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12,632 results for “fish”

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edi52/100

Data package supporting manuscript "Widespread Heterogeneity in Density-Dependent Mortality of Nearshore Fishes"

This repository contains the complete data synthesis and analysis pipeline for a global meta-analysis on density-dependent mortality in reef fishes. We estimated mortality parameters (α and β) from >30 ecological studies and explored how ecological traits, experimental methods, and phylogenetic history explain variation in density dependence. It comprises eight data tables in csv format, three .tre files for phylogenetic trees (see method document for data sources), and the zipped code folder (including 12 R scripts) to ensure transparent, end-to-end reproducibility of data processing, analysis, and visualization. This package supports the manuscript “Widespread Heterogeneity in Density-Dependent Mortality of Nearshore Fishes” by Stier & Osenberg (Ecology Letters).

openCC (other)Oct 2025View details →
edi52/100

SBC LTER: Reef: Long-term experiment: Kelp removal: Fish abundance

These data describe the abundance and size of reef-associated fish within permanent plots of a long-term experiment designed to examine trajectories of change in the structure and productivity of kelp forest communities in response to changes in the frequency and severity of disturbance to giant kelp. The number, size and species identity of reef fish were recorded within a 2 m wide swath centered along a 40 m long transect extending up to 2 m off the bottom. Fish size was measured as total length estimated to the nearest cm. The experiment was initiated in 2008 at five reef sites along the mainland coast of the Santa Barbara Channel and included an annual kelp removal treatment designed to simulate increases in the frequency and severity of winter wave disturbance and a continual kelp removal treatment that allowed the effects of giant kelp on the community to be evaluated. The last experimental removals of giant kelp occurred in winter 2016 or winter 2017, depending on the site. Data collection continued in all plots until spring 2023 to document the recovery trajectory of the reef fish community following the cessation of experimental kelp removal.

openCC (other)Sep 2023View details →
edi52/100

SBC LTER: Reef: Abundance, size and fishing effort for California Spiny Lobster (Panulirus interruptus), ongoing since 2012

Data on abundance, size and fishing pressure of California spiny lobster (Panulirus interruptus) are collected along the mainland coast of the Santa Barbara Channel. Spiny lobsters are an important predator in giant kelp forests off southern California. Two SBC LTER study reefs are located in or near the California Fish and Game Network of Marine Protected Areas (MPA), Naples and Isla Vista, both established as MPAs on 2012-01-01. MPAs provide a unique opportunity to investigate the effects of fishing on kelp forest community dynamics. Sampling began in 2012 and is ongoing. This dataset contains two tables. 1) Abundance and size data collected annually by divers in late summer before the start of the fishing season at five SBC LTER long term kelp forest study sites: two within MPAs (Naples and Isla Vista) and three outside (Arroyo Quemado, Mohawk and Carpinteria). 2) Fishing pressure, as determined by counting the number of commercial trap floats. Data are collected every two to four weeks during the lobster fishing season (October to March) at nine sites along the mainland, eight of which are also SBC LTER long-term kelp forest study reefs. See Methods for more information.

openCC (other)May 2024View details →
edi52/100

Fish Counts and Lengths in South Bay and Hog Island Bay, Virginia 2012-2018

To study how seagrass restoration affects coastal fish communities over time, we sampled fishes at each site once or twice per year with beach seines (7.6 m wide × 1.8 m tall; 1.5 m deep pocket with 6.4 mm mesh) hauled along 25-m transects in the summer (May or June) and autumn (September or October) from 2012 through 2018. Researchers ceased sampling at the 4 initially unvegetated sites in South Bay after 2015, when these sites were colonized by seagrass, although seining occurred once more at these sites during the autumn of 2017. During each sampling event, we counted, measured (total length), and identified fish to the lowest possible taxon in the field prior to release. All seine hauls occurred during the day and within 3 hours of low tide for logistical reasons (n = 204). Due to methodological changes, after 2018 surveys are recorded in a different dataset VCR22364 "Abundance and Size of Seagrass-Associated Fishes in the Virginia Coastal Lagoons, 2019-xxxx" https://doi.org/10.6073/pasta/400c84b859e81e9a1e5212bccb37b759.

