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809 results for “planted forest”

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edi60/100

Plant biomass dynamics following logging, burning, and thinning in Watersheds 6 and 7, Andrews Experimental Forest, 1979 to 2021

Watersheds 6 (WS06) and 7 (WS07) at the HJ Andrews are part of a three-watershed study initiated in the 1970’s to examine the response of hydrology and forest vegetation to logging. In 1974, Watershed 6 was clearcut logged; Watershed 7 was shelterwood cut, leaving 75-100 overstory trees per hectare (comprising about 40% of the original basal area). A nearby watershed (WS08) serves as an unlogged control. In 1975, all of Watershed 6 and the portion of WS07 below the road were broadcast-burned. In 1976, both watersheds were planted with Douglas-fir seedlings. Natural regeneration of Douglas-fir and western hemlock also established. In 1984, the remnant overstory trees in WS07 were harvested, and in 2001 the young stand in WS07 was thinned to about 550 trees per hectare. The thinning was not planned but provides an interesting twist to the study. The watersheds are located along the northern boundary of the HJA off the 327 and 328 roads, at elevations ranging from 850 to 1,160 m. Initial vegetation measurements were taken in the summer of 2002 in watersheds 6 and 7 for the purpose of characterizing plant succession after thinning in a small, high-elevation watershed. Understory vegetation plots are remeasured at approximately 6 year intervals.

openCC (other)Jan 2023View details →
edi60/100

Baseline Plant Abundances on Garlic Mustard Experiment Plots at Harvard Forest 2013

This is a five year project that investigates the reassembly of soil fungi and native plants in forests affected by biological invasion. The experiment brings together regional land managers to create comparative eradications of garlic mustard at nine distinct sites along a natural climate and nitrogen deposition gradient in New England. This dataset represents baseline plant abundances from 2013 at nine study plots in Harvard Forest. Species richness, Shannon diversity, and Pielou’s evenness were not different between invaded and non-invaded plots at Harvard Forest.

openCC0Dec 2023View details →
edi60/100

Leaf and Flower Phenology of Woody Plant Species at Harvard Forest and Southern Quebec 2015

Accurate predictions of spring plant phenology with climate change are critical for projections of growing seasons, plant communities and a number of ecosystem services, including carbon storage. Progress towards prediction, however, has been slow because the major cues known to drive phenology – temperature (including winter chilling and spring forcing) and photoperiod – generally covary in nature and may interact, making accurate predictions of plant responses to climate change complex and nonlinear. Alternatively, recent work suggests many species may be dominated by one cue, which would make predictions much simpler. Here, we manipulated all three cues across 28 woody species from two North American forests. Study sites were Harvard Forest and St. Hipplolyte, Quebec. Species were selected for this study based on their prevalence at the study sites; 28 species are included in this study. At each site, multiple cuttings of six or more representative individuals were collected. In total, we tracked the phenology of 2,137 cuttings from 275 individual source plants. All species responded to all cues examined. Chilling exerted a strong effect, especially on budburst (-15.8 d), with responses to forcing and photoperiod greatest for leafout (-19.1 and -11.2 d, respectively). Interactions between chilling and forcing suggest that each cue may compensate somewhat for the other. Cues varied across species, leading to staggered leafout within each community and supporting the idea that phenology is a critical aspect of species’ temporal niches. Our results suggest that predicting the spring phenology of communities will be difficult, as all species we studied could have complex, nonlinear responses to future warming.

openCC0Dec 2023View details →
edi56/100

Construction Costs of Carnivorous and Non-Carnivorous Plants at Harvard Forest 2006-2008

