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Fig. 1 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 1. Late Paleocene Gashatan localities for multituberculates in the Mongolian Plateau. A. Shabarakh Usu, Mongolia, where Sphenopsalis nobilis and Prionessus lucifer were first discovered. B. Erlian Basin, Inner Mongolia, China. Lambdopsalis bulla, P. lucifer, and Mesodmops tenuis were reported from Subeng (Missiaen and Smith 2008). L. bulla and P. lucifer were present in Nuhetingboerhe (Wang et al. 2010) and Bayan Ulan (Meng et al. 1998). L. bulla, S. nobilis, and P. lucifer were present in Haliut (Chow and Qi 1978) and Erden (Urtyn) Obo area (this study).
Fig. 6 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 6. Lower incisors of multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. A. IVPP V19025, symphysis of mandibles with partial incisors in lateral right (A1) and left (A2), dorsal (A3), and ventral (A4) views. B. IVPP V19034, right incisor in medial (B1) and lateral (B2) views.
Fig. 1. A in Middle Miocene conoidean gastropods from western Ukraine (Paratethys): Integrative taxonomy, palaeoclimatogical and palaeobiogeographical implications
Fig. 1. A. Schematic map of Ukraine and the location of the study area. B. Distribution of the principal lithostratigraphic units in the area of study and location of the three sampled sites (asterisks).
Fig. 8 in Middle Miocene conoidean gastropods from western Ukraine (Paratethys): Integrative taxonomy, palaeoclimatogical and palaeobiogeographical implications
Fig. 8. SEM images of shell features of conoidean gastropods from early Serravallian of western Ukraine, Horodok (A, B) and Varovtsi (C–J). A, B. Pyrgocythara turrispiralata sp. nov. A. MGGC-24515/11. B. MGGC-24515/9. C, D. Raphitoma cf. R. ringicula (Boettger, 1902). C. MGGC-24522/1. D. MGGC-24522/3. E, F. Andonia sp. aff. A. transsilvanica (Hoernes and Auinger, 1890). E. MGGC-24523/1. F. MGGC-24523/3. G, H. Teretia cf. T. turritelloides (Bellardi, 1847). G. MGGC-24524/3. H. MGGC-24524/5. I, J. Haedropleura sp. aff. H. septangularis (Montagu, 1803). I. MGGC-24520/6. J. MGGC-24520/11. Views: A1, C1, E1, G1, I1, apertural; B, D, E2, H, I2, dorsal; A2, C2, F, G2, J, lateral. Scale bars 1 mm.
Fig. 17 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 17. Phylogenetic position of Sphenopsalis nobilis within multituberculates. A. The strict consensus tree of 138 trees obtained in the PAUP search where 19 characters were ordered (see SOM). B. The 50% majority rule consensus tree with 19 characters ordered. See additional supporting data in the SOM.
Fig. 5 in Middle Miocene conoidean gastropods from western Ukraine (Paratethys): Integrative taxonomy, palaeoclimatogical and palaeobiogeographical implications
Fig. 5. SEM images of shell features of new conoidean gastropods from early Serravallian of western Ukraine, Varovtsi (A–E, I–M), Horodok (G), and Velyka Levada (F, H). A. Mangelia angulicosta sp. nov., MGGC-24506/6. B–D. Mangelia larga sp. nov. B. MGGC-24508/11. C. MGGC-24508/1. D. MGGC-24508/12. E. Mangelia pseudorugulosa sp. nov., MGGC-24510/9. F–H. Mangelia odovychenae sp. nov. F. MGGC-24512/1. G. MGGC- 24512/10. H. MGGC-24512/topotype. I–K. Bela varovtsiana sp. nov. I. MGGC-24517/8. J. MGGC-24517/5. K. MGGC-24517/6. L, M. Bela? robusta sp. nov. L. MGGC-24519/8. M. MGGC-24519/1. Views: A1–L1, B, F, I, apertural; A2−L2, C, G, J, dorsal; A3, D, E3, H, K, M, lateral. Scale bars 1 mm.
