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Fig. 3 in The Body Size, Age Structure And Growth Pattern Of The Endemic Balkan Mosor Rock Lizard (Dinarolacerta Mosorensis Kolombatović, 1886)
Fig. 3. The distributions of the first and second visible LAGs. The first deposited LAG has been resorbed in sections in which the diameter of the first visible LAG is greater than 0.60 µm
Fig. 3 in Altitudinal Variation In Population Density, Body Size And Morphometric Structure In C A R A B U S O D O R At U S S H I L, 1996 (C O L E O P T E R A: Carabidae)
Fig. 3. Illustration of measurements: 1-2 – elytra length (hereafter "A", 3-4 – elytra width ("B"), 5-6 – pronotum length "C"), 7-8 – pronotum width (D), 9-10 – head length (E), 11–12 – distance between the eyes (signed as "head width" or "F" in the figures).
Fig. 7 in Altitudinal Variation In Population Density, Body Size And Morphometric Structure In C A R A B U S O D O R At U S S H I L, 1996 (C O L E O P T E R A: Carabidae)
Fig. 7. Descriptive statistics of elytra length means in C. odoratus at the plots on different altitudes.
PSSdb-Merged: A Pelagic Size Structure database merged product to support biogeochemical modeling: First release of Merged products
<p>This dataset represents the first release of <strong>merged products</strong> from the Pelagic Size Structure database (PSSdb,<a href="https://pssdb.net/"> </a><a href="https://pssdb.net/">https://pssdb.net</a>), a scientific project investigating the global particle size distributions measured from multiple pelagic imaging systems. These devices include the Imaging Flow Cytobot (Olson and Sosik 2007), benchtop scanners like the ZooScan (Gorsky et al. 2010), and the Underwater Vision Profiler (Picheral et al. 2010). The data sources originate from Ecotaxa (<a href="https://ecotaxa.obs-vlfr.fr/">https://ecotaxa.obs-vlfr.fr/</a>), Ecopart (<a href="https://ecopart.obs-vlfr.fr/">https://ecopart.obs-vlfr.fr/</a>), and Imaging FlowCytobot dashboards (<a href="https://ifcb.caloos.org/dashboard">https://ifcb.caloos.org/dashboard</a> and<a href="https://ifcb-data.whoi.edu/dashboard"> </a><a href="https://ifcb-data.whoi.edu/dashboard">https://ifcb-data.whoi.edu/dashboard</a>).</p> <p><em><strong>Merged products</strong></em> correspond to the most complete datasets in PSSdb, whereby all instrument-specific datasets are merged together to produce a single, quasi-continuous size spectrum where only optimal values in overlapping size classes are selected for each spatio-temporal bin. The resulting spectra are produced after generating the taxa-specific products following the recent approach of Soviadan et al. (2023). Briefly, this approach assumes that one device is best suited in detecting certain taxa (amongst the living functional groups, see documentation), and size classes (depending on the resolution of the camera). As a result, we consider the maximum observed normalized biovolume/biomass and abundance amongst a set of non-null values from different instruments as the optimal measure for detection.</p> <p>Links to the PSSdb code (including the taxonomic and allometric look-up tables) and documentation are available on the PSSdb webpage (<a href="https://pssdb.net/">https://pssdb.net</a>).</p> <p> </p> <p><em><strong> For additional information, please see the PDF documentation available below ...</strong></em></p>
Рис. 2. Линейный (А) и весовой (Б) рост бурого морского петушка Alectrias alectrolophus из разных районов Тауйской губы Охотского моря Fig. 2. Linear (A) and weight (Б) growth of stone cockscomb Alectrias alectrolophus from different regions of Taui Bay, the Sea of Okhotsk in Size-age structure, growth, and feeding of stone cockscomb Alectrias alectrolophus (Stichaeidae) from different areas of Taui Bay, the Sea of Okhotsk
Рис. 2. Линейный (А) и весовой (Б) рост бурого морского петушка Alectrias alectrolophus из разных районов Тауйской губы Охотского моря Fig. 2. Linear (A) and weight (Б) growth of stone cockscomb Alectrias alectrolophus from different regions of Taui Bay, the Sea of Okhotsk