Leaf traits, including photosynthetic rates, leaf mass area, and leaf nutrient content covary in a coordinated way for a wide range of plant taxa. This covariation results from trade-offs between the costs of constructing plant tissues and the benefits accrued from photosynthesis. Carnivorous plants have been found to be outliers in the "universal spectrum of leaf traits" because they have very low photosynthetic rates for the amount of nitrogen in their leaves and traps. But no studies have measured simultaneously the actual construction costs of carnivorous traps and rates of photosynthesis to determine the amortization required to recover the investment (the "payback time") and thereby calculate the "marginal gain" of "investing" in carnivorous structures. The objective of this study was to measure construction costs (CCmass, grams of glucose required to build 1g of ash-free dry mass of tissue) and photosynthesis (Amass, nmol CO2 g-1 s-1) for traps, leaves, roots, and rhizomes of 15 carnivorous plant species with differing mechanisms of prey capture and consumption (pitfall traps, snap-traps, sticky pads) grown under greenhouse conditions. Payback time (h) was calculated as the quotient of CCmass and Amass after conversion to nmol of carbon per gram of ash-free dry mass. There were highly significant differences amongst species for CCmass of traps but there were no significant differences for CCmass amongst traps, roots and rhizomes. Mean (+- SD) CCmass for traps (1.14 +- 0.24 g glucose g-1) was significantly lower than the mean CCmass of leaves of 267 non-carnivorous plant species (1.47 +- 0.17 g glucose g-1). However, all 15 carnivorous plants examined in this study had low Amass and thus, the marginal gain of carnivory is small with a long payback time (524-1641 h). Our results of low CCmass for carnivorous traps is contrary to the oft-stated expectation of a high cost to construct elaborate carnivorous traps. Payback time integrates traits used to assess leaf

openCC0Dec 2023View details →
edi56/100

Moths, Ants and Pitcher Plants in Bogs at Harvard Forest and Belchertown MA 2007-2013

Ecologists have long recognized that coexistence of interacting species depends on a diversity of separate, but linked habitats. Most models of species coexistence treat these habitat "patches" as unchanging elements of the landscape, but in reality, they are constantly changing in size and shape. The structure and dynamics of the food webs that inhabit them both control and depend on these changes. In this five-year (2006-2011) collaborative project, we are using a combination of extensive field surveys and intensive field experiments to understand how species interactions change the spatial distribution of dynamic habitat patches across the landscape, and to determine how food webs are structured within and among these patches. The experimental system for this five-year research project is the Sarracenia "microecosystem": the northern pitcher-plant Sarracenia purpurea; the unique food web of bacteria, protozoa, rotifers, mites, and fly larvae that live within its rainwater-filled leaves; three species of bog-inhabiting ants that are the primary prey for this carnivorous plant; and larvae of the pitcher-plant moth, Exyra fax, which cut and drain pitchers and remove food web habitat. Results from surveys of bogs in all six New England state and field experiments conducted at bogs at Harvard Forest and Belchertown, Massachusetts will be used to parameterize a simulation model to predict changes in spatial structure of ant, moth, and plant populations, and the structure and composition of the aquatic food web associated with the plant. This work is funded by the U.S. National Science Foundation, through collaborative awards 0541680 and 0541936.

openCC0Dec 2023View details →
edi56/100

Candida Pseudoglaebosa Ecology in Sarracenia Purpurea Pitcher Plants at Harvard Forest since 2021

Fungi and bacteria are common members of the microbiomes of carnivorous plants. In the pitcher plant Sarracenia purpurea these microorganisms enter carnivorous pitchers shortly after pitchers develop, and may be relevant for pitcher functioning. We are sampling pitchers repeatedly over several years to better understand the culturable diversity in this habitat, with a focus on the common pitcher yeast Candida pseudoglaebosa and fungi that have the potential to interact with it. C. pseudoglaebosa dominates pitcher plants by arriving early in pitchers, and we are interested in how this yeast’s populations change over time and in response to other pitcher microorganisms. Between 2021 and 2023, we collected pitcher water from Tom Swamp in Harvard Forest and cultured 118 yeast and bacteria colonies from this water. We have found C. pseudoglaebosa and some other yeasts (Papiliotrema, Rhodotorula, and Sporidiobolus); microbial identification is ongoing. We are planning to investigate changes in C. pseudoglaebosa genetic diversity and changes in C. pseudoglaebosa interactions with other pitcher microorganisms over time.

openCC0Feb 2024View details →
edi56/100

Microbial, Plant, and Soil Impacts on Soil Nutrient Cycling in Harvard Forest and Greater Boston 2021-2022

