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FIG. 12 in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 12. Volviceramus involutus (Sowerby, 1828), TMP 2016.041.0243, LV, Wapiabi Formation, West Thistle Creek, 72.5 m, A, lateral view of the adult stage, B, anterior view, C, oblique, posterodorsal view, D, dorsal view, the photographs are ×1.
FIG. 11 in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 11. Volviceramus koeneni (Müller, 1888), TMP 2016.041.0184, double-valve specimen, Wapiabi Formation, Chungo Creek, 45.5 m, A, dorsal view, B, lateral view of the LV, C, anterior view, D, lateral view of the RV. All photographs are ×0.95.
FIG. 10 in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 10. Cremnoceramus crassus inconstans (Woods, 1912), TMP 2016.041.0101, LV, Wapiabi Formation, Wapiabi Creek, 7.9 m, A, anterior view, B, oblique, posterodorsal view, C, lateral view of the juvenile stage. All photographs are ×1.
FIG. 8 in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 8. Tethyoceramus sp., TMP 2016.041.0395 (two left valves), Wapiabi Formation, Bighorn Dam, 8.5 m: A, D, smaller specimen; A, lateral view; D, anterior view. B, C, larger specimen; B, anterior view, C, lateral view. All photographs are ×1.
FIG. 3 in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 3. Inoceramid zonation of the Coniacian and basal Santonian as recognized herein, and its correlation with the zonations of Tröger, 1989, Kauffman et al., 1993, and Collom, 2001.
FIG. 26 in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 26. Summary representation, to scale, of stratal geometry viewed in strike (NW-SE) and three dip (NE- SW) sections spanning the study area. Lower Coniacian strata fill a saucer-shaped depocenter that thins to both NW and SE, whereas Middle Coniacian strata are thickest in the south but are erosionally truncated toward the NW. Upper Coniacian strata fill a depocenter in the NW but are truncated toward the SE, and are largely absent over most of southern Alberta and northern Montana. Sections summarized from figures 4, 8, 11, and 13.
FIG. 25 in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 25. Comparison of the organic carbon isotope stratigraphy at Cutpick Creek with the carbonate carbon isotope reference curve for the English Chalk succession (after Jarvis et al., 2006, recalibrated to GTS2012 after Laurin et al., 2015). The Cutpick section, and corresponding carbon-isotope curve, has been "expanded" to show the location of hiatuses determined on the basis of regional subsurface correlation (i.e., fig. 4). Biostratigraphic collections made in all the Coniacian sections included in this study (fig. 24), allow three tiepoints to the UK Chalk to be established at the lowest occurrence (LO) of Cremnoceramus crassus crassus, and the lowest occurrence of Volviceramus. The base of the Santonian is defined at the co-appearance level of Clioscaphites saxitonianus and Sphenoceramus ex gr. pachti, which corresponds to surface SS0 of this study. The lowest occurrence of C . crassus, Volviceramus and Scaphites (S .) depressus allows tentative correlation to the Portland core, which does not extend as high as the Coniacian–Santonian boundary (Joo and Sageman, 2014). The highest local occurrence of Inoceramus gibbosus, which is widely distributed in allomembers CA3 and CA4 in the western Alberta foredeep, is marked by the lag-strewn erosion surface CS4, suggestive of significant sea-level fall and subsequent transgression. The absence of the I . ex gr. gibbosus interval in most sections of topmost lower Coniacian strata in other parts of the world suggests that a significant hiatus exists at the base of the overlying Volviceramus Zone.
FIG. 15. A in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 15. A. Overview of surface CS1 exposed at river level at the mouth of Oldfort Creek (fig. 10). At right, a coarse-grained wave ripple composed of granules and small pebbles of chert and quartz rests sharply on regional erosion surface CS1. Traced laterally over only 3 m, the coarse lag pinches out and surface CS1 is manifest simply as a sharp mud-on-mud contact; scale bar = 20 cm. B. Detail of the coarse-grained wave ripple.
FIG. 2 in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 2. Inoceramid ranges and zonation plotted against interpreted bathymetric changes in the interval studied. E5 through E7; CS1 through CS23, and SS0–erosional surfaces; CA1 through CA24–allomembers.
FIG. 20. A in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 20. A. The upper part of the Marshybank Member at the Bighorn Dam section (fig. 7). Surface CS23, which is mantled with chert and siderite pebbles, marks a maximum regressive surface and is overlain by four subtle upward-coarsening successions culminating in surface SS0. B. Upper part of the Marshybank Member exposed on the Bighorn River (fig. 7) showing bioturbated sandy siltstone grading up into weakly stratified silty sandstone, the top of which is marked by surface CS23.