openCustomJul 2024View details →
zenodo48/100

Background data: Untangling the effects of multiple human stressors and their impacts on fish assemblages in European running waters

<p>This dataset presents some backkground data from the EFI+ database. Related work addresses human stressors and their impacts on fish assemblages at pan-European scale by analysing single and multiple stressors and their interactions. Based on an extensive dataset with 3105 fish sampling sites, patterns of stressors, their combination and nature of interactions, i.e. synergistic, antagonistic and additive were investigated. </p> <p>Data were derived within the EU-project "Improvement and Spatial extension of the European Fish Index (EFI+)". EFI+, an EU FP6 research project from 2007-2009 was designed to gain new knowledge and to further develop and improve new biological assessment methods to meet needs of the Water Framework Directive (WFD). </p> <p>Background data are available for boxplots and barplots shown in the related research article in STOTEN.</p>

opencc-by-nc-nd-4.0May 2017View details →
zenodo48/100

Modelled distributions of fish and epibenthic invertebrates in the southern North Sea

<p>These data include distribution maps of fish and invertabrate species in the southern North Sea from 2014 until 2023. The maps are modelled using point data of presence/absence and biomass (per trawled km&sup2;) from scientific fisheries surveys to estimate the distribution of the probability of occurrence (POC) or biomass (kg per km&sup2;), respectively. Also included are forecasts of species' distributions assuming increasing water temperatures in the southern North Sea according to the ICCP scenario RCP8.5.</p> <p>Each files contains a raster stack with layers for each species. The data can be read into the R using the 'stack'-command from the 'raster'-package. The raster stacks contain layers with headers, which code the species and size group. For some species of relevance to fisheries managment, Numbers behind the latin names of the species give information on the included size classes in cm with 'no' indicating no size class information was available.</p> <p>The file names are composed of the follwing elements:</p> <p>'bio' = biomass</p> <p>'poc' = probability of occurrence</p> <p>'emp' = observed occurrence/abundance data from fisheries surveys with employed spatial smoother</p> <p>'sdm' = modelled distributin data from random forests</p> <p>'fc' = forecast distributions based on temperature predictors according to RCP8.5</p> <p>'rel.ca2' = core areas (CA) of distribution representing values &gt; then the mid-point of modelled POC value range</p> <p>Year numbers give the time frame of empirical data or model predictions.&nbsp;</p> <p>&nbsp;</p> <p><strong>You can access the .tiff-files with the following R-commands using the directory path where you have stored the files:</strong></p> <p><em><strong>library(raster)</strong></em></p> <p><em><strong>poc&lt;-stack("your_path/poc.sdm.2014_2023.tiff")</strong></em></p> <p><em><strong>poc$gadus.morhua_5_113 </strong># Plots distribution of Atlantic cod as probability of occurrence observed at a size range from 5 - 113 cm tail length</em></p>

opencc-by-4.0Nov 2023View details →
zenodo48/100

Data: An experimental sound exposure study at sea: No spatial deterrence of free-ranging pelagic fish

