Dataset Search Results

Historical census data collected at Trelease Woods from 1986 to 2004 with information on tree species, diameter at breast height (DBH), and plot location.

Census data collected at Trelease Woods in 1936 with information on tree species, stem count, diameter at breast height (DBH), and basal area. The plot boundaries from the 1936 census were georeferenced to subset 2018 census data for a direct comparison between the two census years.

A mechanistic functional structural plant model. The .gsz file includes a parameterised maize and soybean to be used in GRoIMP software https://grogra.de/. The current model is parameterised to maize cultivar DKC63-21RIB and soybean cultivar AG36X6 for the 2019 growing season in Champaign, IL USA.

The included files are the alignments of DNA or amino acid sequences used for phylogenetic analyses of Auchenorrhyncha (Insecta: Hemiptera) in the manuscript by Bin et al. submitted to the journal “Systematic Entomology.” The files are plain text in either FASTA (.fa or .fas suffix) or PHYLIP (.phy suffix) format. Matrix0 is the set of all loci after multiple sequence alignment and trimming (hereafter called). Matrix1 consists of loci having 75% average bootstrap support and 80% taxon completeness (hereafter called Matrix1). Matrix2 consists of loci having 75% average bootstrap support and 95% completeness. Matrix2_nt12 is the same as Matrix2 but with third codon positions excluded. More details on how the datasets were compiled is provided in the Methods section of the manuscript file, also included as a PDF. Supplemental figures for the submitted manuscript are also provided as a PDF for additional information.

Data at the lake summary and individual crayfish level that supports the manuscript Sawyer, E.K., Kreps, T. A., Lodge, D. M. and E.R. Larson. “Long-term declines in body size of the invasive rusty crayfish (Faxonius rusticus) in temperate lakes." Includes size measurements of 69,303 individual rusty crayfish (Faxonius rusticus) for 17 lakes of Vilas County, Wisconsin, United States collected between 1980 and 2020.

Dataset used for the paper entitled "Morphological differences between wild and game-farm Mallards in North America". Large-scale releases of domesticated, game-farm Mallards to supplement wild populations have resulted in wide-spread introgressive hybridization that changed the genetic constitution of wild populations in eastern North America. The resulting gene flow is well-documented between game-farm and wild Mallards, but the mechanistic consequences from such interactions remain unknown in North America. We provide the first study to characterize and investigate potential differences in morphology between genetically known, wild and game-farm Mallards in North America. We used nine morphological measurements to discriminate between wild and game-farm Mallards with 96% accuracy. Compared to their wild counterparts, game-farm Mallards had longer bodies and tarsi, shorter heads and wings, and shorter, wider, and taller bills. The nail on the end of the bill of game-farm Mallards was longer, and game-farm Mallard bills had a greater lamellae:bill length ratio than wild Mallards. Differences in body morphologies between wild and game-farm Mallards are consistent with an artificial, terrestrial life whereby game-farm Mallards are fed pelleted foods resulting in artificial selection for a more “goose-like” bill. We posit that 1) game-farm Mallards have diverged from their wild ancestral traits of flying and filter feeding towards becoming optimized to run and peck for food; 2) game-farm morphological traits optimized over the last 400 years in domestic environments are likely to be maladaptive in the wild; and 3) the introgression of such traits into wild populations is likely to reduce fitness. Understanding effects of game-farm Mallard introgression requires analysis of various game-farm × wild hybrid generations to determine how domestically-derived traits persist or diminish with each generation.

Raw data associated with PMID: 38925247

This page contains the data for the publication "The pioneer transcription factor Zelda controls the exit from regeneration and restoration of patterning in Drosophila" published in the journal Science Advances.

This dataset provides instructions for procedures to use heat transfer analyses to estimate thermal conditions in artificial roosts for bats. The dataset contains scripts to employ in the program GNU Octave, example meteorology data, and example text files specifying roost dimensions and material properties.

This dataset contains measurements of water loss as white-tailed deer (Odocoileus virginianus) retroypharyngeal lymph nodes air-dried in a refrigerator for 31 days. Daily weights for lymph nodes are recorded every 24 hours, as are the variables "firmness" and "surface wetness". "Firmness" is a categorical variable measuring how much the tissue deforms to the touch (soft, medium, or hard). "Surface wetness" is the amount of visible moisture on the outside of the lymph node (all, some, or none). Lymph node weights were measured until their weights stabilized for 3 consecutive days at two decimal places (ex. 3.02, 3.02, 3.02) or until the weights fluctuated only by 0.01 (ex. 3.02, 3.03, 3.02). Lymph nodes were from northern Illinois white-tailed deer collected as part of the Illinois Department of Natural Resources' ongoing chronic wasting disease (CWD) management efforts.

