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FIG. 1 Early pygostylian Sapeornis STM 15-15 shows faint soft-tissue details that A in Pennaraptoran Theropod Dinosaurs Past Progress And New Frontiers
FIG. 1 Early pygostylian Sapeornis STM 15-15 shows faint soft-tissue details that A, under white light are vivid and B, under LSF, extensive.
◂Fig. 5 Gametogenesis in male and female Veneriserva pygoclava. A–D Semi-thin histological sections of female Veneriserva pygoclava, stained with toluidine blue. A Cross-section of a female Veneriserva. B Close-up of large mature oocytes without discernible nurse cells. C Developing oocytes attached to mesenteries (mes), and oogonia proliferating from the ventral side of the dorsal blood vessel (bv). D Details of vitellogenic oocytes and nurse cells. Arrowheads indicate brownstained yolk platelets and yolk bodies. E Live sperm cells captured in a light micrograph. F–G Cross-sections of male Veneriserva. Note the absence of a gut in the cross-sections. Abbreviations—ac acicula, acr acrosome, bv blood vessel, coe coelomic cavity, mes mesentery, nc nurse cell, nn nurse cell nucleus, nu sperm cell nucleus, Oo oocyte, on oocyte nucleus, sp spermatogonia, vnc ventral nerve cord in Hardly Venus's servant-morphological adaptations of Veneriserva to an endoparasitic lifestyle and its phylogenetic position within Dorvilleidae (Annelida)
◂Fig. 5 Gametogenesis in male and female Veneriserva pygoclava. A–D Semi-thin histological sections of female Veneriserva pygoclava, stained with toluidine blue. A Cross-section of a female Veneriserva. B Close-up of large mature oocytes without discernible nurse cells. C Developing oocytes attached to mesenteries (mes), and oogonia proliferating from the ventral side of the dorsal blood vessel (bv). D Details of vitellogenic oocytes and nurse cells. Arrowheads indicate brownstained yolk platelets and yolk bodies. E Live sperm cells captured in a light micrograph. F–G Cross-sections of male Veneriserva. Note the absence of a gut in the cross-sections. Abbreviations—ac acicula, acr acrosome, bv blood vessel, coe coelomic cavity, mes mesentery, nc nurse cell, nn nurse cell nucleus, nu sperm cell nucleus, Oo oocyte, on oocyte nucleus, sp spermatogonia, vnc ventral nerve cord
Map 1 in First detailed record of Nemausus sordidatus (Stṏl, 1858) (Hemiptera: Alydidae) from mainland Portugal
Map 1.- Iberian distribution of Nemausus sordidatus (Stṏl, 1858), with the previously known Spanish provinces (in grey), the new Portuguese district (in cyan) and the MGRS 10x10 km square of the observation site in Portugal (in blue).
Fig. 1 in First detailed record of Nemausus sordidatus (Stṏl, 1858) (Hemiptera: Alydidae) from mainland Portugal
Fig. 1.- Specimen of Nemausus sordidatus (Stṏl, 1858) photographed by Guilherme Ramos on 12 January 2021 in Lisbon, Portugal.
Figs. 15–19 in A detailed updated description of the morphology of the larva of Reesa vespulae (Coleoptera: Dermestidae: Megatominae: Megatomini)
Figs. 15–19. Mature larva of Reesa vespulae (Milliron): 15, pronotum (dorsal, right half; large circles represent points of insertion of large spicisetae, small circles represent points of insertion of hastisetae); 16, right foreleg (dorsal); 17, abdominal tergum I (dorsal, right half; large circles represent points of insertion of large spicisetae, small circles represent points of insertion of hastisetae); 18, abdominal tergum VII (dorsal, right half); 19, abdominal tergum VIII (dorsal, right half). Scale bar = 0.1 mm.
