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.

78

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

78 results for “soil nematodes”

Learn how ShareScore rates datasets ↗
dryad32/100

Data from: Nematode community responses to range-expanding and native plant communities in original and new range soils

Open the record for dataset details and reuse information.

publicAug 2019View details →
dryad32/100

Data from: High-throughput amplicon sequencing of rRNA genes requires a copy number correction to accurately reflect the effects of management practices on soil nematode community structure

Open the record for dataset details and reuse information.

publicAug 2013View details →
dryad32/100

The functional role and diversity of soil nematodes are stronger at high elevation in the lesser Himalayan mountain ranges

Open the record for dataset details and reuse information.

publicAug 2022View details →
dryad28/100

Data from: Grazing and resource availability control soil nematode body size and abundance-mass relationship in semi-arid grassland

1. Body size is a central functional trait in ecological communities. Despite recognition of the importance of above-belowground interactions, effects of aboveground herbivores on size and abundance-size relationships in soil fauna are almost uncharted. Depending on climate and soil properties, herbivores may increase basal resources of soil food webs, or reduce pore space, mechanisms expected to have contrasting effects on soil animal body size. 2. We investigated how body size and shape of soil nematodes responded to mammalian grazers in three semi-arid grassland sites, along a gradient of soil texture and organic matter (OM) in a long-term herbivore removal study. We analysed nematode mass, length, diameter, body size distribution, and biomass distribution. We formulated two mechanistic hypotheses to assess whether resource availability or pore space was the dominant abiotic control and modulated the effects of grazing. 3. In ungrazed soils, average and maximum nematode size, as well as abundance and biomass of large nematodes, were greater in the high-OM than in the low-OM soil, and intermediate in the medium-OM soil. Grazing promoted larger sizes in the low-OM soil, where it had been shown to increase organic matter and microbial biomass, and led to more homogeneous average size and body size distribution across sites. The results support the hypothesis that nematode size was controlled by basal resource availability rather than by pore space. However, body shape might have been constrained by small pores in the fine-texture, high-OM soil, where nematodes were more elongated. 4. Grazing may facilitate larger sizes in soil nematode communities by boosting basal resources where these are limiting, with important implications for estimations of nematode biomass and contribution to carbon and nutrient cycling. These findings contribute to the insofar-limited mechanistic understanding of how herbivores can shape functional traits of soil fauna, and demonstrate that animals at one trophic level may control patterns in body size and abundance-size relationships in other trophic levels without a direct predator-prey or competitive linkage between them.

opencc-zeroDec 2017View details →
dryad28/100

Data from: Integrating quantitative morphological and qualitative molecular methods to analyze soil nematode community responses to plant range expansion

1. Belowground nematodes are important for soil functioning, as they are ubiquitous and operate at various trophic levels in the soil food web. However, morphological nematode community analysis is time consuming and requires ample training. qPCR-based nematode identification techniques are well available, but high throughput sequencing (HTS) might be more suitable for non-targeted nematode community analysis. 2. We compared effectiveness of qPCR and HTS-based approaches with morphological nematode identification while examining how climate warming-induced plant range expansion may influence belowground nematode assemblages. We extracted nematodes from soil of Centaurea stoebe and C. jacea populations in Slovenia, where both plant species are native, and Germany, where C. stoebe is range expander and C. jacea is native. Half of each nematode sample was identified morphologically and the other half was analysed using targeted qPCR and a novel HTS approach. 3. HTS produced the highest taxonomic resolution of the nematode community. Nematode taxa abundances correlated between the methods. Therefore, especially relative HTS and relative morphological data revealed nearly identical ecological patterns. All methods showed lower numbers of plant feeding nematodes in rhizosphere soils of C. stoebe compared to C. jacea. However, a profound difference was observed between absolute and relative abundance data; both sampling origin and plant species affected relative abundances of bacterivorous nematodes, whereas there was no effect on absolute abundances. 4. Taken together, as HTS correlates with relative analyses of soil nematode communities, while providing highest taxonomic resolution and sample throughput, we propose a combination of HTS with microscopic counting to supplement important quantitative data on soil nematode communities. This provides the most cost-effective, in-depths methodology to study soil nematode community responses to changes in the environment. This methodology will also be applicable to nematode analyses in aquatic systems.

opencc-zeroDec 2017View details →
zenodo28/100

Supplementary material 2 from: Ahmed M, Back MA, Prior T, Karssen G, Lawson R, Adams I, Sapp M (2019) Metabarcoding of soil nematodes: the importance of taxonomic coverage and availability of reference sequences in choosing suitable marker(s). Metabarcoding and Metagenomics 3: e36408. https://doi.org/10.3897/mbmg.3.36408

