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Fig. 2 in A huge caseid pelycosaur from north-western Sardinia and its bearing on European Permian stratigraphy and palaeobiogeography
Fig. 2. Stratigraphy of the three major Permian and Triassic sequences of Nurra. BC, basal conglomerate.
Fig. 11 in A new titanosaur sauropod dinosaur from the Upper Cretaceous of North Patagonia, Argentina
Fig. 11. Posterior appendicular skeleton of the titanosaur sauropod Narambuenatitan palomoi gen. et sp. nov. from the Campanian (Late Cretaceous) Anacleto Formation of Neuquén Province, Argentina; MAU−Pv−N− 425 (holotype). A. Left femur in posterior (A1) and distal (A2) views. B. Left pubis in ventral view. C. Left ischium in ventral view. D. Peduncle of the left ilium in posterolateral (D1) and medial (D2) views.
Fig. 10 in A new titanosaur sauropod dinosaur from the Upper Cretaceous of North Patagonia, Argentina
Fig. 10. Anterior appendicular skeleton of the titanosaur sauropod Narambuenatitan mm palomoi gen. et sp. nov. from the Campanian (Late Cretaceous) Anacleto For− 100 mation of Neuquén Province, Argentina; MAU−Pv−N−425 (holotype). A. Left ulna in lateral (A1), proximal (A2), and distal (A3) views. B. Left humerus in anterior (B1) and posterior (B2) views. C. Right coracoid in lateral view. D. Left sternal plate in anterior view.
Fig. 8 in A new titanosaur sauropod dinosaur from the Upper Cretaceous of North Patagonia, Argentina
Fig. 8. Anterior caudal vertebrae of the titanosaur sauropod Narambuenatitan palomoi gen. et sp. nov. from the Campanian (Late Cretaceous) Anacleto Formation of Neuquén Province, Argentina; MAU−Pv−N−425 (holotype). A. First caudal vertebra in anterior (A1), lateral (A2), and posterior (A3) views. B–F. Anterior caudal vertebrae in left lateral (B, C, D) and in rigth lateral (E, F) views.
Fig. 7 in A new titanosaur sauropod dinosaur from the Upper Cretaceous of North Patagonia, Argentina
Fig. 7. Posterior dorsal vertebra of the titanosaur sauropod Narambuenatitan palomoi gen. et sp. nov. from the Campanian (Late Cretaceous) Anacleto Formation of Neuquén Province, Argentina; MAU−Pv−N−425 (holotype), in anterior (A), posterior (B), dorsal (C), and lateral (D) views.
Fig. 9 in A new titanosaur sauropod dinosaur from the Upper Cretaceous of North Patagonia, Argentina
Fig. 9. Middle caudal vertebrae of the titanosaur sauropod Narambuenatitan palomoi gen. et sp. nov. from the Campanian (Late Cretaceous) Anacleto Formation of Neuquén Province, Argentina; MAU−Pv−N−425 (holotype). A–D. Middle caudals in rigth lateral views.
Fig. 6 in A new titanosaur sauropod dinosaur from the Upper Cretaceous of North Patagonia, Argentina
Fig. 6. Anterior cervical vertebra of the titanosaur sauropod Narambuenatitan palomoi gen. et sp. nov. from the Campanian (Late Cretaceous) Anacleto Formation of Neuquén Province, Argentina; MAU−Pv−N−425 (holotype), in lateral (A) and posterior (B) views.
Fig. 3 in A new titanosaur sauropod dinosaur from the Upper Cretaceous of North Patagonia, Argentina
Fig. 3. Braincase of the titanosaur sauropod Narambuenatitan palomoi gen. et sp. nov. from the Campanian (Late Cretaceous) Anacleto Formation of Neuquén Province, Argentina; MAU−Pv−N−425 (holotype), in lateral (A), dorsal (B), and caudal (C) views.
Fig. 5 in A new titanosaur sauropod dinosaur from the Upper Cretaceous of North Patagonia, Argentina
Fig. 5. Quadrate of the titanosaur sauropod Narambuenatitan palomoi gen. et sp. nov. from the Campanian (Late Cretaceous) Anacleto Formation of Neuquén Province, Argentina; MAU−Pv−N−425 (holotype), in posterior (A) and medial (B) views.
Fig. 2 in A new titanosaur sauropod dinosaur from the Upper Cretaceous of North Patagonia, Argentina
Fig. 2. Stratigraphic column of the Campanian (Upper Cretaceous) Anacleto Formation in the Narambuena area, showing fossiliferous levels.
Fig. 4 in A new titanosaur sauropod dinosaur from the Upper Cretaceous of North Patagonia, Argentina
Fig. 4. Premaxilla−maxilla of the titanosaur sauropod Narambuenatitan palomoi gen. et sp. nov. from the Campanian (Late Cretaceous) Anacleto Formation of Neuquén Province, Argentina; MAU−Pv−N−425 (holotype), in ventral (A) and medial (B) views.
Fig. 2 in Anisodontherium from the Late Miocene of north-western Argentina
Fig. 2. Megatheriine Anisodontherium sp. (PVL 6425), Cerro Castillo de Las Brujas, Tucumán Province, Argentina. Saladillo Formation (Upper Miocene). A–C. Mandible in left lateral (A), right lateral (B), and occlusal (C) views. D. Digit III of the manus in lateral view.
