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Text-fig. 4. Distribution of Glyptostroboxylon rudolphii in the Miocene (solid circles) and Glyptostrobus pensilis at present (open circles). It grows in the subtropical swamps of Vietnamese and China (Eckenwalder 2009, Farjon 2010). in The First Glyptostroboxylon And Taxodioxylon Descriptions From The Late Miocene Of Turkey And Palaeoclimatological Evaluation
Text-fig. 4. Distribution of Glyptostroboxylon rudolphii in the Miocene (solid circles) and Glyptostrobus pensilis at present (open circles). It grows in the subtropical swamps of Vietnamese and China (Eckenwalder 2009, Farjon 2010).
Text-fig. 3. a–g, i, j: Quinquala obovata gen. et sp. nov., fruits from Wyoming and Oregon. a, b: Kisinger Lakes flora, Wyoming. a: Enlarged lateral view of split wing displaying venation along outer edge. Note the seed present in the locular area (arrow). UF 19376-60023b. b: Enlarged lateral view of split wing containing seeds within the locular area (arrow). UF 19376-60023c. c: Lateral view of fruit from White Cliffs, Oregon. UF 262-17690. d: Lateral view of fruit from West Branch Creek, Oregon. UF 229-53091. in Winged Fruits Of Rutaceous Affinity From The Eocene Of Western North America
Text-fig. 3. a–g, i, j: Quinquala obovata gen. et sp. nov., fruits from Wyoming and Oregon. a, b: Kisinger Lakes flora, Wyoming. a: Enlarged lateral view of split wing displaying venation along outer edge. Note the seed present in the locular area (arrow). UF 19376-60023b. b: Enlarged lateral view of split wing containing seeds within the locular area (arrow). UF 19376-60023c. c: Lateral view of fruit from White Cliffs, Oregon. UF 262-17690. d: Lateral view of fruit from West Branch Creek, Oregon. UF 229-53091.
Text-fig. 6. The skeletal remains of the European bison from Gladbeck as reconstruction and presentation in the anatomical position. GMM A5.K 517. in Everything Is A Question Of Time - Age Of Important Quaternary Palaeontological Finds From Westphalia
Text-fig. 6. The skeletal remains of the European bison from Gladbeck as reconstruction and presentation in the anatomical position. GMM A5.K 517.
Text-fig. 7. a. Worn section through a horizontally bedded body-chamber and phragmocone, body-chamber showing oyster attached to inside of aperture as well as burrow mottling. Tape measure provides scale. b. Body-chamber and crushed phragmocone with body-chamber and phragmocone entirely filled with bioturbated matrix containing stringers of crinoid and molluscan debris. Flank of phragmocone encrusted by oysters. Tape measure for scale. c. Complex of Thallassinoides and Diplocraterion burrows associated with conch that has been eroded out by wave action. A few 'Ghostly' fragments of ammonite are also present. Original scope of the image approximately 400 mm. c. Verically embedded conch with largely intact septa and camera infilled with burrowed matrix containing crinoid debris. Tape measure for scale. in 'Cenoceras Islands' In The Blue Lias Formation (Lower Jurassic) Of West Somerset, Uk: Nautilid Dominance And Influence On Benthic Faunas
Text-fig. 7. a. Worn section through a horizontally bedded body-chamber and phragmocone, body-chamber showing oyster attached to inside of aperture as well as burrow mottling. Tape measure provides scale. b. Body-chamber and crushed phragmocone with body-chamber and phragmocone entirely filled with bioturbated matrix containing stringers of crinoid and molluscan debris. Flank of phragmocone encrusted by oysters. Tape measure for scale. c. Complex of Thallassinoides and Diplocraterion burrows associated with conch that has been eroded out by wave action. A few 'Ghostly' fragments of ammonite are also present. Original scope of the image approximately 400 mm. c. Verically embedded conch with largely intact septa and camera infilled with burrowed matrix containing crinoid debris. Tape measure for scale.
