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4,568 results for “planting year”
Assessing Plant Phenological Patterns in the Eastern United States Over the Last 120 Years
Phenology is a key biological trait of an organism’s success and is one of the best indicators of its response to recent climate change. Plants are among the most well-studied organisms in this regard, but observational data bearing on this topic are largely restricted to woody species of the northern hemisphere, mostly from ca. the last three decades. Recent research has demonstrated that mobilized online herbarium specimens provide important, albeit mostly neglected, information on plant phenology. Here, we use the web tool CrowdCurio to crowdsource phenological data from more than 10,000 herbarium specimens representing 30 flowering plant species broadly distributed across the eastern United States. Our results, spanning 120 years and generated from over 2,000 crowdsourcers, clarify numerous aspects of plant phenology. First, they reveal that plant reproductive phenology is significantly advancing in response to warming, which is consistent with previous studies. Second, among those species with broad latitudinal ranges, populations from more southern latitudes are significantly more phenologically sensitive to temperature than those from northern populations. Last, contrary to some recent findings, plants in warmer, less variable climates may be much more dynamic, on average, in their phenological sensitivity. Our results are robust to a variety of confounding factors and span large phylogenetic distances and myriad life histories. These may represent more global trends in the latitudinal gradient of phenological response with myriad potential ecological and evolutionary consequences, and leads us to hypothesize that phenological sensitivity across species' ranges is driven by adaptation to local climates.
The Biomass and Plant Functional Traits of Leymus chinensis Affected by Genotypic Diversity and Soil Nitrogen Addition through a Two-year Experiment, Tianjin, China, 2021-2023
In order to investigate the effects of soil nitrogen addition on the genotypic diversity of Leymus chinensis, 12 genotypes of Leymus chinensis were used as plant material and a two-factor experimental design was carried out in this study. Factor one was genotypic diversity of L. chinensis, including three levels: mono-genotype (G1), three genotypes (G3), and six genotypes (G6). Factor two was the soil nitrogen addition level, which included four levels: no nitrogen addition (N0), 2.5 g N/(m²·a) nitrogen application (N2.5), 5 g N/(m²·a) nitrogen application (N5), and 10 g N/(m²·a) nitrogen application (N10). Each treatment had 12 combinations as replicates, and 12 genotypes of L. chinensis were used. The frequency of each genotype was standardized across all treatment levels of genotypic diversity × soil nitrogen addition. The experiment commenced in September 2021 and soil nitrogen was applied every 2 months. Plants were cultivated in the experimental field at Nankai University, but were moved to a greenhouse for overwintering from November to February each year. During the experiment, there were no stresses or disturbances such as shading, drought, or insect feeding; weeds were regularly removed.
Multi-year census of arthropod abundance on the plant Ligusticum porteri near Gothic, CO
The purpose of this study was to track year-to-year variation in aphid abundance on the host plant Ligusticum porteri (Apiaceae). We censused arthropod abundance on the flowering stalks of L. porteri weekly in June-August from 2012 to 2022. The censuses took place in ten L. porteri populations near the Rocky Mountain Biological Laboratory in Gothic, CO. While the same populations were used across years, we randomly selected ten flowering plants in each population in each year (N = 100 plants per year). Observations focused on colonization by the aphid Aphis asclepiadis, its mutualist ants, and natural enemies. When found, we counted other arthropods as well, identifying them to Family or Order in the field. We also counted the number of host plant flowering stalks and inflorescences (umbel). In 2016, we began tracking flowering phenology using a numerical score (0-8). To track senescence, we used a qualitative score (TB=turning brown and AB=all brown) for terminal and primary umbels.
Multi-year census of arthropod abundance on the plant Ligusticum porteri near Crested Butte, CO
The purpose of this study was to track year-to-year variation in aphid abundance on the host plant Ligusticum porteri (Apiaceae). We censused arthropod abundance on the flowering stalks of L. porteri weekly in June-August from 2017 to 2022. The censuses took place in ten L. porteri populations near Crested Butte, CO. The sites were by Brush Creek, Lake Irwin, and Washington Gulch. While the same populations were used across years, we randomly selected ten flowering plants in each population in each year (N = 100 plants per year). Observations focused on colonization by the aphid Aphis asclepiadis, its mutualist ants, and natural enemies. When found, we counted other arthropods as well, identifying them to Family or Order in the field. We also counted the number of host plant flowering stalks and inflorescences (umbel). We tracked flowering phenology using a numerical score (0-8). To track senescence, we used a qualitative score (TB=turning brown and AB=all brown) for terminal and primary umbels.
