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1,604 results for “Wintering”
Figure 4 in Diurnal time-activity budget and foraging techniques of red-crested pochards (Netta rufina) wintering at the wetlands of West Bengal, India
Figure 4. Comparison of the aggregated proportional time budget (values in percentages of the time spent) of the diurnal foraging activities of male and female RCPs in January and December; deep water conditions prevailed in both December and January at Sites 1, 2, and 4, while shallow water conditions prevailed at Site 3 in January.
Figure 2 in Diet composition, guild structure and trophic relationships of wintering birds of prey in an estuarine wetland (The Evros Delta National Park, Greece)
Figure 2. Cluster analysis (dendrogram) based on the biomass proportions of the diets of the seven species of birds of prey studied in Evros Delta.
Figure 1 in Diet composition, guild structure and trophic relationships of wintering birds of prey in an estuarine wetland (The Evros Delta National Park, Greece)
Figure 1. Diet compiled for the most important prey taxa of the seven species of birds of prey studied in the Evros Delta, a) by biomass (upper graph) and b) by numbers (lower graph) (Shannon index/Evenness are shown below each species name).
Figures 6–10 in A new species of the winter stonefly genus Capniella Klapálek, 1920 (Plecoptera: Capniidae) from Korea
Figures 6–10. Male genital structures of Capniella gibba sp. n. — 6: epiproct and tergite X, oblique dorsocaudal view; 7: same, oblique dorsobasal view; 8: same, ventral view; 9: fusion plate, retractoral plate and paraprocts, oblique ventrocaudal view; 10: same, oblique dorsobasal view — scale 0.25 mm.
Fig. 3 in High winter loads of Oestrid larvae and Elaphostrongylus rangiferi are associated with emaciation in wild reindeer calves
Fig. 3. Visualization of fat reserves in the bone marrow of femur (row 1), knee joint (row 2), vertebral canal (row 3), orbital cavity (row 4), and heart surface (row 5). The three categories used are illustrated from left to right: clearly visible white and stiff fat (+); low amounts of visible fat with a soft consistency (+÷); absence of visible fat (serous adipose atrophy) (÷). All figures are from wild reindeer calves killed on Hardangervidda in spring 2015, except for the heart to the bottom right which is from a moose that died from winter starvation.
Fig. 6 in High winter loads of Oestrid larvae and Elaphostrongylus rangiferi are associated with emaciation in wild reindeer calves
Fig. 6. Photograph from the inside of the skin showing Hypoderma tarandi larvae removed from the lower part of the back of a calf killed on Hardangervidda in spring 2015.
Fig. 9 in High winter loads of Oestrid larvae and Elaphostrongylus rangiferi are associated with emaciation in wild reindeer calves
Fig. 9. Calculated mean air temperature (◦C) in the main summer pasture area of the Hardangervidda wild reindeer population for individual summers (June–August) 1989–2018. The summers of 2014 and 2015 are marked with a black circle. The dotted horizontal line shows the mean (7.4 ◦C) for the 30- year-period.
Fig. 5 in High winter loads of Oestrid larvae and Elaphostrongylus rangiferi are associated with emaciation in wild reindeer calves
Fig. 5. Cephenemyia trompe larvae in the pharynx/nasopharynx of a calf killed on Hardangervidda in spring 2015. Note the paired, swollen retropharyngeal lymph nodes (Ln).
Fig. 4 in High winter loads of Oestrid larvae and Elaphostrongylus rangiferi are associated with emaciation in wild reindeer calves
Fig. 4. Translucent white first stage Cephenemyia trompe larvae (1 mm) in the nasal mucosa of a calf killed on Hardangervidda in autumn 2014.
Fig. 10 in High winter loads of Oestrid larvae and Elaphostrongylus rangiferi are associated with emaciation in wild reindeer calves
Fig. 10. Calculated number of summer days (June–August) with a mean air temperature ≥12 ◦C in the main summer pasture area of the wild reindeer population on Hardangervidda. The figure shows the mean and range for the 30-year period 1989–2018, and the mean for individual years 2014 and 2015 as well as for the five years with a higher mean temperature than in 2014.
Fig. 8 in High winter loads of Oestrid larvae and Elaphostrongylus rangiferi are associated with emaciation in wild reindeer calves
Fig. 8. Group of adult hair-thin, about 3–5 cm long Elahostrongylus rangiferi nematodes in the muscle fascia of a calf killed on Hardangervidda in spring 2015.
Fig. 1 in High winter loads of Oestrid larvae and Elaphostrongylus rangiferi are associated with emaciation in wild reindeer calves
Fig. 1. Map of southern Norway showing the location of the 24 Norwegian wild tundra reindeer populations. The Hardangervidda population (No. 16) is marked with brighter tan.
