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2,885 results for “transfers”
Data from: Dynamics of diet-egg transfer of fatty acids in the teleost fish, red drum (Sciaenops ocellatus)
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Data from: Evaluating temporal and spatial transferability of a tidal inundation model for foraging waterbirds
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Data from: Assisted migration of cloud forest trees: Unearthing the effects of climatic transfer distance
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Nuclear quantum effects slow down the energy transfer in biological light-harvesting complexes
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Data from: RockNet: Rockfall and earthquake detection and association via multitask learning and transfer learning
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Eddy flux measurements and transfer velocities of momentum, water vapor, and sulfur dioxide over the coastal Atlantic ocean
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What could explain 13C signature of dryland biocrusts? Evaluating potential resource transfer between plants and biocrusts.
Dryland ecosystems are increasing in geographic extent and contribute greatly to interannual variability in global carbon dynamics. Disentangling interactions among dominant primary producers can help partition their contributions to dryland C dynamics. We measured the δ13C signatures of biological soil crusts and dominant plant species (C3 and C4) across a regional scale in the southwestern USA to determine if biocrust cyanobacteria were coupled to plant productivity (using plant-derived C mixotrophically), or independent of plant activity (and therefore purely autotrophic).
Air-sea gas transfer velocities measured at wind speeds up to 85m/s in fresh water and seawater
<p>This data set contains gas transfer velocities of 12 tracers (CF4, He, SF6, He, Kr, Pentafluoroethane, Xe, Acetylene, Hexafluorobenzene, Difluoromethane, 1,4-Difluorobenzene, Dimethyl Sulfide, Methyl Acetate) measured in the Kyoto High Speed Wind-Wave tank with fresh water and modeled seawater and the Miami SUSTAIN wind-wave tank with seawater at wind speeds up to 85m/s.</p> <p> </p>
Supplementary data files for: Huston, D.C., Cribb, T.H. and Smales, L.R. 20XX. Molecular characterisation of acanthocephalans from Australian marine teleosts: proposal of a new family, synonymy of another and transfer of taxa between orders. Systematic Parasitology, Jan 2020.
<p>These are the supplementary data files for the manuscript "<strong>Molecular characterisation of acanthocephalans from Australian marine teleosts: proposal of a new family, synonymy of another and transfer of taxa between orders." </strong>Published in the Journal Systematic Parasitology on the 7 of January 2020.</p> <p>Included are the Nexus and Phylip alignment files used for the phylogenetic analyses, and the resulting tree files (in nexus format).</p> <p> </p>
Data and code for figures: Ultralow-Noise Photonic Microwave Synthesis using a Soliton Microcomb-based Transfer Oscillator
<p>This repository contains the data and code for the paper "Ultralow-Noise Photonic Microwave Synthesis using a Soliton Microcomb-based Transfer Oscillator".</p>
Dataset of Paper "Enhanced numerical simulation of photocatalytic reactors with an improved solver for the radiative transfer equation"
<p>Dataset of Paper "Enhanced numerical simulation of photocatalytic reactors with an improved solver for the radiative transfer equation":</p> <p>- Data of the incident radiation profiles in the annular reactor.</p> <p>- Average and net values of main radiation magnitudes in the tubular reactor at different photocatalyst concentration </p> <p> </p>
Intermolecular Vibrational Energy Transfer Enabled by Microcavity Strong Light-Matter Coupling
<p>The datasets are for the work by UCSD Xiong lab and Yuen lab, where light-matter strong coupling enables selective liquid-phase intermolecular energy transfer which is virtually absent in nature.</p>
Supplementary material for "Measurement of volume change and mass transfer during serpentinisation: insights from the Oman Drilling Project" (JGR Solid Earth)
<p>The three supplementary files include one figure displaying the results of X-ray microtomography (File S1), two compilations of figures dealing with the volume change measurement (Files S2 and S3) and a table with the measured compositions in major and trace elements (Table S1).</p> <p>File S1 (Malvoisin_ds01.pdf). Result of X-ray microtomography. Olivine and Fe-brucite have a similar attenuation. The grains segmented by selecting this attenuation are displayed with a circle with a size proportional to the radius of a sphere of equivalent volume. The color of each circle depends on <em>e</em>, the aspect ratio (ratio of the length of the minimum and maximum axes of an ellipsoid fitted to each grain). The white arrow indicates the location of the main central vein. Grains near the main central vein have a lower <em>e</em> attributed to the platy habitus of Fe-brucite. The other grains are considered as olivine and used for the calculation of the extent of reaction.</p> <p>File S2 (Malvoisin_ds02.pdf). Optical photomicrographs used to calculate volume change during reaction (see main text for details about the calculation). Olivine grains (white) are surrounded by the serpentine + brucite mixture (light green to yellowish). The magnetite/clinopyroxene platelets are mapped in blue in olivine and in red in the serpentine + brucite mixture. The results of the model fitting the best the average orientation of the platelets in olivine are shown in green. The title of each photomicrograph provides the minimum and maximum estimates for volume change calculated with this model (see details about the calculation in the main text), and the size of the bottom right scale bar.</p> <p>File S3 (Malvoisin_ds03.pdf). Histograms of magnetite/clinopyroxene platelet orientation (in degree). Each histogram corresponds to a photomicrograph of File S1. The order of the histograms and the photomicrographs is the same. The orientations in the olivine grains, the serpentine + brucite mixture and for the model fitting the best the average orientation in olivine are displayed in blue, red and green, respectively. The title of the histograms provides the standard deviation of the platelet orientation in the olivine grains (STD<sub>oli</sub>), the serpentine + brucite mixture (STD<sub>ori</sub>) and calculated with the model fitting the best the orientation in olivine (STD<sub>cal</sub>).</p> <p>Table S1 (Malvoisin_ds01.xlsx). Composition in major and trace elements measured with LA-ICPMS along five profiles perpendicular to the main vein. The composition as a function of the distance to the main vein is provided. The name of the tabs indicates if the profile was acquired in spot or in continuous mode (the two modes are described in the main text).</p>
Figures 87-99 in Neotropical Acanthoderini (Coleoptera, Cerambycidae, Lamiinae): Synonymies and new status in some genera, new species, transferences and new distributional records
Figures 87-99. (87‑91) Aegomorphus albosignus, male from Mexico (Jalisco). (87) Dorsal habitus. (88) Ventral habitus. (89) Lateral habitus. (90) Head, frontal view. (91) Lower eye lobe. (92‑99) Specimens from Mexico, dorsal habitus. (92) Female from Jalisco. (93) Female from Jalisco. (94) Female from Michoacán. (95) Male from Michoacán. (96) Female from Michoacán. (97) Female from Michoacán. (98) Male from Guerrero. (99) Female from Michoacán.
