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721 results for “ABI”

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zenodo40/100

Abies alba Miller (BR0000012558872)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0Dec 2018View details →
zenodo40/100

Abies alba Miller (BR0000024495981)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0Dec 2018View details →
zenodo40/100

Abies alba Miller (BR0000024496018)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0Dec 2018View details →
zenodo40/100

Abies alba Miller (BR0000009463493)

<p>Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.</p>

opencc-by-sa-4.0Dec 2018View details →
zenodo40/100

Abies alba Miller (BR0000009462960)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0Dec 2018View details →
zenodo40/100

Abies amabilis Douglas ex J.Forbes (BR0000009238145)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0Dec 2018View details →
zenodo40/100

Abies alba Miller (BR0000024495974)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0Dec 2018View details →
zenodo40/100

Abies alba Miller (BR0000015233622V)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0Dec 2018View details →
zenodo40/100

Abies amabilis Douglas ex J.Forbes (BR0000024496117)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0Dec 2018View details →
zenodo40/100

Abies amabilis Douglas ex J.Forbes (BR0000024496100)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0Dec 2018View details →
zenodo40/100

Abies alba Miller (BR0000009305885)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0Dec 2018View details →
dryad40/100

Ecoregion and community structure influences on the foliar elemental niche of balsam fir (Abies balsamea (L.) Mill.) and white birch (Betula papyrifera Marshall)

Open the record for dataset details and reuse information.

publicAug 2022View details →
dryad40/100

Data from: Bioelectrical synchronization of Picea abies during a solar eclipse

Open the record for dataset details and reuse information.

publicMay 2025View details →
dryad36/100

Adaptation to drought is coupled with slow growth, but independent from phenology in marginal silver fir (Abies alba Mill.) populations

Drought is one of the most important selection pressures for forest trees in the context of climate change. Yet, the different evolutionary mechanisms, and their environmental drivers, by which certain populations become more drought tolerant than others is still little understood. We studied adaptation to drought in 16 silver fir (<i>Abies alba</i> Mill.) populations from the French Mediterranean Alps by combining observations on seedlings from a large scale greenhouse experiment (N=8199) and on adult tress in situ (N=315). In the greenhouse, we followed half-sib families for four growing seasons for growth traits and bud break phenology, and tested their water stress response in a "drought until death" experiment. Adult trees in the field were assessed for δ<sup>13</sup>C, a proxy for water use efficiency and genotyped at 357 SNP loci. SNP data was used to generate a null expectation for trait divergence between populations to detect the signature of selection, and 31 environmental variables to identify the selective environment. We found that seedlings originating from populations with low soil water capacity grew more slowly, attained a smaller stature, and resisted the water stress treatment for a longer period of time in the greenhouse. Additionally, adult trees of these populations exhibited a higher water use efficiency as evidenced by δ<sup>13</sup>C. These results suggest a correlated evolution of the growth-drought tolerance trait complex. Population divergence in bud break phenology was adaptive only in the second growing season, and evolved independently from the growth-drought tolerance trait complex. Adaptive divergence in bud break phenology was principally driven by the inter- and intra-annual variation in temperature at the geographic origin of the population. Our results illustrate the different evolutionary strategies used by populations to cope with drought stress at the range limits across a highly heterogeneous landscape, and can be used to inform assisted migration programs.

opencc-zeroMay 2020View details →
zenodo36/100

Selection for 2nd generation plus tree in Abies sachalinensis in eastern Hokkaido, Japan

