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79 results for “plant plasticity”
Data from: Effects of plastic fragments on plant performance are mediated by soil properties and drought
<p>In recent years, the effects of plastic contamination on soil and plants have received growing attention. Plastic can affect soil water content and thus may interact with the effects of drought on soil and plants. However, the effects of plastic on soil are highly context-dependent, and interactions with drought have been hardly tested. We conducted two greenhouse experiments to test the combined effects of plastic fragments (of varying size and concentration), water availability and soil texture, on soil water content and performance of the plant <em>Arabidopsis thaliana</em>. Plastic fragments had stronger negative effects on soil water content in low water availability, and the shape of this response (linear <em>vs.</em> unimodal) was mediated by soil texture. Conversely, increasing concentration of plastic had positive effects on plant growth. We suggest that plastic fragments introduce fracture points within soil aggregates. This increases number and size of soil pores favoring water loss but also facilitating root growth. Our results suggest complex interactive effects of plastic and drought, that may lead to a decoupling of plant and soil response. These processes should be taken into account in ecological studies and agricultural practices.</p>
The terrestrial carnivorous plant Utricularia reniformis sheds light on environmental and life-form genome plasticity: Annotation, Gene Ontology and raw data
<p><strong>Description:</strong> In this work, we deeply sequenced (genome and transcriptome of different organs), assembled, and analyzed the 311-Mbp genome of the terrestrial carnivorous plant <em>U. reniformis</em> (Lentibulariaceae). This project presents great importance to the understanding of genomic, evolutive and functional aspects of<em> U. reniformis</em>, which may, with the next-generation sequencing and computational biology approaches shed light to a better understanding not only for the biology and evolution of <em>Utricularia</em> genus, but also for other genera and lineages of the Lentibulariaceae family. Here we present all the raw data generated, including annotation and gene ontology files.</p> <p><strong>External Information</strong></p> <p><a href="https://genomevolution.org/coge/GenomeInfo.pl?gid=54799">Genome Browser</a> avaliable at CoGe Portal (https://genomevolution.org/coge/GenomeInfo.pl?gid=54799)</p> <p><a href="http://https://www.ncbi.nlm.nih.gov/bioproject/290588">GenBank </a><a href="http://https://www.ncbi.nlm.nih.gov/bioproject/290588">Bioproject</a> (https://www.ncbi.nlm.nih.gov/bioproject/290588) for raw genomic and transcriptomic reads</p> <p><a href="https://bv.fapesp.br/en/auxilios/84264/genomics-and-transcriptomics-of-utricularia-reniformis-lentibulariaceae-an-evolutive-and-function/">FAPESP grant website</a> contaning the project abstract and other information.</p> <p><strong>Papers published related to <em>Utricularia reniformis</em> genome</strong></p> <pre><strong>[1]</strong> Silva SR, Diaz YC, Penha HA, Pinheiro DG, Fernandes CC, Miranda VF, MichaelTP, Varani AM. <strong>The Chloroplast Genome of Utricularia reniformis Sheds Light on the Evolution of the ndh Gene Complex of Terrestrial Carnivorous Plants from the Lentibulariaceae Family</strong>. PLoS One. 2016 Oct 20;11(10):e0165176. doi:<strong><a href="https://www.ncbi.nlm.nih.gov/pubmed/27764252">10.1371/journal.pone.0165176</a></strong>. </pre> <pre><strong>[2] </strong>Silva SR, Alvarenga DO, Aranguren Y, Penha HA, Fernandes CC, Pinheiro DG, Oliveira MT, Michael TP, Miranda VFO, Varani AM. <strong>The mitochondrial genome of the terrestrial carnivorous plant Utricularia reniformis (Lentibulariaceae): Structure, comparative analysis and evolutionary landmarks.