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.
164
datasets available to search
ShareScore release 0.9.0
Dataset results
164 results for “relative position”
Bern3D model output related to: Hysteresis of the Earth system under positive and negative CO2 emissions
<p>The data below is output from the Bern3D intermediate complexity model and idealized CO2 increase-decrease simulations used in Jeltsch-Thömmes et al., Environ. Res. Lett. 15 (2020) 124026, https://doi.org/10.1088/1748-9326/abc4af</p> <p><br> The data are provided as .csv and .nc files<br> There are different types of data</p> <p><br> 1) TIMESERIES DATA (Fig. 1 and 2)<br> =================================<br> The name of the files indicates the variable:<br> co2_ts.csv change in atm. co2 [ppm]<br> cumulativeEmissions_ts.csv cumulative emissions [GtC]<br> cumulativeAOflux_ts.csv cumulative atm-ocean C flux [GtC]<br> cumulativeABflux_ts.csv cumulative atm-land C flux [GtC]<br> sat_ts.csv change in surface air temperature [degC]<br> ohc_ts.csv change in ocean heat content [10^24 J]<br> amoc_ts.csv change in Atlantic meridional overturning circulation strength [Sv]<br> seaice_ts.csv fraction of pre-industrial sea-ice area remaining [fraction of PI]<br> <br> The first row in the .csv files contains the header, which indicates the experiment. The naming convention is as follows:<br> c4k#_###</p> <p>c4 indicates the maximum co2 as times pre-industrial (4 times)<br> k# indicates the equilibrium climate sensitivity of the respective simulation in degrees C (k2 to k5)<br> ### indicates the rate of CDR:<br> 010: 0.1% yr^-1<br> 010: 0.3% yr^-1<br> 010: 0.5% yr^-1<br> 010: 0.7% yr^-1<br> 100: 1% yr^-1<br> 200: 2% yr^-1<br> 400: 4% yr^-1<br> 600: 6% yr^-1</p> <p><br> 2) HYSTERESIS DATA (Fig. 3)<br> ===========================<br> The name of the files indicates the variables:<br> cumulativeEmissions_sat.csv cumulative emissions and change in surface air temperature [degC]<br> cumulativeEmissions_OHCsurf.csv cumulative emissions and change in upper ocean heat content (0-700 m) [10^24 J]<br> cumulativeEmissions_o2thermo.csv cumulative emissions and change in thermocline (200-600 m) o2 [mmol m^-3]<br> cumulativeEmissions_OM_arag.csv cumulative emissions and fraction of water in the uppermost 175 m with omegar_aragonite saturation state >3 [fraction]</p> <p>each file contains the time (simulation year) as well as cumulative emissions (cumuEmis) and the respective variable (same naming as in filename) for all the experiments (see timeseries data for naming convention)</p> <p><br> 3) SPATIAL DATA (Fig. 4 and 5)<br> ==============================<br> All data for Fig. 4 and 5 are contained in one single .nc file (fig4_5_data.nc) with a varibale for each map shown in Fig. 4 and 5:<br> c4k2_100_sat hysteresis (down-path minus up-path) in surface air temperature at cumulative emissions of 1000 GtC, ECS=2 degC, in [degC]<br> c4k3_100_sat hysteresis (down-path minus up-path) in surface air temperature at cumulative emissions of 1000 GtC, ECS=3 degC, in [degC]<br> c4k5_100_sat hysteresis (down-path minus up-path) in surface air temperature at cumulative emissions of 1000 GtC, ECS=5 degC, in [degC]<br> <br> c4k2_100_o2thermo hysteresis (down-path minus up-path) in thermocline (200-600 m) o2 at cumulative emissions of 1000 GtC, ECS=2 degC, in [mmol m^-3]<br> c4k3_100_o2thermo hysteresis (down-path minus up-path) in thermocline (200-600 m) o2 at cumulative emissions of 1000 GtC, ECS=3 degC, in [mmol m^-3]<br> c4k5_100_o2thermo hysteresis (down-path minus up-path) in thermocline (200-600 m) o2 at cumulative emissions of 1000 GtC, ECS=5 degC, in [mmol m^-3]<br> <br> c4k3_100_Om_arag_up mean aragonite saturation state of the uppermost 175 m at cumulative emissions of 1000 GtC on the up-path, ECS=3 degC, [unitless]<br> c4k3_100_Om_arag_do mean aragonite saturation state of the uppermost 175 m at cumulative emissions of 1000 GtC on the down-path, ECS=3 degC, [unitless]</p> <p> </p> <p> </p> <p><br> The files can be readily importet in python, for example, by:<br> import pandas as pd<br> import xarray as xr<br> <br> # for the .csv files<br> df = pd.read_csv('path+filename', sep=',', header=0, index_col=None)<br> <br> # for the .nc files<br> ds = xr.open_dataset('path+filename')</p> <p><br> For additional information or in case of questions please contact:<br> Aurich Jeltsch-Thömmes<br> aurich.jeltsch-thoemmes@unibe.ch</p>