<p>Data abstract:</p> <p>All data and scripts to replicate all plots and statistical results of the paper mentioned below. The data are sound recordings and processed echosounder data (raw echosounder data is available on request but &gt; 100 GB in size and require specialized software).</p> <p>&nbsp;</p> <p>Paper reference:</p> <p>Jeroen Hubert<span>,&nbsp;</span>Jozefien M. Demuynck<span>,&nbsp;</span>M. Rafa Remmelzwaal<span>,&nbsp;</span>Carlota Mu&ntilde;iz<span>,&nbsp;</span>Elisabeth Debusschere<span>,&nbsp;</span>Benoit Berges<span>,&nbsp;</span>Hans Slabbekoorn; An experimental sound exposure study at sea: No spatial deterrence of free-ranging pelagic fish.&nbsp;<em>J. Acoust. Soc. Am.</em>&nbsp;1 February 2024; 155 (2): 1151&ndash;1161.&nbsp;<a href="https://doi.org/10.1121/10.0024720" target="_blank" rel="noopener">https://doi.org/10.1121/10.0024720</a></p> <p>&nbsp;</p> <p>Paper abstract:</p> <p>Acoustic deterrent devices are used to guide aquatic animals from danger or toward migration paths. At sea,&nbsp;moderate sounds can potentially be used to deter fish to prevent injury or death due to acoustic overexposure. In&nbsp;sound exposure studies, acoustic features can be compared to improve deterrence efficacy. In this study, we played&nbsp;200&ndash;1600 Hz pulse trains from a drifting vessel and investigated changes in pelagic fish abundance and behavior by&nbsp;utilizing echosounders and hydrophones mounted to a transect of bottom-moored frames. We monitored fish presence and tracked individual fish. This revealed no changes in fish abundance or behavior, including swimming speed&nbsp;and direction of individuals, in response to the sound exposure. We did find significant changes in swimming depth&nbsp;of individually tracked fish, but this could not be linked to the sound exposures. Overall, the results clearly show that&nbsp;pelagic fish did not flee from the current sound exposures, and we found no clear changes in behavior due to the&nbsp;sound exposure. We cannot rule out that different sounds at higher levels elicit a deterrence response; however, it&nbsp;may be that pelagic fish are just more likely to respond to sound with (short-lasting) changes in school formation.</p> <p>&nbsp;</p> <p>&nbsp;</p>

opencc-by-4.0Dec 2023View details →
zenodo48/100

Dictionary of FAO major fishing areas

<p>This JSON-formatted dictionary of fishing areas as organised by the Food and Agriculture Organization (FAO) of the United Nations (UN) is based on data published on the websites of the European Commission (<a href="https://fish-commercial-names.ec.europa.eu/fish-names/fishing-areas_en">English</a>, <a href="https://fish-commercial-names.ec.europa.eu/fish-names/fishing-areas_de">German</a>). If no German name could be determined, the English name is given instead.</p> <p>The concept and rationale of the FAO Major Fishing Areas is described on the&nbsp;<a href="https://data.apps.fao.org/catalog/dataset/cwp-fishing-area">FAO website</a>.</p> <p>This dictionary implements three hierarchical levels: Areas, Subareas and Divisions.</p>

opencc-by-4.0Apr 2024View details →
zenodo48/100

RivFISH - An European database on fish species presence across river basins

<p>The RivFISH database aggregates the available data on freshwater-dependent fish presence in Europe, validated at the river basin level and considering taxonomical synonyms for species names, thus allowing for a maximization of data usage and robustness. This database also promotes interoperability with other datasets, including the IUCN Red List of Threatened Species, FishBase and the Catchment Characterisation and Modelling (CCM2) &ndash; River and Catchment Database v2.1. It is, as far as the authors know, the most up-to-date and comprehensive database on the presence of freshwater-dependent fish species for European river basins. The structure of the database is also prepared to deal with future alterations in species taxonomy, as well as new records of species occurrence in river basins.</p>

opencc-by-4.0Sep 2024View details →
zenodo48/100

Finite amplitude sound propagation effects in volume backscattering measurements for fish abundance estimation

<p>The upload contains measurement and simulation data for finite-amplitude sound propagation effects in volume backscattering measurements. The experimental data are from a trawl survey conducted in the North Sea with R/V &quot;G. O. Sars&quot;, 6-7&nbsp;November 2004, passing several times over a group of Atlantic mackerel schools. The measurements are of the relative area backscattering coefficient, relative to 38 kHz, 2000 W power setting,&nbsp;at</p> <p>(1) 120 kHz with 250 W transmit power setting, 200 kHz with 120 W transmit power setting<br> (2) 120 kHz with 1000 W power setting, 200 kHz with 1000 W power setting.</p> <p>A&nbsp;Simrad EK60 echosounder system was used, alternating between the low (1) and high (2) power settings through&nbsp;the measurement series.</p> <p>The corresponding simulation data are calculated using the Bergen Code numerical solver of the KZK Equation. The medium parameters input to the simulations are based on CTD data from the field survey . The transducer and amplitude data were found by laboratory measurements on echo sounders of the same type as used in the survey.</p> <p>.m files are included for both .mat data files, with details on how to read the data.</p> <p>An article describing the data has been submitted by the authors to Acta Acustica, 2022.</p>