Figs. 4–14 in A detailed updated description of the morphology of the larva of Reesa vespulae (Coleoptera: Dermestidae: Megatominae: Megatomini)
Figs. 4–14. Mature larva of Reesa vespulae (Milliron): 4, antenna (dorso-fronto-lateral); 5, spiciseta; 6, hastiseta; 7, right mandible (dorsal); 8, mandible (latero- ventral); 9, epipharynx (ventral); 10, lacinia (dorsal); 11, lacinia (ventral); 12, maxilla (ventral); 13, labium (ventral); 14, labial palp (ventral). Scale bar = 0.1 mm.
Figs. 1–3 in A detailed updated description of the morphology of the larva of Reesa vespulae (Coleoptera: Dermestidae: Megatominae: Megatomini)
Figs. 1–3. Mature larva of Reesa vespulae (Milliron): 1, dorsal view; 2, lateral view; 3, ventral view. Scale bar = 1.0 mm.
Fig. 4. Morphological details P in Figs. 10-16 in Taxonomic Review of Zavreliella Kieffer from East Asia
Fig. 4. Morphological details P. brachychaeta of male: (a) ANT I-V; (b) ANT III with secondary rhinaria (sr) and ANT IV with secondary rhinaria and primary rhinarium on the apex (black arrow); (c) end of ANT IV and ANT V with secondary rhinaria (sr) and primary rhinaria (black arrows). Primary rhinaria on ANT V present as large major rhinarium (black arrow) and small accessory rhinaria (white arrow); (d) dorsum of abdomen with siphunculi (s) and ventrally located genitalia (G) out of focus; (e) ventral view of the genitalia with paramere projections (pp) fused basally and connected to the basal part of phallus (bp) and the broad, sclerotic, genitalic ring; (f) posterior ventral view of the genitalia showing the size and shape of paramere projections (pp) and the basal part of phallus (bp).
BRAIN Journal-Cursor Movement – a Valuable Indicator in Intelligent System Design-Figure 2. Detailed view of the individual response
<p>The application that measures the way the user interacts with the PC mouse simulates a simple strategy game. The goal is to choose between different objects in random pattern a particular one. The learning curve of the game is designed to be very fast in order for the subject to quickly understand all the principles and thus the results collected during the test to not be influenced by accommodation to the mechanics. Each 77 individual response were evaluated using the mouse acceleration (reaction) and the number of mouse clicks as indicators for one’s emotional state. Simply plotting acceleration over time provides little information; reaction seems to be very chaotic, and somewhat similar between the two states (Figure 2). </p>
BRAIN Journal-ANNSVM: A Novel Method for Graph-Type Classification by Utilization of Fourier Transformation, Wavelet Transformation, and Hough Transformation-Figure 10. Detailed accuracy separated by classes and a confusion matrix which belongs to the dataset of Coiflet 1 applied by our main method (ANNSVM)
<p>With regard to accuracy values of each class as presented in Figure 10, we observed that the accuracy of the two-dimensional chart class was the lowest (i.e., 0.875), while others were over 0.9. Results here suggested that both the bar and pie classes have their own unique characteristics, as opposed to the 2Dchart class. For example, the graph images that contained some rectangles were individually categorized in the bar graph class. A similar phenomenon occurred for circles in the pie chart class. In contrast, the 2Dchart class contained mixed types of graphs; hence, the graph characteristics belonging to the 2Dchart class varied. </p>
Amarāvatī, Andhra Pradesh. Pillar with inscription, detail.
<p>Amarāvatī, Andhra Pradesh. Pillar with inscription, detail. Chennai, Government Museum.</p>
Prototyping 3D Virtual Learning Environments with X3D-based Content and Visualization Tools-Figure 2. The model of the 3D virtual campus - details from the building interior (3D modeling by Marius Hodea)
<p>The processing workflow for 3D modeling and design for a 3DVLE represents a time- consuming stage in the overall pipeline production. One reason is that a range of technologies and tools are typically used. In (Cudworth 2014) a 3-week period is indicated for experienced users to perform the 3D modeling of a virtual space. In our case, a 3-month work was needed for designing a working model of a 3D virtual campus (see Figure 1 and Figure 2 for final results).</p>
Udaypur, Madhya Pradesh. Hero-stone, detail of inscription.