Supplementary material for "Genes divided according to the relative position of the longest intron show increased representation in different KEGG pathways"
<p>This is a 4th version of the Supplementary Information related to the article "Genes divided according to the relative position of the longest intron show increased representation in different KEGG pathways". It contains upgraded primary and control data used for gene set enrichment analyzes, results of these analyzes as well as our code for calculation of intron lenghts. Detailed information can be found in the above-mentioned article, which deals with the connection between the position of the longest introns in genes and biological functions of genes.</p>
Text-fig. 6. Most parsimonious tree obtained after addition of Acaciaephyllum to the data set of Doyle (2008), with modifications discussed in the text, and with relationships of other taxa fixed with a backbone constraint tree based on results of Doyle (2008). Relative parsimony of alternative positions of Acaciaephyllum is indicated as in Text-fig. 2. Gnet = Gnetales. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 6. Most parsimonious tree obtained after addition of Acaciaephyllum to the data set of Doyle (2008), with modifications discussed in the text, and with relationships of other taxa fixed with a backbone constraint tree based on results of Doyle (2008). Relative parsimony of alternative positions of Acaciaephyllum is indicated as in Text-fig. 2. Gnet = Gnetales.
Text-fig. 4. Most parsimonious trees obtained after addition of Virginianthus (with "Liliacidites" minutus pollen) to the (A) D&E and (B) J/M trees. Relative parsimony of alternative positions of Virginianthus is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 4. Most parsimonious trees obtained after addition of Virginianthus (with "Liliacidites" minutus pollen) to the (A) D&E and (B) J/M trees. Relative parsimony of alternative positions of Virginianthus is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1.
Text-fig. 3. One of two most parsimonious trees obtained after addition of Anacostia (with Similipollis pollen) to the D&E tree. Relative parsimony of alternative positions of Anacostia is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 3. One of two most parsimonious trees obtained after addition of Anacostia (with Similipollis pollen) to the D&E tree. Relative parsimony of alternative positions of Anacostia is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1.
Text-fig. 5. Most parsimonious trees obtained after addition of the Pennipollis plant to the (A) D&E and (B) J/M trees. Relative parsimony of alternative positions of the Pennipollis plant is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 5. Most parsimonious trees obtained after addition of the Pennipollis plant to the (A) D&E and (B) J/M trees. Relative parsimony of alternative positions of the Pennipollis plant is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1.
Text-fig. 11. Eospondylus cf. primigenius (STÜRTZ) "Prastav" quarry at Praha-Holyně, Třebotov Limestone, Lower Devonian, Dalejan, NM L 36905, x 65. Overlay of proximal and distal articulations. Upper photo is proximal surface with distal bird-like articulation knobs superposed in ink. Lower photo is distal surface with proximal articulation knobs superposed in ink. The architecture of articulation surfaces is both zygospondylous and auluroid. This architecture occurs also in vertebrae of Furcaster and indicates that families Eospondylidae and Furcasteridae are closely related. in Isolated Ossicles Of The Family Eospondylidae Spencer Wright, 1966, In The Lower Devonian Of Bohemia (Czech Republic) And Correction Of The Systematic Position Of Eospondylid Brittlestars (Echinodermata: Ophiuroidea: Oegophiurida)
Text-fig. 11. Eospondylus cf. primigenius (STÜRTZ) "Prastav" quarry at Praha-Holyně, Třebotov Limestone, Lower Devonian, Dalejan, NM L 36905, x 65. Overlay of proximal and distal articulations. Upper photo is proximal surface with distal bird-like articulation knobs superposed in ink. Lower photo is distal surface with proximal articulation knobs superposed in ink. The architecture of articulation surfaces is both zygospondylous and auluroid. This architecture occurs also in vertebrae of Furcaster and indicates that families Eospondylidae and Furcasteridae are closely related.
