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Figure 2 in Red-bellied Piranha Pygocentrus nattereri Kner, 1858 (Characiformes: Serrasalmidae) in open waters in R. Macedonia
Figure 2. Morphometric measurements of P. nattereri. Abbreviations are given in material and methods. Length of pelvic fin was not possible to be marked in the photograph.
Fig. 2 in Diet Composition Of The Red Fox, Vulpes Vulpes Linnaeus, 1758 (Canidae, Carnivora) In Western Ukraine
Fig. 2. Cluster analysis. sa – summer-autumn season, ws – winter-spring season; LV – Lviv region, VO – Volyn region, ZA – Zakarpattia region, N/A – Western Ukraine (exact data on region of origin are not available), KH – Khmelnytskyi region, TE – Ternopil region, RI – Rivne region, IV – Ivano-Frankivsk region; d – stomach contents (dissection), f – faeces sample.
Fig.1 in A Review Of Latvian Saproxylic Beetles From The European Red List
Fig.1. Red List Categories taken from International Union for Conservation of Nature (IUCN) (Nieto & Alexander 2010).
Fig. 1 in Comparative Analysis Of Alien Red Oak (Quearcus Rubra L.) And Native Common Oak (Quercus Robur L.) Vegetation In Lithuania
Fig. 1. Detrented Correspondence Analysis of Quercus rubra () and Quercus robur of TilioCarpinetum stachyetosum () and Tilio-Carpinetum typicum types () plots
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
Рис. 1. Seychelliceps cooperi comb. nov., ЗММУ № 23252, 155 мм SL (1, 3, 5, 7, 9) и Suggrundus macracanthus, ИОРАН, Вьетнам, заΛ. Нячанг, 124 мм SL (2, 4, 6, 8, 10, 11), ΑетаΛи строения: 1, 2 — верхний преоперкуΛярный шип; 3, 4 — гребешки и/иΛи бугорки костей крыши черепа в загΛазничной части; 5, 6 — заΑний конец премаксиΛΛярных зубных Λент; 7, 8 — форма небных зубных Λент; 9, 10 — чешуи преΑорсаΛьной обΛасти; 11 — восьмая чешуйка боковой Λинии (окрашена аΛизарином красным S). Масштаб: 1, 2, 4, 7, 8 — 2,5 мм (7, 8 — Λинейка общая); 3 — 5 мм; 5, 9, 10 — 3 мм; 6 — 2 мм; 11 — 0,3 мм Fig. 1. Seychelliceps cooperi comb. nov., ZMMU no. 23252, 155 mm SL (1, 3, 5, 7, 9) and Suggrundus macracanthus, IORAS, Vietnam, Nha Trang Bay, 124 mm SL (2, 4, 6, 8, 10, 11), details: 1, 2 — uppermost preopercular spine; 3, 4 — crests and/or tubercles of cranial roofing bone in postorbital portion of head; 5, 6 — posterior ending of premaxillary tooth band; 7, 8 — shape of tooth band on palatine; 9, 10 — predorsal scales; 11 — eighth scale of lateral line (stained by alizarine red S). Scale bars: 1, 2, 4, 7, 8 — 2.5 mm (7, 8 — common bar); 3 — 5 mm; 5, 9, 10 — 3 mm; 6 — 2 mm; 11 — 0.3 mm in Of The Genus (Teleostei: Scorpaeniformes)
Рис. 1. Seychelliceps cooperi comb. nov., ЗММУ № 23252, 155 мм SL (1, 3, 5, 7, 9) и Suggrundus macracanthus, ИОРАН, Вьетнам, заΛ. Нячанг, 124 мм SL (2, 4, 6, 8, 10, 11), ΑетаΛи строения: 1, 2 — верхний преоперкуΛярный шип; 3, 4 — гребешки и/иΛи бугорки костей крыши черепа в загΛазничной части; 5, 6 — заΑний конец премаксиΛΛярных зубных Λент; 7, 8 — форма небных зубных Λент; 9, 10 — чешуи преΑорсаΛьной обΛасти; 11 — восьмая чешуйка боковой Λинии (окрашена аΛизарином красным S). Масштаб: 1, 2, 4, 7, 8 — 2,5 мм (7, 8 — Λинейка общая); 3 — 5 мм; 5, 9, 10 — 3 мм; 6 — 2 мм; 11 — 0,3 