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Fig. 3 in Giant theropod dinosaurs from Asia and North America: Skulls of Tarbosaurus bataar and Tyrannosaurus rex compared
Fig. 3. Right premaxilla of Tarbosaurus bataar ZPALMgD−I/4 mirrored to be comparable to other bones form the left side of the skull in lateral (A, B) and medial (C) views.
Fig. 5. A in Giant theropod dinosaurs from Asia and North America: Skulls of Tarbosaurus bataar and Tyrannosaurus rex compared
Fig. 5. A. Nasal of Tarbosaurus bataar ZPALMgD−I/4 in lateral (A 1) and ventral (A2, A3) views. B. Ventral view of the nasal of Tyrannosaurus rex BHI−3033.
Fig. 2. A in Giant theropod dinosaurs from Asia and North America: Skulls of Tarbosaurus bataar and Tyrannosaurus rex compared
Fig. 2. A. Generalized skulls of Tarbosaurus bataar in lateral (A1) and dorsal (A2) views. B. Tyrannosaurus rex in lateral (B1) and dorsal (B2) views compared (not to scale). Light grey, lacrimal; dark grey, nasal.
Figure 1 in First record of Chaetopteroides kosovarorum Ibrahimi & Oláh, 2013 (Insecta: Trichoptera) from the Republic of North Macedonia
Figure 1. Distribution of the Chaetopteroides kosovarorum. Yellow dots - previous records (Olah et al. 2013). Red dots – records from this investigation.
Planetary Boundary Layer Height Retrievals from the Cloud-Aerosol Transport System (CATS) around the US Southern Great Plains and the Eastern North Atlantic
<p>Planetary Boundary Layer Height (PBLH) retrievals in kilometers from the Cloud-Aerosol Transport System (CATS) around the DOE ARM US Southern Great Plains (SGP) and the Eastern North Atlantic (ENA), using a modified version of the Different Thermo-Dynamics Stability (DTDS) algorithm. Quality control Flags are included as follows:</p> <ul> <li>0 = 'Good Quality'</li> <li>1 = 'Mediate Quality'</li> <li>2 = 'Bad Quality'</li> </ul> <p>In addition, -999 values in the dataset represent no data. <br>The PBLH for daytime denoised CATS photon counts at SGP is named: "daytime-denoised-dtds-pblh-sgp.csv"<br>The PBLH for the original daytime and nighttime data at SGP and ENA, without denoising the data, are named: "original-cats-dtds-pblh-daytime-nighttime-sgp.csv" and "original-cats-dtds-pblh-daytime-nighttime-ena.csv"</p> <p>References: </p> <p>Roldán-Henao, N., Yorks, J., Su, T., Selmer, P., & Li, Z. (2024). Statistically Resolved Planetary Boundary Layer Height Diurnal Variability Using Spaceborne Lidar Data. <em>Remote Sensing. </em></p> <p>Su, T., Li, Z., & Kahn, R. (2020). A new method to retrieve the diurnal variability of planetary boundary layer height from lidar under different thermodynamic stability conditions. <em>Remote Sensing of Environment</em>, <em>237</em>, 111519.</p>
Figure 2. - Trachinus pellegrini. A in On the presence of Trachinus pellegrini (Trachinidae) in the Canary and Cape Verde Islands (north-eastern Atlantic)
Figure 2. - Trachinus pellegrini. A: Juvenile from the Canary Islands (TFMC-VP/1947, 68.0 mm TL, 59.6 mm SL); B: Subadult from the Cape Verde Islands (MMF42285, 119 mm TL, 101 mm SL). Scale bars = 25 mm.
Figure 3 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 3. - Monthly percentage of each maturity stage for males (A) and females (B) black-bellied anglerfish. Maturity stages: I, Immature; II, Maturing; III, Mature; IV, Spawning; V, Post-Spawning.
Figure 2 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 2. - Length-number distribution of Lophius budegassa sampled in the Saros Bay by commercial vessel between September 2006 and September 2008.
