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677 results for “forest community”

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zenodo44/100

Fruit-feeding butterfly community data analysed in "Recovery patterns in community composition of fruit-feeding butterflies following 26 years of active forest restoration"

<p>Community data of fruit-feeding butterflies collected from Kibale National Park, Uganda, in the periods 2011-2012 and 2020-2021 analysed in our paper Korkiatupa et al. 2023: "Recovery patterns in community composition of fruit-feeding butterflies following 26 years of active forest restoration" (<em>Ecosphere</em> <span>14</span>(<span>5</span>): e4514. <a href="https://doi.org/10.1002/ecs2.4514">https://doi.org/10.1002/ecs2.4514</a>).</p> <p>The table consists of two parts. First part shows counts of individuals of butterfly species in each study site. Second part shows the metadata: code of studysite, census (2011-2012/2020-2021), planting year (planting year or "Primary forest"), and coordinates (WGS 84 coordinate system).</p>

opencc-by-4.0Mar 2023View details →
zenodo44/100

Models simulating abrupt changes in the Chilika lagoon fishery, the Easter Island community, forest dieback and lake water quality

<p>This deposit is in support of Willcock et al &quot;Earlier collapse of Anthropocene ecosystems driven by multiple faster and noisier drivers&quot;. It&nbsp;covers the following items: (i) A list of the files contained within this data deposit; (ii) How to access and download the specialist software required to view and simulate the system dynamics models (STELLA &lsquo;isee Player&rsquo;); (iii) How to run isee Player to simulate the models; (iv) How to access and download the standard statistical software &lsquo;R&rsquo; to run the R scripts; (v) How to load &lsquo;R&rsquo; and modify the standard R script to analyse a subset of the model runs. This file will also details the &lsquo;required content&rsquo; (e.g. software versions), as specified in the &lsquo;nr-software-policy.pdf&rsquo; document.</p> <p>The full descriptions of each of the four system dynamics models used in this manuscript can be read in the following papers:</p> <ol> <li>Lake Chilika &ndash; Cooper, G. S. &amp; Dearing, J. A. Modelling future safe and just operating spaces in regional social-ecological systems. <em>Sci. Total Environ.</em> <strong>651</strong>, 2105&ndash;2117 (2019), <a href="https://doi.org/10.1016/j.scitotenv.2018.10.118">https://doi.org/10.1016/j.scitotenv.2018.10.118</a></li> <li>Easter Island &ndash; Brandt, G. &amp; Merico, A. The slow demise of Easter Island: Insights from a modeling investigation. <em>Front. Ecol. Evol.</em> <strong>3</strong>, 13 (2015), <a href="https://www.frontiersin.org/article/10.3389/fevo.2015.00013">https://www.frontiersin.org/article/10.3389/fevo.2015.00013</a></li> <li>Lake phosphorus &ndash; Wang, R. <em>et al.</em> Flickering gives early warning signals of a critical transition to a eutrophic lake state. <em>Nature</em> <strong>492</strong>, 419&ndash;22 (2012), <a href="http://dx.doi.org/10.1038/nature11655">http://dx.doi.org/10.1038/nature11655</a></li> <li>TRIFFID - Ritchie, P. D. L., Clarke, J. J., Cox, P. M. &amp; Huntingford, C. Overshooting tipping&nbsp;point thresholds in a changing climate. <em>Nat. 2021 5927855</em> <strong>592</strong>, 517&ndash;523 (2021), <a href="http://dx.doi.org/10.1038/nature11655">http://dx.doi.org/10.1038/nature11655</a></li> </ol>

opencc-by-4.0Feb 2023View details →
zenodo44/100

The effect of a political crisis on performance of community- and state-managed forests in Madagascar