Carbon and nitrogen isotopes and concentrations in terrestrial plants from a six-year (2006-2012) fertilization experiment at the Arctic LTER, Toolik Field Station, Alaska.
The data set describes stable carbon and nitrogen isotopes and carbon and nitrogen concentrations from an August 2012 pluck of a fertilization experiment begun in 2006. Fertilization was with nitrogen (N) and phosphorus (P). Fertilization levels included control, F2, F5, and F10, with F2 corresponding to yearly additions of 2 g/m2 N and 1 g/m2 P, F5 corresponding to yearly additions of 5 g/m2 N and 2.5 g/m2 P, and F10 corresponding to yearly additions of 10 g/m2 N and 5 g/m2 P. After harvest, plants were separated by species and then by tissue. Tissues were then dried, ground and analyzed for stable isotopes and concentrations at the University of New Hampshire stable isotope laboratory.
Relative percent cover of plant species in low nutrient LTER moist acidic tundra experimental plots (MAT06) established in 2006 for years 2008, 2010-2025, Arctic LTER Toolik Field Station Alaska.
Relative percent cover of plant species was measured in low nutrient LTER moist acidic tundra experimental plots (MAT06). Treatments include a gradient of nitrogen and phosphorus additions along with ammonium and nitrate alone.
Phenology of flowers and leaves following experimental warming in the initiation and maturation years for 7 understory boreal plants at the Bonanza Creek Long Term Ecological Research (BNZ LTER) site in Interior Alaska: 2017-2019
This dataset contains the results of experimental warming of flower and leaf buds for 7 understory boreal plants: Rhododendron groenlandicum, Rosa acicularis, Rubus chamaemorus, Shepherdia canadensis, Viburnum edule, Vaccinium uliginosum, and Vaccinium vitis-idaea. Plants in two cohorts were subjected to one of four treatments: warming in the initiation year (the year prior to flowering or leaf-out) only, warming in the maturation year (the year of flowering or leaf-out) only, warming in both years, or no warming (controls). The timing of flowering (both cohorts) and leaf-out (usually one cohort) was monitored. We also tracked developmental stages of the flower bud primordia using repeated desctructive sampling followed scanning electron microscopy throughout the initiation years. Environmental data associated with the plots, including air temperature throughout the summer, soil temperature and depth of ground thaw in late May, and canopy cover, are also reported.
warmXtrophic: plant community responses to the individual and interactive effects of climate warming and herbivory across multiple years at Kellogg Biological Station Long-Term Ecological Research Sites (KBS LTER), Michigan, USA, and University of Michigan Biological Station (UMBS), Michigan, USA.
Climate change has both direct and indirect effects on ecological communities. Whereas most climate change ecology experiments manipulate abiotic drivers to measure direct effects of climate on species or communities, fewer quantify the indirect effects through biotic interactions, especially over multiple sites and years. In this factorial experiment we manipulate temperature through open-top chambers, and the level of insect herbivory through insecticide. At two early successional field sites separated by 3 degrees of latitude and 3°C of mean annual temperature (University of Michigan Biological Station, Pellston, MI and Kellogg Biological Station, Hickory Corners, MI), 6 replicate 1-m2 plots per treatment were installed in May 2015. 12 plots per site are at ambient temperature, 12 are warmed with year-round non-UV filtering polycarbonate and wood frame construction OTCs for tall-stature plants (Welshofer et al. 2018 MEE). Insecticide reduces insect herbivory in half the plots (Welshofer et al. 2018 Oecologia). Over the course of the experiment, OTCs warmed the plant communities by 1.9°C-3.0°C on average over the growing season. Each year, through 2021, plant traits and community responses were measured at the species level: plant phenology (green-up, flowering, flowering duration, seed set); plant percent cover (aerial % cover of the 1m2 plot); plant traits (specific leaf area, C and N content), herbivory damage to leaves, and plant species biomass (only in 2021). Further methodological details are found within each response variable metadata. This experiment is ongoing and further data package updates are planned. L0 data is available upon request. R scripts can be found here: https://github.com/SpaCE-Lab-MSU/warmXtrophic. The biotic and abiotic community context and relative strengths of direct vs. indirect effects may yield ecological surprises under climate change unless addressed together. Large-scale experiments like this one can improve our ability to unde