opencc-by-4.0Sep 2021View details →
zenodo48/100

Multiplexed DNA-FISH imaging dataset, drosophila embryos, nuclear cycles 11-14

<p>Multiplexed DNA-FISH imaging dataset from Drosophila embryos at nuclear cycles 11-14.</p> <p>Examples on how to load and use this dataset can be found at this <a href="https://github.com/NollmannLab/Goetz_etal">GitHub repository</a>.</p> <p><strong>Data processing details</strong></p> <p>Barcodes were segmented using a neural network (<a href="https://github.com/stardist/stardist"><em>stardist</em></a>) specifically trained for the detection of 3D diffraction limited spots produced by our microscope. To extract the position of the barcode with sub-pixel accuracy, a subsequent 3D Gaussian fit of the regions segmented by <em>stardist</em> was performed with Big-FISH (<a href="https://github.com/fish-quant/big-fish">https://github.com/fish-quant/big-fish</a>). Barcode localizations with intensities lower than 1.5 times that of the background were filtered out.</p> <p>Nuclei were segmented from projected DAPI images using <em><a href="https://github.com/stardist/stardist">stardist</a> </em>with a neural network trained for detection of nuclei from <em>Drosophila</em> embryos under our imaging conditions. Barcodes were then attributed to single nuclei by using the XY coordinates of the barcodes and the DAPI masks of the nuclei. Finally, pairwise distance matrices were calculated for each single nucleus.</p> <p><strong>Processed data in Figures</strong></p> <p>This new version of the dataset contains the raw data for each of the figures in the manuscript:</p> <p><strong>Associated publication</strong></p> <p><strong>Multiple parameters shape the 3D chromatin structure of single nuclei at the doc locus in </strong><em>Drosophila</em>.</p> <p>Markus G&ouml;tz, Olivier Messina, Sergio Espinola, Jean-Bernard Fiche, Marcelo Nollmann</p> <p>Nature Communications (2022).</p>

opencc-by-4.0Jan 2022View details →
zenodo48/100

Arctic specimens in the NHMO Fish collection 2022

<p>All Arctic specimens in the NHMO Fish collection as of August 2022. See Johannessen et al. 2023 &quot;Arctic specimens in the<br> zoological collections at the Natural History Museum, University of Oslo, Norway (NHMO)&quot; for further details.</p>

opencc-by-4.0Aug 2022View details →
zenodo48/100

Barley as a production platform for oral vaccines in sustainable fish aquaculture

<p>Experimental data for the study "Barley as a production platform for oral vaccines in sustainable fish aquaculture"</p>

opencc-by-4.0Sep 2024View details →
zenodo48/100

Two decades of body length measurements in size-structured larval and juvenile fish populations in English rivers.