Text-fig. 2. Latest Albian – Late Cretaceous palaeobotanical-palaeogeographical subregions of the North Pacific Region (a); modern outline of North-eastern Asia is shown for the Coniacian (after Smith et al. 1981): 1 – the Verkhoyansk-Chukotka Subregion, 2 – the Okhotsk-Chukotka Subregion, 3 – the Anadyr-Koryak Subregion (modified from Herman 2013) and geographical and geological position of the Turonian – Coniacian floras (b) (present-day map, modified from Shczepetov and Herman 2013). in On The Likely Palaeoelevation Of The Turonian - Coniacian Arman Flora Site (North-Eastern Asia)
Text-fig. 2. Latest Albian – Late Cretaceous palaeobotanical-palaeogeographical subregions of the North Pacific Region (a); modern outline of North-eastern Asia is shown for the Coniacian (after Smith et al. 1981): 1 – the Verkhoyansk-Chukotka Subregion, 2 – the Okhotsk-Chukotka Subregion, 3 – the Anadyr-Koryak Subregion (modified from Herman 2013) and geographical and geological position of the Turonian – Coniacian floras (b) (present-day map, modified from Shczepetov and Herman 2013).
Figure 8. Comparison between Trinomys lower teeth, which presents a in Relationships among extant and fossil echimyids (Rodentia: Hystricognathi)
Figure 8. Comparison between Trinomys lower teeth, which presents a deep sulcus between hypolophid and hypoconid (indicated by an arrow in the dP4), resulting in a hypoflexid continuous to the metaflexid ('deep main fold' of Moojen, 1948); and Proechimys lower teeth, which do not present a sulcus or have it quite shallow (feature considered in characters 8 and 20). A, Trinomys dimidiatus (MN 4016; left series); B, Proechimys gularis (AMNH 67323, left series). The arrows, in the dP4 of both specimens, show the area between the hypolophid and hypoconid. Note that, although the Trinomys specimen is older (has all teeth already worn), the sulcus is present in all teeth (state 1); by contrast, in Proechimys, only the unworn M3 presents the sulcus, which is already absent in dP4–M2 (state 0).
Figure 13. Comparison between Trinomys upper teeth, which presents a in Relationships among extant and fossil echimyids (Rodentia: Hystricognathi)
Figure 13. Comparison between Trinomys upper teeth, which presents a deep sulcus between protoloph and the protocone region in little-worn teeth (indicated by an arrow in the dP4), resulting in a hypoflexus continuous to the paraflexus ('deep main fold' of Moojen, 1948), and Proechimys upper teeth, which do not present a sulcus or have it quite shallow (character 32). A, Trinomys dimidiatus (MN 4016, left series); B, Proechimys gularis (AMNH 67323, right series reversed to the left side). The arrows, in the dP4 of both specimens, show the area between the protoloph and the protocone region. Note that, although the Trinomys specimen is older (has all teeth already worn), the sulcus is present in all teeth; by contrast, in Proechimys, only the unworn M3 presents the sulcus, which is already absent in dP4–M2.
Source: Photos courtesy of M.M. Le Roux (a–d) and K.S. Mashego (e–f) FIGURE 1: Morphological characters of Thesium confine (a, d, e) and T. durum (b, c, f) showing (a) the scale-like leaves found in both species; (b) involucral bracts that are invariably present in T. durum; (c) longitudinal section of a flower showing the dense hairs on the perianth lobes, stigma opposite the anthers and the twisted placental column; the habit of (d) T. confine and typical herbarium specimens of (e) T. confine and (f) T. durum. in A taxonomic evaluation of the Thesium confine species complex (Santalaceae)
Source: Photos courtesy of M.M. Le Roux (a–d) and K.S. Mashego (e–f) FIGURE 1: Morphological characters of Thesium confine (a, d, e) and T. durum (b, c, f) showing (a) the scale-like leaves found in both species; (b) involucral bracts that are invariably present in T. durum; (c) longitudinal section of a flower showing the dense hairs on the perianth lobes, stigma opposite the anthers and the twisted placental column; the habit of (d) T. confine and typical herbarium specimens of (e) T. confine and (f) T. durum.