Fig. 2 in High winter loads of Oestrid larvae and Elaphostrongylus rangiferi are associated with emaciation in wild reindeer calves
Fig. 2. Kernel Density Analysis, visualizing the main pasture area of radio-collared females in the wild reindeer population in Hardangervidda during June, July, and number of GPS positions recorded. Calculated center at UTM 32V: 426706–6650377 and average altitude at 1283m. The center in the previously used summer area with an asterisk. The red lines represent summer trails for hikers marked by the Norwegian Tourist Association. (For interpretation of the references to color in this figure of this article.)
Fig. 7 in High winter loads of Oestrid larvae and Elaphostrongylus rangiferi are associated with emaciation in wild reindeer calves
Fig. 7. Verminous pneumonia in a calf killed on Hardangervidda in spring 2015. Numerous confluent granulomas containing Elaphostrongylus rangiferi eggs and hatched first stage larvae. Haematoxylin and eosin stain. Bar, 100 μm.
Winter Precipitation-Type Models for "Evidential Deep Learning: Enhancing Predictive Uncertainty Estimation for Earth System Science Applications"
<p>This contains trained model weights, scalers, and evaluation metrics for the winter precipitation-type models trained as part of the paper "Evidential Deep Learning: Enhancing Predictive Uncertainty Estimation for Earth System Science Applications". </p>
Data from: Autumn and winter plankton composition and size structure in the North Sea
<p><span>Plankton dynamics in temperate ecosystems have been mainly studied during productive seasons, with comparatively less research conducted during the winter, particularly on microplankton. Implementing plankton sampling during a regular fishery cruise, we investigated the North Sea micro- and mesozooplankton community composition, abundance and size structure (55-2000 µm) during autumn (Buchan/Banks area) and winter (Downs area) between 2013 and 2019. Samples were analyzed using image-based techniques. Community diversity (broad taxa) was relatively similar across years in both areas, with diatoms and tripos taxa sets dominating the microplankton community and gastropods and copepods the mesozooplankton one. The average micro- to mesoozooplankton ratio (in abundance) was 90:1 for Buchan/Banks, resulting in average Normalized Abundance Size Spectra (NASS) slopes of -1.45 ±0.18 SD. For Downs, the micro- to mesoozooplankton ratio was 235:1 and steeper NASS slopes of -1.67 ±0.20 SD due to a lower contribution of large organisms. Interannual changes in the planktonic community for each area and their potential environmental drivers were examined using a redundancy analysis (including taxonomy and size) and a correlation analysis using NASS slopes (size only). Both approaches highlighted the importance of water mass properties (e.g. salinity, temperature, turbidity) in shaping plankton dynamics, although the amount of explained variance differed between approaches (11 versus 46%). <span><span>Our results contribute to a better understanding of standing stocks of plankton and their environmental drivers. Specifically, novel insights were gained into microplankton dynamics, which play an important role in supporting the growth and survival of winter-spawned fish larvae in the North Sea. </span></span></span></p>
Future winter blocking data and codes
<p>Here, you can find data and codes required to reproduce analyses from Michel et al. (in rev.). Please refer to the readMe file.</p>
Linked collectors and determiners for: Description of new apterous winter species of Leuctra (Plecoptera: Leuctridae) based morphology and DNA barcoding and further records to stonefly fauna of the Caucasus, Georgia.
Natural history specimen data linked to collectors and determiners held within, "Description of new apterous winter species of Leuctra (Plecoptera: Leuctridae) based morphology and DNA barcoding and further records to stonefly fauna of the Caucasus, Georgia". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/9b404efd-c9b4-4d83-bc6d-1fa39672a9c6">https://bionomia.net/dataset/9b404efd-c9b4-4d83-bc6d-1fa39672a9c6</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/9b404efd-c9b4-4d83-bc6d-1fa39672a9c6">https://gbif.org/dataset/9b404efd-c9b4-4d83-bc6d-1fa39672a9c6</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: A new micropterous winter species of Leuctra (Plecoptera: Leuctridae) and little known endemic stoneflies from the Greater Caucasus.
Natural history specimen data linked to collectors and determiners held within, "A new micropterous winter species of Leuctra (Plecoptera: Leuctridae) and little known endemic stoneflies from the Greater Caucasus". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/5be94d4e-9f7e-477d-ad93-1320f4446885">https://bionomia.net/dataset/5be94d4e-9f7e-477d-ad93-1320f4446885</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/5be94d4e-9f7e-477d-ad93-1320f4446885">https://gbif.org/dataset/5be94d4e-9f7e-477d-ad93-1320f4446885</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Larvae Of The Winter Stonefly Genus Allocapnia (Plecoptera: Capniidae) In Mississippi, Usa.
Natural history specimen data linked to collectors and determiners held within, "Larvae Of The Winter Stonefly Genus Allocapnia (Plecoptera: Capniidae) In Mississippi, Usa". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/866eda6e-74f1-4508-85eb-974ffc7bdae8">https://bionomia.net/dataset/866eda6e-74f1-4508-85eb-974ffc7bdae8</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/866eda6e-74f1-4508-85eb-974ffc7bdae8">https://gbif.org/dataset/866eda6e-74f1-4508-85eb-974ffc7bdae8</a>. Formatted as a Frictionless Data package.
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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.