<p>Data associated with paper: "The effect of a political crisis on performance of community forests and protected areas in Madagascar"</p> <p>For code and selected tabular data outputs, also see: https://github.com/raenb0/madagascar</p> <p>Includes a number of files with raster (tif)&nbsp;data. All data is for Madagascar:</p> <p>⦁&nbsp;&nbsp; &nbsp;for2000.tif is forest cover in the year 2000<br>⦁&nbsp;&nbsp; &nbsp;for2000_0.tif is the same as above but contains 0 values instead of NA values (better for analysis)<br>⦁&nbsp;&nbsp; &nbsp;defor_year_90m is annual deforestation as a proportion of each 90 m pixel that is deforested, values range from 0-1.</p> <p>data on all time-invariant covariates used for matching, including:<br>⦁&nbsp;&nbsp; &nbsp;dist_cart (distance from cart tracks, meters)<br>⦁&nbsp;&nbsp; &nbsp;dist_road (distance from roads, meters)<br>⦁&nbsp;&nbsp; &nbsp;dist_urb (distance from villages, meters)<br>⦁&nbsp;&nbsp; &nbsp;dist_urb (distance from urban centers, meters)<br>⦁&nbsp;&nbsp; &nbsp;dist_vil (distance from villages, meters)<br>⦁&nbsp;&nbsp; &nbsp;edge_05&nbsp;(distance from forest edge in 2005, meters)<br>⦁&nbsp;&nbsp; &nbsp;elev (elevation, meters)<br>⦁&nbsp;&nbsp; &nbsp;q1_materials (index of self-reported development level, based on material assets)<br>⦁&nbsp;&nbsp; &nbsp;rain (average precipitation 1970-2000, mm)<br>⦁&nbsp;&nbsp; &nbsp;rice (rice suitability, 0 for unsuitable or 1 for suitable)<br>⦁&nbsp;&nbsp; &nbsp;slope (slope, meters)<br>⦁&nbsp;&nbsp; &nbsp;v7_security (self-reported indicator of security and risk of theft)<br>⦁&nbsp;&nbsp; &nbsp;veg_type (vegetation type, 1= eastern humid forest, 2= western deciduous forest, 3 = southern dry spiny forest)</p> <p>time-variant covariates include (for years 2005-2020):<br>⦁&nbsp;&nbsp; &nbsp;distance_year (distance from forest edge of each forest pixel, in meters,&nbsp;in each year)<br>⦁&nbsp;&nbsp; &nbsp;drght_year (drought severity, Palmer Index Score)<br>⦁&nbsp;&nbsp; &nbsp;pop_year (human population density, people per sq km)<br>⦁&nbsp;&nbsp; &nbsp;precip_year (maximum accumulated precipitation, mm)<br>⦁&nbsp;&nbsp; &nbsp;rice_av_year (annual average rice prices, in USD)<br>⦁&nbsp;&nbsp; &nbsp;rice_sd_year (standard deviation of rice price, in USD)<br>⦁&nbsp;&nbsp; &nbsp;temp_year (maximum annual temperature, degrees C)<br>⦁&nbsp;&nbsp; &nbsp;wind_year (maximum annual windspeed, meters/sec)</p> <p>Shapefile polygons for Community Forest Managed areas (CFM) and protected areas administered by Madagascar National Parks can be requested from the corresponding author: ran63 (at) cornell (dot) edu</p> <p>Shapefile polygons for protected areas in Madagascar are available from the World Database of Protected Areas:&nbsp;https://www.protectedplanet.net/country/MDG</p>

opencc-by-4.0Jul 2023View details →
edi44/100

Kelp forest fish communities environmental DNA samples from Santa Barbara Channel

The dataset in this package is the processed fish community structure inferred from 12S eDNA metabarcoding in the Santa Barbara Channel. 49 water samples were collected across 11 sites in 2017 and the taxa were identified to the highest resolution possible. The raw DNA sequence has been archived in the Sequence Read Archive (SRA) database (https://www.ncbi.nlm.nih.gov/sra) under the accession number PRJNA667508. This dataset is used to support manuscript: Lamy, T., Pitz, K.J., Chavez, F.P. et al. Environmental DNA reveals the fine-grained and hierarchical spatial structure of kelp forest fish communities. Sci Rep 11, 14439 (2021). https://doi.org/10.1038/s41598-021-93859-5

openCC (other)May 2022View details →
edi44/100

FRAME (FoRests Among Managed Ecosystems) – Plant community and seed bank composition in forests, Philadelphia metropolitan area, USA, 2017-2019