Рис. 3. Возрастная Δинамика относитеΛьных приростов ΔΛины (А) и массы теΛа (А) бурого морского петушка Alectrias alectrolophus из разных районов Тауйской губы Охотского моря Fig. 3. Age-related dynamics of relative gains in length (A) and body weight (A) of stone cockscomb Alectrias alectrolophus from different regions of Taui Bay, the Sea of Okhotsk in Size-age structure, growth, and feeding of stone cockscomb Alectrias alectrolophus (Stichaeidae) from different areas of Taui Bay, the Sea of Okhotsk
Рис. 3. Возрастная Δинамика относитеΛьных приростов ΔΛины (А) и массы теΛа (А) бурого морского петушка Alectrias alectrolophus из разных районов Тауйской губы Охотского моря Fig. 3. Age-related dynamics of relative gains in length (A) and body weight (A) of stone cockscomb Alectrias alectrolophus from different regions of Taui Bay, the Sea of Okhotsk
Рис. 1. Возрастной (А), размерный (Б) и весовой (В) состав бурого морского петушка Alectrias alectrolophus из разных районов Тауйской губы Охотского моря in Size-age structure, growth, and feeding of stone cockscomb Alectrias alectrolophus (Stichaeidae) from different areas of Taui Bay, the Sea of Okhotsk
Рис. 1. Возрастной (А), размерный (Б) и весовой (В) состав бурого морского петушка Alectrias alectrolophus из разных районов Тауйской губы Охотского моря
Anterior, lateral, and posterior aspects of the mounted skeleton of Tyrannosaurus rex, chiefly from Amer. Mus. 5027, partly from the type specimen Amer. Mus. 973. The sternal ribs are not restored. The structure of the manus is unknown as yet; the restoration of the digits is conjectural. About natural size. in Skeletal Adaptations of Ornitholestes, Struthiomimus, Tyrannosaurus
Anterior, lateral, and posterior aspects of the mounted skeleton of Tyrannosaurus rex, chiefly from Amer. Mus. 5027, partly from the type specimen Amer. Mus. 973. The sternal ribs are not restored. The structure of the manus is unknown as yet; the restoration of the digits is conjectural. About natural size.
Pelvic arcade and vertebral structure of the second chief specimen of Tyrannosaurus rex, Amer. Mus. 5027, discovered in 1908. An orthogonal projection executed on a very large scale and reproduced one-twelfth natural size. C 1-C 10 cervical series, D 1-D 13 dorsal or thoracic series, S 1-S 5 sacral series, Cd 1- Cd 53 caudal series. The caudals actually preserved are shaded; those drawn in outline are conjectural and restored. The total number of caudals is conjectural. in Skeletal Adaptations of Ornitholestes, Struthiomimus, Tyrannosaurus
Pelvic arcade and vertebral structure of the second chief specimen of Tyrannosaurus rex, Amer. Mus. 5027, discovered in 1908. An orthogonal projection executed on a very large scale and reproduced one-twelfth natural size. C 1-C 10 cervical series, D 1-D 13 dorsal or thoracic series, S 1-S 5 sacral series, Cd 1- Cd 53 caudal series. The caudals actually preserved are shaded; those drawn in outline are conjectural and restored. The total number of caudals is conjectural.
Figure 1 in The body size, age structure, and growth of Bosc's fringe-toed lizard, Acanthodactylus boskianus (Daudin, 1802)
Figure 1. Cross-sections (18 µm thick) at the diaphysis level of a phalange of juvenile (A) and male (B) Acanthodactylus boskianus. A) Four-year-old juvenile, 45.14 mm body length. Four LAGs were observed in the periosteal bone. B) Eight-yearold male, 79.86 mm body length. Eight LAGs were observed in the periosteal bone (arrow heads). Endosteal resorption and endosteal bone were present. Periphery (black arrow) was not regarded as a LAG (m.c. = marrow cavity, r.l. = reversal line, e.r. = endosteal resorption, e.b. = endosteal bone).
Figure 2 in Age structure and body size of the Strauch's racerunner, Eremias strauchi strauchi Kessler, 1878
Figure 2. Age frequency distributions for males and females of an Eremias strauchi strauchi sample population.