Figures 67-76 in Neotropical Acanthoderini (Coleoptera, Cerambycidae, Lamiinae): Synonymies and new status in some genera, new species, transferences and new distributional records
Figures 67-76. (67‑71) Scythropopsis barrerai, female. (67) Dorsal habitus. (68) Ventral habitus. (69) Lateral habitus. (70) Head, frontal view. (71) Lower eye lobe. (72‑76) Scythropopsis intricata sp. nov. holotype female. (72) Dorsal habitus. (73) Ventral habitus. (74) Lateral habitus. (75) Head, frontal view. (76) Lower eye lobe.
Figures 55-66 in Neotropical Acanthoderini (Coleoptera, Cerambycidae, Lamiinae): Synonymies and new status in some genera, new species, transferences and new distributional records
Figures 55-66. (55) Psapharochrus sallei, holotype female, dorsal habitus. (56‑61) Scythropopsis cornuta. (56) Holotype female, dorsal habitus. (57) Dorsal habitus, male. (58) Ventral habitus, male. (59) Lateral habitus, male. (60) Head, frontal view, male. (61) Lower eye lobe, male. (62‑66) Scythropopsis wappesi, male. (62) Dorsal habitus. (63) Ventral habitus. (64) Lateral habitus. (65) Head, frontal view. (66) Lower eye lobe.
Figures 19-34 in Neotropical Acanthoderini (Coleoptera, Cerambycidae, Lamiinae): Synonymies and new status in some genera, new species, transferences and new distributional records
Figures 19-34. Symperasmus alboniger. (19‑22) Male from Brazil (Amazonas, Benjamin Constant). (19) Dorsal habitus. (20) Ventral habitus. (21) Lateral habitus. (22) Head, frontal view. (23‑26) Male from Peru (Huánuco, Tingo Maria). (23) Dorsal habitus. (24) Ventral habitus. (25) Lateral habitus. (26) Head, frontal view. (27‑34) Elytral apex. (27) Female, Bolivia. (28) Female, Bolivia. (29) Female, Peru. (30) Male, Peru. (31) Male, Peru. (32) Male, Peru. (33) Male, Bolivia. (34) Male, Brazil.
Figures 1-9 in Neotropical Acanthoderini (Coleoptera, Cerambycidae, Lamiinae): Synonymies and new status in some genera, new species, transferences and new distributional records
Figures 1-9. (1‑3) Acanthoderes daviesii, male. (1) Dorsal habitus. (2) Head, frontal view. (3) Lower eye lobe. (4‑6) Aegomorphus modestus, female. (4) Dorsal habitus. (5) Head, frontal view. (6) Lower eye lobe. (7‑9) Aegomorphus cylindricus, male. (7) Dorsal habitus. (8) Head, frontal view. (9) Lower eye lobe.
Figures 110-120 in Neotropical Acanthoderini (Coleoptera, Cerambycidae, Lamiinae): Synonymies and new status in some genera, new species, transferences and new distributional records
Figures 110-120. (110‑114) Aegomorphus circumflexus, male from Cuba. (110) Dorsal habitus. (111) Ventral habitus. (112) Lateral habitus. (113) Head, frontal view. (114) Lower eye lobe. (115‑120) Aegomorphus irumus. (115) Dorsal habitus, female. (116) Ventral habitus, female. (117) Lateral habitus, female. (118) Head, frontal view, female. (119) Lower eye lobe, female. (120) Dorsal habitus, male.
Figures 130-141 in Neotropical Acanthoderini (Coleoptera, Cerambycidae, Lamiinae): Synonymies and new status in some genera, new species, transferences and new distributional records
Figures 130-141. (130‑135) Aegomorphus robustus sp. nov. (130) Dorsal habitus, holotype male. (131) Ventral habitus, holotype male. (132) Lateral habitus, holotype male. (133) Head, frontal view, holotype male. (134) Lower eye lobe, holotype male. (135) Dorsal habitus, paratype female. (136‑141) Plagiosarus literatus. (136) Dorsal habitus, male. (137) Ventral habitus, male. (138) Lateral habitus, male. (139) Head, frontal view, male. (140) Lower eye lobe, male. (141) Dorsal habitus, female.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.