Set of cross sections presented in "Electronic excitation of benzene by low energy electron impact and the role of higher lying Rydberg states"
<p>Contents:</p> <p>117_ch_thresholds.txt: TCIS excitation energies obtained from the 117CH-B1 calculation.</p> <p>305_ch_thresholds.txt: TCIS excitation energies obtained from the 305CH-B2 calculation.</p> <p>117_ch_DCS.tar.gz: differential cross sections obtained from the 117CH-B1 calculation.</p> <p>305_ch_DCS.tar.gz: differential cross sections obtained from the 305CH-B2 calculation.</p> <p>305_ch_DCS_BC.tar.gz: differential cross sections obtained from the 305CH-B2 calculation with the Born-Closure procedure for the dipole-allowed transitions of band V.</p> <p>305_ch_ICS_and_ICS_BC.tar.gz: elastic and summed electronic excitation integral cross sections and total cross sections, obtained from the 305CH-B2 calculation, with and without the Born-Closure procedure for the dipole-allowed transitions of band V.</p>
REMODEL. WP4. Vision-Based Perception. T4-2. Dynamic environment reconstruction. Data related to a paper presented at 2021 IEEE/RSJ International Conference on Intelligent Robots and Systems (IROS) (2021)
<p>Dataset with evaluation results of the paper "New Metrics for Industrial Depth Sensors Evaluation for Precise Robotic Applications", DOI <a href="https://doi.org/10.1109/IROS51168.2021.9636322">10.1109/IROS51168.2021.9636322</a></p>
REMODEL. WP4. Vision-Based Perception. T4-4. Functional component detection. Data related to a paper presented at 27th International Conference on Automation and Computing (ICAC) (2022)
<p>Dataset with evaluation parameters of the paper "Real-Time Instance Segmentation of Pedestrians using Transfer Learning", DOI: <a href="https://doi.org/10.1109/ICAC55051.2022.9911121">10.1109/ICAC55051.2022.9911121</a></p>
Tan-Tári Bricks Presentation Video in iGEM Design League 2022
<p>Tan Tári Bricks is this year's iDL Chilean Team. We propose a platform based on synthetic and computational biology to evaluate the risk of Antarctic beta-lactamases for developing inhibitory proteins.<br> By focusing on three key areas: a new scientific approach, education for the Chilean people, and taking political action to tackle this problem, we aim to develop an integrated solution in the Chilean territory for the Antimicrobial Resistance problem.<br> </p>
Fig. 5 in A new genus and species of Polynoidae (Annelida: Polychaeta) from the Canary Islands, and update on taxa present in the Northeast Atlantic
Fig. 5. Webbnesia maculata gen. et sp. nov., holotype (TFMCBM-AN/246). Distal part of neuropodium (posterior view), showing shorter rounded postchaetal lobe and elongate prechaetal acicular lobe with minute supra-acicular process (arrow). Scale bar = 70 µm.
Fig. 1 in A new genus and species of Polynoidae (Annelida: Polychaeta) from the Canary Islands, and update on taxa present in the Northeast Atlantic
Fig. 1. Map of the Canary Islands with type localities. Gran Canaria: 1. East coast, off Tufía (holotype, TFMCBM-AN/246). 2–3. South coast, off Castillo del Romeral (paratypes, TFMCBM-AN/247 and AN/248). Tenerife: 4. South coast, off Granadilla (paratype, SMF 32262).
Fig. 2 in A new genus and species of Polynoidae (Annelida: Polychaeta) from the Canary Islands, and update on taxa present in the Northeast Atlantic
Fig. 2. Webbnesia maculata gen. et sp. nov., holotype (TFMCBM-AN/246). A. Anterior end, elytra removed and left dorsal cirrus of segment 3 missing. B. Right elytron of segment 21. C. Right cirrigerous parapodium of segment 20, posterior view. D. Left elytragerous parapodium of segment 21, posterior view. E. Notochaetae. F. Upper, middle and lower neurochaetae. Scale bar: A= 1.3 mm; B = 1.9 mm; C–D = 0.4 mm; E–F = 40 µm.
