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Figure 2 in Neurovascular evidence for a co-occurrence of teeth and baleen in an Oligocene mysticete and the transition to filter-feeding in baleen whales
Figure 2. Neurovascular canals through rostrum of Aetiocetus weltoni (UCMP 122900). A, ventral view of 3D rendering of skull (top), skull rendered semi-transparent to reveal internal canals of rostrum (middle), and digital segmentation of rostral canals (bottom). B, lateral view of 3D rendering of skull (top), skull rendered semi-transparent to reveal internal canals of rostrum (middle), and digital segmentation of rostral canals (bottom).
Modelled data - Energy Transition in Bolivia
<p>Model structure, input data and output files from MoManI </p>
Supplementary data for: "Transition from sub-Rayleigh anticrack to supershear crack propagation in snow avalanches"
<p>This Folder contains supplementary data for the paper "Transition from sub-Rayleigh anticrack to supershear crack propagation in snow avalanches". Please see ReadMe.txt for more details.</p> <p> </p>
Elastic Anomalies across the α-β Phase Transition in Orthopyroxene: Implication for the Metastable Wedge in the Cold Subduction Slab
<p>Here are the expeirmental data</p>
Guiding antiferromagnetic transitions by substitution in Ca2RuO4
<p>Data and analysis scripts for the publication "Guiding antiferromagnetic transitions by substitution in Ca<sub>2</sub>RuO<sub>4</sub>" .</p> <p>Characterisation and Resonant x-ray diffraction data from single crystals of Mn doped Ca2RuO4.</p> <p>Included in this repository are the following data:</p> <ul> <li>Single Crystal X-Ray Diffraction <ul> <li>Refined CIFs from x-ray diffraction experiments on Ca<sub>2</sub>Ru<sub>1-x</sub>Mn<sub>x</sub>O<sub>4</sub> with x=0,3,5,10,20% at temperatures 90-500K.</li> <li>Python scripts to determine the exchange path distances</li> <li>Python scripts to create figures</li> </ul> </li> <li>Magnetisation Data <ul> <li>Data files from Quantum Design SQUID VSM measurements of Ca<sub>2</sub>Ru<sub>1-x</sub>Mn<sub>x</sub>O<sub>4</sub> with x=0,3,5,10,20%. Field Cooled measurements in different orientations relative to the external field are included.</li> </ul> </li> <li>Resonant X-Ray Diffraction Data <ul> <li>Raw scan files from I16 measurements covering multiple beamtime allocations on samples of Ca<sub>2</sub>Ru<sub>1-x</sub>Mn<sub>x</sub>O<sub>4</sub> with x=0,3,5,10,20%.</li> <li>Analysed datasets including python scripts with descriptions of data analysis and figure plots.</li> </ul> </li> </ul>
5.0 EVALUATING CHANGES IN TRANSIT ACCESSIBILITY FOR TRANSPORTATION-DISADVANTAGED POPULATIONS IN THE CITY OF GAINESVILLE
<p>This dataset contains four parts: 1. A geodatabase of street network in Alachua County ; 2. Shapefiles of places (hospitals, parks, schools, etc.) in Florida that were defined as "trip destinations" in our research; 3. GTFS (General Transit Feed Specification) data used to developed different transit service scenarios; 4. Data of the transit service scenarios that we developed. </p>
The rehydration attributes and quality characteristics of 'Quick-cooking' dehydrated beans: Implications of glass transition on storage stability
<p>The data set was used to generate the figures.</p>
Subspecies and Distribution. D. m. merriami Mearns, 1890 — SW USA and NW Mexico (desert regions from N Nevada and extreme SW Utah, through SE California and SW Arizona, to NE Baja California and Sonora). D. m. ambiguus Merriam, 1890 — SW USA and NW Mexico (N portion of the Chihuahuan Desert from NC New Mexico and W Texas, through E Chihuahua and Coahuila, to NE Durango, N Zacatecas, and C Nuevo Leon). D. m. annulus Huey, 1951 — NW Mexico (coastal plains of the Gulf of California, SE Baja California). D. m. arenivagus Elliot, 1904 — SW USA and NW Mexico (S Mojave Desert of SC California and E of Sierra Juarez and Sierra San Pedro Martir to C Baja California). D. m. atronasus Merriam, 