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355 results for “northeast Atlantic”
FIGURE 22 in Revision of the genus Harmothoe Kinberg, 1856 (Polychaeta: Polynoidae) in the Northeast Atlantic
FIGURE 22. Harmothoe imbricata (additional specimens, SMF 16582). (A) left elytron from segment 5 of large specimen; (B) right elytron from segment 9 of smaller specimen. (Scales: A = 2 mm; B = 1 mm).
FIGURE 21 in Revision of the genus Harmothoe Kinberg, 1856 (Polychaeta: Polynoidae) in the Northeast Atlantic
FIGURE 21. Harmothoe imbricata (neotype, SMNH-type-7728). (A) anterior end; left palp bent downwards; (B) left 2nd elytron from segment 4; (C) detail of lateral margin of same; (D) left elytragerous parapodium from segment 15, posterior view; (E) distal half of long notochaeta; (F) tip of same; (G) distal part of middle neurochaeta; (H) tip of same; (I) tip of upper neurochaeta, secondary tooth abraded; (J) tip of lowermost neurochaeta. (Scales: A, B = 2 mm; C, E, G = 250 µm; D = 1 mm; F, H–J = 100 µm).
FIGURE 15 in Revision of the genus Harmothoe Kinberg, 1856 (Polychaeta: Polynoidae) in the Northeast Atlantic
FIGURE 15. Harmothoe extenuata (neotype, NHMW ZooEv 274). (A) anterior end; styles of left and right dorsal and left ventral tentacular cirri missing; style of right dorsal cirrus regenerating; (B) second right elytron from segment 4; (C) detail of posterior margin of same; (D) left cirrigerous parapodium from segment 16, posterior view, style of dorsal cirrus missing; (E) distal part of long notochaeta; (F) tip of same; (G) distal part of middle neurochaeta; (H) tip of same; (I) tip of uppermost neurochaeta; (J) tip of lower neurochaeta. (Scales: A, B = 1 mm; C, E, G = 100 µm; D = 500 µm; F, H–J = 50 µm).
FIGURE 24 in Revision of the genus Harmothoe Kinberg, 1856 (Polychaeta: Polynoidae) in the Northeast Atlantic
FIGURE 24. Harmothoe ingolfiana (largest syntype, ZMUC-POL 1316). (A) anterior end; left palp and styles of median antenna and tentacular cirri missing; (B) left anterior elytron from unknown segment, free in vial; (C) detail of posterior margin of same; (D) detail of lateral margin of same; (E) right elytragerous parapodium from unknown segment, free in vial, posterior view; (F) tip of long notochaeta; (G) tip of upper neurochaeta; (H) tip of lower neurochaeta. (Scales: A, B = 1 mm; C, D = 250 µm; E = 500 µm, F = 100 µm; G, H = 50 µm).
FIGURE 25 in Revision of the genus Harmothoe Kinberg, 1856 (Polychaeta: Polynoidae) in the Northeast Atlantic
FIGURE 25. Harmothoe longisetis (additional specimen, SMF 12445). (A) anterior end; styles of median antenna, left tentacular cirri, and left dorsal cirrus mising; (B) right anterior elytron from unknown segment; (C) microtubercles; (D) right cirrigerous parapodium from segment 14, posterior view, style of dorsal cirrus missing; (E) long notochaeta; (F) tip of same; (G) middle neurochaeta; (H) tip of same; (I) tip of upper neurochaeta. (Scale: A, B = 2 mm; C = 100 µm; D = 1 mm; E, G = 250 µm; F, H, I = 50 µm).
Data from: Descriptive multi-agent epidemiology via molecular screening on Atlantic salmon farms in the northeast Pacific Ocean
<p>Rapid expansion of salmon aquaculture has resulted in high-density populations that host diverse infectious agents, for which surveillance and monitoring are critical to disease management. Screening can reveal infection diversity from which disease arises, differential patterns of infection in live and dead fish that are difficult to collect in wild populations, and potential risks associated with agent transmission between wild and farmed hosts. We report results from a multi-year infectious-agent screening program of farmed salmon in British Columbia, Canada, using quantitative PCR to assess presence and load of 58 infective agents (viruses, bacteria, and eukaryotes) in 2931 Atlantic salmon (Salmo salar). Our analysis reveals temporal trends, agent correlations within hosts, and agent-associated mortality signatures. Multiple agents, most notably Tenacibaculum maritimum, were elevated in dead and dying salmon. We also report detections of agents only recently shown to infect farmed salmon in BC (Atlantic salmon calicivirus, Cutthroat trout virus-2), detection in freshwater hatcheries of two marine agents (Kudoa thyrsites and Tenacibaculum maritimum), and detection in the ocean of a freshwater agent (Flavobacterium psychrophilum). Our results provide information for farm managers, regulators, and conservationists, and enable further work to explore patterns of multi-agent infection and farm/wild transmission risk.</p>
FIGURE 5 in A new genus and two new species of Luzarinae cricket from the Atlantic Forest of Northeast Brazil (Orthoptera, Grylloidea)
FIGURE 5. Marcgraviella christianae Desutter-Grandcolas & Souza-Dias, n. sp. Male holotype. A–D, male genitalia in dorsal (A), ventral (B), lateral (C), and apical view (D); E–F, forewing, dorsal field (E), lateral field (F). Abbreviations, see page 500. Scale bar: 1 mm.
