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4,276 results for “Estimation”
Annual occupancy estimates for butterflies, grasshoppers and dragonflies in Bavaria (Germany), 1980-2019
<p>Recent climate and land-use changes are having substantial impacts on biodiversity, including population declines, range shifts, and changes in community composition. However, few studies have compared these impacts among multiple taxa, particularly because of a lack of standardized time series data over long periods. Existing datasets are typically of low resolution or poor coverage, both spatially and temporally, thereby limiting the inferences that can be drawn from such studies. Here, we compare climate and land-use driven occupancy changes in butterflies, grasshoppers, and dragonflies using an extensive dataset of highly heterogeneous observation data collected in the central European region of Bavaria (Germany) over a 40-year period. Using occupancy models, we find occupancies (the proportion of sites occupied by a species in each year) of 37% of species have decreased, 30% have increased and 33% showed no significant trend. Butterflies and grasshoppers show strongest declines with 41% of species each. By contrast, 52% of dragonfly species increased. Temperature preference and habitat specificity appear as significant drivers of species trends. We show that cold-adapted species across all taxa have declined, while warm-adapted species have increased. In butterflies, habitat specialists have decreased, while generalists increased or remained stable. The trends of habitat generalists and specialists both in grasshoppers and semi-aquatic dragonflies however did not differ. Our findings indicate strong and consistent effects of climate warming across insect taxa. The decrease of butterfly specialists could hint towards a threat from land-use change, as especially butterfly specialists' occurrence depends mostly on habitat quality and area. Our study not only illustrates how these taxa showed differing trends in the past, but also provides hints on how we might mitigate the detrimental effects of human development on their diversity in the future.</p>
Paleobotanical precipitation estimates used in Williams et al.: African hydroclimate monsoon during the early Eocene from the DeepMIP simulations, Paleoceanography and Paleoclimatology, 2022
<p>Paleobotanical precipitation estimates used in Williams et al.: African hydroclimate monsoon during the early Eocene from the DeepMIP simulations, Paleoceanography and Paleoclimatology, 2022.</p>
Estimation of groundwater flow rate by an actively heated fiber optics based thermal response test in a grouted borehole
<p>The dataset contains the numerical data and the <em>in-situ</em> measurements in the manuscript titled "Estimation of groundwater flow rate by an actively heated fiber-optics-based thermal response test in a grouted borehole". The data is stored in MAT files, which are Binary MATLAB files. There are a series of codes used in this manuscript to estimate groundwater flow rates. The codes were written in MATLAB Live Script, version 2021b.</p> <ul> <li>The numerical data contains temperatures of the heating stage in different thermal response tests in a numerical model, which considers the borehole effects. The model is set up by COMSOL Multiphysics, and a series of flow rates is set to the model respectively for different thermal response tests.</li> <li>The <em>in-situ</em> measurements include temperatures of the heating stage in an actively heated fiber-optics-based thermal response test, which was performed in July 2021 in the grouted borehole, which is located in the lower section of the Sima bend of the Yangtze River. The temperature for the flow rate estimation was thinned to 120 s records from 10s records for the limited computing resources.</li> <li>The <em>data_process.mlx</em> provides pre-processing for the observational data recorded by Silixa Ultima-M MK2 DTS. The <em>estimation_process.mlx </em>gives a groundwater flow estimation case in a grouted borehole.</li> </ul>
R_JAGS code for estimation and analysis of species-area-relationship (SAR) parameters from NEON (National Ecological Observatory Network) data on plant surveys