Microbes are the driving force behind nutrient cycling within soils, secreting enzymes necessary to break down organic matter, immobilizing nutrients and C, or transferring nutrients to plant hosts. Even though nutrients would almost never move through ecosystems without microbes, we know little about how their composition and activity is related to ecosystem nutrient cycling, and their importance relative to plant and soil abiotic factors. In this study, we sought to determine which commonly measured soil microbial community characteristics best explain soil N and P cycling, and the relative contributions of microbial, plant, and abiotic factors in explaining these processes.

openCC0Mar 2025View details →
edi56/100

Vascular Plant Species at Harvard Forest 1992

This dataset contains a list of vascular plant species found in 269 22.5 x 22.5 m plots sampled in the 1992 Prospect Hill vegetation survey. The species list was compiled on 5 May 1993.

openCC0Dec 2023View details →
edi52/100

Plant succession and biomass dynamics following logging and burning in Watersheds 1 and 3, Andrews Experimental Forest, 1962 to Present

Watersheds 1 and 3 in the HJ Andrews Experimental Forest have a long history of hydrologic, geomorphic, and ecological study. Long-term successional studies in the two watersheds are unprecedented in their scope and duration (1962 to present), spanning more than 50 years of post-logging measurements. To date, studies have focused on understory responses to logging and burning, early stand developmental processes (tree growth and mortality), and understory responses to canopy closure. Understory sampling was initiated in 1962, prior to harvest, and includes approximately 190, 2 x 2 m permanent understory plots. Measurements include estimates of ground-surface conditions and abundance (cover and biomass) of herbaceous, shrub, and tree species. After broadcast burning (1963 in WS3, 1966 in WS1) plots were sampled annually through 1972/1973, but less frequently thereafter (every 2-6 years). Studies of early stand development were initiated in 1979/1980, with sample plots collocated with the understory plots. In each of approximately 190, 250 m2 tree plots, all conifer and hardwood stems greater than or equal to 1.4 m tall are tagged, measured for diameter, and assessed for status (live or dead, including the cause of mortality). Both watersheds experienced recent snow-related windthrow (2019, 2020) and parts of WS1 burned in 2020 during the Holiday Farm Fire, adding complexity to the structure and composition of the understory and overstory communities.

openCC (other)Aug 2022View details →
edi52/100

Plant Pollinator data at HJ Andrews Experimental Forest, 2011 to 2021

Despite the importance of plant-pollinator interactions for ecological communities, few long-term observational studies have been conducted of plant-pollinator networks. This study involves the annual collection of plant-pollinator interaction data from up to 18 meadows in the Willamette National Forest, Oregon, including 12 meadows in the HJ Andrews Forest. This study addresses how meadow size, the amount of nearby meadow habitat, weather, degree days, and soil moisture are related to the flowering of meadow plants and the frequency of plant-pollinator interactions.

openCC (other)Aug 2022View details →
edi52/100

May to July 2018 regions of interest (ROIs) of tidal marsh and tidal forest plant species to be used as ground reference data in habitat mapping

We collected field data from sites distributed in habitats along the salinity axis of the Altamaha River estuary and the Duplin River to be used as ground reference data for habitat mapping. Regions of interest (ROIs) for tidal marsh (salt, brackish, tidal fresh) and tidal fresh forest vegetation species were generated near ground control points (GCP) by digitizing vegetation areas in ArcGIS 10.4 based on field maps.These observations will be used to create habitat maps from aerial photographs of the Altamaha River estuary, GA taken following Hurricane Irma to better understand how the storm surge affected tidal vegetation and to examine any shifts in vegetation type.

openCustomSep 2021View details →
zenodo48/100

Data from 'Tracability of Forest Reproductive Material with the quality label 'Plant van Hier': A DNA database with genetic profiles of native autochthonous tree and shrub species of Flanders, Belgium'