Figure 2. The relationship between relative gut length and trophic position for the 6 in Tissue pH and gut ecomorphology in six freshwater teleosts occupying different trophic levels
Figure 2. The relationship between relative gut length and trophic position for the 6 freshwater fish species. (a) Relative gut length is presented in percent of body length; (b) Relative gut length is presented in percent of total length. Averaged values of trophic position (TP) from the study by Zhang et al. (2013). Grey and black circle dots correspond to TP for stable isotope analysis (SIA) and for gut content analysis (GCA), respectively. Dashed line represents the linear fitting of relative gut length and TP for SIA, while solid line represents the linear fitting of relative gut length and TP for GCA.
Text-fig. 3 Ternary diagram of the relative abundance (in %) of juvenile, prime adult, and old adult specimens in samples of Castor fiber (data from Table 3). The red dots indicate the Pleistocene samples of Bilzingsleben II (B), Weimar- Ehringsdorf (E), and Weimar-Taubach (T), the black dot represents an extant population from Telemark in Norway (data from Campbell 2009). Abbreviations of zones (after Discamps and Costamagno 2015): JOP – Juveniles-Old-Prime dominated zone, JPO – Juveniles-Prime-Old dominated zone, O – Old dominated zone, P – Prime dominated zone. The diagram shows the position of all three fossil samples in the prime dominated zone. in Mortality Profiles Of Castor And Trogontherium (Mammalia: Rodentia, Castoridae), With Notes On The Site Formation Of The Mid-Pleistocene Hominin Locality Bilzingsleben Ii (Thuringia, Central Germany)
Text-fig. 3 Ternary diagram of the relative abundance (in %) of juvenile, prime adult, and old adult specimens in samples of Castor fiber (data from Table 3). The red dots indicate the Pleistocene samples of Bilzingsleben II (B), Weimar- Ehringsdorf (E), and Weimar-Taubach (T), the black dot represents an extant population from Telemark in Norway (data from Campbell 2009). Abbreviations of zones (after Discamps and Costamagno 2015): JOP – Juveniles-Old-Prime dominated zone, JPO – Juveniles-Prime-Old dominated zone, O – Old dominated zone, P – Prime dominated zone. The diagram shows the position of all three fossil samples in the prime dominated zone.
FIG. 6 in Relations et position systématique du genre Cuisitherium Sudre et al., 1983, le plus dérivé des artiodactyles de l'Éocène inférieur d'Europe
FIG. 6. — Lophiobunodon minervoisensis Deperet, 1908; A, maxillaire gauche avec la série PM1-M3, FSL3016, lectotype de l'espèce, coll. Faculté des Sciences de Lyon, La Livinière; B, mandibule droite avec la dp3 (incomplète) et la série dp4-m2, FSL 3017, coll. Fac. Sc. Lyon, La Livinière. Échelle: 2 mm.
FIG. 5 in Relations et position systématique du genre Cuisitherium Sudre et al., 1983, le plus dérivé des artiodactyles de l'Éocène inférieur d'Europe
FIG. 5. — Rhagatherium kowalevskyi Stehlin, 1908, maxillaire gauche avec M2-M3, FSL 2627, coll. Faculté des Sciences de Lyon, Lissieu, pièce étant à l'origine de la mention du Lophiobunodon rhodanicum Deperet, 1908. Échelle: 2 mm.
FIG. 3 in Relations et position systématique du genre Cuisitherium Sudre et al., 1983, le plus dérivé des artiodactyles de l'Éocène inférieur d'Europe
FIG. 3. — Cuisitherium sp., m3 inférieure gauche, AV 15585, coll. MNHN, Paris, Avenay. Échelle: 2 mm.
FIG. 4 in Relations et position systématique du genre Cuisitherium Sudre et al., 1983, le plus dérivé des artiodactyles de l'Éocène inférieur d'Europe
FIG. 4. — Hallebune krumbiegeli Erfurt & Sudre, 1995, maxillaire supérieur droit avec la série PM3-M3 (cassée), Ce IV-3925, holotype, collections du Giseltal Museum, Halle, niveau obereMittelkohle du Geiseltal. Échelle: 2 mm.
FIG. 1 in Relations et position systématique du genre Cuisitherium Sudre et al., 1983, le plus dérivé des artiodactyles de l'Éocène inférieur d'Europe
FIG. 1. — Cuisitherium lydekkeri (Lemoine, 1891); A, fragment de mandibule gauche avec m1-m3 (hypoconulide de m3 cassé), AL 5236, holotype de l'espèce, coll. MNHN, Paris, formation des sables à Unios et Térédines; B, fragment de mandibule gauche avec m1-m2, MT 9-L, coll. MNHN, Paris, Monthelon; C, fragment de mandibule gauche avec m1-m3, GR 109, coll. Université de Montpellier 2, Grauves. Échelle: 2 mm.
