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1,604 results for “Wintering”
Data for: Resource landscapes explain contrasting patterns of aggregation and site fidelity by red knots at two wintering sites
<p>This repository contains data for the paper: Oudman et al. 2018. Resource landscapes explain contrasting patterns of aggregation and site fidelity by red knots at two wintering sites. <em>Movement Ecology</em> 6(14) 1-12. https://doi.org/10.1186/s40462-018-0142-4.</p> <p>Please cite the original publication when using this data.</p>
The TRIple-frequency and Polarimetric radar Experiment for improving process observation of winter precipitation (version 2)
<p>The combined TRIple-frequency and Polarimetric radar Experiment for improving process observation of winter precipitation (TRIPEx) was a joint field experiment of the University of Cologne, the University of Bonn, the Karlsruhe Institute of Technology (KIT), and the Research Center Jülich. TRIPEx took place at the Jülich Observatory for Cloud Evolution (JOYCE) from 11 November 2015 until 04 January 2016. During this experiment, the X, Ka and W Band ground-based Doppler radars were used vertically pointing to observe the clouds. Here we provide level 2 of the dataset collected during this campaign. Several step processing were applied to minimize the radar offset and attenuation. In addition, we provide the attenuation correction and the quality flags for each processing steps to allow the user to retrieve the data without our correction. The raw and the level 1 of the dataset are available for the users on request from the corresponding author.</p>
Data and code: Gut microbiota structure differs between honey bees in winter and summer
<p>This dataset contains data and code underlying the qPCR, amplicon sequencing, and statistical analysis of the research article "Gut microbiota structure differs between honey bees in winter and summer”. Short read datasets are available under NCBI Bioproject accession PRJNA578869.</p>
Fig. 2 in Unusual Age Structure Of The Winter Aggregation Of Nyctalus Noctula (Mammalia, Chiroptera) In Kyiv
Fig. 2. Age of common noctule bats in the examined sample: A — total sample, n = 113, the model of the logarithmic regression is indicated with the line; B — females, n = 31; C — males, n = 77.
Figure 2 in Soil fauna contribution to winter decomposition in subalpine grasslands
Figure 2. Litter mass loss of Patzkea paniculata, Dactylis glomerata and the mixture in small mesh (white bars) and large mesh (grey bars) and litterbags, for each location (pots and field), after winter decomposition. The results of the 6 pairwise tests are shown for each location and litter type (ns: p> 0.3, **: p <0.01, ***: p <0.001).
Figure 2 in Unusual wintering records of pipits (Aves: Motacillidae) in Hatay, Eastern Mediterranean Region of Turkey
Figure 2. The total number of observations in comparison with the number of records of each pipit species during the 4 months of the winter period in the study.
Fig. 2 in The Distribution of Soil Testate Amoebae under Winter Snow Cover at the Plot-scale Level in Arctic Tundra (Qeqertarsuaq/Disko Island, West Greenland)
Fig. 2. Maps of the spatial distribution of the explanatory environmental variables (A – microtopography; B – snow depth; C – loge(substrate density)) plotted against their spatial coordinates at 57 sampling locations within an 8 × 15 m plot in arctic tundra in Qeqertarsuaq/Disko Island (West Greenland). All data are centred on 0, so square sizes are proportional to the deviations from the mean values at the plot. Open symbols are used for negative values and the filled symbols are used for positive values. Spatial patterns are visualised as aggregations of similar size and colour.
Figure 2 in Time-activity budgets of wintering Ferruginous Duck, Aythya nyroca, at Gajoldoba wetland, Jalpaiguri, India
Figure 2. Mean percentage of nocturnal time spent in various activities by the Ferruginous Duck in different time blocks, with standard error bars.
Figure 1 in Time-activity budgets of wintering Ferruginous Duck, Aythya nyroca, at Gajoldoba wetland, Jalpaiguri, India
Figure 1. Percentage of time allocated to different activities by Ferruginous Duck at different parts of winter season.
Figure 1 in Selective predation on common voles by Tawny Owls and Long-eared Owls in winter and spring
Figure 1. Distribution of the body mass of Microtus arvalis individuals, trapped in October–April and preyed upon by both Strix aluco and Asio otus in winter and spring, as estimated from mandibles.
Figure 6 in A comparative study of the diurnal behaviour of the Northern Shoveller (Anas clypeata) during the wintering season at Garaet Hadj-Tahar (North-East Algeria) and Garaet Timerganine (Algerian highlands)
Figure 6. Balance of the rhythms of daytime activities of the Shovellers in Garaet Hadj-Tahar during the 2 wintering seasons of 2007 and 2009.
Figure 4 in A comparative study of the diurnal behaviour of the Northern Shoveller (Anas clypeata) during the wintering season at Garaet Hadj-Tahar (North-East Algeria) and Garaet Timerganine (Algerian highlands)
Figure 4. Percentage of time allocated by the Shoveller for diurnal activities at (A) Garaet Hadj-Tahar and (B) Garaet Timerganine.
Figure 6 in Unusual winter zooplankton bloom in the open southern Adriatic Sea
Figure 6. Box-and-whisker plot of the abundance of protozoan shown by depth layers (February/March 2015, all investigated stations).
Figure 5 in Unusual winter zooplankton bloom in the open southern Adriatic Sea
Figure 5. Spatial distribution of total microzooplankton and mesozooplankton abundance along the investigated profile in February/March 2015.
Figure 3 in Unusual winter zooplankton bloom in the open southern Adriatic Sea
Figure 3. Vertical profiles of temperature, salinity, and density (sigma-t) over the investigated profile in February/March 2015.
Figure 4 in Unusual winter zooplankton bloom in the open southern Adriatic Sea
Figure 4. Vertical profiles of chlorophyll a fluorescence (Chl F) concentration and picophytoplankton,nanophytoplankton, and microphytoplankton abundance along the investigated profile in February/March 2015.
Figure 7 in Unusual winter zooplankton bloom in the open southern Adriatic Sea
Figure 7. Box-and-whisker plot of the total copepod developmental stages abundance shown by depth layers (February/March 2015, all investigated stations).
Figure 1 in Movement and home range of cinereous vulture Aegypius monachus during the wintering and summering periods in East Asia
Figure 1. Migration route of cinereous vultures (a) VK 1501, (b) VK 1502, (c) VK 1503, (d) VK 1504, (e) VK 1505, (f) VK 1506, (g) VK 1507, and (h) total birds tracked using the GPS-WCDMA-based transmitter in East Asia from January 2015 to March 2017.
Figure 2 in Diurnal time-activity budget and foraging techniques of red-crested pochards (Netta rufina) wintering at the wetlands of West Bengal, India
Figure 2. Canonical correspondence analysis (CCA with 95% ellipses) ordination diagram showing the scatter plot for the month-wise and site-wise density of the wintering RCPs together with the selected environmental variables. Vector lines represent the relationship of significant environmental variables to the ordination axes; their length is proportional to their relative significance.
Figure 1 in Diurnal time-activity budget and foraging techniques of red-crested pochards (Netta rufina) wintering at the wetlands of West Bengal, India
Figure 1. Study site (Adra saheb bandh,Purulia saheb bandh, Kadamdeuli Dam, and Gangdoa Dam) locations inWest Bengal, India (India and West Bengal maps not in scale).
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