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FIG. 16 in Deep-sea "lithistid" assemblages from the Norfolk Ridge (New Caledonia), with description of seven new species and a new genus (Porifera, Demospongiae)
FIG. 16. — Anaderma rancureli Lévi & Lévi, 1983; A, B, outer surface of the choanosomal skeleton; note long spines of megaclones; C, D, details of articulation of megaclones; E, F, smooth megaclone choanosomal desma. Scale bars: A-C, E, F, 500 µm; D, 100 µm.
FIG. 7 in Deep-sea "lithistid" assemblages from the Norfolk Ridge (New Caledonia), with description of seven new species and a new genus (Porifera, Demospongiae)
FIG. 7. — Scleritoderma flabelliforme Sollas, 1888; A, outer surface of the choanosomal skeleton with large openings; B, choanosomal skeleton; C, details of choanosomal skeleton of rhizoclones; D, details of choanosomal skeleton of rhizoclones; E, outer surface with crust of curved microstrongyles; F, detail of outer surface with crust of curved microstrongyles. Scale bars: A, 1 mm; B, 500 µm; C, 100 µm; D, E, 200 µm; F, 50 µm.
Fig. 1 in Changes in Assemblages and Diversity Patterns of Carabidae (Coleoptera) from 1997 to 2014 in a Desalinized, Intensively Cultivated Agricultural Landscape in Northern China
Fig. 1. Map of sampling field margin plots in 2014.
Text-fig. 5. Fossils of some mammalian taxa from Gánovce-Hrádok Neanderthal site. a) Castor fiber – mandible dext. et sin. with incisors and p4 – m3 in lateral (mandible) and occlusal (cheek teeth) views (OF 6664–6665); b) Ursus ex gr. spelaeus – right mandible fragment with m1 – m3 in lateral view (P-unnumbered); c) Coelodonta antiquitatis – p2 sin. in buccal view (OF 7188); d) Equus sp. I (cf. taubachensis) – P3 – M3 dext. in travertine, buccal view (P-14302); e) Equus sp. II (cf. germanicus) – Mt sin. fragment in anterior view (OF unnumbered); f) Alces alces – left maxilla fragment with M1 – M3 in occlusal view (P-14303); g) Mammuthus primigenius – m2 sin. in occlusal view (P-14312); h) Palaeoloxodon antiquus – palate fragment with M3 dext. et sin. in occlusal view (P-14281). 50 mm scale is for a–c, 100 mm scale is for d–h. in Revised Floral And Faunal Assemblages From Late Pleistocene Deposits Of The Gánovce-Hrádok Neanderthal Site -Biostratigraphic And Palaeoecological Implications
Text-fig. 5. Fossils of some mammalian taxa from Gánovce-Hrádok Neanderthal site. a) Castor fiber – mandible dext. et sin. with incisors and p4 – m3 in lateral (mandible) and occlusal (cheek teeth) views (OF 6664–6665); b) Ursus ex gr. spelaeus – right mandible fragment with m1 – m3 in lateral view (P-unnumbered); c) Coelodonta antiquitatis – p2 sin. in buccal view (OF 7188); d) Equus sp. I (cf. taubachensis) – P3 – M3 dext. in travertine, buccal view (P-14302); e) Equus sp. II (cf. germanicus) – Mt sin. fragment in anterior view (OF unnumbered); f) Alces alces – left maxilla fragment with M1 – M3 in occlusal view (P-14303); g) Mammuthus primigenius – m2 sin. in occlusal view (P-14312); h) Palaeoloxodon antiquus – palate fragment with M3 dext. et sin. in occlusal view (P-14281). 50 mm scale is for a–c, 100 mm scale is for d–h.
Fig. 1 in Spatio-temporal segregation and size distribution of fish assemblages as related to non-native species occurrence in the middle rio Doce Valley, MG, Brazil
Fig. 1. Study region, indicating the ten sampled lakes. The lakes Capim (Ca), Ferrugem (Fe) and Nova (No) have only native fish species, lakes Crentes (Cr), Poço Redondo (Po), Romoalda (Ro), and Timburé (Ti) have non-piscivorous non-native fish species present, and lakes Águas Claras (Ag), Ariranha (Ar), and Palmeirinha (Pa) have non-native piscivores present.
Fig. 2 in Spatial pattern of a fish assemblage in a seasonal tropical wetland: effects of habitat, herbaceous plant biomass, water depth, and distance from species sources
Fig. 2. Distribution of the relative abundance of the 49 species of fish captured in the 22 plots in Site of Long-Term Sampling (SLTS), related to the depth at each of the collection plots.
Fig. 3. Fish assemblage ordination resulting from a in Flow seasonality and fish assemblage in a tropical river, French Guiana, South America
Fig. 3. Fish assemblage ordination resulting from a CA analysis using species (a), family (b), trophic guild (c), and MOS (d) descriptors in the upstream site, Comté River. Bold text indicates the species, family, trophic guild or MOS which contributes most to axes. Dots = samples taken during high waters; triangles = samples taken during low waters. Numbers correspond to fish species in Table 1. Axis scales are indicated in the small box.