FIG. 2 in Relations et position systématique du genre Cuisitherium Sudre et al., 1983, le plus dérivé des artiodactyles de l'Éocène inférieur d'Europe
FIG. 2. — Cuisitherium lydekkeri (Lemoine, 1891), maxillaire supérieur avec PM2-M3, CH 206 LG, coll. de l'Association des géologues du Noyonnais (Grisolles), Monthelon, moulage déposé dans les collections de l'Université de Montpellier 2, vue occlusale. Échelle: 2 mm.
Text-fig. 4. Tooth replacement by the barbary ground squirrel (Atlantoxerus getulus). a – right maxillary with DP3–M3 (MNCN- 5522) showing the relative position of the two deciduous teeth; b – right maxillary with P3–M3 (MNCN-5538) showing the replacement of the DP4 by the P4 (not erupted). Blue: DP4; green: P4; yellow DP3; red: P3. in Dental Anomaly In A Middle Miocene Fossil Of The Genus Spermophilinus (Rodentia, Sciuridae) From Southern Germany
Text-fig. 4. Tooth replacement by the barbary ground squirrel (Atlantoxerus getulus). a – right maxillary with DP3–M3 (MNCN- 5522) showing the relative position of the two deciduous teeth; b – right maxillary with P3–M3 (MNCN-5538) showing the replacement of the DP4 by the P4 (not erupted). Blue: DP4; green: P4; yellow DP3; red: P3.
Text-fig. 1. Spermophilinus bredai (VON MEYER, 1848): 3D models of a right upper jaw with (abnormal) P3, P4 and all molars (mirrored; NMA-2019-1/2352). a – the specimen in occlusal view showing the relative position of the three roots in place of P3 (yellow) compared to P4 (green); b – same view, with focus on P3–P4; c – lingual view; d – mesial view. Scale bars 2 mm. in Dental Anomaly In A Middle Miocene Fossil Of The Genus Spermophilinus (Rodentia, Sciuridae) From Southern Germany
Text-fig. 1. Spermophilinus bredai (VON MEYER, 1848): 3D models of a right upper jaw with (abnormal) P3, P4 and all molars (mirrored; NMA-2019-1/2352). a – the specimen in occlusal view showing the relative position of the three roots in place of P3 (yellow) compared to P4 (green); b – same view, with focus on P3–P4; c – lingual view; d – mesial view. Scale bars 2 mm.
Habitat corridors alter relative trophic position of fire ants
Habitat fragmentation disrupts species movement, leading to local extinctions and altered community structure. Habitat corridors, which connect isolated patches of habitat and facilitate movement between patches, provide a potential solution to these negative impacts. However, most studies to date have examined the movement of species alone without considering emergent effects on the community (e.g., altered trophic structure). We use large-scale, experimental landscapes and nitrogen stable isotopes ratios (delta-N-15) of a common generalist consumer (the fire ant, Solenopsis invicta) to determine how corridors affect trophic structure. Thus, because the fire ant is a species whose trophic position is flexible and whose diet typically reflects local prey availability, we assume that shifts in fire ants' trophic position between connected and isolated patches are likely to reflect shifts in patch trophic structure. We found that colonies in isolated patches had lower means and ranges of delta-N-15 than colonies in otherwise similar connected patches, suggesting that corridors may increase fire ants' trophic position and breadth, respectively. Previous work in our landscapes documented higher species richness of plants in connected than unconnected patches. Patch means of ant delta-N-15 were positively correlated with plant richness, suggesting that increased plant richness may influence the observed responses in fire ant delta-N-15. Together these results suggest that fragmentation may reduce trophic position and narrow trophic breadth of dietary generalists such as the fire ant. These shifts likely reflect an alteration of food webs in isolated patches. Our results suggest that corridors may be effective in preventing or reducing such alterations.
Experimental evidence for the incorporation of two metals at equivalent lattice positions in mixed metal organic frameworks. Dataset related to publication. Version: 1
<p>Experimental evidence for the incorporation of two metals at equivalent lattice positions in mixed metal organic frameworks. Dataset related to publication. Version: 1</p>
Electrical impedance tomography - Depency of cardiac related impedance change amplitudes on body position and reconstruction algorithm
<p>Dataset of a publication investigating the influence of body position and reconstruction algorithm on the amplitudes of cardiac related impedance changes in healthy adult volunteers.</p>
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.