</strong> PLoS One. 2017 Jul19;12(7):e0180484. doi: <strong><a href="https://www.ncbi.nlm.nih.gov/pubmed/28723946">10.1371/journal.pone.0180484</a></strong>.</pre> <pre><strong>[3] </strong>Silva SR, Moraes AP, Penha HA, Julião MHM, Domingues DS, Michael TP, Miranda VFO, Varani AM. <strong>The Terrestrial Carnivorous Plant Utricularia reniformis Sheds Light on Environmental and Life-Form Genome Plasticity.</strong> Int J Mol Sci. 2019 Dec 18;21(1). pii: E3. doi: <strong><a href="https://www.ncbi.nlm.nih.gov/pubmed/31861318">10.3390/ijms21010003</a></strong>.</pre> <p><strong>Acknowledgements</strong></p> <p>This work was supported by Sao Paulo Research Foundation FAPESP, Grant ID: [1325164-6]</p> <p> </p> <p><strong>---------------------------------------------------------</strong><br> <strong>FILES DESCRIPTION</strong><br> <strong>---------------------------------------------------------</strong><br> <br> ----------------<br> <strong>ANNOT-vFinal.sql: </strong>MySQL database containing all integrated annotation information of Urenif and Ugibba<br> ----------------<br> <strong>TABLE fields description</strong><br> gene_name gene name generated by EVidence Modeler + PASA<br> length gene lenght<br> status duplicate_gene_classifier status (0:singleton, 1:dispersed, 2:proximal, 3: tandem, 4:WGD)<br> product gene product <br> GOterms Blast2GO/OmicsBox GOterms<br> GO_mapping Blast2GO/OmicsBox GOterms derived from direct mapping (UniProt)<br> GO_annotation Blast2GO/OmicsBox annotated GOterms<br> GO_interpro Blast2GO/OmicsBox derived from InterProScan<br> EC Blast2GO/OmicsBox EC number<br> EC_name Blast2GO/OmicsBox enzyme name<br> NOG_annot EggNOG annotation description<br> NOG_EC EggNOG EC number<br> NOG_GO EggNOG GOterms<br> NOG_class EggNOG COG/KOG classfication<br> KEGG_Pathway EggNOG KEGG pathyways<br> KEGG_ko EggNOG KEGG ko<br> CAZy EggNOG CAZy enzymes<br> TAIR_gene Closest A. thaliana gene name (homologous) TAIR database lasted version<br> TAIR_annot Closest A. thaliana gene product (homologous) TAIR database lasted version <br> ortho MCL clustering among Vvinifera, Athaliana, and Slycopersicum (S:singleton, C: clustered, Y: shared)<br> ortho_two MCL clustering among Urenif and Ugibba (S:singleton, C: clustered, Y: shared)<br> -<br> -<br> ----------------<br> <strong>CEGs.zip </strong> 336 shared and concatenated CEGs from Urenif, U. gibba, Genlisea nigrocaulis, G. hispidula, G. aurea, G. pygmaea, and G. repens.<br> ----------------</p> <p><strong>ProcessRepeats_mod</strong> Modified version of RepeatMasker, ProcessRepeats script for detection of plant evolutionary lineages<br> ----------------</p> <p><strong>----------------------------------------------------------------------------------------------------------------------------------------------<br> <em>Utricularia gibba</em> files<br> ----------------------------------------------------------------------------------------------------------------------------------------------</strong><br> <strong>Ugibba</strong><strong>-no-masked.fa </strong> Ugibba genome excluding organellar genomes (provided by Lan et al., 2017)<br> <strong>Ugibba-softmasked.fa</strong> Ugibba genome RepeatMasker softmasked and excluding organellar genomes (provided by Lan et al., 2017)<br> <strong>Ug.collinearity </strong> MCScanX collinearity file<br> <strong>Ug-duplicates.txt</strong> MCScanX duplicate_gene_classifier short report<br> <strong>Ug.gene_type </strong> MCScanX duplicate_gene_classifier full report<br> <strong>Ug.tandem </strong> Ugibba tandem genes generated by MCScanX tool<br> <strong>Ugibba_annot.annot </strong> Blast2GO/OmicsBox annotation file (eudicotyledons filtered and Viridiplantae GOSlim) <strong>Ugibba_annot-</strong><strong>noclean</strong><strong>.