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Fig. 12 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 12. Left lacrimal of the holotype specimen of Alioramus altai (IGM 100/1844) in lateral (A), medial (B), dorsal (C), anterior (D) views.Scale bar 5 5 cm. Abbreviations: air, arcuate internal ridge within lacrimal recess; all, lateral lamina of anterior ramus; aml, medial lamina of anterior ramus; aof, antorbital fossa; antpf, pneumatic fossae on anterior surface of ventral ramus; antpp, pneumatic pocket at posteroventral corner of antorbital fossa; apo, accessory pneumatic openings on anterior ramus; cle, cleft
Fig. 9 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 9. Closeup photos of the left maxilla of the holotype specimen of Alioramus altai (IGM 100/1844) in medial view. A, medial antorbital sinus region; B, anterior end of maxilla; C, posterior end of ascending ramus. Scale bar 5 2 cm. Abbreviations as in figure 6, plus: gap, apparent gap between the medial bounding wall of the maxillary antrum and the medial maxillary shelf (but probably a result of damage and not genuine); mant, maxillary antrum.
Fig. 13 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 13. Right lacrimal of the holotype specimen of Alioramus altai (IGM 100/1844) in lateral (A), medial (B), and dorsal (C) views. Scale bar 5 5 cm. Abbreviations as in figure 12, plus: fro ov, facet on dorsal surface of posterior ramus of lacrimal that is overlapped by the frontal.
Fig. 5 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 5. Plot of total skull length vs. femur length (logarithmic scale) for several tyrannosaurid specimens, based on Currie (2003b). Squares represent tyrannosaurine specimens (Tarbosaurus, Tyrannosaurus); closed circles represent albertosaurines (Albertosaurus, Gorgosaurus); star represents holotype of Alioramus altai (IGM 100/1844). Note that the A. altai holotype falls above the regression lines, demonstrating that its skull is longer than those of other tyrannosaurids with a similar femur length (and hence body size, as femur length and body size are tightly correlated in theropods). The Alioramus data point is closer to the tyrannosaurine regression line, which is consistent with its phylogenetic position as a tyrannosaurine.
Fig. 3 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 3. The holotype skull of Alioramus altai (IGM 100/1844) partially prepared in the original field jacket.
Fig. 15 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 15. Left jugal of the holotype specimen of Alioramus altai (IGM 100/1844) in lateral (A), medial (B), and dorsal (C) views. Scale bar 5 5 cm. Abbreviations: aap, anterior ascending process; app, anterior pocket of jugal pneumatic recess; cor, cornual process; dmax, dorsally positioned groove for maxilla
Fig. 2 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 2. The Tsaggan Khuushuu locality in the Gobi Desert of Mongolia, where the holotype of Alioramus altai (IGM 100/1844) was discovered in Maastrichtian-aged rocks of the Nemegt Formation (top). The right maxilla, in medial view, as preserved in the field (bottom).
Fig. 1 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 1. Skeletal reconstruction of the holotype specimen of the Late Cretaceous tyrannosaurid Alioramus altai (IGM 100/1844). Bones in light gray (e.g., skull) are preserved and those in dark gray (e.g., forearm) are absent but reconstructed based on comparison to close relatives (Appalachiosaurus, Tarbosaurus, and Tyrannosaurus of similar body size). Entire scale bar 5 2 m. Reconstruction delineated by Frank Ippolito, American Museum of Natural History.
Fig. 27 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 27. Closeup photo of the right palatine of the holotype specimen of Alioramus altai (IGM 100/ 1844) in lateral view. Scale bar 5 2 cm. This figure is not labeled, but refer to figure 25 for corresponding labels on the right palatine.
Fig. 11 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 11. Closeup photo of the conjoined nasals of the holotype specimen of Alioramus altai (IGM 100/
Fig. 8 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 8. Closeup photos of the left maxilla of the holotype specimen of Alioramus altai (IGM 100/1844) in lateral view. A, antorbital fossa region; B, posterior end of maxilla. Scale bar 5 2 cm. Abbreviations as in figure 6.
Fig. 10 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 10. Conjoined nasals of the holotype specimen of Alioramus altai (IGM 100/1844) in dorsal (A), ventral (B), right lateral (C), and left lateral (D) views. Scale bar 5 5 cm. Abbreviations: for, foramina; lac, lacrimal articular facet; max, maxillary articular facet; nar, external naris; ons, open internarial suture; pmp, premaxillary process; prf, prefrontal articular facet; rug, discrete rugosities; sgr, secondary groove of lacrimal facet; snp, subnarial process.
