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.

44

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

44 results for “Native conservation”

Learn how ShareScore rates datasets ↗
zenodo44/100

Supplementary material 3 from: Bongard C, Butler K, Fulthorpe R (2013) Investigation of fungal root colonizers of the invasive plant Vincetoxicum rossicum and co-occurring local native plants in a field and woodland area in Southern Ontario. Nature Conservation 4: 55-76. https://doi.org/10.3897/natureconservation.4.3578

Supplementary material 3 from: Bongard C, Butler K, Fulthorpe R (2013) Investigation of fungal root colonizers of the invasive plant Vincetoxicum rossicum and co-occurring local native plants in a field and woodland area in Southern Ontario. Nature Conservation 4: 55-76. https://doi.org/10.3897/natureconservation.4.3578

opencc-by-4.0Jun 2013View details →
edi44/100

Data for "Pollinator Conservation Paradox: Exotic Forbs Support Native Pollinators Under Global Changes" by Nelson, Seabloom and Borer 2025, California grasslands, 2023-2024

Data for analysis on how plant provenance mediates plant-pollinator interaction responses to fertilization and herbivore exclusion, associated with Nelson, Seabloom, and Borer 2025. Data on pollinator visitation and floral abundance were collected in plots that received factorial experimental treatments of combined nitrogen, phosphorus and potassium with micronutrients by herbivore exclusion fencing in three California grasslands in 2023-2024.

openCustomMay 2025View details →
zenodo40/100

Figure 1 in Helminth fauna of the invasive American red-eared slider Trachemys scripta in eastern Spain: potential implications for the conservation of native terrapins

Figure 1. Sampling localities of the American red-eared slider, Trachemys scripta in eastern Spain. (A) Protected wetland 'Marjal de Peñíscola'; (B) 'Cabanes-Torreblanca' Natural Park; (C) Protected Landscape 'Desembocadura del Mijares'; (D) Protected wetland 'Marjal de Gandía'; (E) Site of Community Importance 'Marjal de La Safor'.

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 4 in The threat of free-ranging domestic dog to native wildlife: implication for conservation in Southeast Asia

Fig. 4. The spatial distribution of perceived risk from domestic dog (Canis familiaris) across mainland Southeast Asia. Excluded human settlements and water bodies have been marked in white.

opencc-by-4.0Apr 2022View details →
zenodo40/100

Fig. 3 in The threat of free-ranging domestic dog to native wildlife: implication for conservation in Southeast Asia

Fig. 3. Percentage perceived risk in Avian and Mammalian orders. Height of peaks represent number of species scaled to 2, see Supplementary Materials 4 and 5. Orders with two or less species, including Otidiformes, Dermoptera, Perissodactyla, Pholidota, and Proboscidea, were removed for visualisation.

opencc-by-4.0Apr 2022View details →
zenodo40/100

Fig. 2 in The threat of free-ranging domestic dog to native wildlife: implication for conservation in Southeast Asia

Fig. 2. Percentage perceived risk in Red List categories. Height of peaks represent number of species scaled to 2, see Supplementary Materials 4 and 5.

opencc-by-4.0Apr 2022View details →
zenodo40/100

Fig. 1 in The threat of free-ranging domestic dog to native wildlife: implication for conservation in Southeast Asia

Fig. 1. Bayesian networks modelling (a) perceived risk to carnivore mammalian species, (b) perceived risk to non-carnivore mammalian species, (c) perceived risk to Avian species and, (d) the spatial distribution of perceived risk from domestic dogs in mainland Southeast Asia.

opencc-by-4.0Apr 2022View details →
zenodo40/100

Supplementary material 1 from: Bongard C, Butler K, Fulthorpe R (2013) Investigation of fungal root colonizers of the invasive plant Vincetoxicum rossicum and co-occurring local native plants in a field and woodland area in Southern Ontario. Nature Conservation 4: 55-76. https://doi.org/10.3897/natureconservation.4.3578

