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Fig. 2 in New Stratigraphic Data from the Erlian Basin: Implications for the Division, Correlation, and Definition of Paleogene Lithological Units in Nei Mongol (Inner Mongolia)
Fig. 2. Above, Paleogene outcrops at the Nuhetingboerhe locality. The arrow points to the lower hiatus between the Nomogen (lower) and Arshanto (upper) formations; Below, Close-up view of the lower hiatus showing the lithology and erosional surface.
Fig. 1. A in New Stratigraphic Data from the Erlian Basin: Implications for the Division, Correlation, and Definition of Paleogene Lithological Units in Nei Mongol (Inner Mongolia)
Fig. 1. A. Localities (black dots) of the Erlian Basin, Nei Mongol (Inner Mongolia). The shaded area indicates the location of the Nuhetingboerhe-Huheboerhe area (NHA). B. Topographic map of NHA. The black bars indicate positions of measured sections at the Daoteyin Obo, Nuhetingboerhe, Wulanboerhe (Huheboerhe of Meng et al., 2004), and Huheboerhe.
Text-fig. 2. Stratigraphic ranges of Microtoscoptini-bearing sites. Correlation of ELMA and NALMA with earth years is according to Hilgen et al. (2012). Localities of very broad stratigraphic range (e.g., the entire Turolian or Hemphillian, as for Vasilivka 1, Lobkove, Little Valley, Cambridge), do not contribute to detail the range, and are omitted in this figure. in Comments On The Age And Dispersal Of Microtoscoptini (Rodentia: Cricetidae)
Text-fig. 2. Stratigraphic ranges of Microtoscoptini-bearing sites. Correlation of ELMA and NALMA with earth years is according to Hilgen et al. (2012). Localities of very broad stratigraphic range (e.g., the entire Turolian or Hemphillian, as for Vasilivka 1, Lobkove, Little Valley, Cambridge), do not contribute to detail the range, and are omitted in this figure.
Text-fig. 19. Position of the studied faunas correlated to chronostratigraphic and biochronological charts. in Late Miocene (Early Turolian) Vertebrate Faunas And Associated Biotic Record Of The Northern Caucasus: Geology, Taxonomy, Palaeoenvironment, Biochronology
Text-fig. 19. Position of the studied faunas correlated to chronostratigraphic and biochronological charts.
Text-fig. 3. Correlation model of the studied sections of Late Miocene deposits. a. Tuapse highway bridge. b. Gaverdovsky. c. Volchaya Balka. 1. reversed polarity; 2. normal polarity; 3. unstudied interval. in Late Miocene (Early Turolian) Vertebrate Faunas And Associated Biotic Record Of The Northern Caucasus: Geology, Taxonomy, Palaeoenvironment, Biochronology
Text-fig. 3. Correlation model of the studied sections of Late Miocene deposits. a. Tuapse highway bridge. b. Gaverdovsky. c. Volchaya Balka. 1. reversed polarity; 2. normal polarity; 3. unstudied interval.
Text-fig. 2. Lithostratigraphy and magnetostratigraphy of the Rigi section with correlation to the MPTS (Magnetostratigraphic Polarity Time Scale) according to Schlunegger (1995). Asterisk = mammal site. in Eomys Helveticus N. Sp. And Eomys Schluneggeri N. Sp., Two New Small Eomyids Of The Chattian (Mp 25/Mp 26) Subalpine Lower Freshwater Molasse Of Switzerland
Text-fig. 2. Lithostratigraphy and magnetostratigraphy of the Rigi section with correlation to the MPTS (Magnetostratigraphic Polarity Time Scale) according to Schlunegger (1995). Asterisk = mammal site.
Fig. 5. Correlation between PCA axis 1 in Fish assemblages of tropical floodplain lagoons: exploring the role of connectivity in a dry year
Fig. 5. Correlation between PCA axis 1 and species richness (a), density (b), and biomass (c) in connected [February (), May (), November ()] and disconnected lagoons, May (), August (), November ()]. Arrows indicate the direction of the limnological variables influence.
FIG. 6. A. IGM 100 in A new specimen of the ornithischian dinosaur Haya griva, cross-Gobi geologic correlation, and the age of the Zos Canyon beds
FIG. 6. A. IGM 100/3181.Two carpals in unknown orientation. B. Metacarpal I and manual phalanx I-1 in dorsal view. C. Metacarpal II or III and manual phalanx in dorsal view. D. Manual phalanx in dorsal view. E. Three ungual phalanges in partial dorsal view.