: Data type: source code

opencc-zeroNov 2019View details →
zenodo28/100

Supplementary material 1 from: Ahmed M, Back MA, Prior T, Karssen G, Lawson R, Adams I, Sapp M (2019) Metabarcoding of soil nematodes: the importance of taxonomic coverage and availability of reference sequences in choosing suitable marker(s). Metabarcoding and Metagenomics 3: e36408. https://doi.org/10.3897/mbmg.3.36408

: Data type: species data

opencc-zeroNov 2019View details →
zenodo28/100

Fig. 3 in Review paper Interactions between Bacteria, Protozoa and Nematodes in Soil

Fig. 3. Effect of soil texture on protozoa and nematodes. The graph shows the abundance of amoebae (a), flagellates (b), and nematodes (c) in soils with varying clay content. The soils were amended with glucose and incubated for two weeks before enumeration of organisms. Data from Rønn et al. (1995).

opencc-by-4.0Dec 2012View details →
zenodo28/100

Fig. 1 in Review paper Interactions between Bacteria, Protozoa and Nematodes in Soil

Fig. 1. Diagram of a simplified soil food web showing important trophic links. The diagram is combined and modified from several sources (see e.g. Holtkamp 2008, Hunt et al. 1987).

opencc-by-4.0Dec 2012View details →
zenodo28/100

Fig. 2. A in Review paper Interactions between Bacteria, Protozoa and Nematodes in Soil

Fig. 2. A diagram illustrating the interactions between bacteria, protozoa and nematodes, which are treated in this paper. Numbers in circles refer to the section of the paper in which the particular interaction is discussed.

opencc-by-4.0Dec 2012View details →
zenodo28/100

Figure 4 in Positioning entomopathogenic nematodes for the future viticulture: exploring their use against biotic threats and as bioindicators of soil health

Figure 4. Evaluation of the impact of cover crops (CC) in the entomopathogenic nematode (EPN) soil food web in a Spanish vineyard. A. Impact in the presence and activity of native EPNs. B. Presence of natural enemies (nematophagous fungi and ectoparasitic bacteria) and competitors for the resource (Free-living nematodes) (Data from Blanco-Pérez et al., 2020, modified for this figure).

opencc-by-4.0Aug 2021View details →
zenodo28/100

Figure 3. Preventive inhibition growth effect against Botrytis cinerea over grapevine leaves three days after the infection. A in Positioning entomopathogenic nematodes for the future viticulture: exploring their use against biotic threats and as bioindicators of soil health

Figure 3. Preventive inhibition growth effect against Botrytis cinerea over grapevine leaves three days after the infection. A. Destilled water (control treatment). B. Xenorhabdus nematophilus natural products treatment.

opencc-by-4.0Aug 2021View details →
dryad28/100

Data from: Integrating quantitative morphological and qualitative molecular methods to analyze soil nematode community responses to plant range expansion

Open the record for dataset details and reuse information.

publicMar 2019View details →
dryad28/100

Data from: Grazing and resource availability control soil nematode body size and abundance-mass relationship in semi-arid grassland

Open the record for dataset details and reuse information.

publicMay 2019View details →
geo16/100

Toxicogenomic effects of nano- and bulk TiO2 particles in the soil nematode Carnorhabditis elegans using juglone as a positive control for oxidative stress

GEO Series GSE59519. Caenorhabditis elegans. 62 samples. Type: Expression profiling by array.

openGEO-OpenJul 2014View details →
geo16/100

Toxicogenomic effects of nano- and bulk TiO2 particles in the soil nematode Carnorhabditis elegans

GEO Series GSE59470. Caenorhabditis elegans. 38 samples. Type: Expression profiling by array.

openGEO-OpenJul 2014View details →
geo12/100

Ecotoxicity of silver nanoparticles on the soil nematode Caenorhabditis elegans using functional ecotoxicogenomics

GEO Series GSE14932. Caenorhabditis elegans. 2 samples. Type: Expression profiling by array.

openGEO-OpenFeb 2009View details →
geo12/100

Ecotoxicogenomic analysis on the soil nematode Caenorhabditis elegans exposed to BPA, DEHP and NP

GEO Series GSE15016. Caenorhabditis elegans. 4 samples. Type: Expression profiling by array.

openGEO-OpenFeb 2009View 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