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Figure 3 in Large dendrinids meet giant clam: the bioerosion trace fossil Neodendrina carnelia igen. et isp. n. in a Tridacna shell from Pleistocene-Holocene coral reef deposits, Red Sea, Egypt
Figure 3. SEM images (BSE detector) of Neodendrina carnelia igen. et isp. n. of the inner side of a Tridacna maxima bivalve shell from the Pleistocene–Holocene coral reef deposits in the Marsa Alam area, Red Sea, Egypt. (a–c) Overview and close-ups of the holotype. (d–e) Overview and close-up of an early ichnogenetic stage. (f–g) Overview and close-up of a specimen with authigenic gypsum crystals, calcite spar, and clay minerals within the boring as well as on the host's shell surface. (h) Different morphologies possibly developed in the trace, comprising deep open canals (1), isolated deep pits (2), shallow open canals (3), pits in shallow canals (4) and discontinuities (5). (i) Cross section of a trace showing deep (1) and shallow (2) open canals. (j–k) Overview and detail of an epoxy resin cast of a specimen, illustrating the smooth surface texture and the high degree of microbioerosion in the surrounding (partly mechanically removed to gain a view of the dendrinid).
75 Coral Endolith Bacterial Genomes (MAGs) from Red Sea corals Goniastrea edwardsi and Porites lutea
<p>The skeleton of reef-building corals harbors diverse microbial communities that can supply energy to the coral host tissues and might have an integral role in holobiont nutrient cycling. However, we are lacking functional insight of the endolithic microbiome at large. In particular, the link between endolithic microbiome diversity and encoded genomic potential to supply energy to the coral host during coral bleaching, in the absence of their Symbiodiniaceae photosymbionts, remains poorly understood. Here we assembled endolith bacterial MAGs from DNA of coral skeletons from Goniastrea edwardsi and Porites lutea, two common reef‐building corals from the central Red Sea.</p>
Figs 1–2 in New Intestinal Trematodes From Siganid Fishes Off The Saudi Coast Of The Red Sea
Figs 1–2. Holotypes (whole-mount, ventral view): 1 = Hexangium saudii sp. n. from Siganus rivulatus, Red Sea. 2 = Progyliauchen magnacetabulum sp. n. from Siganus luridus, Red Sea. Scale bar= 500 μm.
Fig. 4 in The Amount And Distribution Of The Red Data Book Bird Wetland Species In The Azov-Black Sea Region Of Ukraine According To The Results Of August Counts 2004-2015
Fig. 4. Distribution of wetlands number depending on number of species in them (axis X — number of species, axis Y — number of wetlands).
Fig. 5 in The Amount And Distribution Of The Red Data Book Bird Wetland Species In The Azov-Black Sea Region Of Ukraine According To The Results Of August Counts 2004-2015
Fig. 5. Distribution of wetlands depending on species number (axis X) and average amount of birds in them (axis Y).
Fig. 7 in Red Sea Leucothoidae (Crustacea: Amphipoda) including new and re-described species
Fig. 7. Leucothoe minoculis sp. nov., holotype, ♂, 5.0 mm (MVRCr 7729); paratype, ♀, 3.5 mm (MVRCr-7729).
Fig. 12. Leucothoe squalidens Ledoyer, 1984 in Red Sea Leucothoidae (Crustacea: Amphipoda) including new and re-described species
Fig. 12. Leucothoe squalidens Ledoyer, 1984, juv., length 1.6 mm (MVRCr 7732); ♂, length 2.0 mm (MVRCr 7733).
Fig. 3. A. Leucothoe acutilobata Ledoyer, 1978 in Red Sea Leucothoidae (Crustacea: Amphipoda) including new and re-described species
Fig. 3. A. Leucothoe acutilobata Ledoyer, 1978, ♀, length 6.0 mm. B. Leucothoe predenticulata Ledoyer, 1978, length 4.5 mm.
Fig. 10 in Red Sea Leucothoidae (Crustacea: Amphipoda) including new and re-described species
Fig. 10. Leucothoe reimeri sp. nov., holotype, ♂, length 5.9 mm (ZMB 29750, slide 5096); paratype, ♀, length 5.5 mm (ZMB 29751, slide 5097).
