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17 results for “matrix habitat”

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zenodo40/100

Fig. 3 in Composition and structure of the helminth community of rodents in matrix habitat areas of the Atlantic forest of southeastern Brazil

Fig. 3. Bipartite plot of the interactions between the mammal hosts and the helminth parasites identified in the present study.

opencc-by-4.0Aug 2021View details →
zenodo40/100

Fig. 2 in Composition and structure of the helminth community of rodents in matrix habitat areas of the Atlantic forest of southeastern Brazil

Fig. 2. Species accumulation curve of the helminths recorded in each mammalian host: a. Akodon cursor b. Mus musculus c. Necromys lasiurus.

opencc-by-4.0Aug 2021View details →
zenodo40/100

Fig. 1 in Composition and structure of the helminth community of rodents in matrix habitat areas of the Atlantic forest of southeastern Brazil

Fig. 1. Location of the sampling sites within the REBIO Poço das Antas and the APA-BRSJ in Rio de Janeiro state (RJ), southeastern Brazil, showing the distribution of the different vegetation types and the canals that separate the two reserves.

opencc-by-4.0Aug 2021View details →
dryad40/100

Time and matrix quality increase the relative habitat value of smaller patches in fragmented landscapes

Open the record for dataset details and reuse information.

publicJan 2025View details →
dryad36/100

From nature reserve to mosaic management: improving matrix survival, not permeability, benefits regional populations under habitat loss and fragmentation

<p>Although matrix improvement in fragmented landscapes is a promising conservation measure, matrix permeability (willingness of an organism to enter the matrix) and movement survival in the matrix are usually aggregated. Consequently, it is unknown which matrix property needs to be improved. It also remains unclear whether matrix upgrading from dispersal passage to providing reproduction opportunities has large conservation benefits and whether there are interactive effects between habitat and matrix management.</p> <p>We examined matrix effects on regional populations across a gradient of habitat loss and fragmentation using simulation experiments that integrated demographic processes and movement modeling based on circuit theory. We separately modified the levels of matrix permeability and movement survival to evaluate their individual effects. We also altered the amount and configuration of not only habitat but also improved matrix to assess their effects on population vital rates (size, survival and density).</p> <p>In binary landscapes comprising habitat and unimproved matrix, matrix movement survival had larger effects on population vital rates than matrix permeability. Increasing movement survival increased vital rates, yet, increasing matrix permeability decreased vital rates. Increased permeability required corresponding increased movement survival to offset potential negative population outcomes.</p> <p>When subsets of the matrix functioning as dispersal passage only (where no reproduction opportunities existed) were improved, increasing matrix permeability but holding movement survival constant reduced all vital rates, especially with increasing habitat fragmentation. In contrast, when movement survival increased, vital rates increased given strong habitat fragmentation. The benefits of upgrading dispersal passage to provide reproduction opportunities for population survival were greatest when habitat amount was moderate. We also found synergetic effects between amounts of habitat and improved matrix, and the benefits of matrix improvement were promoted when improvement was achieved in a spatially aggregated manner.</p> <p><em>Synthesis and applications</em>: Matrix improvement and connectivity modeling aimed at increasing movement survival will likely bring larger conservation benefits than those for improving permeability alone. Buffering and connecting habitat remnants with improved matrix could provide benefits as long as movement survival is increased. Simultaneous implementation of habitat management and matrix improvement would yield synergistic conservation benefits.</p>

opencc-zeroMar 2022View details →
dryad36/100

From nature reserve to mosaic management: improving matrix survival, not permeability, benefits regional populations under habitat loss and fragmentation

Open the record for dataset details and reuse information.

publicMar 2022View details →
dryad36/100

Activity-pressure-habitat linkage matrix: Identifying impact chains to assess impact risk to tropical marine ecosystems from human activities in four Southeast Asian case studies Version 1.0

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publicOct 2024View details →
dryad32/100

Data from: Matrix type and landscape attributes modulate avian taxonomic and functional spillover across habitat boundaries in the Brazilian Atlantic Forest

Land use intensification drives biodiversity loss worldwide. In heterogeneous landscape mosaics, both overall forest area and anthropogenic matrix structure induce changes in biological communities in primary habitat remnants. However, community changes via cross-habitat spillover processes along forest-matrix interfaces remain poorly understood. Moreover, information on how landscape attributes affect spillover processes across habitat boundaries are embryonic. Here, we quantify avian  and β-diversity (as proxies of spillover rates) across two dominant types of forest-matrix interfaces (forest-pasture and forest-eucalyptus plantation) within the Atlantic Forest biodiversity hotspot in southeast Brazil. We also assess the effects of anthropogenic matrix type and landscape attributes (forest cover, edge density and land-use diversity) on bird taxonomic and functional β-diversity across forest-matrix boundaries. Alpha taxonomic richness was higher in forest edges than within both matrix types, but between matrix types, it was higher in pastures than in eucalyptus plantations. Although significantly higher in forests edges than in the adjacent eucalyptus, bird functional richness did not differ between forest edges and adjacent pastures. Community changes (β-diversity) related to species and functional replacements (turnover component) were higher across forest-pasture boundaries, whereas changes related to species and functional loss (nested component) were higher across forest-eucalyptus boundaries. Forest edges adjacent to eucalyptus had significant higher species and functional replacements than forest edges adjacent to pastures. Forest cover negatively influenced functional β-diversity across both forest-pasture and forest-eucalyptus interfaces. We show the importance of matrix type and the structure of surrounding landscapes (mainly forest cover) on rates of bird assemblage spillover across forest-matrix boundaries, which has profound implications to biological fluxes, ecosystem functioning and land-use management in human-modified landscapes.