<h2>Background</h2> <p>Indigenous trees and shrubs play an important role in multifunctional forest management. They form a significant part of the biodiversity in our forests. Forest reproductive material (FRM) of autochthonous Flemish origin is sold under the quality label &lsquo;Plant van Hier&rsquo;, a certification mark of the Agency for Nature and Forests. To ensure the provenance of the seedlings, we developed a DNA-database of genetic profiles of potential parent trees, using species-specific genetic markers. This database enables the traceability of FRM of the &lsquo;Plant van Hier&rsquo; label throughout the entire production chain; from seed harvesting and cultivation to planting by the end user.</p> <p>This database contains the genetic profiles of almost all possible parent trees present within 27 Flemish autochthonous seed orchards of eight ecologically important tree and shrub species: <em>Carpinus betulus</em>, <em>Corylus avellana</em>, <em>Frangula alnus</em>, <em>Populus tremula</em>, <em>Sorbus aucuparia</em>, <em>Tilia cordata</em>, <em>Tilia platyphyllos,</em> and <em>Ulmus laevis</em>. The profiles were established using microsatellite markers (11 to 24 markers per species).&nbsp;&nbsp;New genetic markers were developed for&nbsp;<em>Carpinus betulus</em> and <em>Ulmus laevis</em>. PCR products were run on an ABI 3500 Genetic Analyser (Thermo Fisher Scientific).</p> <h2>Files</h2> <p>The files will be updated when new genotypes are added to the seed orchards. The current data files contain data from genotypes collected in the period 2018-2023.&nbsp;</p> <h3>Species_genotypes</h3> <p>These files contain the genetic fingerprints of the parent trees of autochthonous Flemish seed orchards. Missing data is indicated as &lsquo;MD&rsquo;. For <em>Carpinus betulus</em>, an octoploid species, the allelic phenotype is given instead of the genotype as the number of times that an allele occurs on a specific locus is not known.</p> <p>The next metadata is additionally given:<br>- Species: the Latin name of the species<br>- Seed_orchard: the name of the seed orchard in which the genotypes are located<br>- Code_seed_orchard: the code of the seed orchard in which the genotypes are located as given in the Register of Flemish Forest Reproductive Material (&lsquo;Register bosbouwkundig uitgangsmateriaal&rsquo;; inbo.be)<br>- Genotype: the fieldname given to the genotype<br>- Origin: the location where the genotype was collected in Flanders, Belgium. Genotypes were collected from natural stands which are assumed to have an autochthonous origin. When the specific location is unknown, the location &lsquo;Flanders&rsquo; is given.&nbsp;<br>- Year_sampled: the year in which the genotypes were sampled in the respective seed orchard for genetic analysis.</p> <h3>Species_binsets</h3> <p>These files contain the binsets and allele names that are used to score the alleles of the genotypes in the programme Geneious Prime 2019.3.2 (<a href="https://www.geneious.com">https://www.geneious.com</a>). For <em>Tilia platyphyllos </em>and <em>Tilia cordata</em>, the same binsets were used.</p>

opencc-by-4.0Nov 2024View details →
edi48/100

Understory plant community data from repeated plot sampling (1978-2019) in old-growth northern hardwood forest, northern Michigan (Dukes RNA, Hiawatha National Forest)

This data-set includes long-term, permanent-plot-based data for understory plant communities in old-growth mixed northern hardwood-hemlock forest and forested peatland in the Upper Great Lakes region. Data for over 900 understory quadrats (all associated with long-term canopy data from larger permanent plots) included multiple (2-5) remeasurements over 23-40 years, with longest periods and most remeasurements for upland forest types. The Dukes Research Natural Area (RNA) (https://www.fs.usda.gov/research/nrs/rnas/locations/dukes) in the Hiawatha National Forest (Marquette Co., MI) includes ca. 100 ha of largely unlogged, original forest. Publications cited below include more detailed information about the site. About half of the RNA supports upland forests intergrading from hemlock (Tsuga candensis) dominance to mixtures of hemlock and northern hardwoods species. Sugar maple (Acer saccharum) is dominant over much of the upland area, with, locally, significant admixtures of beech (Fagus grandifolia), yellow birch (Betula alleghaniensis), and red maple (Acer rubrum). Topographic relief is very slight with total elevational change within the RNA only about 10 m. The stand is within a few km of the western limit of the continuous range of beech. In 1935, 248 continuing forest inventory (CFI) plots (circular, 0.2 acre) were established on a regular grid throughout the RNA, and these have been the subject of repeated sampling through 2018-2019 and support continuing long-term study addressing canopy tree communities (canopy data to be deposited in a separate project). Examples of resulting publications are cited elsewhere in metadata, and can provide more detailed information about the RNA. In 1978-80, U.S. Forest Service researchers, directed by Jan Schultz and Frederick Metzger, initiated studies of understory communities, including herbaceous species and woody seedlings. Data were derived from four sub-quadrats within each of the CFI plots. These quadrats were re-estab

openCC (other)Apr 2023View details →
edi48/100

Understory percent cover, plant traits, canopy LAI, PAR, temperature, and soil moisture data at multiple time points for sites in the burn chronosequence and Indian Point forest at the University of Michigan Biological Station, Pellston, MI (2022-2023)