мм Fig. 1. Seychelliceps cooperi comb. nov., ZMMU no. 23252, 155 mm SL (1, 3, 5, 7, 9) and Suggrundus macracanthus, IORAS, Vietnam, Nha Trang Bay, 124 mm SL (2, 4, 6, 8, 10, 11), details: 1, 2 — uppermost preopercular spine; 3, 4 — crests and/or tubercles of cranial roofing bone in postorbital portion of head; 5, 6 — posterior ending of premaxillary tooth band; 7, 8 — shape of tooth band on palatine; 9, 10 — predorsal scales; 11 — eighth scale of lateral line (stained by alizarine red S). Scale bars: 1, 2, 4, 7, 8 — 2.5 mm (7, 8 — common bar); 3 — 5 mm; 5, 9, 10 — 3 mm; 6 — 2 mm; 11 — 0.3 mm
Fig. 1 in Golden jackal (Canis aureus Linnaeus, 1758) and Red fox (Vulpes vulpes Linnaeus, 1758) population dynamics in Sarnena Sredna Gora Mts., Bulgaria based on hunting statistics
Fig. 1. Golden jackal (Canis aureus L.) and Red fox (Vulpes vulpes L.) population dynamics trends in Sarnena Sredna Gora Mts., Bulgaria, for a period of 11 years based on the analysis of the hunting data base (number of shot individuals)
Fig. 2. After 73 in Osmotic induction marking with Alizarin Red S on juveniles of pejerrey, Odontesthes bonariensis (Atherinopsidae)
Fig. 2. After 73 days post-treatment, clear marks were observed for both marking procedures, in otoliths (Figs. 2a, b), scales (Figs. 2c, d) and caudal fin rays (Figs. 2e, f). The intensity of the signal in scales was higher in fish marked with OI+ARS (Fig. 2d). After 385 days, only marks in caudal fin rays were observed in fish treated with OI+ARS (Fig 2g). All control fish structures and, otoliths and scales for 385 days post- immersion showed no marks under fluorescence microscope (Fig. 2h). a, c, e: ARS treatment; b, d, f, g: OI+ARS treatment. Scale bar = 200 µm.
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.
Fig. 3 in Diet shift of Red Belly Pacu Piaractus brachypomus (Cuvier, 1818) (Characiformes: Serrasalmidae), a Neotropical fish, in the Sepik-Ramu River Basin, Papua New Guinea
Fig. 3. Bray Curtis (Polar) ordination of arcsine-square root transformed volumetric proportions of food categories. Abbreviations: AP, aquatic plants; AI, aquatic invertebrates; Fi, fish remains; TP, terrestrial plants; TI, terrestrial invertebrates. Other includes: mammals, arthropods, plant material of unknown origin, and debris (Sepik); detritus (Tarapoto); gravel (Caquetá FW). Site abbreviations follow those in Fig. 2.
Fig. 2 in Diet shift of Red Belly Pacu Piaractus brachypomus (Cuvier, 1818) (Characiformes: Serrasalmidae), a Neotropical fish, in the Sepik-Ramu River Basin, Papua New Guinea
Fig. 2. Comparison of the relative contribution of food categories to the diet (% volume) of Piaractus brachypomus of introduced (Sepik River) and natural populations (Colombia: Tarapoto Lake and Caquetá River; Brazil: Tocantins River and Tucuruí Reservoir; Venezuela: Caura River). Food items included in each category are listed in Table 1. Category "Other" includes: mammals, arthropods, plant material of unknown origin, and debris (Sepik); detritus (Tarapoto); gravel (Caquetá FW). Abbreviations: FW, falling water season, LW, low water season; RW, rising water season; DS, downstream from reservoir; RS, reservoir.