SI for Cherns et al "Correlative tomography of exceptionally preserved Jurassic ammonite implies hyponome-propelled swimming"
<p>================================================================================<br> About<br> ================================================================================</p> <p>This repository is associated with:</p> <p>"Correlative tomography of exceptionally preserved Jurassic ammonite implies hyponome-propelled swimming"</p> <p>Authored by:</p> <p>Lesley Cherns (1), Alan R. T. Spencer (2,3), Imran A. Rahman (3,4), Russell J. Garwood (3,5), Chris Reedman (1,6), Genoveva Burca (7,8), Martin J. Turner (9), Neville T. J. Hollingworth (10), and Jason Hilton (11)</p> <p>1 School of Earth and Environmental Sciences, Cardiff University, Cardiff, UK<br> 2 Department of Earth Science and Engineering, Imperial College London, London, UK<br> 3 Earth Sciences Department, Natural History Museum, London, UK<br> 4 Oxford University Museum of Natural History, University of Oxford, Oxford, UK<br> 5 Department of Earth and Environmental Sciences, University of Manchester, Manchester, UK<br> 6 Jurassic Coast Trust HQ, Bridport, Dorset, UK<br> 7 Science and Technology Facilities Council, Rutherford Appleton Laboratory, ISIS Facility, Harwell, UK<br> 8 Faculty of Science and Engineering, University of Manchester, Manchester, UK<br> 9 Department of Computer Science, University of Manchester, Manchester, UK<br> 10 Science and Technology Facilities Council, Swindon, UK<br> 11 School of Geography, Earth and Environmental Sciences, University of Birmingham, Birmingham, UK</p> <p>================================================================================<br> Contents<br> ================================================================================</p> <p>This archive contains the following file(s):</p> <p>- ct_dataset.zip<br> - dragonfly_sigaloceras_enodatum.zip<br> - neutron_dataset.zip<br> - neutron_dataset_cropped_cleaned.zip<br> - photogrammetry_block_model.ply<br> - photogrammetry_dataset.zip<br> - stl_model_meshes.zip<br> - video.mkv<br> - video_blender.zip</p> <p>+ metadata.txt (this file)</p> <p>================================================================================<br> Note on .zip archives:<br> ================================================================================</p> <p>All .zip archive where created using 7-zip (https://www.7-zip.org/), using the<br> default .zip settings.</p> <p>================================================================================<br> File Descriptions and Metadata:<br> ================================================================================</p> <p>--------------------------------------------------------------------------------<br> ct_dataset.zip<br> --------------------------------------------------------------------------------</p> <p>X-ray CT data. A Nikon Metrology XTek XT H 225 at the University of Manchester<br> was used. The scan used a 0.5mm Copper filter, 145 kV, uA 85, capturing 6000 <br> projections on a 3192 x 2296 detector. The projection data was reconstructed <br> using Nikon Metrology NV’s XT 5.1.4.3 software.</p> <p>Dataset is consists of a .vol and .vgi (metadata) file. The .vol contains the<br> raw data for the individual slices. Each image has the following properties:</p> <p>Images format: 32-bit float (raw)<br> Image x/y: 3189 x 3191 px <br> Number of images: 1150<br> Caculated voxel size: 19.6419 µm</p> <p>Uncompressed total size: 45 GB</p> <p>--------------------------------------------------------------------------------<br> dragonfly_sigaloceras_enodatum.zip<br> --------------------------------------------------------------------------------</p> <p>Contains: sigaloceras_enodatum_final.ORSSession | 8.8 GB (uncompressed)</p> <p>The sigaloceras_enodatum_final.ORSSession file is a save DragonFly session.<br> The session conatains the full setup (aligned Nutron and CT datasets, ROIs, <br> segments, and meshes) used to produce and interpret the ammonite. </p> <p>DragonFly version: 2021.1.0.977<br> See: https://www.theobjects.com/dragonfly/index.html</p> <p>DragonFly was used under the terms of its Non-Commercial Use License.<br> Non-commercial licenses are granted free-of-charge to qualified researchers, <br> academics, and non-commercial developers for non-profit research or development <br> purposes. Non-commercial licenses are valid for a one-year period and can be renewed <br> annually at no charge.