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Fig. 5 in Systematic and biostratigraphic significance of a chinchillid rodent from the Pliocene of eastern Argentina
Fig. 5. The chinchillid rodent Lagostomus (Lagostomopsis) incisus (Ameghino, 1888) from the Chapadmalal Formation, Buenos Aires Province, Argentina (early Late Pliocene). A. MLP 91−IV−5−258, skull in ventral (A1), dorsal (A2) and lateral (A3) views. B. MLP 88−VI−1−2, palate with right P4–M3 and left P4–M2 in ventral view (B1), and left mandible with p4–m3 in occlusal (B2) and labial (B3) views. C. MLP 91−IV−5−214, left mandible with p4–m2 in occlusal (C1) and labial (C2) views.
Fig. 8 in Systematic and biostratigraphic significance of a chinchillid rodent from the Pliocene of eastern Argentina
Fig. 8. Differences between Lagostomus (Lagostomopsis) incisus (Ameghino, 1888) from the Pliocene of Buenos Aires Province, Argentina (A, B, D, E) and the living Lagostomus maximus (Desmarest, 1817) (C, F). A–C. Skulls in ventral view. A. MLP 91−IV−5−258, juvenile. B. MLP 91−III−1−18, adult. C. MACN−Mz 49.48, adult. D–F. Mandibles in occlusal view. D. MLP 94−II−1−146, juvenile. E. MLP 91−III−1−9 adult. F. MACN−Mz 49.48, adult.
Fig. 4 in Systematic and biostratigraphic significance of a chinchillid rodent from the Pliocene of eastern Argentina
Fig. 4. The chinchillid rodent Lagostomus (Lagostomopsis) incisus (Ameghino, 1888) from the Irene "Formation", Buenos Aires Province, Argentina (late Early–early Late Pliocene). A. MLP 91−III−1−18, skull with complete tooth rows in ventral (A1), dorsal (A2), and lateral (A3) views. B. MLP 63−VI−10−59, partial skull with complete tooth rows in ventral (B1) and dorsal (B2) views. C. MLP 91−III−1−36, palate with complete tooth rows. D. MLP 94−II−1−136, palate with complete tooth rows. E. MLP 91−III−1−9, right mandible with p4–m3 in occlusal (E1) and labial (E2) views. F. MLP 91−III−1−88, mandibles with complete tooth rows in occlusal (F1) and labial (F2) views, and left humerus (F3) in anterior view.
Fig. 7 in Systematic and biostratigraphic significance of a chinchillid rodent from the Pliocene of eastern Argentina
Fig. 7. Scatterplot of transverse and anteroposterior diameters of the upper (A) and lower (B) incisors of Lagostomus (Lagostomopsis) incisus (gray squares), and Lagostomus maximus male (black circles) and female (open circles) specimens.
Fig. 1 in Systematic and biostratigraphic significance of a chinchillid rodent from the Pliocene of eastern Argentina
Fig. 1. Map of Buenos Aires Province, Argentina (A), showing the localities mentioned in the text (B). Black circles indicate fossil localities, while open circles indicate towns and cities.
Fig. 6 in Systematic and biostratigraphic significance of a chinchillid rodent from the Pliocene of eastern Argentina
Fig. 6. The chinchillid rodent Lagostomus (Lagostomopsis) incisus (Ameghino, 1888) from the Irene "Formation", Buenos Aires Province, Argentina (late Early–early Late Pliocene); MLP 94−II−1−146. A. Mandibles with incisors and complete tooth rows in occlusal (A1) and labial (A2) views. B. Right mandible with p4–m3 in occlusal (B1) and labial (B2) views. C. Right maxilla with P4–M3 in ventral view. D. Right humerus in anterior view.
Fig. 3 in A new turtle species of Brodiechelys from the Early Cretaceous of Spain: Systematic and palaeobiogeographic implications
Fig. 3. Phylogenetic hypotheses of the new taxon Brodiechelys royoi based on the modified data set of Sterli and de la Fuente (2011) proposed here (A), and on the data matrix proposed by Tong et al. (2012) (B). Values refer percentages under 100% obtained in the majority rule analyses.
Fig. 2 in A new turtle species of Brodiechelys from the Early Cretaceous of Spain: Systematic and palaeobiogeographic implications
Fig. 2. Type specimens of Brodiechelys royoi sp. nov. from Morella (Castellón, Spain). A. CMP-3b/181, holotype, shell in dorsal (A1, A2) and ventral (A3, A4) views. B. CMP-3c/293, second right costal plate in dorsal (B1, B2) and ventral (B3, B4) views. C. CMP-3c/122, first right costal in dorsal (C1, C2) and ventral (C3, C4) views.
Fig. 1 in A new turtle species of Brodiechelys from the Early Cretaceous of Spain: Systematic and palaeobiogeographic implications
Fig. 1. Geographical location of Morella (Castellón, Spain), the type locality of Brodiechelys royoi.
Fig. 5 in Cranial morphology, systematics and succession of beavers from the middle Miocene Valentine Formation of Nebraska, USA
Fig. 5. The beaver Prodipoides burgensis (Korth, 2002) from the middle Miocene Valentine Formation of Nebraska, USA. A. UNSM 49029, left p4–m3, from the Crookston Bridge Member in occlusal (A1) and medial (A2) views. B. FAM 64857, left p4–m2, from Devil's Gulch Member. Anterior to right.
