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opencc-by-4.0Mar 2007View details →

Fig. 14 in A Small Derived Theropod from Öösh, Early Cretaceous, Baykhangor Mongolia

Fig. 14. Systematic variation in tooth denticle size among theropod dinosaurs. Dromaeosaurus albertensis (AMNH FR 5356), top, illustrating anterior and posterior denticles not significantly different in size (character 247.0). Velociraptor mongoliensis (IGM 100/1252), bottom, illustrating anterior denticles that are significantly smaller than posterior denticles (character 247.1). Images not to scale.

Global dataset of Sentinel-1 azimuth shift values and derived horizontal displacements from COMET LiCSAR system

For this dataset, we were exploiting spatio-temporal behaviour of side-products of coregistration of Sentinel-1 radar images, that were generated in last couple of years, within the COMET LiCSAR system for computing interferograms. These side-products are sub-pixel (azimuth) offsets, allowing for a very precise match of the images (up to a 0.0005 pixels). We have shown that by a proper approach, these offsets can be used as measurements of large-scale horizontal motion - in our case, using 250x250 km resolution cells, we aimed to measure motion of tectonic plates. Our measurements are fitting well to the latest ITRF2014 plate motion model, although the E component contains an extra overall shift, not explained at the moment of sharing the outputs. The sub-pixel offsets (result of intensity cross correlation and spectral diversity estimation, w.r.t. precise orbit ephemerides) were corrected for solid Earth tides and ionospheric phase advance, using external models. The code shared within the dataset includes the correction functions. The data contains both original and corrected values. Also, the data contains ITRF2014 plate motion values. The dataset contains outputs from both COMET LiCSAR frame units and their decomposition into N, E motion vectors, as well as some metadata on the frames that are necessary for the reprocessing if needed.

EO-derived water quality parameters using aerial imaging spectrometry for Lake Mulargia (Sardinia, Italy) (2020/09/24)

This dataset contains Hyspex-derived water quality (WQ) products of Lake Mulargia (Sardinia, Italy) for the 24 September 2020. The acquisition was done by CGR Spa (Italy). Available parameters are: True-color image (RGB), Colored Dissolved Organic Matter (CDOM), Chlorophyll-a (CHL), and Suspended Particulate Matter (SPM). WQ parameters have been calculated using CNR’s bio-optical model BOMBER parameterized with the inherent optical properties specific of the case study. The data are available as GeoTiff files in WGS 84 / UTM zone 32N (EPSG: 32632).

opencc-by-4.0Oct 2009View details →

Figure 5. Comparative cranial morphology for derived metriorhynchid species. A in What is Geosaurus? Redescription of Geosaurus giganteus (Thalattosuchia: Metriorhynchidae) from the Upper Jurassic of Bayern, Germany

Figure 5. Comparative cranial morphology for derived metriorhynchid species. A, Dakosaurus maximus neotype, SMNS 8203. B, Enaliosuchus schroederi holotype, MMGLV. C, Geosaurus araucanensis holotype, MLP 72-IV-7-1. The relative position of the orbit is indicated for Dakosaurus. Scale bars: 20 mm.

Figure 9 in Developmental patterns of the crocodilian and avian columella auris: reappraisal of interpretations of the derivation of the dorsal hyoid arch in archosaurian tetrapods

Figure 9. Development of the columella auris in Gallus domesticus and Coturnix japonica. A, day-8 chick embryo, ventro-right lateral view. B, day-10 chick embryo, postero-right lateral view. C, day-11 chick embryo, antero-right lateral view. D, day-7 quail embryo, left lateral view. E, day-9 quail embryo, ventro-right lateral view. F, day-9 quail embryo, ventro-left lateral view. G, day-10 quail embryo, ventropostero-right lateral view. For abbreviations see the Appendix. A–G: whole mounts.

Figure 8 in Developmental patterns of the crocodilian and avian columella auris: reappraisal of interpretations of the derivation of the dorsal hyoid arch in archosaurian tetrapods

Figure 8. Development of the columella auris and surrounding tissues in Struthio camelus. A, day-16 embryo, posteroleft lateral and anteroventro-left lateral view. B, day-17 embryo, ventro-left lateral view. C, day-18 embryo, left lateral view. D, day-20 embryo, postero-left lateral view. E, day-25 embryo, antero-left lateral view. F, day-29 embryo,

Figure 6 in Developmental patterns of the crocodilian and avian columella auris: reappraisal of interpretations of the derivation of the dorsal hyoid arch in archosaurian tetrapods

Figure 6. Development of the columella auris and surrounding tissues in Struthio camelus. A, day-11 embryo, ventro-right lateral view. B, day-12 embryo, ventro-right lateral view. C and D, day-13 embryo, postero-left lateral view. E, day-13 embryo, posterior view. F, day-13 embryo, postero-dorsal and posterior view. G, day-13 embryo, anterior view. For abbreviations see the Appendix. The dotted yellow circle represents the region of the tympanic process. The dotted red circle represents tympanic invagination. A and B, whole mounts; C–G, graphic reconstructions.

