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FIG. 21 in Eomakhaira molossus, A New Saber-Toothed Sparassodont (Metatheria: Thylacosmilinae) from the Early Oligocene (?Tinguirirican) Cachapoal Locality, Andean Main Range, Chile
FIG. 21. Temporal durations of major lineages of mammalian saber-toothed carnivores, with metatherian lineage in grey and placental lineages in black. A representative skull of each clade is depicted to the right; from top to bottom: Thylacosmilus atrox (Thylacosmilinae), Machaeroides eothen (Machaeroidinae), Hoplophoneus primaevus (Nimravidae), Barbourofelis fricki (Barbourofelidae) and Smilodon fatalis (Machairodontinae). Images of Machaeroides, Barbourofelis, and Smilodon modified from Antón (2013), Thylacosmilus from Riggs (1934), and Hoplophoneus from Scott and Jepsen (1936) and Bryant (1996). Tick mark on Thylacosmilinae record represents the oldest occurrence of this clade (~20.2 Ma) prior to the discovery of Eomakhaira. Abbreviations: Plio., Pliocene; Ple., Pleistocene.
FIG. 2 in New material of Eocene Helaletidae (Perissodactyla, Tapiroidea) from the Irdin Manha Formation of the Erlian Basin, Inner Mongolia, China and comments on Related Localities of the Huheboerhe Area
FIG. 2. Cranium and mandible of Paracolodon fissus (IVPP V 22640). A, lateral view of cranium and mandible; B−C, dorsal and ventral views of the cranium.
FIG. 3 in New material of Eocene Helaletidae (Perissodactyla, Tapiroidea) from the Irdin Manha Formation of the Erlian Basin, Inner Mongolia, China and comments on Related Localities of the Huheboerhe Area
FIG. 3. Right petrosal of Paracolodon fissus (IVPP V 22640). Parallel lines indicate damaged surfaces. The anteroposterior length of the promontorium is about 14.66 mm. Abbreviations: bg, basicapsular groove; bo, basiocciptial; bs, basisphenoid; ci, crista interfenestralis; ctp, caudal tympanic process; eam, external acoustic meatus; fc, fenestra cochleae; fs, facial sulcus; fv, fenestra vestibuli; gpns, greater petrosal nerve sulcus; hf, hypoglossal foramen; mlf, middle lacerate foramen; oc, occipital condyle; p, promontorium; pgp, postglenoid process; pcop, paracondylar process; s, squamosal; sf, stapedial muscle fossa; sff, secondary facial foramen; ts, transpromontorial sulcus; ttf, fossa for the tensor tympani muscle.
FIG. 11 in New material of Eocene Helaletidae (Perissodactyla, Tapiroidea) from the Irdin Manha Formation of the Erlian Basin, Inner Mongolia, China and comments on Related Localities of the Huheboerhe Area
FIG. 11. The single most parsimony tree and the distribution of selected taxa. The left column showing Polarity Chrons, NALMA, and ALMA was modified from Vandenberghe et al. (2012). Numbers on the cladogram are node numbers, and numbers in the parentheses are Bremer Support which is greater than 1. Abbreviations: ALMA, Asian Land Mammal Ages; Ck., Clarkforkian; Du., Duchesnean; Er., Ergilian; Ga., Gashatan; Hs., Hsandagolian; 55 NALMA, North American Land Mammal Ages; Or., Orellan; Pa., Paleocene; Ta., Tabenbulakian; Th., Thanetian; Ul., Ulangochuian; Wt., Whitneyan.
FIG. 1 in New material of Eocene Helaletidae (Perissodactyla, Tapiroidea) from the Irdin Manha Formation of the Erlian Basin, Inner Mongolia, China and comments on Related Localities of the Huheboerhe Area
FIG. 1. Topographic map of the Huheboerhe area (modified from Meng et al., 2007: fig. 1). 1, presumed location of Camp Margetts; 2, Daoteyin Obo (5 miles east of Camp Margetts); 3, Nuhetingboerhe (6 miles west of Camp Margetts); 4, Wulanboerhe; 5, Huheboerhe (7 miles west and southwest [235°] of Camp Margetts); 6, Changanboerhe (10 miles southwest of Camp Margetts); 7, Jibuqilehasha.
FIG. 4 in New material of Eocene Helaletidae (Perissodactyla, Tapiroidea) from the Irdin Manha Formation of the Erlian Basin, Inner Mongolia, China and comments on Related Localities of the Huheboerhe Area
FIG. 4. Occlusal view of upper cheek teeth of Paracolodon fissus, Paracolodon inceptus, and Desmatotherium mongoliense. A−B, P. fissus; A, left P2−M3 (IVPP V 22640); B, left P2−P4 (AMNH FM 20161); C−D, P. inceptus; C, left P1−P3 (AMNH FM 20355); D, left P3−M3 (AMNH FM 20357); E−G, D. mongoliense; E, left P1−M2 (IVPP V 14692); F, left P3−P4 (AMNH FM 20156); G, left P2−M3 (AMNH FM 19161, reversed).