FIG. 22 in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 22. Offshore facies typical of the Muskiki Member. A. Weakly bioturbated (BI 0-1) cm-scale beds of very fine-grained sandstone interstratified with mudstone forming an upward-coarsening succession culminating at flooding surface CS4. The rusty-weathering colour is typical of this facies and is due to abundant disseminated pyrite. Overlying rock comprises weakly bioturbated mudstone with mm-scale siltstone interbeds. Example: "Brown Creek" section (fig. 6, 11–19 m). B. Stratified mudstone (BI 1-2) with mm-scale coarse siltstone interbeds and abundant, dispersed siderite nodules; scale bar = 20 cm. Example: Oldfort Creek (fig. 10, 42–46 m). C. Heavily bioturbated (BI 4-5) sandy siltstone with dispersed siderite nodules. Example: Oldfort Creek (fig. 10, 49–52 m).
FIG. 1 in Allostratigraphy And Biostratigraphy Of The Upper Cretaceous (Coniacian-Santonian) Western Canada Foreland Basin
FIG. 1. Map of localities and the location of the study area with respect to the outline map of North America.
Fig. 1 in Short communication An evidence of asp viper (Vipera aspis) consumption by a western European hedgehog (Erinaceus europaeus) on Elba Island (Italy)
Fig. 1 - Map of Italy. The red arrow points to the Elba Island. / Mappa d'Italia. La freccia rossa indica l'Isola d'Elba. (Google Earth. Data SIO, NOAA, U.S. Navy, NGA, GEBCO. Image Landsat / Copernicus).
Fig. 2 - A in Short communication An evidence of asp viper (Vipera aspis) consumption by a western European hedgehog (Erinaceus europaeus) on Elba Island (Italy)
Fig. 2 - A hedgehog consuming an asp viper on Elba. / Un riccio che consuma un aspide all'Elba. (Photo/foto: Walter Costa).
Fig. 2 in The western European hedgehog Erinaceus europaeus L. 1758 on San Pietro Island (southern Sardinia, Italy) and an updated review of its presence on the Italian small islands
Fig. 2 - The small Italian islands with evidence of western European hedgehog presence. Thick-bordered circles: probable occurrence of stable populations; thin-bordered circles: only occasional presence of individuals (low probability of short-term persistence). See Tab. 2 for details. / Evidenze di presenza di riccio europeo occidentale nelle piccole isole italiane. Cerchi con bordo spesso: probabile presenza di popolazioni stabili; cerchi con bordo sottile: probabile presenza di singoli individui (bassa probabilità di persistenza a breve termine). Vedasi Tab. 2 per dettagli. 1) Elba; 2) Capraia; 3) Pianosa; 4) Alicudi; 5) Salina; 6) Favignana; 7) Ustica; 8) Procida; 9) Vivara; 10) Capraia; 11) La Maddalena; 12) Asinara; 13) San Pietro.
Fig. 1 in The western European hedgehog Erinaceus europaeus L. 1758 on San Pietro Island (southern Sardinia, Italy) and an updated review of its presence on the Italian small islands
Fig. 1 - The study area (San Pietro Island, Sulcis archipelago; South Sardinia) with the evidence of presence of western European hedgehog. Black circles: direct observations; grey circles: indirect data. See Table 1 for details and numbers. / L'area di studio (Isola di San Pietro, arcipelago del Sulcis; Sardegna meridionale) con i siti di presenza del riccio europeo occidentale. Cerchi neri: osservazione dirette; cerchi grigi: dati indiretti. Vedere Tabella 1 per dettagli e numerazione.
Figure 2 in Communities of the Bidentetea class of small coastal river valleys of the Western Pomerania (Poland)
Figure 2. The numerical classification of relevés from rivers of the Wałcz Plain – dendrogram (1-68 – numbers of relevés; A – comm. with Polygonum minus; B – Chenopodietum rubri Timar 1947; C – Bidentetum cernui Kobendza 1948; Da-Df – Bidenti-Polygonetum hydropiperis (Miljan 1933) Lohmeyer in R.Tx. 1950 nom invers).
Fig. 1 in Heavy metals in bones from Harbour Porpoises Phocoena phocoena from the Western Black Sea Coast
Fig. 1. Map of the Western Black Sea showing the sampling sites along the Bulgarian Black Sea Coast.
Fig. 2 in Heavy metals in bones from Harbour Porpoises Phocoena phocoena from the Western Black Sea Coast
Fig. 2. (a) Correlation matrix between heavy metals and age in bone tissue of harbour porpoises (Phocoena phocoena) beached at Black Sea, Bulgaria (significant correlations highlighted in bold). (b) Zink (Zn) concentration in the bones of common harbour porpoises (mg/kg) as a function of age (years).
Fig.1 in Home range, movements and activity patterns of an exceptionally large male Brown Bear (Ursus arctos L.) in the area of the Bulgarian-Greek border (Western Rhodope Mts.)
Fig.1. Dominant male (supposed age of at least 15 years old) with scars of battles with rivals. Hunting Forestry Adjilarska (photo from a kamera-trap, D. Bukovsky, 17.03.2014 at a game-feeding station).
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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.