1894 — NC Mexico (southern portion of the Chihuahuan Desert from EC Zacatecas, SE Coahuila, and SW Nuevo Leon to Aguascalientes and San Luis Potosi). D. m. brunensis Huey, 1951 — NW Mexico (Gulf of California coast of NE Baja California Sur). D. m. collinus Lidicker, 1960 — SW USA (San Felipe, Earthquake, La Puerta, and Aguanga valleys of SW California). D. m. frenatus Bole, 1936 — SW USA (SW Utah and NW Arizona). D. m. insularis Merriam, 1907 — NW Mexico (San José I, Gulf of California, Baja California Sur). D. m. margaritae Merriam, 1907 — NW Mexico (Santa Margarita I, Baja California Sur). D. m. mayensis Goldman, 1928 — NW Mexico (Gulf of California coastal plains of S Sonora and N Sinaloa). D. m. melanurus Merriam, 1893 — NW Mexico (Magdalena Plains and Cape Region of S Baja California Sur). D. m. mitchelli Mearns, 1897 — NW Mexico (Tiburon I, Gulf of California, Sonora). D. m. olivaceus Swarth, 1929 — SW USA and NW Mexico (transitional zone between the Sonoran Desert of SE Arizona and NE Sonora, and the Chihuahuan Desert of SW New Mexico and NW Chihuahua). D. m. parvus Rhoads, 1894 — SW USA (San Bernardino and San Jacinto valleys of SW California). D. m. platycephalus Merriam, 1907 — NW Mexico (Pacific slope S of the Sierra San Pedro Martir, S Baja California to the Vizcaino Desert of N Baja California Sur). D. m. quintinensis Huey, 1951 — NW Mexico (San Quintin Plain, Pacific coast of NW Baja California). D. m. trinidadensis Huey, 1951 — SW USA and NW Mexico (S California and N Baja California). D. m. vulcani Benson, 1934 — SW USA (disjunct and restricted distribution in Toroweap Valley, NW Arizona). in Heteromyidae
Subspecies and Distribution. D. m. merriami Mearns, 1890 — SW USA and NW Mexico (desert regions from N Nevada and extreme SW Utah, through SE California and SW Arizona, to NE Baja California and Sonora). D. m. ambiguus Merriam, 1890 — SW USA and NW Mexico (N portion of the Chihuahuan Desert from NC New Mexico and W Texas, through E Chihuahua and Coahuila, to NE Durango, N Zacatecas, and C Nuevo Leon). D. m. annulus Huey, 1951 — NW Mexico (coastal plains of the Gulf of California, SE Baja California). D. m. arenivagus Elliot, 1904 — SW USA and NW Mexico (S Mojave Desert of SC California and E of Sierra Juarez and Sierra San Pedro Martir to C Baja California). D. m. atronasus Merriam, 1894 — NC Mexico (southern portion of the Chihuahuan Desert from EC Zacatecas, SE Coahuila, and SW Nuevo Leon to Aguascalientes and San Luis Potosi). D. m. brunensis Huey, 1951 — NW Mexico (Gulf of California coast of NE Baja California Sur). D. m. collinus Lidicker, 1960 — SW USA (San Felipe, Earthquake, La Puerta, and Aguanga valleys of SW California). D. m. frenatus Bole, 1936 — SW USA (SW Utah and NW Arizona). D. m. insularis Merriam, 1907 — NW Mexico (San José I, Gulf of California, Baja California Sur). D. m. margaritae Merriam, 1907 — NW Mexico (Santa Margarita I, Baja California Sur). D. m. mayensis Goldman, 1928 — NW Mexico (Gulf of California coastal plains of S Sonora and N Sinaloa). D. m. melanurus Merriam, 1893 — NW Mexico (Magdalena Plains and Cape Region of S Baja California Sur). D. m. mitchelli Mearns, 1897 — NW Mexico (Tiburon I, Gulf of California, Sonora). D. m. olivaceus Swarth, 1929 — SW USA and NW Mexico (transitional zone between the Sonoran Desert of SE Arizona and NE Sonora, and the Chihuahuan Desert of SW New Mexico and NW Chihuahua). D. m. parvus Rhoads, 1894 — SW USA (San Bernardino and San Jacinto valleys of SW California). D. m. platycephalus Merriam, 1907 — NW Mexico (Pacific slope S of the Sierra San Pedro Martir, S Baja California to the Vizcaino Desert of N Baja California Sur). D. m. quintinensis Huey, 1951 — NW Mexico (San Quintin Plain, Pacific coast of NW Baja California). D. m. trinidadensis Huey, 1951 — SW USA and NW Mexico (S California and N Baja California). D. m. vulcani Benson, 1934 — SW USA (disjunct and restricted distribution in Toroweap Valley, NW Arizona).