Dataset presented in the recently submitted AGU manuscript "Constraining the crustal and mantle conductivity structures beneath islands by a joint inversion of multi-source magnetic transfer functions"
<p>Dataset (observed tippers, solar quiet global-to-local transfer functions, and global Q responses) presented in the recently submitted AGU manuscript "Constraining the crustal and mantle conductivity structures beneath islands by a joint inversion of multi-source magnetic transfer functions".</p>
SNAPPING PSI surface motion measurements over selected sites presented in MDPI Remote Sensing paper "SNAPPING Services on the Geohazards Exploitation Platform for Copernicus Sentinel-1 Surface Motion Mapping"
<p>SNAPPING PSI surface motion measurements over selected sites as presented in the paper with the title "SNAPPING Services on the Geohazards Exploitation Platform for Copernicus Sentinel-1 Surface Motion Mapping" by Michael Foumelis, Jose Manuel Delgado Blasco, Fabrice Brito, Fabrizio Pacini, Elena Papageorgiou, Panteha Pishehvar and Philippe Bally on Remote Sensing Open Access Journal.</p> <p>Whenever using this dataset, please cite its original paper (<a href="https://doi.org/10.3390/rs14236075">https://doi.org/10.3390/rs14236075</a>) and include the reference to this dataset (<a href="https://doi.org/10.5281/zenodo.7369653">https://doi.org/10.5281/zenodo.7369653</a>).</p> <p>This dataset includes average Line-of-Sight velocities for the following sites and dates:</p> <table> <tbody> <tr> <td><strong>Site name</strong></td> <td><strong>Country</strong></td> <td><strong>Period</strong></td> <td><strong>Relative orbit</strong></td> <td><strong>Orbit direction</strong></td> </tr> <tr> <td>Cap-Haïtien</td> <td>Haiti</td> <td>Jan-2017 / Dec-2019</td> <td>106</td> <td>ascending</td> </tr> <tr> <td>Gran Renaissance Ethiopian Dam</td> <td>Ethiopia</td> <td>Jan-2019 / Jun-2021</td> <td>50</td> <td>descending</td> </tr> <tr> <td>La Palma Volcano</td> <td>Spain</td> <td>Jun-2019 / Dec-2021</td> <td>169</td> <td>descending</td> </tr> <tr> <td>Santorini Volcano</td> <td>Greece</td> <td>Apr-2015 / May-2021</td> <td>29</td> <td>ascending</td> </tr> <tr> <td>San Francisco</td> <td>USA</td> <td>Jan-2016 / Dec-2020</td> <td>115</td> <td>descending</td> </tr> <tr> <td>Thessaloniki International Airport (SKG)</td> <td>Greece</td> <td>Apr-2015 / Dec-2020</td> <td>102</td> <td>ascending</td> </tr> </tbody> </table>
Eviterbo brief presentation
<p>This video is a brief presentation of eViterbo platform, in development under the scope of TechNetEMPIRE (PTDC/ART-DAQ/31959/2017) and anchored in the “Art, History and Heritage” group and in the “Heritage and Memory” line of CHAM – Centre for the Humanities.</p> <p>Version 1 was a video presentation for Linked Pasts VII, Ghent University 2021.</p> <p>Version 2 Video was modified from an original video presentation to serve as an <em>e</em>Viterbo generic presentation.</p>
Deep margin elevation – present status and future directions
<p>BibTex database file, containing the records identified in the electronic search, and the datasets generated and analyzed in this article on deep margin elevation.</p> <p>Information on the risk of bias of included studies is presented in supplementary tables (Tables S1-S38 and Questionnaire SQ1). The ROBFEAD, MINORS, RoBDEMAT, and AMSTAR tools were used for <em>in silico</em> studies, clinical studies, <em>in vitro</em> studies, and reviews respectively. The CASP qualitative research checklist was used for healthcare survey studies.</p>
MEG data during the presentation of Gabor patterns and word sets
<p><strong>Subjects</strong></p> <p>MEG was recorded in 7 healthy subjects (5 young right-handed and 1 left-handed and 1 elderly) in the waking state with their eyes open or closed, who were sitting in a comfortable chair. The experimental technique was approved by the ethical commission of the Institute of Higher Nervous Activity and Neurophysiology of RAS (protocol No. 5 dated 02.12.2020).</p> <p><strong>Equipment</strong></p> <p>MEG was recorded on a VectorView device (Elekta Neuromag Oy, Finland), which was placed inside a magnetically protected chamber made of multilayer permalloy (AK3b, Vacuumschmelze GmbH, Germany). Before MEG recording, the coordinates of anatomical reference points (left and right preauricular points and nasion) were determined, as well as indicator coils attached to the surface of the scalp of the subject in the upper part of the forehead and behind the auricles. These points were determined using a FASTRAK 3D digitizer (Polhemus, USA). Each subject had a virtual model of the brain and head obtained from an anatomical 3D MRI taken the day before (file: MRI_V1_7.zip).