Figure 1 in The first record of age structure and body size of the Suphan Racerunner, Eremias suphani Başoğlu & Hellmich, 1968
Figure 1. Cross-section (18 µm thick) at the diaphysis level of a phalanx of male E. suphani, 60.52 mm SVL, 7 years old. Six LAGs were observed in the periosteal bone. The first LAG was destroyed by endosteal resorption and endosteal bone was present. Periphery was not regarded as a LAG. Arrows indicate endosteal resorption and periphery, and arrowheads indicate LAGs. e.b. = endosteal bone, m.c. = marrow cavity, r.l. = reversal line, p = periphery.
Figure 4 in The song structure and repertoire size of Daurian Redstarts (Phoenicurus auroreus) in South Korea
Figure 4. Cumulative plot showing the number of new syllable types produced by 20 Daurian Redstart males against the nth bird sampled in South Korea. The number of the new syllable types leveled off at approximately the 15th male sampled; the equation shown is for the curve-fit.
Figure 5 in The song structure and repertoire size of Daurian Redstarts (Phoenicurus auroreus) in South Korea
Figure 5. Cumulative number of syllable types per each song part produced by 20 Daurian Redstart males against the nth bird sampled in South Korea.
Figure 3 in The song structure and repertoire size of Daurian Redstarts (Phoenicurus auroreus) in South Korea
Figure 3. Cumulative plot showing the number of syllable types produced by 20 Daurian Redstart males against the nth song sampled. Most of the songs reached the peak syllable types at approximately the 18th song. A1 to E4 is the ID of each individual.
Figure S1 in The song structure and repertoire size of Daurian Redstarts (Phoenicurus auroreus) in South Korea
Figure S1. Syllable types in whistle, subsyllable, and syllable parts of 400 songs of 20 individuals from five population samples in 2015 and 2016 in South Korea.
Data from: Autumn and winter plankton composition and size structure in the North Sea
<p><span>Plankton dynamics in temperate ecosystems have been mainly studied during productive seasons, with comparatively less research conducted during the winter, particularly on microplankton. Implementing plankton sampling during a regular fishery cruise, we investigated the North Sea micro- and mesozooplankton community composition, abundance and size structure (55-2000 µm) during autumn (Buchan/Banks area) and winter (Downs area) between 2013 and 2019. Samples were analyzed using image-based techniques. Community diversity (broad taxa) was relatively similar across years in both areas, with diatoms and tripos taxa sets dominating the microplankton community and gastropods and copepods the mesozooplankton one. The average micro- to mesoozooplankton ratio (in abundance) was 90:1 for Buchan/Banks, resulting in average Normalized Abundance Size Spectra (NASS) slopes of -1.45 ±0.18 SD. For Downs, the micro- to mesoozooplankton ratio was 235:1 and steeper NASS slopes of -1.67 ±0.20 SD due to a lower contribution of large organisms. Interannual changes in the planktonic community for each area and their potential environmental drivers were examined using a redundancy analysis (including taxonomy and size) and a correlation analysis using NASS slopes (size only). Both approaches highlighted the importance of water mass properties (e.g. salinity, temperature, turbidity) in shaping plankton dynamics, although the amount of explained variance differed between approaches (11 versus 46%). <span><span>Our results contribute to a better understanding of standing stocks of plankton and their environmental drivers. Specifically, novel insights were gained into microplankton dynamics, which play an important role in supporting the growth and survival of winter-spawned fish larvae in the North Sea. </span></span></span></p>
Effect of Organic Cation Size on Structural, Thermochromic, Dielectric and Photoluminescence Properties of Two-Dimensional Lead Iodide Perovskites with Extremally Reduced Dielectric Confinement
<p>Dataset for scientific publication entitled Effect of Organic Cation Size on Structural, Thermochromic, Dielectric and Photoluminescence Properties of Two-Dimensional Lead Iodide Perovskites with Extremally Reduced Dielectric Confinement. </p> <p>This research was supported by the National Science Center (Narodowe Centrum Nauki) in Poland under project No. 2020/38/A/ST3/00214. JKZ acknowledges support from Academia Iuvenum, Wroclaw University of Science and Technology.</p>