Our study objectives were to conduct a Rosa multiflora (multiflora rose) removal experiment in three forest sites experiencing different invasion intensities and to restore native plant biodiversity while preventing secondary invasion. The study was conducted in and around Newark, DE, from 2017-2019, and data collection is complete. We utilized three management strategies: invasive plant removal, removal followed by native seed addition, and removal plus native seed and mulched invasive stem addition. We investigated the similarity between seed bank species composition and existing vegetation before and after removal to assess the potential for passive restoration. Two seasons after removal, we found that simply removing rose increased native species richness, Native Floristic Quality Assessment (FQAIN), and native shrub abundance in our medium invasion site, and total species richness in our low and medium invasion sites. Compared to removal alone, native seed addition, with and without mulch addition, resulted in larger native and total species richness and FQAIN increases at all sites, larger increases in native shrub abundance and exotic species richness in our medium invasion site, and larger reductions in exotic and total shrub abundance in our low and medium invasion sites. Following removal, species similarity between seed bank and vegetation improved for all three sites. Our results indicate that removal of Rosa multiflora (multiflora rose) alone increased native plant biodiversity in the medium invasion scenario, but the seed bank may not provide a large native species pool. Additional management strategies lead to improved outcomes, especially in our most invaded forest, demonstrating the need to conduct multiple plant removal treatments across forests with varying site conditions and plant invasion intensity to improve management recommendations.

openCC (other)Sep 2022View details →
edi44/100

Peeking under the canopy: anomalously short fire-return intervals alter subalpine forest understory plant communities

Changing climate and fire regimes are profoundly affecting temperate coniferous forests, driving greatly reduced tree cover postfire. However, whether similar changes are present in the understory of these forests remains less well-understood. We sampled understory plant communities in 20 plot pairs across Greater Yellowstone (Wyoming, USA) in July and August 2021, with each including one plot burned at short (<30 year) fire-return interval and one plot burned in the same most recent fire but not burned previously for >125 years. We also included 11 plot pairs meeting our definition of short- and long-interval fire that were sampled 12 years after the 1988 Yellowstone fires in summer 2000. We also used previously collected published and unpublished data to compare understory communities following recent (2016) short-interval fires to those following the previous long-interval fire in the same general area. In each plot, percent cover of understory plant species was estimated in 0.25-m2 quadrats, and species richness determined via a whole-plot sweep. Understory plant community cover, richness, and diversity did not differ by interval class, but species able to persist in drier conditions and in lower vegetation zones became more abundant following shot interval fire. Further, previously distinct understory communities following long-interval fire in two regions of Greater Yellowstone became slightly more similar following recent short-interval fire. Dissimilarity between plot pairs increased with greater historical snowfall and decreased with time since fire and postfire winter snowfall. These changes to understory plant communities may continue with ongoing shifts in climate and fire across temperate and boreal forests.

openCC (other)May 2023View details →
edi44/100

Data for: Sparse subalpine forest recovery pathways, plant communities, and carbon stocks 34 years after stand-replacing fire (Greater Yellowstone Ecosystem, Wyoming, USA; 2022)

We assessed postfire forest recovery pathways, stem densities, understory plant communities, and carbon stocks across 55 plots in areas exhibiting sparse and reduced forest recovery 34 years after the 1988 Yellowstone Fires in the Greater Yellowstone Ecosystem, Wyoming, USA. Recovery pathways were identified using plot-level frequency distributions of tree ages and correlated with potentially important biotic and abiotic variables (e.g., elevation, seed source distance). Species- and age-specific stem densities were similarly regressed across environmental factors to determine variability in forest recovery across the sampled landscape. Understory plant communities were sampled in 0.25m-square quadrats and environmental drivers of individual species occurrence and whole compositional shifts were determined. Finally, carbon stock sizes were derived from field measures of tree characteristics, understory cover, and soil combined with regionally derived allometric equations. Data collection is complete and is part of a forthcoming manuscript at Ecological Monographs.

openCC (other)Sep 2024View details →
edi44/100

Plant community typing (2009 update), Andrews Experimental Forest

Plant Communities of the HJ Andrews Experimental Forest (revised 2009). A total of 23 forest communities have been identified and characterized in a preliminary manner. Data used in formatting the classification had previously been collected on 300 reconnaissance plots located on the H. J. Andrews Forest and surrounding area. Vegetation classification was facilitated by similarity analysis and stand ordination procedures developed by Dr. Will Moir, formerly of Colorado State University. Results of stand ordination indicate the presence of strong moisture and temperature gradients along which forest stands array themselves. The forest communities recognized in this classification are listed in the following internal report: http://andrewsforest.oregonstate.edu/pubs/pdf/pub1741.pdf

openCustomJan 2014View details →
edi44/100

SBC LTER: Reef: Kelp Forest Community Dynamics: Kelp Forest Data to support "Estimating biomass of benthic kelp forest invertebrates from body size and percent cover"