<p><span>Invasive species science is heavily geared toward the invasive agent. </span>However, management to protect native species also requires a proactive approach focused on understanding the features affecting community vulnerability to invasion impacts<span>. </span><span>Vulnerability </span><span>is likely the result of </span><span>factors acting across spatial scales, from </span><span>local to regional, and it is the combined effects of these factors that will determine the magnitude of vulnerability.</span><span> We introduce an analytical framework that quantifies the scale-dependent impact of biological invasions from the shape of the native species-area-relationship (SAR). We leverage newly available, biogeographically extensive vegetation data from the US National Ecological Observatory Network to assess plant community vulnerability to invasion impact as a function of factors acting across scales. We analyzed more than 1000 SARs widely distributed across the USA along environmental gradients and under different levels of invasion. </span>Results show that a decrease in native richness is consistently associated with invasive species cover<span>, but it is only at relatively high levels of invasion that native richness is compromised. After accounting for variation in baseline ecosystem diversity, net primary productivity, and human modification, ecoregions that are colder and wetter seem to be most vulnerable to losses of native plant species at the local level, while warmer and wetter areas seem most susceptible at the landscape level. We also document how the combined effects of cross-scale factors result in a heterogenous spatial pattern of vulnerability. </span><span>This pattern </span><span>cannot be predicted by analyses at any single scale, underscoring the importance of accounting for factors acting across scales. Simultaneously assessing differences in vulnerability between distinct plant communities at local, landscape and regional scales provided outputs that can be used to inform policy and management aimed at reducing vulnerability to the impact of plant invasions.</span></p>
SCADIE: simultaneous estimation of cell type proportions and cell type-specific gene expressions using SCAD-based iterative estimating procedure
<p>This repository contains the source code and data used in the paper: SCADIE: simultaneous estimation of cell type proportions and cell type-specific gene expressions using SCAD-based iterative estimating procedure.1.</p>
Chronogram or phylogram for ancestral state estimation? Model-fit statistics indicate the branch lengths underlying a binary character's evolution: R scripts and simulated trees
<p>All R scripts used in this study, and the set of simulated phylogenetic trees used in the study.</p> <p>1. Modern methods of ancestral state estimation (ASE) incorporate branch length information, and it has been demonstrated that ASEs are more accurate when conducted on the branch lengths most correlated with a character's evolution; however, a reliable method for choosing between alternate branch length sets for discrete characters has not yet been proposed.<br><br>2. In this study, we simulate paired chronograms and phylograms, and generate binary characters that evolve in correlation with one of these. We then investigate (1) the effect of alternate branch lengths on ASE error, and (2) whether phylogenetic signal statistics and/or model-fit statistic can be used to select the branch lengths most correlated with a binary character.<br><br>3. In agreement with previous studies, we find that ASEs are more accurate when conducted on the branch lengths most correlated with the character. Phylogenetic signal statistics show limited utility for selecting the correct branch lengths, but model-fit statistics are found to be more accurate, with the correct branch lengths generally returning greater model-fit (lower AICc and BIC values). Using this method to choose between alternate branch length sets is more accurate when tree and character properties are more favorable for model optimization, and when shape differences between alternate phylogenies are greater.<br><br>4. Our results indicate that researchers conducting ASEs on discrete characters should carefully consider which branch lengths are appropriate, and, in the absence of other evidence, we suggest estimating model-fit values over alternate branch length sets and evolutionary models and choosing the branch length/model combination that returns better model fit.</p>
Riverscape heterogeneity in estimated Chinook Salmon emergence phenology and implications for size and growth
<p>Many salmonid-bearing rivers exhibit thermal and hydrologic heterogeneity at multiple spatial and temporal scales, but how this translates into spatiotemporal patterns of fry emergence is poorly understood. Understanding this variability is important because emergence timing determines the biophysical conditions fish first experience (e.g., temperature, flow, food supply), thereby influencing growth opportunities and survival during this critical life stage. We predicted spring Chinook Salmon (<em>Oncorhynchus tshawytscha</em>) emergence phenology across four NE Oregon subbasins over 5-9 years using empirical spawning and temperature data. We then related inter-annual emergence timing estimates to juvenile salmon size and growth rates at consistent sampling locations. There were clear longitudinal patterns of predicted emergence timing in each subbasin: the shape of these patterns was consistent among years, but not among subbasins. In two subbasins