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.
2,135
datasets available to search
ShareScore release 0.9.0
Dataset results
2,135 results for “stabling”
Dataset for "Alternative stable states of forest types"
<p>Source data to reproduce figures in the main manuscript</p>
Rational design of stable bimetallic and trimetallic nickel-based single-atom alloys for acetic acid dehydrogenation
<p>Data access for the paper publication.</p>
Dataset for "Model diagnostic analysis in a cold basin influenced by frozen soils with the aid of stable isotope"
Open the record for dataset details and reuse information.
Stable Trajectory of tRNA_HRM, PolyA_HRM, PGC_HRM
Open the record for dataset details and reuse information.
Holocene Hydroclimate Variability of the Baltic Region Inferred from Stable Isotopes, d Excess and Multi-Proxy Data at Lake Nuudsaku, Estonia (NE Europe)
Open the record for dataset details and reuse information.
Fig. 3. a in Stable isotope evidence for trophic overlap of sympatric Mexican Lake Chapala silversides (Teleostei: Atherinopsidae: Chirostoma spp.)
Fig. 3. a) Arrow diagram for the distribution of angles (θ) for Chirostoma jordani in Lake Chapala, Mexico. Angles are calculated from δ15N and δ13C values for C. jordani individuals. The red line is the mean vector of movement (in isotopic food web space) for the species; the curved thicker line on the rim indicates the 95% confidence interval around the mean vector of movement. b) Angle scatter diagram of isotopic distribution of the "charales" group (including C. jordani, C. labarcae and C. consocium) (crosses) and the "pescados blancos" group (including C. sphyraena and C. promelas) (triangles).
Fig. 2. a in Stable isotope evidence for trophic overlap of sympatric Mexican Lake Chapala silversides (Teleostei: Atherinopsidae: Chirostoma spp.)
Fig. 2. a) Lake Chapala food web plot resulting from the analysis of δ13C and δ15N stable isotope values. Values for both plots are mean δ15N and δ13C (± 1SE). Shaded area corresponds to species in gen. Chirostoma, which is plotted in detail in b) In note jaw morphology differences among silverside species (n indicates the number of specimens in each species for which isotopic values were determined). Acronyms for both figures: Chapalichthys encaustus = Chap.; Lepomis macrochirus = Lep.; Goodea atripinnis = Goo.; Oreochromis sp. = Ore.; Zooplankton = Zoop.; Poecilia sp. = Poe.; benthic invertebrates = Ben.; C. sphyraena = Cs; C. labarcae = Cl; C. consocium = Cc; C. promelas = Cp; C. jordani = Cj.
Figure 7 from: Derkarabetian S, Starrett J, Tsurusaki N, Ubick D, Castillo S, Hedin M (2018) A stable phylogenomic classification of Travunioidea (Arachnida, Opiliones, Laniatores) based on sequence capture of ultraconserved elements. ZooKeys 760: 1-36. https://doi.org/10.3897/zookeys.760.24937
Figure 7 Representative penis morphology of Travunioidea. Clockwise from left: Trojanella serbica redrawn from Karaman (2005), Travunia hofferi redrawn from Karaman (2005), Cryptomaster behemoth adapted from Starrett et al. (2016), Holoscotolemon jaqueti redrawn from Martens (1978), Briggsus hamatus, Yuria pulcra, Paranonychus brunneus, Metanonychus setulus navarrus, Nippononychus japonicus redrawn from Suzuki (1975), Kaolinonychus coreanus coreanus redrawn from Suzuki (1975), Izunonychus ohruii, Zuma acuta. All Travuniidae and Cladonychiidae are drawn in ventral view; Cryptomastridae, Yuria, and Paranonychidae drawn in lateral. For simplicity, not all travunioid genera are included.
Figure 5 from: Derkarabetian S, Starrett J, Tsurusaki N, Ubick D, Castillo S, Hedin M (2018) A stable phylogenomic classification of Travunioidea (Arachnida, Opiliones, Laniatores) based on sequence capture of ultraconserved elements. ZooKeys 760: 1-36. https://doi.org/10.3897/zookeys.760.24937
Figure 5 Phylogenomic relationships among travunioid genera. Left: 70% SVDQuartets. Right: 70% ASTRAL. Nodes are fully supported (100% bootstrap), unless indicated.