Community ecology has sought to understand the mechanisms by which plant communities are assembled through time and space. One prominent way to address how communities are assembled is by quantifying functional traits. While there is a tremendous body of literature on functional traits, debate persists about how to account for variation in measured traits. For example, intraspecific trait variation (ITV) can be equal to or greater than interspecific trait variation and ITV has also been found to vary greatly across years. Therefore, there is a need to account for variability in functional trait measures among and within species and through time to improve our understanding of community assembly. Chronosequences are a powerful tool to address temporal changes in community dynamics, however, the inclusion of understory plants in forest chronosequence studies is still relatively uncommon. Previous chronosequence studies have been primarily performed in grasslands or in a limited subset of forest types, so further work is needed in understory plant traits across other ecosystems and climates to improve trait-based understanding of understory plant communities through time. Additionally, because plant traits change as ecosystems age, community interactions are likely to change with ecosystem age. Interactions of particular interest are herbivory, arthropod predation, and the influence of plant traits on arthropod diversity.

openCC (other)Nov 2024View details →
edi48/100

May to July 2018 ground control points GPS coordinates of tidal marsh and tidal forest plant species to be used as ground control points in habitat mapping.

We collected field data from sites distributed in habitats along the salinity axis of the Altamaha River estuary and the Duplin River to be used as ground control points (GCP) and ground reference data for habitat mapping. GCPs for tidal marsh (salt, brackish, tidal fresh) and tidal fresh forest vegetation species were acquired. A real time kinematic (RTK) GPS survey of GPS coordinates and ground elevations for tidal marsh vegetation was carried out in May of June of 2018. A handheld GPS was used to collect GPS coordinates for tidal forest plant species in July of 2018. A total of 101 GCPs were collected in tidal habitats, with 26 in salt, 28 in brackish and 29 in tidal fresh marsh, and another 18 in tidal fresh forest. These observations will be used to create habitat maps from aerial photographs of the Altamaha River estuary, GA taken following Hurricane Irma to better understand how the storm surge affected tidal vegetation and to examine any shifts in vegetation type.

openCustomJan 2020View details →
zenodo44/100

global interpreted planted forest, natural forests validation samples

<p>This dataset provided the global validation dataset including planted forest, natural forest, and non-forest in 2015. This dataset was visually interpreted using the high spatial resolution (&lt;1 m) images from Google Earth, and combining the spatial distribution of planted forets, and forest gain map.</p> <p>1 denotes planted forest, 2 denotes the natural forest, and 3 denotes the nonforest.</p> <p>Detailed information about how the global validation dataset was visually interpreted can be seen in the following reference:</p> <p>Xu,&nbsp;H.,&nbsp;He,&nbsp;B.,&nbsp;Guo,&nbsp;L.,&nbsp;Yan,&nbsp;X.,&nbsp;Zeng,&nbsp;Y.,&nbsp;Yuan,&nbsp;W., et al. (2024).&nbsp;Global forest plantations mapping and biomass carbon estimation.&nbsp;Journal of Geophysical Research: Biogeosciences,&nbsp;129,&nbsp;e2023JG007441.</p>

opencc-by-4.0Mar 2024View details →
zenodo44/100

1-km forest tree height, cover, plant area index, and foliage height diversity for the CONUS