emergence occurred progressively later with distance upstream, whereas in the other two subbasins emergence was earliest at upstream sites. Within each year, median emergence dates among sites within each subbasin ranged between 44 and 58 days. This spatial variation was comparable to inter-annual variation, with median emergence dates for a given location in each subbasin ranging between 47 to 74 days among years. Contrary to our expectations, juvenile salmon were not larger in years with earlier emergence, owing to slower spring and summer growth rates compared to years with later emergence. Despite large inter-annual variation in emergence dates, these results suggest that other factors (e.g., stream flow, temperature, density-dependence) were more important than growth duration in determining juvenile salmon growth rates and size among years. We demonstrated considerable spatial and inter-annual variation in emergence phenology within these subbasins. Understanding how this variation translates to spatiotemporal patterns of juvenile salmon habitat use, growth, and survival has important implications for guiding restoration efforts and understanding how climate change may impact these populations.</p>
A comparison of density estimation methods for monitoring marked and unmarked animal populations
<p>These data were generated to compare different methods of estimating population density from marked and unmarked animal populations. We compare conventional live trapping with two more modern, non-invasive field methods of population estimation: genetic fingerprinting from hair-tube sampling and camera trapping for the European pine marten (Martes martes). We used arrays of camera traps, live traps, and hair tubes to collect the relevant data in the Ring of Gullion in Northern Ireland. We apply marked spatial capture-recapture models to the genetic and live trapping data where individuals were identifiable, and unmarked spatial capture-recapture (uSCR), distance sampling (CT-DS), and random encounter models (REM) to the camera trap data where individual ID was not possible. All five approaches produced plausible and relatively consistent point estimates (0.41 – 0.99 animals per km<sup>2</sup>), despite differences in precision, cost, and effort being apparent.</p> <p>In addition to the data, we provide novel code for running unmarked spatial capture-recapture (uSCR) and random encounter models (REM) to the camera trap data where individual ID was not possible. </p>
Validating marker-less pose estimation with 3D x-ray radiography
<p class="MsoNormal"><span>These data were generated to evaluate the accuracy of DeepLabCut (DLC), a deep learning marker-less motion capture approach, by comparing it to a 3D x-ray video radiography system that tracks markers placed under the skin (XROMM). We recorded behavioral data simultaneously with XROMM and RGB video as marmosets foraged and reconstructed three-dimensional kinematics in a common coordinate system. We used XMALab to track 11 XROMM markers, and we used the toolkit Anipose to filter and triangulate DLC trajectories of 11 corresponding markers on the forelimb and torso. We performed a parameter sweep of relevant Anipose and post-processing parameters to characterize their effect on tracking quality. We compared the median error of DLC+Anipose to human labeling performance and placed this error in the context of the animal's range of motion. </span></p>
Assets for 'Phase correlation on the edge for estimating cloud motion' submitted to Atmospheric Measurement Techniques
<p>1. CMV-26-07-2016_ARM-SGP.gif Sample cloud motion vectors from TSI camera images over the United States Atmospheric Radiation Measurement user facility’s Southern Great Plains site.</p> <p>2. raindrop_02-01-2017_ARM-SGP.gif Rotation of cloud motion vectors from raindrop contaminated TSI camera.</p>
Copper River, Alaska, Chinook Salmon Inriver Abundance Estimate 2018-2021 DATA ARCHIVE
<p>Long-term monitoring of returning adult Chinook salmon (<em>Oncorhynchus tshawytscha</em>) abundance on the Copper River, AK, has been conducted using fishwheels and two-sample mark-recapture methods since 2003. This data archive is from from the 2018-2021 field seasons. The annual objective was to estimate the inriver abundance of Copper River Chinook salmon such that the estimate was within 25% of the true abundance 95% of the time. This data represents annual catch, bycatch, tagging site data, recapture site data, session data, QC check tables, CPUE, mark-recapture matrix, mark-recapture stratification tables, effort, and daily catch matrix. </p> <p>See annual report for methodology, analyses and results @ http://akssf.org/default.aspx?id=3477 or contact the Alaska Sustainable Salmon Fund or U.S. Fish and Wildlife Service Office of Subsistence Management Fisheries Resource Monitoring Program or Native Village of Eyak DENR. </p> <p> </p>
