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Figure 4. MCT 1723-R in New material of Pepesuchus (Crocodyliformes; Mesoeucrocodylia) from the Bauru Group: implications about its phylogeny and the age of the Adamantina Formation
Figure 4. MCT 1723-R, rostrum in lateral views. A, B, left lateral views. C, D, right lateral views. Grey areas are associated sediments; hatched areas are broken parts. Scale bars represent 5 cm.
Figure 8 in Reconstruction of the pharyngeal corpus of Aphelenchus avenae (Nematoda: Tylenchomorpha), with implications for phylogenetic congruence
Figure 8. Diagrammatic representation of the pharyngeal corpus of Caenorhabditis elegans and three different Tylenchomorpha showing positions of pharyngeal neurone nuclei. Neurone homologies in Aphelenchus avenae are based on similarity to C. elegans in cell body position, dendrite topology, and connectivity. Homologies in Heterodera glycines and Aphelenchoides blastophthorus are proposed based on positions of nuclei as described by Endo (1984) and Shepherd et al. (1984), respectively. The top of each diagram shows dorsal neurone nuclei; the bottom is one of the two subventral rows of nuclei. Diagram of C. elegans redrawn from Chiang et al. (2006); nucleus positions in Aphelenchoides blastophthorus redrawn from Shepherd et al. (1984). Abbreviated names of neurones are consistent with Albertson & Thomson (1976). Abbreviations: I1–3, interneurones 1–3; M1, M3, M4, motor neurones 1, 3, 4; MC, marginal cell neurone; NSM, neurosecretory motor neurone.
Figure 5 in A juvenile skull of Dysalotosaurus lettowvorbecki (Ornithischia: Iguanodontia), and implications for cranial ontogeny, phylogeny, and taxonomy in ornithopod dinosaurs
Figure 5. Comparison of two preserved jugals of Dysalotosaurus in lateral view. A, left jugal of the juvenile skull BSPG AS I 834. B, left jugal of the relatively older individual dyB (MB.R.1333). Note the ontogenetic differences of the lacrimal facet (lf) and the postorbital facet (pof). Scale bar: 1 cm.
Figure 3 in A juvenile skull of Dysalotosaurus lettowvorbecki (Ornithischia: Iguanodontia), and implications for cranial ontogeny, phylogeny, and taxonomy in ornithopod dinosaurs
Figure 3. Stereo pairs of the skull BSPG AS I 834 and explanatory sketches. The sketches are relatively enlarged for better resolution. Dark grey illustrates sediment, light grey illustrates inner views of, e.g. the frontals or the dentaries, and hatched areas illustrate broken or corroded surfaces. The label affixes -r and -l stand for right and left of the respective element, where the distinction of each side is difficult to see. A, right lateral view. B, outline drawing of the ventral view. C, outline drawing of the right lateral view. D, ventral view. See Material and methods for a list of the abbreviations. Scale bars: 1 cm.
Figure 7 in A juvenile skull of Dysalotosaurus lettowvorbecki (Ornithischia: Iguanodontia), and implications for cranial ontogeny, phylogeny, and taxonomy in ornithopod dinosaurs
Figure 7. Comparison of the cranial base of two individuals of Dysalotosaurus. Small arrows indicate the location of the suture between the basioccipital and the basisphenoid. Larger arrows indicate the location of the tuberi basioccipitalia. Note also the shape of the ventral lip of the occipital condyle. A, the large cranial base of dyA (MB.R.1373) consists of the basioccipital, the basisphenoid with the long ventral basipterygoid processes, and the anteriorly incomplete parasphenoid; left lateral view. B, the smallest known cranial base (MB.R.3536) consists of the basioccipital and the posterior half of the basisphenoid; left lateral view. C, same as (B); ventral view. D, Same as (A), ventral view. Scale bar: 1 cm.
Taxonomic revision of the genus Miltotranes Zimmerman, 1994 (Coleoptera: Curculionidae: Molytinae), the Bowenia-pollinating cycad weevils in Australia, with description of a new species and implications for the systematics of Bowenia
<p>Unedited photos used in the taxonomic research.</p>
Snow albedo dataset for "Divergence of apparent and intrinsic snow albedo over a season at a sub-alpine site with implications for remote sensing"
<p>See DataExplanation.pdf</p> <p> </p>
FIGURE 2 in Implications of combined taxonomic, morphometric, and molecular characteristics for the species status of Paracentrobia tapajosae and Paracentrobia subflava (Hymenoptera: Trichogrammatidae), egg parasitoids of different leafhopper hosts in the Americas
FIGURE 2. Forewings of Paracentrobia. Paracentrobia tapajosae from Tapajosa rubromarginata, Argentina, A) female and B) male. Paracentrobia tapajosae from Dalbulus maidis, Argentina, C) female and D) male. Paracentrobia subflava from Dalbulus maidis, Mexico, E) female and F) Male.
Figure 36 in Diversity of schizomids (Arachnida: Schizomida) revealed by new fossil genera and species from mid-Cretaceous Burmese amber with implications for a Gondwanan origin of the Burma Terrane
Figure 36. Undescribed schizomid specimens with particular morphological characters (all from the Müller collection). A, BUB562. B, BUB3545. C, BUB3564.
FIGURE 5 in Late Devonian-early Carboniferous bryozoans from Zhankurgan (Greater Karatau, Kazakhstan)-taxonomy and palaeobiogeographical implications
FIGURE 5. Palaeobiogeographical affinities of bryozoan assemblages from Karatau and other regions in Famennian (A) and Tournaisian (B) performed by cluster analysis.
