Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
129
datasets available to search
ShareScore release 0.9.0
Dataset results
129 results for “jays”
Henry Jaye (j0621)
<b>-- <a href="https://doi.org/10.5281/zenodo.11582199">Documentation</a> --</b><br><br><u>Name</u>: Henry Jaye<br><u>musiXplora-ID</u>: j0621<br><u>musiXplora-URI</u>: <a href="https://musixplora.de/mxp/j0621">https://musixplora.de/mxp/j0621</a><br><u>Gender</u>: m<br><u>Date of Death</u>: 1676<br><u>Place of Death</u>: Undefined<br><u>First Mentioned</u>: 1611<br><u>Sectors</u>: Geigenbau<br><u>Professions (Musical)</u>: Geigenbauer<br><u>Other Places of Activity</u>: London, Southwark<br><br><br><u>Titel/Medien:</u><br><table><tbody><tr><th>Role</th><th>Sigel</th><th>Title</th><th>mXp-ID</th></tr><tr><td>Related</td><td>Lütgendorff 1922</td><td>Die Geigen- und Lautenmacher vom Mittelalter bis zur Gegenwart. 2 Bände. Lüt2</td><td><a href="https://musixplora.de/mxp/5002059">5002059</a></td></tr><tr><td>Related</td><td>Kinsky 1921a</td><td>Verkauf der Sammlung Galpin nach Amerika</td><td><a href="https://musixplora.de/mxp/5033592">5033592</a></td></tr></tbody></table><br><br><u>Changelog</u>:<br> - v0.0.1: Initial Upload.<br>
JWST spectrum of galaxy COSMOS-11142 from the Blue Jay survey.
<p>Spectroscopic and photometric data for galaxy COSMOS-11142, studied in Belli et al. (2024).</p> <ul> <li>The JWST/NIRSpec spectroscopy is stored as a FITS table which includes wavelength (in angstrom), calibrated flux, uncertainty, and best-fit model (in erg/(s cm2 A)).</li> <li>The JWST and HST photometry is stored as a FITS table which includes the name of each filter, the effective wavelength (in angstrom), the observed flux and its uncertainty (in microJy).</li> </ul>
Multistate modeling of Florida scrub-jay adult survival and breeding transitions
<p><strong>Metadata for data file “MS4APR2020 ALL ENTER 2 STATES.txt” for the research published in Ecosphere Article ECS21-0698</strong></p> <p>Multistate modeling of Florida scrub-jay adult survival and breeding transitions</p> <p>David R. Breininger<sup>1</sup>†, Geoffrey M. Carter<sup>1</sup>, Stephanie A. Legare<sup>1</sup> William V. Payne<sup>1</sup>, Eric D. Stolen<sup>1</sup>, Daniel J. Breininger<sup>2</sup>, James E. Lyon<sup>3</sup></p> <p><sup>1</sup>Herndon Solutions Group, LLC, NASA Environmental and Medical Contract, NEM-022, Kennedy Space Center, FL 32899, U.S.A.</p> <p><sup>2</sup>Department of Mathematics, Florida Institute of Technology, Melbourne FL, 32899 U.S.A.</p> <p><sup>3</sup>Merritt Island National Wildlife Refuge, Titusville FL 32901, U.S.A.</p> <p>†<em> Corresponding author: </em>e-mail: <a href="mailto:david.r.breininger@nasa.gov">david.r.breininger@nasa.gov</a></p> <p>The data uses input file format described in the Program MARK manual (White and Burnham 1999, Cooch and White 2006). Each record (row) starts with an adult bird’s capture history, followed by group variables (each bird belongs to only one group) and then covariates, which here are all time specific. Time starts with 2001 and ends with 2015. Periods “.” in the capture history represented birds that were censored because the study sites were discontinued. </p> <table> <tbody> <tr> <td> <p> </p> <p>The first 15 columns represent states from 2001 to 2015 where “I” refers to nonbreeder, “2” refers to breeder and “0” occurs when the bird is not observed.