Fig. 5 in Red Sea Leucothoidae (Crustacea: Amphipoda) including new and re-described species
Fig. 5. Leucothoe bannwarthi (Schellenberg, 1928), ♂, length 3.0 mm (MCRCr 7726); ♀, length 3.0 mm (MVRCr 7725).
Fig. 4 in Red Sea Leucothoidae (Crustacea: Amphipoda) including new and re-described species
Fig. 4. Leucothoe bannwarthi (Schellenberg, 1928), ♂, length 3.0 mm (MCRCr 7726); ♀, length 3.0 mm (MVRCr 7725).
А – типовые местонахоЖдениЯ: Зал. ЛаврентиЯ (красный маркер), б. ПровидениЯ (Зеленый маркер); B, B' – иЗобраЖениЯ раковины (B) и Зуба радулы (B') Bela violacea var. nodulosa. Вр=14.5 мм, ДЗ=0.25 мм, иЗ: Krause [1885, pl. 18, figs. 4, 12]; C, C' – синтип Bela violacea var. nodulosa (C) и увеличенный участок предпоследнего оборота (C'), ZMB 37860, Вр=12 мм (фотографиЯ – с раЗрешениЯ ZMB); D–I – иЗменчивость Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN беЗ номера, ЗФИ, о-в Аполлонова, Американский Залив, 3–4 м. Вр=8.2 мм; E – Defrancia becki. ZIN беЗ номера, ЗФИ, о-в Кука, 3–4 м. Вр=9.1 мм; F – Bela violacea var. laevior. Вр=12 мм, иЗ: Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Баренцево море, Югорский Шар, 13 м. Вр=8.7 мм; H – Pleurotoma bicarinata. ZIN 41203/156, ЗФИ, о-в ГрЭм-БЭм, 12–15 м. Вр=8.4 мм; I, I' – Зубы радулы типичной (I) и беЗкилевой (I') форм. ДЗ=0.12 мм и 0.21 мм, соответственно, иЗ: [Sars, 1878, pl. 9, figs. 7, 8]; J – иЗобраЖение раковины Lora inequita. Вр=11 мм, иЗ: Dall [1919, pl. 16, fig. 9]; K – голотип Lora inequita, USNM 222238. Вр=11 мм (фотографиЯ – с раЗрешениЯ USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: раковины (L) и Зуб радулы (L'). Вр=12 мм и 11.6 мм, соответственно, ДЗ=0.15 мм, иЗ: Богданов [1990, рис. 175, 176, 422 (7)]. A – type localities: Lawrence Bay (red circle), Providence Bay (green circle); B, B' – images of the shell (B) and tooth of the radula (B') of Bela violacea var. nodulosa. H=14.5 mm, L=0.25 mm, after Krause [1885, pl. 18, figs. 4, 12]; C, C' – a syntype of Bela violacea var. nodulosa (C) and the enlarged section of the penultimate whorl (C'), ZMB 37860, H=12 mm (photo – courtesy of ZMB); D–I – variability of Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN uncatalogued, Franz Josef Land, Apollonova Isl., American Gulf, 3–4 m. H=8.2 mm; E – Defrancia becki. ZIN uncatalogued, Franz Josef Land, Cook Isl., 3–4 m. H=9.1 mm; F – Bela violacea var. laevior. H=12 mm, after Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Barents Sea, Ugra Shar, 13 m. H=8.7 mm; H – Pleurotoma bicarinata. ZIN 41203/156, Franz Josef Land, Graham-Bam Isl., 12–15 m. H= 8.4 mm; I, I' – teeth of typical (I) and keelless (I') forms. L=0.12 mm and 0.21 mm, respectively; after Sars [1878, pl. 9, figs. 7,8]; J – image of Lora inequita. H=11 mm, after Dall [1919, pl.16, fig. 9]; K – the holotype of Lora inequita, USNM 222238. H=11 mm (photo – courtesy of USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: shells (L) and tooth (L'). H=12 mm and 11.6 mm, respectively, L=0.15 mm, after Bogdanov [1990, figs. 175, 176, 422 (7)]. in Curtitoma nodulosa (Krause, 1885) comb. nov. (Gastropoda: Mangeliidae), a rare species twice described from the northern part of Bering Sea
