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Text-fig. 6. Occurrence of p3 in mandibles from brown bears, data after Table 3 (presence = p3 or alveoli observed, absence = no p3 developed, broken = diastema fragmented). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 6. Occurrence of p3 in mandibles from brown bears, data after Table 3 (presence = p3 or alveoli observed, absence = no p3 developed, broken = diastema fragmented).
Text-fig. 5. Occurrence of p1 in mandibles from brown bears, data after Table 3 (presence = p1 or alveoli observed, absence = no p1 developed, broken = diastema fragmented). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 5. Occurrence of p1 in mandibles from brown bears, data after Table 3 (presence = p1 or alveoli observed, absence = no p1 developed, broken = diastema fragmented).
Text-fig. 1. Occurrence of P1 in maxillae from brown bears, data after Table 1 (presence = P1 or alveoli observed, absence = no P1 developed, broken = rostral part of maxilla broken). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 1. Occurrence of P1 in maxillae from brown bears, data after Table 1 (presence = P1 or alveoli observed, absence = no P1 developed, broken = rostral part of maxilla broken).
Text-fig. 3. Occurrence of P1 in maxillae from Deninger bears and cave bears, data after Table 1 (presence = P1 or alveoli observed, absence = no P1 developed, broken = rostral part of maxilla broken). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 3. Occurrence of P1 in maxillae from Deninger bears and cave bears, data after Table 1 (presence = P1 or alveoli observed, absence = no P1 developed, broken = rostral part of maxilla broken).
Text-fig. 7. Occurrence of p1 in mandibles from Deninger bears and cave bears, data after Table 3 (presence = p1 or alveoli observed, absence = no p1 developed, broken = diastema fragmented). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 7. Occurrence of p1 in mandibles from Deninger bears and cave bears, data after Table 3 (presence = p1 or alveoli observed, absence = no p1 developed, broken = diastema fragmented).
Text-fig. 18. Carnivore chewing traces on medial trochlear ridge of humerus 98-594-A-Př (2), for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 18. Carnivore chewing traces on medial trochlear ridge of humerus 98-594-A-Př (2), for the metrics of this bone see Table 12.
Text-fig. 17. Percussion marks on the diaphysis of humerus 98-594-A-Předm, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 17. Percussion marks on the diaphysis of humerus 98-594-A-Předm, for the metrics of this bone see Table 12.
Text-fig. 15. Oblique cut marks on the mid-shaft of tibia 98-596-B (1) Př15/5 83, root traces visible on the shaft, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 15. Oblique cut marks on the mid-shaft of tibia 98-596-B (1) Př15/5 83, root traces visible on the shaft, for the metrics of this bone see Table 12.
Text-fig. 16. Impact marks on the ventral edge of mandible 98-583-C-Př5-90-92, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 16. Impact marks on the ventral edge of mandible 98-583-C-Př5-90-92, for the metrics of this bone see Table 12.
Text-fig. 13. "Repetive" marks on femur P12403 Předmostí 1928, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 13. "Repetive" marks on femur P12403 Předmostí 1928, for the metrics of this bone see Table 12.
Text-fig. 8. Disarticulation marks on tibia 98-589-B-Předmostí 1928, transversal cut marks on the tibial tuberosity and on the tibial crest are visible, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 8. Disarticulation marks on tibia 98-589-B-Předmostí 1928, transversal cut marks on the tibial tuberosity and on the tibial crest are visible, for the metrics of this bone see Table 12.
Text-fig. 10. Defleshing marks on femur 98-601a-D to cut loose the quadriceps femoris muscle, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 10. Defleshing marks on femur 98-601a-D to cut loose the quadriceps femoris muscle, for the metrics of this bone see Table 12.
Text-fig. 12. "Repetitive" marks on humerus P12404 Předmostí 1928, root traces visible on the shaft, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 12. "Repetitive" marks on humerus P12404 Předmostí 1928, root traces visible on the shaft, for the metrics of this bone see Table 12.
Text-fig. 6. Disarticulation marks on humerus 98-594-C-P (2) for disarticulation from the scapula, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 6. Disarticulation marks on humerus 98-594-C-P (2) for disarticulation from the scapula, for the metrics of this bone see Table 12.
Text-fig. 9. Defleshing marks on ulna 98-596-D on the olecranon related to the cutting of caput longum and the caput laterale of the m. triceps, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 9. Defleshing marks on ulna 98-596-D on the olecranon related to the cutting of caput longum and the caput laterale of the m. triceps, for the metrics of this bone see Table 12.
Text-fig. 7. Disarticulation marks on the neck of femur 98-598-D to dismember it from the hip joint, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 7. Disarticulation marks on the neck of femur 98-598-D to dismember it from the hip joint, for the metrics of this bone see Table 12.
Text-fig. 20. Carnivore puncture mark on tibia 97-597-C-Př82, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 20. Carnivore puncture mark on tibia 97-597-C-Př82, for the metrics of this bone see Table 12.
Text-fig. 5. Disarticulation marks on the head of humerus 98- 594-B-P (1) to disarticulate the shoulder joint, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 5. Disarticulation marks on the head of humerus 98- 594-B-P (1) to disarticulate the shoulder joint, for the metrics of this bone see Table 12.
Text-fig. 10. Phylogenetic relationships of Miocene hyaenodonts (for definitions of character states see Table 2). The data matrix was compiled in MacClade 4.05 and run in PAUP 4.0b10 (Macintosh version). We chose Cimolestes magnus CLEMENS et RUSSELL, 1965, (additional data from Lillegraven 1969), as the outgroup. The unordered and unweighted analysis produced 16 trees. a: Majority-rule consensus. b: Strict consensus. Consistency index (CI): 0.5882; Homoplasy index (HI): 0.4118; Retention index (RI): 0.7742. in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 10. Phylogenetic relationships of Miocene hyaenodonts (for definitions of character states see Table 2). The data matrix was compiled in MacClade 4.05 and run in PAUP 4.0b10 (Macintosh version). We chose Cimolestes magnus CLEMENS et RUSSELL, 1965, (additional data from Lillegraven 1969), as the outgroup. The unordered and unweighted analysis produced 16 trees. a: Majority-rule consensus. b: Strict consensus. Consistency index (CI): 0.5882; Homoplasy index (HI): 0.4118; Retention index (RI): 0.7742.
Text-fig. 13. Stereo occlusal views of SQU 290, juvenile left mandible of Omanitherium dhofarense, part of the holotype (scale bar 5 cm). Table 2. Measurements (in mm) of the teeth of Omanitherium dhofarense. in Large Mammals From The Rupelian Of Oman - Recent Finds
Text-fig. 13. Stereo occlusal views of SQU 290, juvenile left mandible of Omanitherium dhofarense, part of the holotype (scale bar 5 cm). Table 2. Measurements (in mm) of the teeth of Omanitherium dhofarense.
ScienceDex guides
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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.