<p>Long term ecological datasets are valuable in providing context and understanding to complex ecological processes that occur over broad temporal scales, and provide a baseline for analysing change. Monitoring of fish populations in UK waterbodies and elsewhere is typically through measuring the length of individual fish caught in surveys. Through this method, the age structure of fish populations can be determined, as well as over winer survival rates and future recruitment success and cohort sizes can be predicted. The larval and juvenile period are when fish are considered most vulnerable to predation, competition, disease and environmental perturbations.&nbsp;</p> <p><br>This study presents the first long-term larval and juvenile fish lengths dataset for 67 survey sites over two decades (1999-2018) from the rivers Ancholme, Warwickshire Avon, Don, Trent, and Yorkshire Ouse&nbsp;(including the Swale, Ure, Nidd and Wharfe) in the United Kingdom. These rivers represent a range of topographical and biotopical characteristics. For the majority of this study, surveys were conducted on a monthly or fortnightly basis making both annual and seasonal analyses of size structure, growth and body length possible. Although there is some variation in the sampling frequency and some locations varied throughout the study according to requirements. In total, more than 380,000 larval or juvenile fish of 30 species were measured, likely representing one of the most comprehensive datasets of its type.</p> <p>Surveys were conducted in river margins, where the velocity was slowest and larval and juvenile fish tend to aggregate. Fish were captured using a 25 x 3 m micromesh (3 mm mesh size) seine net that was set in a rectangle parallel to the bank. This net capture fish as small as 5 mm and is the most appropriate method of catching larvae and juvenile fish,&nbsp;although occasionally some larger adult fish may have also been captured and measured as part of this dataset for completeness. All fish were identified to species and measured to standard length (mm) and released at the point of capture. The exception was the smallest larvae, which were euthanised with an overdose of methanesulphonate (MS-222) and preserved in 4% formalin solution for microscopic examination.</p> <p><br>The dataset contains 384,090 rows and 13 columns. Each row corresponds to a single fish that was measured at each site and date. Associated site information (site name, location, area fished (m<sup>2</sup>) and survey date) is reported for each row. When only a fraction of the catch was processed, the sub-sample size was reflected in the Count column (e.g. when half the sample was processed, the numbers of fish measured or only counted were multiplied by two). This enables accurate densities to be calculated as the total number of both measured and unmeasured fish is recorded.</p> <p>Description of columns found in the dataset:</p> <p>&nbsp;</p> <table> <tbody> <tr> <td> <p><strong>Column heading</strong></p> </td> <td> <p><strong>Column description</strong></p> </td> <td> <p><strong>Data type</strong></p> </td> <td> <p><strong>Units</strong></p> </td> </tr> <tr> <td> <p>Fish _Catchment</p> </td> <td> <p>The river catchment/basin location of each fish site</p> </td> <td> <p>Text</p> </td> <td> <p>n/a</p> </td> </tr> <tr> <td> <p>Fish_River</p> </td> <td> <p>The river/watercourse location of each fish site.</p> </td> <td> <p>Text</p> </td> <td> <p>n/a</p> </td> </tr> <tr> <td> <p>Fish_SiteName</p> </td> <td> <p>The name of each fish site</p> </td> <td> <p>Text</p> </td> <td> <p>n/a</p> </td> </tr> <tr> <td> <p>Fish_Latitude</p> </td> <td> <p>The latitude of each fish site (WGS 1984)</p> </td> <td> <p>Integer</p> </td> <td> <p>Decimal degrees</p> </td> </tr> <tr> <td> <p>Fish_Longitude</p> </td> <td> <p>The longitude of each fish site (WGS 1984)</p> </td> <td> <p>Integer</p> </td> <td> <p>Decimal degrees</p> </td> </tr> <tr> <td> <p>Fish_Area</p> </td> <td> <p>Area of fish site surveyed</p> </td> <td> <p>Integer</p> </td> <td> <p>m<sup>-2</sup></p> </td> </tr> <tr> <td> <p>Fish_SurveyDate</p> </td> <td> <p>Date fish survey was carried out</p> </td> <td> <p>Integer</p> </td> <td> <p>dd/mm/yyyy</p> </td> </tr> <tr> <td> <p>Fish_Year</p> </td> <td> <p>Year fish survey was carried out</p> </td> <td> <p>Integer</p> </td> <td> <p>yyyy</p> </td> </tr> <tr> <td> <p>Common_Name</p> </td> <td> <p>The common/vernacular name of each fish taxon recorded in the dataset.</p> </td> <td> <p>Text</p> </td> <td> <p>n/a</p> </td> </tr> <tr> <td> <p>Latin_Name</p> </td> <td> <p>The scientific name of each fish taxon recorded in the dataset</p> </td> <td> <p>Text</p> </td> <td> <p>n/a</p> </td> </tr> <tr> <td> <p>Net_Number</p> </td> <td> <p>The net number the fish in a given survey were caught on</p> </td> <td> <p>Integer</p> </td> <td> <p>n/a</p> </td> </tr> <tr> <td> <p>Length_mm</p> </td> <td> <p>Length of individual fish caught</p> </td> <td> <p>Integer</p> </td> <td> <p>mm</p> </td> </tr> <tr> <td> <p>Count</p> </td> <td> <p>Count of fish caught accounting for sub- sampling</p> </td> <td> <p>Integer</p> </td> <td> <p>Number of fish</p> </td> </tr> </tbody> </table> <p>&nbsp;</p>

