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Fig. 16 Aceroxylon palaeosaccharinum Greguss, 1943 emend. a in New Trees Identified In The Petrified Forest Of Middle Miocene From Zarand, Apuseni Mountains, Romania.
Fig. 16 Aceroxylon palaeosaccharinum Greguss, 1943 emend. a - cross section: diffuse-porous to semi-ring-porous wood, solitary vessels, two sized rays, ray dilation at the ring boundary - x50; b, c - cross-section: multiseriate rays with obvious dilations at the ring boundary, solitary vessels, thick-walled fibres - x100; d - tangential section: multiseriate fusiform rays, tall - x100; e-f - tangential section: crystalliferous parenchyma, alternate vascular pitting - x200; g, h, i - radial section: simple perforations, cross-fields, chambered parenchyma with rows of crystals - x200.
Fig. 17 in New Trees Identified In The Petrified Forest Of Middle Miocene From Zarand, Apuseni Mountains, Romania.
Fig. 17 Aceroxylon zarandense sp.nov. a - cross section: diffuse-porous wood, solitary and small grouped vessels, two sized rays with slight dilation at the ring boundary - x50; b, c - cross-section: fine and multiseriate rays with slight dilations at the ring boundary, solitary and grouped vessels - x100; d - tangential section: fine and multiseriate fusiform rays, tall, vessels with tilted simple perforated plates - x100; e-f - tangential section: remains of spiral thickenings and badly preserved pitting (e), intervascular alternate pitting - x200; g, h, i - radial section: simple perforations (h), bad preserved cross-field (i), bad preserved alternate pitting (g, h) - x200.
Fig. 13 in New Trees Identified In The Petrified Forest Of Middle Miocene From Zarand, Apuseni Mountains, Romania.
Fig. 13 Quercoxylon sarmaticum Starostin et Trelea, 1969. a, b - cross section: semi-ring-porous wood, two sized rays, ray dilation at the growth-ring boundary - x100; c - cross-section: usually solitary vessels, thick to very thick walled fibres - x200; d, e, f - tangential section: broad fusiform rays, high, dissected - x100; g, h, i - radial section: simple perforations (g, i), alternate pitting on vessels and on vascular tracheids pitted parenchyma (g, i), bad preserved cross-field (h, i) - x200.
Fig. 12 Fagoxylon cristallophorum van der Burgh, 1973. a, b in New Trees Identified In The Petrified Forest Of Middle Miocene From Zarand, Apuseni Mountains, Romania.
Fig. 12 Fagoxylon cristallophorum van der Burgh, 1973. a, b - cross section: difuse-porous wood, two sized rays, ray dilation at the distinct growth-ring boundary - x50; c - cross-section: vessels, fibres, rays - x100; Photo d - tangential section: broad fusiform rays, high, disected, vessels - x100; e, f - tangential section: fusiform broad rays, scalariform perforation (e), scalariform intervascular pitting (f) - x200; g, h, i - radial section: scalariform piting on vessels (g), scalariform perforation (h), cross field with vessels (i) - x200.
Fig. 10 Liquidambaroxylon speciosum Felix, 1884. a in New Trees Identified In The Petrified Forest Of Middle Miocene From Zarand, Apuseni Mountains, Romania.
Fig. 10 Liquidambaroxylon speciosum Felix, 1884. a - cross section: polygonal vessels, linear rays 1-3-seriate, less distinct growth-ring boundary, solitary and grouped vessels - x50; b, c - cross-section: polygonal vessels, solitary or grouped, thick-walled fibers x100; d, e - tangential section: 2-3-seriate rays, vessels - x200; f - tangential section: scalariform perforation - x200; g - radial section: cross-field with rounded crystals in the ray-cells - x200; h - radial section: scalariform perforation – x200; i - radial section: scalariform pitting in cross field marginal ray-cells - x200.
Fig. 9 in New Trees Identified In The Petrified Forest Of Middle Miocene From Zarand, Apuseni Mountains, Romania.
