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3,015 results for “occurrences”
Figure 1 in The occurrence of three tick-borne pathogens in Ixodes ricinus ticks collected from the area of the Kraków-Częstochowa Upland (Southern Poland)
Figure 1 Locations of the Kraków-Częstochowa Upland in Poland and the location of the studied areas.
Figure 2 in Occurrence of the introduced snake mite, Ophionyssus natricis (Gervais, 1844), in the wild in Australia
Figure 2 The locality inside the dried-up earth dam where the infested lizard was caught and where it as recaptured four months later (photographed by Gerrut Norval).
Figure 3 in Occurrence of the introduced snake mite, Ophionyssus natricis (Gervais, 1844), in the wild in Australia
Figure 3 One of the four engorged females ofOphionyssus natricis that were collected from a sleepy lizard (Tiliqua rugosa) on 17 August 2019 at the study site surrounding the Bundey Lutheran Church ruins in the Mid North of South Australia (photographed by Gerrut Norval).
Figure 1 in Occurrence of the introduced snake mite, Ophionyssus natricis (Gervais, 1844), in the wild in Australia
Figure 1 The sleepy lizards (Tiliqua rugosa) were checked for mite by holding them within a plastic container and brushing the areas under their scales with a fine paintbrush (photographed by Jessica Clayton).
FIG. 4. — Torbenia calvata n in New species and new occurrence of Galatheoidea (Crustacea, Decapoda) from New Caledonia
FIG. 4. — Torbenia calvata n. sp., holotype, ovigerous ♀ 4.5 mm: A, carapace and abdomen, dorsal view; B, sternal plastron; C, ventral view of cephalic region, showing antennular and antennal peduncles; D, right third maxilliped, lateral view; E, right cheliped, dorsal view; F, left first walking leg, lateral view; G, dactylus of left first walking leg, lateral view. Setae of carapace, abdomen and pereiopods not illustrated. Scale bars: A, E, F, 2 mm; B-D, G, 1 mm.
FIG. 3. — Munida devestiva n in New species and new occurrence of Galatheoidea (Crustacea, Decapoda) from New Caledonia
FIG. 3. — Munida devestiva n. sp., holotype, ovigerous ♀ 5.8 mm: A, carapace and abdomen, dorsal view; B, sternal plastron; C, ventral view of cephalic region, showing antennular and antennal peduncles; D, right third maxilliped, lateral view; E, right cheliped, dorsal view of the merus, palm and fingers; F, left first walking leg, lateral view; G, dactylus of left first walking leg, lateral view. Setae of carapace, abdomen and pereiopods not illustrated. Scale bars: A, E, F, 2 mm; B-D, G, 1 mm.
FIG. 1. — Eumunida spinosa n in New species and new occurrence of Galatheoidea (Crustacea, Decapoda) from New Caledonia
FIG. 1. — Eumunida spinosa n. sp., holotype, ♂ 18.3 mm: A, carapace, dorsal view; B, anterior part of sternal plastron; C, left lateral side of the second abdominal somite; D, ventral view of left antennal peduncle; E, merus of right third maxilliped, lateral view; F, right cheliped, mesial view of the carpus and palm; G, right cheliped, mesial view of the fingers; H, right first walking leg, lateral view. Scale
FIG. 2. — Munida aulakodes n in New species and new occurrence of Galatheoidea (Crustacea, Decapoda) from New Caledonia
FIG. 2. — Munida aulakodes n. sp., holotype, ♂ 8.0 mm: A, carapace and abdomen, dorsal view; B, sternal plastron; C, ventral view of cephalic region, showing antennular and antennal peduncles; D, right third maxilliped, lateral view; E, right cheliped, dorsal view of the merus, palm and fingers; F, right first walking leg, lateral view; G, dactylus of right first walking leg, lateral view. Setae of carapace, abdomen and pereiopods not illustrated. Scale bars: A, E, F, 2 mm; B-D, G, 1 mm.
Text-fig. 2. (A) Orientation of Schizocrania filosa (HALL, 1847) on articulated shells of benthic brachiopod Rafinesquina sp. (A1–A3 – on dorsal valve of articulated shells, A4 – on ventral valve of articulated shell; forward growth direction is unclear in three specimens) from Upper Ordovician, Corryville Formation, Lawrenceburg, Indiana (after www.drydredgers.org/scizo.htm). (B) Orientation of Schizocrania multistriata (REED, 1905) shells on outer face of conulariid Metaconularia imperialis test (Dobrotivá Formation, Kařízek mine, Barrandian area; after Havlíček and Vaněk 1996); preserved conulariid shell in white, suggested outline of incomplete conulariid test in grey. Arrows indicate direction of forward growth of Schizocrania specimens. in Schizocrania (Brachiopoda, Discinoidea): Taxonomy, Occurrence, Ecology And History Of The Earliest Epizoan Lingulate Brachiopod
Text-fig. 2. (A) Orientation of Schizocrania filosa (HALL, 1847) on articulated shells of benthic brachiopod Rafinesquina sp. (A1–A3 – on dorsal valve of articulated shells, A4 – on ventral valve of articulated shell; forward growth direction is unclear in three specimens) from Upper Ordovician, Corryville Formation, Lawrenceburg, Indiana (after www.drydredgers.org/scizo.htm). (B) Orientation of Schizocrania multistriata (REED, 1905) shells on outer face of conulariid Metaconularia imperialis test (Dobrotivá Formation, Kařízek mine, Barrandian area; after Havlíček and Vaněk 1996); preserved conulariid shell in white, suggested outline of incomplete conulariid test in grey. Arrows indicate direction of forward growth of Schizocrania specimens.
