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Text-fig. 3. Nomenclature of tooth parts. Upper row left to right: M1, P4, DP4; lower row left to right m1, p4, dp4. Loc. = location. The anterolophulid is not on this picture, it is the mid-line connection between anteroconid and the metalophulid. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 3. Nomenclature of tooth parts. Upper row left to right: M1, P4, DP4; lower row left to right m1, p4, dp4. Loc. = location. The anterolophulid is not on this picture, it is the mid-line connection between anteroconid and the metalophulid.
Post-Perovskite Phase Transition in the Pyrolitic Lowermost Mantle: Implications for Ubiquitous Occurrence of Post-Perovskite Above CMB
<p><strong>Table 1.</strong> Experimental Results</p>
Figure 9 in The postcranial anatomy of Whatcheeria deltae and its implications for the family Whatcheeriidae
Figure 9. Articulated vertebrae of Whatcheeria. FMNH PR 1953 articulated caudal vertebrae in left lateral view (A); FMNH PR 1879 articulated vertebrae in left lateral view (B); FMNH PR 1745 articulated vertebrae in left lateral view (C). In all specimens, anterior is on the left and posterior is on the right.
Figure 6 in The postcranial anatomy of Whatcheeria deltae and its implications for the family Whatcheeriidae
Figure 6. FMNH PR 1875, articulated specimen of Whatcheeria. A, specimen photo; B, interpretive drawing with labels. Arrows point anteriorly.
Figure 18 in The skeletal remains of the euryhaline sclerorhynchoid †Onchopristis (Elasmobranchii) from the 'Mid'-Cretaceous and their palaeontological implications
Figure 18. Phylogenetic trees recovered by the different analysis used in the present study. A, strict consensus and majority rule trees produced by the TNT analysis. B, strict consensus and majority rule trees produced by the TreeSearch analysis: clade support values from the Jackknife analysis displayed inside the parenthesis. Character supporting nodes of TNT's majority rule tree (MRT): black circles, characters recovered by both consensus methods; white circles, characters recovered only by MRT.
Figure 5 in The skeletal remains of the euryhaline sclerorhynchoid †Onchopristis (Elasmobranchii) from the 'Mid'-Cretaceous and their palaeontological implications
Figure 5. Enlarged rostral denticles of † Onchopristis. A–C, micro-CT-based volume rendering of denticle collected along with the specimen IPUW 353500 from Morocco: A, dorsoventral; B, anterior; C, posterior views. D–G, denticles collected in Egypt (Werner, 1989; pl. 19, fig. 2a–d): D, posterior view; E, dorsoventral; F, anterior; G, base. Scale bar: 1 mm.
Figure 6 in Jurassic mammaliaform petrosals from Western Siberia (Russia) and implications for early mammalian inner-ear anatomy
Figure 6. Virtual horizontal cut through the three?haramiyidan promontoria, specimens PIN 5087/37 (A), PIN 5087/69 (B), and PIN 5087/70 (C). Remnants of a bony bar on the medial side of the cochlear nerve foramen are visible in each specimen inside the cochlear canal (indicated by black arrow heads). White rectangle in B depicts area seen close up in D, light source was virtually adjusted in D to make the sulci visible. E, reconstruction of the perforated bony bar with single cochlear nerve fibres (yellow) piercing through; number of holes random and only for illustration purpose. Anterior to the top, not to scale.
Figure 1 in Taxonomic, palaeobiological and evolutionary implications of a phylogenetic hypothesis for Ornithischia (Archosauria: Dinosauria)
Figure 1. Hypotheses of the phylogenetic relationships of dinosaurs compared: A, the traditional ('Seeley') hypothesis (e.g. Nesbitt 2011; Langer et al., 2017) incorporating the clade Silesauridae. B, the 'Phytodinosauria' hypothesis (e.g. Paul 1984; Bakker, 1986). C, the 'Ornithoscelida' hypothesis (e.g. Baron et al., 2017a, 2017b; Cau, 2018). D, the 'Seeley' hypothesis with Silesauridae placed as the sister-taxon to traditional ornithischians (e.g. Langer & Ferigolo, 2013; Cabreira et al., 2016). E, paraphyletic silesaurs as stem-lineage ornithischians (Müller & Garcia, 2020a). Silhouettes are based on artwork by Márcio L. Castro.
