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4,563 results for “correlations”
Correlation between LA Crimes and Museum Visitors Dataset Files
<p>Raw data for an experiment where I test the correlation between number of museums visitors and crimes in Los Angles city.</p>
Correlation of global temperature change and the number of children born in Vienna per year
<p>The datasets contains values from 2002 to 2017<br> The first row of the file contains the column titles (= the header).<br> Every row afterwards contains values separated by a semi-colon:<br> index; year; mean near surface temperature deviation; number of children born in Vienna<br> <br> </p>
Subpixel optical correlation co-seismic offsets for the Mw 6.4 and Mw 7.1 Ridgecrest, California earthquakes, from Copernicus Sentinel 2 data
<p>Two strong earthquakes (Mw 6.4 and Mw 7.1) took place near Ridgecrest, California, on July 4 2019 and July 6, respectively.</p> <p><a href="https://earthquake.usgs.gov/earthquakes/eventpage/ci38443183/executive">https://earthquake.usgs.gov/earthquakes/eventpage/ci38443183/executive</a></p> <p><a href="https://earthquake.usgs.gov/earthquakes/eventpage/ci38457511/executive">https://earthquake.usgs.gov/earthquakes/eventpage/ci38457511/executive</a></p> <p>In order to assess surface ruptures and the displacement field from the earthquakes, we used subpixel image correlation with Copernicus Sentinel-2 optical imagery (Band 4). MicMac and CosiCorr software was used to to extract the 2D (East-West and North-South) horizontal co-seismic displacement field.</p> <p>Four high-resolution figures are given per method and component (EW and NS). Road network (white lines - from OpenStreetMap) and Quaternary Faults (black polylines) from USGS (<a href="https://earthquake.usgs.gov/hazards/qfaults/">https://earthquake.usgs.gov/hazards/qfaults/</a>) are used for overlay.</p> <p>Rasters are given per software used (MICMAC_ for MicMac and COSI for CosiCorr), with a pixel resolution of 20m. Final product is corrected with detrending (to remove mostly registration errors) and filtered to remove noise. Stripes resulting from pushbroom scanner and orbit errors were not removed at this product (visible as WNW-ESE and NNE-SSW linear parallel stripes).</p> <p>-North-South displacement: positive values to the North.</p> <p>- East-West displacement: positive values to the East.</p> <p>Raster files are projected in UTM Zone 11North WGS84 ( EPSG:32611)</p> <p> </p> <p>A contribution to <strong>CEOS Working Group Disasters:</strong> Seismic Demonstrator</p> <p><strong>Copyright:</strong> Contains modified Copernicus Sentinel data (2019), OpenStreetMap data (2019), Quaternary Fault and Fold Database of the United States - USGS (2019)</p>
РИС. 3. Графики Зависимости: А – Ширины (D) и В – фронтальной кривиЗны (D/L) раковины Corbicula fluminea от длины (L). В качестве Зависимых переменных (y) в формулах укаЗаны Ширина (D) и фронтальнаЯ кривиЗна раковины (D/L). FIG. 3. Graphs of correlations between (A) width (D), (B) frontal curvature (H/L) and the shell length (L) of Corbicula fluminea. The formulas include shell width (D) and frontal curvature (D/L) as dependent variables (y). in Особенности аллометрического роста двустворчатого моллюска-вселенца Corbicula fluminea (Bivalvia: Cyrenidae) иЗ бассейна реки Дон
РИС. 3. Графики Зависимости: А – Ширины (D) и В – фронтальной кривиЗны (D/L) раковины Corbicula fluminea от длины (L). В качестве Зависимых переменных (y) в формулах укаЗаны Ширина (D) и фронтальнаЯ кривиЗна раковины (D/L). FIG. 3. Graphs of correlations between (A) width (D), (B) frontal curvature (H/L) and the shell length (L) of Corbicula fluminea. The formulas include shell width (D) and frontal curvature (D/L) as dependent variables (y).
Fig. 6 in Biozonation And Correlation Of Two Wells In Niger Delta Using Calcareous Nannofossils
Fig. 6 Correlation of the MAY-01 and MAY-02 wells based on calcareous nannofossil zones, MFS and SB.
Fig. 2 in Biozonation And Correlation Of Two Wells In Niger Delta Using Calcareous Nannofossils
Fig. 2 Stratigraphy and paleoenvironment of the Eocene-Pliocene interval of the Niger Delta (modified from Doust & Omatsola, 1990)
Figure. Constrained ordination plot as produced from canonical correspondence analysis (CCA). The variability of environmental variables is summarized on Axis 1 and Axis 2 of the constrained biplot, explaining the variability of the trophic groups included in the red fox's diet. Trophic groups are shown with black line (unfilled) pyramids, whereas environmental variables are shown with black filled pyramids. Proximity and distance of response centroids to predictor centroids indicate positive and negative correlations between them, respectively. in Factors affecting the diet of the red fox (Vulpes vulpes) in a heterogeneous Mediterranean landscape
Figure. Constrained ordination plot as produced from canonical correspondence analysis (CCA). The variability of environmental variables is summarized on Axis 1 and Axis 2 of the constrained biplot, explaining the variability of the trophic groups included in the red fox's diet. Trophic groups are shown with black line (unfilled) pyramids, whereas environmental variables are shown with black filled pyramids. Proximity and distance of response centroids to predictor centroids indicate positive and negative correlations between them, respectively.