</p> </td> </tr> <tr> <td> <p>Spaces occur after the capture history and between group variables and covariates.</p> </td> </tr> <tr> <td> <p>The first group variable identifies males if given a "1".</p> </td> </tr> <tr> <td> <p>The second group variable identifies females if given a :1".</p> </td> </tr> <tr> <td> <p>The third and final group membership identifies birds of unknown sex if given a "1".</p> </td> </tr> <tr> <td> <p>All following data refer to time-specific covariates except for the semicolon at the end of each individual's record.</p> </td> </tr> <tr> <td> <p>The first 14 covariates refer to whether a bird resided on the study site edge (0) or interior (1).</p> </td> </tr> <tr> <td> <p>The 2nd set of 14 covariates refer density (number of pairs/potential pairs) within the local population.</p> </td> </tr> <tr> <td> <p>The 3rd set of 14 covariates refer to population breeder mortality rates (number of banded breeders that died/number of banded breeders).</p> </td> </tr> <tr> <td> <p>The final set of 14 covariates refer to mean family group size of adults in each local population.</p> </td> </tr> </tbody> </table>
Рис. 6. Морские двустворчатые моллюски иЗ раскопа 5 поселениЯ Константиновка-1: A–H – Mizuhopecten yessoensis (Jay, 1857) (слои 1, 2 – бровка). Длина фрагментов от 51 до 121 мм. Fig. 6. Marine bivalves from excavation 5 of the Konstantinovka-1 settlement excavations: A–H – Mizuhopecten yessoensis (Jay, 1857) (levels 1, 2 – cross section). Sizes of shell fragments are from 51 to 121 mm. in Mollusks from the archaeological site Konstantinovka-1 in Primorye (Russian Far East)
Рис. 6. Морские двустворчатые моллюски иЗ раскопа 5 поселениЯ Константиновка-1: A–H – Mizuhopecten yessoensis (Jay, 1857) (слои 1, 2 – бровка). Длина фрагментов от 51 до 121 мм. Fig. 6. Marine bivalves from excavation 5 of the Konstantinovka-1 settlement excavations: A–H – Mizuhopecten yessoensis (Jay, 1857) (levels 1, 2 – cross section). Sizes of shell fragments are from 51 to 121 mm.
Рис. 7. Морские двустворчатые моллюски иЗ раскопа 1 поселениЯ Константиновка-1: A–M – Glycymeris (Glycymeris) yessoensis (Sowerby III, 1889) (A, B – данные не расшифрованы, длина раковины 44.6 мм; C, D – данные не расшифрованы, длина раковины 38.7 мм; E, F – раскоп 5, пл. 6, кв. Б-6, длина раковины 30.7 мм; G, H –?подъемный материал, длина раковины 33.8 мм; I, J – раскоп 3, кв. З-6, длина раковины 40.4 мм; K–M – раскоп 2, пл. 7, кв. Д-6, длина раковины 23.5 мм; N, O – Mya (Arenomya) japonica Jay, 1857 – подъемный материал, длина раковины 61.7 мм. Fig. 7. Marine bivalves from excavation 1 of the Konstantinovka-1 site: A–M – Glycymeris (Glycymeris) yessoensis (Sowerby III, 1889) (A, B – data not available, shell length 44.6 mm; C, D – data not available, shell length 38.7 mm; E, F – excavation 5, layer 6, square Б-6, shell lenth 30.7 mm; G, H –?surface scatter, shell length 33.8 mm; I, J – excavation 3, square З-6, shell length 40.4 mm; K–M – excavation 2, layer 7, square Д-6, shell length 23.5 mm; N, O – Mya (Arenomya) japonica Jay, 1857 – surface scatter, shell length 61.7 mm. in Mollusks from the archaeological site Konstantinovka-1 in Primorye (Russian Far East)
