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Fig. 1. Sanitheriid mammal Diamantohyus africanus Stromer, 1922 in Suidae and Sanitheriidae from Wadi Moghra, early Miocene, Egypt
Fig. 1. Sanitheriid mammal Diamantohyus africanus Stromer, 1922 from early Miocene of Wadi Moghra, Egypt. A. Palate of a young adult (WM 05−50) in buccal (A1) and occlusal (A2) views (arrow points to the palatine foramen opposite front of M2). B. Left mandible (DPC 6618), m2–3 in buccal (B1), occlusal (B2), and lingual (B3) views. C. Juvenile left mandible (DPC 8997), m1–2, p4 erupting in lingual (C1) and occlusal (C2) views. D. Juvenile right mandible (DPC 6469) with part of dp3, complete dp4 and m1, m2 in crypt in occlusal view.
Fig. 7 in Suidae and Sanitheriidae from Wadi Moghra, early Miocene, Egypt
Fig. 7. Length versus breadth scatter plots of suid molars from early Miocene of Wadi Moghra (black diamond) compared with early and middle Miocene suids from other localities in Africa. Abbreviations: A, Libycochoerus anchidens (Van der Made, 1996); B, Megalochoerus marymuunguae (Van der Made, 1996); J, Libycochoerus jeanneli (Arambourg, 1933); K, Nguruwe kijivium (Wilkinson, 1976); M, Libycochoerus massai Arambourg, 1961; N, Nguruwe namibensis (Pickford, 1986); Q, Kenyasus namaquensis Pickford and Senut, 1997; R, Kenyasus rusingensis Pickford, 1986; Z, Megalochoerus khinzikebirus (Wilkinson, 1976).
Fig. 3. Sanitheriid mammal Diamantohyus africanus Stromer, 1922 in Suidae and Sanitheriidae from Wadi Moghra, early Miocene, Egypt
Fig. 3. Sanitheriid mammal Diamantohyus africanus Stromer, 1922 from early Miocene of Wadi Moghra, Egypt. A. Left mandible (DPC 12599) preserving both central incisors, and left i2–p2, roots of p3, p4 and anterior root of m1 in buccal (A1), occlusal (A2), and lingual (A3) views. B. Edentulous symphysis (DPC 14581) in inferior (B1) and superior (B2) views.
Fig. 6 in Suidae and Sanitheriidae from Wadi Moghra, early Miocene, Egypt
Fig. 6. Kubanochoerin suid cf. Libycochoerus sp. (size of Libycochoerus jeanneli and Libycochoerus anchidens) sensu Drake et al. (1988) from early Miocene of Wadi Moghra, Egypt, (DPC 8947), left mandible fragment with wind−abraded m1–m3 in buccal (A), occlusal (B), and lingual (C) views.
Fig. 2. Sanitheriid mammal Diamantohyus africanus Stromer, 1922 in Suidae and Sanitheriidae from Wadi Moghra, early Miocene, Egypt
Fig. 2. Sanitheriid mammal Diamantohyus africanus Stromer, 1922 from early Miocene of Wadi Moghra, Egypt, snout (DPC 17688) in right lateral (A), occlusal (B), left lateral (C), anterior (D), and superior (E) views (note palatine foramina opposite middle of M2).
Fig. 15 in Kasimovian (late Pennsylvanian) cornute rugose corals from Egypt: taxonomy, facies and palaeogeography of a cool-water fauna from northern Gondwana
Fig. 15 Depositional environments of the Aheimer Formation (lower member). A Microphotograph of calcareous silty mudstone; disarticulated crinoid ossicles (Cr), tiny shell fragments (in part ostracods) and indeterminable microbioclasts associated with silt-sized quartz grains, all set in a ferruginous calcareous cement. B Microphotograph of silty dolostone; large brachiopod shell (B), crinoid ossicles (Cr) and other undifferentiated fossil fragments, all altered and dolomitized, associated with silt-sized quartz grains. Brownish-black ferruginous oxides are filling the pore spaces. C, D Microphotographs of calcareous siltstone bearing crinoids (Cr), bryozoa (Br) and other altered fossil fragments. All components set in ferruginous– calcareous cement. E, F Vertical, elongated burrows of the Tisoa siphonalis in mudstone in the uppermost part of the lower member of the Aheimer Formation
Fig. 1 in Short communication Antecedent description and depiction of the recently described cetacean behaviour of trap/tread-water feeding inferred from a nineteenth-century sighting of a 'sea monster' in the Gulf of Suez, Egypt
Fig. 1 - Illustration of a nineteenth-century encounter with a purported sea monster observed in the Gulf of Suez (Andrews, 1879). The vertical body position and open mouth of what is obviously a baleen whale (the rightward animal in the group) closely resembles the photographs and digital reconstructions of the recently described, so-called 'new' or 'first' descriptions of the stationary hunting behaviour of trap/tread-water feeding, as shown in Iwata et al. (2017), McMillan et al. (2018), McCarthy et al. (2023a, 2023b), and Lu (2023). The illustration, drawn in concordance to the eyewitness report, is emblematic of the instance of such whales 'rapidly closing them [their mouths] to trap prey' (McCarthy et al., 2023a). Note the presence of seabirds, something common to all modern recorded instances of such feeding documented in humpback whales, an association which may be related to shoaling fish being driven to seek the apparent shelter of the whale's open mouth (McMillan et al., 2018).