Fig. 1 in Feeding ecology of a stream fish assemblage in an Atlantic Forest remnant (Serra do Japi, SP, Brazil)
Fig. 1. Location of the Serra Japi in the APAs of Jundiaí, Cabreúva, Cajamar and in the municipality of Pirapora do Bom Jesus (SP), showing sampling sites in the different streams. Adapted from "Atlas das Unidades de Conservação Ambiental do Estado de São Paulo- Parte II-Interior, SMA, 1998".
Fig. 5 in Stability and spatio-temporal structure in fish assemblages of two floodplain lagoons of the lower Orinoco River
Fig. 5. Variability by hydrological phases and habitats of the diversity and equitability (Shanon) and richness. a and b = the Arhuacas; c and d = the Cardonales. The abbreviations of the hydrological phases and habitats are explained in the Fig. 2.
Fig. 2 in Influence of environmental variables and anthropogenic perturbations on stream fish assemblages, Upper Paraná River, Central Brazil
Fig. 2. Ordination of the co-structure between (a) fish assemblages (arrows) and stream sites (squares) and (b) fish species and environmental variables resulting from the co-inertia analysis. Only species that most contributes to each axis are displayed. Black and white squares represent stream sites sampled in the wet and dry season, respectively. Codes correspond to names listed in Tables 1 and 2. Small boxes indicate the graphic scale.
Fig. 1 in Fish larvae assemblages in two floodplain lakes with different degrees of connection to the Paraná River, Brazil
Fig. 1. Locations of the sampling sites in Ilha Grande National Park, upper Paraná River. X1 - Xambrê stream; X2 - Xambrê middle; S1 - Saraiva channel; and S2- Saraiva middle.
Fig. 2 in Influence of environmental parameters on fish assemblage of a Neotropical river with a flood pulse regime, Central Brazil
Fig. 2. Ordination of the co-structure resulting from the co-inertia analysis between the fish assemblages and quantitative (a) and qualitative (b) environmental parameters (square arrow edge = stretch; circle = fish assemblage). Numbers represent the stretch sampled at low (L) or high (H) waters. Letter codes correspond to the main fish species that contributed to the costructure and are listed in Table 1. CD = channel depth; CW = channel width; DO = dissolved oxygen; ST = Secchi transparency; RS/S/L/R = river substrate/sand/leaves/roots; RVC/H = river vegetation cover/high; RVC/A/H = river vegetation cover absent/ high; RS/S/L = river substrate/sand/leaves; RVC/F = river vegetation cover/flooded. Boxes indicate scales.
Fig. 3 in Fish larvae assemblages in two floodplain lakes with different degrees of connection to the Paraná River, Brazil
Fig. 3. Variations in mean fish larvae abundance per sampling for Xambrê Lake and Saraiva Lake sites (S1 - Saraiva channel, S2- Saraiva middle, X1 - Xambrê stream and X2 - Xambrê middle) in Ilha Grande National Park, upper Paraná River, during the three studied spawning seasons (s.d. = standard deviation).
Fig. 3 in Simple relationships to predict attributes of fish assemblages in patches of submerged macrophytes
Fig. 3. Relationships between macrophyte biomass and fish density (a) and species richness (b), in patches dominated by E. densa and E. najas.
Fig. 3 in Fish assemblage structure in tributaries of the Meia Ponte River, Goiás, Brazil
Fig. 3. Ordination of the sampling stations resulting from detrended correspondence analysis (DCA) applied to abundance data matrix. Squares = dry season; black circles = rainy season.
Fig. 6 in Testing the ecomorphological hypothesis in a headwater riffles fish assemblage of the rio São Francisco, southeastern Brazil
Fig. 6. Apareiodon ibitiensis specimen using its expanded and horizontally orientated paired fins to hold its position over a rocky surface while grazing on periphyton in the riffles substrate, during daytime (photo: Ricardo M.C. Castro).
Fig. 4 in A remarkable sand-dwelling fish assemblage from central Amazonia, with comments on the evolution of psammophily in South American freshwater fishes
Fig. 4. The minute and translucent Stauroglanis gouldingi (not preserved) poised on the sandy stream bottom.
Fig. 3 in Fish assemblages of tropical floodplain lagoons: exploring the role of connectivity in a dry year
Fig. 3. Average values (± standard error) of species richness (a), density (b), and biomass (c) in connected () and disconnected () lagoons.
FIGURE 5. Typhlotanais froufesae, female. Holotype. A, maxilliped. B, pleopod. Scale bar 0.1 in The tanaidacean assemblage from the Central Pacific Manganese Nodule Province. II. The genera Stenotanais and Typhlotanais (Crustacea)
FIGURE 5. Typhlotanais froufesae, female. Holotype. A, maxilliped. B, pleopod. Scale bar 0.1 mm.
Figure 3 from: Tajovsky K, Hosek J, Hofmeister J, Wytwer J (2012) Assemblages of terrestrial isopods (Isopoda, Oniscidea) in a fragmented forest landscape in Central Europe. ZooKeys 176: 189-198. https://doi.org/10.3897/zookeys.176.2296
Figure 3 - A triplot of the RDA block analyses of terrestrial isopod assemblages at the sites studied. For the abbreviations of the species see Table 1, FA – fragment area, C/N – carbon-nitrogen ratio, Ca2+ – calcium content of the soil, pHH2O – soil acidity. TO, MOH, TOH, AO, BO, BOH, MDF, DP and CP – vegetation at the different sites, see text.
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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.