MIRCA-BC-USMX: Irrigated and planted fractions over the continental United States and Mexico for years 1992, 2002, and 2012
<p>The MIRCA-BC-USMX project contains a spatially explicit mean annual cycle of monthly planted and irrigated fractions at 0.0625 degree (6 km) spatial resolution over the continental United States and Mexico for years 1992, 2002, and 2012.</p> <p>These fractions were generated by (1) reconciling the MIRCA2000 Global Monthly Irrigated and Rainfed Crop Areas dataset (Portmann et al., 2010) with the cropland and pasture classes of year 2001 of the harmonized NLCD_INEGI land cover dataset (Bohn and Vivoni, 2019b); (2) bias-correcting the irrigated and planted fractions to match state-by-state total irrigated and planted areas from government records in the United States (USDA, 2016) and Mexico (SADER, 2014; SAGARPA, 2016).</p> <p>These fractions have been added to land surface parameter files for the Variable Infiltration Capacity (VIC) model (Liang et al., 1994) version 5.1 (Hamman et al., 2018), extended to include the irrigation module of Haddeland et al. (2006), available on <a href="https://github.com/tbohn/VIC/tree/feature/irrig.imperv.deep_esoil">GitHub</a>. The parameter files were taken from the MOD-LSP project, available on <a href="https://zenodo.org/record/2612560">Zenodo</a> (Bohn and Vivoni, 2019a). The VIC 5 image driver requires a "domain" file to accompany the parameter file. This domain file is also necessary for disaggregating the daily gridded meteorological forcings to hourly for input to VIC via the disaggregating tool <a href="https://github.com/UW-Hydro/MetSim">MetSim</a> (Bennett et al., 2018). We have provided a domain file compatible with the meteorological forcings of Livneh et al (2015) and the MIRCA-BC-USMX parameters, on <a href="https://zenodo.org/record/2564019">Zenodo</a> (Bohn et al., 2019a,b).</p> <p>Contents:</p> <ul> <li>Input Files <ul> <li>county_codes.csv - table mapping the numerical codes for counties with the county names used by the US Census Bureau and USDA. This was created by parsing this information from US Census tables from years 1990, 2000, and 2010 and USDA tables from years 1992, 2002, and 2012 and manually reconciling discrepancies across years. Thus the names may not match county names in the original files exactly from year to year, but rather represent my own naming convention. However these discrepancies were rare.</li> <li>mun_us.0.01_deg.asc.tgz and mun_mx.0.0.01_deg.asc.tgz - gzipped tar archives containing mun_us.0.01_deg.asc and mun_mx.0.01_deg.asc, which are ascii-format ESRI grid files created by rasterizing publicly available shapefiles of US and Mexican counties/municipios. These have 0.01 degree (1 km) spatial resolution and pixels have numerical values equal to the codes in county_codes.csv.</li> </ul> </li> <li>Output Files <ul> <li>fplant_firr_bc.$LCYEAR.nc, where $LCYEAR is one of ("s1992","2001", or "2011") - NetCDF-format files at 0.0625 degree (6 km) resolution containing 12 monthly maps each of bias-corrected "fplant" (planted area fraction) and "firr" (irrigated area fraction) for a specific historical year.The value of $LCYEAR indicates the snapshot of the NLCD_INEGI harmonized land cover classification with which fplant and firr were reconciled (so that these area fractions would not exceed the total agricultural/pastoral area given by NLCD_INEGI). Values of fplant and firr were bias corrected so that state-wide total areas matched government records from USDA (USDA, 2014) and SAGARPA (SADER, 2014; SAGARPA, 2016). For $LCYEAR = ("s1992", "2001", "2011"), the agricultural census year used in the bias correction was (1992, 2002, 2012).