</p> <p>See: https://www.theobjects.com/dragonfly/get-non-commercial-licensing-program.html</p> <p>--------------------------------------------------------------------------------<br> neutron_dataset.zip<br> --------------------------------------------------------------------------------</p> <p>Neutron tomography was performed at the IMAT beamline of ISIS Neutron and Muon <br> Source, UK. Imaging was undertaken using an optical camera box with a <br> field-of-view of 120 x 120 mm2. A total of 1801 projections were acquired <br> over 360° rotation, with an exposure time of 30 s per projection, giving a total <br> duration of ~15 hours. Projections were reconstructed as two-dimensional <br> slices using Octopus Imaging Software. These slices have an uncompressed total <br> size of 15.4 GB. Each slice in the stack has the following properties:</p> <p>Images format: 16-bit .tiff<br> Image x/y: 2048 x 2048 px <br> Number of images: 2048<br> Caculated voxel size: 58 µm<br> Image size (uncompressed): 8192 MB each.</p> <p>--------------------------------------------------------------------------------<br> neutron_dataset_cropped_cleaned.zip<br> --------------------------------------------------------------------------------</p> <p>Neutron tomographic slices that have been cropped and cleaned (ie. had background <br> noise removed) based on images in neutron_dataset.zip. Images in .tiff format.<br> 1715 images in stack.</p> <p>--------------------------------------------------------------------------------<br> photogrammetry_block_model.ply<br> --------------------------------------------------------------------------------</p> <p>Model in .ply format (with coloured vertex) showing the limestone block and <br> counter-part of the ammonite. 257136 vertices and 513513 faces.</p> <p>--------------------------------------------------------------------------------<br> photogrammetry_dataset.zip<br> --------------------------------------------------------------------------------</p> <p>Photographs, with backgrounds removed, used to generate the 3D block model via<br> photogrammetry. The .zip archive contains 142 photographs.</p> <p>--------------------------------------------------------------------------------<br> stl_model_meshes.zip<br> --------------------------------------------------------------------------------</p> <p>.zip archive containing the 49 .stl meshes used in the creation of the 3D<br> reconstructions. These meshes have been smoothed within DragonFly prior to <br> exportation.</p> <p>--------------------------------------------------------------------------------<br> video.mkv<br> --------------------------------------------------------------------------------</p> <p>Video showing annimation starting with the limestone block and ammonite in<br> place, ammonite is then shown on its own, before the combinded neutron and x-ray<br> tomography results are presented.</p> <p>Length: 00:43 min<br> Size: 23.9MB<br> Format: .mkv</p> <p>--------------------------------------------------------------------------------<br> video_blender.zip<br> --------------------------------------------------------------------------------</p> <p>This .zip contains the Blender file used in the creation of the video.</p>
Data characteristic and spurious correlation
<p>Database and scripts in R of the doctoral thesis "Análisis composicional del acceso a servicios de agua, saneamiento e higiene y medida de sus desigualdades"</p>
Electronic correlations and universal long-range scaling in kagome metals
<p>Dataset for the constrained Random Phase Approximation calculations shown in the manuscript. The VASP OUTCAR (ascii plain texy file) contains the whole cRPA U_iijj, U_ijij and U_ijji tensors, from which the numbers in the table of the paper (Supplementary Material) are extracted. Input files necessary to reproduce the results are also in the repository.</p>
Data from: A rallid ballad: Communal signaling is correlated with year-round territoriality in the most duet-rich family of birds (Gruiformes: Rallidae)
<p>Duetting, in which two or more individuals call in coordinated unison, is common in birds, yet most research investigating the function of avian duets has focused only on oscine passerines. However, we have discovered that duetting occurs in 61 species (59%) in the family Rallidae (rails), one of the highest known rates in any bird clade, and that rail duets are also significantly associated with year-round territoriality and habitat type. We applied a comparative approach to study the occurrence of duetting relative to socio-ecological traits and call properties in 103 rail species, with the prediction that duetting rails produce low-frequency calls that spread well over short distances in densely vegetated habitats. Using a model correcting for phylogenetic signal, we found that duetting is the ancestral state in Rallidae, and that duetting rails show a trending effect for being sedentary and non-migratory. Contrary to our predictions, there was no significant correlation between rail duetting and social bond length, breeding system, breeding latitude from the equator, or sexual dimorphism, as year-round territoriality and forest or heterogeneous habitats were the strongest predictors of duets. Despite the prevalence of duetting in Rallidae, few studies have tested duet functions such as territory defense in this family, and our comparative phylogenetic study lays the groundwork for future research, as little remains known about the behavioral ecology and vocal interactions of many rails.</p>