</p> <p><strong>Registration and pre-processing</strong></p> <p>The subject's head was covered by a helmet, which is part of a fiberglass Dewar vessel with an array of sensors immersed in liquid helium. The subject sat down in such a way that the surface of the head was as close as possible to the sensors. The magnetic signal was recorded from 102 triplets, each of which consisted of 1 magnetometer and 2 gradiometers at rest with eyes closed and upon presentation of visual and speech stimuli. Recording was performed with a sampling frequency of 1000 Hz in a bandwidth of 0.1–330 Hz and was processed by the MaxFilter program (Elekta Neuromag Oy, Finland), which eliminates artifacts (the tSSS method—spatio-temporal separation of signals). The signal levels were corrected in accordance with the data on the position of the subject's head in relation to the MEG sensors. The position of the head during the experiment was controlled using special inductors.</p> <p><strong>Visual and verbal stimuli</strong></p> <p>After recording the background MEG for 3 minutes with closed eyes, the subject opened his eyes on command and observed the fixation point on the projection screen. After 15 seconds, stimulation was started and the subject's responses were received in the form of pressing a button. In response to the 0 degrees and 90 degrees stimuli, the subject had to press the button with the index finger, and to the 45 degrees and 135 degrees inclined stimuli, the adjacent button with the middle finger. Stimuli lasting 100 ms were presented randomly every 3100±100 ms (intervals between stimuli varied randomly). In two series, 42 stimuli of each orientation were presented. Between the series, the subject rested for 2-3 minutes. Visual stimuli in the form of Gabor contrast gratings (1.9 cycles per angular degree) with dimensions of 5.25 angular degrees and an average brightness of 4 lux were projected onto a screen located at a distance of 95 cm from the subject's eyes using a Panasonic PT-stimulating projector D7700E-K, which is part of the MEG facility. Visual stimulus patterns were generated at http://www.cogsci.nl/pages/gabor-generator with edge parameters: Circular (sharp edge). The samples are contained in the GaborStim.zip file (the names of the sample files correspond to their name in the script file, but do not match their geometric meaning, see table below). The stimulator was programmed using the Presentation software (USA, Neurobehavioral Systems, Inc). Stimulation scripts are contained in the sce.zip file.</p> <p><strong>Table</strong></p> <p><em>Stimulus or response code Type of stimulus or response</em></p> <p>STI101_1 Fixation point<br> STI101_2 90 degrees<br> STI101_4 135 degrees</p> <p>STI101_8 0 degrees<br> STI101_16 45 degrees<br> STI101_32 First button (index finger)</p> <p>STI101_64 Second button (middle finger)</p> <p>After 2 series of visual stimuli, the subject closed his eyes and was presented with 3 series of speech stimuli for 2 minutes with a break of 1 minute. In each series, recordings of audio files of 8 separate adjectives of the Russian language were presented, which were repeated 5 times in a pseudo-random order. The series began with 3 words, which were not taken into account in further analysis. The subject listened to the words and had to press the button after he understood the meaning of the presented word. After pressing or no response, the next word followed in 2±1 s. The audio files are contained in the words101_343.zip file (the names correspond to the script file).</p> <p><strong>Data received</strong></p> <p>The records are contained in files with the name of the type V1m24r, where V1 is the number of the subject, m is the sex (m/f), 24 is the age, and r is the right-handed subject. This dataset can be easily loaded into the Brainstorm program. Spontaneous and evoked MEG can be used for source localization and reconstruction of traveling waves.</p> <p><strong>Acknowledgments</strong></p> <p>The reported study was funded by RFBR, project number 20-015-00475.</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.