opencc-by-4.0Aug 2024View details →
zenodo48/100

Modulation of bioelectric cues in the evolution of flying fishes [Data set]

<p>Assembled reference contigs for protein-coding exons and conserved non-coding regions from targeted sequence enrichment of beloniform&nbsp;fishes.&nbsp;</p> <p>Current citation:&nbsp;Daane JM, Blum&nbsp;N, Lanni&nbsp;J, Boldt&nbsp;H, Iovine&nbsp;MK, Johnson&nbsp;SL, Lovejoy&nbsp;NR,&nbsp;and MP Harris. (2021).&nbsp;Novel regulators of growth identified in the evolution of fin proportion in flying fish. <em>bioRxiv. </em>doi: 10.1101/2021.03.05.434157</p> <p>-contigs.tar.gz contains the assembled contigs for each species. Each contig represents a targeted region with the addition of flanking DNA sequence</p> <p>-cnes.tar.gz contains the targeted conserved non-coding regions isolated from the larger contigs in contigs.tar.gz</p> <p>-exons.tar.gz contains the targeted protein coding exons isolated from the larger contigs in contigs.tar.gz</p> <p>-translated_exons.tar.gz&nbsp;contains the translated protein coding exons from exons.tar.gz</p> <p>-Beloniformes.tre is the species tree&nbsp;</p> <p>-medaka_cne_great.txt contains the associations between the assembled CNEs and neighboring protein-coding genes based on the GREAT approach&nbsp;</p>

opencc-by-4.0Jul 2021View details →
zenodo48/100

Dataset for Semantic Segmentation of Fishing Trajectories

<p>This is the dataset that was manually labelled by the author during his research work for the paper &quot;Semantic Segmentation of AIS Trajectories for Detecting Complete Fishing Activities&quot; in MDM 2022.</p>

opencc-by-4.0Nov 2022View details →
zenodo48/100

Arctic specimens in the NHMO DNA bank Fish & Herptile collection 2022

<p>All Arctic specimens in the NHMO DNA bank Fish &amp; Herptile collection as of August 2022. See Johannessen et al. 2023 &quot;Arctic specimens in the zoological collections at the Natural History Museum, University of Oslo, Norway (NHMO)&quot; for further details.</p>

opencc-by-4.0Aug 2022View details →
edi48/100

Knights Landing, California Department of Fish and Wildlife, Genetic Determination of Population of Origin 2017 through 2019

Central Valley Chinook Salmon populations differ in their Endangered Species Act listing status. It is often difficult to distinguish individuals from the different Evolutionarily Significant Units. As such, many of the salmon monitoring and evaluation efforts in the Central Valley and San Francisco Bay-Delta are hampered by uncertainty about population (stock) identification and proportional effects of management actions (Dekar et al. 2013; IEP 2019). Studies have identified that the current identification method (length-at-date models) of juvenile Chinook salmon (Fisher 1992) captured in the watershed vary in their accuracy, particularly for spring-run (NMFS 2013; Harvey et al. 2014; Merz et al. 2014). The inaccuracy of the size-based methods is likely due to differences in fish distribution during early rearing, habitat-specific growth rates, and inter-annual variability in temperatures and food availability that lead to overlap in size ranges among stocks. The primary objective of this project was the genetic classification (to race; Evolutionary Significant Unit) of Chinook Salmon captured from State Water Project and Central Valley Project fish protection facilities and Interagency Ecological Program monitoring programs. The population-of-origin was determined for sampled fish by comparing their genotypes to reference genetic baselines. Genetic methods, having less statistical uncertainty that size-based models for population identification, were intended to directly target (and reduce) one source of uncertainty in the estimation of loss (take) from water diversions (operations) and develop the information necessary for understanding stock-specific distribution, habitat utilization, abundance, and life history variation. This project supports recommendations from the Interagency Ecological Program’s Salmon and Sturgeon Assessment of Indicators by Life Stage and Interagency Ecological Program Science Agenda efforts to improve Central Valley salmonid monitoring