Anatomy of a Mare Basalt-filled Lunar Silicic Construct: The Wolf Crater Complex on Mare Nubium and implications for early silicic magmatism on the Moon
Open the record for dataset details and reuse information.
Short-term modifications in the chemical structure of wood charcoals: implications for anthracological investigations (under review in Journal of Archaeological Research: Reports)
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Fig. 3 in Systematics of limbless scincid lizards from northern Madagascar: morphology, phylogenetic relationships and implications for classification (Squamata: Scincidae)
Fig. 3 Paracontias rothschildi (ZSM 1579/2008), head. a Dorsal view. b Lateral view. c Ventral view. Scale bar = 1 mm
Fig. 5 Gynoecial architecture and intraspecific variability. A–C, F, G, C in Flower and fruit anatomy of Cordia nodosa Lam. and Varronia bonplandii Desv. (Cordiaceae, Boraginales) with phylogenetic implications
Fig. 5 Gynoecial architecture and intraspecific variability. A–C, F, G, C. nodosa (blue frames). D, E, H–K, V. bonplandii (yellow frames). A, LS of carpel with two hemianatropous ovules. B, LS of stigma with pollen. C, LS of gynoecium. D, LS of hemianatropous ovule. E, F, LS of egg apparatus (white arrow indicates stalk under chalazal haustorium). G, TS of gynoecium with four locules and only two fertile ovules (i.e., one ovule per carpel). H, flower at anthesis with two styles, ten stamens and ten petals (arrow indicates dehiscence line of thecae). J, flower after
Fig. 2 Flower and perianth. A–E, G, V in Flower and fruit anatomy of Cordia nodosa Lam. and Varronia bonplandii Desv. (Cordiaceae, Boraginales) with phylogenetic implications
Fig. 2 Flower and perianth. A–E, G, V. bonplandii (yellow frames). F, H–L, C. nodosa (blue frames). A, inflorescence. B, bud (arrow indicates detached adaxial calyx epidermis). C, flower. D, gynoecium after anthesis in opened calyx (arrow indicates delaminated adaxial calyx epidermis). E, F, TS of sepals, petals and gynoecium (level of corolla tube). G, LSs of bud (left) and developing fruit (right; upper arrow indicates delaminated adaxial calyx epidermis, lower arrow indicates abscission area of the detached corolla tube). H, inflorescence. J, bud (right) and flower. K, operculate calyx (corolla shed). L, LSs of bud (left; arrow indicates constriction between the receptacle and the pedicel), flower at anthesis (middle) and flower after anthesis (right). Abbreviations: a, anther; c, corolla; d, disc; g, ovary; k, calyx; LS, longisection; o, ovule (or young seed); stg, stigma; sty, style; tr, trichomes; TS, transverse section
Fig. 3 Anthers and pollen. A, C, D, F, K–M, V in Flower and fruit anatomy of Cordia nodosa Lam. and Varronia bonplandii Desv. (Cordiaceae, Boraginales) with phylogenetic implications
Fig. 3 Anthers and pollen. A, C, D, F, K–M, V. bonplandii (yellow frames). B, E, G–J, C. nodosa (blue frames). A, opened corolla tube with trichomes (arrow). B–D, TS of anthers (arrows indicate dehiscence line, note crystals under phase-contrast microscopy in D). E, flower, stamens and yellow trichomes (arrow). F–H, TS of anther walls (arrows indicate binuclear tapetum cells). J, K, tricolporate and triporate pollen
FIGURE 6 in Taxonomic and systematic implications of the revision of the phylogenetic relations in the genus Ectinogonia Spinola 1837 (Coleoptera: Buprestidae) of Central Chile
FIGURE 6. BI majority consensus trees for the species of Ectinogonia studied; A: Majority consensus tree constructed with COI, 16S and Wg genes concatenated. B: Majority consensus tree constructed with COI. C: Majority consensus tree constructed with 16S gene. D: Majority consensus tree constructed with Wg gene. The black dots are nodes with a posteriori probabilities (pp) over 0.95. E: Taxa under study with the old taxinomic asignation.
FIGURE 4 in Taxonomic and systematic implications of the revision of the phylogenetic relations in the genus Ectinogonia Spinola 1837 (Coleoptera: Buprestidae) of Central Chile
FIGURE 4. Haplotype network of 16S fragment from Ectinogonia species studied. Each color represents a species. Circle size indicates the frequency of the haplotype. Mutational steps between haplotypes are indicated by hash marks on the axis that unites haplotypes.
Fig. 4 in Phylogeography of three closely related myrmecophytic pioneer tree species in SE Asia: implications for species delimitation
Fig. 4 Results of species-specific Bayesian structure analyses of M. griffithiana (optimal K =2) and M. motleyana (optimal K =4). Bar plots were obtained with the admixture model and are illustrated on the map. Numbers in parentheses are locality numbers as used in Fig. 3
Fig. 1 in Phylogeography of three closely related myrmecophytic pioneer tree species in SE Asia: implications for species delimitation
Fig. 1 Study sites and geographic distribution of cpDNA haplotypes found in M. constricta, M. griffithiana, and M. motleyana. Circle sizes are proportional to population sample sizes. Individual haplotypes are defined by different colors (for haplotype numbers see Table 1, Fig. 2)
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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.