Figure 5 in Developmental patterns of the crocodilian and avian columella auris: reappraisal of interpretations of the derivation of the dorsal hyoid arch in archosaurian tetrapods

Figure 5. Development of the columella auris of Crocodylus niloticus. A, day-17 embryo, left lateral view. B, day-21 embryo, left lateral view. C, day-25 embryo, left lateral view. D, day-26 embryo, left lateral view. E, day-26 embryo, right lateral view. F, day-27 embryo, right lateral view. G, day-29 embryo, right lateral view. H, day-29 embryo, left lateral view. I, day-30 embryo, left lateral view. J, day-35 embryo, left lateral view. K, day-40 embryo, left lateral view. For abbreviations see the Appendix. A–K, whole mounts.

Figure 4 in Developmental patterns of the crocodilian and avian columella auris: reappraisal of interpretations of the derivation of the dorsal hyoid arch in archosaurian tetrapods

Figure 4. Development of the columella auris and surrounding tissues of Alligator mississippiensis. A and B, day-40 embryo, left lateral and right lateral view. C, day-40 embryo, right lateral view. D, day-42 embryo, right lateral and medial view. E, day-42 embryo, right lateral view. F, day-47 embryo, right lateral view. G, day-51 embryo, right lateral view. For abbreviations see the Appendix. A, B, and E–G, whole mounts; C and D, graphic reconstructions.

Figure 3 in Developmental patterns of the crocodilian and avian columella auris: reappraisal of interpretations of the derivation of the dorsal hyoid arch in archosaurian tetrapods

Figure 3. Development of the columella auris and surrounding tissues of Alligator mississippiensis. A, day-30 embryo, left lateral and medial view. B, day-33 embryo, left lateral view. C, day-37 embryo, right lateral and medial view. D and E, day-39 embryo, right lateral view. For abbreviations see the Appendix. A and C, graphic reconstructions; B, D, and E,

Figure 2 in Developmental patterns of the crocodilian and avian columella auris: reappraisal of interpretations of the derivation of the dorsal hyoid arch in archosaurian tetrapods

Figure 2. Development of the columella auris and surrounding tissues of Alligator mississippiensis. A–C, day-21 embryos, transverse sections through the external and middle ear region. D, day-21 embryo, posterior view. E, day-22 embryo, right lateral view. F, day-25 embryo, right lateral view. G, day-27 embryo, postero-right lateral view. H, day-28 embryo, right lateral view. For abbreviations see the Appendix. A–C, histological sections; D and G, graphic reconstructions; E, F, and H, whole mounts.

Figure 1 in Developmental patterns of the crocodilian and avian columella auris: reappraisal of interpretations of the derivation of the dorsal hyoid arch in archosaurian tetrapods

Figure 1. Development of the columella auris and surrounding tissues of Alligator mississippiensis. A, day-12 embryo, right lateral view. B, C, and E, day-14 embryo, postero-left lateral, posterior, and right lateral view. D and F, day-14 embryo, transverse sections through the external and middle ear region. G and H, day-16 embryo, transverse sections through the external and middle ear region. I, day-18 embryo, right lateral view. For abbreviations see the Appendix. In all figures hyal elements are distinguished in all whole mounts by yellow labels. A and I, whole mounts; B, C, and E, graphic reconstructions; D, and F–H, histological sections.

opencc-by-4.0Mar 2003View details →

Figure 3. Synthetic tree derived from the 12S in Evolutionary systematics of the Indian mouse Mus famulus Bonhote, 1898: molecular (DNA/DNA hybridization and 12S rRNA sequences) and morphological evidence

Figure 3. Synthetic tree derived from the 12S rRNA datasets with the inclusion of all substitutions (TV + TI). The thin lines indicate nodes that are not robustly supported by all kinds of analysis. The robustness of the different nodes are indicated as follows: [BP(BPweighted analysis)/BSI (Parsimony)]/[BP(NJ)/Reliability Percentage (ML)].

opencc-by-4.0Aug 2008View details →

Figure 3. A, the single most parsimonious tree derived from 2129 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)