Fig. 12 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 12. The femur of multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 (IVPP V19030) from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. A. Proximal portion of the left femur in anterior (A1), posterior (A2), and proximal end (A3) views. B. Right femur (with proximal end broken) in anterior (B1), posterior (B2), and distal end (B3) views.
Fig. 8 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 8. Occlusal views of molars of multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. A. IVPP V19037, right m2. B. IVPP V19030, left m2. C. IVPP V19028, right m2. D. IVPP V19029, right m2 (D1), right M1–2 (D2), left M1–2 (D3). E. IVPP V19025, right M1, which belongs to the same individual as in Fig. 4. F. IVPP V19027, a developing right m2? G. IVPP V19033, a deeply worn left m2. H. IVPP V19026, right M2. I. IVPP V19036, right m2.
Fig. 9 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 9. Skull fragments of multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. A. IVPP V19025, skull fragment showing the orbital crest in lateral (A1) and dorsal (A2, A3) views. B. IVPP V19029, skull fragment showing the temporal crest in lateral (B1) and dorsal (B2, B3) views. The anterior end of each element is toward upside. Photographs (A1, A2, B1, B2), explanatory drawings (A3, B3).
Fig. 11 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 11. Fragmentary scapula and humerus of multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. A. IVPP V19030, proximal portion of the right scapula in lateral (A1), medial (A2), and ventral (glenoid fossa) (A3) views. B. IVPP V19031, left humerus in anterior (B1), posterior (B2), lateral (B3), and medial (B4) views. Due to the breakage, the proximal (top) and distal (bottom) portions may not be displayed in their precise anatomical positions.
Fig. 5 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 5. Multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 (IVPP V19032) from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. Left upper molars (M1–2) from the same individual as the lower ones in Fig. 7 in occlusal (A), medial (B), and lateral (C) views. The arrow indicates the broken anterior root of the zygomatic arch. Photographs (A1–C1), SEM images (A2–C2).
Fig. 4 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 4. Multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 (IVPP V19025) from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. Partial left maxilla with M1 and M2 in occlusal (A), medial (B), and lateral (C) views. The arrow indicates the broken anterior root of the zygomatic arch; wear facets: 1, on buccal sides of the lingual cusps of M2; 2, on lingual sides of the medial cusps of M2; 3, on buccal sides of the medial cusps of M2; 4, on the cusp of the buccal (external) row, which is aligned with the buccal wear facets of medial cusps of M2. Photographs (A1–C1), SEM images (A2–C2).
Fig. 14 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 14. The upper and lower left molars of multituberculate mammal Lambdopsalis bulla Matthew, Granger, and Simpson, 1928 (IVPP V20101) from the upper Paleocene Nomogen beds at the Bayan Ulan locality, Inner Mongolia, China. Crown view of m1–2 (A) and M1–2 (B). Wear facets: 1, on lingual sides of the buccal cusps of m2; 2, on buccal sides of the lingual cusps of m2; 3, on lingual sides of the lingual cusps of m2; 4, on buccal sides of the lingual cusps of M2; 5, on lingual sides of medial cusps of M2; 6, on the buccal sides of medial cusps of M2; 7, on buccal sides of the buccal cusps of m1; 8, on lingual sides of the buccal cusps of m1; 9, on buccal sides of the lingual cusps of m1; 10, on lingual sides of the lingual cusps of m1; no wear facet was developed yet on the cusp of the buccal (external) cusp row of M2 in this specimen.
Fig. 7 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 7. Multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 (IVPP V19032) from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. Left lower cheek teeth (p4–m2) from the same individual as in Fig. 5 in occlusal (A), medial (B), and lateral (C) views. Photographs (A1–C1), SEM images (A2–C2).