opencc-zeroJun 2019View details →
dryad32/100

Recent population differentiation in the habitat specialist Glossy Antshrike (Aves: Thamnophilidae) across Amazonian seasonally flooded forests: Complete matrix

<p>We assessed population structure and the spatio-temporal pattern of diversification in the Glossy Antshrike <i>Sakesphorus luctuosus</i> (Aves, Thamnophilidae) to understand the processes shaping the evolutionary history of Amazonian floodplains and address unresolved taxonomic controversies surrounding its species limits. By targeting ultraconserved elements (UCEs) from 32 specimens of <i>S. luctuosus</i>, we identified independent lineages and estimated their differentiation, divergence times and migration rates. We also estimated current and past demographic histories for each recovered lineage. We found evidence confirming that <i>S. luctuosus</i> consists of a single species, comprising at least four populations, with some highly admixed individuals and overall similar levels of migration between populations. We confirmed the differentiation of the Araguaia River basin population (<i>S. l.</i> <i>araguayae</i>), and gathered circumstantial evidence indicating that the taxon <i>S. hagmanni</i> may represent a highly introgressed population between 3 distinct phylogroups of <i>S. luctuosus</i>. Divergence time estimates between populations seem to be recent, occurring during the last 183 kya. Signs of population expansions were detected for populations attributed to subspecies <i>S. l. luctuosus</i>, but the <i>S. l. araguayae </i>population had probably maintained its effective size through time. Our results support<b> </b>that <i>S. luctuosus</i> has had a complex population history, resulting from a high dependence on southeastern "clear-water" habitats and their availability through time. Spatial and demographic expansions towards the western "white water" flooded forests might still be ongoing. Our study reinforces the view that isolation due to absence of suitable habitat has been an important driver of population differentiation within Amazonian flooded forests, but also that differences between <i>várzeas</i> ("white water" floodplains, mostly in southwestern Amazonia) and <i>igapós</i> ("clear- water" floodplains, especially located in the east) should be further explored as powerful drivers of micro-evolution.</p>

opencc-zeroJul 2021View details →
dryad32/100

Data from: Matrix type and landscape attributes modulate avian taxonomic and functional spillover across habitat boundaries in the Brazilian Atlantic Forest

Open the record for dataset details and reuse information.

publicJun 2019View details →
dryad32/100

Recent population differentiation in the habitat specialist Glossy Antshrike (Aves: Thamnophilidae) across Amazonian seasonally flooded forests: Complete matrix

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publicSep 2022View details →
zenodo28/100

Supplementary material 1 from: Cirino DW, Lupinetti-Cunha A, Freitas CH, de Freitas SR (2022) Do the roadkills of different mammal species respond the same way to habitat and matrix? In: Santos S, Grilo C, Shilling F, Bhardwaj M, Papp CR (Eds) Linear Infrastructure Networks with Ecological Solutions. Nature Conservation 47: 65-85. https://doi.org/10.3897/natureconservation.47.73010

Correlation plot and R script for building and selecting best models

opencc-zeroMar 2022View details →
zenodo28/100

Figure 4 from: Gandhi K, Epstein M, Koehle J, Purrington F (2011) A quarter of a century succession of epigaeic beetle assemblages in remnant habitats in an urbanized matrix (Coleoptera, Carabidae). ZooKeys 147: 667-689. https://doi.org/10.3897/zookeys.147.1954

Figure 4 - Dendrogram for the similarity/dissimilarity in standardized per trap catches of epigaeic beetle assemblages in sampling years 1980 and 2005 (A) and 1981 and 2005 (B) in cottonwood and oak stands, and old fields.

opencc-by-4.0Nov 2011View details →
zenodo28/100

Figure 2 from: Gandhi K, Epstein M, Koehle J, Purrington F (2011) A quarter of a century succession of epigaeic beetle assemblages in remnant habitats in an urbanized matrix (Coleoptera, Carabidae). ZooKeys 147: 667-689. https://doi.org/10.3897/zookeys.147.1954

Figure 2 - Mean (+SE) standardized total catches of epigaeic beetles (A), and Cyclotrachelus sodalis sodalis LeConte (B) caught in 1980 and 2005 in cottonwood (N = 3) and oak (N =4) stands, and old fields (N = 2).

opencc-by-4.0Nov 2011View details →
zenodo28/100

Figure 3 from: Gandhi K, Epstein M, Koehle J, Purrington F (2011) A quarter of a century succession of epigaeic beetle assemblages in remnant habitats in an urbanized matrix (Coleoptera, Carabidae). ZooKeys 147: 667-689. https://doi.org/10.3897/zookeys.147.1954

Figure 3 - Estimated mean species richness of epigaeic beetles using rarefaction analyses in sampling years 1980 and 2005 (A) and 1981 and 2005 (B) in cottonwood and oak stands, and old fields.

opencc-by-4.0Nov 2011View details →
dryad28/100

Data from: Heterogeneous matrix habitat drives species occurrences in complex, fragmented landscapes

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publicMar 2020View details →
zenodo24/100

Figure 1 from: Gandhi K, Epstein M, Koehle J, Purrington F (2011) A quarter of a century succession of epigaeic beetle assemblages in remnant habitats in an urbanized matrix (Coleoptera, Carabidae). ZooKeys 147: 667-689. https://doi.org/10.3897/zookeys.147.1954

Figure 1 - Location of study sites in Ramsey County and major cities in Minnesota, USA.

opencc-by-4.0Nov 2011View 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

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