Polymorphism-aware estimation of species trees and evolutionary forces from genomic sequences with RevBayes
<p>Supplementary files of Polymorphism-aware estimation of species trees and evolutionary forces from genomic sequences with RevBayes by Borges, Boussau, Höhna, Pereira and Kosiol<br> </p>
Estimating the abundance of the critically endangered Baltic Proper harbour porpoise (Phocoena phocoena) population using passive acoustic monitoring
<p>Knowing the abundance of a population is a crucial component to assess its conservation status and develop effective conservation plans. For most cetaceans, abundance estimation is difficult given their cryptic and mobile nature, especially when the population is small and has a transnational distribution. In the Baltic Sea, the number of harbour porpoises (<i>Phocoena phocoena</i>) has collapsed since the mid-20<sup>th</sup> century and the Baltic Proper harbour porpoise is listed as Critically Endangered by the IUCN and HELCOM; however, its abundance remains unknown. Here, one of the largest ever passive acoustic monitoring studies was carried out by eight Baltic Sea nations to estimate the abundance of the Baltic Proper harbour porpoise for the first time. By logging porpoise echolocation signals at 298 stations during May 2011-April 2013, calibrating the loggers' spatial detection performance at sea, and measuring the click rate of tagged individuals, we estimated an abundance of 71-1,105 individuals (95% CI, point estimate 491) during May-October within the population's proposed management border. The small abundance estimate strongly supports that the Baltic Proper harbour porpoise is facing an extremely high risk of extinction, and highlights the need for immediate and efficient conservation actions through international cooperation. It also provides a starting point in monitoring the trend of the population abundance to evaluate the effectiveness of management measures and determine its interactions with the larger neighbouring Belt Sea population. Further, we offer evidence that design-based passive acoustic monitoring can generate reliable estimates of the abundance of rare and cryptic animal populations across large spatial scales.</p>
Data from: Robust Estimation of Field Inhomogeneity Map Following Magnitude-Based Water-Fat Separation with Resolved Ambiguity
<p>These data have been uploaded and shared as part of "Robust Estimation of Field Inhomogeneity Map Following Magnitude-Based Water-Fat Separation with Resolved Ambiguity". The data may be used for field inhomogeneity mapping and PDFF/R2* reconstruction. </p> <p>These data were acquired by Perspectum Ltd (https://perspectum.com/) on a healthy volunteer. Informed consent was obtained from the participant. The dataset includes a localizer series and a multi-slice series (magnitude and phase) acquired from a volunteer covering the dome of the liver, heart and lungs:</p> <ul> <li>1-localizer_haste_bh</li> <li>2-I_6_Echo_3D_32_Slice_IDEAL</li> <li>3-I_6_Echo_3D_32_Slice_IDEAL</li> </ul> <p>These data were gathered using a Siemens Prisma 3 Tesla scanner. The main dataset comprises an acquisition with thirty-two slices including the abdominal region, with slices placed away from the isocenter. The acquisition consisted of a 6‐echo (TE1=1.3 ms, ΔTE=1 ms) gradient-recalled echo (GRE) protocol designed to minimize T1 bias (3° flip angle), Pixel Bandwidth = 1565 Hz, and 232 x 256 reconstructed image size, with 5 mm slice thickness and 1.72 x 1.72 mm^2 in-plane resolution. </p>
Teller 47 solifluction: Sentinel-1 deformation estimates
<p>Sentinel-1 deformation estimates from orbit 15/377</p> <p>Specifications:</p> <ul> <li>Location: Seward, Peninsula, AK</li> <li>Spatial resolution: ~100 m</li> <li>Unit: m</li> <li>Sign convention: positive: increasing distance to satellite</li> </ul> <p>Files:</p> <ul> <li>avg_disp171819.tif: average thaw-season displacement for years 2017, 2018, 2019; normalized to a 90-day period</li> <li>subseasonal.txt: subseasonal displacement time series for four points J1-J4 in years 2017-2019. Coordinates and measurement times are included.</li> </ul>
Data from: Improving quartet graph construction for scalable and accurate species tree estimation from gene trees