А – типовые местонахоЖдениЯ: Зал. ЛаврентиЯ (красный маркер), б. ПровидениЯ (Зеленый маркер); B, B' – иЗобраЖениЯ раковины (B) и Зуба радулы (B') Bela violacea var. nodulosa. Вр=14.5 мм, ДЗ=0.25 мм, иЗ: Krause [1885, pl. 18, figs. 4, 12]; C, C' – синтип Bela violacea var. nodulosa (C) и увеличенный участок предпоследнего оборота (C'), ZMB 37860, Вр=12 мм (фотографиЯ – с раЗрешениЯ ZMB); D–I – иЗменчивость Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN беЗ номера, ЗФИ, о-в Аполлонова, Американский Залив, 3–4 м. Вр=8.2 мм; E – Defrancia becki. ZIN беЗ номера, ЗФИ, о-в Кука, 3–4 м. Вр=9.1 мм; F – Bela violacea var. laevior. Вр=12 мм, иЗ: Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Баренцево море, Югорский Шар, 13 м. Вр=8.7 мм; H – Pleurotoma bicarinata. ZIN 41203/156, ЗФИ, о-в ГрЭм-БЭм, 12–15 м. Вр=8.4 мм; I, I' – Зубы радулы типичной (I) и беЗкилевой (I') форм. ДЗ=0.12 мм и 0.21 мм, соответственно, иЗ: [Sars, 1878, pl. 9, figs. 7, 8]; J – иЗобраЖение раковины Lora inequita. Вр=11 мм, иЗ: Dall [1919, pl. 16, fig. 9]; K – голотип Lora inequita, USNM 222238. Вр=11 мм (фотографиЯ – с раЗрешениЯ USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: раковины (L) и Зуб радулы (L'). Вр=12 мм и 11.6 мм, соответственно, ДЗ=0.15 мм, иЗ: Богданов [1990, рис. 175, 176, 422 (7)]. A – type localities: Lawrence Bay (red circle), Providence Bay (green circle); B, B' – images of the shell (B) and tooth of the radula (B') of Bela violacea var. nodulosa. H=14.5 mm, L=0.25 mm, after Krause [1885, pl. 18, figs. 4, 12]; C, C' – a syntype of Bela violacea var. nodulosa (C) and the enlarged section of the penultimate whorl (C'), ZMB 37860, H=12 mm (photo – courtesy of ZMB); D–I – variability of Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN uncatalogued, Franz Josef Land, Apollonova Isl., American Gulf, 3–4 m. H=8.2 mm; E – Defrancia becki. ZIN uncatalogued, Franz Josef Land, Cook Isl., 3–4 m. H=9.1 mm; F – Bela violacea var. laevior. H=12 mm, after Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Barents Sea, Ugra Shar, 13 m. H=8.7 mm; H – Pleurotoma bicarinata. ZIN 41203/156, Franz Josef Land, Graham-Bam Isl., 12–15 m. H= 8.4 mm; I, I' – teeth of typical (I) and keelless (I') forms. L=0.12 mm and 0.21 mm, respectively; after Sars [1878, pl. 9, figs. 7,8]; J – image of Lora inequita. H=11 mm, after Dall [1919, pl.16, fig. 9]; K – the holotype of Lora inequita, USNM 222238. H=11 mm (photo – courtesy of USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: shells (L) and tooth (L'). H=12 mm and 11.6 mm, respectively, L=0.15 mm, after Bogdanov [1990, figs. 175, 176, 422 (7)].
