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.

129

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

129 results for “Biodiversity change”

Learn how ShareScore rates datasets ↗
dryad24/100

Data from: Proportional mixture of two rarefaction/extrapolation curves to forecast biodiversity changes under landscape transformation

Progressive habitat transformation causes global changes in landscape biodiversity patterns, but can be hard to quantify. Rarefaction/extrapolation approaches can quantify within‐habitat biodiversity, but may not be useful for cases in which one habitat type is progressively transformed into another habitat type. To quantify biodiversity patterns in such transformed landscapes, we use Hill numbers to analyse individual‐based species abundance data or replicated, sample‐based incidence data. Given biodiversity data from two distinct habitat types, when a specified proportion of original habitat is transformed, our approach utilises a proportional mixture of two within‐habitat rarefaction/extrapolation curves to analytically predict biodiversity changes, with bootstrap confidence intervals to assess sampling uncertainty. We also derive analytic formulas for assessing species composition (i.e. the numbers of shared and unique species) for any mixture of the two habitat types. Our analytical and numerical analyses revealed that species unique to each habitat type are the most important determinants of landscape biodiversity patterns.

opencc-zeroAug 2019View details →
dryad24/100

Data from: How do different aspects of biodiversity change through time? A case study on an Australian bird community

The study of ecological communities through time can reveal fundamental ecological processes and is key to understanding how natural and human pressures will affect biodiversity. Most studies of ecological communities through time consider only one or a few summary measures (e.g. species richness, total abundance), which might neglect important aspects of community structure or function. We studied temporal variation in several measures of species diversity, size diversity, and species composition in an intensively sampled bird community to determine whether different biodiversity measures change synchronously. We used a novel function regression model, which supports the study of diversity measures that are distributions (e.g. species abundance distributions) alongside measures that are scalar values (e.g. species richness). Most diversity measures changed predictably within years, but inter-annual changes in size diversity and species composition were not reflected in species diversity. Within and among years, there was considerable variation in distributional measures that was not captured in scalar measures. Predictable variation within years probably was related to seasonal variation in weather patterns or food availability, but variation in size diversity among years probably resulted from stochastic changes in species composition. These results suggest that species and size diversity may be decoupled, and that inferences on scalar diversity measures might not reflect fundamental changes to community structure or function. Our method supports the inclusion of size-based measures and distributional measures in ecological analyses, and broader uptake of our approach is likely to provide new insight into the processes structuring ecological communities, and inform the links between structure and function in ecological communities.

opencc-zeroDec 2015View details →
zenodo24/100

Selected data sets for Marsh et al. 2024 'Tropical forest clearance impacts biodiversity and function whereas logging changes structure'

<p>Data sets used in the for the manuscript <strong>Marsh<em> </em>et<em> </em>al. 2024 'Tropical forest clearance impacts biodiversity and function whereas logging changes structure'</strong>. The DOIs that link to all other data sets used in the publication are available in Tables S2-5 of the supplementary information. The z-score standardised data, and outputs of RMarkdown documents outline all the steps in the processing and analysis of the data are available at https://zenodo.org/uploads/13161799.</p> <p>&nbsp;</p> <p>This repository contains data used for:</p> <h3><strong><em>Mean canopy height</em></strong></h3> <p>Canopy height and vertical profiles of forest structure were compiled using airborne remote sensing with LiDAR collected by NERC&rsquo;s Airborne Research Facility (ARF) in November 2014, using a Leica ALS50-II LiDAR.&nbsp;A Beer-Lambert approximation was used to convert point clouds to plant area density (PAD) distributions, a similar measure to leaf-area index, but where methods do not distinguish between leaves and branches or trunks.&nbsp;LiDAR measurements for the carbon plots were converted to rasters with 0.5 &times; 0.5 m cell size. Plots were rotated to a North-South axis if necessary</p> <h3><br><em><strong>Spectral diversity</strong></em></h3> <p>Spectral measurements were made on five leaves attached to tree branches used to measure leaf chemical traits. Leaves were randomly selected but we avoided damaged and young plant material to avoid potential confounding factors. Reflectance spectra (350&ndash;2500 nm) were acquired using a FieldSpec 4, produced by Analytical Spectral Devices (ASD, Boulder, Colorado, USA). The spectroradiometer's contact probe was mounted on a clamp and firmly pushed down onto the sample against a black background so that no extraneous light was included in the measurement.&nbsp;Spectral measurements were taken halfway between the petiole and leaf tip, and between the main vein and the leaf edge, with the abaxial surface pointing towards the probe. The readings were calibrated against a Spectralon white reference panel every five samples. Leaf reflectance measured&nbsp;at 430 nm, 660 nm, 1450, 1980 nm and 2350 nm align closely with absorption features for pigments, water content, proteins and cellulose. Spectral diversity calculated from these absorption features can provide an integrated measure of the functional trait variability within plant communities and may be used as a proxy for functional diversity.</p> <p>&nbsp;</p> <h3><em><strong>Liana abundance</strong></em></h3> <p>Percentage liana cover for large canopy and emergent trees. The four quadrants of the canopy were scored as 0 (no lianas), 1 (1-20%), 2 (20-40%), 3 (40-60%), 4 (60-80%) and 5 (80-100%).</p> <p>&nbsp;</p> <h3><em><strong>Leaf-area index<br></strong></em></h3> <p>Leaf area index (LAI) for carbon plots was derived from hemispherical photos (Sigma 8mm SRL fish eye lens and Canon EOS 600D digital camera, mounted on a tripod at 1 m height). Between 5-27 photos were taken over time in each subplot. Images were&nbsp;processed with Hemisfer&reg; software (www.wsl.ch/dienstleistungen/produkte/software/hemisfer/index_EN). LAI was calculated with the method by Thimonier et <em>al</em>. (2010) <em>European Journal of Forest Research</em> 129, 543&ndash;562 (2010), with a canopy clumping correction applied from Chen &amp; Cihlar (1995) <em>IEEE Transactions on Geoscience and Remote Sensing</em> 33, 777&ndash;787.</p> <p>&nbsp;</p> <h2>Funding</h2> <p>Analyses were carried out, and data were collected, as part of the BALI (Biodiversity And Land-use Impacts on tropical ecosystem function) using the following funding:</p> <ul> <li>NERC's Human Modified Tropical Forests research programme (grant number NE/K016377/1 awarded to the BALI consortium)</li> <li>MHN was supported by a PhD scholarship from the Conselho Nacional de Pesquisa e Desenvolvimento (CNPq, grant No. 201516/2014-4) from Brazil</li> </ul>

