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112 results for “Scandinavia”
Data from: Weak geographical structure in sperm morphology across the range of two willow warbler Phylloscopus trochilus subspecies in Scandinavia
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Data from: Impact of a recolonizing, cross-border carnivore population on ungulate harvest in Scandinavia
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Fig. 10 in Redescription and taxonomic notes on Cyclops bohater Koźmiński, 1933 and Cyclops lacustris G.O. Sars, 1863 (Arthropoda, Crustacea), with an identification key to the Cyclops species of Fenno-Scandinavia
Fig. 10. Original drawings of Cyclops lacustris, made by G.O. Sars (Archives of the National Library of Norway, archive items – Ms.Fol. 1109: 333; Ms.Fol. 1109: 421). A. Habitus, dorsal. B. Antenna, caudal – note the long setules on the inner medial seta of the coxobasis. C. Leg 5, third endopodal segment of leg 4, and caudal rami with setae. All drawings show specimens from Lake Mjøsa, Norway.
Fig. 9. A−B. Cyclops lacustris G.O. Sars, 1863 in Redescription and taxonomic notes on Cyclops bohater Koźmiński, 1933 and Cyclops lacustris G.O. Sars, 1863 (Arthropoda, Crustacea), with an identification key to the Cyclops species of Fenno-Scandinavia
Fig. 9. A−B. Cyclops lacustris G.O. Sars, 1863, Ƌ (ZMO: Sars Coll. 12976 Ƌ-1). A. Leg 1, frontal. B. Leg 4, caudal. C. Cyclops vicinus Uljanin, 1875, maxilliped syncoxopodite, frontal (Lake Østensjøvann, Norway ̅ MIZ 2/2016/30). Scale bars = 50 µm.
Fig. 4 in Redescription and taxonomic notes on Cyclops bohater Koźmiński, 1933 and Cyclops lacustris G.O. Sars, 1863 (Arthropoda, Crustacea), with an identification key to the Cyclops species of Fenno-Scandinavia
Fig. 4. Cyclops bohater Koźmiński, 1933, Ƌ. A. Habitus, dorsal. B. Prosome with distinctly wide pediger 2. C. Pediger 5, genital segment, and first abdominal segment, ventral. D−E. Antennal coxobasis. D. Frontal. E. Caudal. F. Labrum. Except for B (Lake Largen, Sweden ̅ MIZ 2/2016/15) all drawings show a paralectotype (NHMUK 2016. 40). Scale bars: A̅B = 500 µm; C̅F = 100 µm.
Fig. 10 in On the genus Halirages (Crustacea, Amphipoda), with the description of two new species from Scandinavia and Arctic Europe
Fig. 10. Halirages stappersi sp. nov., holotype ♂, 20 mm, Kara Sea, RV Belgica stn 132. A. original. B-G. after Stappers (1911). A-B. anterior part of body. C. article 2 of peduncle of left A2. D. lower lip. E. palp of left Md. F. right Mx1 (medial face). G. palp of left Mx1 (medial face).
The importance of Canadian Arctic Archipelago gateways for glacial expansion in Scandinavia
<p><strong>Reference:</strong> <em>Lofverstrom, M., Thompson, D. M., Otto-Bliesner, B. L. & Brady, E. C. (2022): The importance of Canadian Arctic Archipelago gateways for glacial expansion in Scandinavia, Nature Geoscience, doi:10.1038/s41561-022-00956-9</em></p> <p><strong>Description:</strong><br> 30 year monthly climatologies and monthly timeseries from the <em>CESM2</em> pre-industrial control simulation (<em>piControl</em>), as well as the 116 ka simulations with open and closed ocean gateways in the Canadian Arctic Archipelago (<em>openCAA</em> and <em>closedCAA</em>, respectively). This is version 2 of this dataset that includes an extension of simulation <em>openCAA<strong> </strong></em>to model year 815 (similar to simulation <em>closedCAA</em>).</p> <p><strong>The pre-industrial data is derived from:</strong><br> https://www.earthsystemgrid.org/dataset/ucar.cgd.cesm2.b.e21.B1850.f09_g17.CMIP6-piControl.001.html</p> <p><strong>Proxy datasets:</strong><br> vo.imcce.fr/insola/earth/online/earth/earth.html<br> doi.pangaea.de/10.1594/PANGAEA.854045<br> doi.pangaea.de/10.1594/PANGAEA.55501<br> doi.pangaea.de/10.1594/PANGAEA.840727<br> doi.pangaea.de/10.1594/PANGAEA.777694<br> doi.pangaea.de/10.1594/PANGAEA.742858</p>
Large and small herbivores have strong effects on tundra vegetation in Scandinavia and Alaska
<p>Large and small mammalian herbivores are present in most vegetated areas in the Arctic, and often have large impacts on plant community composition and ecosystem functioning. The relative importance of different herbivores and especially how their specific impact on the vegetation varies across the Arctic is however poorly understood.</p> <p>Here, we investigate how large and small herbivores influence vegetation density and plant community composition in four arctic vegetation types in Scandinavia and Alaska. We used a unique set of exclosures, excluding only large (reindeer and muskoxen) or all mammalian herbivores (also voles and lemmings) for at least 20 years.</p> <p>We found that mammalian herbivores in general decreased Leaf Area Index, NDVI and abundance of vascular plants in all four locations, even though the strength of the effect and which herbivore type caused these effects differed across locations. In three locations, herbivore presence caused contrasting plant communities, but not in the location with lowest productivity. Large herbivores had a negative effect on plant height, whereas small mammalian herbivores increased species diversity by decreasing dominance of the initially dominating plant species. Above- or belowground disturbances caused by herbivores were found to play an important role in shaping the vegetation in all locations.</p> <p>Synthesis: Based on these results, we conclude that both small and large mammalian herbivores influence vegetation in Scandinavia and Alaska in a similar way, some of which can mitigate effects of climate change. We also see important differences across locations, but these depend rather on local herbivore- and plant community composition than large biogeographical differences among continents.</p>
Figure 6 in Cranial variation in the European badger Meles meles (Carnivora, Mustelidae) in Scandinavia
Figure 6. Histograms for length between the angular process and infradentale in different forms of the European badger: 1, 'south-western Norwegian' form; 2, 'main Fennoscandian' form; 3, 'non–Fennoscandian' form.
