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Fig. 3 in Captive management, reproduction, and comparative larval development of Klappenbach's Red-bellied Frog, Melanophryniscus klappenbachi Prigioni and Langone, 2000
Fig. 3. Developing coloration in young toadlets of different ages. (A) Recently metamorphosed toadlet. (B) Ten days after metamorphosis. (C) Twenty-three days after metamorphosis. (D) Two months after metamorphosis.
Development of new PET radiotracers for CXCR3 chemokine receptors
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DEVELOPMENT OF HIGH PERFORMANCE SPORTS IN RUSSIA AT THE PRESENT STAGE
<p><span>This article examines the implementation of a common strategy and standards in the field of sport development, where fair and equal competition between athletes is necessary, which is important for preserving reputation and fairness in the sport environment, as well as protecting the health of athletes. Increasing transparency and ethics in sport contributes to its development and attractiveness for both participants and spectators. The formation of the sports industry through integration and joint sports events plays a key role not only in changing the economic situation in Russia, but also in improving relations between countries and popularizing sports as a means of maintaining health and friendship.</span></p>
Рис. 1. ЖорЖ Кювье – официальный портрет (источник: http://www.napoleon-empire.com/pictures/cuvier.php). in Contribution of Georges Cuvier and Jean-Baptiste de Lamarck to development of the system of Mollusca
Рис. 1. ЖорЖ Кювье – официальный портрет (источник: http://www.napoleon-empire.com/pictures/cuvier.php).
Fig. 2 in Contribution of Georges Cuvier and Jean-Baptiste de Lamarck to development of the system of Mollusca
Fig. 2. Jean-Baptiste de Lamarck in the period of preparation of «Systéme des animaux sans vertébres» (source: Wikimedia Commons).
Figure 3 in Filtrates from cultures of endophytic fungi isolated from leaves of Copaifera oblongifolia (Fabaceae) affect germination and seedling development differently
Figure 3. Variations (mean ± standard error) of aerial mass (A), root mass (B) and total seedling mass (C) of Copaifera oblongifolia as a function of treatments with inoculation of different species of endophytic fungi. Different letters on the bars indicate statistical variations between treatments (P <0.05) according contrast analysis
Figure 1 in Filtrates from cultures of endophytic fungi isolated from leaves of Copaifera oblongifolia (Fabaceae) affect germination and seedling development differently
Figure 1. Variations (mean ± standard error) of the germination percentage (A) and the time required for germination (B) of Copaifera oblongifolia seeds as a function of treatments with inoculation of different species of endophytic fungi. Different letters on the bars indicate statistical variations between treatments (P <0.05) according contrast analysis.
Figure 4 in Filtrates from cultures of endophytic fungi isolated from leaves of Copaifera oblongifolia (Fabaceae) affect germination and seedling development differently
Figure 4. The relationship between aerial mass (A), root mass (B) and total seedling mass (C) with seed mass of Copaifera oblongifolia.
Fig. 1 in Embryonic development of the ornamental shrimp, Urocaridella arabianensis Akash et al., 2020
Fig. 1 — Embryonic development of U. arabianensis: (a) Brooder animals; (b) Stage I - Fertilized eggs; (c) Stage II - Cleavage (Cv); (d) Stage III - Blastula; (e) Stage IV - Gastrula, Tp - Translucid area; (f) Stage V - Nauplius; (g) Stage VI - Post-Nauplius I; (h) Stage VII - Post-Nauplius II; (i) Stage VIII - Pre-hatching; and (j) Stage IX - Newly hatched larva (Zoea I). Scale bar: 0.5 mm
Dataset for 'The State of Data Curation at NeurIPS: An Assessment of Dataset Development Practices in the Datasets and Benchmarks Track'
<p>This packages comprises of analyses and evaluations of 60 datasets from the NeurIPS Datasets and Benchmarks track. It is part of a paper currently under review at the 2024 the NeurIPS Datasets and Benchmarks track, titled, "The State of Data Curation at NeurIPS: An Assessment of Dataset Development Practices in the Datasets and Benchmarks Track". </p>
Figure 3 in Postembryonic Ventral Nerve Cord Development and Gonad Migration in Steinernema carpocapsae
Figure 3: Lateral left view (anterior to left) differential interference contrast (DIC) micrograph (top) and with transparent color overlay (bottom) of a 96 HET female Steinernema carpocapsae gonad posterior arm. The gonad morphology at 96 HET is similar to that seen at 72 HET. However, by 96 HET, numerous fertilized embryos are seen in the uterus (red). The spermathecal-uterine complex (green) is located at the farthest point away from the mid-body and contains a single oocyte (inset) surrounded by numerous sperm (arrowhead). The ovary (blue) is much longer than in 72 HET females, frequently extending beyond the mid-body plane. In this image, the distal tip cell of the anterior gonad arm (arrow) extends into the posterior half of the female. Scale bars, 50 µm (main figure) 10 µm (inset).
