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156 results for “biotic interactions”
Supplementary material 3 from: Eisenhauer N, Bonkowski M, Brose U, Buscot F, Durka W, Ebeling A, Fischer M, Gleixner G, Heintz-Buschart A, Hines J, Jesch A, Lange M, Meyer S, Roscher C, Scheu S, Schielzeth H, Schloter M, Schulz S, Unsicker S, van Dam NM, Weigelt A, Weisser WW, Wirth C, Wolf J, Schmid B (2019) Biotic interactions, community assembly, and eco-evolutionary dynamics as drivers of long-term biodiversity–ecosystem functioning relationships. Research Ideas and Outcomes 5: e47042. https://doi.org/10.3897/rio.5.e47042
Plant species lists of the Field Experiment and the Ecotron Experiment
Figure 2 from: Rasoloariniaina JR, Ganzhorn JU, Riemann JC, Raminosoa N (2016) Water quality and biotic interaction of two cavefish species: Typhleotris madagascariensis Petit, 1933 and Typhleotris mararybe Sparks & Chakrabarty, 2012, in the Mahafaly Plateau groundwater system, Madagascar. Subterranean Biology 18: 1-16. https://doi.org/10.3897/subtbiol.18.8321
Figure 2 - Significant relationships between the abundance of Typhleotris madagascariensis and Typhleotris mararybe and water characteristics.
Effects of ants on riparian poplars: an ex situ experiment of biotic interaction
<p>Poplars establish on alluvial bars within sand and gravel-bed rivers. Alluvial bars also provide particularly suitable habitats<br> for the proliferation of ants. We hypothesized that ants, by modifying substrate structure and resource availability in fluvial<br> habitats, positively influence poplar growth during its establishment stage. We conducted a preliminary nine-month ex situ<br> greenhouse experiment with one ant species (Lasius niger L.) and six different genotypes of poplar cuttings (Populus nigra<br> L.), both collected on the Garonne River, SW France. Three main treatments: ‘P. nigra alone’, ‘P. nigra without ants and with<br> ant food’ and ‘P. nigra with ants and ant food’ were applied. After one growing season, we tested differences in branching<br> length and biomass of stems, roots and leaves. Certain genotypes showed significant differences in growth, but there were<br> no significant differences in stem length, dry mass of stems and roots between the three treatments. The total biomass of<br> poplars after the first growing season was positively affected by the initial size of the cuttings and was modulated by the<br> genotype independently from the treatments. However, an increased poplar growth for the treatment without ants and with<br> ant food was observed according to significant differences in dry weight of leaves and total biomass (i.e. dry mass of stems,<br> roots and leaves) for the pooled genotypes across treatments. We discuss our results with the aim of serving as a reference<br> for future in situ and ex situ experiments and field measurements exploring interactions between ants and poplars, specifically<br> in riparian ecosystems.en</p>
Data from: Understanding nutrient dynamics in an African savanna: local biotic interactions outweigh a major regional rainfall gradient
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Data from: Density and biotic interactions modify the combined effects of global and local stressors
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Data from: Biotic interactions and seed deposition rather than abiotic factors determine recruitment at elevational range limits of an alpine tree
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Data from: The interplay of nested biotic interactions and the abiotic environment regulates populations of a hypersymbiont
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Data for: Effects of biotic interactions on plant fecundity depend on spatial and functional structure of communities and time since disturbance
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Data from: Geographic variation of parasitic and predatory traces on mollusks in the northern Adriatic Sea, Italy: implications for the stratigraphic paleobiology of biotic interactions
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Data from: Process-based species pools reveal the hidden signature of biotic interactions amid the influence of temperature filtering
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Data from: Evidence of functional species sorting by rainfall and biotic interactions: A community monolith experimental approach
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Data from: Predicting biotic interactions and their variability in a changing environment
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Data from: Biotic interactions govern genetic adaptation to toxicants
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Links between prey assemblages and poison frog toxins: a landscape ecology approach to assess how biotic interactions affect species phenotypes
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Figure 1 from: Rasoloariniaina JR, Ganzhorn JU, Riemann JC, Raminosoa N (2016) Water quality and biotic interaction of two cavefish species: Typhleotris madagascariensis Petit, 1933 and Typhleotris mararybe Sparks & Chakrabarty, 2012, in the Mahafaly Plateau groundwater system, Madagascar. Subterranean Biology 18: 1-16. https://doi.org/10.3897/subtbiol.18.8321
Figure 1 - Study area and survey sites for Typhleotris spp.
The small RNA diversity from Medicago truncatula roots under biotic interactions evidences the environmental plasticity of the miRNAome
GEO Series GSE49226. Medicago truncatula. 23 samples. Type: Non-coding RNA profiling by high throughput sequencing.
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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.
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.
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.
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.
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.