Figure 2 in Ostracoda (Crustacea) species composition and environmental correlates in different aquatic habitats of the Zonguldak and Bartın regions (Turkey)
Figure 2. CCA diagrams for (a) 4 variables (water temperature [Tw]; electrical conductivity [EC]; dissolved oxygen [DO]; pH) and (b) 15 ostracods in 68 sampling sites.
Figure 3 in Ostracoda (Crustacea) species composition and environmental correlates in different aquatic habitats of the Zonguldak and Bartın regions (Turkey)
Figure 3. Relationships among air temperature (Ta), water temperature (Tw), and number of species (Nuspp) in Bartın and Zonguldak.
Fig. 2. Correlations between diversity and abundance across collections. Each record represents a in Streetlights attract a broad array of beetle species
Fig. 2. Correlations between diversity and abundance across collections. Each record represents a night of collection in a given trap. Colors represent traps, with color code being the same as in Figs. 1, 3 and 4. Line represents the regression line between the two variables with intercept forced to 0.
Fig. 2. The PCR products identified within the 18S in Usefulness of PCR-RFLP of 18S rRNA gene for rapid post-mortem diagnostics of highly pathogenic Eimeria spp. (Apicomplexa: Eimeriidae) of European bison, Bison bonasus L. with histopathological correlation
Fig. 2. The PCR products identified within the 18S rRNA of Eimeria bovis following digestion with two restriction endonucleases: AluI recognising AG∧CT and Hin1II recognising CATG∧. M1: GeneRuler 100 bp Plus DNA Ladder (Thermo Fisher Scientific); M2: GeneRuler 50bp DNA Ladder (Thermo Fisher Scientific); lane 1: European bison colon wall tissue; lane 2: European bison colon wall tissue after digestion; lane 3: E. bovis oocysts of European bison; lane 4: E. bovis oocysts of European bison after digestion.
Fig. 3 in Usefulness of PCR-RFLP of 18S rRNA gene for rapid post-mortem diagnostics of highly pathogenic Eimeria spp. (Apicomplexa: Eimeriidae) of European bison, Bison bonasus L. with histopathological correlation
Fig. 3. The virtual double digestion of the 18S rRNA gene of eimerians infecting the large intestine of the European bison with the restriction enzymes Mval (BstNI) recognising CC∧WGG, and KpnI recognising GGTAC∧C, simulated with SnapGene version 5.0.6 (GSL Biotech LLC); M: GeneRuler 50 bp DNA Ladder (Thermo Fisher Scientific). (A) A three-band pattern for E. bovis (20 bp, 210 bp, 343 bp). (B) A four-band pattern for E, zuernii (20 bp, 100 bp, 210 bp, 242 bp). (C) A two-band pattern for E. alabamensis (212 bp, 362 bp).
Fig. 1 in Usefulness of PCR-RFLP of 18S rRNA gene for rapid post-mortem diagnostics of highly pathogenic Eimeria spp. (Apicomplexa: Eimeriidae) of European bison, Bison bonasus L. with histopathological correlation
Fig. 1. Histopathological lesions associated with endogenous stages of Eimeria spp. in sections of the ileum and colon of European bison (H-E staining). (A) Shortening and blunting of the intestinal villi of the ileum with diffuse infiltration of mononuclear inflammatory cells within the lamina propria, edematous stroma, dilated crypt containing necrotic debris (arrow), and atrophy of submucosal lymphoid follicles (× 20 magnification). (B) Schizonts and degenerating merozoites in the crypt lumen of the colon (arrows); immature macrogamont with a central nucleus (arrowhead) (× 1000 magnification). (C) Immature microgamonts in the epithelial cells of the colon crypt (arrows) (× 400 magnification). (D) Mature microgamont in the epithelial cells of the colon crypt (arrow) (× 1000 magnification). (E) Gametogonic stages of Eimeria development in the epithelial cells of the colon. Microgamont with peripheral microgames (arrowhead), (a) nearly mature microgamonts, (b) macrogamont with eosinophilic wall-forming bodies, (c) early oocyst (× 400 magnification). (F) Mature macrogamont in the epithelial cells of the cecum (arrow) (× 1000 magnification).
Fig. 1 in Imperfect nanorings with superconducting correlations
Fig. 1. Fragments of the stolon system of the Crustoidea. Wysoczki outcrop (Holy Cross Mts., Poland), upper Tremadocian. SEM micrographs. A, B, D. Specimens with two nodes (ZPAL G.36/1–3). C, E. Specimens with one node (ZPAL G.36/4–5). s., stolon.