Figure 4 in Cranial variation in the European badger Meles meles (Carnivora, Mustelidae) in Scandinavia
Figure 4. The range of the 'Fennoscandian badgers' based on posterior classification probabilities (females and males are combined): 0–0.3, 'non–Fennoscandian' badgers; 0.3–0.6, unclear classified specimens (2.2%), 0.6–1.0, 'Fennoscandian' badgers.
Figure 6 from: Westberg M, Timdal E, Asplund J, Bendiksby M, Haugan R, Jonsson F, Larsson P, Odelvik G, Wedin M, Millanes A (2015) New records of lichenized and lichenicolous fungi in Scandinavia. MycoKeys 11: 33-61. https://doi.org/10.3897/mycokeys.11.6670
Figure 6 - Lecidea degeliana. a With the host, Acarospora sp., still visible (S F265204) b Independent thallus (S F265201). Scale: 1 mm.
Figure 12 from: Westberg M, Timdal E, Asplund J, Bendiksby M, Haugan R, Jonsson F, Larsson P, Odelvik G, Wedin M, Millanes A (2015) New records of lichenized and lichenicolous fungi in Scandinavia. MycoKeys 11: 33-61. https://doi.org/10.3897/mycokeys.11.6670
Figure 12 - Sarcogyne hypophaeoides. a Apothecia (S F123697) b Apothecia (Kocourkova & Hafellner 46366 (GZU)) c Section of an apothecium showing a carbonized margin and a brownish black hypothecium (S F265197). Scale: 1 mm (a–b); 100 µm (c).
Figure 11 from: Westberg M, Timdal E, Asplund J, Bendiksby M, Haugan R, Jonsson F, Larsson P, Odelvik G, Wedin M, Millanes A (2015) New records of lichenized and lichenicolous fungi in Scandinavia. MycoKeys 11: 33-61. https://doi.org/10.3897/mycokeys.11.6670
Figure 11 - Sarcogyne algoviae. a Apothecia (S F122537) b Apothecia (S L2741, holotype) c Section of an apothecium showing a strongly carbonized margin and a colourless hypothecium (S F122537). Scale: 1 mm (a–b); 100 µm (c).
Figure 15 from: Westberg M, Timdal E, Asplund J, Bendiksby M, Haugan R, Jonsson F, Larsson P, Odelvik G, Wedin M, Millanes A (2015) New records of lichenized and lichenicolous fungi in Scandinavia. MycoKeys 11: 33-61. https://doi.org/10.3897/mycokeys.11.6670
Figure 15 - Tremella wirthii. a Basidiomata on the thallus of Protoparmelia oleagina (S F262967) b Basidium with one longitudinal septum (S F262963) c Basidium with one oblique septum (S F262963) d Basidium with one transeverse septum (S F262963) e Catenulate conidia (S F262963). Scale: 0.5 mm (a); 10 mm (b–e).
Figure 14 from: Westberg M, Timdal E, Asplund J, Bendiksby M, Haugan R, Jonsson F, Larsson P, Odelvik G, Wedin M, Millanes A (2015) New records of lichenized and lichenicolous fungi in Scandinavia. MycoKeys 11: 33-61. https://doi.org/10.3897/mycokeys.11.6670
Figure 14 - Tremella lobariacearum. Galls induced by Tremella lobariacearum on Lobaria pulmonaria (S F263902). Scale: 1 mm.
A Study of Open Angle Glaucoma or Ocular Hypertension in Patients Within Scandinavia
ClinicalTrials.gov study NCT00751062. IPD Sharing: Not stated. Countries: 4. Publications: 1.
Large and small herbivores have strong effects on tundra vegetation in Scandinavia and Alaska
Open the record for dataset details and reuse information.
Figure 9 from: Westberg M, Timdal E, Asplund J, Bendiksby M, Haugan R, Jonsson F, Larsson P, Odelvik G, Wedin M, Millanes A (2015) New records of lichenized and lichenicolous fungi in Scandinavia. MycoKeys 11: 33-61. https://doi.org/10.3897/mycokeys.11.6670
Figure 9 - Phacographa protoparmeliae (S F265200). Scale: 1 mm.
Figure 5 from: Westberg M, Timdal E, Asplund J, Bendiksby M, Haugan R, Jonsson F, Larsson P, Odelvik G, Wedin M, Millanes A (2015) New records of lichenized and lichenicolous fungi in Scandinavia. MycoKeys 11: 33-61. https://doi.org/10.3897/mycokeys.11.6670
Figure 5 - Cladonia albonigra (O L-195662). Scale: 5 mm.
Figure 13 from: Westberg M, Timdal E, Asplund J, Bendiksby M, Haugan R, Jonsson F, Larsson P, Odelvik G, Wedin M, Millanes A (2015) New records of lichenized and lichenicolous fungi in Scandinavia. MycoKeys 11: 33-61. https://doi.org/10.3897/mycokeys.11.6670
Figure 13 - Tephromela grumosa (O L-190787). Scale: 5 mm.
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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.