Data from: Accuracy of assignment of Atlantic salmon (Salmo salar L.) to rivers and regions in Scotland and northeast England based on single nucleotide polymorphism (SNP) markers.
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Data from: SNPs reveal a genetic cline across the northeast Atlantic and enable powerful population assignment in the European lobster
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Data from: Vocal foragers and silent crowds: context-dependent vocal variation in Northeast Atlantic long-finned pilot whales
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Data from: Feeding ecology of Northeast Atlantic mackerel, Norwegian spring-spawning herring and blue whiting in the Norwegian Sea
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Data from: Bioenergetics modeling of the annual consumption of zooplankton by pelagic fish feeding in the Northeast Atlantic
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Genomic survey of edible cockle (Cerastoderma edule) in the Northeast Atlantic: a baseline for sustainable management of its wild resources
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Data from: Habitat risk assessment for regional ocean planning in the U.S. Northeast and Mid-Atlantic
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Data from: Descriptive multi-agent epidemiology via molecular screening on Atlantic salmon farms in the northeast Pacific Ocean
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Fig. 7 in A new deepwater species of Calliopiidae, Halirages helgae (Crustacea, Amphipoda), with a synoptic table to Halirages species from the northeast Atlantic
Fig. 7. Halirages helgae sp. nov., holotype, ♀, 10 mm long. A. Uropod 1. B. Uropod 2. C. Telson. D. Epimeron 2–3.
Figure 18 in Tanaidacea (Crustacea: Peracarida) of the northeast Atlantic: Chauliopleona Dojiri and Sieg, 1997 and Saurotipleona n. gen. from the 'Atlantic Margin'
Figure 18. Distribution of Chauliopleona species in the Atlantic Margin area. Filled triangles C. amdrupii, filled squares C. armata, and filled circles C. hastata; crosses indicate Ingolf records of C. hastata.
Figure 19 in Tanaidacea (Crustacea: Peracarida) of the northeast Atlantic: Chauliopleona Dojiri and Sieg, 1997 and Saurotipleona n. gen. from the 'Atlantic Margin'
Figure 19. Distribution of Chauliopleona bamberi and Saurotipleona julii in the Atlantic Margin area. Filled squares indicate C. bamberi, and filled circles S. julii.
Figure 16. Saurotipleona julii n. gen. n in Tanaidacea (Crustacea: Peracarida) of the northeast Atlantic: Chauliopleona Dojiri and Sieg, 1997 and Saurotipleona n. gen. from the 'Atlantic Margin'
Figure 16. Saurotipleona julii n. gen. n. sp. Non-ovigerous female paratype, BIOICE Stn 3522: (A–F) pereopods 1–6, respectively; (G) pleopod (setae very finely plumose, omitted for clarity). Scale bar 0.25 mm.
Figure 14. Saurotipleona julii n. gen. n in Tanaidacea (Crustacea: Peracarida) of the northeast Atlantic: Chauliopleona Dojiri and Sieg, 1997 and Saurotipleona n. gen. from the 'Atlantic Margin'
Figure 14. Saurotipleona julii n. gen. n. sp. Non-ovigerous female, holotype, BIOICE Stn 3504: (A) habitus; (B) pleonal sternites, lateral. Non-ovigerous female, paratype, BIOICE Stn 3522: (C) pleonite-5 sternal spur; (D) antennule; (E) antenna; (F) uropod. Preparatory male, allotype, BIOICE Stn 3522: (G) habitus; (H) pleonite-5 sternal spur; (J) antennule. Scale bars: (i) 1 mm for A, G; (ii) 0.5 mm for B–C, H; (iii) 0.25 mm for D–F, J.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.