FIG. 10 in New material of Eocene Helaletidae (Perissodactyla, Tapiroidea) from the Irdin Manha Formation of the Erlian Basin, Inner Mongolia, China and comments on Related Localities of the Huheboerhe Area
FIG. 10. Longitudinal section of the ectoloph of upper right P4 of Paracolodon fissus and Desmetotherium mongoliense showing the curved HSB configuration. A, P. fissus with continuous and relatively narrower HSB pattern; B, D. mongoliense with waved and relatively wider HSB pattern. Abbreviations: if, interface; me, metacone; pa, paracone; pas, parastyle.
Text-fig. 2. Field photograph of the sampling locality, together with a schematic profile. Stratigraphic horizon from which the fossil wood fragment was extracted (white arrow) (Modified from Pires and Da Rosa 2000). in A New Fossil Fabaceae Wood From The Pleistocene Touro Passo Formation Of Rio Grande Do Sul, Brazil
Text-fig. 2. Field photograph of the sampling locality, together with a schematic profile. Stratigraphic horizon from which the fossil wood fragment was extracted (white arrow) (Modified from Pires and Da Rosa 2000).
Text-fig. 1. Map of westernmost part of Rio Grande do Sul showing the position of the sampling locality (star). Adapted from Oliveira and Kerber (2009). in A New Fossil Fabaceae Wood From The Pleistocene Touro Passo Formation Of Rio Grande Do Sul, Brazil
Text-fig. 1. Map of westernmost part of Rio Grande do Sul showing the position of the sampling locality (star). Adapted from Oliveira and Kerber (2009).
Text-fig. 1. a – Discosauriscidae indet., DE K 396, skull in dorsal view. b – reconstruction of skull of DE K 396 in dorsal view. c – reconstruction of skull of Discosauriscus austriacus in dorsal view (on the basis of specimen Z 15529 from the locality Kochov-Horka, Boskovice Basin, deposited in the Slovak National Museum, Bratislava, Slovakia; Klembara 1997). in A New Find Of Discosauriscid Seymouriamorph From The Lower Permian Of Boskovice Basin In Moravia (The Czech Republic)
Text-fig. 1. a – Discosauriscidae indet., DE K 396, skull in dorsal view. b – reconstruction of skull of DE K 396 in dorsal view. c – reconstruction of skull of Discosauriscus austriacus in dorsal view (on the basis of specimen Z 15529 from the locality Kochov-Horka, Boskovice Basin, deposited in the Slovak National Museum, Bratislava, Slovakia; Klembara 1997).
Text-fig. 1. Geological overview map of Saar-Nahe Basin (modified from Stapf (1990) and Uhl et al. (2004)). Asterisk (✽) marks position of localities at Remigiusberg. in New Data On The Macroflora Of The Basal Rotliegend Group (Remigiusberg Formation; Gzhelian) In The Saar-Nahe Basin (Sw-Germany)
Text-fig. 1. Geological overview map of Saar-Nahe Basin (modified from Stapf (1990) and Uhl et al. (2004)). Asterisk (✽) marks position of localities at Remigiusberg.
Figs. 22–23. Collection localities for Brachistosternus Pocock, 1893 in The genus Brachistosternus (Scorpiones: Bothriuridae) in Chile, with Descriptions of Two New Species
Figs. 22–23. Collection localities for Brachistosternus Pocock, 1893 in Chile. 22. Los Vilos, 30 km S (near Pichidangui), habitat of Brachistosternus (L.) chango, n.sp. 23. Pan de Azúcar National Park, Sector Las Lomitas, habitat of Brachistosternus (L.) kamanchaca, n.sp.
Text-fig. 3. Tumidopteris astra sp. nov., holotype GIN 4851/343h, morphology of sori. a: part of fertile pinnule; b: one practically complete sorus located on the terminal part of a lateral vein; c: sorus with four visible sporangia; d: partly damaged sorus with three visible sporangia; e: two neighbouring sori. Locality: the borehole IK-675, depth 961.7 m. Scale 1 mm (a, b, e), 500 Μm (c), 100 Μm (d). in A New Species Of The Genus Tumidopteris Naugolnykh From The Permian Of The Pechora Cis-Urals, Russia
Text-fig. 3. Tumidopteris astra sp. nov., holotype GIN 4851/343h, morphology of sori. a: part of fertile pinnule; b: one practically complete sorus located on the terminal part of a lateral vein; c: sorus with four visible sporangia; d: partly damaged sorus with three visible sporangia; e: two neighbouring sori. Locality: the borehole IK-675, depth 961.7 m. Scale 1 mm (a, b, e), 500 Μm (c), 100 Μm (d).