openCC (other)Dec 2021View details →
edi48/100

Sacramento trawl, Delta Juvenile Fish Monitoring Program, Genetic Determination of Population of Origin 2017-2021

Central Valley Chinook Salmon populations differ in their Endangered Species Act listing status. It is often difficult to distinguish individuals from the different Evolutionarily Significant Units. As such, many of the salmon monitoring and evaluation efforts in the Central Valley and San Francisco Bay-Delta are hampered by uncertainty about population (stock) identification and proportional effects of management actions (Dekar et al. 2013; IEP 2019). Studies have identified that the current identification method (length-at-date models) of juvenile Chinook salmon (Fisher 1992) captured in the watershed vary in their accuracy, particularly for spring-run (NMFS 2013; Harvey et al. 2014; Merz et al. 2014). The inaccuracy of the size-based methods is likely due to differences in fish distribution during early rearing, habitat-specific growth rates, and inter-annual variability in temperatures and food availability that lead to overlap in size ranges among stocks. The primary objective of this project was the genetic classification (to race; Evolutionary Significant Unit) of Chinook Salmon captured from State Water Project and Central Valley Project fish protection facilities and Interagency Ecological Program monitoring programs. The population-of-origin was determined for sampled fish by comparing their genotypes to reference genetic baselines. Genetic methods, having less statistical uncertainty that size-based models for population identification, were intended to directly target (and reduce) one source of uncertainty in the estimation of loss (take) from water diversions (operations) and develop the information necessary for understanding stock-specific distribution, habitat utilization, abundance, and life history variation. This project supports recommendations from the Interagency Ecological Program’s Salmon and Sturgeon Assessment of Indicators by Life Stage and Interagency Ecological Program Science Agenda efforts to improve Central Valley salmonid monitoring

openCC (other)Dec 2021View details →
edi48/100

Chipps Island trawl, Delta Juvenile Fish Monitoring Program, Genetic Determination of Population of Origin 2017-2021

Central Valley Chinook Salmon populations differ in their Endangered Species Act listing status. It is often difficult to distinguish individuals from the different Evolutionarily Significant Units. As such, many of the salmon monitoring and evaluation efforts in the Central Valley and San Francisco Bay-Delta are hampered by uncertainty about population (stock) identification and proportional effects of management actions (Dekar et al. 2013; IEP 2019). Studies have identified that the current identification method (length-at-date models) of juvenile Chinook salmon (Fisher 1992) captured in the watershed vary in their accuracy, particularly for spring-run (NMFS 2013; Harvey et al. 2014; Merz et al. 2014). The inaccuracy of the size-based methods is likely due to differences in fish distribution during early rearing, habitat-specific growth rates, and inter-annual variability in temperatures and food availability that lead to overlap in size ranges among stocks. The primary objective of this project was the genetic classification (to race; Evolutionary Significant Unit) of Chinook Salmon captured from State Water Project and Central Valley Project fish protection facilities and Interagency Ecological Program monitoring programs. The population-of-origin was determined for sampled fish by comparing their genotypes to reference genetic baselines. Genetic methods, having less statistical uncertainty that size-based models for population identification, were intended to directly target (and reduce) one source of uncertainty in the estimation of loss (take) from water diversions (operations) and develop the information necessary for understanding stock-specific distribution, habitat utilization, abundance, and life history variation. This project supports recommendations from the Interagency Ecological Program’s Salmon and Sturgeon Assessment of Indicators by Life Stage and Interagency Ecological Program Science Agenda efforts to improve Central Valley salmonid monitoring

openCC (other)Dec 2021View 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