MADFORWATER: WP1: Water and water-related vulnerabilities in Egypt, Morocco and Tunisia: Task1.2: Analysis and mapping of water stress, water vulnerability and potential for water reuse in Egypt, Morocco and Tunisia: Subtask1.2.b: Data collection on water stress and vulnerability: Souss-Massa Region Subset
<p>This folder contains the dataset that I used to write my conference paper "Groundwater Resources Scarcity in Souss-Massa Region and Alternative Solutions for Sustainable Agricultural Development"</p>
Figure 1 in Collyriclum faba (Digenea: Collyriclidae) in migrant Phylloscopus trochilus (Aves: Sylvidae) in Egypt: the first record of the parasite on the African continent
Figure 1. Subcutaneous cysts with Collyriclum faba in the leg (A) and head (B) of Phylloscopus trochilus found naturally infected in Egypt. Photos by I Rząd, Wadi Allaqi, Egypt, 24 September 2012.
Figure 3 in Tintinnina (Ciliophora) and Foraminifera in plankton of hypersaline Lagoon Bardawil (Egypt): spatial and temporal variability
Figure 3. Dependence of number of found tintinnid species on number of analyzed samples in Lagoon Bardawil (a) and the Mediterranean Sea (b).
Figure 2 in Tintinnina (Ciliophora) and Foraminifera in plankton of hypersaline Lagoon Bardawil (Egypt): spatial and temporal variability
Figure 2. Dependence of total tintinnid abundance on number of tintinnid species in Lagoon Bardawil during 2009 and 2010 (a- winter, b- all seasons).
Figures 1–4 in Mesostigmata mites (Acari: Parasitiformes) associated with birds and their nests from Egypt
Figures 1–4. Kleemannia nova Nasr & Abou-Awad, 1986: 1- General view of dorsum; 2- close-up of anterodorsal area showing the fanlike vertical setae; 3. Blattisocius keegani Fox, 1947, dorsal view, and the one-toothed movable digit of chelicera (bottom right); 4- Blattisocius tarsalis (Berlese, 1918), dorsal view, and the tridentate movable digit of chelicera (bottom right). Scale bars = 100 µm.
Fig. 4 in A new species of the neopterygian fish Enchodus from the Duwi Formation, Campanian, Late Cretaceous, Western Desert, central Egypt
Fig. 4. Majority rule consensus of 222 equally parsimonious trees (TL = 263, CI = 0.53, HI = 0.47, RI = 0.75, and RC = 0.4). Numbers next to branches indicate the percentage of trees in which each clade is present.
Fig. 3 in A new species of the neopterygian fish Enchodus from the Duwi Formation, Campanian, Late Cretaceous, Western Desert, central Egypt
Fig. 3. Digital reconstructions of the aulopiform teleost Enchodus tineidae sp. nov. holotype (MUVP 59) from the Campanian of central Egypt. Right dentary showing its caudal extent, otherwise obscured by matrix, in lateral (A) and medial (B) views. Caudal portion of the left anguloarticular in lateral view (C), showing its dorsal aspect, otherwise obscured by matrix. Right ectopterygoid showing its caudal extent and dorsal aspect, otherwise obscured by matrix, in lateral (D), caudodorsal (E), showing V-shaped trough for articulation with the dermopalatine, and medial (F) views. Abbreviations: d, dentary tooth; E, ectopterygoid tooth; numbers 1–13 indicate tooth position in the respective bone.
Fig. 2 in A new species of the neopterygian fish Enchodus from the Duwi Formation, Campanian, Late Cretaceous, Western Desert, central Egypt
Fig. 2. Aulopiform teleost Enchodus tineidae sp. nov. holotype (MUVP 59) from the Campanian of central Egypt. A, B. Photographs of specimen in lateral (A1) and medial (B1) views; photographs with identifiable elements outlined, in lateral (A2) and medial (B2) views. C. Close up of denticles of the lateral tooth row.