</strong><strong>annot</strong><strong> </strong> Blast2GO/OmicsBox annotation file (not filtered)<br> <strong>Ugibba</strong><strong>.cDNA</strong> Ugibba cDNAs fasta file<br> <strong>Ugibba</strong><strong>.CDS </strong> Ugibba CDSs fasta file<br> <strong>Ugibba</strong><strong>-EVM.all-no-TEs-PASA-ANNOTATED.gff3</strong> Ugibba GFF3 file fully annotated (including gene products and GO terms)</p> <p><strong>Ugibba</strong><strong>-EVM.all-no-TEs-PASA.gff3</strong> Ugibba GFF3 file fully annotated (genes only)<br> <strong>Ugibba_export.txt</strong> Blast2GO/OmicsBox full exported table<br> <strong>Ugibba_fasta.fasta</strong> Blast2GO/OmicsBox Ugibba fasta proteins containg annotation (product and GO terms)<br> <strong>ugibba_frozen_cleaned-validated.box</strong> Full Blast2GO/OmicsBox file</p> <p><strong>ugibba_frozen.box</strong> Full Blast2GO/OmicsBox file (containing TEs genes annotation)</p> <p><strong>ugibba_nogs_emapper_annotations.box</strong> Full Blast2GO/OmicsBox EggNOG file (containing TEs genes annotation)</p> <p><strong>Ugibba_GAF.txt</strong> GAF file<br> <strong>Ugibba</strong><strong>.gene</strong> Ugibba gene fasta file<br> <strong>Ugibba_GOstat.txt </strong> GOstat file<br> <strong>Ugibba</strong><strong>-PASA-assemblies.fasta </strong> Ugibba PASA assemblies<br> <strong>Ugibba</strong><strong>-PASA.stats </strong> Ugibba annotation STATS<br> <strong>Ugibba</strong><strong>.</strong><strong>prot</strong><strong> </strong> Ugibba protein fasta file<br> <strong>Ugibba</strong><strong>-RepeatMasker.gff </strong> Ugibba RepeatMasker gff file<br> <strong>Ugibba</strong><strong>-RepeatMasker.gff3 </strong> Ugibba RepeatMasker gff3 file<br> <strong>Ugibba</strong><strong>-RepeatMasker.tbl </strong> Ugibba RepeatMasker results<br> <strong>Ugibba</strong><strong>-RepeatMasker-v2.gff3</strong> Ugibba RepeatMasker gff3 second version file<br> <strong>Ugibba</strong><strong>-RNAseq-assembled.fasta </strong> Ugibba RNAseq assembled transcriptome (Trinity)<br> <strong>Ugibba_TEs_DANTE_2019.fa </strong> Ugibba TEs library, detected by REPET and annotated by PASTEC and DANTE<br> <strong>Ugibba_WEGO.txt </strong> WEGO file</p> <p><strong>----------------------------------------------------------------------------------------------------------------------------------------------<br> <em>Utricularia reniformis</em> files<br> ----------------------------------------------------------------------------------------------------------------------------------------------</strong><br> <strong>Urenif</strong><strong>-no-masked.fa </strong> Urenif genome excluding organellar genomes<br> <strong>Urenif</strong><strong>-</strong><strong>softmasked</strong><strong>.fa</strong> Urenif genome RepeatMasker softmasked and excluding organellar genomes<br> <strong>Ur.collinearity </strong> MCScanX collinearity file<br> <strong>Ur-duplicates.txt </strong> MCScanX duplicate_gene_classifier short report<br> <strong>Ur.gene_type</strong> MCScanX duplicate_gene_classifier full report<br> <strong>Ur.tandem</strong> Urenif tandem genes generated by MCScanX tool<br> <strong>Urenif_annot.annot</strong> Blast2GO/OmicsBox annotation file (eudicotyledons filtered and Viridiplantae GOSlim)<br> <strong>Urenif_annot-</strong><strong>noclean</strong><strong>.</strong><strong>annot</strong> Blast2GO/OmicsBox annotation file (not filtered)<br> <strong>Urenif</strong><strong>.cDNA</strong> Urenif cDNAs fasta file<br> <strong>Urenif</strong><strong>.CDS </strong> Urenif cDNAs fasta file<br> <strong>Urenif</strong><strong>-EVM.all-no-TEs-PASA-ANNOTATED.gff3</strong> Urenif GFF3 file fully annotated (including gene products and GO terms)</p> <p><strong>Urenif</strong><strong>-EVM.all-no-TEs-PASA.gff3</strong> Urenif GFF3 file fully annotated (genes only)<br> <strong>Urenif_export.txt</strong> Blast2GO/OmicsBox full exported table<br> <strong>Urenif_fasta.fasta</strong> Blast2GO/OmicsBox Urenif fasta proteins containg annotation (product and GO terms)<br> <strong>urenif_frozen_cleaned-validated.box</strong> Full Blast2GO/OmicsBox