Fig. 1 in Diet shift of Red Belly Pacu Piaractus brachypomus (Cuvier, 1818) (Characiformes: Serrasalmidae), a Neotropical fish, in the Sepik-Ramu River Basin, Papua New Guinea
Fig. 1. Map of sampling site and locations of comparative studies. Circles represent sites in the Amazon Basin (Colombia: Tarapoto Lake and Caquetá River; Brazil: Tocantins River). The triangle represents a site in the Orinoco Basin (Venezuela: Caura River). The star represents the sampling site at the lower Sepik River, Papua New Guinea (PNG).
Figure 1 in Applicability of the vital dyes neutral red and fluorescein diacetate to differentiate between alive and dead non-copepod zooplankton
Figure 1. Intensity of staining of the Black Sea zooplankton with neutral red (NR) and fluorescein diacetate (FDA). 1 (FDA), 2 (NR) – Penilia avirostris; 3, 4 (FDA), 5, 6 (NR) – Pleopis polyphemoides; 7, 8 (FDA), 9 (NR) – Evadne spinifera; 10 (FDA), 11 (NR) – Pseudevadne tergestina; 12, 13 (FDA), 14, 15 (NR) – Cirripedia nauplii; 16 (NR), 17 (FDA) – Rotifera; 18, 19 (FDA), 20, 21 (NR) – Polychaeta larvae; 22, 23 (FDA), 24 (NR) – Decapoda larvae; 25 (NR), 26 (FDA) – Pisces ova; 27 (NR) – Pisces larvae; 28 (FDA), 29 (NR) – Parasagitta setosa; 30 (FDA), 31 (NR) – Oikopleura dioica; 32, 33 (FDA), 34 (NR) – Noctiluca sсintillans; 35 (NR) – Hydromedusae; 36 (NR), 37 (FDA) – Bivalvia larvae; 38, 41 (NR), 39, 40 (FDA) – Gastropoda larvae.
Figure 5 in Red deer on the move: home range size and mobility in Bulgaria
Figure 5. Comparison between male and female red deer mobility. Boxes – the interquartile range (25-75 percentiles); middle line in boxes – median values; diamonds – average values; whiskers – minimum and maximum values within the 95.0% confidence level; circles – outliers; the perimeter outside boxes shows the probability density of the of the 12 hours step-length displacement in males and females.
Figure 3 in Red deer on the move: home range size and mobility in Bulgaria
Figure 3. Comparison of the core and total area in males and females. Boxes – the interquartile range (25-75 percentiles); middle line in boxes – median values; diamonds – average values; whiskers – minimum and maximum values within the 95.0% confidence level; circles – outliers; circles with plus sign - "Far outside" outliers, points more than 3 times above the interquartile range.
Figure 1. Study area and 100 in Red deer on the move: home range size and mobility in Bulgaria
Figure 1. Study area and 100 % minimum convex polygons from the locations of the GPS-collared red deer
Figure 2. A–G, Madagascan Scarabaeini species. A, B in Rediscovery of Scarabaeus sevoistra Alluaud, 1902 (Coleoptera: Scarabaeinae): biological notes and IUCN Red Listing
Figure 2. A–G, Madagascan Scarabaeini species. A, B, holotype male of Scarabaeus sevoistra Alluaud, 1902 and the associated labels from the MNHN; C, habitus drawing of a female S. sevoistra (from Paulian & Lebis (1960: 14)) for comparison; note the dimorphism in the shape and form of the protibiae of the male (A) and female (C); D, Scarabaeus radama Fairmaire, 1895; E, F, Scarabaeus viettei (Paulian, 1953), holotype female and the associated labels from the MNHN. Scale bar is 10 mm.
Figure 1. A–F in Rediscovery of Scarabaeus sevoistra Alluaud, 1902 (Coleoptera: Scarabaeinae): biological notes and IUCN Red Listing
Figure 1. A–F, Recent photographic observations of Scarabaeus sevoistra Alluaud, 1902. A, B, C, photographed by Joseph Thompson, 04 November 2015; D, photographed by Bitty Roy, 17 November 2019; E, F, photographed by Maxim Nuraliev, 01 August 2015.
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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.