative of each season.

opennotspecifiedAug 2008View details →
zenodo32/100

Figure 4 in Temporal changes in burrow structure of the thalassinidean ghost shrimps Trypaea australiensis and Biffarius arenosus

Figure 4. Dendrogram showing how casts of Biffarius arenosus burrows cluster together based on overall morphological similarities (W denotes casts made in winter, P are casts made in spring, S are casts made in summer and A are casts made in autumn). The horizontal dashed line shows 80% similarity with two main groups of casts, each containing representatives of each season.

opennotspecifiedAug 2008View details →
zenodo32/100

Monitoring temporal changes of velocity and attenuation from ultrashort diffuse records

<p>This repository contains the raw field data in the manuscript entitled &quot;Monitoring temporal changes of velocity and attenuation from ultrashort diffuse records&quot; by Ning Gu, Haoran Meng, Bo Yang,&nbsp;Xin Liu,&nbsp;Yehuda Ben-Zion, Junxin Guo, Bin Luo, Zhen Guo, Shuye Huang, Shichuan Yuan, Xiaofei Chen.</p>

opencc-by-4.0Mar 2023View details →
zenodo32/100

Carbonate record of temporal change in oxygen fugacity and gaseous species in asteroid Ryugu

<p>Supplementary Table 1. Carbon- and oxygen-isotope data of carbonates&nbsp;obtained&nbsp;with&nbsp;SIMS.</p> <p>Supplementary Table 2.&nbsp;Chemical compositions of carbonates measured with&nbsp;EDS.</p> <p>&nbsp;</p>

opencc-by-4.0May 2023View details →
zenodo32/100

Temporal changes of gene expression in health and mental disorders. Supporting Data

<p>This dataset provides data necessary to replicate the results of the time-perturbation analysis of gene expression in health and mental disorders. The corresponding code is available in the GitHub repository <a href="https://github.com/susieavagyan/BrainExp-TemporalDynamics">https://github.com/susieavagyan/BrainExp-TemporalDynamics</a>․</p> <p>The content of the data archive is following:</p> <ul> <li><strong>"GTEX_unzipped"</strong> folder contains &nbsp;GTEx single-tissue cis-eQTL dataset (v8)</li> <li><strong>"pheno"</strong> folder &nbsp;contains sample phenotype data for datasets used in the analysis&nbsp;</li> <li><strong>"scRNA-Ruzicka_data"</strong> folder &nbsp;contains gene signatures for neuronally associated processes and brian cell populations from Ruzicka, W. Brad, Shahin Mohammadi, Jose Davila-Velderrain, Sivan Subburaju, Daniel Reed Tso, Makayla Hourihan, and Manolis Kellis. 2020. &ldquo;Single-Cell Dissection of Schizophrenia Reveals Neurodevelopmental-Synaptic Axis and Transcriptional Resilience.&rdquo; MedRxiv, January, 2020.11.06.20225342. https://doi.org/10.1101/2020.11.06.20225342 paper.</li> <li><strong>"v5_results.SOM - Results"</strong> folder &nbsp;contains the transcriptome analysis results generated with oposSOM pipeline &nbsp;</li> <li><strong>"BM.table.Rdata"</strong> file contains gene symbol ENSEMBL ID conversion table required for eQTL analysis&nbsp;</li> <li><strong>"Brain_development_v3.Rdata"</strong> file contains combined raw gene expression data of datasets used in this analysis</li> <li><strong>"som_input_v5.Rdata"</strong> file contains batch adjusted and normalized gene expression matrix that was used as an input for oposSOM pipeline.</li> </ul>

opencc-by-4.0May 2023View details →
ClinicalTrials.gov32/100

Temporal Change in Parasternal Thickening Fraction as a Predictor for Weaning

ClinicalTrials.gov study NCT07083128. IPD Sharing: UNDECIDED. Countries: 1. Publications: 5.

restrictedIPD-UNDECIDEDFeb 2026View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated 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.

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