</li> <li>fplant_firr_bc.2011.mun_mx.nc - same as fplant_firr_bc.2011.nc, but bias-corrected at the municipio level in Mexico. County-level bias correction was not possible in the US due to lack of sufficient resolution USDA records. Similarly, municipio-level records were not available in Mexico prior to year 2003.</li> <li>params.USMX.NLCD_INEGI.$LCYEAR.$YEAR1_$YEAR2.with_irrig.nc - VIC 5 image driver-compliant input parameter files into which fplant and firr of the given $LCYEAR have been inserted. $YEAR1 and $YEAR2 indicate the first and last years of MODIS data used to estimate the annual cycle of monthly LAI, fcanopy, and albedo (independent of the values of fplant and firr).</li> <li>params.USMX.NLCD_INEGI.2011.$YEAR1_$YEAR2.with_irrig.mun_mx.nc - same as params.USMX.NLCD_INEGI.2011.$YEAR1_$YEAR2.with_irrig.nc but with fplant and firr bias-corrected at the municipio level in Mexico.</li> </ul> </li> </ul> <p>These parameters were created with scripts archived on <a href="https://github.com/tbohn/MIRCA-BC-USMX/releases/tag/v1.1">GitHub</a> (Bohn, 2019).</p>
N fertilization and recovery experiment (2-4-6) plant species composition data for East of Tvan from 1997 to 2017, yearly
The realization that anthropogenic nitrogen (N) deposition is causing significant environmental change in many ecosystems has led to lower emissions of reactive N and deposition rates in many regions. However, the impacts of N deposition on terrestrial ecosystems can be long-lasting, with significant inertia in the return of the biota and biogeochemical processes to baseline levels. To better understand patterns of recovery and the factors that may contribute to slow or no responses following declines in N deposition, we followed plant species composition, microbial abundance, N cycling rates, soil pH, and pools of NO3- and extractable cations in an impacted alpine ecosystem following cessation of 12-year experiment increasing N deposition rates by 0, 20, 40, and 60 kg N/ha/yr. Simulated N deposition had resulted in a tripling in the cover of the nitrophilic species Carex rupestris, while the dominant sedge Kobresia myosuroides had decreased by more than half at the highest N input level. In addition nitrification rates were elevated, soil extractable magnesium (Mg2+) and pH decreased, and aluminum (Al3+) and manganese (Mn2+) were elevated at the highest N treatment inputs. Over the nine years following cessation of N additions to the impacted plots only the cover of the nitrophilic C. rupestris showed any recovery to prior levels. Abundances of both bacteria and fungi were lower with N addition in both treatment and recovery plots. Rates of nitrification and pools of NO3- remained elevated in the recovery plots, likely contributing to the lack of biotic response to the cessation of N inputs. In addition, nutrient base cations (Ca2+ and Mg2+) and soil pH remained depressed, and the toxic metal cations (Al3+ and Mn2+) remained elevated in recovery plots, also potentially influencing biotic recovery. These results emphasize the importance of considering long-term environmental impacts of N deposition associated with legacy effects, such as elevated N cycling and losse
G-quadruplex in the gene of the large subunit of plant RNA polymerase II: billion years old story
<p><strong>Supplementary material to the journal article</strong></p> <p>Consist of:</p> <p>Supplementary material S1: Analyzed <em>RPB1 </em>sequences in 40 plant species together with detailed characteristics and G-quadruplex prediction using four different computational approaches.