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FIG. 1 in Bajocian (Middle Jurassic) ammonites of stratigraphical and palaeobiogeographical importance from Mombasa, Kenya, East Africa
FIG. 1. — The Upper Bajocian ammonite locality in East Africa (A), near Mombasa (B), where the Garantiana garantiana Zone elements (at MR 1) and the Strenoceras niortense Zone ammonites (at MR 2) were collected from the shales respectively above and below the dividing limestone of the Kambe Formation.
FIG. 5. — A, B in Bajocian (Middle Jurassic) ammonites of stratigraphical and palaeobiogeographical importance from Mombasa, Kenya, East Africa
FIG. 5. — A, B, Phylloceras trifoliatum Neumayr, 1871 MR 1, EMNH.2015.286; C, D, Phylloceras trifoliatum Neumayr, 1871 MR 2, EMNH.2015.285; E, F, Ptychophylloceras lardyi (Ooster, 1860) MR 1, EMNH.2015.303; G, H, Calliphylloceras disputabile (Zittel, 1868) MR 1, EMNH.2015.304; I, J, Holcophylloceras zignodianum (d'Orbigny, 1848) MR 1, EMNH.2015.259; K, L, Nannolytoceras polyhelictum (BÖckh, 1881) MR 2, EMNH.2015.257; M, N, Trimarginia sp. MR 2, EMNH.2015.279; O, P, Lissoceras oolithicum (d'Orbigny, 1845) MR 2, EMNH.2015.268; Q, R, Oecotraustes sp. MR 1, EMNH.2015.249; S,?Diplesioceras sp. MR 1, EMNH.2015.180; T, U, Cadomites (Cadomites) sp. MR 1, EMNH.2015.232; V, W, Normannites egyptiacus Arkell, 1952 MR 2, EMNH.2015.288; X, Y, Spiroceras annulatum (Deshayes, 1831) MR 2, EMNH.2015.287. Scale bar: 10 mm.
FIG. 2. — A in Bajocian (Middle Jurassic) ammonites of stratigraphical and palaeobiogeographical importance from Mombasa, Kenya, East Africa
FIG. 2. — A rock sample from the Upper Shaley member of the Kambe Formation (locality MR 1) showing the preservation of pyritic ammonite nucleus. Scale bar: 10 mm.
FIG. 3 in Bajocian (Middle Jurassic) ammonites of stratigraphical and palaeobiogeographical importance from Mombasa, Kenya, East Africa
FIG. 3. — Occasional preservation of big ammonite specimens (Lytoceras eudesianum eudesianum (d'Orbigny, 1846)), as shown here with an imprint in the Upper Shaley member of the Kambe Formation (locality MR 1). Scale bar: 10 mm.
FIG. 6. — A, B in Bajocian (Middle Jurassic) ammonites of stratigraphical and palaeobiogeographical importance from Mombasa, Kenya, East Africa
FIG. 6. — A, B, Lytoceras eudesianum eudesianum (d'Orbigny, 1846) MR 1, EMNH.2015.184; C, Masckeites cf. psilacanthoides (Sandoval, 1983) MR 2, EMNH.2015.278; D, Leptosphinctes cf. schmiereri (Bentz, 1924) MR 2, EMNH.2015.224. Scale bar: 10 mm.
FIG. 6 in Felidae from Cooper's Cave, South Africa (Mammalia: Carnivora)
FIG. 6. — Length of P3 plotted against anterior breadth of P3 for Felis nigripes (Burchell, 1824), Felis silvestris lybica Forster, 1780 and CD 675, Felis sp.
FIG. 5 in Felidae from Cooper's Cave, South Africa (Mammalia: Carnivora)
FIG. 5. — Craniodental felid specimens; A-D, Megantereon whitei (Broom, 1937); A, CD 5963, buccal view of right mandible; B, CD 5997, buccal view of left mandible; C, D, CD 10452 in buccal (C) and lingual (D) views of lower M; E, cf. Megantereon whitei, CD 10497, left upper I3 with two cusplets on medial surface; 1 F, G, Machairodontinae indet., CD 3835, right upper P3 in lingual (F) and occlusal (G) views; Acinonyx jubatus (Schreber, 1775), CD 3871, left upper P4 lacking protocone in occlusal (H) and lingual (I) views; J, K, Felis sp.: CD 675, right mandible with lower P3 and partial P4 in buccal (J) and lingual (K) views. Scale bars: 1 cm.
FIG. 4. — Log10 in Felidae from Cooper's Cave, South Africa (Mammalia: Carnivora)
FIG. 4. — Log10 total length of P4 plotted against metastyle length of the P4 for six African Dinofelis Zdansky, 1924 species. Data from Werdelin & Lewis (2001), Lacruz et al. (2006) and this study.
FIG. 2 in Felidae from Cooper's Cave, South Africa (Mammalia: Carnivora)
FIG. 2. — Postcranial specimens of Dinofelis cf. aronoki: A, B, right third metatarsal (CD 19953) in medial (A) and lateral (B) views; C-E, CD 3233, left tibia in lateral (C), medial (D) and superior views (E); F, G, CD 7359 right ulna fragment in lateral (F) and medial (G) views. Scale bars: 1 cm.