This dataset is associated with the manuscript "Residual tau-fluvalinate, a beehive acaricide, disrupts growth and metabolism in the greater wax moth, Galleria mellonella" This dataset includes 2 Excel files: 1) raw_data_bioassay.xlsx: this file contains the raw data for waxworm bioassay. There are 2 worksheets within this file: - LC50: raw data for measuring the LC50 of Galleria mellonella (greater wax moth) in laboratory and field strains exposed to tau-fluvalinate. - RGR: Relative Growth Rate, raw data for measuring body weight of field strain of Galleria mellonella exposed to tau-fluvalinate. 2) raw-data_RT-qPCR.xlsx: this file contains raw data (Ct value) of RT-qPCR.

The dataset shows all poison frogs (superfamily Dendrobatoidea) in private U.S. collections during 1990–2020. For each species and color morph, there is a date of arrival, the way it arrived in U.S. collections, and detailed notes related to its presence in the pet trade.

The materials used to provide Continuing Medical Education on ticks and tick-borne diseases in Illinois on February 1, 2023 at Carle Hospital, along with the pre- and post-quiz and deidentified data of the quiz takers. Files: "Ticks and Tick-borne Diseases of Illinois_Final_w_speaker_notes.pptx": Presentation slides used for CME course, with notes to indicate verbal commentary "CME assessment_final.docx": Pre- and post-CME quiz questions and answers, annotated to indicate correct answers and reasoning for incorrect answers "CME_prequiz_data_for_sharing.csv": De-identified data from pre-CME quiz "CME_postquiz_data_for_sharing.csv": De-identified data from post-CME quiz, including demographics "DataCleaning_forSharing.R": R file used to clean the raw data and calculate the scores "ReadMe.txt":

GIS data and geoprocessing tools associated with White and Lambert (2025) modeling paper that assesses the potential impact of development on the archaeological resources of Illinois.

These datasets contain the complete output from a Monte Carlo simulation of the number of wild cervids to test for chronic wasting disease (CWD) depending on true prevalence. Five CSVs of the simulation results are provided, split due to limitations in file size. The R code used to run the simulation and process the data is included. The data to replicated Table 1 and the data used to compare the simulation results to the CWD surveillance efforts of the Illinois Department of Natural Resources (IDNR) are also provided.

This is a peptide imaging data obtained by mtarix assisted laser desoption ionization trapped ion mobility datasets from the central nervous sytem and select ganglion of aplysia Californica.

This dataset includes the original data (including photographs as .jpg files and sound recordings as .wav files) and detailed descriptions of workflows for analyses of acoustic and morphometric data for the Neoaliturus tenellus (beet leafhopper) species complex. Files needed for different parts of the two analytical workflows are included in the "Acoustics.zip" and "PCA.zip" archives. The "Folder Structure.png" file contains a diagram of the folder structure of the two archives. Each archive contains a "ReadMe" file with instructions for repeating the analyses. File and folder names including the two-letter abbreviations TB, TD, TN and TP refer to four different putative species (operational taxonomic units, or OTUs, of the Neoaliturus tenellus complex.

These data files were used for phylogenomic analyses of Darnini and related Membracidae (Hemiptera: Auchenorrhyncha) in the referenced article by Gonzalez-Mozo et al. - The "mem_50p_alignment.fas" file contains the aligned, concatenated nucleotide sequence data for 51 species and 492 genetic loci included in the phylogenetic analyses ("N" indicates missing data and "-" indicates an alignment gap). - The file "Table1.rtf" lists the included species, country of origin and genbank accession number. Species newly sequenced for this study have a Sample ID with prefix "DAR"; previously sequenced species for which data were downloaded from genbank have "NCBI" indicated in the same column of the table. - The file "partition_def.txt" lists the 492 genetic loci included in the alignment with their exact positions indicated by the range of numbers given at the end of each line (e.g., locus "uce-1" occupies positions 1-280 in the alignment). - The substitution model file "mem_50p.model" contains information on the substitution models used in the partitioned maximum likelihood analysis, including the models used for different data partitions and parameter values, as output by the phylogenetic software IQ-TREE. - Individual tree files in Newick format (plain text) are provided for the phylogeny from concatenated analysis with the best likelihood score ("mem_50p_bestLikelihoodScore"), concatenated likelihood analysis with gene concordance factors ("mem_50p_gcf") and site concordance factors ("mem_50p_scf"). - The tree file from the ASTRAL analysis is "mem_50p_astral". - The zip archive entitled “IQ-TREE analysis results.zip” includes output from the maximum likelihood analysis of the concatenated nucleotide sequence data, including the following: (1) main output file “mem_50p.iqtree” summarizing model selection, partitioning schemes, likelihood scores, and run parameters; (2) “mem_50p.mldist” including pairwise ML distances between taxa; (3) “mem_50p.best_scheme.nex” with the best partitioning scheme identified by ModelFinder in NEXUS format and (4) “mem_50p.best_scheme” the RAxM-compatible version of the same file. - The “Ultrafast bootstrap results.zip” zip archive contains: (1) “mem_50p.ufboot” with the bootstrap replicate trees; (2) “mem_50p.contree” with the majority-rule consensus tree with support values; (3) “mem_50p.splits.nex”, with split support values across the replicates; (4) “mem_50p.log” is the log file. - The “gene_trees.zip” zip archive contains the individual gene trees as input for subsequent coalescent gene tree analysis in the phylogenetic program ASTRAL. - The file "DarniniAHE_Character Matrix.csv" contains the data for 6 morphological characters for which the ancestral states were reconstructed using the phylogenetic results from analysis of anchored-hybrid data (see article text for details). - The file "scriptACRDarnini.txt" contains the commands used to reconstruct ancestral morphological characters states using the corHMM 2.8 R package. See the Methods section of the article for more details.