Text-fig. 6. Scanning electron micrographs of multicarpellate and apocarpous floral structures from the Early Cretaceous Puddledock locality, Virginia, USA (a, b: PP43701, Puddledock sample 001; c: PP43000x, Puddledock sample 073). a) Anacostia? sp., strongly compressed, elongated receptacle with spirally arranged carpels (red dots; not all shown); note larger size compared to the other floral structures; b) Numerous Anacostia type pollen grains in proximal view from the base of floral structure in (a); note graded reticulum over the proximal pole of the pollen grains; c) Elongated receptacle with numerous carpels in a spiral arrangement, possibly representing an earlier developmental stage of Anacostia? sp. Scale bars = 1 mm (a, c), 10 µm (b). in Multiparted, Apocarpous Flowers From The Early Cretaceous Of Eastern North America And Portugal
Text-fig. 6. Scanning electron micrographs of multicarpellate and apocarpous floral structures from the Early Cretaceous Puddledock locality, Virginia, USA (a, b: PP43701, Puddledock sample 001; c: PP43000x, Puddledock sample 073). a) Anacostia? sp., strongly compressed, elongated receptacle with spirally arranged carpels (red dots; not all shown); note larger size compared to the other floral structures; b) Numerous Anacostia type pollen grains in proximal view from the base of floral structure in (a); note graded reticulum over the proximal pole of the pollen grains; c) Elongated receptacle with numerous carpels in a spiral arrangement, possibly representing an earlier developmental stage of Anacostia? sp. Scale bars = 1 mm (a, c), 10 µm (b).
Influence of feature size and shape on corrosion of 316L lattice structures fabricated by laser powder bed fusion
<p><strong>An open dataset for the paper with the same title: "<em>Influence of feature size and shape on corrosion of 316L lattice structures fabricated by laser powder bed fusion</em>". </strong></p> <p><strong>The dataset contains, for example, 3D models, original and analyzed microCT data, video visualizations, tensile testing .csv files, microscopy images, and code resources. Selected works are presented as part of the paper.</strong></p> <p><strong>Abstract:</strong></p> <p><em>Laser powder bed fusion (LPBF) has become an established method for manufacturing end-use metal components. Exploiting the geometric freedom of additive manufacturing (AM) offers broad possibilities for part optimization and enables performance enhancements across industry sectors. However, part shape and feature size have been found to locally affect residual stresses, melt pool cooling rates, microstructure, and thus the mechanical properties of </em><em>components. Even though the mesoscale structure can locally induce microstructural changes, there are no prior studies on how it influences corrosion. </em><em>Using AM-produced, optimized parts in critical applications necessitates a better understanding of their long-term performance. In this study, lattice structures were used to probe the influence of feature size and shape on corrosion susceptibility and its spatial localization.</em></p> <p><em>The susceptibility of submillimeter LPBF-fabricated 316L stainless steel </em><em>lattice structures to corrosion was investigated by conducting a 21-day immersion corrosion test in an aqueous 3.5wt% NaCl solution. Schoen gyroid and Schwarz </em><em>diamond triply periodic minimal surface lattices were manufactured with three unit cell sizes and wall thicknesses (0.867, 0.515, and 0.323 mm). The nominal surface and cross-sectional areas were the same for the two geometries. X-ray microcomputed tomography (microCT) scans before and after the corrosion test were compared for volumetric losses. <em>In addition, the </em>mechanical properties and microstructure of the samples were evaluated.</em></p> <p><em>As part of the study, a workflow to register, index, and analyze volumetric changes of consecutive microCT image stacks was developed. The method is fully reported and applicable to time-lapse studies with microCT. Three out of five of the 0.323 mm wall thickness lattices displayed visually aggressive pitting. Based on the microcomputed tomography data, the mass losses were localized either in the entrapped powder particles or partially melted surface globules. Corrosion did not occur in the dense base material. The total mass losses ranged from 8 to 19 mg. Despite visual indications to support a higher corrosion susceptibility for the smallest lattice sizes, the mass loss values did not confirm this conclusion. The tensile test results did not provide any clear indications of latent corrosion effects on mechanical properties.</em></p> <p> </p> <p><em>Version 1.1: 'Microstructure.zip' was revised. Metallographic preparation and Beraha II etching was redone for selected samples. New images and grain size (and grain distribution) measurements were added.</em></p> <p><em>Version 1.2: 'CT_Data_Heatmap_example.zip' was added. </em></p>
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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.