file</p> <p><strong>urenif_frozen.box</strong> Full Blast2GO/OmicsBox file (containing TEs genes annotation)</p> <p><strong>urenif_nogs_emapper_annotations.box</strong> Full Blast2GO/OmicsBox EggNOG file (containing TEs genes annotation)<br> <strong>Urenif_GAF.txt </strong> GAF file<br> <strong>Urenif</strong><strong>.gene</strong> Urenif gene fasta file<br> <strong>Urenif_GOStat.txt </strong> GOstat file<br> <strong>Urenif</strong><strong>-PASA-assemblies.fasta</strong> Urenif PASA assemblies<br> <strong>Urenif</strong><strong>-PASA.stats </strong> Urenif annotation STATS<br> <strong>Urenif</strong><strong>.</strong><strong>prot</strong><strong> </strong> Urenif protein fasta file<br> <strong>Urenif</strong><strong>-RepeatMasker.gff </strong> Urenif RepeatMasker gff file<br> <strong>Urenif</strong><strong>-RepeatMasker.gff3 </strong> Urenif RepeatMasker gff3 file<br> <strong>Urenif</strong><strong>-RepeatMasker.tbl </strong> Urenif RepeatMasker results<br> <strong>Urenif</strong><strong>-RepeatMasker-v2.gff3 </strong> Urenif RepeatMasker gff3 second version file<br> <strong>Urenif</strong><strong>-RNAseq-assembled.fasta </strong> Urenif RNAseq assembled transcriptome (Trinity)<br> <strong>Urenif_TEs_DANTE_2019.fa </strong> Urenif TEs library, detected by REPET and annotated by PASTEC and DANTE<br> <strong>Urenif_WEGO.txt </strong> WEGO file<br> <strong>----------------------------------------------------------------------------------------------------------------------------------------------<br> ----------------------------------------------------------------------------------------------------------------------------------------------</strong></p>
Code and Data for: "Signs of local adaptation and phenotypic plastic response to elevation shifted between environmental backgrounds in Snapdragon plants"
<p>Code and data for manuscript: "Signs of local adaptation and phenotypic plastic response to elevation shifted between environmental backgrounds in Snapdragon plants"</p>
ARCHIMED-φ simulation files for the simulation of Design A from the article "When architectural plasticity fails to counter the light competition imposed by planting design: an in silico approach using a functional-structural model of oil palm"; in silico Plants journal
<p>Input files for the simulation of Design A in ARCHIMED-φ from the article "When architectural plasticity fails to counter the light competition imposed by planting design: an in silico approach using a functional-structural model of oil palm"; in silico Plants journal.</p> <p>See https://archimed-platform.github.io/archimed-phys-user-doc/ for more details on the model.</p> <p>Make a simulation by opening a terminal at the root of the folder and type: `java -jar .\archimed-phys.jar .\DesignA_MockUpA_seed1_MAP_72.yml`.</p>
Plant responses to urban gradients: extinction, plasticity, adaptation
<p><span>Individual functional traits (LMA – leaf mass per area, plant height and flower length), population performance traits (seed mass and germination rate), as well as species frequency in the plant community, of four herbaceous plant species present in the metropolitan area of Strasbourg: Dactylis glomerata, Medicago lupulina, Plantago lanceolata, Trifolium pratense. Traits were measured <em>in situ</em> at 60 mesophilic herbaceous sites, and <em>ex situ</em> in a common garden experiment in the Botanical Garden of the University of Strasbourg. Environmental data include mowing frequency, soil characteristics (composition and structure), air temperature, air humidity, and surrounding landscape variables: mean building height, population density, NDVI, road density, and distance to the city center. <br></span></p>
Data from: Soil microbes influence the ecology and evolution of plant plasticity
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Data from: Testing the evolutionary potential of an alpine plant: Phenotypic plasticity in response to growth temperature outweighs parental environmental effects and other genetic causes of variation
