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30 results for “tree characteristics”

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zenodo32/100

FIG. 8. Bayesian tree inferred from 18S in Analyses of morphological and molecular characteristics of Telotylenchinae from Iran point at the validity of the genera Bitylenchus and Sauertylenchus

FIG. 8. Bayesian tree inferred from 18S rDNA sequences. Posterior probabilities (pp) exceeding 0.65 are given on appropriate clades, bifurcations with pp above 0.95 are considered to be well-supported. Nematode species and GenBank numbers are listed for each taxon. In bold: newly generated 18S rDNA sequences. With regard to Telotylenchinae Clades (indicated in Roman figures) we adhered to Handoo et al. (2014).

opennotspecifiedAug 2022View details →
dryad32/100

Density and characteristics of tree cavities inside and outside Volcanoes National Park, Rwanda

<p>Tree cavities, formed by animal excavation or processes of fungal decay and mechanical damage, may provide nesting, roosting, or resting opportunities to many invertebrate and vertebrate species. Although cavity availability has been linked to patterns of biodiversity and ecosystem functioning elsewhere, there have been few such studies in the Afrotropics. Here, we present a baseline survey of cavity availability inside the high elevation (<span>2,200</span>–<span>3,714 </span>m) Afromontane forest ecosystems of Volcanoes National Park (VNP), Rwanda. We aimed to provide such reference data in the form of summary statistics on cavity density and characteristics in a collection of 400 m<sup>2</sup> plots that together cover 8.8 ha inside and 0.68 ha outside VNP. We also explored the relative importance of fungal decay vs. excavators in the formation of cavities, tested for the relative role of standing dead trees and living trees as cavity substrates, considered differences in diameter and height between cavity-bearing trees and trees without cavities, determined the orientation of cavity entrances, and tested whether cavity density varies across elevation. We found 109 cavities in 52 cavity-bearing trees (dominated by <em>Hagenia</em> <em>abyssinica</em>) inside VNP, for a density of 12.4 cavities and 5.9 cavity-bearing trees per hectare, and none outside the park. More cavities were decay-formed (n = 90) than excavated (n = 19) and though most cavities were found in living trees (n = 44) the number of cavities in dead trees (n = 8) was high relative to dead tree substrate availability. We also found that cavity-bearing trees were larger than those without cavities, that excavated cavities were predominantly oriented towards the southeast and decay-formed cavities to the northeast, and that cavity density peaked near ~3,000 m. Our results show that large and dead trees of particular species are important cavity substrates that need to be given attention in conservation and management as is clearly illustrated by the lack of cavities in the highly managed Eucalyptus stands outside VNP.</p>

opencc-zeroAug 2023View details →
dryad32/100

Density and characteristics of tree cavities inside and outside Volcanoes National Park, Rwanda

Open the record for dataset details and reuse information.

publicAug 2023View details →
dryad32/100

Data from: Seed quality and seed quantity in red maple depends on weather and individual tree characteristics

Open the record for dataset details and reuse information.

publicJan 2021View details →
dryad32/100

Data from: Long term impacts of selective logging on two Amazonian tree species with contrasting ecological and reproductive characteristics: inferences from Eco-gene model simulations

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publicDec 2013View details →
dryad32/100

Characteristics of households that were interviewed in a study that investigated factors driving tree species in cocoa farms in Cote d'Ivoire

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publicNov 2020View details →
dryad28/100

Data from: Sylleptic branching in winter-headed apple (Malus × domestica) trees: accession-dependent responses and their relationships with other tree architectural characteristics

Well-feathered apple trees are essential for commercial orchards to optimize yields. However, most cultivars do not form these sylleptic branches readily in commercial nurseries due to high apical dominance. Several treatments exist to promote their formation in the nurseries, one of which is heading. However, not all cultivars are expected to react similarly to these treatments. We studied the branching response of 155 genotypes following heading and its relation to other architectural traits as a function of the cultivar's genetic background. Trees were grown for two consecutive years after grafting in a nursery, and the main axes were headed in the winter following growth in year 1. After heading, a single shoot was retained when growth resumed in the second year. Plant architectural traits such as growth of the main shoot, internode length, sylleptic branching, etc. were measured before and after heading and were statistically compared using a mixed model. This model showed the effect of heading for all architectural traits studied. In addition significant genotype and genotype × treatment interactions were found. In general, genotypes that showed a more vigorous growth during the first year also reacted more vigorously to heading. Accounting for the genetic substructure of this collection, no clear distinction in tree response could be found except in a small group of individuals that belonged to an F1 mapping population. This study shows that heading is not favorable for all genotypes to promote sufficient sylleptic branching and that other methods are needed to promote branching in these accessions.

opencc-zeroDec 2015View details →
dryad28/100

Data from: Sylleptic branching in winter-headed apple (Malus × domestica) trees: accession-dependent responses and their relationships with other tree architectural characteristics

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publicDec 2016View details →
geo24/100

A single-nucleus transcriptomic atlas reveals cellular and genetic characteristics in the hippocampus of natural aging-inducing Alzheimer’s disease tree shrews

GEO Series GSE235838. Tupaia belangeri. 6 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenMar 2025View details →
geo16/100

Transcriptome analysis of Botrytis cinerea in response to tea tree oil and its two characteristic components

GEO Series GSE138291. Botrytis cinerea. 15 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenOct 2019View 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