Figure 4 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 4. - Monthly variation of gonadosomatic index for males (A) Figure 5. - Percentage of sexually mature males (A) and females and females (B) Lophius budegassa between September 2006 and (B) Lophius budegassa according to total length. September 2008. Vertical bars represent standard error with sample size values indicated between brackets. and GSI values in females and males. Therefore, the results suggest a main spawning period from December to March decreases with increasing depth that may reflect a seasonal for blackbellied anglerfish. In females, spawning and postsegregation (García-Rodríguez et al., 2005). Laurenson et spawning stages have been seen from December to March al. (2008) found that the proportion of L. piscatorius varies and in males from January to March (Fig. 3A, B). At the same with both depth and season in Scottish waters. Several state- time, GSI values in males were high except in August and ments can explain this difference. Differentiation in growth November, while female GSI values were the highest in Janrate between sexes can cause an unbalanced proportion, uary (Fig. 4A, B). The spawning males can be seen almost all since the sex presenting faster growth rate will go through year around (Duarte et al., 2001; Landa et al., 2014), and this the most vulnerable smaller size phase quickly and, there- could increase the chances for a mature female to encounter fore decrease the predation proportion. Conversely, the sex with slower growth rate will be more likely to pass predation, with its abundance decreased disproportion- Table I. - Length at 50% maturity (L50) of Lophius budegassa obtained by other authors. ately in next development phases (Vicentini and Araújo,
Figure 3. - Collection locations for the new records from the Canaries. 1 in New records of non-indigenous fishes (Perciformes and Tetraodontiformes) from the Canary Islands (north-eastern Atlantic)
Figure 3. - Collection locations for the new records from the Canaries. 1: Holocentrus adscensionis, 2: Cephalopholis taeniops, 3: Paranthias furcifer, 4: Prognathodes marcellae, 5: Abudefduf saxatilis, 6: Abudefduf hoefleri, 7: Acanthurus bahianus, 8: Acanthurus coeruleus, 9: Acanthurus chirurgus, 10: Acanthurus monroviae, 11: Cantherhines pullus.
Figure 2 in New records of non-indigenous fishes (Perciformes and Tetraodontiformes) from the Canary Islands (north-eastern Atlantic)
Figure 2. - Non-native species introduced to the Canaries. A: Holocentrus adscensionis; B: Cephalopholis taeniops; C: Paranthias furcifer; D: Prognathodes marcellae; E: Abudefduf saxatilis; F: Abudefduf hoefleri; G: Acanthurus bahianus; H: Acanthurus coeruleus; I: Acanthurus chirurgus; J: Acanthurus monroviae; K: Cantherhines pullus. Scale bars = 5 cm.
Fig. 2 in Morphometry of the teeth of western North American tyrannosaurids and its applicability to quantitative classification
Fig. 2. Schematic illustration of tooth and denticle measurements obtained for this study. Diagram is an outline of tooth specimen TMP 86.130.214. Denticles on tooth outline in lateral (A), basal (B), and enlarged (C) views, not to scale. For measurements, tooth is aligned so that the basal termination of enamel (broken line in A) is approximately horizontal. 1, fore−aft basal length (FABL); 2, tooth crown height (THEIGHT); 3, cross−sectional thickness (XSTHICK); 4, curvature (CURVATUR); 5, distance from the base of the mesial carina to the base of the tooth (DMCTOB); 6, denticle width (DW); 7, denticle height (DH).
Fig. 4. A in Morphometry of the teeth of western North American tyrannosaurids and its applicability to quantitative classification
Fig. 4. A. Ordination plot for PC I versus PC II for the teeth in jaws. B. Ordination plot for PC I versus PC III for the teeth in jaws. C. Ordination plot for PC II versus PC III for the teeth in jaws.
Fig. 1 in Morphometry of the teeth of western North American tyrannosaurids and its applicability to quantitative classification
Fig. 1. Longitudinal section through the crown of a small, broken, tyrannosaurid tooth (TMP 86.130.214, Judith River Group, Campanian, Alberta, Canada). The plane of the break resulted in the loss of the mesial carina, so only the distal carina is preserved on the tooth. A. Enlargement of the area outlined in B shows the enamel and the denticles. B. Photograh of the whole specimen showing dentine (light−colored area).
Fig. 3 in Morphometry of the teeth of western North American tyrannosaurids and its applicability to quantitative classification
Fig. 3. The five major types of teeth found in the tyrannosaurid jaw, Judith River Group, Campanian, Upper Cretaceous, Alberta, Canada. A. Premaxillary, TMP 65.26.3. B, C. Mesial maxillary, MM1 TMP 98.68.65 (B), MM2 TMP 66.31.36 (C). D. Distal maxillary, TMP 85.36.342. E, F. Mesial dentary, MD1 TMP 79.14.538 (E), MD2 TMP 89.79.4 (F). G. Distal dentary, TMP 97.12.43. Cross−sectional shape and location of carinae are as indicated, and are to scale relative to each other. Scale bars 10 mm.
Supplemental data for: Evaluation of SARS-CoV-2 response at the University of North Carolina (UNC) at Charlotte using percent positivity data and viral genomic sequence data.