Fig. 7 in A new Oligocene site with terrestrial mammals and a selachian fauna from Minqar Tibaghbagh, the Western Desert of Egypt
Fig. 7. Bivariate plots of Phiomia sp. cheek teeth from the BOTM, early Oligocene, Minqar Tibaghbagh, Qattara Depression, Egypt (stars) compared with Phiomia spp. from the early Oligocene Jebel Qatrani Formation, Fayum Depression, Egypt (diamonds) and Phiomia major from the late Oligocene, Chilga Formation of the Chilga Region, Ethiopia (triangles). Comparative dimensions of Phiomia serridens from Matsumoto (1924: 48, tables B, C, E, G); dimensions of Phiomia major from Sanders et al. (2004: table 2). A. M3? (or M2?) and M3?, originally the latter molar would have been larger in width (see text). B. m3, the width is based on estimated dimensions.
Fig. 12. A–C in A new Oligocene site with terrestrial mammals and a selachian fauna from Minqar Tibaghbagh, the Western Desert of Egypt
Fig. 12. A–C. Carcharhiniformes and Myliobatiformes from the BOTM, early Oligocene, Minqar Tibaghbagh, Qattara Depression, Egypt; photographed and left in the field. A. Carcharhinus sp., incomplete upper tooth in lingual view. B, C. "Aetobatus" sp. B. Lower tooth in occlusal (B1) and basal (B2) views. C. Lower tooth in occlusal view. D–M. Carcharhiniformes and Lamniformes from the BOS, early Oligocene, Minqar Tibaghbagh, Qattara Depression, Egypt. D. Hemipristis cf. serra Agassiz, 1835 (1843) (CGM67195), upper lateral teeth in lingual (D1, D2, D4) and labial (D3) views. E. Carcharhinus cf. perseus Adnet, Antoine, Hassan Baqri, Crochet, Marivaux, Welcomme, and Métais, 2007 (CGM67194), upper antero-lateral teeth in lingual view. F. Carcharhinus sp. (CGM67195), upper teeth in lingual (F1, F4, F5, F6) and labial (F2, F3) views. G. Negaprion frequens (Dames, 1883) (CGM67191), lower teeth in lingual (G1, G3, G4) and lateral (G2, G5) views. H. Galeocerdo sp. (CGM67195) in lingual view. I–L. Otodus (Carcharocles) cf. sokolowi. I. CGM67195, upper tooth in lingual view. J. CGM69186 upper tooth in lingual (J1) and labial (J2) views. K. CGM69186, lower tooth in labial view. L. CGM69186, lower tooth in lingual (L1) and labial (L2) views. M. Carcharias? sp. (CGM67195), lower teeth in lateral (M1) and lingual (M2) views.
Fig. 8 in A new Oligocene site with terrestrial mammals and a selachian fauna from Minqar Tibaghbagh, the Western Desert of Egypt
Fig. 8. Left hyracoid astragalus, cf. Antilohyrax sp. (CGM67188) from the BOTM, early Oligocene, Minqar Tibaghbagh, Qattara Depression, Egypt, in plantar (A), lateral (B), and mediodorsal (C) views (photographs: A1–C1; explanatory drawings: A2–C2). D. Outline drawing of Antilohyrax pectidens from the Fayum Depression, Egypt in dorsal view, showing the similarities with the astragalus from Minqar Tibaghbagh (based on Rasmussen and Simons 2000: fig. 6b). Arrows point at the characteristic saddle-shaped navicular facet, broken parts indicated by dotted lines.
Fig. 3 in A new Oligocene site with terrestrial mammals and a selachian fauna from Minqar Tibaghbagh, the Western Desert of Egypt
Fig. 3. Comparison between Eocene and Oligocene strata at Minqar Tibaghbagh, El-Qara, El-Arag, and the Fayum Depression, Egypt.
Fig. 10 in A new Oligocene site with terrestrial mammals and a selachian fauna from Minqar Tibaghbagh, the Western Desert of Egypt
Fig. 10. Right anthracotheriid astragalus, cf. Bothriogenys sp. from the BOTM, early Oligocene, Minqar Tibaghbagh, Qattara Depression, Egypt, in plantar (A), lateral (B), and dorsal (C) views (photographs, A1–C1; explanatory drawings, A2–C2). Missing, reconstructed parts indicated by dotted lines. Drawings reconstructed by projection on pictures from Sileem and Hewaidy (2015: fig. 5B2, B4, B1, respectively).
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Allen Brain Atlas
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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.
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