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.

8

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

8 results for “paleo-endemism”

Learn how ShareScore rates datasets ↗
zenodo40/100

Figure 3 in Phylogenetic measures of biodiversity and neo- and paleo-endemism in Australian Acacia

Figure 3 | CANAPE, a two-step procedure described in text. (a) Map of centres of endemism discovered. White cells contain no records; beige cells are not significant. The red values indicate grid cells that contain significantly lower RPE than expected given random sampling of the same number of species from a null tree, termed 'centres of neo-endemism'. The blue values indicate grid cells that contain significantly higher RPE than expected, termed 'centres of paleo-endemism'. The purple values indicate grid cells that are a mix of neo-endemism and paleo-endemism; the most highly significant of which (darker purple) are termed 'centres of superendemism'. (b) Bivariate plot showing the relationship between the numerator (y axis) and denominator (x axis) of RPE, applied following the two-step CANAPE procedure described in text, for comparison with a. The grey points in the background are results of the randomization, the beige points are actual values for grid cells that are not significant, the red points are actual values for grid cells that are interpreted as significantly dominated by neo-endemism, the blue points are actual values for grid cells that are interpreted as significantly dominated by paleo-endemism, and the purple points are actual values for grid cells significant for both the y-axis and x-axis variables separately, the most highly significant of which (darker purple) are termed 'centres of super-endemicity'.

opencc-by-4.0Jul 2014View details →
zenodo40/100

Figure 2 in Phylogenetic measures of biodiversity and neo- and paleo-endemism in Australian Acacia

Figure 2 | Maps showing significance levels resulting from of a randomization test in Australian Acacia. White cells contain no records; beige cells are not significant. (a) PD: the red values indicate grid cells that contain significantly less PD than expected; the blue values indicate grid cells that contain significantly more PD than expected. (b) RPD: the red values indicate grid cells that contain significantly less RPD than expected; the species present in that cell are significantly more closely related than expected. The blue values indicate grid cells that contain significantly more RPD than expected; the species present in that cell are significantly more distantly related than expected. (c) Phylogenetic endemism (PE). The red values indicate grid cells that contain significantly less PE than expected; the blue values indicate grid cells that contain significantly more PE than expected. (d) Relative phylogenetic endemism (RPE). The red values indicate grid cells that contain significantly lower RPE than expected; the blue values indicate grid cells that contain significantly higher RPE than expected.

opencc-by-4.0Jul 2014View details →
dryad32/100

Data from: Phylogenetic measures of biodiversity and neo- and paleo-endemism

Understanding spatial patterns of biodiversity is critical for conservation planning, particularly given rapid habitat loss and human-induced climatic change. Diversity and endemism are typically assessed by comparing species ranges across regions. However, investigation of patterns of species diversity alone misses out on the full richness of patterns that can be inferred using a phylogenetic approach. Here, using Australian Acacia as an example, we show that the application of phylogenetic methods, particularly two new measures, relative phylogenetic diversity and relative phylogenetic endemism, greatly enhances our knowledge of biodiversity across both space and time. We found that areas of high species richness and species endemism are not necessarily areas of high phylogenetic diversity or phylogenetic endemism. We propose a new method called categorical analysis of neo- and paleo-endemism (CANAPE) that allows, for the first time, a clear, quantitative distinction between centres of neo- and paleo-endemism, useful to the conservation decision-making process.

opencc-zeroDec 2013View details →
dryad32/100

Data from: Islands within islands: two montane paleo-endemic birds impacted by recent anthropogenic fragmentation

Anthropogenic habitat fragmentation of species that live in naturally patchy metapopulations such as mountaintops or sky islands experiences two levels of patchiness. Effects of such multilevel patchiness on species have rarely been examined. Metapopulation theory suggests that patchy habitats could have varied impacts on persistence, dependent on differential migration. It is not known whether montane endemic species, evolutionarily adapted to natural patchiness, are able to disperse between anthropogenic fragments at similar spatial scales as natural patches. We investigated historic and contemporary gene flow between natural and anthropogenic patches across the distribution range of a Western Ghats sky-island-endemic bird species complex. Data from 14 microsatellites for 218 individuals detected major genetic structuring by deep valleys, including one hitherto undescribed barrier. As expected, we found strong effects of historic genetic differentiation across natural patches, but not across anthropogenic fragments. Contrastingly, contemporary differentiation (DPS) was higher relative to historic differentiation (FST) in anthropogenic fragments, despite the species' ability to historically traverse shallow valleys. Simulations of recent isolation resulted in high DPS/FST values, confirming recent isolation in Western Ghats anthropogenic fragments and also suggesting that this ratio can be used to identifying recent fragmentation in the context of historic connectedness. We suggest that in this landscape, in addition to natural patchiness affecting population connectivity, anthropogenic fragmentation additionally impacts connectivity, making anthropogenic fragments akin to islands within natural islands of montane habitat, a pattern that may be recovered in other sky-island systems.

opencc-zeroDec 2014View details →
dryad32/100

Data from: Islands within islands: two montane paleo-endemic birds impacted by recent anthropogenic fragmentation

Open the record for dataset details and reuse information.

publicJun 2015View details →
dryad32/100

Data from: Phylogenetic measures of biodiversity and neo- and paleo-endemism

Open the record for dataset details and reuse information.

publicMay 2015View details →
zenodo28/100

Figure 4 in Phylogenetic measures of biodiversity and neo- and paleo-endemism in Australian Acacia

Figure 4 | Map (a) and cluster analysis (b) showing phylogenetic similarity relationships among centres of endemism for Australian Acacia. The cluster analysis used PD-dissimilarity and a phylo-jaccard metric with link-average linkage. Areas that cluster closely, indicating that they share many branches of their phylogenetic subtrees, are shown in the same colour and lettered for reference in the text. The number given by each letter is the proportion of grid cells in that cluster that are at least partly covered by currently protected areas; Eand F, the most poorly protected, are marked with an asterisk. The arrows on the map point to the grid cells in clusters Eand F that lie completely outside of protected areas and are thus of highest conservation concern.

opencc-by-4.0Jul 2014View details →
zenodo28/100

Figure 1 in Phylogenetic measures of biodiversity and neo- and paleo-endemism in Australian Acacia

Figure 1 | Maps showing basic biodiversity patterns in Australian Acacia. (a) SR; (b) WE; (c) PD; and (d) PE.

opencc-by-4.0Jul 2014View 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

ScienceDex for faculty

Your academic CV and NIH biosketch

Make your CV in your school's format and your NIH biosketch from it, then download both as Word files.