<p>Supplemental data for:</p> <p>Evaluation of SARS-CoV-2 response at the<br>University of North Carolina (UNC) at Charlotte<br>using percent positivity data and viral genomic<br>sequence data.</p> <p>Submitted to Biocarla 2024</p> <p>https://carla2024.org/portfolios/biocarla/</p> <p>Authors:</p> <p>Daniel Janies 1,2,3 [0000−0002−7890−9906], Shirish Yasa 1,2,3 [0000−0003−3217−4921],<br>Colby T. Ford 1,3,4 [0000−0002−7859−3622] Jannatul Ferdous 2,3 [0000−0003−3053−9616],<br>William Taylor 2,3 [0009−0000−6204−1172], April Harris 2,3 [0009−0009−2557−7926],<br>Sam Kunkleman 2,3 [0000−0002−2309−6418], Juan Bolanos 2,3, Kevin Lambirth 2,3 [0000-0002-6568-543X], Denis<br>Jacob Machado 1,2,3 [0000−0001−9858−4515], Cynthia Gibas 1,2,3 [0000−0002−1288−9543],<br>and Jessica Schlueter 1,2,3 [0000−0002−6490−0580]</p> <p>Affiliations:</p> <p>1) Center for Computational Intelligence to Predict Health and Environmental Risks<br>(CIPHER), University of North Carolina at Charlotte 28223, USA<br>Correspondence to: djanies@charlotte.edu<br>https://cipher.charlotte.edu<br>2) Department of Bioinformatics and Genomics, University of North Carolina at<br>Charlotte 28223, USA https://cci.charlotte.edu/departments/<br>department-of-bioinformatics-and-genomics/<br>3) College of Computing and Informatics, University of North Carolina at Charlotte<br>28223, USA https://cci.charlotte.edu<br>4) School of Data Science, University of North Carolina at Charlotte 28223, USA<br>https://sds.charlotte.edu<br>5) Division of Research, University of North Carolina at Charlotte 28223, USA<br>https://research.charlotte.edu/</p> <p> </p>
Fig. 5 in New species of Kontrimavichusia Makarikov & Binkienė, 2022 (Eucestoda: Hymenolepididae) from arvicoline rodents (Rodentia: Cricetidae) from the North Caucasus
Fig. 5. Maximum likelihood phylogenetic tree of Kontrimavichusia Makarikov & Binkienė, 2022 and Hymenolepis Weinland, 1858 based on analysis of partial sequences of the 28S rRNA gene. Bootstrap support given for maximum likelihood analysis based on 1000 replicates. Bootstrap support values lower than 70% are not shown.
Fig. 4 in New species of Kontrimavichusia Makarikov & Binkienė, 2022 (Eucestoda: Hymenolepididae) from arvicoline rodents (Rodentia: Cricetidae) from the North Caucasus
Fig. 4. Kontrimavichusia hobergi sp. nov. A. Paratype (ISEA AM17-236#1), cirrus and vagina, ventral view. B. Holotype (ISEA AM17-236#3), pregravid proglottis, showing appearance of uterine diverticula, dorsal view. C. Holotype, gravid proglottis, showing labyrinthine uterus, dorsal view. D. Holotype, egg. E. Holotype, embryonic hooks. Abbreviations: al = anterolateral; m = median; pl = postero-lateral. Scale bars: A = 50 µm; B–C = 300 µm; D = 20 µm; E = 10 µm.
Fig. 1 in New species of Kontrimavichusia Makarikov & Binkienė, 2022 (Eucestoda: Hymenolepididae) from arvicoline rodents (Rodentia: Cricetidae) from the North Caucasus
Fig. 1. Kontrimavichusia testiculata sp. nov. A. Holotype (ISEA AM14-134#1), scolex, dorso-ventral view. B. Paratype (ISEA AM14-147#2), scolex, sub-lateral view. C. Paratype (ISEA AM14-142#2), rostellar hooks in profile and frontal view (note narrow hook guard). D. Holotype, male mature proglottides, dorsal view. E. Holotype, hermaphroditic mature proglottis, dorsal view. F. Paratype (ISEA AM14-147#2), genital ducts, dorsal view. Scale bars: A–B, F = 100 µm; C = 10 µm; D–E = 300 µm.
Fig. 6 in New species of Kontrimavichusia Makarikov & Binkienė, 2022 (Eucestoda: Hymenolepididae) from arvicoline rodents (Rodentia: Cricetidae) from the North Caucasus
Fig. 6. Maximum likelihood phylogenetic tree of species of Kontrimavichusia Makarikov & Binkienė, 2022 based on analysis of partial sequences of the nad1 gen. Bootstrap support given for maximum likelihood analysis based on 1000 replicates. Bootstrap support values lower than 70% are not shown.
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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.