These data describe quantitative relationships between wet mass and length or wet mass and percent cover, and conversion factors to transform wet mass into dry mass, shell-free and decalcified dry mass, and ash-free dry mass for 84 species of benthic macroinvertebrates common to giant kelp forests in southern California. Data are based on organisms collected from sites in the Santa Barbara Channel between April 2010 and May 2014. These measurements are intended to facilitate the conversion of invertebrate abundance into common metrics of biomass, for quantitative studies of community dynamics, trophic interactions, energy flow and biodiversity. Converting numerical abundance (i.e., organism density) to biomass requires information on the relationship between individual size and biomass. For colonial and small aggregating taxa that are numerous and indistinct, measures of abundance are usually proportional (e.g., percent cover). Hence, converstions are taxa-specific, based on either size or cover, and a variety of metrics of species biomass are included, e.g., wet mass, shell-free wet mass, ash-free dry mass. Data are published in Reed, D. C, J. C. Nelson, S. L. Harrer, and R. J. Miller, Estimating biomass of benthic kelp forest invertebrates from body size and percent cover data. Marine Biology. DOI: 10.1007/s00227-016-2879-x. From the paper abstract: The inability to compare different measures of species abundance (such as density and percent cover) or different metrics of species biomass (such as wet mass and ash-free dry mass) hampers quantitative studies of community dynamics, trophic interactions, energy flow and biodiversity. This has been especially problematic for the dynamic and highly productive communities inhabiting shallow reefs in temperate seas where varied metrics are commonly used to characterize the abundance and biomass of different suites of species. Regressions for all 84 species were highly significant and regression fits were very good for mos

openCC (other)Oct 2022View details →
zenodo40/100

Fig. 1 in Saproxylic beetle (Coleoptera) communities and forest management practices in coniferous stands in southwest Nova Scotia, Canada

Fig. 1. Map of Bowater Mersey Paper Company Ltd land in Nova Scotia. Bowater Mersey lands highlighted. Site descriptions: 1 &amp; 2 – 40-80 yr, CT; 3 &amp; 4 – 40-80 yr, none; 5 – 80-120 yr, US; 6 &amp; 7 – 80- 120, none; 8 – 120+ yr, S; 9 – 120+ yr, S/SH; 10 &amp; 11 – 120+ yr, none. CT = Commercial thinning; US = Uniform selection harvest; SH = Shelterwood harvest; S = Selection harvest.

opencc-by-4.0Sep 2008View details →
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Fig. 2 in Saproxylic beetle (Coleoptera) communities and forest management practices in coniferous stands in southwest Nova Scotia, Canada

Fig. 2. Overstory composition for dominant tree species based on importance value (Importance Value = Relative Density + Relative Dominance + Relative Frequency). Site descriptions: 1 &amp; 2 – 40-80 yr, CT; 3 &amp; 4 – 40-80 yr, none; 5 – 80-120 yr, US; 6 &amp; 7 – 80-120, none; 8 – 120+ yr, S; 9 – 120+ yr, S/SH; 10 &amp; 11 – 120+ yr, none. CT = Commercial thinning; US = Uniform selection harvest; SH = Shelterwood harvest; S = Selection harvest.

opencc-by-4.0Sep 2008View details →
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Fig. 7 in Saproxylic beetle (Coleoptera) communities and forest management practices in coniferous stands in southwest Nova Scotia, Canada

Fig. 7. Mean species richness of beetles in different forest stand age classes, including standard deviation from both the present study and Bishop (1998).

opencc-by-4.0Sep 2008View details →
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Fig. 5 in Saproxylic beetle (Coleoptera) communities and forest management practices in coniferous stands in southwest Nova Scotia, Canada

Fig. 5. Rarefaction curve demonstrating projected species richness for number of individuals based on Bishop (1998), and the present study (Dollin et al.) beetle collections.

opencc-by-4.0Sep 2008View details →
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Fig. 8 in Saproxylic beetle (Coleoptera) communities and forest management practices in coniferous stands in southwest Nova Scotia, Canada

Fig. 8. Mean species richness across harvest treatment, including standard deviation, for 11 stands in southwestern Nova Scotia.

opencc-by-4.0Sep 2008View details →
zenodo40/100

Fig. 3 in Saproxylic beetle (Coleoptera) communities and forest management practices in coniferous stands in southwest Nova Scotia, Canada