Fig. 2 in A new Metapolygnathus platform conodont species and its implications for Upper Carnian global correlations
Fig. 2. SEM photographs of gondolellid conodonts. A. Holotype of Paragondolella noah (Hayashi, 1968). B. Holotype of Metapolygnathus communisti Hayashi, 1968 from the original plates of Hayashi (1968: 79, pl. 3). Both specimens are from chert at the base of the Adoyama Formation within a mixed Middle–Upper Triassic fauna (Ashio Mountains, Central Japan). C–J. Metapolygnathus praecommunisti sp. nov. from the Upper Triassic of "Calcari con Selce", Pizzo Mondello section (Sicani Mountains, Sicily). C. Holotype (sample NA12). D, E. Asymmetric morphotypes, samples NA14 and NA18 respectively. F, G. Rounded morphotypes, samples PM11A and NA19 respectively. H, I. More advanced forms with short platform (sample NA19). J. Advanced form, NA19 (from Mazza et al. 2010).
Fig. 4. A in A new Metapolygnathus platform conodont species and its implications for Upper Carnian global correlations
Fig. 4. A schematic figure illustrating the evolution of Paragondolella noah (Hayashi, 1968) into its descendant species. The main evolutionary trends from P. noah to the last representative of the lineage, Metapolygnathus parvus Kozur, 1972, are observable: the gradual shortening of the platform, the forward shifting of the pit, the posterior lengthening of the keel termination and the development of nodes at the geniculation point. In M. parvus the nodes disappear for the extreme reduction of the platform. A, B. Metapolygnathus parvus Kozur, 1972 (sample NA37, Lower Norian, PMs). C, D. Metapolygnathus communisti Hayashi, 1968 (samples NA39 and PM27 respectively, Lower Norian, PMs). Metapolygnathus praecommunisti sp. nov. from the Upper Carnian of the PMs and P2s: E, F. Very advanced specimens (samples NA22 and NA19 respectively, PMs). G, H. Intermediate specimens (samples NA12 and NA14 respectively, PMs). I, J. Primitive specimens (sample P25 of P2s and sample NA8 of PMs respectively). K, L. Paragondolella noah (sample NA2 of PMs and sample P21 of P2s respectively). Abbreviations: PMs, Pizzo Mondello section; P2s, Pignola 2 section.
Fig. 3 in A new Metapolygnathus platform conodont species and its implications for Upper Carnian global correlations
Fig. 3. SEM photographs of gondolellid conodonts Metapolygnathus praecommunisti sp. nov. from the Calcari con Selce of the Pizzo Mondello section (Sicani Mountains, Sicily) (A, C, D, F–H) and from the Upper Triassic of Calcari con Selce of the Pignola 2 section (southern Apennines, Basilicata) (B, E). A–C. Primitive forms, closer to Paragondolella noah (Hayashi, 1968), samples NA8, P25 and FNP53 respectively. D, E. Late juvenile growth stage, samples NA15A and P34 respectively. F. Advanced form, sample PM11A. G, H. Extremely mature stages, samples NA11 and PM11A.
Fig. 1 in Ecological correlates of ectoparasite load in a rodent: Complex roles of seasonality
Fig. 1. Interactive effects of season and body weight (centralized) on tick load in S. dauricus (A); and interactive effects of season and trappability on tick load in S. dauricus (B).
Correlation between Radiation Enhancements at Aviation Altitudes and Energetic Precipitation Electrons
<p>Figures, data, and code used in my paper describing "Correlation between Radiation Enhancements at Aviation Altitudes and Energetic Precipitation Electrons"</p>
FIGURE 7 in Telychian (Llandovery, Silurian) conodonts from the LaPorte City Formation of eastern Iowa, USA (East-Central Iowa Basin) and their implications for global Telychian conodont biostratigraphic correlation
FIGURE 7. Simple cone elements from Garrison Core. All specimens in lateral view except for 6. 1-2, Panderodus equicostatus, graciliform, GC 124.66–124.93 m, SUI 142251 (1) and graciliform, GC 121.92-121.88 m, SUI 142253 (2). 3-5, Panderodus panderi, graciliform, GC 124.66–124.93 m, SUI 142252 (3); arcuatiform, GC 131.95–132.23 m, SUI 142254 (4); and graciliform, GC 111.38–111.63 m, SUI 142255 (5). 6, Psuedooneotodus beckmanni, oral view, GC 135.65–136.10 m, SUI 142256. 7, Panderodus cf. P. unicostatus, falciform, GC 135.65–136.10 m, SUI 142257. 8- 11, Panderodus unicostatus, falciform, GC 131.95–132.23 m, SUI 142258 (8); fused cluster of 8 elements, GC 130.20–130.48 m, specimen destroyed processing for SEM (9); fused cluster of 6 elements, GC 131.95–132.23 m, SUI 142260 (10); and tortiform element, GC 131.95–132.23 m, SUI 142261 (11); 12-13, Walliserodus curvatus, dyscritiform, GC 134.06–134.31 m, SUI 142262 (12) and curvatiform, GC 128.85–129.11 m, SUI 142263 (13). 14-15, Panderodus greenlandensis, arcuatiform GC 118.20–118.41 m, SUI 142264 (14) and graciliform, GC 134.06–134.31 m, SUI 142265 (15). White scale bar represents 0.5 mm.
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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.