<p>Consistent and spatially explicit periodic monitoring of forest structure is essential for estimating forest-related carbon emissions, analyzing forest degradation, and supporting sustainable forest management policies.&nbsp; To date, few products are available that allow for continental to global operational monitoring of changes in canopy structure.&nbsp; In this study, we explored the synergy between the NASA&rsquo;s spaceborne Global Ecosystem Dynamics Investigation (GEDI) waveform LiDAR and the Visible Infrared Imaging Radiometer Suite (VIIRS) data to produce spatially explicit and consistent annual maps of canopy height (CH), percent canopy cover (PCC), plant area index (PAI), and foliage height diversity (FHD) across the conterminous United States (CONUS) at 1-km resolution for 2013-2020.&nbsp; The accuracies of the annual maps were assessed using forest structure attribute derived from airborne laser scanning (ALS) data acquired between 2013 and 2020 for the 48 National Ecological Observatory Network (NEON) field sites distributed across the CONUS.&nbsp; The root mean square error (RMSE) values of the annual canopy height maps as compared with the ALS reference data varied from a minimum of 3.31-m for 2020 to a maximum of 4.19-m for 2017.&nbsp; Similarly, the RMSE values for PCC ranged between 8% (2020) and 11% (all other years).&nbsp; Qualitative evaluations of the annual maps using time series of very high-resolution images further suggested that the VIIRS-derived products could capture both large and &ldquo;more&rdquo; subtle changes in forest structure associated with partial harvesting, wind damage, wildfires, and other environmental stresses.</p>

opencc-by-4.0May 2022View details →
zenodo44/100

dataset: Responses of the structure and function of the understory plant communities to precipitation reduction across forest ecosystems in Germany

<p><strong>Context</strong>: Understory plant communities play a central role in forest biogeochemistry and the recruitment of trees making up the future forest. It is so far poorly understood how climate change will affect understory structure and functions in forest of different management intensity.</p> <p>  </p><p><strong>Aims</strong>: We monitored understory functional traits including transpiration and carbon isotope discrimination, community structure and diversity during two growing seasons as affected by drought in forests subjected to different management intensities. We hypothesized that drought would affect ecophysiological traits such as transpiration but not species richness and diversity. Moreover, we assumed that stand-specific characteristics and forest management intensity modify the drought-resistance of the understory community.</p> <p></p> <p><strong>Methods</strong>: We set up roofs in beech and conifer stands with different management intensity in three different regions across Germany and a drought event close to the 2003 drought was imposed in two consecutive years.</p> <p><strong>Results</strong>: Precipitation reduction decreased soil water content by 2 to 8%, depending on stand and region, in comparison to the control subplots. In the first year, leaf level transpiration was reduced for different functional groups, which scaled to community transpiration modified by additional effects of drought on functional group specific leaf area. Acclimation effects in most functional groups were observed in the second year. We did not observe a significant reduction of plant diversity or a consistent management effect upon drought.</p> <p><strong>Conclusion</strong>: Our results indicate high plasticity and acclimation responses of the forest understory vegetation to changing climate conditions and recurrent drought events.</p> <p><strong>Abbreviations:</strong></p> <p>sp12 - campaign spring 2012; ls12 - campaign late summer 2012; es13 - campaign early summer 2013; ls13-campaign late summer 2013</p> <p>SEW16 - Schorfheide plot 16; SEW49 - Schorfheide plot 49; SEW48 - Schorfheide plot 48;HEW03 - Hainich plot 03; HEW12 - Hainich plot 12; HEW47-  Hainich plot 47; AEW13 -  Alb plot 13; AEW29 - Alb plot 29; AEW08 -  Alb plot 08<br> explo - exploratory<br> SEW - Schorfheide; HEW - Hainich; AEW - Schwäbische Alb<br> in - conifer intensive managed; ma - beech managed; un - beech unmanaged<br> c- control; r - roof<br> LAIs - community leaf area index m<sup>2</sup>/m<sup>2</sup>; H - Shannon´s diversity index; Ts - community transpiration rate (weighted by LAI) mmol H<sub>2</sub>O m-<sup>2</sup> leaf area s-<sup>1</sup>; Ets - Evapotranspiration (mmol/m2/sec); E - Evaporation (mmol/m2/sec); C - leaf photosynthetic carbon isotope discrimination (∆<sup>13</sup>C) according to Farquhar et al. (1982); Cs - community photosynthetic carbon isotope discrimination (∆<sup>13</sup>C) according to Farquhar et al. (1982) (weighted by LAI)</p> <p> </p>

opencc-by-4.0Nov 2017View details →
zenodo44/100

The role of the intraspecific variability of hydraulic traits for modelling the plant water use in different European forest ecosystems: scripts, model output, and parameter files