Рис. 7. Морские двустворчатые моллюски иЗ раскопа 1 поселениЯ Константиновка-1: A–M – Glycymeris (Glycymeris) yessoensis (Sowerby III, 1889) (A, B – данные не расшифрованы, длина раковины 44.6 мм; C, D – данные не расшифрованы, длина раковины 38.7 мм; E, F – раскоп 5, пл. 6, кв. Б-6, длина раковины 30.7 мм; G, H –?подъемный материал, длина раковины 33.8 мм; I, J – раскоп 3, кв. З-6, длина раковины 40.4 мм; K–M – раскоп 2, пл. 7, кв. Д-6, длина раковины 23.5 мм; N, O – Mya (Arenomya) japonica Jay, 1857 – подъемный материал, длина раковины 61.7 мм. Fig. 7. Marine bivalves from excavation 1 of the Konstantinovka-1 site: A–M – Glycymeris (Glycymeris) yessoensis (Sowerby III, 1889) (A, B – data not available, shell length 44.6 mm; C, D – data not available, shell length 38.7 mm; E, F – excavation 5, layer 6, square Б-6, shell lenth 30.7 mm; G, H –?surface scatter, shell length 33.8 mm; I, J – excavation 3, square З-6, shell length 40.4 mm; K–M – excavation 2, layer 7, square Д-6, shell length 23.5 mm; N, O – Mya (Arenomya) japonica Jay, 1857 – surface scatter, shell length 61.7 mm.
Fig. 1 in High prevalence of haemosporidian parasites in Eurasian jays
Fig. 1 Median-joining network of mitochondrial cytochrome b lineages (476 bp, n = 60 sequences) of haemosporidian parasites found in Eurasian jays Garrulus glandarius. Circle size is proportional to the lineage frequency. Lineage names are noted at the associated circles together with one exemplary GenBank association number in parentheses. One hatch mark represents one mutation. Sample origins are represented by different colours, 'MalAvi' referring to sequences from other studies deposited in the MalAvi database (MalAvi 2023). Morphospecies names for GAGLA07 (H. homopicae) and TURDUS2 (H. minutus) are not provided within the figure
Figure 4 in Distribution of Pinyon Jay Gymnorhinus cyanocephalus in Chihuahua, Mexico: new records and environmental characterisation
Figure 4. GAM regression showing relationship between environmental suitability index (ESI) against elevation (m).
Figure 2 in Distribution of Pinyon Jay Gymnorhinus cyanocephalus in Chihuahua, Mexico: new records and environmental characterisation
Figure 2. Sampling bias file generated using the Gaussian kernel density of sampling localities tool (spatially rarefied records as input).
Figure 1 in Distribution of Pinyon Jay Gymnorhinus cyanocephalus in Chihuahua, Mexico: new records and environmental characterisation
Figure 1. Cluster analysis showing correlation between bioclimatic and topographic layers supported by AU (approximately unbiased) P-value (left) and bootstrap values (right).
Figure 3 in Distribution of Pinyon Jay Gymnorhinus cyanocephalus in Chihuahua, Mexico: new records and environmental characterisation
Figure 3. Tenfold cross-validation MaxEnt 'year-round' distribution model in a scale of maximum–minimum values showing the potential distribution for Pinyon Jay Gymnorhinus cyanocephalus in our study area and plotting the spatially rarefied records and the new Chihuahuan record.