Redox-independent low water solubility in quartz and implications for water storage in the crust
<p>The data for quartz samples in the work.</p>
Fig 1 in The oldest known bat skeletons and their implications for Eocene chiropteran diversification
Fig 1. Skeleton of Holotype of Icaronycteris gunnelli (FM.145747A) A) Dorsal view; B) Counterpart (FM.145747B). https://doi.org/10.1371/journal.pone.0283505.g001
Fig 6 in The oldest known bat skeletons and their implications for Eocene chiropteran diversification
Fig 6. Phylogentic position of Icaronycteris gunnelli and other Eocene bat fossils with respect to extant bat lineages. A) Strict consensus of three most parsimonious trees of 1511 steps resulting from analyses including all taxa; B) Strict consensus of two most parsimonious trees of 1455 steps for analyses excluding Icaronycteris? menui and Icaronycteris sigei. Bootstrap values from 10,000 bootstrap replicates are shown above and to the left of nodes. Fossil taxa are represented by a dagger (†). https://doi.org/10.1371/journal.pone.0283505.g006
Fig. 6 in Multigenic resistance to Xylella fastidiosa in wild grapes (Vitis sps.) and its implications within a changing climate
Fig. 6 Climate predictions and projections of the prevalence of X. fastidiosa for focal crops. a The map portrays the number of climate models (out of 54 total) that support movement across the BIO8 = 10 °C threshold. The warmer colors reflect regions that are moving from below (in the present) to above the threshold, while the cooler colors portray areas that are moving from above (in the present) to below the threshold. The intensity of color in the scale bar reflects the number of 54 climate models that agree with the threshold transition. The generation of this map, as well as the maps in Figures S1 and S18, relied on publicly available information from WorldClim2 (https://www.worldclim.org/) and CMIP6 (https://pcmdi.llnl.gov/CMIP6/). b A summary of the percentage of locations associated with movement from above the 8 C °C or 10 °C threshold (in the present) to below that threshold for five crops and for V. arizonica. c. A summary of the percentage of locations associated with movement from above the threshold (in the present) to below the threshold for five crops and V. arizonica. Both b and c are based on 6204 locations for coffee; 3386 locations for almonds, 1111 locations for V. arizonica; 5256 locations for Citrus; 174,713 locations for olives and 33,225 locations for grapevines. In both b and c, each dot represents an estimate based on one of the 54 climate models.
Fig. 3 in Multigenic resistance to Xylella fastidiosa in wild grapes (Vitis sps.) and its implications within a changing climate
Fig. 3 Genetic analyses of the PdR1 region. a A plot of linkage disequilibrium (LD) across chromosome 14, where darker colors represent higher levels of LD. The two dark squares on the diagonal include GWA peak 4 (on the left, from 0 to 7 Mb on the chromosome) and the GWA peak that corresponds to PdR1 (on the right, from 22 to 28 Mb on the chromosome). The two off-diagonal squares reflect LD between these two distinct regions. b A Manhattan plot of chromosome 14 indicating the locations of peak 4 and the PdR1 region. c An expanded representation of the PdR1 region showing the location of significant SNPs (red circles denote SNP significant with two GWA methods), significant kmers (green triangles) and CNVs (blue triangles). The dashed vertical lines represent the 361 kb region defined by SSR markers and the 106 kb region defined by the location of significant markers. The schematics below represent genes in PdR1 and a summary of gene expression results. Genes are denoted by rectangles and colored if they are related to R genes, with the category of R gene indicated by its color. Expression information shows expression, in transcripts per million (TPM) for leaves, for stems during four stages after infection and for mock controls.