Figure 6 in Postembryonic Ventral Nerve Cord Development and Gonad Migration in Steinernema carpocapsae
Figure 6: Lateral right (A) and left (B) views of gonad (red) morphology in male Steinernema carpocapsae at 72 HET. In most males (A), the gonad migration pattern is similar to C. elegans. However, 30% of males examined have a gonad that never extends away from the ventral wall (B). Scale bar, 50 µm.
Figure 5 in Postembryonic Ventral Nerve Cord Development and Gonad Migration in Steinernema carpocapsae
Figure 5: Lateral left views (anterior to left) of female gonad (red overlay) development in Steinernema carpocapsae at various time points. The gonad of newly hatched S. carpocapsae (A) contained four nuclei with two central larger nuclei and two smaller cap nuclei. By 25 HET (B), the number of nuclei in the gonad noticeably increased and began elongating along the ventral body wall. At 33 HET (C), the gonad extended toward the dorsal surface. Between 44 HET (D) and 54 HET (E), we observed an expansion of the gonad along the dorsal surface. Note that the anterior arm typically wraps around the right side of the intestine and is out of frame at this focal plane, whereas the posterior arm wraps around the left side. Scale bar, 50 µm.
Figure 1 in Postembryonic Ventral Nerve Cord Development and Gonad Migration in Steinernema carpocapsae
Figure 1: Lateral left view (anterior to left) fluorescent micrographs of J2 (top) and J1 (bottom) Steinernema carpocapsae following 4′, 6-diamidino2-phenylindole (DAPI) staining. The ventral nerve cord (VNC) comprises a series of putative neurons extending from the retrovesicular ganglion (RVG) (arrowhead) to the preanal ganglion (PAG) (arrow) along the ventral edge of the animal. Between J1 and J2, there is a large increase in the number of VNC neuronal-like nuclei. Scale bar, 10 µm.
Figure 2 in Postembryonic Ventral Nerve Cord Development and Gonad Migration in Steinernema carpocapsae
Figure 2: Cartoons of Caenorhabditis elegans (A) and Steinernema carpocapsae (B) gonads and lateral left view (anterior to left) micrograph of posterior S. carpocapsae gonad arm (C): differential interference contrast (DIC) alone (top); DIC color overlay (bottom). Unlike C. elegans, which undergoes stereotypical development to a 'U-shaped' gonad, the most common S. carpocapsae gonad shape does not include extensive migration along the ventral wall. As shown in the stitched DIC micrograph (C) (top) and with transparent color overlay (bottom), the gonad extends from the central region of the animal near the vulva (position indicated with straight arrow) and immediately extends to the dorsal side where it extends away from the mid-body. It eventually makes a u-turn (curved arrow) and then extends along the dorsal wall back to the midbody where it then migrates back to the ventral wall. The posterior gonad arm typically wraps around the left side of the intestine, whereas the anterior arm typically wraps around the right side of the intestine. The proximal end of the gonad, including the uterus and spermathecal-uterine complex, is colored red. The distal end of the gonad following the turn includes the ovary and is colored blue. Scale bar, 50 µm.
Figure 4 in Postembryonic Ventral Nerve Cord Development and Gonad Migration in Steinernema carpocapsae
Figure 4: Cartoon depicting the variability in the gonad migration pattern among 72 HET Steinernema carpocapsae females that deviate from the most common phenotype seen in figure 2C. Numbers indicate the ratio of the particular gonad phenotype among the 28 females whose gonads were fully traced.