Фототаблица 2 Plate 2 A, B – Crassostrea gigas (Thunberg, 1793): СевернаЯ КореЯ, провинциЯ Северный Хамгён, высота 91.3 мм, ЗМ ДВФУ № 38379/Bv-5785; C, D – Pododesmus (Monia) macrochisma (Deshayes, 1839): СевернаЯ КореЯ, провинциЯ Северный Хамгён, Чипсам, длина 49.6 мм, ЗМ ДВФУ № 38635/Bv-5915; E, F – Mactra (Mactra) chinensis Philippi, 1846: СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 47.5 мм, ЗМ ДВФУ № 38353/Bv-5769; G, H – Spisula (Pseudocardium) sachalinensis (Schrenck, 1861): СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 95.0 мм, ЗМ ДВФУ № 38355/Bv-5771; I, J – Mactromeris polynyma (Stimpson, 1860): СевернаЯ КореЯ, провинциЯ Северный Хамгён, Чипсам, длина 45.6 мм, ЗМ ДВФУ № 38625/Bv-5905; K–N – Mizuhopecten yessoensis (Jay, 1857): СевернаЯ КореЯ, провинциЯ Северный Хамгён, г. ЧхондЖин, рынок, длина 65.9 мм, ЗМ ДВФУ № 38377/Bv-5783; O–P – Chlamys (Swiftopecten) swiftii (Bernardi, 1858): СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 70.8 мм, ЗМ ДВФУ № 38378/Bv-5784. A, B – Crassostrea gigas (Thunberg, 1793): North Korea, North Hamgyong Province, shell height 91.3 mm, ZMFU no. 38379/Bv-5785; C, D – Pododesmus (Monia) macrochisma (Deshayes, 1839): North Korea, North Hamgyong Province, Jipsam, shell length 49.6 mm, ZMFU no. 38635/Bv-5915; E, F – Mactra (Mactra) chinensis Philippi, 1846: North Korea, North Hamgyong Province, shell length 47.5 mm, ZMFU no. 38353/Bv-5769; G, H – Spisula (Pseudocardium) sachalinensis (Schrenck, 1861): North Korea, North Hamgyong Province, shell length 95.0 mm, ZMFU no. 38355/Bv-5771; I, J – Mactromeris polynyma (Stimpson, 1860): North Korea, North Hamgyong Province, Jipsam, shell length 45.6 mm, ZMFU no. 38625/Bv-5905; K–N – Mizuhopecten yessoensis (Jay, 1857): North Korea, North Hamgyong Province, Chongjin City, market, shell length 65.9 mm, ZMFU no. 38377/Bv-5783; O–P – Chlamys (Swiftopecten) swiftii (Bernardi, 1858): North Korea, North Hamgyong Province, shell length 70.8 mm, ZMFU no. 38378/Bv-5784. in On the bivalve molluscan fauna of North Hamgyong Province (North Korea)
Фототаблица 2 Plate 2 A, B – Crassostrea gigas (Thunberg, 1793): СевернаЯ КореЯ, провинциЯ Северный Хамгён, высота 91.3 мм, ЗМ ДВФУ № 38379/Bv-5785; C, D – Pododesmus (Monia) macrochisma (Deshayes, 1839): СевернаЯ КореЯ, провинциЯ Северный Хамгён, Чипсам, длина 49.6 мм, ЗМ ДВФУ № 38635/Bv-5915; E, F – Mactra (Mactra) chinensis Philippi, 1846: СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 47.5 мм, ЗМ ДВФУ № 38353/Bv-5769; G, H – Spisula (Pseudocardium) sachalinensis (Schrenck, 1861): СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 95.0 мм, ЗМ ДВФУ № 38355/Bv-5771; I, J – Mactromeris polynyma (Stimpson, 1860): СевернаЯ КореЯ, провинциЯ Северный Хамгён, Чипсам, длина 45.6 мм, ЗМ ДВФУ № 38625/Bv-5905; K–N – Mizuhopecten yessoensis (Jay, 1857): СевернаЯ КореЯ, провинциЯ Северный Хамгён, г. ЧхондЖин, рынок, длина 65.9 мм, ЗМ ДВФУ № 38377/Bv-5783; O–P – Chlamys (Swiftopecten) swiftii (Bernardi, 1858): СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 70.8 мм, ЗМ ДВФУ № 38378/Bv-5784. A, B – Crassostrea gigas (Thunberg, 1793): North Korea, North Hamgyong Province, shell height 91.3 mm, ZMFU no. 38379/Bv-5785; C, D – Pododesmus (Monia) macrochisma (Deshayes, 1839): North Korea, North Hamgyong Province, Jipsam, shell length 49.6 mm, ZMFU no. 38635/Bv-5915; E, F – Mactra (Mactra) chinensis Philippi, 1846: North Korea, North Hamgyong Province, shell length 47.5 mm, ZMFU no. 38353/Bv-5769; G, H – Spisula (Pseudocardium) sachalinensis (Schrenck, 1861): North Korea, North Hamgyong Province, shell length 95.0 mm, ZMFU no. 38355/Bv-5771; I, J – Mactromeris polynyma (Stimpson, 1860): North Korea, North Hamgyong Province, Jipsam, shell length 45.6 mm, ZMFU no. 38625/Bv-5905; K–N – Mizuhopecten yessoensis (Jay, 1857): North Korea, North Hamgyong Province, Chongjin City, market, shell length 65.9 mm, ZMFU no. 38377/Bv-5783; O–P – Chlamys (Swiftopecten) swiftii (Bernardi, 1858): North Korea, North Hamgyong Province, shell length 70.8 mm, ZMFU no. 38378/Bv-5784.