Fig. 2 in The mitochondrial genomes of ladybird beetles and implications for evolution and phylogeny
Fig. 2. Heterogeneous sequence divergence within datasets including only the first, the second, the third codon positions or all codon positions. The obtained mean similarity score between sequences was represented by a colored square. The scores were ranging from 1, indicating full random similarity, to +1, non-random similarity. The darker red indicated the higher randomized similarities between pairwise sequence comparisons. Blue indicated the opposite. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)
Fig. 4 in The mitochondrial genomes of ladybird beetles and implications for evolution and phylogeny
Fig. 4. Maximum likelihood tree inferred from the dataset of PCG_AA using the predefined partition schemes under the best-fitting models selected by ModelFinder. Node numbers show bootstrap support values (left) and Bayesian posterior probability support values (right). Scale bar represents substitutions/site. ''–" indicates that the node is not recovered by BI analysis.
Fig. 3 in The mitochondrial genomes of ladybird beetles and implications for evolution and phylogeny
Fig. 3. Maximum likelihood tree inferred from the dataset of PCGRNA using the predefined partition schemes under the best-fitting models selected by ModelFinder. Node numbers show bootstrap support values (left) and Bayesian posterior probability support values (right). Scale bar represents substitutions/site. ''–" indicates that the node is not recovered by BI analysis.
Figure 4 in The first record of fossilized soft parts in ossified tendons and implications for the understanding of tendon mineralization
Figure 4. SEM images and EDS spectra of fossil and recent tendon samples. A–I, fibrous matrix in the vascular canals of: A, B, Edmontosaurus regalis (UAMES 52615); C–F, Homalocephale calathocercos (MPC-D 100/1201); G, Pinacosaurus grangeri (ZPAL MgD-II/32); H, I, mineralized tendon of modern turkey (Meleagris gallopavo, GIUS-12-3741), note the presence the of fibres both in the vascular canals (white asterisks) and in the bone matrix (black asterisks). J–L, EDS spectra of: J, Edmontosaurus regalis (UAMES 52615); K, Homalocephale calathocercos; L, Meleagris gallopavo showing calcium, phosphorus and oxygen as dominant components in tendon mineral matrix in fossil and recent tendon samples. Note that carbon signal is omitted in the spectra (see Material and methods).
Figure 8 in The first record of fossilized soft parts in ossified tendons and implications for the understanding of tendon mineralization
Figure 8. Restoration of tube-shaped blood vessels with attached cells based on SEM images of the extract obtained from Edmontosaurus regalis sample and etched surfaces of a tendon; artwork by Jakub Zalewski. Not to scale.
Figure 7 in The first record of fossilized soft parts in ossified tendons and implications for the understanding of tendon mineralization
Figure 7. FTIR spectra of studied tendon samples of ornithischian dinosaurs: A, powdered samples of a fossilized tendon of Homalocephale calathocercos; B, powdered samples of the extract obtained after demineralization of H. calathocercos tendon; C, powdered samples of a fossilized tendon of Edmontosaurus regalis; D, powdered samples of the extract obtained after demineralization of E. regalis tendon; E, powdered sample of demineralized tendon of Meleagris gallopavo, note that phosphate (PO)3– and carbonate (CO)2– signals are masked by the high input of organic residues; F, amide I region of 4 3 samples extract after demineralization of H. calathocercos as well as (G) E. regalis and (H) M. gallopavo ossified tendons.
FIGURE 1. 1–18 in Taxonomic implications of leaf epidermal characteristics in subfamily Caesalpinioideae (Leguminosae)
FIGURE 1. 1–18 Light micrographs of non-glandular trichomes of adaxial surface of 1. Bauhinia acuminata; 2. Bauhinia purpurea; 3. Cassia fistula; 4. Cassia javanica; 5. Delonix regia; 6. Guilandina bonduc; 7. Phanera retusa; 8. Senna alata; 9. Senna pallida; 10. Senna siamea; 11. Senna sophera; 12. Senna tora; 13. Tamarindus indica and abaxial surface of; 14. Bauhinia acuminata; 15. Bauhinia purpurea; 16. Bauhinia tomentosa; 17. Cassia fistula; 18. Cassia javanica.
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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.