Supplementary material 1 from: Bongard C, Butler K, Fulthorpe R (2013) Investigation of fungal root colonizers of the invasive plant Vincetoxicum rossicum and co-occurring local native plants in a field and woodland area in Southern Ontario. Nature Conservation 4: 55-76. https://doi.org/10.3897/natureconservation.4.3578

opencc-by-4.0Jun 2013View details →
dryad40/100

Data from: Native shade trees aid bird conservation in tea plantations in southern India

<p>In the Western Ghats, India, we study how different intensities of tea cultivation influence birds. We compared bird communities in conventional monoculture tea and mixed-shade tea plantations, both of which use agrochemicals, with organic tea plantations, a rainforest fragment, and continuous rainforest within the Anamalai Tiger Reserve. In 225 point count surveys, overall bird species richness and abundance were lowest in conventional tea and up to 33% higher in organic tea. Mixed-shade tea had 40% higher species richness (including 15 canopy and 4 shrub and mid-storey species – primarily frugivores, nectarivores and insectivores), and 83% higher bird abundance than conventional tea, with a greater proportion of forest-affiliated birds and similarity in species composition with forest sites. The rainforest fragment and continuous rainforest had a higher proportion, richness and abundance of forest-affiliated birds and fewer open-country birds, unlike tea plantations where the pattern was reversed. Habitat associations of 62 bird species in indicator species analysis revealed similar patterns. Thus organic tea is better than conventional tea for birds, but mixed-shade tea is even better, although still poorer than forests. Retaining or promoting native shade trees in tea plantations will increase bird diversity and abundance, including of forest-affiliated species and support landscape-level bird conservation.</p>

opencc-zeroJul 2021View details →
dryad40/100

Data from: Native shade trees aid bird conservation in tea plantations in southern India

Open the record for dataset details and reuse information.

publicJul 2021View details →
dryad40/100

Riverscape genetics of non-native Brook Trout to inform native Cutthroat Trout conservation

Open the record for dataset details and reuse information.

publicSep 2025View details →
zenodo36/100

Replication data for: Conservation Gaps in Traditional Vegetables Native to Europe and Fennoscandia

<p>Vegetables are rich in vitamins and other micronutrients and are important crops for healthy diets and diversification of the food system, and many traditional (also termed underutilized or indigenous) species may play a role. The current study analyzed 35 vegetables with a European region of diversity with the effort to map the conservation status in Fennoscandia and beyond. We mapped georeferenced occurrences and current genebank holdings based on global databases and conducted conservation gaps analysis based on representativeness scores in situ and ex situ. Out of the 35 target species, 19 got at a high priority score for further conservation initiatives, while another 14 species got a medium priority score. We identified a pattern where traditional vegetables are poorly represented in genebank holdings. This corresponds well to a lack of attention in the scientific community measured in number of published papers. Considering the grand challenges ahead in terms of climate change, population growth and demand for sustainability, traditional vegetables deserve greater attention. Our contribution is to provide a basis for conservation priorities among the identified vegetables species native to Fennoscandia.</p>

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

Data from: What shapes the genetic diversity of the <em>Alnus cordata</em> species across its Italian native range? informing conservation strategies

Open the record for dataset details and reuse information.

publicSep 2025View details →
dryad36/100

Dancing with the devil: Could native predators inside 'predator free' havens be good for the conservation of threatened native prey species?