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Local thermal extremes shape the nature of herbivore plasticity that controls plant communities
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Data from: Phenological plasticity is a poor predictor of subalpine plant population performance following experimental climate change
<p>Phenological shifts, changes in the seasonal timing of life cycle events, are among the best documented responses of species to climate change. However, the consequences of these phenological shifts for population dynamics remain unclear. Population growth could be enhanced if species that advance their phenology benefit from longer growing seasons and gain a pre-emptive advantage in resource competition. However, it might also be reduced if phenological advances increase exposure to stresses, such as herbivores and, in colder climates, harsh abiotic conditions early in the growing season. We exposed subalpine grasslands to ~ 3 K of warming by transplanting intact turfs from 2000 m to 1400 m elevation in the eastern Swiss Alps, with turfs transplanted within the 2000 m site acting as a control.<i> </i>In the first growing season after transplantation, we recorded species' flowering phenology at both elevations. We also measured species' cover change for three consecutive years as a measure of plant performance. We used models to estimate species' phenological plasticity (the response of flowering time to the change in climate) and analysed its relationship with cover changes following climate change. The phenological plasticity of the 18 species in our study varied widely but was unrelated to their changes in cover. Moreover, early- and late-flowering species did not differ in their cover response to warming, nor in the relationship between cover changes and phenological plasticity. These results were replicated in a similar transplant experiment within the same subalpine community, established one year earlier and using larger turfs. We discuss the various ecological processes that can be affected by phenological shifts, and argue why the population-level consequences of these shifts are likely to be species- and context-specific. Our results highlight the importance of testing assumptions about how warming-induced changes in phenotypic traits, like phenology, impact population dynamics.</p>
Data from: Plasticity of plant defense and its evolutionary implications in wild populations of Boechera stricta
Phenotypic plasticity is thought to impact evolutionary trajectories by shifting trait values in a direction that is either favored by natural selection ("adaptive plasticity") or disfavored ("nonadaptive" plasticity). However, it is unclear how commonly each of these types of plasticity occurs in natural populations. To answer this question, we measured glucosinolate defensive chemistry and reproductive fitness in over 1,500 individuals of the wild perennial mustard Boechera stricta, planted in four common gardens across central Idaho, USA. Glucosinolate profiles—including total glucosinolate concentration as well as the relative abundances and overall diversity of different compounds—were strongly plastic both among habitats and within habitats. Patterns of glucosinolate plasticity varied greatly among genotypes. Plasticity among sites was predicted to affect fitness in 27.1% of cases; more often than expected by chance, glucosinolate plasticity increased rather than decreased relative fitness. In contrast, we found no evidence for within-habitat selection on glucosinolate reaction norm slopes (i.e., plasticity along a continuous environmental gradient). Together, our results indicate that glucosinolate plasticity may improve the ability of B. stricta populations to persist after migration to new habitats.