Рис. 3. Схема миграций виΑов рыб, участвующих в современной Αинамике ихтиофауны на территории НТТ: 1 — разΛивы; 2 — намывы. Черным цветом обозначены направΛения миграций из реки Туманной; красным — из оз. Хасан и РазΛивов; синим — с мест зимовки в реках южного Приморья; зеΛеным — сезонные миграции из южных морей Fig. 3. Scheme of migration of fish species involved in the modern dynamics of ichthyofauna on the territory of LRT: 1 — spills; 2 — alluvial. Black color indicates the direction of migration from the Tumannaya river; red — from lake Khasan and spills; blue — from wintering places in the rivers of southern Primorye; green — seasonal migration from the south seas in Transboundary Migration And The Local Constraints In The Dynamic Of Fish Fauna In The Lower Reaches Of Tumannaya River
Рис. 3. Схема миграций виΑов рыб, участвующих в современной Αинамике ихтиофауны на территории НТТ: 1 — разΛивы; 2 — намывы. Черным цветом обозначены направΛения миграций из реки Туманной; красным — из оз. Хасан и РазΛивов; синим — с мест зимовки в реках южного Приморья; зеΛеным — сезонные миграции из южных морей Fig. 3. Scheme of migration of fish species involved in the modern dynamics of ichthyofauna on the territory of LRT: 1 — spills; 2 — alluvial. Black color indicates the direction of migration from the Tumannaya river; red — from lake Khasan and spills; blue — from wintering places in the rivers of southern Primorye; green — seasonal migration from the south seas
Figure 4 in New record of the rare flounder Parabothus budkeri (Chabanaud, 1943) (Teleostei: Bothidae) from the Gulf of Aqaba, northern Red Sea, with a key to the genus Parabothus
Figure 4. – Parabothus budkeri (Chabanaud, 1943), HUJ 1635, 1 male, 49.7 mm SL, Red Sea, Gulf of Aqaba, Israel, Eilat. X-ray.
Figure 2 in New record of the rare flounder Parabothus budkeri (Chabanaud, 1943) (Teleostei: Bothidae) from the Gulf of Aqaba, northern Red Sea, with a key to the genus Parabothus
Figure 2. – Parabothus budkeri (Chabanaud, 1943), HUJ 1635, 1 male, 49.7 mm SL, Red Sea, Gulf of Aqaba, Israel, Eilat. Photograph by D. Golani. Blind side.
Figure 1 in New record of the rare flounder Parabothus budkeri (Chabanaud, 1943) (Teleostei: Bothidae) from the Gulf of Aqaba, northern Red Sea, with a key to the genus Parabothus
Figure 1. – Parabothus budkeri (Chabanaud, 1943), HUJ 1635, 1 male, 49.7 mm SL, Red Sea, Gulf of Aqaba, Israel, Eilat. Photograph by D. Golani. Ocular side.
Figure 5 in In vitro antifungal and antibacterial potentials of organic extracts of Avicennia marina collected from Rabigh Lagoon, Red Sea Coasts in Saudi Arabia
Figure 5. Comparison of MIC with MBC values (mg/mL) of A. marina in different solvents: a: Petroleum ether; b: Ethyl acetate. All tests were performed in triplicates (n = 3) and the error bars represent the SD. * p <0.05, ** p <0.01, *** p <0.001 with respect to the control. NS: not significant.
Figure 3 in In vitro antifungal and antibacterial potentials of organic extracts of Avicennia marina collected from Rabigh Lagoon, Red Sea Coasts in Saudi Arabia
Figure 3. Comparison of MIC values (mg/mL) of A. marina different extracts. All tests were performed in triplicates (n = 3) and the error bars represent the SD. * p <0.05, ** p <0.01, *** p <0.001 with respect to the control.
Figure 2 in In vitro antifungal and antibacterial potentials of organic extracts of Avicennia marina collected from Rabigh Lagoon, Red Sea Coasts in Saudi Arabia
Figure 2. Antagonistic effect expressed by the inhibition zone of Ethyl acetate extract on the growth of: (A):A. fumigatus; (B):C. albicanis.
Figure 1 in In vitro antifungal and antibacterial potentials of organic extracts of Avicennia marina collected from Rabigh Lagoon, Red Sea Coasts in Saudi Arabia
Figure 1. The antifungal effect of plant extracts from Avicennia marina against some pathogenic fungi expressed by zones of inhibition (ZI in mm). All tests were performed in triplicates (n = 3) and the error bars represent the SD. * p <0.05, ** p <0.01, *** p <0.001 with respect to the control. NS: not significant.
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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.