<p>Summary methods are one of the dominant approaches for estimating species trees from genome-scale data. However, they can fail to produce accurate species trees when the input gene trees are highly discordant due to gene tree estimation error as well as biological processes, like incomplete lineage sorting. Here, we introduce a new summary method TREE-QMC that offers improved accuracy and scalability under these challenging scenarios. TREE-QMC builds upon the algorithmic framework of QMC (Snir and Rao 2010) and its weighted version wQMC (Avni et al. 2014). Their approach takes weighted quartets (four-leaf trees) as input and builds a species tree in a divide-and-conquer fashion, at each step constructing a graph and seeking its max cut. We improve upon this methodology in two ways. First, we address scalability by providing an algorithm to construct the graph directly from the input gene trees. By skipping the quartet weighting step, TREE-QMC has a time complexity of O(n^3 k) with some assumptions on subproblem sizes, where n is the number of species and k is the number of gene trees. Second, we address accuracy by normalizing the quartet weights to account for "artificial taxa," which are introduced during the divide phase so that solutions on subproblems can be combined during the conquer phase. Together, these contributions enable TREE-QMC to outperform the leading methods (ASTRAL-III, FASTRAL, wQFM) in an extensive simulation study. We also present the application of these methods to an avian phylogenomics data set.</p>
Data: Guiding the design of SARS-CoV-2 genomic surveillance by estimating the resolution of outbreak detection
<p>Contains data necessary to reproduce the quantitative results related to a SARS-CoV-2 outbreak in NSW, Australia in the associated paper.</p> <p><strong>icpmr_delta_gisaid.csv</strong><br> Tabular data containing the GISAID accession numbers, dates of collection and submission for all sequences used in the NSW outbreak analysis. The epi set is available on GISAID as EPI_SET_220919ef. The <code>wgs_cluster</code> column contains identifiers of genomic clusters defined at ICPMR, NSW Health Pathology. A value of "Other" means that the sequence either did not belong to a cluster or was part of a cluster that contained fewer than 30 sequences in the study period, and sequences with this value should not be considered to form a single cluster.</p> <p><strong>icpmr_delta_gisaid.dists.tsv.gz</strong><br> Compressed pairwise SNP distance matrix in the format output by snp-dists. The script that creates this file from sequence data is available in the linked code archive.</p>
Estimating drivers and pathways for hydroelectric reservoir methane emissions using a new mechanistic model (estimated methane emissions for hydropower reservoir surfaces and potential dam emissions)
<p>Methane emissions data from hydropower reservoir surfaces and dams, as estimated with the ResME model. Emissions estimates available for hydropower reservoirs in the GRanD database (Lehner et al., 2011). </p> <p> </p> <p>References:</p> <p>Lehner, B., Liermann, C. Reidy, Revenga, C., Vörösmarty, C., Fekete, B., Crouzet, P., Döll, P., Endejan, M., Frenken, K., Magome, J., Nilsson, C., Robertson, J.C., Rodel, R., Sindorf, N., and Wisser, D. (2011). High-resolution mapping of the world’s reservoirs and dams for sustainable river-flow management. Frontiers in Ecology and the Environment, 9 (9): 494-502. https://doi.org/10.1890/100125.</p>
Dataset for "Intercomparison of methods to estimate gross primary production based on CO2 and COS flux measurements"
<p>The final dataset used in manuscript "Intercomparison of methods to estimate gross primary production based on CO2 and COS flux measurements" by Kohonen et al. (2022). The dataset contains carbonyl sulfide (COS) and carbon dioxide (CO2) eddy covariance flux data and in-situ meteorological data measured at Hyytiälä forest in Juupajoki, Southern Finland, as well as GPP estimates derived from COS and CO2 flux measurements as described in the manuscript from January 2013 to December 2017. Raw data are available upon request from the author.</p>
An ensemble of 48 perturbed-physics model (Noah-MP) estimates of the 1/8° runoff over the conterminous United States, 1980–2015 (time-merged version)
<p>This dataset contains the 1980–2015 monthly evapotranspiration simulated by a 48-member perturbed-physics ensemble configured from the Noah LSM with multi-physics options (Noah‑MP v3.6). Simulation outputs include the surface and subsurface runoff. The file name has four parts: the variable collection, the used parameterization, the time period, the suffix, and the compression format.</p> <p>The 48 physics configurations are generated by combining four runoff parameterizations (run1: SIMGM, run2: SIMTOP, run3: NOAHR, run4: BATS), two parameterizations of stomatal conductance (can1: Ball–Berry, can2: Jarvis), three parameterizations of soil moisture stress factor (btr1:NOAHB, btr2: CLM, btr3: SSiB), and two parameterizations of near-surface atmospheric turbulence (tub1: M-O, tub2: Chen97).</p> <p>The simulation domain covers the all of conterminous United States (25°–53°N, 125°–67°W), which is also called the NLDAS-2 testbed (Xia et al., 2012a, b). The simulations were performed at a spatial resolution of 0.125°, which is the same as for NLDAS-2 models. Details of the simulation settings and spin-up run can be found in Section 2.3 of Zheng et al. (2019) and Section 2.2 of Fei et al. (2021).</p>
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
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.