Data from: Adaptive responses and transgenerational plasticity of a submerged plant to benthivorous fish disturbance
<p>Benthivorous fish dominance in some subtropical lakes may alter submerged plant growth, reproduction, and progeny germination by changing water-submerged plant-algae interactions. We conducted mesocosm experiments to examine the effects of three densities of benthivorous fish, <em>Misgurnus anguillicaudatus</em>, on the water properties, the growth, asexual reproduction, and the germination of turions of <em>Potamogeton crispus</em> L.</p> <p>The dataset includes water environment characteristics, macrophyte traits, algae traits, and sediment nutrient characteristics. Macrophyte traits include morphological, stoichiometric, turion traits, and germination traits.</p>
Climate-induced plasticity in leaf traits of riparian plants
<p><strong>Aim:</strong> Leaf inputs from riparian vegetation and its decomposition play a key role in energy and nutrients transfer in many stream ecosystems. Instream leaf-litter decomposition is mainly driven by leaf traits. Therefore, understanding and predicting leaf traits variation with current environmental changes and its putative effects on stream food webs is a critical challenge. Most studies have focused on the assumed higher interspecific leaf traits variability, with little research addressing an intraspecific perspective.</p> <p><strong>Location:</strong> Andalusia, Spain</p> <p><strong>Methods:</strong> We assessed the relative effects of climate and soil on the intraspecific variability in leaf traits of four common woody riparian species in permanent low-order Mediterranean streams along a wide aridity gradient. We used a space-for-time substitution approach to predict leaf traits changes and consequences for stream food webs in a future climate change scenario.</p> <p><strong>Results:</strong> We found that climate had a major influence on intraspecific variability of leaf traits, but with opposite patterns depending on plant functional type. Results indicated that leaf quality—linked to palatability and decomposability—of Alnus glutinosa, Salix atrocinerea and Rubus ulmifolius (deciduous/semideciduous) will decrease with the forecasted aridification, whereas that of the evergreen Nerium oleander will increase.</p> <p><strong>Main conclusions:</strong> Our findings suggest a decrease of intraspecific leaf-quality in riparian deciduous species with global warming in a relatively short term, which, in a longer term, may add to the forecasted dieback of deciduous species in riparian corridors of temperate climate zones. These forecasted changes have the potential to significantly impair ecosystem functioning of Mediterranean mountain streams currently under deciduous gallery forests.</p>
Plastic mulch film residues in agriculture: impact on soil suppressiveness, plant growth, and microbial communities
<p>Plastic mulch film residues have been accumulating in agricultural soils for decades, but so far, little is known about its consequences on soil microbial communities and functions. Here, we tested the effects of plastic residues of low-density polyethylene and biodegradable mulch films on soil suppressiveness and microbial community composition. We investigated how plastic residues in a Fusarium culmorum suppressive soil affect the level of disease suppressiveness, plant biomass, nutrient status, and microbial communities in rhizosphere using a controlled pot experiment. The addition of 1% plastic residues to the suppressive soil did not affect the level of suppression and the disease symptoms index. However, we did find that plant biomasses decreased, and that plant nutrient status changed in the presence of plastic residues. No significant changes in bacterial and fungal rhizosphere communities were observed. Nonetheless, bacterial and fungal communities closely attached to the plastisphere were very different from the rhizosphere communities with overrepresentation of potential plant pathogens. The plastisphere revealed a high abundance of specific bacterial phyla (Actinobacteria, Bacteroidetes, and Proteobacteria) and fungal genera (Rhizoctonia and Arthrobotrys). Our work revealed new insights and raises emerging questions for further studies on the impact of microplastics on the agroecosystems.</p>
Data from: Associations between developmental stability, canalization and phenotypic plasticity in plants with temporally heterogeneous environmental experience
<p>We subjected eight plant species to a first round of alternating inundation and drought vs. constantly moderate water treatments and a second round of water conditions. Fluctuating asymmetry (FA), intra- and inter-individual variations (CV<sub>intra</sub> and CV<sub>inter</sub>), and plasticity in traits were measured and correlations between variables were calculated for each species. Early temporally heterogeneous experience decreased the leaf size of half of the species, but had complex effects on leaf fluctuating asymmetry (FA) and inter-individual variation (CV<sub>inter</sub>) in traits immediately or in late conditions, with little effects on intra-individual variation (CV<sub>intra</sub>). There were several positive correlations between FA and CV<sub>inter</sub>, while there were correlations between CV<sub>inter</sub> and plasticity in early treatments, but negative ones in late treatments.</p>
Evolutionary and plastic changes in a native annual plant after a historic drought
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Climate-induced plasticity in leaf traits of riparian plants
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Data from: Plasticity of plant defense and its evolutionary implications in wild populations of Boechera stricta
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Data from: Phenotypic integration limits the variation in plant phenotypic plasticity among traits: a meta-analysis
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Data from: Phenotypic plasticity accounts for changes in plant phosphorus-acquisition strategies from mining to scavenging along a gradient of soil phosphorus availability in South American Campos grasslands
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Data and code from: Temperature affects the relative importance of phenotypic plasticity and natural selection contributing to the niche breadth of invasive plants
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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)
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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.
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