Homeostatic regulation through strengthening of neuronal network correlated synaptic inputs
<p>Data from "Homeostatic regulation through strengthening of neuronal network correlated synaptic inputs" by Barnes SJ, Keller GB & Keck T.</p> <p> </p>
Correlation of the kinetics of viral antigen and genomic RNA with restoration of normal cell homeostasis
<p>The main objective of the studies within COCID Work Package 6 is to understand basic mechanisms by which viral replication machineries are removed from cells after pharmacological interruption of viral replication using functional as well as imaging techniques, including soft X-ray tomography.</p> <p>In this document, we highlight the progress in establishing the HCV replication models (replicons), the antiviral treatment chosen to eliminate viral structures from the host cells and the correlation between elimination of the viral replication machinery and restoration of a normal host cell homeostasis, using markers of HCV-induced stress. These data are essential to frame the experimental setup chosen for the imaging process required in subsequent stps of the project.</p>
Data for: Distinguishing intrinsic photon correlations from external noise with frequency-resolved homodyne detection
<p>Data for the publication C. Lüders, M. Aßmann, Distinguishing intrinsic photon correlations from external noise with frequency-resolved homodyne detection, Scientific Reports 10 (1), 1-11 (2020).</p> <p>In this work, we apply homodyne detection to investigate the frequency-resolved photon statistics of a cw light field emitted by a driven-dissipative semiconductor system in real time. We demonstrate that studying the frequency dependence of the photon number noise allows us to distinguish intrinsic noise properties of the emitter from external noise sources such as mechanical noise while maintaining a sub-picosecond temporal resolution. We further show that performing postselection on the recorded data opens up the possibility to study rare events in the dynamics of the emitter. By doing so, we demonstrate that in rare instances, additional external noise may actually result in reduced photon number noise in the emission.</p> <p>Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) – SFB-Geschäftszeichen TRR142/3-2022 – Projektnummer 231447078, Project A04.</p>
Figs 9, 10 in Scorpions of the Brandberg Massif, Namibia: Species richness inversely correlated with altitude
Figs 9, 10. Adult females, habitus in life: (9) Hottentotta conspersus (Thorell, 1876); (10) Parabuthus brevimanus (Thorell, 1876).
Figs 15, 16 in Scorpions of the Brandberg Massif, Namibia: Species richness inversely correlated with altitude
Figs 15, 16. Uroplectes adults, habitus in life: (15) U. gracilior Hewitt, 1913, male; (16) U. planimanus (Karsch, 1879), female with brood.
Fig. 1 in Scorpions of the Brandberg Massif, Namibia: Species richness inversely correlated with altitude
Fig. 1. Brandberg Massif (Namibia), gravel plains southwest, facing northeast to Massif in distance, dry year. Gravel plains, habitat of Parabuthus brevimanus (Thorell, 1876), Parabuthus namibensis Lamoral, 1979 and Uroplectes gracilior Hewitt, 1913.
Fig. 4 in Scorpions of the Brandberg Massif, Namibia: Species richness inversely correlated with altitude
Fig. 4. Brandberg Massif (Namibia), base of Massif at entrance to Goaseb (Ga-Asab) Gorge, facing north to Orabeskopf at summit, wet year. Dominant vegetation, Boscia foetida Schinz and Commiphora sp. Rocky flats, habitat of Hottentotta conspersus (Thorell, 1876), Parabuthus brevimanus (Thorell, 1876), Parabuthus villosus (Peters, 1862), and Opistophthalmus lamorali Prendini, 2000.
Figs 13, 14 in Scorpions of the Brandberg Massif, Namibia: Species richness inversely correlated with altitude
Figs 13, 14. Parabuthus adults, habitus in life: (13) P. kraepelini Werner, 1902, female; (14) P. villosus (Peters, 1862), male.
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Allen Brain Atlas
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