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Figure 4 in Ecomorphological patterns and shape indices of otoliths in the Pagellus acarne (Actinopterygii, Sparidae) from the Aegean and Marmara Seas
Figure 4. Principal component analysis (PCA) plot showing similarities/ differences between both Pagellus acarne stocks and left and right side otoliths: (AS) Aegean Sea and (MS) Sea of Marmara.
Figure 1 in The importance of shape analysis of the first upper molar in the separation of two subspecies of the Hazel dormouse (Muscardinus avellanarius (Linnaeus, 1758)) in Northern Anatolia
Figure 1. Worldwide distribution of Muscardinus avellanarius (a) and trapped localities in Northern Anatolia, Turkey (b) [Number of specimens: in the West; Bolu = 23, Bursa = 3, Düzce = 6, and in the East; Giresun = 4, Ordu = 6, Trabzon = 14].
Figure 8 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 8. Relationships between values of distribution coefficients (Kd Shell/Water Zn (A), Kd Shell/Water Sr (B) and Kd Shell/Water Al (C)) and principal component 1, revealed from the shell shape analysis of Beringiana beringiana. For the numbers of localities see caption for Figure 7.
Figure 6. Normed PCA factorial graph F1 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 6. Normed PCA factorial graph F1 × F2 of two revealed geographical groups of Beringiana beringiana samples (blue circles indicate samples from Primorsky Krai, Kunashir, Sakhalin, and Iturup islands; red circles indicate samples from Kamchatka Peninsula). Ellipses show 95 % confidence interval.
Figure 5 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 5. Relationships between Kd Shell/Sediment Al and Kd Shell/Water Al: (1) Peschanoye Lake, Kunashir Island, (2) Bolshoye Vavayskoye Lake, Sakhalin Island, (3) Vaskovskoye Lake, Primorsky Krai, (4) Lebedinoe Lake, Iturup Island, (5) Kurazhechnoye Lake, Kamchatka Peninsula, (6) Khalaktyrskoye Lake, Kamchatka Peninsula, (7) Chernoye Lake, Sakhalin Island.
Figure 4 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 4. Median joining networks of Beringiana beringiana (N = 50) based on the COI gene fragment. The circle size is proportional to the number of available sequences belonging to the given haplotype (the smallest = 1 sequence). The red numbers near branches indicate the number of nucleotide substitutions between haplotypes.
Figure 2 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 2. Shells of Beringiana beringiana specimens, collected from studied waterbodies: A – Kurazhechnoye Lake, Kamchatka Peninsula (voucher number RMBH biv1212/2), B – Vaskovskoye Lake, Primorsky Krai (RMBH biv1181/1), C – Lebedinoye Lake, Iturup Island (RMBH biv1254/2), D – Bolshoye Vavayskoye Lake, Sakhalin Island (RMBH biv1250/1), E - Peschanoye Lake, Kunashir Island (RMBH biv1251/1), F – Khalaktyrskoye Lake, Kamchatka Peninsula (RMBH biv1213/3). Scale bar = 50 mm.
Figure 1 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 1. Map of the studied region. Lakes: (1) Kurazhechnoye, Kamchatka Peninsula (n = 5), (2) Khalaktyrskoye, Kamchatka Peninsula (n = 5), (3) Lebedinoye, Iturup Island (n = 3), (4) Peschanoye, Kunashir Island (n = 3), (5) Chernoye, Sakhalin Island (n = 3), (6) Bolshoye Vavayskoye, Sakhalin Island (n = 3), (7) Vaskovskoye, Primorsky Krai (n = 3). n reveals the number of collected shells of Beringiana beringiana.
Figure 3. Principal components 1 and 2 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 3. Principal components 1 and 2 visualized by drawing synthetic outlines of extreme (±2SD) and mean shell shapes of Beringiana beringiana. The umbo position marked by star.
Figure 11 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 11. Relationships between values of KAl and longitudinal cross-sectional area of shell (mm2), d Shell/Sediment revealed from the shell shape analysis of Beringiana beringiana. For the numbers of localities see caption for Figure 7.
Figure 7 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 7. Relationships between Ca-normalized concentration of zinc in shells and principal component 1, (A), copper in shells and principal component 1 (B), revealed from the shell shape analysis of Beringiana beringiana: (1) Peschanoye Lake, Kunashir Island, (2) Lebedinoe Lake, Iturup Island, (3) Bolshoye Vavayskoye Lake, Sakhalin Island, (4) Kurazhechnoye Lake, Kamchatka Peninsula, (5) Vaskovskoye Lake, Primorsky Krai, (6) Khalaktyrskoye Lake, Kamchatka Peninsula.
Figure 10 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 10. Relationships between values of Kd Shell/Water Al (A), Kd Shell/Water P (B), Kd Shell/Water Fe (C) and longitudinal cross-sectional area of shell (mm2), revealed from the shell shape analysis of Beringiana beringiana. For the numbers of localities see caption for Figure 7.
Figure 9 in Impact of aquatic habitat environment on the elemental composition and shell shape variability of the Beringian freshwater mussel Beringiana beringiana (Bivalvia, Unionidae)
Figure 9. Relationships between Zn: Ca – ratio in Beringiana beringiana shells and longitudinal cross-sectional area of shell (mm2), revealed from shell shape analysis of Beringiana beringiana. For the numbers of localities see caption for Figure 7.