Distribution. Amazonian Brazil, S of the Rio Amazonas, between the rios Xingu and Tocantins-Araguaia; the exact S limits of its distribution are unknown, but it has been recorded in the lower rio Tapirapé in NE Mato Grosso State, near the forestsavanna transition. in Phitheciidae
Distribution. Amazonian Brazil, S of the Rio Amazonas, between the rios Xingu and Tocantins-Araguaia; the exact S limits of its distribution are unknown, but it has been recorded in the lower rio Tapirapé in NE Mato Grosso State, near the forestsavanna transition.
Distribution. Brazilian Amazon, S of the Rio Amazonas, between the Tapajos/Juruena system and the Tocantins/Araguaia river system to the E, in the Brazilian states of Para and Mato Grosso; the exact S limit ofits distribution is unclear, but it seems likely that it coincides with the transition between the Amazon rainforest and the cerrado savannas of C Brazil; this ecotone encompasses headwaters of the Xingu and Tapajos river systems in N Mato Grosso. Vieira's Titi (C. vieirai) is also known to occur in this region, but there are too few records to confirm whether their distributions intergrade, or in fact where the exact limits of their distributions are. One recent study also found that the Red-bellied Titi may be absent from or present at extremely low densities in large areas of the Tocantins-Xingu interfluvium. Given the overall lack of records, while it is clear that the Red-bellied Titi occurs over a vast area of the SE Amazon Basin, the exact limits of its distribution within this area remain unclear. in Phitheciidae
Distribution. Brazilian Amazon, S of the Rio Amazonas, between the Tapajos/Juruena system and the Tocantins/Araguaia river system to the E, in the Brazilian states of Para and Mato Grosso; the exact S limit ofits distribution is unclear, but it seems likely that it coincides with the transition between the Amazon rainforest and the cerrado savannas of C Brazil; this ecotone encompasses headwaters of the Xingu and Tapajos river systems in N Mato Grosso. Vieira's Titi (C. vieirai) is also known to occur in this region, but there are too few records to confirm whether their distributions intergrade, or in fact where the exact limits of their distributions are. One recent study also found that the Red-bellied Titi may be absent from or present at extremely low densities in large areas of the Tocantins-Xingu interfluvium. Given the overall lack of records, while it is clear that the Red-bellied Titi occurs over a vast area of the SE Amazon Basin, the exact limits of its distribution within this area remain unclear.
Distribution. Most of Europe, from the British Is and NW France E to W Siberia as far E as Irtysh and Ob rivers, and from S Sweden, S Finland, and S Karelia (Russia) S to N Italy and N Balkans; marginally present also in NW Kazakhstan. In E Europe and in Asia the border roughly follows the extreme extension of the taiga in the N (northernmost record is from Pechora River close to 68°N) and the steppe-forest—steppe transition in the S. Present on some Is in the Baltic Sea and around Denmark (Oland, Funen, Zeeland, Bjgrng, Tasinge, Tung, Langeland, Riigen, Usedom, and Wollin), around Great Britain (Sky, Mull, Anglesey, Wight, and Jersey), offshore W coast of France (Ouessant and Ré), and on Cres (Croatia) as the only Mediterranean I. in Talpidae
Distribution. Most of Europe, from the British Is and NW France E to W Siberia as far E as Irtysh and Ob rivers, and from S Sweden, S Finland, and S Karelia (Russia) S to N Italy and N Balkans; marginally present also in NW Kazakhstan. In E Europe and in Asia the border roughly follows the extreme extension of the taiga in the N (northernmost record is from Pechora River close to 68°N) and the steppe-forest—steppe transition in the S. Present on some Is in the Baltic Sea and around Denmark (Oland, Funen, Zeeland, Bjgrng, Tasinge, Tung, Langeland, Riigen, Usedom, and Wollin), around Great Britain (Sky, Mull, Anglesey, Wight, and Jersey), offshore W coast of France (Ouessant and Ré), and on Cres (Croatia) as the only Mediterranean I.