opencc-by-4.0Aug 2024View details →
zenodo24/100

Supplementary material 1 from: Fernandez D, Millán A, Rizzo V, Comas J, Lleopard E, Pastor J, Pallarés S, Abellán P, Spada M, Bilton DT, Ribera I (2018) The CAVEheAT project: climate change, thermal niche and conservation of subterranean biodiversity. ARPHA Conference Abstracts 1: e30105. https://doi.org/10.3897/aca.1.e30105

The CAVEheATproject: climate change, thermal niche and conservation of subterranean biodiversity

opencc-zeroMar 2022View details →
dryad24/100

Data from: How do different aspects of biodiversity change through time? A case study on an Australian bird community

Open the record for dataset details and reuse information.

publicApr 2016View details →
dryad24/100

Data from: Proportional mixture of two rarefaction/extrapolation curves to forecast biodiversity changes under landscape transformation

Open the record for dataset details and reuse information.

publicAug 2019View details →
zenodo20/100

Fig. 5 in How might sea level change affect arthropod biodiversity in anchialine caves: a comparison of Remipedia and Atyidae taxa (Arthropoda: Altocrustacea)

Fig. 5 Scatterplot of the distances of cave openings from the current coastline and the coastline 18,000 years ago during the last glacial maximum. Analysis limited to caves in regions where both remipedes and atyid shrimp co-occur (Table 2). Box in the lower corner of (a) is enlarged to show finer scale remipede distributions in (b). Regressions. (a) Shrimp: y = 0.2376x+10.0617, r 2 =0.4297; Neither: y =0.2610x +9.0827, r 2 = 0.4568. (b) Remipede: y =- 0.3130x+0.3040, r 2 =0.6379

opennotspecifiedFeb 2014View details →
zenodo20/100

Fig. 2 in How might sea level change affect arthropod biodiversity in anchialine caves: a comparison of Remipedia and Atyidae taxa (Arthropoda: Altocrustacea)

Fig. 2 Atyid species richness in (a) the Yucatan Peninsula, (b) the Caribbean, (c) southern Europe, (d) Australia, and (e) global species richness. Species richness by cave correlates with the size of white circles. For (e), only the caves with the highest richness in the region are shown. The present-day coastlines are outlined in black, and the

opennotspecifiedFeb 2014View details →
zenodo20/100

Nutrient enrichment changes species composition, taxonomic and functional diversity in a global biodiversity hotspot

<p>This data set was presented in the article "Nutrient enrichment changes species composition, taxonomic and functional diversity in a global biodiversity hotspot", by Castro and collaborators. &nbsp;</p><p>We collected plant traits from a Brazilian savanna known as Cerrado.&nbsp;</p>

restrictedcc-by-4.0Oct 2023View 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