Fig. 9 Sequoioxylon multiseriatum (Ramanujam et Stewart) nov. comb. a-c - cross section: less distinct growth-ring boundary, few parenchyma disperse - x100; d - tangential section: uniseriate rays – x100?; e, f - tangential section: - broad rays 2-5-seriate, dispersed parenchyma - x100; g - tangential section: multiseriate rays, parenchyma with thin end wall with a single knot – x200; h-i - radial section: radial pitting on tracheids, cross-fields with 2-4 taxodioid pits on 1-2 storeys - x200.
Fig. 8 in New Trees Identified In The Petrified Forest Of Middle Miocene From Zarand, Apuseni Mountains, Romania.
Fig. 8 Sequoioxylon gypsaceum (Goeppert) Greguss, 1967. a - cross-section: less distinct growth-ring boundary, parenchyma disperse - x50; b, c - cross-section: thin-walled polygonal tracheids, dispersed parenchyma - x100; d-f - tangential section: - unpitted tracheids, parenchyma with globular resin content and smooth and thin horizontal end walls, uniseriate high rays, or with biseriate storeys or even biseriate - x200; g-i - radial section: radial pitting on tracheids, typical cross-fields with 1-6 taxodioid pits on 1-2 storeys, sometimes alternate - x200.
Fig. 3 in Air sac trematodes: Morishitium polonicum as a newly identified cause of death in the common blackbird (Turdus merula)
Fig. 3. Morishitium polonicum from the air sacs of Turdus merula. A. Tongue-shaped specimen of M. polonicum. In the posterior part of the body are clearly visible the two large testes and the ovary lying between them. (scale bar = 200 μm). B. Anterior end of M. polonicum showing the eggs inside the uterus. (scale bar = 100 μm). C. Posterior end of M. polonicum showing two globular testes situated obliquely to each other, an intertesticular oval ovary placed in a longitudinal straight line with the testes, two caeca joined posteriorly and two symmetrical vitelline glands not confluent posteriorly. (scale bar = 300 μm). D. The oral sucker, the pharynx, the genital pore of M. polonicum in the anterior end (scale bar = 50 μm).
Fig. 2 in Air sac trematodes: Morishitium polonicum as a newly identified cause of death in the common blackbird (Turdus merula)
Fig. 2. Turdus merula female, histology of different coelomic organs. A. Lower power magnification of an area where flukes are adherent to the liver. The presence of inflammatory infiltrate is observed on the Glissonian capsule (arrow) in the contact area with the parasite. At this magnification a general overview of the parasite is also clear: the cephalic portion (arrow-head), different internal organs and the uterus filled by the ova (asterisk) are appreciated (H&E, scale bar = 0.2 cm). B. Detail of the contact area between the fluke tegument and liver serosa, involved in the inflammatory reaction (arrow). Note the pyogranulomatous exudate represented by large amounts of mononuclear cells with interspersed heterophils in the area of close contact with the parasite (asterisk). Trematode eggs and an internal gland (arrow-head) are also visible (H&E, scale bar = 200 μm). C. Fluke localization on the kidney capsule: note the same inflammatory reaction (arrow) described in the liver, in the areas of more close contact (H&E, scale bar = 2 mm). D. Air sacs inflammation and modification in the site of parasite attachment (arrow). Note the previously described inflammatory infiltrate and the altered lung parenchyma (asterisk) in the area of the affected air sac. The pulmonary parenchyma is congested and collapsed, as observed also at gross examination (H&E, scale bar = 200 μm).
Text-fig. 8. Sex estimation of Moča skull (Komárno district, southern Slovakia), linear discriminant analysis using Henke's Late Upper Palaeolithic and Mesolithic database (n = 129, f = 46, m = 83) with variables M1 (GOL) and M45 (ZYB). As the closest to the Moča skull, the following fossil samples from Mesolithic could be identified: Vlasac, Arruda 2, Moita 16, Moita 17, Téviec 2, Téviec 3. in A Late Upper Palaeolithic Skull From Moča (The Slovak Republic) In The Context Of Central Europe
Text-fig. 8. Sex estimation of Moča skull (Komárno district, southern Slovakia), linear discriminant analysis using Henke's Late Upper Palaeolithic and Mesolithic database (n = 129, f = 46, m = 83) with variables M1 (GOL) and M45 (ZYB). As the closest to the Moča skull, the following fossil samples from Mesolithic could be identified: Vlasac, Arruda 2, Moita 16, Moita 17, Téviec 2, Téviec 3.