Open the record for dataset details and reuse information.

publicDec 2024View details →
dryad32/100

Conservation genetics of native and European-introduced Chinese Water Deer (Hydropotes inermis)

<p><span><span><span><span><span><span><span><span><span><span><span>The Chinese water deer (<i>Hydropotes inermis</i>) belongs to a relatively early-divergence lineage of Cervidae and is thought to have retained some ancestral features of the group. This species is classified as Vulnerable on the IUCN Red List (accessed 2020), and populations in its native range have declined drastically in recent years.  However, a number of individuals were introduced to the UK about a century ago; these have flourished and now make up over 40% of global numbers.  To infer the population genetic structure and genetic diversity of Chinese water deer both in their native China and in populations introduced to the UK and France, mitochondrial DNA sequence variation was investigated (control region and cytochrome B) for near 100 individuals. The distribution of haplotypes among the regions shows distinct geographic structure, and only one cytochrome B haplotype was common to both China and European populations. Our results reveal lower levels of genetic diversity in the British populations, differentiation between native and introduced populations, and that the source population of British deer is likely to be extinct. Some recommendations are made for the conservation of different populations.</span></span></span></span></span></span></span></span></span></span></span></p>

opencc-zeroAug 2020View details →
zenodo32/100

Supplementary material 1 from: Huang J, Guo Z, Tang S, Ren W, Chu G, Wang L, Zhao L, Yu R, Xu Y, Ding Y, Zang R (2020) Floristic composition and plant diversity in distribution areas of native species congeneric with Betula halophila in Xinjiang, northwest China. Nature Conservation 42: 1-17. https://doi.org/10.3897/natureconservation.42.54735

Figure S1. The correlation between environmental variables in distribution areas of five congeneric species with Betula halophila

opencc-zeroSep 2020View details →
dryad32/100

Data from: An invasive non-native mammal population conserves genetic diversity lost from its native range

Invasive, non-native species are one of the major causes of global biodiversity loss. Although they are, by definition, successful in their non-native range, their populations generally show major reductions in their genetic diversity during the demographic bottleneck they experience during colonization. By investigating the mitochondrial genetic diversity of an invasive non-native species, the stoat Mustela erminea, in New Zealand and comparing it to diversity in the species' native range in Great Britain, we reveal the opposite effect. We demonstrate that the New Zealand stoat population contains four mitochondrial haplotypes that have not been found in the native range. Stoats in Britain rely heavily on introduced rabbits Oryctolagus cuniculus as their primary prey and were introduced to New Zealand in a misguided attempt at biological control of rabbits, which had also been introduced there. While invasive stoats have since decimated the New Zealand avifauna, native stoat populations were themselves decimated by the introduction to Britain of Myxoma virus as a control measure for rabbits. We highlight the irony that while introduced species (rabbits) and subsequent biocontrol (myxomatosis) have caused population crashes of native stoats, invasive stoats in New Zealand, which were also introduced for biological control, now contain more genetic haplotypes than their most likely native source.

opencc-zeroDec 2014View details →
dryad32/100

Does urbanization favor exotic bee species? Implications for the conservation of native bees in cities

A growing body of research indicates that cities can support diverse bee communities. However, urbanization may disproportionately benefit exotic bees, potentially to the detriment of native species. We examined the influence of urbanization on exotic and native bees using two datasets from Michigan, USA. We found that urbanization positively influenced exotic – but not native – bee abundance and richness, and that this association could not be explained by proximity to international ports of entry, prevalence of exotic flora, or urban warming. We found a negative relationship between native and exotic bee abundance at sites with high total bee abundance, suggesting that exotic bees may negatively affect native bee populations. These effects were not driven by the numerically dominant exotic honeybee, but rather by other exotic bees. Our findings complicate the emerging paradigm of cities as key sites for pollinator conservation.

opencc-zeroDec 2019View details →
zenodo32/100

Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008). in Muridae

Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae &amp; Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser &amp; Carleton (2005), Richardson &amp; Hussain (2006), Stuart (2008).

opennotspecifiedNov 2017View details →
zenodo32/100

FIGURE 6 in Diversity and conservation of native Argentine species of Gratioleae (Plantaginaceae)

FIGURE 6. Map showing the geographical distribution of threatened Argentinean Gratioleae in relation to the existing protected areas in the country. Abreviations: NPIB=National Park Iberá, NPIG= National Park Iguazú, NPM= National Parks Mburucuyá, HCR= Ramsar Site Network.

opennotspecifiedMay 2024View 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