Figure 3. A, the single most parsimonious tree derived from 2129 aligned characters of mitochondrial genes (12S, 16S, cyt-b) (CI = 0.40; TL = 31; RI = 0.58) using maximum parsimony. Of these, 1229 characters are constant and 708 characters are parsimony-informative. Numbers above branches are bootstrap values and below are Bremer values. B, strict consensus of 96 trees generated from 1244 aligned characters of nuclear genes (Rag1 and Cmos) (CI = 0.82; TL = 205; RI = 0.84) using maximum parsimony. Of these, 1086 characters are constant and 90 are parsimonyinformative. Numbers above branches are bootstrap values and below are Bremer values.

opencc-by-4.0Apr 2000View details →

Fig. 61. One cladogram derived from successive weighting approach using NONA. See fig. 60 in A Cladistic Analysis of the Therini: A New Synonym of the Cidariini (Lepidoptera: Geometridae, Larentiinae)

Fig. 61. One cladogram derived from successive weighting approach using NONA. See fig. 60 for generic abbreviations and symbols. Each node number is indicated.

Biomarker Signatures of Quality for Engineering Nasal Chondrocyte-Derived Cartilage

Data underlying the figures in the publication “Biomarker Signatures of Quality for Engineering Nasal Chondrocyte-Derived Cartilage”, published in Front Bioeng Biotechnol., 2020, 8: 283. (DOI: 10.3389/fbioe.2020.00283). Table of contents: 1. biochem_summary; Biochemistry data and MBS of pellets made from NC and PC mixtures in the titration experiment. 2. dirty-clean-biochem; Biochemistry data and MBS of pellets made from passage 2 cells from dirty/clean biopsies. 3. identity_all; All passage 1 and passage 2 cells of type pure NC and pure PC from the titration and dirty/clean datasets. All PCR data included. 4. identity_titration; Passage 1 and 2 and pellets made from pure NC and PC populations in the titration experiment. All PCR data included. Average (avg) refers to the average of the biologicsl replicates (which are already the average of the experimental replicates of Data 5). 5. identity_titration_avg; Passage 1 and 2 and pellets made from pure NC and PC populations in the titration experiment. All PCR data included. All experimental replicate information is included (which are the average of the technical replicates). 6. PCR_cells_summary; For the purity and potency assays, mixtures of increasing NC to PC cell ratios were created. The PCR data from those mixtures are here for passage 2 and for the pure populations as passage 1. 7. PCR_pellet_summary; For the purity and potency assays, mixtures of increasing NC to PC cell ratios were created. PCR data from engineered pellets are here included. 8. PCRdirty-clean; PCR data of cells obtained from dirty/clean biopsies at passage 0,1, and 2. 9. PCRsummary_all; Combined Data 5, 7, and 8. 10. Proliferation_TOT; Proliferation rates of cells from clean and dirty biopsies.

Code and data archive to accompany "A derivative-free optimisation method for global ocean biogeochemical models", Oliver et. al. 2021

This archive is to accompany the article: A derivative-free optimisation method for global ocean biogeochemical models, Sophy Oliver, Coralia Cartis, Iris Kriest, Simon Tett, and Samar Khatiwala. The optimisation framework used in this study can be found here: https://doi.org/10.5281/zenodo.5517610 The original source code of MOPS were from the Supplement of Kriest et al. (2017). The most recent TMM source code is available at https://github.com/samarkhatiwala/tmm. In this archive: Supplement/Configurations/OxfordMOPS_Configs contains: - ReadOnlyFiles (Files and Code specifically used to run the global ocean biogeochemical model MOPS model with   the Transport Matrix Method, which have been edited to differ from the versions downloaded from the sources above.) - RunCode (runscripts to run the MOPS model with the TMM) - TWIN_Configs (JSON files required by each optimisation experiment carried out). Supplement/OxfordMOPS_EXP contains data for each iteration of all optimisation experiments carried out. Supplement/OPTCLIMSO_PlottingScripts contains MATLAB plotting scripts used to create results figures of these experiments.

Dataset to paper YWang and SWillett Escarpment retreat rates derived from detrital cosmogenic nuclide concentrations

This is dataset used in paper Wang, Y. and Willett, S. D.: Escarpment retreat rates derived from detrital cosmogenic nuclide concentrations, Earth Surf. Dynam., 9, 1301–1322, https://doi.org/10.5194/esurf-9-1301-2021, 2021.

opencc-by-4.0Oct 2021View details →

Microscale termophoresis fluorescence time traces testing the interaction between human survivin and a peptide derived from hSgol2

Microscale termophoresis fluorescence time traces testing the interaction between human survivin and a peptide derived from hSgol2 ( sequence: ECQVKKVNKMTSKSKKRKTS). Survivin was chemically labelled and titrated with different concentrations of hSgol2 peptide.