</p> <p>Supplementary material S2: G4 locus is the most conserved within the <em>RPB1</em> gene (40 bp long potential G4 locus is the most conserved site in the whole ~ 6000 bp long <em>RPB1</em> gene. See the histogram below the alignment: the position of the G4 locus is depicted, together with the horizontal red dashed line indicating relative nucleotide conservation among aligned sequences of<em> RPB1</em>)</p> <p>Supplementary material S3: Multiple alignment of G4 locus of <em>RPB1</em> paralogs in <em>Arabidopsis thaliana </em>centered to G4 locus of <em>RPB1 </em></p> <p>Supplementary material S4: Modelled 3D structure of G4 from <em>Bathycoccus prasinos</em> in PDB format</p> <p>Supplementary material S5: Gel electrophoresis and ThT staining of the selected G4-forming sequences</p> <p>Supplementary material S6: All analyzed <em>RPB1</em> sequences in FASTA format</p> <p>Supplementary material S7: Aligned <em>RPB1</em> sequences in FASTA format</p> <p>Supplementary material S8: <em>RPB1</em> paralogs in <em>Arabidopsis thaliana</em></p> <p>Supplementary material S9: Spectral composition of light used in the UV experiment. Analysis of emitted light was performed by Ocean Optics (HR4000CG-UV-NIR, USA) device.</p> <p>Supplementary material S10: Difference CD spectra - comparison without and with previous UV treatment</p>
Data for: Sparse subalpine forest recovery pathways, plant communities, and carbon stocks 34 years after stand-replacing fire (Greater Yellowstone Ecosystem, Wyoming, USA; 2022)
We assessed postfire forest recovery pathways, stem densities, understory plant communities, and carbon stocks across 55 plots in areas exhibiting sparse and reduced forest recovery 34 years after the 1988 Yellowstone Fires in the Greater Yellowstone Ecosystem, Wyoming, USA. Recovery pathways were identified using plot-level frequency distributions of tree ages and correlated with potentially important biotic and abiotic variables (e.g., elevation, seed source distance). Species- and age-specific stem densities were similarly regressed across environmental factors to determine variability in forest recovery across the sampled landscape. Understory plant communities were sampled in 0.25m-square quadrats and environmental drivers of individual species occurrence and whole compositional shifts were determined. Finally, carbon stock sizes were derived from field measures of tree characteristics, understory cover, and soil combined with regionally derived allometric equations. Data collection is complete and is part of a forthcoming manuscript at Ecological Monographs.
Relative percent cover of plant species for years 2012-2017 in the Arctic Long-term Ecological Research (ARC-LTER) 1989 moist acidic tundra (MAT89) experimental plots, Toolik Field Station, Alaska.
Relative percent cover of plant species was measured in ARC-LTER 1989 moist acidic tundra experimental plots. Treatments include Control (CT), Nitrogen Phosphorus (NP), Nitrogen (N), Phosphorus (P), and Greenhouse Control (GHCT). In 1996 on unassigned plots, an experiment that manipulate herbivory presence and nutrients was started. Treatments include Control Unfenced (NFCT), Nitrogen Phosphorus Unfenced (NFNP), and Small Fenced Control (CTSF). Not all treatments were measured each year.
Relative percent cover of plant species for years 2013 2014 2016 2017 in LTER dry heath tundra experimental plots established in 1989, Arctic LTER Toolik, Field Station Alaska
Relative percent cover of plant species was measured in Arctic Long-Term Ecological Research (ARC-LTER) Dry Heath experimental plots. Treatments include Nitrogen Phosphorus (NP), and Control (CT), Nitrogen Phosphorus Unfenced (NFNP), Nitrogen Phosphorus Small Fenced (SFNP), Nitrogen Phosphorus Large Fenced (LFNP), Control (CT), Control Small Fenced (CTSF), and Control Large Fenced (LFCT).
N fertilization experiment plant species composition data for north of the saddle from 2011 to ongoing, yearly
In August 2010, N fertilization plots were established over a gradient of Geum rossii (Aco) and Deschampsia caespitosa (Des) cover in an area of moist-wet meadow alpine tundra north of the Saddle on Niwot Ridge. A total of 20 plots were set up, with 1X-10X being control plots where no nitrogen (N) was added, and 1N-10N being fertilization plots where N was added. Control and fertilized plots were paired so that pairs had the same percent cover of Aco and Des. Initially in 2010, N addition plots were fertilized at a rate of 28.8 g N x m^2 x yr^-1 (72 g of slow-release Osmocote (40-0-0)). In 2011 fertilization rate was reduced to N x m^2 x yr^-1 (25 g Osmocote (2011-2013), Duration Urea 120, 40-0-0, SGN 150 (2014-on).