Figure 3 from: Derkarabetian S, Starrett J, Tsurusaki N, Ubick D, Castillo S, Hedin M (2018) A stable phylogenomic classification of Travunioidea (Arachnida, Opiliones, Laniatores) based on sequence capture of ultraconserved elements. ZooKeys 760: 1-36. https://doi.org/10.3897/zookeys.760.24937
Figure 3 Phylogenetic relationships among major laniatorean lineages. Lower phylogenies correspond to results presented in this study. Nodes are fully supported (100% bootstrap or 1.0 posterior probability), unless indicated otherwise. Numbers in lower left phylogeny correspond to support values from 50% RAxML concatenated (top), and from 70% RAxML partitioned (bottom) analyses. Numbers in ASTRAL phylogeny based on 50% (top) and 70% (bottom) matrices.
Figure 2 from: Derkarabetian S, Starrett J, Tsurusaki N, Ubick D, Castillo S, Hedin M (2018) A stable phylogenomic classification of Travunioidea (Arachnida, Opiliones, Laniatores) based on sequence capture of ultraconserved elements. ZooKeys 760: 1-36. https://doi.org/10.3897/zookeys.760.24937
Figure 2 Geographic distribution of travunioid genera. Colors correspond to classification proposed in this study. Abbreviations: wNA = western North America, eNA = eastern North America, EUR = central and southern Europe, JPN/KOR = Japan and South Korea.
Figure 1 from: Derkarabetian S, Starrett J, Tsurusaki N, Ubick D, Castillo S, Hedin M (2018) A stable phylogenomic classification of Travunioidea (Arachnida, Opiliones, Laniatores) based on sequence capture of ultraconserved elements. ZooKeys 760: 1-36. https://doi.org/10.3897/zookeys.760.24937
Figure 1 Photographs of live travunioid harvestmen. A Theromaster brunneus B Erebomaster sp. C Cryptomaster leviathan D Holoscotolemon lessiniense E Peltonychia leprieurii F Trojanella serbica G Briggsus sp. H Isolachus spinosus I Speleonychia sengeri J Yuria pulcra K Paranonychus brunneus L Sclerobunus nondimorphicus M Metanippononychus sp. N Zuma acuta O Kainonychus akamai. All photos by MH, except D, E (courtesy of and copyright A. Schönhofer), and F (courtesy of and copyright I. Karaman).
Figure 4 from: Derkarabetian S, Starrett J, Tsurusaki N, Ubick D, Castillo S, Hedin M (2018) A stable phylogenomic classification of Travunioidea (Arachnida, Opiliones, Laniatores) based on sequence capture of ultraconserved elements. ZooKeys 760: 1-36. https://doi.org/10.3897/zookeys.760.24937
Figure 4 Phylogenomic relationships among travunioid genera. Left: RAxML and 50% BEAST concatenated topologies, with bootstrap support from the partitioned analysis. All nodes in the BEAST topology have posterior probability of 1.0. Abbreviations indicate placement in classification at the time of Kury et al. (2014): Tt = Travuniidae, Travuniinae; Tc = Travuniidae, Cladonychiinae; Tb = Travuniidae, Briggsinae; Pp = Paranonychidae, Paranonychinae; Ps = Paranonychidae, Sclerobuninae; N = Nippononychidae. Right: 70% BEAST concatenated. Nodes are fully supported (100% bootstrap or 1.0 posterior probability), unless indicated.
Figure 6 from: Derkarabetian S, Starrett J, Tsurusaki N, Ubick D, Castillo S, Hedin M (2018) A stable phylogenomic classification of Travunioidea (Arachnida, Opiliones, Laniatores) based on sequence capture of ultraconserved elements. ZooKeys 760: 1-36. https://doi.org/10.3897/zookeys.760.24937
Figure 6 Morphology of Cryptomastridae. A) male Cryptomaster, arrow denotes sexually dimorphic swelling diagnostic of Cryptomastridae; B) Speleomaster, habitus; C) Scanning electron micrograph of tibial swelling, from Starrett et al. (2016); D) Cryptomastrid distribution.
Supplementary material 2 from: Derkarabetian S, Starrett J, Tsurusaki N, Ubick D, Castillo S, Hedin M (2018) A stable phylogenomic classification of Travunioidea (Arachnida, Opiliones, Laniatores) based on sequence capture of ultraconserved elements. ZooKeys 760: 1-36. https://doi.org/10.3897/zookeys.760.24937
Figures : Explanation note:
Mechanochemically-derived Fe atoms on defective boron nitride for stable propylene production
Open the record for dataset details and reuse information.