Distribution. SW & S Madagascar, in the W up to the Tsiribihina River, in the SE it is found near to (just N of) Tolagnaro (= Fort-Dauphin) in the Nahampoana Reserve, although it was probably introduced there; the distributional limit in the SE is the transitional and spiny forest patches of the Mangatsiaka Parcel of Andohahela National Park. in Indriidae
Distribution. SW & S Madagascar, in the W up to the Tsiribihina River, in the SE it is found near to (just N of) Tolagnaro (= Fort-Dauphin) in the Nahampoana Reserve, although it was probably introduced there; the distributional limit in the SE is the transitional and spiny forest patches of the Mangatsiaka Parcel of Andohahela National Park.
Effectiveness of interventions to support the transition home after acute stroke: systematic review and meta-analysis
<p>Raw data used in systematic review</p>
Assignment of structural transitions during mechanical unwrapping of nucleosomes and their disassembly products
<p>Optical tweezer data of the mechanical unwrapping of nucleosomes</p>
Complementary hepatic metabolomics and proteomics reveal the adaptive mechanisms of dairy cows to the transition period
<p>Gas chromatography quadrupole-time-of-flight mass spectrometry-based metabolomics and data-independent acquisition-based quantitative proteomics methods were used to analyze liver tissues collected from eight healthy multiparous Holstein dairy cows on 21 days before and after calving.</p>
[Dataset] Determining the origin of tidal oscillations in the ionospheric transition region with EISCAT radar and global simulation data
<p>Preprocessed data</p>
Replication package for: Culture and the Historical Fertility Transition
<p>Replication package for: Beach, Brian and Hanlon, W. Walker (Forthcoming). "Culture and the Historical Fertility Transition," Review of Economic Studies. Package contains data, processing and analysis code, and results tables.</p>
Supplementary material for the manuscript "Transition to chaos and modal structure of magnetized Taylor–Couette flow"
<p>These data and codes are the supplementary materials for the manuscript "Transition to chaos and modal structure of magnetized Taylor–Couette flow". The description of the data is in the file "DATA_OVERVIEW.txt".</p>
Data from: Examining competition during the agnathan/gnathostome transition using distance-based morphometrics
<p class="MsoNormal">The rise of jawed vertebrates (gnathostomes) and extinction of nearly all jawless vertebrates (agnathans) is one of the most important transitions in vertebrate evolution, but the causes are poorly understood. Competition between agnathans and gnathostomes during the Devonian period is the most commonly hypothesized cause; however, no formal attempts to test this hypothesis have been made. Generally, competition between species increases as morphological similarity increases; therefore, this study uses the largest-to-date morphometric comparison of Silurian and Devonian agnathan and gnathostome groups to determine which groups were most and least likely to have competed. Five agnathan groups (Anaspida, Heterostraci, Osteostraci, Thelodonti, and Furcacaudiformes) were compared with five gnathostome groups (Acanthodii, Actinopterygii, Chondrichthyes, Placodermi, Sarcopterygii) including taxa from most major orders. Morphological dissimilarity was measured by Gower's dissimilarity coefficient, and the differences between agnathan and gnathostome body forms across early vertebrate morphospace were compared using principal coordinate analysis. Our results indicate competition between some agnathans and gnathostomes is plausible, but not all agnathan groups were similar to gnathostomes. Furcacaudiformes (fork-tailed thelodonts) are distinct from other early vertebrate groups and the least likely to have competed with other groups.</p>
Figure 7 in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 7. Live coloration of the three species of Diogenes: A–C, left cheliped, outer aspect; D–F, cephalothorax and cephalic appendages; G–I, detailed photographs of the inner face of palms, showing the shape of the row of tubercles; J–L, left pereiopod 2. A, D, G, J, Diogenes pugilator; B, E, H, K, Diogenes armatus sp. nov. C, F, I, L, Diogenes curvimanus.
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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.
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.