Text-fig. 4. Lithostratigraphy of the BCB and standard ammonite zonation in relation to Schloenbachia lymensis occurrence. a. Plaňany. b. Slaný. Dashed lines indicate chronostratigraphic ranges of marine strata in both localities. For detailed litho- and biostratigraphy of the Pecínov Member see Košťák et al. (2018). in Taxonomy And Stratigraphic Distribution Of The Ammonite Schloenbachia Neumayr, 1875 From The Bohemian Cretaceous Basin
Text-fig. 4. Lithostratigraphy of the BCB and standard ammonite zonation in relation to Schloenbachia lymensis occurrence. a. Plaňany. b. Slaný. Dashed lines indicate chronostratigraphic ranges of marine strata in both localities. For detailed litho- and biostratigraphy of the Pecínov Member see Košťák et al. (2018).
Text-fig. 3. Palaeogeographic distribution of Schloenbachia lymensis (red dots) in the Upper Cenomanian Calycoceras guerangeri through the Metoicoceras geslinianum Zones. Light blue – shallow epicontinental sea, dark blue – deep marine settings, yellow – land. * asterisk – occurrence in the BCB (modified after Wilmsen 2012). in Taxonomy And Stratigraphic Distribution Of The Ammonite Schloenbachia Neumayr, 1875 From The Bohemian Cretaceous Basin
Text-fig. 3. Palaeogeographic distribution of Schloenbachia lymensis (red dots) in the Upper Cenomanian Calycoceras guerangeri through the Metoicoceras geslinianum Zones. Light blue – shallow epicontinental sea, dark blue – deep marine settings, yellow – land. * asterisk – occurrence in the BCB (modified after Wilmsen 2012).
Text-fig. 4. Occurrence of P3 in maxillae from Deninger bears and cave bears, data after Table 1 (presence = P3 or alveoli observed, absence = no P3 developed, broken = caudal part of maxilla broken). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 4. Occurrence of P3 in maxillae from Deninger bears and cave bears, data after Table 1 (presence = P3 or alveoli observed, absence = no P3 developed, broken = caudal part of maxilla broken).
Text-fig. 2. Occurrence of P3 in maxillae from brown bears, data after Table 1 (presence = P3 or alveoli observed, absence = no P3 developed, broken = caudal part of maxilla broken). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 2. Occurrence of P3 in maxillae from brown bears, data after Table 1 (presence = P3 or alveoli observed, absence = no P3 developed, broken = caudal part of maxilla broken).
Text-fig. 8. Occurrence of p3 in mandibles from Deninger bears, data after Table 3 (presence = p3 or alveoli observed, absence = no p3 developed, broken = diastema fragmented). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 8. Occurrence of p3 in mandibles from Deninger bears, data after Table 3 (presence = p3 or alveoli observed, absence = no p3 developed, broken = diastema fragmented).
Text-fig. 6. Occurrence of p3 in mandibles from brown bears, data after Table 3 (presence = p3 or alveoli observed, absence = no p3 developed, broken = diastema fragmented). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 6. Occurrence of p3 in mandibles from brown bears, data after Table 3 (presence = p3 or alveoli observed, absence = no p3 developed, broken = diastema fragmented).
Text-fig. 5. Occurrence of p1 in mandibles from brown bears, data after Table 3 (presence = p1 or alveoli observed, absence = no p1 developed, broken = diastema fragmented). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 5. Occurrence of p1 in mandibles from brown bears, data after Table 3 (presence = p1 or alveoli observed, absence = no p1 developed, broken = diastema fragmented).
Text-fig. 1. Occurrence of P1 in maxillae from brown bears, data after Table 1 (presence = P1 or alveoli observed, absence = no P1 developed, broken = rostral part of maxilla broken). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 1. Occurrence of P1 in maxillae from brown bears, data after Table 1 (presence = P1 or alveoli observed, absence = no P1 developed, broken = rostral part of maxilla broken).
Text-fig. 3. Occurrence of P1 in maxillae from Deninger bears and cave bears, data after Table 1 (presence = P1 or alveoli observed, absence = no P1 developed, broken = rostral part of maxilla broken). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 3. Occurrence of P1 in maxillae from Deninger bears and cave bears, data after Table 1 (presence = P1 or alveoli observed, absence = no P1 developed, broken = rostral part of maxilla broken).
Text-fig. 7. Occurrence of p1 in mandibles from Deninger bears and cave bears, data after Table 3 (presence = p1 or alveoli observed, absence = no p1 developed, broken = diastema fragmented). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 7. Occurrence of p1 in mandibles from Deninger bears and cave bears, data after Table 3 (presence = p1 or alveoli observed, absence = no p1 developed, broken = diastema fragmented).
Text-fig. 10. List of Siwalik murine rodents. a) Stratigraphic occurrence of fossil localities of the Potwar Plateau, Pakistan. b) Murine species recovered from the Siwaliks, updated from Kimura et al. (2015). All localities but DP 13 have Y as prefix. in Early Late Miocene Murine Rodents From The Upper Part Of The Nagri Formation, Siwalik Group, Pakistan, With A New Fossil Calibration Point For The Tribe Apodemurini (Apodemus/Tokudaia)
Text-fig. 10. List of Siwalik murine rodents. a) Stratigraphic occurrence of fossil localities of the Potwar Plateau, Pakistan. b) Murine species recovered from the Siwaliks, updated from Kimura et al. (2015). All localities but DP 13 have Y as prefix.
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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)
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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.