This data comprises image files used in the analysis of Analysis of Nematode Ventral Nerve Cords Suggests Multiple Instances of Evolutionary Addition and Loss of Neurons by Han et al. (bioRxiv, 2025: doi: https://doi.org/10.1101/2025.03.20.644414). It is separated into two folders. The first comprise data using DAPI staining to quantify the number of VNC nuclei in diverse nematodes. The second includes dye-filling data of Mononchus aquaticus.

___________________________________SUMMARY This dataset contains derivative data from concurrent fMRI and scalp EEG recordings used in: Mostame Parham, Wirsich Jonathan, Alderson Thomas H, Ridley Ben, Giraud Anne-Lise, Carmichael David W, Vulliemoz Serge, Guye Maxime, Lemieux Louis, Sadaghiani Sepideh (2024) A multiplex of connectome trajectories enables several connectivity patterns in parallel eLife 13:RP98777. doi: https://doi.org/10.7554/eLife.98777.3 ___________________________________RAW DATA The data has been originally published and described as part of other studies (Morillon et al., 2010; Sadaghiani et al., 2012). Briefly, 10 minutes of eyes-closed resting state were analyzed from 26 healthy subjects (average age = 24.39 years; range: 18-31 years; 8 females) with no history of psychiatric or neurological disorders. Informed consent was given by each participant and the study was approved by the local Research Ethics Committee (CPP Ile de France III). FMRI was acquired using a 3T Siemens Tim Trio scanner with a GE-EPI pulse sequence (TR = 2 s; TE = 50 ms; 40 slices; 300 volumes; field of view: 192×192; voxel size: 3×3×3 mm3). Structural T1-weighted scan were acquired using the MPRAGE pulse sequence (176 slices; field of view: 256×256; voxel size: 1×1×1 mm3). 62-channel scalp EEG (Easycap, with an additional EOG and an ECG channel) was recorded using an MR-compatible amplifier (BrainAmp MR, Brain Products) at 5Hz sampling rate. ___________________________________PREPROCESSING fMRI and EEG data were preprocessed with standard preprocessing steps as explained in detail elsewhere (Wirsich et al., 2020). In brief, fMRI underwent standard slice-time correction, spatial realignment (SPM12, http://www.fil.ion.ucl.ac.uk/spm/software/spm12). Structural T1-weighted images were processed using Freesurfer (recon-all, v6.0.0, https://surfer.nmr.mgh.harvard.edu/) in order to perform non-uniformity and intensity correction, skull stripping and gray/white matter segmentation. The cortex was parcellated into 68 regions of the Desikan-Kiliany atlas (Desikan et al., 2006). This atlas was chosen because —as an anatomical parcellation— avoids biases towards one or the other functional data modality. The T1 images of each subject and the Desikan-Killiany were co-registered to the fMRI images (FSL-FLIRT 6.0.2, https://fsl.fmrib.ox.ac.uk/fsl/fslwiki). We extracted signals of no interest such as the average signals of cerebrospinal fluid (CSF) and white matter from manually defined regions of interest (ROI, 5 mm sphere, Marsbar Toolbox 0.44, http://marsbar.sourceforge.net) and regressed out of the BOLD timeseries along with 6 rotation, translation motion parameters and global gray matter signal (Wirsich et al., 2017a). Then we bandpass-filtered the timeseries at 0.009–0.08 Hz. Average timeseries of each region was then used to calculate connectivity. EEG underwent gradient and cardio-ballistic artifact removal using Brain Vision Analyzer software (Allen et al., 1998, 2000) and was down-sampled to 250 Hz. EEG was projected into source space using the Tikhonov-regularized minimum norm in Brainstorm software (Baillet et al., 2001; Tadel et al., 2011). Source activity was then averaged to the 68 regions of the Desikan-Killiany atlas. Band-limited EEG signals in each canonical frequency band and every atlas region were then used to calculate frequency-specific connectome dynamics. Note that the MEG-ROI-nets toolbox in the OHBA Software Library (OSL; https://ohba-analysis.github.io/osl-docs/) was used to minimize source leakage in the band-limited source-localized EEG data (Colclough et al., 2015). ___________________________________FOLDER STRUCTURE The dataset includes five separate folders as described below: 1) EEGfMRI_dFC folder: connectome dynamics of scalp data This folder contains 26 single MATLAB (.mat) files for each subject. Inside each `.mat` is a structure with fields `A`, `B`, and `C`, corresponding to fMRI, amplitude-coupling, and phase-coupling connectome dynamics, respectively. The fMRI data are 3-dimensional (ROI × ROI × timepoints). The EEG data are stored in a 1×5 cell array (Delta, Theta, Alpha, Beta, Gamma), each cell containing a 3-D ROI × ROI × timepoints matrix. 2) EEGfMRI_dFC_SourceOrtho foldeR: connectome dynamics of source-orthogonalized scalp data Same format as above, except that EEG connectome dynamics are derived from source-orthogonalized signals. The MEG-ROI-nets toolbox in the OHBA Software Library (OSL; https://ohba-analysis.github.io/osl-docs/) was used to minimize source leakage in the band-limited, source-localized EEG data (Colclough et al., 2015). 3-5) Cross-modal Recurrence Plot (CRP) data Each subject has an Excel file with five sheets (Delta through Gamma), corresponding to the five frequency bands. Each sheet contains a 2-D CRP matrix (rows = fMRI timepoints, columns = band-limited EEG timepoints). - Scalp EEG–fMRI CRPs (CRP_EEGfMRI and CRP_EEGfMRI_SourceOrtho folder): two versions (with and without source-orthogonalization), each has 52 Excel files, including amplitude- and phase-coupling CRPs. - Intracranial EEG–fMRI CRPs (CRP_iEEGfMRI folder): one version, 27 Excel files, containing three cases: amplitude coupling, HRF-convolved amplitude coupling, and phase coupling.