Effects of inhaled double-branch dilator Umeclidinium/Vilanterol on pulmonary function and inflammatory factors in patients with stable chronic obstructive pulmonary disease
Open the record for dataset details and reuse information.
Linked collectors and determiners for: (Appendix 9) Stable oxygen isotope record of Globigerina bulloides, and abundances of Neogloboquadrina pachyderma and ice-rafted debris in sediment core MD03-2697.
Natural history specimen data linked to collectors and determiners held within, "(Appendix 9) Stable oxygen isotope record of Globigerina bulloides, and abundances of Neogloboquadrina pachyderma and ice-rafted debris in sediment core MD03-2697". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/7c8d2b88-f762-11e1-a439-00145eb45e9a">https://bionomia.net/dataset/7c8d2b88-f762-11e1-a439-00145eb45e9a</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/7c8d2b88-f762-11e1-a439-00145eb45e9a">https://gbif.org/dataset/7c8d2b88-f762-11e1-a439-00145eb45e9a</a>. Formatted as a Frictionless Data package.
Data from: Stable isotope labeled n-alkanes to assess digesta passage kinetics through the digestive tract of ruminants
We describe the use of carbon stable isotope (13C) labeled n-alkanes as a potential internal tracer to assess passage kinetics of ingested nutrients in ruminants. Plant cuticular n-alkanes originating from intrinsically 13C labeled ryegrass plants were pulse dosed intraruminally in four rumen-cannulated lactating dairy cows receiving four contrasting ryegrass silage treatments that differed in nitrogen fertilization level (45 or 90 kg nitrogen ha−1) and maturity (early or late). Passage kinetics through the gastrointestinal tract were derived from the δ13C (i.e. the ratio 13C:12C) in apparently undigested fecal material. Isotopic enrichment was observed in a wide range of long-chain n-alkanes (C27–C36) and passage kinetics were determined for the most abundant C29, C31 and C33 n-alkanes, for which a sufficiently high response signal was detected by combustion isotope ratio mass spectrometry. Basal diet treatment and carbon chain length of n-alkanes did not affect fractional passage rates from the rumen (K1) among individual n-alkanes (3.71–3.95%/h). Peak concentration time and transit time showed a quantitatively small, significant (p≤0.002) increase with carbon chain length. K1 estimates were comparable to those of the 13C labeled digestible dry matter fraction (3.38%/h; r = 0.61 to 0.71; p≤0.012). A literature review has shown that n-alkanes are not fermented by microorganisms in the rumen and affirms no preferential depletion of 13C versus 12C. Our results suggest that 13C labeled n-alkanes can be used as nutrient passage tracers and support the reliability of the δ13C signature of digestible feed nutrients as a tool to measure nutrient-specific passage kinetics.
Data from: Starvation effects on nitrogen and carbon stable isotopes of animals: an insight from meta-analysis of fasting experiments
Nitrogen and carbon stable isotopic compositions (δ15N and δ13C) of consumers have been used for physiological and food web studies. Previous studies have shown δ15N and δ13C values are affected by several biological and environmental factors during starvation, but the generality of the effect of starvation on δ15N and δ13C values has not yet been tested. Here, we performed a meta-analysis to evaluate the effects of starvation on δ15N and δ13C values of consumers, and the underlying factors that may explain the observed variation. The δ15N and δ13C values were calculated as the differences between the final δ15N and δ13C values of consumers (post-starvation) and the pre-starvation values on each experiment. Our meta-analysis showed a large variation in the δ15N and δ13C values of consumers (δ15N range: –0.82 to 4.30‰; mean: 0.47‰ and δ13C range: –1.92 to 2.62‰; mean: 0.01‰). The δ15N values of most consumers increased along the length of the starvation period and were influenced by nitrogen excretion and thermoregulation types, probably because differences in nitrogen metabolism and thermoregulation affect nitrogen processing and excretion rates. None of our predictor variables accounted for the variation in δ13C values, which showed both increases and decreases due to fasting. Our findings suggest that starvation results in changes in consumer δ15N values which are mainly explained by the length of the fasting period and by nitrogen and energy metabolism, but the underlying mechanisms of the starvation effects on δ13C values seem to be more complex than previously thought.
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.