Fig. 15 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 15. Teeth of multituberculate mammal from the lower Paleocene Puercan in the San Juan Basin, New Mexico. A. Taeniolabis sp., AMNH 117415, cast, occlusal view of right p4–m2. B, C. Taeniolabis taoensis Cope, 1882. B. AMNH 16310, occlusal view of the left p4–m2. C. AMNH 16321, occlusal view of the right P4–M2.
Fig. 4 in Early Miocene evolution of the rodent Megacricetodon in Europe and its palaeobiogeographical implications
Fig. 4. Biostratigraphic distribution of Early Miocene Megacricetodon species from Europe with indication of the proposed migrations events among South-eastern Europe (Greece), Central Europe (Czech Republic, Switzerland, and Germany) and South-western Europe (France and Spain), modified from Oliver and Peláez-Campomanes (2013). The silhouettes of the cricetid indicate indicate three phases of immigration of Megacricetodon species into Europe.
Fig. 3 in Early Miocene evolution of the rodent Megacricetodon in Europe and its palaeobiogeographical implications
Fig. 3. Micro-CT images, showing the relative height of the five main cusps. In Megacricetodon hellenicus sp. nov. (A, IAUU AL-N-2096; B, IAUU AL-N-2097) from Aliveri South quarry, Greece (MN4, Early Miocene) the anteroconid is lower than the rest of the cusps. In Megacricetodon primitivus (Freudenthal, 1963) (C, VLT-167) from Valtorres, Spain (MN5, Middle Miocene) the anteroconid is of similar height than the other cusps. Labial (A1–C1) and occlusal (A2–C2) views.
Fig. 2 in Early Miocene evolution of the rodent Megacricetodon in Europe and its palaeobiogeographical implications
Fig. 2. Cricetodontid rodent Megacricetodon hellenicus sp. nov. from the Aliveri South quarry, Greece (MN4, Early Miocene). A. IAUU AL- S-1112, M1 right. B. IAUU AL-S-1114, M1 left. C. IAUU AL-S-1118, M3 left. D. IAUU AL-S-1119, M3 left. E. IAUU AL-S-1122, m1 left. F. IAUU AL-S-1124, m1 right. G. IAUU AL-S-1115, M2 left. H. IAUU AL-S-1128, m3 right. I. IAUU AL-S-1129, m3 right.
Fig. 1 in Early Miocene evolution of the rodent Megacricetodon in Europe and its palaeobiogeographical implications
Fig. 1. Cricetodontid rodent Megacricetodon hellenicus sp. nov. from type locality Aliveri North quarry, Greece (MN4, Early Miocene). A. IAUU AL-N-2051, M1 left. B. IAUU AL-N-2052, M1 left. C. IAUU AL-N-2053, M1 left. D. IAUU AL-N-2055, M1 left. E. IAUU AL-N-2056, M1 left. F. IAUU AL-N-2057, M1 left. G. IAUU AL-N-2059, M1 left. H. IAUU AL-N-2060, M1 left. I. IAUU AL-N-2071, M2 left. J. IAUU AL-N-2072, M2 left. K. IAUU AL-N-2077, M2 right. L. IAUU AL-N-2078, M2 right. M. IAUU AL-N-2091, m1 left. N. IAUU AL-N-2092, m1 left. O. Holotype IAUU AL-N-2096, m1 right. P. IAUU AL-N-2097, m1 right. Q. IAUU AL-N-2101, m2 left. R. IAUU AL-N-2102, m2 left. S. IAUU AL-N-2104, m2 left. T. IAUU AL-N-2105, m2 left. U. IAUU AL-N-2111, m2 right. V. IAUU AL-N-2126, m3 right.
Fig. 4 in Pathological phalanges in a camarasaurid sauropod dinosaur and implications on behaviour
Fig. 4. Photo (A) and drawing (B) of the right pedal ungual II of the camarasaurid sauropod SMA 0002 (Upper Jurassic Morrison Formation, HoweStephens Quarry, Wyoming, USA) in proximal view, showing the broken surface indicating overgrowth attachment. Modified from Tschopp et al. (2015).
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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.