Fig. 4 in Cranial morphology, systematics and succession of beavers from the middle Miocene Valentine Formation of Nebraska, USA
Fig. 4. The beavers from the middle Miocene Valentine Formation of Nebraska, USA. A–C. Monosaulax skinneri Stout, 1999. D–F. Prodipoides dividerus (Stirton, 1935). Cheek teeth: A. FAM 64315, right p4–m2 from Devil's Gulch Member in occlusal (A1) and medial (A2) views. B. FAM 64317, right p4–m2 from Devil's Gulch Member. C. UNSM 49027, left P4–M3 from Crookston Bridge Member. D. FAM 64319, left p4–m3 from Devil's Gulch Member; in occlusal (D1) and medial (D2) views. E. FAM 64316, right p4–m2 from Devil's Gulch Member. F. FAM 64314, right p4–m2 (partial) from Crookston Bridge Member. Anterior to left for specimens of M. skinneri, anterior to right for specimens of P. dividerus.
Fig. 8 in Cranial morphology, systematics and succession of beavers from the middle Miocene Valentine Formation of Nebraska, USA
Fig. 8. The beaver Temperocastor valentinensis (Stout, 1999), specimen UNSM 45392 from the Crookston Bridge Member equivalent at Myers Farm Quarry. Cranium in dorsal (A) and right lateral (B) views. C. Mandible in lateral view. Anterior to right.
Fig. 7. The beavers. A, B in Cranial morphology, systematics and succession of beavers from the middle Miocene Valentine Formation of Nebraska, USA
Fig. 7. The beavers. A, B. Eucastor tortus (Leidy, 1858) from th latest Barstovian Devil's Gulch Member of the Valentine Formation. C, D. Temperocastor valentinensis (Stout, 1999) from the late Barstovian Crookston Bridge Member equivalent of the Valentine Formation. Cheek teeth: A. FAM 65262, right p4–m2 in occlusal (A1) and medial (A2) views. B. CM 18876, left p4–m2. C. UNSM 46392, right P4–M3. D. UNSM 45385, right p4–m3. A, B, anterior to left; C, D, anterior to right.
Fig. 6 in Cranial morphology, systematics and succession of beavers from the middle Miocene Valentine Formation of Nebraska, USA
Fig. 6. The beavers from the middle Miocene Valentine Formation of Nebraska, USA. A. Prodipoides burgensis (Korth, 2002). B. Eucastor tortus (Leidy, 1858). Left mandibles in lateral view. A. FAM 64857, from Crookston Bridge Member. B. FAM 64966, from the Devil's Gulch Member.
Fig. 3. The beaver Monosaulax skinneri Stout, 1999, specimen UNSM 49028 in Cranial morphology, systematics and succession of beavers from the middle Miocene Valentine Formation of Nebraska, USA
Fig. 3. The beaver Monosaulax skinneri Stout, 1999, specimen UNSM 49028 from the middle Miocene Valentine Formation of Nebraska, USA. Posterior fragment of skull. A. Cranial basis in ventral view (anterior to the top). B. Occipital plate in posterior view.
Fig. 1 in Cranial morphology, systematics and succession of beavers from the middle Miocene Valentine Formation of Nebraska, USA
Fig. 1. Generalized stratigraphic section of the middle Miocene Valentine Formation in northern Nebraska (modified after Skinner and Johnson 1984: fig. 4 and Tedford et al. 2004: fig. 6.2). Striped area represents time gap of unconformity between members.
Fig. 9 in Cranial morphology, systematics and succession of beavers from the middle Miocene Valentine Formation of Nebraska, USA
Fig. 9. Occurrence of the castoroidine species through the middle Miocene Valentine Formation of Nebraska. Width of members not intended to represent time or stratigraphic thickness of layers. Arrows indicate continued occurrence in superjacent layers.
Fig. 4 in Systematic relationships of the blind phacopine trilobite Trimerocephalus, with a new species from Causses-et-Veyran, Montagne Noire
Fig. 4. Trimerocephalus (Trifoliops) trifolius (Osmólska, 1958) subgen. nov. Montagne Noire, France, Famennian, Upper Devonian. A. Reconstruction of a mature cephalon, in dorsal view. B. Reconstruction of a young cephalon, in dorsal view. Scale bars 1 mm.
Fig. 3. A in Systematic relationships of the blind phacopine trilobite Trimerocephalus, with a new species from Causses-et-Veyran, Montagne Noire
Fig. 3. A. Trimerocephalus (Trifoliops) trifolius (Osmólska, 1958) subgen. nov. Montagne Noire, France, Famennian, Upper Devonian. Reconstruction of the cephalon, in dorsal (A1) and in ventral (A2) views. B. Trimerocephalus (Trifoliops) nigritus subgen. et sp. nov. Montagne Noire, France, Famennian, Upper Devonian. Reconstruction of the cephalon, in dorsal (B1) and in ventral (B2) views. Scale bars 1 mm.
Fig. 5 in Systematic relationships of the blind phacopine trilobite Trimerocephalus, with a new species from Causses-et-Veyran, Montagne Noire
Fig. 5. Scatter diagram of length (cm) versus width (cm) of cephalon and glabella in specimens of Trimerocephalus (Trifoliops) trifolius (Osmólska, 1958) subgen. nov, Trimerocephalus (Trifoliops) nigritus subgen. et sp. nov. and Trimerocephalus? trifolius, the specimen ilustrated (ZPAL Tr. D. I/16) by Osmólska in 1963.
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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.