Density dependence maintains long-term stability despite increased isolation and inbreeding in the Florida Scrub-Jay
<p>Isolation caused by anthropogenic habitat fragmentation can destabilize populations. Populations relying on the inflow of immigrants can face reduced fitness due to inbreeding depression as fewer new individuals arrive. Empirical studies of the demographic consequences of isolation are critical to understanding how populations persist through changing conditions. We used a 34-year demographic and environmental dataset from a population of cooperatively-breeding Florida Scrub-Jays (<em>Aphelocoma coerulescens</em>) to create mechanistic models linking environmental and demographic factors to population growth rates. We found that the population has not declined despite both declining immigration and increasing inbreeding, owing to a coinciding response in breeder survival. We find evidence of density-dependent immigration, breeder survival, and fecundity, indicating that interactions between vital rates and local density play a role in buffering the population against change. Our study elucidates the impacts of isolation on demography and how long-term stability is maintained via demographic responses.</p>
Figs. 6–10. 6. Cerithium magnum Jay, 1836 in Catalog Of Recent Type Specimens In The Division Of Invertebrate Zoology, American Museum Of Natural History. V. Mollusca, Part 2 (Class Gastropoda [Exclusive Opisthobranchia And Pulmonata With Supplements To Gastropoda [Opisthobranchia], And Bivalvia
Figs. 6–10. 6. Cerithium magnum Jay, 1836 (lectotype—AMNH 56067), X 0.75. 7. Conus Bernardi and Crosse, 1861 (syntype—AMNH 47629), X 1.75. 8. Conus pseudoaustini Usticke, (holotype—AMNH 195452), X 2. 9. Cyclostoma maculosa Jay, 1839 (syntype—AMNH 56086), 10. Cyclostoma multilineata Jay, 1839 (syntype—AMNH 56087), X 2.6.
Deep ecomorphological and genetic divergence in Steller's Jays (Cyanocitta stelleri, Aves: Corvidae)
<p>The relationship between ecology and morphology is a cornerstone of evolutionary biology, and quantifying variation across environments can shed light on processes that give rise to biodiversity. Three morphotypes of the Steller’s Jay (<em>Cyanocitta stelleri</em>) occupy different ecoregions in western North America that vary in climate and landcover. These morphotypes (Coastal, Interior, Rocky Mountain) differ in size, plumage coloration, and head pattern. We sampled 1,080 Steller’s Jays from 68 populations (plus 11 outgroups) to address three main questions using data on morphology, plumage, genetics (mtDNA, microsatellites), and ecological niches: (1) How do phenotypic and genetic traits vary within and among populations, morphotypes, and ecoregions? (2) How do population-level differences in Steller’s Jays compare to other sister species pairs of North American birds? (3) What can we infer about the population history of Steller’s Jays in relation to past climates, paleoecology, and niche evolution? We found substantial morphological, genetic, and ecological differentiation among morphotypes. The greatest genetic divergence separated Coastal and Interior morphotypes from the Rocky Mountain morphotype, which was associated with warmer, drier, and more open habitats. Microsatellites revealed additional structure between Coastal and Interior groups. The deep mtDNA split between Coastal/Interior and Rocky Mountain lineages of Steller’s Jay (ND2 ~7.8%) is older than most North American avian sister species and dates to approximately 4.3 mya. Interior and Rocky Mountain morphotypes contact across a narrow zone with steep clines in traits and reduced gene flow. The distribution of the three morphotypes coincides with divergent varieties of ponderosa pine and Douglas fir. Species distribution models support multiple glacial refugia for Steller’s Jays. Our integrative dataset combined with extensive geographic sampling provides compelling evidence for recognizing at least two species of Steller’s Jay.</p>
Survival of juvenile Florida Scrub-Jays is positively correlated with month and negatively correlated with male breeder death