Text-fig. 2. Tumidopteris astra sp. nov., macromorphology. a, c: sterile pinna, spec. GIN 4851/340; b, d: holotype GIN 4851/343h; e: sterile pinna, spec. GIN 4851/344. Localities: the city of Vorkuta, Section 49, layer 254 (a, c), the borehole IK-675, depth 961.7 m (b, d), the borehole IK-677, depth 147.8 m (e). Scale 1 cm (a, b, c, e), 1 mm (d). in A New Species Of The Genus Tumidopteris Naugolnykh From The Permian Of The Pechora Cis-Urals, Russia
Text-fig. 2. Tumidopteris astra sp. nov., macromorphology. a, c: sterile pinna, spec. GIN 4851/340; b, d: holotype GIN 4851/343h; e: sterile pinna, spec. GIN 4851/344. Localities: the city of Vorkuta, Section 49, layer 254 (a, c), the borehole IK-675, depth 961.7 m (b, d), the borehole IK-677, depth 147.8 m (e). Scale 1 cm (a, b, c, e), 1 mm (d).
Text-fig. 4. Bivariate plots of the upper teeth (M2 – P3) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1914, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2007), Holroyd (1999), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017). in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 4. Bivariate plots of the upper teeth (M2 – P3) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1914, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2007), Holroyd (1999), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017).
Text-fig. 3. Bivariate plots of the lower teeth (m3 – m2) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2003, 2007, 2008, 2010), Holroyd (1999), Morlo et al. (2007), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017). in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 3. Bivariate plots of the lower teeth (m3 – m2) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2003, 2007, 2008, 2010), Holroyd (1999), Morlo et al. (2007), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017).
Text-fig. 7. Bivariate plots of the upper teeth (M2, M1, P4) and lower teeth (m3, m2, p4) of large Miocene hyaenodonts from Eurasian and African localities. Data source: Stromer (1926), Savage (1965), Barry (1988), Ginsburg (1999), Holroyd (1999), Morales et al. (2003, 2007, 2008, 2010), Morlo et al. (2007), Rasmussen and Gutiérrez (2009), Borths et al. (2016). in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 7. Bivariate plots of the upper teeth (M2, M1, P4) and lower teeth (m3, m2, p4) of large Miocene hyaenodonts from Eurasian and African localities. Data source: Stromer (1926), Savage (1965), Barry (1988), Ginsburg (1999), Holroyd (1999), Morales et al. (2003, 2007, 2008, 2010), Morlo et al. (2007), Rasmussen and Gutiérrez (2009), Borths et al. (2016).
Text-fig. 9. Biostratigraphy of African Miocene localities, with the temporal ranges of the diverse species of hyaenodonts found therein. See Pickford (1986a), Pickford and Senut (2003), Reynoso (2014) and Werdelin (2010). in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 9. Biostratigraphy of African Miocene localities, with the temporal ranges of the diverse species of hyaenodonts found therein. See Pickford (1986a), Pickford and Senut (2003), Reynoso (2014) and Werdelin (2010).
Text-fig. 1. Geographical setting. Topographic map (swissALTI3D) showing the position of the Rigi localities (asterisks) in Central Switzerland. in Eomys Helveticus N. Sp. And Eomys Schluneggeri N. Sp., Two New Small Eomyids Of The Chattian (Mp 25/Mp 26) Subalpine Lower Freshwater Molasse Of Switzerland
Text-fig. 1. Geographical setting. Topographic map (swissALTI3D) showing the position of the Rigi localities (asterisks) in Central Switzerland.
Text-fig. 7. Molars referred to Karnimata fejfari sp. nov. from type locality Y 311. Right M2, a) YGSP 34588 and b) 54187, buccal upward. Lower teeth c) YGSP 34528 and d) 36166 both left m1, and e) 36170 and f) 54176, left and right m2; c–f figured lingual side upward. All teeth same scale. in Early Late Miocene Murine Rodents From The Upper Part Of The Nagri Formation, Siwalik Group, Pakistan, With A New Fossil Calibration Point For The Tribe Apodemurini (Apodemus/Tokudaia)
Text-fig. 7. Molars referred to Karnimata fejfari sp. nov. from type locality Y 311. Right M2, a) YGSP 34588 and b) 54187, buccal upward. Lower teeth c) YGSP 34528 and d) 36166 both left m1, and e) 36170 and f) 54176, left and right m2; c–f figured lingual side upward. All teeth same scale.
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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.