<p>Data description (update; 6 July, 2015)</p> <p>Head title of &quot;Abies_A-38data.xlsx&quot; file</p> <p>(column) ; (description)<br /> ID ; individual numbering of all 700 trees<br /> Rep (Block) ; three replicates (blocks) in studied site, A-38<br /> Mother tree (Plus tree) ; name of mother trees that was resistrated as the &quot;1st-generation&quot; plus tree. Each name was composed of the name of the city where the plus tree was selected and its series number.<br /> &nbsp; &nbsp; &nbsp;---Containing---<br /> &nbsp; &nbsp; &nbsp;Akkeshi#, Kitami#, Ikeda#, Urahoro#, Urakawa#, Okoppe#, Bifuka#, Nayoro#, Iwamizawa#, Rumoi#, Tomakomai#<br /> Moth. ID ; individual numbering of mother trees. This number has been used in the field survey of A-38 site.<br /> Origin ; provenance region of the mother tree&nbsp;<br /> &nbsp; &nbsp; &nbsp;---Containing---<br /> &nbsp; &nbsp; &nbsp;Peripheral East, East, South, North, West<br /> Tree No. ; the numbering of trees per a mother tree within the replicates<br /> Position ; spatial position of the planting trees (&quot;edge&quot;, &quot;0&quot;; not edge of the block)<br /> Tagged label No. ; label number tagged on each trunk of the tree. This number has been used in the field survey.</p> <p>DBH_35year ; diameter of breast height (DBH, cm) at 35 year after plantation<br /> H_35year ; tree height (m) at 35 year after plantation<br /> V_35year ; estimated trunk volume (m^3) at 35 year after plantation<br /> pilodyn ; inserted depth of pilodyn (mm)<br /> df ; multiple value of DBH and a resonance frequency (df value, cm*kHz)</p> <p>Breeding value for V ; estimated breeding value for the trunk volume (m^3)<br /> Breeding value for pilodyn ; estimated breeding value for the pilodyn (mm)<br /> Breeding value for df; estimated breeding value for the df value (cm*kHz)<br /> Select1 for V; result of 1st selection for the trunk volume (1; selected, 0; not selected)<br /> Select1 for pilodyn; result of 1st selection for pilodyn (1; selected, 0; not selected)<br /> Select1 for df; result of 1st selection for the df value (1; selected, 0; not selected)<br /> select2 for V; result of 2nd selection for the trunk volume (1; selected, 0; not selected)<br /> select2 for pilodyn; result of 2nd selection for pilodyn (1; selected, 0; not selected)<br /> select2 for df; result of 2nd selection for the df value (1; selected, 0; not selected)<br /> Select for traits; summary of the results of 1st and 2nd selection for all traits (1; selected, 0; not selected)<br /> Result of selection ; final result of the selection after considering the number of individuals selected per mother tree (finally, 45 trees were remained)</p> <p><br /> Dr. Wataru Ishizuka has contributed to data collection.</p>

opencc-zeroJul 2015View details →
dryad36/100

Short-term effects of continuous cover forestry on forest biomass production and biodiversity: Applying single-tree selection in forests dominated by Picea abies

AbstractThe rotation forestry system provides high biomass production, but could also have a negative impact on species sensitive to disturbance. Continuous cover forestry (CCF) could contribute to solving these conflicting goals, but its feasibility in nutrient limited boreal forests is yet unresolved. In a unique experiment, we simultaneously assessed the short-term effect of single-tree selection on both biomass production and biodiversity (vascular plants, bryophytes, wood-inhabiting fungi), and tested fertilization as a way to mediate growth-biodiversity trade-offs. We found that unharvested stands and stands subjected to single-tree selection had a similar species assemblage of vascular plants, bryophytes, and wood-inhabiting fungi. Fertilization increased growth by 37% and induced shifts in two understory species (favoring the grass Avenella flexuosa and disfavoring the bryophyte Hylocomium splendens). We conclude that single-tree selection may become a useful tool to enhance biodiversity in managed forests.

opencc-zeroJun 2022View details →
zenodo36/100

Abies concolor (Pinaceae) - cone - female - closed

Image of Abies concolor (Pinaceae) - cone - female - closed

opencc-by-4.0Dec 2009View details →
dryad36/100

Circular genetic structure of the Abies nephrolepis species complex shaped by the circular landform of Northeast Asia