Fig. 3 in Anisodontherium from the Late Miocene of north-western Argentina
Fig. 3. Lower molariforms of megatheriines in occlusal view. A. Anisodontherium sp. (PVL 6425), Cerro Castillo de Las Brujas, Tucumán Province, Argentina. Saladillo Formation (Upper Miocene). B. Pyramiodontherium Rovereto, 1914 (MLP 31−XI−12−25), Bajo de Andalhuala, Catamarca Province, Andalhuala Formation (Upper Miocene). C. Megatherium Cuvier, 1796 (CICYTTP−PV−M−2−356), Entre Ríos Province, Tezanos Pinto Formation (Upper Pleistocene). Explanatory drawings (A1–C1), photographs (A2–C2).
Fig. 2 in The first giant titanosaurian sauropod from the Upper Cretaceous of North America
Fig. 2. Size comparison of Alamosaurus sanjuanensis (Gilmore, 1922) with Futalognkosaurus dukei Calvo, Porfiri, Gonzalez−Riga, and Kellner, 2007a from the Turonian, Argentina. A. A. sanjuanensis caudal vertebrae 2–4 from North Horn specimen (Gilmore 1946: pl. 8). B. A. sanjuanensis caudal vertebra (probably third or fourth) SMP VP−2104 in posterior view. C. Futalognkosaurus dukei caudal vertebra?2, MUCPv−323, in anterior view (after Calvo et al. 2007b).
Fig. 1 in The first giant titanosaurian sauropod from the Upper Cretaceous of North America
Fig. 1. Size comparison of Alamosaurus sanjuanensis (Gilmore, 1922) with Puertasaurus reuili Novas, Salgado, Calvo, and Agnolin, 2005 from the Lower Maastrichtian, Argentina. A. Alamosaurus sanjuanensis cervical vertebra, SMP VP−1850, in posterior (A1) and right lateral (A2) views. B. Puertasaurus reuili cervical vertebra, MPM 10002, in posterior (B1) and right lateral (B2) views (after Novas et al. 2005). C. Alamosaurus sanjuanensis distal end of left femur SMP VP−1625.
Fig. 1. A in Anisodontherium from the Late Miocene of north-western Argentina
Fig. 1. A. Map of Argentina showing the distribution of fossil Megatheriinae during the Late Miocene–Pliocene. 1, Abra Pampa (Jujuy Province); 2, Saladillo Formation (Tucumán Province); 3, Andalhuala and Corral Quemado formations (Catamarca Province); 4, Toro Negro Formation (La Rioja Province); 5, Huayquerías de San Carlos (Mendoza Province); 6, "conglomerado osífero", Ituzaingó Formation (Entre Ríos Province); 7, Arroyo Chasicó Formation (Buenos Aires Province); 8, Río Negro Formation (Río Negro Province). B. Geologic map of Cerro Castillo de Las Brujas area (Tucumán Province). C. Schematic profile of the sequence indicating the position of the fossiliferous level and the dated tuff.
Fig. 2 in Molecular detection of Cryptosporidium parvum in wild rodents (Phyllotis darwini) inhabiting protected and rural transitional areas in north-central Chile
Fig. 2. Phylogram representing analysis of the 18 rRNA region. The evolutionary history was inferred with maximum likelihood method and the Tamura 3-parameter (T92) model with a discrete Gamma distribution (5 categories (+G)). Analysis contains sequences uploaded from GenBank (with Cryptosporidium species, host, country, and accessions numbers in brackets) and those obtained in the present study are shown in triangles (with ID isolate, host, site of sampling and country, and accessions numbers in brackets). Bootstrap values are represented as per cent of internal branches (1000 replicates), and values lower than 50 are hidden. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. Cryptosporidium muris was used to root the tree.
Fig. 1 in Molecular detection of Cryptosporidium parvum in wild rodents (Phyllotis darwini) inhabiting protected and rural transitional areas in north-central Chile
Fig. 1. Map of the Coquimbo region in Chile showing the two types of areas (i.e., Bosque Fray Jorge National Park - BFPNP [in green]; El Tangue Farm [in blue]) in which Darwin's leaf-eared mice (Phyllotis darwini) were sampled. In each area, 4 grids were established, and 200 capture points were allocated per grid. (UTM projection. Datum WGS84, Zone 19J).
Fig. 11 in Discovering high species diversity of Ophiotaenia tapeworms (Cestoda: Proteocephalidae) of watersnakes (Colubridae) in North America
Fig. 11. Maximum likelihood phylograms of cox1 data (Alignment 4; 549 nt) for selected members of the Proteocephalidae. Bootstrap support from maximum likelihood (ML) and Bayesian inference (BI) nodal support are indicated as ML/BI; values <0.90 (BI) and <70 (ML) are not shown. The scale bar indicates the expected number of substitutions per site. The newly generated sequences are highlighted in bold. Abbreviations of the U.S. states where the samples were collected: AR – Arkansas; MS – Mississippi; OK – Oklahoma. Abbreviations of biogeographical regions: NEA – Nearctic; NEO – Neotropical.
Fig. 9 in Discovering high species diversity of Ophiotaenia tapeworms (Cestoda: Proteocephalidae) of watersnakes (Colubridae) in North America
Fig. 9. Maximum likelihood phylogram based on 28S rDNA data for selected members of the Proteocephalidae. Bootstrap support from maximum likelihood (ML) and Bayesian inference (BI) nodal support are indicated as ML/BI; values <0.90 (BI) and <70 (ML) are not shown. The scale bar indicates the expected number of substitutions per site. The newly generated sequences are highlighted in bold. The hosts are indicated by silhouettes. The sequence of O. europaea obtained from a fish intermediate host is indicated by an asterisk. Abbreviations of the U.S. states where the samples were collected: AR – Arkansas; MS – Mississippi; OK – Oklahoma. Abbreviations of biogeographical regions: NEA – Nearctic; NEO – Neotropical; PAL – Palaearctic.
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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.