Includes two files (.csv) behind all analyses and results in the paper published with the same title. <b>1) 'sites.species.counts'</b> is the raw 2018-2022 data from Angella Moorehouse (Illinois Nature Preserves Commission) including her 456 identified pollinator species and her raw counts per site (there may be a few errors of identification or naming, and there will always be name changes over time). Headers in columns F through Q correspond to the remnant-site labels in Figure 1 and Table 1 of the paper. Columns R to AB are the “nonremnant” sites, which have not been uniquely labelled since the specific sites aren't referenced anywhere in the manuscript. <b>2) 'C.scores'</b> has the 265 species assigned empirical C values (empirical.C) along with the four sets of expert C values and their confidence ranks (low, medium, high), and the Illinois/Indiana conservation ranks (S-ranks), following the methods described in the paper. Other headers in these files: - taxa.code: four-letter abbreviation for genus and specific name - genus: genus name - species: specific epithet - common.name: English name - group: general pollinator taxa group - empirical.C: empirically estimated conservatism score - expert#.C: conservatism score assigned by each of four experts - expert#.conf: expert's confidence in their conservatism score Blank cells in the site-species abundance matrix indicates species absence (or non-detection) Blank cells in C.scores.csv indicates missing S-ranks and unassigned C-scores (with associated missing confidence ranks) where experts lacked knowledge or confidence

Coagulation testing (VCM Vet™) was performed on 57 horses with acute abdominal pain at admission to the University of Illinois Veterinary Teaching Hospital. Additional clinical data were recorded retrospectively. ROC analysis was performed to determine the optimal number of abnormal coagulation parameters for coagulopathy diagnosis based on survival. General linear regression (GLM) and random forest (RF) classification models were developed to predict short-term survival. A training cohort of 40 horses was used for model development, and model performance was determined using the remaining 17 horses.

1228 egg hyperspectral images, the wavelength from 400 nm to 900 nm.

Data collected at 71 study sites from 2023 to 2024 for Reves, Olivia P. (2025): Using Environmental DNA Metabarcoding to Inform Biodiversity Conservation in Agricultural Landscapes. Master's thesis, University of Illinois Urbana-Champaign. Files include study site information, taxa by site matrices for vertebrates from environmental DNA metabarcoding using multiple mitochondrial DNA primers (COI, 12S), and bird species audibly detected by a phone app at study sites.

Data was generated from a field and lab study to determine the influence of thermal variation in livewells on largemouth bass recovery from angling tournaments. The field study data includes temperature data from inside angler livewells during a tournament day. This was collected across four tournaments. The laboratory data was generated from a series of experiments simulating tournament practices and trends in thermal variation within livewells observed in the field proponent. Following simulation, blood was collected to determine levels of analytes consistent with primary, secondary, and tertiary stress response in largemouth bass. Reflex impairment was also included.