<p>Aim:</p> <p>Pinaceae have been noted for their tendency towards reticulation as a result of interspecific hybridization. Here, we demonstrated the phylogeographic dynamics of the native Northeast Asian sub-alpine conifer, <em>Abies nephrolepis</em> species complex (ANSC), evolving in circular overlaps along the Northeast Asian landform, which functions as a corridor with the sea, thus acting as a geographic barrier.</p> <p>Location: Northeast Asia: the Korean Peninsula, Japanese Archipelago, Russian Far East, and northeastern China</p> <p>Taxon:<em> Abies nephrolepis</em> species complex (Family Pinaceae, Genus <em>Abies</em>, Section <em>Balsamea</em>, <em>Abies nephrolepis, A. koreana, A. veitchii</em>, and<em> A. sachalinensis</em>)</p> <p>Methods: A total of 728 individuals from 38 ANSC populations were analysed using multiplexed inter-simple sequence repeat genotyping by sequencing to capture variations in bi-parental nuclear genomes. Eight mitochondrial regions and eight chloroplast regions of each individual were sequenced using the MiSeq platform and Sanger sequencing. Species distribution models were generated.</p> <p>Results: Bayesian clustering with 507 nuclear single nucleotide polymorphisms and the discrepancy between cytoplasmic and nuclear genome lineages implied contemporary and ancient connections between neighbouring species in the form of circular overlap. This genetic connectivity was supported by principal component analysis. Strong correlations between genetic distance and geographic distance were observed, suggesting that gene flow occurs through a continuous chain around the sea. We also found that gene flow direction and intensity changed over time, with support from paleodistribution modelling.</p> <p>Conclusion: Past hybridization events were captured in cytoplasmic genomes, generating heterogeneity across maternal ancestries. This intensive phylogeographic study demonstrates speciation with incomplete reproductive isolation (continuous gene flow) among neighbouring species with an alteration of the direction and intensity of gene flow due to climate change. The divergence of ANSC due to repeated isolation and reconnection caused by heterogenous physiological environments and climate fluctuation provides a model to solve evolutionary scenarios for reticulate evolution in Pinaceae and other plants.</p>

opencc-zeroMay 2024View details →
dryad36/100

TreeGrow - Data from: Morphology, bud burst and root fungal communities of Norway spruces (Picea abies)

<p>Our study delved into the relationship between root-associated fungi, gene expression and plant morphology in Norway spruce cuttings derived from both slow-and fast-growing trees. We found no clear link between the gene expression patterns of adventitious roots and the growth phenotype, suggesting no fundamental differences in the receptiveness to fungal symbionts between the phenotypes. Interestingly, saplings from slow-growing parental trees exhibited a higher richness of ectomycorrhizal species and larger roots. Some ectomycorrhizal species, typically found on mature spruces, were more prevalent on saplings from slow-growing spruces. The ericoid mycorrhizal fungus, Hyaloscypha hepaticola, showed a stronger association with saplings from fast-growing spruces. Moreover, saplings from slow-growing spruces had a greater number of Ascomycete taxa and free-living saprotrophic fungi. Aboveground sapling stems displayed some phenotypic variation; saplings from fast-growing phenotypes had longer branches but fewer whorls in their stems compared to those from the slow-growing group. In conclusion, the observed root-associated fungi and phenotypic characteristics in young Norway spruces may play a role in their long-term growth rate. This suggests that the early interactions between spruces and fungi could potentially influence their growth trajectory.</p>

opencc-zeroJun 2024View details →
zenodo36/100

Is tree age or tree size reducing height increment in Abies alba Mill. at its southernmost distribution limit?

<p>Many factors limit height increment of trees when age and size increase in large-statured tree species. Height-diameter allometric relationships are commonly used measures of tree growth.</p> <p>The data were collected in a silver fir forest located in Southern Italy, at the southernmost distribution limit for this species. Through a stratified random sampling, 100 trees were selected. All the selected trees were then felled and the total tree height, height increments (internode distances), diameter at breast height, and diameter increments (ring widths) were measured.</p> <p>Conventional methods for estimating the current annual increment of stand volume are based on the uncertain assumption that height increment decreases with tree age. Conversely, size, rather than age, should be accounted for the observed senescence-related declines in relative growth rate and, consequently, implemented in silvicultural manuals. Results stem from a study on Abies alba Mill. at its southern limit of distribution.</p>

opencc-by-4.0Dec 2018View 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