Figure 3 in Identifying the hotspots of wildlife-vehicle collision on the Çankırı-Kırıkkale highway during summer
Figure 3. Monthly average traffic density by the hour on the Çankırı–Kırıkkale highway (above with moderate traffic density, below with low traffic density).
Figure 4 in Identifying the hotspots of wildlife-vehicle collision on the Çankırı-Kırıkkale highway during summer
Figure 4. The KDE map of the mammals that were killed in accidents on the Çankırı–Kırıkkale highway.
Figure 5 in Occlusal surface variations in genetically-identified specimens of the genus Apodemus (Mammalia: Rodentia) distributed in the Northern Anatolia region and three Turkish islands: Gökçeada, Marmara Island, and Bozcaada
Figure 5. The UPGMA dendrograms based on nonmetric characters. A: Interspesific data, B: A. flavicollis, C: A. mystacinus.
Supplementary Material Requirements Study - Identifying Necessary Green Coding Knowledge for Young Professionals Starting their Careers in the Software Industry Full Audio Transcript with transcribers Notes
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Proteome-wide Mendelian randomization study identifies potential therapeutic targets for Coronary atherosclerosis
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A Potential Method for Identifying Milk Adulteration and Pb(II) Contamination Scenarios Using Principal Component Analysis from Smartphone Photographs
<p>Early Research Data</p>
Can eDNA Present in Aquatic Environments of Rural Areas Help Identify Species Diversity in the Family Anura?
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Table ¹: Model performance in relation to predictor variables combinations and MaxEnt parameters for the two best models identified in our analysis. in Understanding habitat suitability and road mortality for the conservation of the striped hyaena (Hyaena hyaena) in Batna (East Algeria)
<p><b>Table ¹:</b> Model performance in relation to predictor variables combinations and MaxEnt parameters for the two best models identified in our analysis.</p><table><tbody><tr><th><b>Prediction set</b></th><th><b>FC</b></th><th><b>RM</b></th><th><b>P</b> <b>ROC</b></th><th><b>OR</b></th><th><b>AICc</b></th><th><b>ΔAICc</b></th><th><b>WAICc</b></th><th><b>Number of parameters**</b></th></tr></tbody><tbody><tr><th>313</th><td>lqp</td><td>0.7</td><td>0</td><td>0</td><td>752.875</td><td>1.226</td><td>0.0337</td><td>10</td></tr><tr><th>314*</th><td>lqp</td><td>1</td><td>0</td><td>0</td><td>751.649</td><td>0.000</td><td>0.057</td><td>7</td></tr></tbody></table><p>The selected model set (*) met the statistical significance and omission rate criteria during evaluation with train and test data.**Number of environmental variables. FC, feature class; RM, regularization multiplier; OR = omission rate; ΔAICc, Akaike information criterion corrected for small simple sizes; WAICc, weighted AICc.</p>
Natural history specimens collected and/or identified and deposited.
Natural history specimen data collected and/or identified by Alvin Goodale Embree, <a href="http://www.wikidata.org/entity/Q130476233">http://www.wikidata.org/entity/Q130476233</a>. Claims or attributions were made on Bionomia, <a href="http://bionomia.net">https://bionomia.net</a> using specimen data from the Global Biodiversity Information Facility, <a href="https://gbif.org">https://gbif.org</a>.
Linked collectors and determiners for: Four Achnanthidium species (Bacillariophyta) formerly identified as Achnanthidium minutissimum from the Antarctic Region.
Natural history specimen data linked to collectors and determiners held within, "Four Achnanthidium species (Bacillariophyta) formerly identified as Achnanthidium minutissimum from the Antarctic Region". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/b2e284c1-70c1-4e2e-a6ef-cff807e570b5">https://bionomia.net/dataset/b2e284c1-70c1-4e2e-a6ef-cff807e570b5</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/b2e284c1-70c1-4e2e-a6ef-cff807e570b5">https://gbif.org/dataset/b2e284c1-70c1-4e2e-a6ef-cff807e570b5</a>. Formatted as a Frictionless Data package.
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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.