<p>Juvenile survival in birds is difficult to estimate, but this vital rate can be an important consideration for management decisions. We estimated juvenile survival of cooperatively breeding Florida Scrub-Jays (<em>Aphelocoma</em> <em>coerulescens</em>) in a landscape degraded by fire suppression and fragmentation using data from marked (n = 325) and unmarked juveniles (n = 1,306) with an integrated hierarchical Bayesian model. To assess the combined analyses, we also analyzed these datasets separately, with a Cormack–Jolly–Seber model (marked) and a young model (unmarked). Our data consisted of monthly censuses of territorial family groups from Florida Scrub-Jay populations in East Central Florida collected over a 22-year period. Juvenile survival was estimated from July when young Florida Scrub-Jays begin developing independence to March when they become first-year individuals and grouped according to the habitat quality class of their natal territory that were based on shrub height (with intermediate shrub heights being optimal and short and tall shrub heights being suboptimal) and the presence of sandy openings (the preferred open having many sandy openings; closed not having enough). Parameter estimates in the combined analysis were intermediate to the separate analyses. Notable differences among the separate analyses were that suboptimal habitat survival was lower in the unmarked analysis, the unmarked analysis showed a linear effect of time not seen in the marked analysis, and there was an effect of male breeder death in the marked but not unmarked analysis. The combined data analysis provided more inference than did either dataset analyzed separately including juveniles in optimal-closed territories unexpectedly had higher survival than those in optimal-open, survival increased through time, and male breeder death had a negative effect on survival. This study suggests that optimal-closed habitat may play an important role in juvenile Florida Scrub-Jay survival perhaps by providing better cover from predators and warrants further investigation for management implications.</p>
Genetic parallelism underlying repeated bill divergence in Island Scrub-Jays (<em>Aphelocoma insularis</em>) increases at higher genetic levels of organization
Open the record for dataset details and reuse information.
Density dependence maintains long-term stability despite increased isolation and inbreeding in the Florida Scrub-Jay
Open the record for dataset details and reuse information.
Survival of juvenile Florida Scrub-Jays is positively correlated with month and negatively correlated with male breeder death
Open the record for dataset details and reuse information.
Data from: Translocations spur population growth but fail to prevent genetic erosion in imperiled Florida Scrub-Jays
Open the record for dataset details and reuse information.
Identifying drivers of Florida Scrub-Jay reproductive success in the absence of helpers, 1989-2021
Florida Scrub-Jays (FSJ) are federally Threatened, cooperatively breeding birds, where about half of breeding pairs typically have helpers. Factors affecting reproductive success of this species in the absence of helpers has received little attention. This dataset contains reproductive and environmental data relevant to a subset of known age breeding pairs that did not have helpers at Archbold Biological Station (ABS) from 1989 to 2021. Generalized linear mixed models were used to explain variation in reproductive output (offspring survived to 75 days) in relation to: male and female breeding experience and environmental variables (acorn abundance, fire history, and territory size), with year and territory ID included as random effects. Reproductive output was associated with female breeding experience and all three environmental variables. The findings highlight the importance of fire-maintained oak scrub in FSJ reproductive success, which is consistent with management recommendations for this species.
ScienceDex guides
Understand access before you commit
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.