<p>This repository contains the model outputs and R scripts used to process the data to analyze the impact of the plant hydraulic parameterization of the manuscript: &quot;The role of the intraspecific variability of hydraulic traits for modelling the plant water use in different European forest ecosystems&quot;. The following is a detailed description of the content of this repository:</p> <p>model_output.zip: This compressed file contains the results of all the individual numerical experiments per experimental site as produced by the Comunity Land Model version 5. The files are stored in NETCDF format per year. The folder is arranged with subfolders containing the individual results from each experimental site as follows:</p> <ul> <li>rc: model output with the results of the resistant configuration of experiment 1 (RC)</li> <li>vc: model output with the results of the vulnerable&nbsp;configuration of experiment 1 (VC)</li> <li>k_dc:&nbsp;model output with the results of the default configuration used for experiments 1 and 2 (DC or DC<em>k</em><sub>max</sub>)</li> <li>k_rc:&nbsp;model output with the results of the low&nbsp;plant hydraulic conductance (L<em>k</em><sub>max</sub>) for experiment 2</li> <li>k_irc:&nbsp;model output with the results of the intermediate low plant hydraulic conductance (IL<em>k</em><sub>max</sub>) for experiment 2</li> <li>k_vc:&nbsp;model output with the results of the high&nbsp;plant hydraulic conductance (H<em>k</em><sub>max</sub>) for experiment 2</li> <li>k_ivc:&nbsp;model output with the results of the intermediate high&nbsp;plant hydraulic conductance (IH<em>k</em><sub>max</sub>) for experiment 2</li> <li>k_iirc:&nbsp;model output with the results of the additional intermediate low&nbsp;plant hydraulic conductance (IIL<em>k</em><sub>max</sub>) for experiment 2</li> <li>ko_dc:&nbsp;model output with the results of the best <em>k</em><sub>max</sub>&nbsp;and the default configuration of the PVC used in&nbsp;experiment 3</li> <li>ko_rc:&nbsp;model output with the results of the best <em>k</em><sub>max</sub>&nbsp;and the resistant configuration of the PVC used in&nbsp;experiment 3</li> <li>ko_vc:&nbsp;model output with the results of the best <em>k</em><sub>max</sub>&nbsp;and the vulnerable&nbsp;configuration of the PVC used in&nbsp;experiment 3</li> </ul> <p>The scripts were written for use in RStudio, and each contains a&nbsp;detailed description of the data requirements and outputs. Each script was developed to read directly the netcdf files of the model output and the csv files containing the transpiration estimates calculated from the SAPFLUXNET per experimental site (script 1).</p>

opencc-by-4.0Nov 2022View details →
edi44/100

FRAME (FoRests Among Managed Ecosystems) – Plant community and seed bank composition in forests, Philadelphia metropolitan area, USA, 2017-2019

Our study objectives were to conduct a Rosa multiflora (multiflora rose) removal experiment in three forest sites experiencing different invasion intensities and to restore native plant biodiversity while preventing secondary invasion. The study was conducted in and around Newark, DE, from 2017-2019, and data collection is complete. We utilized three management strategies: invasive plant removal, removal followed by native seed addition, and removal plus native seed and mulched invasive stem addition. We investigated the similarity between seed bank species composition and existing vegetation before and after removal to assess the potential for passive restoration. Two seasons after removal, we found that simply removing rose increased native species richness, Native Floristic Quality Assessment (FQAIN), and native shrub abundance in our medium invasion site, and total species richness in our low and medium invasion sites. Compared to removal alone, native seed addition, with and without mulch addition, resulted in larger native and total species richness and FQAIN increases at all sites, larger increases in native shrub abundance and exotic species richness in our medium invasion site, and larger reductions in exotic and total shrub abundance in our low and medium invasion sites. Following removal, species similarity between seed bank and vegetation improved for all three sites. Our results indicate that removal of Rosa multiflora (multiflora rose) alone increased native plant biodiversity in the medium invasion scenario, but the seed bank may not provide a large native species pool. Additional management strategies lead to improved outcomes, especially in our most invaded forest, demonstrating the need to conduct multiple plant removal treatments across forests with varying site conditions and plant invasion intensity to improve management recommendations.

openCC (other)Sep 2022View details →

ScienceDex guides

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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