Fig. 3. Volume of coarse woody debris (CWD) by decay class for 11 stands in southwestern Nova Scotia as measured by Thompson (2004). Decay classes are summarized as follows: "1" is freshly dead, little to no rot; in "2", the bole is mostly sound; "3" has well-established rot and significant bark loss; "4" is advanced decay; and "5" is rotted through but still of wood character. Site descriptions: 1 &amp; 2 – 40-80 yr, CT; 3 &amp; 4 – 40-80 yr, none; 5 – 80-120 yr, US; 6 &amp; 7 – 80-120, none; 8 – 120+ yr, S; 9 – 120+ yr, S/SH; 10 &amp; 11 – 120+ yr, none. CT = Commercial thinning; US = Uniform selection harvest; SH = Shelterwood harvest; S = Selection harvest.

opencc-by-4.0Sep 2008View details →
zenodo40/100

Elevation differently shapes functional diversity patterns in understory forest communities when considering intraspecific and interspecific trait variability

<p>Datasets used for the analysis done for the paper "Elevation differently shapes functional diversity patterns in understory forest communities when considering intraspecific and interspecific trait variability".</p> <p>Files present are:</p> <p>-Species x Plot (vegetation releve&eacute;s).</p> <p>-Plot x Environment.</p> <p>-Plot x CWM_inter for Plant height, Leaf area, Specific Leaf Area (SLA), Leaf Dry Matter Content (LDMC) using the traits fixed for species, i.e., holding traits constant as the species mean, thus incorporating only turnover.</p> <p>-Plot x CWM_intra for Plant height, Leaf area, Specific Leaf Area (SLA), Leaf Dry Matter Content (LDMC) based on an individual by trait matrix, therefore incorporating both turnover and intraspecific trait variation.</p> <p>-Plot x SES-FD_inter (Standard Effect Size Functional Diversity) for Plant height, Leaf area, Specific Leaf Area (SLA), Leaf Dry Matter Content (LDMC) using the traits fixed for species, i.e., holding traits constant as the species mean, thus incorporating only turnover.</p> <p>-Plot x SES-FD_intra (Standard Effect Size Functional Diversity) for Plant height, Leaf area, Specific Leaf Area (SLA), Leaf Dry Matter Content (LDMC) based on an individual by trait matrix, therefore incorporating both turnover and intraspecific trait variation.</p> <p>All analysis were carried out using the software R version 4.1.2 (R Foundation for Statistical Computing, Vienna, Austria, <a href="http://www.R-project.org">http://www.R-project.org</a>) and can be consulted on GitHub https://github.com/AriannaFerrara/Elevation-and-Intraspecific-trait-variability.git</p>

opencc-by-4.0Jan 2024View details →
zenodo40/100

FIG. 2 in Nematode community structure of forest woodlots. I. Relationships based on similarity coefficients of nematode species

FIG. 2. Dendrogram of forest sites in Tippecanoe County, Ind., based on similarity indices of nematode species.

opencc-by-4.0Jun 1972View details →
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FIG. 1 in Nematode community structure of forest woodlots. I. Relationships based on similarity coefficients of nematode species

FIG. 1. Influence of the number of soil cores taken at Tippecanoe County, Ind., at site P on the number of nematode species recovered.

opencc-by-4.0Jun 1972View details →
zenodo40/100

Fig. 1 in Effects of changes in the riparian forest on the butterfly community (Insecta: Lepidoptera) in Cerrado areas

Fig. 1. Butterfly sampling sites at the Pindaíba River Basin, MT – Brazil; (CVS 1, CVS 2, CVS 3, CVS 4 = Caveira stream (1st to 4th order); MS 1, MS 2, MS 3 and MS 4 = Mata Stream (1st to 4th order).

opencc-by-4.0Nov 2016View details →
zenodo40/100

Figure 2 in Epiphytic Bryophyte And Lichen Communities In Relation To Tree And Forest Stand Variables In Populus Tremula Forests Of South-East Latvia

Figure 2. Epiphytic bryophyte and lichen species in the studied territories. Tade Micr – Microreserve in Tadenava, Augs land – Augšzeme Protected Landscape Area, Star Rese – Starinas mežs Nature Reserve. Signal species include all WKH indicator species and red-listed species.

opencc-by-4.0Dec 2010View details →

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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