<p>Udaypur, Madhya Pradesh. Hero-stone, detail of inscription.</p>
Fig. 11 in Redescription of Tapinesthis inermis (Araneae, Oonopidae), with detailed information on its ultrastructure
Fig. 11. Tapinesthis inermis, SEM, A–H dorsal views, I lateral view. – A–D. Ƌ (PBI 33882). A. Leg I. B. Leg II. C. Leg III. D. Leg IV. – E–G. ♀ (PBI 33883). E. Leg I. F. Leg II. G. Leg III. – H–I. Ƌ (PBI 33564). H. Leg IV. I. Tarsal organ, leg IV.
Fig. 8 in Redescription of Tapinesthis inermis (Araneae, Oonopidae), with detailed information on its ultrastructure
Fig. 8. Tapinesthis inermis, SEM views of ♀ genitalia (PBI 33267). A. Overview of genital area, dorsal view. B. Same, close up. C. Same, view slightly anterior. D. Anterior receptaculum (ARe), close up, arrow indicates gland ducts (GD). E. Same, anterior view. F. Same, detail of gland ducts (arrows). G. Lateral protrusion (Pr), detail, dorsal view. – ARe: Anterior Receptaculum; AS: Anterior Sclerite; FA: Flattened Apodeme; GD: Gland Duct; Pr: lateral Protrusion; PRe: Posterior Receptaculum; T: transverse sclerite.
Fig. 7 in Redescription of Tapinesthis inermis (Araneae, Oonopidae), with detailed information on its ultrastructure
Fig. 7. Tapinesthis inermis, SEM views of Ƌ (PBI 33564). A. Palp, frontal view. B. Same, prolateral view. C. Tip of embolus, ventral view. D. Same, retrolateral view.
Fig. 5 in Redescription of Tapinesthis inermis (Araneae, Oonopidae), with detailed information on its ultrastructure
Fig. 5. Tapinesthis inermis, genitalia of ♀ (PBI 33267) A. Genital area, ventral view. B. Same, after digestion, ventral view. C. Same, dorsal view. D. Same, anterior view. – ARe: Anterior Receptaculum; AS: Anterior Sclerite; FA: Flattened Apodeme; Pr: lateral Protrusion; PRe: Posterior Receptaculum.
Fig. 4. Tapinesthis inermis. – A–C in Redescription of Tapinesthis inermis (Araneae, Oonopidae), with detailed information on its ultrastructure
Fig. 4. Tapinesthis inermis. – A–C. Ƌ (PBI 33564), palp. A. Retrolateral view. B. Same, frontal view. C. Same, prolateral view. – D. Ƌ (PBI 09021), palp, prolateral view, transmitted light. – E. Ƌ palp, lateral view after Saaristo & Marusik, 2009 (modiFed). – D: duct; Te: tendon; Tw: thin-walled duct; V: vesicle.
Fig. 3 in Redescription of Tapinesthis inermis (Araneae, Oonopidae), with detailed information on its ultrastructure
Fig. 3. Tapinesthis inermis, Ƌ from the Czech Republic (PBI 32902). A. Habitus, dorsal view. B. Same, lateral view. C. Same, lateral view. D. Prosoma, ventral view.
Fig. 9 in Redescription of Tapinesthis inermis (Araneae, Oonopidae), with detailed information on its ultrastructure
Fig. 9. Tapinesthis inermis, SEM views of spinneret area of Ƌ (PBI 33564) and ♀ (PBI 33267). A. Ƌ, colulus, ventral view. B. Same, anterior lateral spinnerets, ventral view. C. Same, posterior lateral spinnerets. D. Same, focus on posterior median spinnerets. E. ♀, posterior median spinnerets, ventral view. F. Same, anterior lateral spinnerets. G. Same, posterior lateral spinnerets. H. Same, lateral view. – ALS: anterior lateral spinnerets; PLS: posterior lateral spinnerets; PMS: posterior median spinnerets.
ScienceDex guides
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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.