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Figure 6 in The Macrobiotus ariekammensis species complex provides evidence for parallel evolution of claw elongation in macrobiotid tardigrades
Figure 6. Macrobiotus ariekammensis groenlandicus subsp. nov. – cuticular structures on legs: A–C, granulation on the external surface of legs III seen in PCM (A) and SEM (B, C), respectively; C, shows a magnification of leg granulation above the dense granulation patch; D–F, granulation on the internal surface of legs III seen in PCM (D) and SEM (E, F), respectively; F, shows a magnification of leg granulation above the dense granulation patch; G–I, granulation on the dorsal and dorsolateral surface of leg IV seen in PCM (G) and SEM (H, I); I, shows a magnification of leg granulation above the dense granulation patch. Filled flat arrowheads indicate the dense granulation patch on the external leg surface, empty indented arrowhead indicates the cuticular bulge (pulvini), empty flat arrowheads indicate the dense granulation patch on the internal leg surface, filled indented arrowhead indicates cuticular bar under the claws. Scale bars in µm.
Figure 7 in The Macrobiotus ariekammensis species complex provides evidence for parallel evolution of claw elongation in macrobiotid tardigrades
Figure 7. Macrobiotus ariekammensis groenlandicus subsp. nov. – claws: A, B, claws III and IV seen in PCM, respectively; C–E, claws I, III and IV seen in SEM, respectively. Filled flat arrowheads indicate double muscles attachments under the claws, filled indented arrowhead indicates cuticular bar under the claws. Scale bars in µm.
Figure 5. Macrobiotus ariekammensis groenlandicus subsp. nov. A in The Macrobiotus ariekammensis species complex provides evidence for parallel evolution of claw elongation in macrobiotid tardigrades
Figure 5. Macrobiotus ariekammensis groenlandicus subsp. nov. A, habitus, dorsoventral projection (holotype, Hoyer's medium, PCM); B, C, well-visible granulation on the dorsal (B) and ventral (C) parts of the body seen in PCM; D, less-visible granulation on the dorsal part of the body seen in PCM; E, F, granulation on the dorsal part of the body seen in SEM; G, magnification on the cuticular pore and granulation on the dorsal part of the body in SEM. Filled flat arrowheads indicate the granules of granulation seen in SEM. Scale bars in µm.
Figure 4 in The Macrobiotus ariekammensis species complex provides evidence for parallel evolution of claw elongation in macrobiotid tardigrades
Figure 4. Macrobiotus ariekammensis ariekammensis from Svalbard – egg chorion morphology seen in PCM: A, B, surface of the egg under 1000× magnification; C–H, midsections of eggs processes under 1000× magnification. Filled flat arrowheads indicate a crown of dark thickenings and pores arranged alternately around egg processes bases. Scale bars in µm.
Figure 3 in The Macrobiotus ariekammensis species complex provides evidence for parallel evolution of claw elongation in macrobiotid tardigrades
Figure 3. Macrobiotus ariekammensis ariekammensis from Svalbard – buccal apparatus and the oral cavity armature seen in PCM: A, dorsoventral projection of the entire buccal apparatus; B, C, oral cavity armature visible from dorsal (B) and ventral (C) views, respectively; D, E, placoid morphology visible from dorsal (D) and ventral (E) views, respectively. Filled flat arrowheads indicate a single tooth in dorsal portion of the third band of teeth in the oral cavity, empty arrow indicates cuticular spike, empty indented arrowheads indicate central constrictions in first macroplacoids and faint subterminal constriction in second macroplacoid. Scale bars in µm.
Figure 2 in The Macrobiotus ariekammensis species complex provides evidence for parallel evolution of claw elongation in macrobiotid tardigrades
Figure 2. Macrobiotus ariekammensis ariekammensis from Svalbard – claws: A, B, claws II and IV respectively, seen in PCM; C, single continuous cuticular bar and double muscle attachments on leg I seen in PCM; D, details of lunulae on leg IV seen in PCM. Empty flat arrowhead indicates discontinuous cuticular bar, filled flat arrowheads indicate double muscles attachments, filled indented arrowhead indicates cuticular bar. Scale bars in µm.
Figure 1 in The Macrobiotus ariekammensis species complex provides evidence for parallel evolution of claw elongation in macrobiotid tardigrades
Figure 1. Macrobiotus ariekammensis ariekammensis from Svalbard: A, habitus, dorsoventral projection (Hoyer's medium, PCM); B, cuticular pores on the dorsal part of the body seen in PCM; C, granulation on the external surface of leg III seen in PCM; D, granulation on the internal surface of leg III seen in PCM; E, granulation on the dorsal and dorsolateral surface of leg IV seen in PCM. Filled flat arrowhead indicates granulation patch on the external leg surface, empty flat arrowhead indicates the faint granulation patch on the internal leg surface, filled indented arrowhead indicates cuticular bar under claws, empty indented arrowhead indicates the cuticular bulge (pulvini). Scale bars in µm.