FIG. 1 in Felidae from Cooper's Cave, South Africa (Mammalia: Carnivora)
FIG. 1. — Craniodental specimens of Dinofelis cf. aronoki: A-C, CD 19961 in buccal (A), lingual (B) and occlusal (C) views; D, maxillary fragment CD 7323b, c, d in buccal view; E, CD 7323b, c, d in occlusal view; F, buccal view of P4 fragment CD 7323a, associated with 7323b, c, d; G, CD 16765a+b, right premaxilla fragment with roots of I1-I3; H, upper canine fragment CD 16769a+b; I, J, CD 15696, an isolated P3, in lingual (I) and buccal (J) views; K, L, CD 18836, right mandible with P4 and M1 in buccal (K) and occlusal (L) views; M, N, CD 19265, left M1 in mandible fragment in buccal (M) and occlusal (N) views. Scale bars: 1 cm.
Figure 9 in Micromammalian distribution and abundance in the Western Cape Province, South Africa, as evidenced by Barn owls Tyto alba (Scopoli)
Figure 9. Proportional representation of 3-month age classes (C1–8) of Otomys irroratus at Geelbek in the West Coast National Park by month and season.
Figure 10 in Micromammalian distribution and abundance in the Western Cape Province, South Africa, as evidenced by Barn owls Tyto alba (Scopoli)
Figure 10. Proportion of total measured Otomys irroratus individuals born per month at Geelbek in the West Coast National Park during 1984–8, based on material collected during 1985–8, compared with mean monthly rainfall at Langebaanweg for the same period.
Figure 8 in Micromammalian distribution and abundance in the Western Cape Province, South Africa, as evidenced by Barn owls Tyto alba (Scopoli)
Figure 8. Variation in (A) maxillary and (B) mandibular alveolar length in Tatera afra from selected sites with mean annual precipitation increasing from left to right. SFN and SFS, Steenbokfontein North and South (139 mm); AGA, Andriesgrond (248 mm); BBS, Blombos (464 mm); KFN, Kraaifontein (569 mm); STB, Stellenbosch Airfield (629 mm).
Figure 6 in Micromammalian distribution and abundance in the Western Cape Province, South Africa, as evidenced by Barn owls Tyto alba (Scopoli)
Figure 6. Dominant species in quarter-degree squares where the micromammalian sample comprises>100 individuals. Blank squares yielded samples of fewer than 100 individuals. Ch, Cryptomys hottentotus; Da, Desmodillus auricularis; Mm, Mus minutoides; Mv, Myosorex varius; Oi, Otomys irroratus; Rp, Rhabdomys pumilio; Sv, Suncus varilla; Ta, Tatera afra.
Figure 1 in Micromammalian distribution and abundance in the Western Cape Province, South Africa, as evidenced by Barn owls Tyto alba (Scopoli)
Figure 1. Location of the Western Cape Province in South Africa (A) and of Western Cape Province quarterdegree squares yielding Tyto alba pellet samples discussed in this paper (B).
Figure 5 in Micromammalian distribution and abundance in the Western Cape Province, South Africa, as evidenced by Barn owls Tyto alba (Scopoli)
Figure 5. Distribution of Gerbillinae (A, B) and Soricidae (C–F) whose remains have been found in Tyto alba pellets from 10 or more Western Cape Province quarter-degree squares. White circles indicate dominance in squares yielding remains of at least 100 individuals.
Figure 7 in Micromammalian distribution and abundance in the Western Cape Province, South Africa, as evidenced by Barn owls Tyto alba (Scopoli)
Figure 7. Significant correlation of seasonal variation in percentage representation of Suncus varilla and Steatomys krebsii and climate variables in the De Hoop Nature Reserve (Geelbek and Bottelary). (A) Same-season rainfall and proportions of S. varilla; (B) same-season minimum monthly temperature and S. krebsii; (C) previous-season minimum monthly temperature and S. varilla. See text for further details.
Figure 3 in Micromammalian distribution and abundance in the Western Cape Province, South Africa, as evidenced by Barn owls Tyto alba (Scopoli)
Figure 3. Distribution of Murinae whose remains have been found in Tyto alba pellets from 10 or more Western Cape Province quarter-degree squares. White circles indicate dominance in squares yielding remains of at least 100 individuals.
Figure 2 in Micromammalian distribution and abundance in the Western Cape Province, South Africa, as evidenced by Barn owls Tyto alba (Scopoli)
Figure 2. Distribution of Chrysochloridae (A), Macroscelididae (B), Bathyergidae (C, D) and Vespertilionidae (E) whose remains have been found in Tyto alba pellets from 10 or more Western Cape Province quarter-degree squares. White circles indicate dominance in squares yielding remains of at least 100 individuals.
Figure 4 in Micromammalian distribution and abundance in the Western Cape Province, South Africa, as evidenced by Barn owls Tyto alba (Scopoli)
Figure 4. Distribution of Otomyinae (A–C) and Dendromurinae (D–F) whose remains have been found in Tyto alba pellets from 10 or more Western Cape Province quarter-degree squares. White circles indicate dominance in squares yielding remains of at least 100 individuals.
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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.