Fig. 7 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 7. Right maxilla of the holotype specimen of Alioramus altai (IGM 100/1844) in lateral (A), medial
Fig. 18 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 18. Closeup photos of the left postorbital of the holotype specimen of Alioramus altai (IGM 100/ 1844) in medial (A) and lateral (B, C) views. A, region articulating with various cranial bones; B, region of cornual process at posterodorsal corner of orbit; C, ventral ramus. Scale bar 5 2 cm. Abbreviations as in figure 17.
Fig. 17 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 17. Left postorbital of the holotype specimen of Alioramus altai (IGM 100/1844) in lateral (A), medial (B), anterior (C), posterior (D), and dorsal (E) views. Scale bar 5 5 cm. Abbreviations: cor, cornual process; fos, fossa; froab, anterior bulge of frontal articulation; froph, posterior horizontal portion of
Fig. 24 in The Osteology Of Alioramus, A Gracile And Long-Snouted Tyrannosaurid (Dinosauria: Theropoda) From The Late Cretaceous Of Mongolia
Fig. 24. Left quadratojugal and quadrate (in articulation) of the holotype specimen of Alioramus altai (IGM 100/1844) in posterior view. Scale bar 5 1 cm. Abbreviations as in figures 21, 22, and 23.
Data from: Genetic diversity in a long-lived mammal is explained by the past's demographic shadow and current connectivity
<p>Within-species genetic diversity is crucial for the persistence and integrity of populations and ecosystems. Conservation actions require an understanding of factors influencing genetic diversity, especially in the context of global change. Both population size and connectivity are factors greatly influencing genetic diversity; the relative importance of these factors can however change through time. Hence, quantifying the degree to which population size or genetic connectivity are shaping genetic diversity, and at which ecological time scale (past or present), is challenging, yet essential for the development of efficient conservation strategies. In this study, we estimated the genetic diversity of 42 colonies of <i>Rhinolophus hipposideros,</i> a long-lived mammal vulnerable to global change, sampling locations spanning its continental northern range. We present an integrative approach that disentangles and quantifies the contribution of different connectivity measures in addition to contemporary colony size and historic bottlenecks in shaping genetic diversity. In our study, the best model explained 64% of the variation in genetic diversity. It included historic bottlenecks, contemporary colony sizes, connectivity and a negative interaction between the latter two. Contemporary connectivity explained most genetic diversity when considering a 65 km radius around the focal colonies, emphasizing the large geographic scale at which the positive impact of connectivity on genetic diversity is most profound and hence the minimum scale at which conservation should be planned. Our results highlight that the relative importance of the two main factors shaping genetic diversity varies through time, emphasizing the relevance of disentangling them to ensure appropriate conservation strategies.</p>
Reproduction package for 'Limits on long-timescale radio transients at 150 MHz using theTGSS ADR1 and LoTSS DR2 catalogues'
<p>This is a basic reproduction package for 'Limits on long-timescale radio transients at 150 MHz using theTGSS ADR1 and LoTSS DR2 catalogues' by de Ruiter et al (2021). It aims to provide the most important data products to check and reproduce the main results of the paper.</p>
FIG. 1 in Les porcs « long châssis »: le péril des mariages? Comprendre les transformations du bestiaire dotal du Cameroun méridional
FIG. 1 — Porc « long châssis » en vente au marché de Tsinga à Yaoundé. Crédit photo: S. Balla, juillet 2021.
Capture-recapture histories used in our paper "High long-term survival and asymmetric movements in a reintroduced metapopulation of cinereous vultures" published by Ecosphere
<p>These three datasets correspond to the capture-recapture histories used in the E-surge software (in the HEADED format) for both population models (Capture_recapture_histories_ALPS.txt for the Alps and Capture_recapture_histories_CAUSSES.txt for the Causses) and the metapopulation model (Capture_recapture_histories_METAPOPULATION.txt).</p> <p>Columns descriptor:</p> <ul> <li>H:O1 to H:O25 correspond to each occasion (i.e. year)</li> <li>S: correspond to the sample size (i.e. associated number of animals)</li> <li>RC: correspond to the Right Censoring ( -1 if the animal is removed at the last capture or 0 if no right censoring)</li> <li>$COV:Group correspond to the group to which the individual belongs</li> </ul> <p>Individuals were grouped by age (from the 1<sup>st</sup> year until ≥6<sup>th</sup> years), by release status (wild-born / hacking: released juveniles before fledging / aviary: released immatures, sub-adults or adults), by origin (Causses / Alps) and if a missing ring was replaced. All details for the groups are given in the Appendix B for both population models and in the Appendix C for the metapopulation model.</p>
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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.