Figure 8 in Discrete aggregate analysis of ovoid egg shapes in various bird species
Figure 8. Golden proportion manifested in the shape of bird eggs: 1, 13, 25, 37, ovoid profiles; 2, 14, 26, 38, ovoid profile profiles for comparison with bird eggs. Bird eggs: 3 – Alectoris chukar; 4 – Glareola pratincola; 5 – Sturnus vulgaris; 6 – Sylvia nisoria; 7 – Milvus milvus; 8 – Buteo buteo; 9 – Falco cherrug; 10 – Lanius collurio; 11 - Perdix perdix; 12 – Garrulus glandarius; 15 – Sylvia communis; 16 – Perdix perdix; 17 – Numida meleagris; 18 – Alectoris chukar; 19 – Garrulus glandarius; 20 – Coccothraustes coccothraustes; 21 – Larus melanocephalus; 22 – Dendrocopos major; 23 – Picus canus; 24 – Jynx torquilla; 27 – Luscinia svecica; 28 – Oenanthe oenanthe; 29 – Turdus merula; 30– Picus canus; 31– Aquila pomarina; 32 – Perdix perdix; 33 – Lanius collurio; 34 – Anthus trivialis; 35 – Jynx torquilla; 36– Hieraaetus pennatus; 39 – Turdus philomelos; 40 – Oriolus oriolus; 41 – Ficedula albicollis; 42 – Dendrocopos leucotos; 43 – Delichon urbica; 44 – Coccothraustes coccothraustes; 45 – Garrulus glandarius; 46 – Corvus frugilegus; 47 – Turdus merula; 48 – Gallinula chloropus.
Figure 5 in Discrete aggregate analysis of ovoid egg shapes in various bird species
Figure 5. Comparison of geometric standards (1, 7, 13, 19, 25, 31) with profiles of real eggs: 2 – Athene noctua; 3 – Neophron percnopterus; 4 – Merops apiaster; 5 – Phylloscopus sibilatrix; 6 – Alcedo atthis; 8 – Falco vespertinus; 9 – Aegithalos caudatus; 10 – Merops apiaster; 11 – Ficedula hypoleuca; 12 – Jynx torquilla; 14 – Sterna hirundo; 15 – Buteo buteo; 16 – Falco cherrug; 17 – Upupa epops; 18 – Dendrocopos major; 20 – Picus canus; 21 – Perdix perdix; 22 – Phasianus colchicus; 23 – Corvus monedula; 24 – Coccothraustes coccothraustes; 26 – Limosa limosa; 27 – Pica pica; 28 – Luscinia luscinia; 29 – Corvus frugilegus; 30 – Alca torda; 32 – Uria aalge; 33 – Numenius arquata; 34 – Recurvirostra avosetta; 35 – Alca torda; 36 – Corvus corax.
Figure 3 in Discrete aggregate analysis of ovoid egg shapes in various bird species
Figure 3. Discrete variants of combinations of the lateral arcs of the ovoid profiles (matrices): a - 0.75D; b -1.0 D; c - 1.25D; d - 1.5D; e - 1.75D.
Figure 7 in Discrete aggregate analysis of ovoid egg shapes in various bird species
Figure 7. Construction of ovoid profiles with golden ratio: a - construction of ovoids with doubling of radii of circles; b - construction of ovoids with increasing of radii of circles by F=1,618; c - getting golden section by a combination of four circles; d - construction of ovoids with golden section by pentagons.
Figure 11 in Discrete aggregate analysis of ovoid egg shapes in various bird species
Figure 11. Schematics for calculating the complementarity indices of avian eggs: 1, 2, 9, 10 - scheme and geometric profile of eggs with a complementarity index close to unity (rc=ri=(L–D)/2); 3 – Podiceps cristatus; 4 – Cygnus olor; 5 – Egretta alba; 6 – Pelecanus crispus; 7 – Egretta garzetta; 8 – Mergus serrator; 11 – Anser anser; 12 – Casuarius casuarius; 13 – Porzana parva; 14 – Phalacrocorax carbo; 15 – Podiceps nigricollis; 16 – Ardea cinerea; 17, 18 - scheme and geometric profile of eggs with a complementarity index close to 1,333 (rc=ri=lipz=L/3); 19 – Pygoscelis papua; 20 – Nyctea scandiaca; 21 – Strutio camelus; 22 – Dendrocopos minor; 23 – Alcedo atthis; 24 – Buteo chemilasius; 25 – Jynx torquilla; 26 – Asio otus; 27 – Streptopelia decaocto; 28 – Merops apiaster; 29 – Asio flammeus; 30 – Aquila pomarina; 31 – Bubo bubo; 32 – Columba oenas; 33, 34 – scheme and geometric profile of eggs with a complementarity index greater than 1,5 (rc=ri/lipz˃1,5); 35 – Athene noctua; 36 – Otus scops; 37 – Otus brucei; 38 – Merops apiaster; 39 – Strix aluco; 40 – Pygoscelis papua; 41 – Alcedo atthis; 42 – Merops superciliosus; 43 – Milvus migrans; 44 – Asio flammeus; 45 – Strutio camelus; 46 – Hieraaetus pennatus; 47 – Strix aluco; 48 – Accipiter nisus.
Figure 2 in Discrete aggregate analysis of ovoid egg shapes in various bird species
Figure 2. Relationship between the ovoid constructs with the diagonals of the square and the double square.
Figure 6 in Discrete aggregate analysis of ovoid egg shapes in various bird species
Figure 6. Ovoid profiles (a) Erkoca, 2021; (b) Rojas, 2002; (c) Dixon, 1987; (d) Petrović et al., 2010.
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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.