Fig. 12 in Ontogenetic variation in the cranium of Mixosaurus cornalianus, with implications for the evolution of ichthyosaurian cranial development
Fig. 12 Mixosaurus cornalianus, skull roof elements. Interpretative drawings are identified by an apostrophe beside their corresponding letter. A Right-skull roof complex of fetus PIMUZ T 4830 in ventral (internal) view; B left-skull roof complex of juvenile PIMUZ T 4857 in dorsal view; C partial skull roof complex of juvenile PIMUZ T 2134; D skull roof of adult specimen PIMUZ T 2414 in dorsolateral view; E isolated parietal of small? juvenile PIMUZ T 2134 in dorsal view, numbers denote possible anterior margins of the parietal foramen. co ossification centre, epif epipterygoid facet, fr frontal, inv invagination, la lacrimal, na nasal, nac nasal capsule, ocf occipital flange, oli indentation for the olfactory lobe, opi indentation for the optic lobe, pa parietal, paf parietal facet, pde posterodorsal edge supratemporal, pf parietal foramen, pmax premaxilla, prf prefrontal, po postorbital, pof postfrontal, qj quadratojugal, qf quadrate facet, sq squamosal, sqf squamosal facet, st supratemporal, str supratemporal ramus, tfa anterior terrace upper temporal fenestra. Scale bar equals 10 mm
Fig. 13 in Ontogenetic variation in the cranium of Mixosaurus cornalianus, with implications for the evolution of ichthyosaurian cranial development
Fig. 13 Mixosaurus cornalianus (A-E) and Stenopterygius quadriscissus (F) palatal elements. Interpretative drawings are identified by an apostrophe beside the corresponding letter. A Pterygoid of fetus PIMUZ T 4830 in dorsal view; B pterygoid of juvenile specimen PIMUZ T 2416 in dorsal view; C vomer of fetus PIMUZ T 4830 in medial view; D vomer of juvenile specimen PIMUZ T 2416 in medial(?) view; E vomer of fetus PIMUZ T 4830 in medial view; F vomer of stage 3 fetus SMNS 80234 in medial view. avof antimeric vomer facet, bsf basisphenoid facet; co, ossification centre, dr. dorsal ramus, lw lateral wing, pmp posteromedial process, psf/vof parasphenoid and vomer facet, qr quadrate ramus, voc vomer crest. Scale bar equals 5 mm
Fig. 10 in Ontogenetic variation in the cranium of Mixosaurus cornalianus, with implications for the evolution of ichthyosaurian cranial development
Fig. 10 Mixosaurus cornalianus, isolated and disarticulated jugals and postorbitals. Interpretative drawings are identified by an apostrophe beside the corresponding letter. A Isolated jugal of fetus PIMUZ T 4830 in lateral? view; B disarticulated jugal of juvenile PIMUZ T 0077 in lateral view; C disarticulated jugal of juvenile specimen PIMUZ T 2416 in lateral? view; D semi-articulated jugal of adult MSNM BES SC 1001 in lateral view; E isolated postorbital of fetal specimen PIMUZ T 4830 in lateral view; F isolated postorbital of juvenile specimen PIMUZ T 2416 in lateral view. cd central depression, juf jugal facet, maxf maxilla facet, pof postorbital facet, poff postfrontal facet, stf supratemporal facet. Scale bar equals 5 mm
Fig. 9 in Ontogenetic variation in the cranium of Mixosaurus cornalianus, with implications for the evolution of ichthyosaurian cranial development
Fig. 9 Mixosaurus cornalianus, maxillae. Interpretative drawings are identified by an apostrophe beside the corresponding letter. A Fetus PIMUZ T 4830 in medial(?) view; B fetus PIMUZ T 4830 in medial view; C juvenile specimen PIMUZ T 0077 in medial view; D juvenile specimen PIMUZ T 2416 in medial view; E adult MSNM BES SC 1001 in lateral view; F adult GPIT PV 76274 in ventral view. al alveolus, ar anterior ramus, ardp anterior ramus dorsal process, co ossification centre, dmp dorso-medial platform, dr dorsal ramus, en external naris, jr jugal ramus, la lacrimal, max maxilla, na nasal, nuf nutritive foramen, pmax premaxilla, prf prefrontal, t tooth, tr tooth row. Scale bar equals 5 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.