Fig. 2 in A phylogenetic investigation of the taxonomically problematic Eucalyptus odorata complex (E. section Adnataria series Subbuxeales): evidence for extensive interspecific gene flow and reticulate evolution
Fig. 2. Neighbour-net networks of E. odorata complex taxa and co-occurring members of E. section Adnataria created in Splitstree V.4 using uncorrelated-P distances of SNPs generated by A. ddRADseq and B. DArTseq. Tips are coloured by species, with shapes used to distinguish different major groups: E. series Hetereophloiae (inverse triangles), E. series Melliodorae (hexagons), E. series Buxeales (triangles), the grey-box taxa (diamonds), mallee members of E. series Subbuxeales not in the E. odorata complex (squares), and the E. odorata complex (circles) coloured consistent with Fig. 1.
Raw data: Unravelling the mechanistic complexity of oxygen evolution reaction and Ir dissolution in highly dimensional amorphous hydrous iridium oxides
<p>Raw data for the manuscript titled:</p> <p><strong>Unravelling the mechanistic complexity of oxygen evolution reaction and Ir dissolution in highly dimensional amorphous hydrous iridium oxides</strong></p> <p> </p>
FIGURE 14 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 14. Comparison of the subdigital lamellae of G. nana (no additional granules), G. granulum sp. nov. (1 to 3 small granules dividing proximal lamellae, shown in red) and G. spheniscus (small wedge of granules that extends towards tip of digit) (drawing—L. Tedeschi).
FIGURE 1 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 1. Distribution maps of species in the Gehyra nana group. A) Distribution of previously-described species and G. nana as redefined here. The distribution of the G. nana complex is represented in light green and based on over 100 genotyped specimens. For other species, symbols represent genotyped specimens. B) Distribution of the four new species described herein. Dots represent genotyped specimens.
FIGURE 10 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 10. Holotype of Gehyra pseudopunctata sp. nov. (WAM R164776) from Mt Nyulasy, WA, in dorsal, ventral and lateral views (scale bar = 10 mm).
FIGURE 2 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 2. Species tree (from Moritz et al. 2018), obtained using StartBEAST2 of members of the Gehyra nana group. Numbers on the nodes indicate posterior probabilities. Photo credits: P. Doughty, S. Wilson, R.J. Ellis, S. Mahony, H. Cook, B. Maryan, L. Tedeschi.
FIGURE 15 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 15. Holotype of Gehyra pluraporosa sp. nov. (WAM R174024) from King Edward River west, WA, in dorsal, ventral and lateral views (scale bar = 10 mm).
FIGURE 4 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 4. Visualisation of outcomes of linear discriminant analysis on morphological traits of Gehyra nana group specimens across: upper plot) the four phylogenetically divergent lineages we describe here and the G. nana complex (confidence ellipse removed); lower plot) lineages within the G. nana species complex (for nana8 we removed the confidence ellipse due to the small sample sizes for this lineage; n = 5).Vectors indicate the relative contributions of strongly loading traits for the first 2 LDA axes.
FIGURE 8 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 8. Holotype of Gehyra paranana sp. nov. (NTM R37057) from Robin Falls area, NT (scale bar = 10 mm).
FIGURE 3 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 3. Upper) Phylogenetic tree for all samples of the Gehyra nana group subject to exon capture, obtained by RAxML on a concatenated dataset (from Moritz et al. 2018). Lower) Matrix summarising the geographic range and the pairwise geographic relations across all lineages and species within the G. nana group.
FIGURE 5 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 5. Photos in life of the species described herein. A) Gehyra nana (lineage nana2) (NTM R37597) from Bradshaw Field Training Area, NT (S. Mahony), B) G. nana (nanamulti) (WAM R174051) from Drysdale River National Park, WA (R.J. Ellis), C) G. paranana sp. nov. (NTM R37601) from Bradshaw Field Training Area, NT (S. Mahony), D) G. pseudopunctata sp. nov. (not collected) from near Halls Ck, WA (S. Zozaya), E) G. granulum sp. nov. (WAM R171403) from Prince Regent River National Park, WA (P. Doughty), F) G. granulum sp. nov. (WAM R168561) from Byam Martin Island (P. Doughty), G) G. pluraporosa sp. nov. (WAM R174024) from Theda Station, WA (R.J. Ellis).
FIGURE 7 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 7. Variation within the Gehyra nana complex. Lineages from left to right: nana1, nana4, nana4, nanamulti. All specimens from WAM (scale bar = 10 mm).
FIGURE 12 in Species delimitation in the Gehyra nana (Squamata: Gekkonidae) complex: cryptic and divergent morphological evolution in the Australian Monsoonal Tropics, with the description of four new species
FIGURE 12. Holotype of Gehyra granulum sp. nov. (WAM R176212) from Bell Gorge, WA (scale bar = 10 mm).
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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.