Plant community compositional stability over 40 years in a Fraser River Estuary tidal freshwater marsh
<p class="MsoNormal"><span>Long-term data sets documenting temporal changes in vegetation communities are uncommon, yet imperative for understanding trends and triggering potential conservation management interventions. For example, decreasing species diversity and increasing non-native species abundance may be indicative of decreasing community stability. We explored long-term plant community change over a 40-year period through the contribution of data collected in 2019 to two historical datasets collected in 1979 and 1999 to evaluate decadal changes in plant community biodiversity in a tidal freshwater marsh in the Fraser River Estuary in British Columbia, Canada. We found that plant assemblages were characterized by similar indicator species, but most other indicator species changed, and that overall </span><span>α-diversity</span><span> decreased while </span><span>β</span><span>-diversity increased. Further, we found evidence for plant assemblage homogenization through the increased abundance of invasive species such as yellow flag iris (<em>Iris pseudacorus</em>), and reed canary grass (<em>Phalaris arundinacea</em>). These observations may inform concepts of habitat stability in the absence of direct anthropogenic disturbance and corroborate globally observed trends of native species loss and non-native species encroachment. Our results indicate that within the Fraser River Estuary, active threat management may be necessary in areas of conservation concern in order to prevent further native species biodiversity loss. </span></p>
Data from: Mechanical soil disturbance in a pine savanna has multi-year effects on plant species composition
<p>Data used in the manuscript Mechanical soil disturbance in a pine savanna has multi-year effects on plant species composition accepted for publication in Ecosphere. Data included are species lists for all plots and years, percent cover of species in each plot in 2021, and life-history characteristics (life span, dispersal mechanism, seed bank persistence) of all species. See manuscript for site description and data collection methodology. </p>
Dataset of Rainy years counteract negative effects of drought on taxonomic, functional, and phylogenetic diversity: resilience in annual plant communities
<p>Data used in the article: </p> <p><strong>Rainy years counteract negative effects of drought on taxonomic, functional, and phylogenetic diversity: resilience in annual plant communities</strong></p> <p><strong>Abstract</strong></p> <p>1- Climate models forecast changes in the amounts and distribution of rain, which may affect ecosystems worldwide, especially in drylands where water is already the limiting factor for plant life. Annual plant communities are common in drylands where they can complete their entire life cycle during the rainy period while avoiding the dry season. Moreover, seed dormancy allows them to disperse over time by remaining in the seed bank for long periods. However, the extent to which these communities will be able to tolerate increasing drought is uncertain.</p> <p>2- We performed a five-year rainfall reduction treatment under field conditions and determined its effects on annual plant communities in a Mediterranean gypsum ecosystem. We assessed the taxonomic, functional, and phylogenetic diversity of these communities each year for five years.</p> <p>3-The taxonomic and functional diversity decreased under the rainfall reduction treatment whereas the phylogenetic diversity increased. Moreover, the relative importance of species with drought-resistant functional designs increased in the community assemblages. However, after a rainy season with above average rainfall, all of the diversity values recovered completely even under the rainfall reduction treatment.</p> <p>4- Our results provide important insights into the responses of these plant communities under a climate change scenario, where they indicate high losses of diversity during drought events but rapid recovery in milder years.</p> <p><em>Synthesis</em> Our findings highlight the great resilience of annual plant communities in drylands, which may allow them to tolerate increased drought under the present climate change scenario.</p>
Supporting data sets for "Estimating Carbon Fixation of Plant Organs for Afforestation Monitoring using a Process-based Ecosystem Model and Ecophysiological Parameter Optimization". (the survey of tree breast diameter and tree height in 11-year old Eucommia ulmoides plantation, values of simulation results used in figures and tables.)
<p>Supporting data sets for Miyauchi et al., Ecology and Evolution, 2019 (accepted).</p> <p>The files store: </p> <p>(1) The survey of tree breast diameter and tree height in <em>Eucommia ulmoides</em> plantation<em>.</em> The ring and stem analysis and dry weight of seven harvested sample trees in the plantation.</p> <p>(2) Values of optimization result used fig.7.</p> <p>(3) Values of prediction result used fig.8. and table 4.</p> <p>(4) Values of optimized parameters by optimization methods, parameter range and constrain.</p>
Figure 1 in Ten years from propagule to mature plant of Butia purpurascens Glassman (Arecaceae): an endemic and endangered palm of the Brazilian Cerrado
Figure 1. General view of Butia purpurascens population in southwest Goiás, with its leaves extracted (relived crown). In the foreground, some plants with inflorescence and immature infrutescences. In the background, the clearing of natural areas of Cerrado for agricultural use (A). Detail of individuals without extracted leaves. Note the large size (about 6-7 m heigth) of some individuals (B). Photos are from the authors.
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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
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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.
OpenNeuro
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